Robert B. Gennis

Q: What Schools Are Affiliated With Robert B. Gennis

Robert B. Gennis is affiliated with the following schools: Johns Hopkins University, Oregon Health & Science University, Moscow State University, Leiden University, University of California, Santa Cruz, Harvard University, Rensselaer Polytechnic Institute, University of Ulm, University of California, Berkeley, University at Albany, SUNY, University of East Anglia, University of Leeds, University of Oxford, University of Illinois Urbana-Champaign, Kyoto University, University of Helsinki, University of Arkansas, Stockholm University, Ohio State University, Albert Einstein College of Medicine

Robert B. Gennis's AcademicInfluence.com Rankings

Robert B. Gennis

Biology

#5180

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#7603

Historical Rank

Biochemistry

#589

World Rank

#679

Historical Rank

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Biology

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Robert B. Gennis's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Biomembranes: Molecular Structure and Function (1988) (1393)
The superfamily of heme-copper respiratory oxidases (1994) (402)
The cytochrome bd respiratory oxygen reductases. (2011) (397)
Energy Transduction by Cytochrome Complexes in Mitochondrial and Bacterial Respiration: The Enzymology of Coupling Electron Transfer Reactions to Transmembrane Proton Translocation (1994) (308)
The roles of the two proton input channels in cytochrome c oxidase from Rhodobacter sphaeroides probed by the effects of site-directed mutations on time-resolved electrogenic intraprotein proton transfer. (1997) (293)
Properties of the two terminal oxidases of Escherichia coli. (1991) (289)
Cytochrome c oxidase: exciting progress and remaining mysteries (2008) (259)
The aerobic respiratory chain of Escherichia coli (1987) (257)
Cytochrome o (cyoABCDE) and d (cydAB) oxidase gene expression in Escherichia coli is regulated by oxygen, pH, and the fnr gene product (1990) (238)
Protein-lipid interactions. (1977) (230)
The sequence of the cyo operon indicates substantial structural similarities between the cytochrome o ubiquinol oxidase of Escherichia coli and the aa3-type family of cytochrome c oxidases. (1990) (207)
Energy transduction by cytochrome complexes in mitochondrial and bacterial respiration: the enzymology of coupling electron transfer reactions to transmembrane proton translocation. (1994) (196)
Insight into the active-site structure and function of cytochrome oxidase by analysis of site-directed mutants of bacterial cytochromeaa3 and cytochromebo (1993) (194)
Energetic efficiency of Escherichia coli: effects of mutations in components of the aerobic respiratory chain (1993) (181)
Multitarget Drug Discovery for Tuberculosis and Other Infectious Diseases (2014) (180)
Possible proton relay pathways in cytochrome c oxidase. (1995) (174)
Requirement for terminal cytochromes in generation of the aerobic signal for the arc regulatory system in Escherichia coli: study utilizing deletions and lac fusions of cyo and cyd (1990) (171)
Structure of the Alternative Complex III in a supercomplex with cytochrome oxidase (2018) (171)
Relationship between mitochondrial NADH-ubiquinone reductase and a bacterial NAD-reducing hydrogenase. (1991) (166)
Structure and function of the -complex of (1992) (155)
Mechanism of ubiquinol oxidation by the bc(1) complex: different domains of the quinol binding pocket and their role in the mechanism and binding of inhibitors. (1999) (155)
Substitution of asparagine for aspartate-135 in subunit I of the cytochrome bo ubiquinol oxidase of Escherichia coli eliminates proton-pumping activity. (1993) (154)
The cytochrome oxidase superfamily of redox-driven proton pumps. (1994) (151)
Diversity of the heme-copper superfamily in archaea: insights from genomics and structural modeling. (2008) (140)
Transmembrane proton translocation by cytochrome c oxidase. (2006) (138)
Pathways for proton release during ubihydroquinone oxidation by the bc(1) complex. (1999) (134)
Multiple proton-conducting pathways in cytochrome oxidase and a proposed role for the active-site tyrosine (1998) (133)
Glutamate 286 in cytochrome aa3 from Rhodobacter sphaeroides is involved in proton uptake during the reaction of the fully-reduced enzyme with dioxygen. (1997) (132)
A novel cytochrome c oxidase from Rhodobacter sphaeroides that lacks CuA. (1994) (131)
On the role of the K-proton transfer pathway in cytochrome c oxidase (2001) (131)
Proton pumping by cytochrome oxidase: progress, problems and postulates. (2000) (119)
Antiinfectives targeting enzymes and the proton motive force (2015) (119)
Redox enzymes in tethered membranes. (2006) (118)
The purification and characterization of the cytochrome d terminal oxidase complex of the Escherichia coli aerobic respiratory chain. (1983) (116)
Restoration of a lost metal‐binding site: construction of two different copper sites into a subunit of the E. coli cytochrome o quinol oxidase complex. (1992) (113)
One-step purification from Escherichia coli of complex II (succinate: ubiquinone oxidoreductase) associated with succinate-reducible cytochrome b556. (1989) (111)
Aerobic respiratory chain of Escherichia coli is not allowed to work in fully uncoupled mode (2011) (110)
Mutations in the putative H-channel in the cytochrome c oxidase from Rhodobacter sphaeroides show that this channel is not important for proton conduction but reveal modulation of the properties of heme a. (2000) (110)
Adaptation of aerobic respiration to low O2 environments (2011) (109)
Role of the pathway through K(I-362) in proton transfer in cytochrome c oxidase from R. sphaeroides. (1998) (107)
Purification and characterization of the recombinant Na(+)-translocating NADH:quinone oxidoreductase from Vibrio cholerae. (2002) (106)
Thebc1 complexes ofRhodobacter sphaeroides andRhodobacter capsulatus (1993) (106)
Optical studies of a conformational change in DNA before melting. (1972) (106)
The cytochrome ba3 oxygen reductase from Thermus thermophilus uses a single input channel for proton delivery to the active site and for proton pumping (2009) (105)
Demonstration of separate genetic loci encoding distinct membrane-bound respiratory NADH dehydrogenases in Escherichia coli (1993) (103)
The nucleotide sequence of the cyd locus encoding the two subunits of the cytochrome d terminal oxidase complex of Escherichia coli. (1988) (100)
Spectroscopic evidence for a heme-heme binuclear center in the cytochrome bd ubiquinol oxidase from Escherichia coli. (1993) (99)
Identification of heme and copper ligands in subunit I of the cytochrome bo complex in Escherichia coli. (1992) (97)
Two Hydrophobic Subunits Are Essential for the Heme b Ligation and Functional Assembly of Complex II (Succinate-Ubiquinone Oxidoreductase) from Escherichia coli(*) (1996) (94)
Genomic replacement in Escherichia coli K-12 using covalently closed circular plasmid DNA. (1990) (94)
The use of gene fusions to determine the topology of all of the subunits of the cytochrome o terminal oxidase complex of Escherichia coli. (1990) (94)
Isolation and characterization of an Escherichia coli mutant lacking cytochrome d terminal oxidase (1983) (93)
Coulometric and spectroscopic analysis of the purified cytochrome d complex of Escherichia coli: evidence for the identification of "cytochrome a1" as cytochrome b595. (1986) (92)
Assignment of the histidine axial ligands to the cytochrome bH and cytochrome bL components of the bc1 complex from Rhodobacter sphaeroides by site-directed mutagenesis. (1991) (92)
Redox-coupled proton translocation in biological systems: Proton shuttling in cytochrome c oxidase (2003) (92)
Chemical shift assignment of the transmembrane helices of DsbB, a 20‐kDa integral membrane enzyme, by 3D magic‐angle spinning NMR spectroscopy (2008) (90)
Purification and characterization of the cytochrome c oxidase from Rhodopseudomonas sphaeroides. (1982) (89)
The cbb3-type cytochrome c oxidase from Rhodobacter sphaeroides, a proton-pumping heme-copper oxidase. (1998) (87)
Determination of the ligands of the low spin heme of the cytochrome o ubiquinol oxidase complex using site-directed mutagenesis. (1992) (87)
Mass spectrometric determination of dioxygen bond splitting in the "peroxy" intermediate of cytochrome c oxidase. (1999) (86)
Definition of the catalytic site of cytochrome c oxidase: specific ligands of heme a and the heme a3-CuB center. (1992) (84)
Proton transfer in cytochrome bo3 ubiquinol oxidase of Escherichia coli: second-site mutations in subunit I that restore proton pumping in the mutant Asp135-->Asn. (1995) (84)
Identification of the cydC locus required for expression of the functional form of the cytochrome d terminal oxidase complex in Escherichia coli (1987) (82)
Reconstitution of the membrane-bound, ubiquinone-dependent pyruvate oxidase respiratory chain of Escherichia coli with the cytochrome d terminal oxidase. (1984) (81)
Cloning and DNA sequencing of the fbc operon encoding the cytochrome bc1 complex from Rhodobacter sphaeroides. Characterization of fbc deletion mutants and complementation by a site-specific mutational variant. (1990) (80)
Partial 13C and 15N Chemical‐Shift Assignments of the Disulfide‐Bond‐Forming Enzyme DsbB by 3D Magic‐Angle Spinning NMR Spectroscopy (2007) (79)
Coupled proton and electron transfer reactions in cytochrome oxidase. (2004) (79)
Direct observation of protonation reactions during the catalytic cycle of cytochrome c oxidase (2003) (79)
Proposed Structure of Heme d, a Prosthetic Group of Bacterial Terminal Oxidases (1985) (78)
Sequencing and preliminary characterization of the Na+-translocating NADH:ubiquinone oxidoreductase from Vibrio harveyi. (1999) (77)
The cytochrome d complex is a coupling site in the aerobic respiratory chain of Escherichia coli. (1985) (77)
Active site rearrangement and structural divergence in prokaryotic respiratory oxidases (2019) (76)
Effects of mutation of the conserved lysine-362 in cytochrome c oxidase from Rhodobacter sphaeroides. (1997) (75)
Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site. (2005) (75)
Polar residues in helix VIII of subunit I of cytochrome c oxidase influence the activity and the structure of the active site. (1996) (75)
Magic-angle spinning solid-state NMR of a 144 kDa membrane protein complex: E. coli cytochrome bo3 oxidase (2006) (74)
Bacterial NADH-quinone oxidoreductases: Iron-sulfur clusters and related problems (1993) (73)
Mechanism of inhibition of electron transfer by amino acid replacement K362M in a proton channel of Rhodobacter sphaeroides cytochrome c oxidase. (1998) (73)
A Mutation in Subunit I of Cytochrome Oxidase from Rhodobacter sphaeroides Results in an Increase in Steady-State Activity but Completely Eliminates Proton Pumping† (2002) (72)
Transmembrane Charge Separation during the Ferryl-oxo → Oxidized Transition in a Nonpumping Mutant of Cytochrome c Oxidase* (2004) (72)
Aspartate-132 in cytochrome c oxidase from Rhodobacter sphaeroides is involved in a two-step proton transfer during oxo-ferryl formation. (1999) (72)
Comparative genomics and site-directed mutagenesis support the existence of only one input channel for protons in the C-family (cbb3 oxidase) of heme-copper oxygen reductases. (2007) (71)
Use of nonspecific dye labeling for singlet energy-transfer measurements in complex systems. A simple model. (1972) (71)
Ionophoric effects of the antitubercular drug bedaquiline (2018) (71)
Large-scale purification and characterization of a highly active four-subunit cytochrome bc1 complex from Rhodobacter sphaeroides. (1990) (70)
Sequence analysis of cytochrome bd oxidase suggests a revised topology for subunit I. (1999) (70)
Reconstitution of active transport in proteoliposomes containing cytochrome o oxidase and lac carrier protein purified from Escherichia coli. (1983) (70)
Controlled uncoupling and recoupling of proton pumping in cytochrome c oxidase. (2006) (70)
The low-spin heme site of cytochrome o from Escherichia coli is promiscuous with respect to heme type. (1992) (70)
X- and W-band EPR and Q-band ENDOR studies of the flavin radical in the Na+ -translocating NADH:quinone oxidoreductase from Vibrio cholerae. (2003) (69)
The post-translational modification in cytochrome c oxidase is required to establish a functional environment of the catalytic site. (1998) (69)
Subunit CydX of Escherichia coli cytochrome bd ubiquinol oxidase is essential for assembly and stability of the di‐heme active site (2014) (66)
Riboflavin is a component of the Na+-pumping NADH–quinone oxidoreductase from Vibrio cholerae (2002) (66)
The entry point of the K-proton-transfer pathway in cytochrome c oxidase. (2002) (66)
Heme-copper and heme-heme interactions in the cytochrome bo-containing quinol oxidase of Escherichia coli. (1990) (65)
Interactions between heme d and heme b595 in quinol oxidase bd from Escherichia coli: a photoselection study using femtosecond spectroscopy. (2002) (65)
Evolutionary migration of a post-translationally modified active-site residue in the proton-pumping heme-copper oxygen reductases. (2006) (63)
Cloning, sequencing and deletion from the chromosome of the gene encoding subunit I of the aa3‐type cytochrome c oxidase of Rhodobacter sphaeroides (1992) (63)
Structure of cytochrome c oxidase, energy generator of aerobic life (1995) (63)
A mutation in subunit I of cytochrome oxidase from Rhodobacter sphaeroides results in an increase in steady-state activity but completely eliminates proton pumping. (2002) (62)
Location of heme axial ligands in the cytochrome d terminal oxidase complex of Escherichia coli determined by site-directed mutagenesis. (1989) (62)
Methionine-393 is an axial ligand of the heme b558 component of the cytochrome bd ubiquinol oxidase from Escherichia coli. (1995) (61)
Cloning of the cyo locus encoding the cytochrome o terminal oxidase complex of Escherichia coli (1987) (60)
Human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of iron sulfur (Ip) subunit of liver mitochondria. (1990) (60)
One-step purification of histidine-tagged cytochrome bo3 from Escherichia coli and demonstration that associated quinone is not required for the structural integrity of the oxidase. (1997) (60)
Mitochondrial NADH:ubiquinone reductase: complementary DNA sequence of the import precursor of the bovine 75-kDa subunit. (1989) (60)
Proton transfer from glutamate 286 determines the transition rates between oxygen intermediates in cytochrome c oxidase. (2000) (58)
A rapid and robust method for selective isotope labeling of proteins. (2011) (58)
Helix switching of a key active-site residue in the cytochrome cbb3 oxidases. (2005) (57)
Magnetic circular dichroism used to examine the interaction of Escherichia coli cytochrome bd with ligands. (1999) (57)
Single electron reduction of cytochrome c oxidase compound F: resolution of partial steps by transient spectroscopy. (1998) (56)
The gateway to the active site of heme-copper oxidases. (1993) (55)
Identification of subunit I as the cytochrome b558 component of the cytochrome d terminal oxidase complex of Escherichia coli. (1984) (55)
Impaired proton pumping in cytochrome c oxidase upon structural alteration of the D pathway. (2008) (54)
Proton transfer in ba(3) cytochrome c oxidase from Thermus thermophilus. (2012) (54)
Modified, large-scale purification of the cytochrome o complex (bo-type oxidase) of Escherichia coli yields a two heme/one copper terminal oxidase with high specific activity. (1992) (53)
The use of gene fusions to examine the membrane topology of the L-subunit of the photosynthetic reaction center and of the cytochrome b subunit of the bc1 complex from Rhodobacter sphaeroides. (1991) (52)
High-resolution membrane protein structure by joint calculations with solid-state NMR and X-ray experimental data (2011) (52)
Reconstitution of the Ubiquinone-dependent pyruvate oxidase system of Escherichia coli with the cytochrome o terminal oxidase complex. (1985) (51)
Phosphonate analogues of pyruvate. Probes of substrate binding to pyruvate oxidase and other thiamin pyrophosphate-dependent decarboxylases. (1980) (50)
Expression and mutagenesis of the NqrC subunit of the NQR respiratory Na+ pump from Vibrio cholerae with covalently attached FMN (2001) (50)
Intricate role of water in proton transport through cytochrome c oxidase. (2010) (50)
The quinone-binding sites of the cytochrome bo3 ubiquinol oxidase from Escherichia coli. (2010) (50)
Site-directed mutagenesis of highly conserved residues in helix VIII of subunit I of the cytochrome bo ubiquinol oxidase from Escherichia coli: an amphipathic transmembrane helix that may be important in conveying protons to the binuclear center. (1993) (49)
The cytochromes of Escherichia coli (1987) (49)
Perfusion‐induced redox differences in cytochrome c oxidase: ATR/FT‐IR spectroscopy (2001) (49)
Epitopes of monoclonal antibodies which inhibit ubiquinol oxidase activity of Escherichia coli cytochrome d complex localize functional domain. (1990) (49)
Proposed structure for the prosthetic group of the catalase HPII from Escherichia coli (1989) (48)
Characterization of mutations in the cytochrome b subunit of the bc1 complex of Rhodobacter sphaeroides that affect the quinone reductase site (Qc). (1993) (48)
Replacing Asn207 by aspartate at the neck of the D channel in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides results in decoupling the proton pump. (2006) (48)
A single-amino-acid lid renders a gas-tight compartment within a membrane-bound transporter. (2004) (48)
Demonstration by FTIR that the bo-type ubiquinol oxidase of Escherichia coli contains a heme-copper binuclear center similar to that in cytochrome c oxidase and that proper assembly of the binuclear center requires the cyoE gene product. (1992) (48)
High affinity lipid binding sites on the peripheral membrane enzyme pyruvate oxidase. Specific ligand effects on detergent binding. (1977) (48)
The room temperature reaction of carbon monoxide and oxygen with the cytochrome bd quinol oxidase from Escherichia coli. (1994) (47)
How does cytochrome oxidase pump protons? (1998) (47)
Isolation and characterization of an Escherichia coli mutant lacking the cytochrome o terminal oxidase (1985) (47)
Potentiometric analysis of the purified cytochrome d terminal oxidase complex from Escherichia coli (1984) (47)
Mutagenesis study of the 2Fe-2S center and the FAD binding site of the Na(+)-translocating NADH:ubiquinone oxidoreductase from Vibrio cholerae. (2004) (47)
Expression and one-step purification of a fully active polyhistidine-tagged cytochrome bc1 complex from Rhodobacter sphaeroides. (1999) (46)
Vibrational modes of tyrosines in cytochrome c oxidase from Paracoccus denitrificans: FTIR and electrochemical studies on Tyr-D4-labeled and on Tyr280His and Tyr35Phe mutant enzymes. (2002) (46)
Localization of histidine residues responsible for heme axial ligation in cytochrome b556 of complex II (succinate:ubiquinone oxidoreductase) in Escherichia coli. (1998) (45)
Microfluidic Generation of Lipidic Mesophases for Membrane Protein Crystallization. (2009) (45)
Proteolysis of the cytochrome d complex with trypsin and chymotrypsin localizes a quinol oxidase domain. (1991) (45)
Characterization of the type 2 NADH:menaquinone oxidoreductases from Staphylococcus aureus and the bactericidal action of phenothiazines. (2014) (45)
Identification of a ferryl intermediate of Escherichia coli cytochrome d terminal oxidase by resonance Raman spectroscopy. (1991) (44)
Substitutions for glutamate 101 in subunit II of cytochrome c oxidase from Rhodobacter sphaeroides result in blocking the proton-conducting K-channel. (2003) (44)
Two conformations of the catalytic site in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides. (1995) (44)
Preparation and characterization of the water-soluble heme-binding domain of cytochrome c1 from the Rhodobacter sphaeroides bc1 complex. (1991) (43)
Immunological characterization of the cytochrome o terminal oxidase from Escherichia coli. (1983) (43)
Cloning and expression of the gene encoding the soluble cytochrome b562 of Escherichia coli. (1991) (43)
Cloning the cyd gene locus coding for the cytochrome d complex of Escherichia coli. (1984) (43)
Regulation of expression of the cytochrome d terminal oxidase in Escherichia coli is transcriptional (1988) (43)
Vibrational modes of ubiquinone in cytochrome bo(3) from Escherichia coli identified by Fourier transform infrared difference spectroscopy and specific (13)C labeling. (1999) (43)
Kinetic design of the respiratory oxidases (2011) (42)
Spectroscopic and genetic evidence for two heme-Cu-containing oxidases in Rhodobacter sphaeroides (1992) (42)
Strong excitonic interactions in the oxygen-reducing site of bd-type oxidase: the Fe-to-Fe distance between hemes d and b595 is 10 A. (2008) (42)
Structure and function of thebc-complex ofRhodobacter sphaeroides (1992) (41)
The haem b558 component of the cytochrome bd quinol oxidase complex from Escherichia coli has histidine-methionine axial ligation. (1995) (40)
Structure of the disulfide bond generating membrane protein DsbB in the lipid bilayer. (2013) (40)
Site-directed mutagenesis of residues lining a putative proton transfer pathway in cytochrome c oxidase from Rhodobacter sphaeroides. (1996) (40)
Cytochrome bo from Escherichia coli: identification of haem ligands and reaction of the reduced enzyme with carbon monoxide. (1993) (39)
Purification and characterization of the cytochrome bd complex from Azotobacter vinelandii: comparison to the complex from Escherichia coli (1994) (39)
Characterization of the cytochrome d terminal oxidase complex of Escherichia coli using polyclonal and monoclonal antibodies. (1984) (39)
Identification of a stable semiquinone intermediate in the purified and membrane bound ubiquinol oxidase-cytochrome bd from Escherichia coli. (1998) (38)
Properties of Arg481 mutants of the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides suggest that neither R481 nor the nearby D-propionate of heme a3 is likely to be the proton loading site of the proton pump. (2009) (38)
Lipid activation and protease activation of pyruvate oxidase. Evidence suggesting a common site of interaction on the protein. (1977) (38)
Resonance Raman spectroscopic identification of a histidine ligand of b595 and the nature of the ligation of chlorin d in the fully reduced Escherichia coli cytochrome bd oxidase. (1996) (38)
Heme-heme and heme-ligand interactions in the di-heme oxygen-reducing site of cytochrome bd from Escherichia coli revealed by nanosecond absorption spectroscopy. (2010) (38)
Electron and proton transfer in the ba3 oxidase from Thermus thermophilus (2008) (38)
Spectral and Kinetic Equivalence of Oxidized Cytochrome c Oxidase as Isolated and “Activated” by Reoxidation* (2006) (38)
Characterization of the Type III sulfide:quinone oxidoreductase from Caldivirga maquilingensis and its membrane binding. (2013) (37)
Identification of the residues involved in stabilization of the semiquinone radical in the high-affinity ubiquinone binding site in cytochrome bo(3) from Escherichia coli by site-directed mutagenesis and EPR spectroscopy. (2002) (37)
The oxygenated complex of cytochrome d terminal oxidase : direct evidence for iron-oxygen coordination in a chlorin-containing enzyme by resonance Raman spectroscopy (1993) (37)
Exploring the proton pump and exit pathway for pumped protons in cytochrome ba3 from Thermus thermophilus (2012) (37)
Proximity mapping the surface of a membrane protein using an artificial protease: demonstration that the quinone-binding domain of subunit I is near the N-terminal region of subunit II of cytochrome bd. (1995) (37)
Glutamate-89 in subunit II of cytochrome bo3 from Escherichia coli is required for the function of the heme-copper oxidase. (1999) (37)
Assembly of the Rieske iron-sulfur subunit of the cytochrome bc1 complex in the Escherichia coli and Rhodobacter sphaeroides membranes independent of the cytochrome b and c1 subunits. (1993) (36)
The fully oxidized form of the cytochrome bd quinol oxidase from E. coli does not participate in the catalytic cycle: Direct evidence from rapid kinetics studies (2008) (36)
Characterization of the Exchangeable Protons in the Immediate Vicinity of the Semiquinone Radical at the QH Site of the Cytochrome bo3 from Escherichia coli* (2006) (36)
Affinity of intact Escherichia coli for hydrophobic membrane probes is a function of the physiological state of the cells. (1977) (35)
Structure and function of the bc-complex of Rhodobacter sphaeroides. (1992) (35)
Expression of cyoA and cyoB demonstrates that the CO-binding heme component of the Escherichia coli cytochrome o complex is in subunit I. (1990) (35)
Single-electron photoreduction of the P(M) intermediate of cytochrome c oxidase. (2006) (35)
Some recent advances relating to prokaryotic cytochrome c reductases and cytochrome c oxidases. (1991) (35)
Role of the K-channel in the pH-dependence of the reaction of cytochrome c oxidase with hydrogen peroxide. (2001) (35)
Time-resolved step-scan Fourier transform infrared spectroscopy of the CO adducts of bovine cytochrome c oxidase and of cytochrome bo(3) from Escherichia coli. (2002) (35)
Examination of the functional roles of 5 highly conserved residues in the cytochrome b subunit of the bc1 complex of Rhodobacter sphaeroides. (1992) (35)
Kinetics of electron and proton transfer during the reaction of wild type and helix VI mutants of cytochrome bo3 with oxygen. (1996) (34)
Division of labor in transhydrogenase by alternating proton translocation and hydride transfer (2015) (34)
Entrance of the proton pathway in cbb3-type heme-copper oxidases (2011) (34)
Glutamate 107 in subunit I of the cytochrome bd quinol oxidase from Escherichia coli is protonated and near the heme d/heme b595 binuclear center. (2007) (34)
Singlet energy-transfer studies on associating protein systems. Distance measurements on trypsin, -chymotrypsin, and their protein inhibitors. (1972) (34)
Oriented immobilization and electron transfer to the cytochrome c oxidase (2011) (34)
FTIR studies of internal proton transfer reactions linked to inter-heme electron transfer in bovine cytochrome c oxidase. (2004) (33)
Activation of C55-isoprenoid alcohol phosphokinase from Staphylococcus aureus. I. Activation by phospholipids and fatty acids. (1976) (33)
The active form of the cytochrome d terminal oxidase complex of Escherichia coli is a heterodimer containing one copy of each of the two subunits. (1988) (33)
Preparation of Escherichia coli pyruvate oxidase utilizing a thiamine pyrophosphate affinity column. (1976) (33)
Direct infrared detection of the covalently ring linked His-Tyr structure in the active site of the heme-copper oxidases. (2002) (33)
Binding of nickel and zinc ions to bacitracin A. (1980) (32)
Cytochrome c Oxidase: One Enzyme, Two Mechanisms? (1998) (32)
Effects of pH and detergent on the kinetic and electrochemical properties of the purified cytochrome d terminal oxidase complex of Escherichia coli. (1984) (32)
Spectroscopic and quantitative analysis of the oxygenated and peroxy states of the purified cytochrome d complex of Escherichia coli. (1989) (32)
Site-directed mutations of conserved residues of the Rieske iron-sulfur subunit of the cytochrome bc1 complex of Rhodobacter sphaeroides blocking or impairing quinol oxidation. (1993) (32)
Gene fusions with β‐lactamase show that subunit I of the cytochrome bd quinol oxidase from E. coli has nine transmembrane helices with the O2 reactive site near the periplasmic surface (2004) (32)
Identification of the axial heme ligands of cytochrome b 556 in succinate: Ubiquinone oxidoreductase from Escherichia coli (1994) (32)
The gene encoding cytochrome c oxidase subunit II from Rhodobacter sphaeroides; comparison of the deduced amino acid sequence with sequences of corresponding peptides from other species. (1991) (32)
Decoupling mutations in the D-channel of the aa(3)-type cytochrome c oxidase from Rhodobacter sphaeroides suggest that a continuous hydrogen-bonded chain of waters is essential for proton pumping. (2010) (32)
Peroxide complex of cytochrome bd: kinetics of generation and stability. (1995) (32)
Characterization of the proteolytic activation of pyruvate oxidase. Control by specific ligands and by the flavin oxidation-reduction state. (1977) (31)
Accommodation of two diatomic molecules in cytochrome bo: insights into NO reductase activity in terminal oxidases. (2009) (31)
Identity of the axial ligand of the high-spin heme in cytochrome oxidase: spectroscopic characterization of mutants in the bo-type oxidase of Escherichia coli and the aa3-type oxidase of Rhodobacter sphaeroides. (1993) (31)
Characterization of Mutants That Change the Hydrogen Bonding of the Semiquinone Radical at the QH Site of the Cytochrome bo3 from Escherichia coli* (2007) (31)
Beta-galactosidase gene fusions as probes for the cytoplasmic regions of subunits I and II of the membrane-bound cytochrome d terminal oxidase from Escherichia coli. (1988) (30)
Site-directed mutagenesis studies on subunit I of the aa3-type cytochrome c oxidase of Rhodobacter sphaeroides: a brief review of progress to date. (1992) (30)
Site-directed mutation of the highly conserved region near the Q-loop of the cytochrome bd quinol oxidase from Escherichia coli specifically perturbs heme b595. (2001) (30)
Substitution of lysine-362 in a putative proton-conducting channel in the cytochrome c oxidase from Rhodobacter sphaeroides blocks turnover with O2 but not with H2O2. (1998) (30)
Functional interactions between membrane-bound transporters and membranes (2010) (30)
Trypsin proteolysis of the cytochrome d complex of Escherichia coli selectively inhibits ubiquinol oxidase activity while not affecting N,N,N',N'-tetramethyl-p-phenylenediamine oxidase activity. (1988) (30)
Identification of the ubiquinol-binding site in the cytochrome bo3-ubiquinol oxidase of Escherichia coli. (1994) (30)
Subunit II of the cytochrome bo3 ubiquinol oxidase from Escherichia coli is a lipoprotein. (1997) (30)
Recent studies of the cytochrome o terminal oxidase complex of Escherichia coli. (1990) (30)
Activation of C55-isoprenoid alcohol phosphokinase from Staphylococcus aureus. III. Activation by detergents. (1976) (29)
Single-particle cryo-EM studies of transmembrane proteins in SMA copolymer nanodiscs. (2019) (29)
FTIR spectroscopic evidence for the involvement of an acidic residue in quinone binding in cytochrome bd from Escherichia coli. (2002) (29)
Activity of membrane proteins immobilized on surfaces as a function of packing density. (2008) (29)
EPR studies of the cytochrome-d complex of Escherichia coli. (1989) (29)
CtaM Is Required for Menaquinol Oxidase aa3 Function in Staphylococcus aureus (2016) (28)
Specific overproduction and purification of the cytochrome b558 component of the cytochrome d complex from Escherichia coli. (1986) (28)
pH-dependent structural changes at the Heme-Copper binuclear center of cytochrome c oxidase. (2001) (28)
A new ruthenium complex to study single-electron reduction of the pulsed O(H) state of detergent-solubilized cytochrome oxidase. (2007) (28)
Interactions of Small Molecules with Membranes: Partitioning, Permeability, and Electrical Effects (1989) (28)
INTERACTION OF CYTOCHROME BD FROM ESCHERICHIA-COLI WITH HYDROGEN-PEROXIDE (1995) (28)
Partial steps of charge translocation in the nonpumping N139L mutant of Rhodobacter sphaeroides cytochrome c oxidase with a blocked D-channel. (2010) (28)
Immunological investigation of the distribution of cytochromes related to the two terminal oxidases of Escherichia coli in other gram-negative bacteria (1985) (28)
A pH-dependent polarity change at the binuclear center of reduced cytochrome c oxidase detected by FTIR difference spectroscopy of the CO adduct. (1996) (28)
Potentiometric analysis of the cytochromes of an Escherichia coli mutant strain lacking the cytochrome d terminal oxidase complex (1984) (27)
Cytochrome O from Escherichia coli Is Structurally Related to Cytochrome aa3 a (1988) (27)
Cu XAS shows a change in the ligation of CuB upon reduction of cytochrome bo3 from Escherichia coli. (1999) (27)
Purification and reconstitution of the cytochrome d terminal oxidase complex from Escherichia coli. (1986) (27)
Identification of the nitrogen donor hydrogen bonded with the semiquinone at the Q(H) site of the cytochrome bo3 from Escherichia coli. (2008) (26)
The diheme cytochrome c(4) from Vibrio cholerae is a natural electron donor to the respiratory cbb(3) oxygen reductase. (2010) (26)
Mutations which decouple the proton pump of the cytochrome c oxidase from Rhodobacter sphaeroides perturb the environment of glutamate 286 (2006) (26)
Reconstitution of respiratory oxidases in membrane nanodiscs for investigation of proton‐coupled electron transfer (2012) (26)
Site-directed mutants of the cytochrome bo ubiquinol oxidase of Escherichia coli: amino acid substitutions for two histidines that are putative CuB ligands. (1993) (26)
Flash photolysis of the carbon monoxide compounds of wild-type and mutant variants of cytochrome bo from Escherichia coli. (1994) (26)
Relocation of internal bound water in bacteriorhodopsin during the photoreaction of M at low temperatures: an FTIR study. (2000) (26)
Ca2+-Binding Site in Rhodobacter Sphaeroides Cytochrome c Oxidase† (2002) (25)
Interactions of intermediate semiquinone with surrounding protein residues at the Q(H) site of wild-type and D75H mutant cytochrome bo3 from Escherichia coli. (2012) (25)
Exposure of Bovine Cytochrome c Oxidase to High Triton X-100 or to Alkaline Conditions Causes a Dramatic Change in the Rate of Reduction of Compound F* (2001) (25)
The two terminal oxidases of the aerobic respiratory chain of Escherichia coli each yield water and not peroxide as a final product. (1988) (25)
Direct measurement of proton release by cytochrome c oxidase in solution during the F-->O transition. (2004) (25)
Interaction of internal water molecules with the schiff base in the L intermediate of the bacteriorhodopsin photocycle. (2002) (25)
EPR evidence on the structure of the copper(II)-bacitracin A complex (1983) (25)
Cyanide‐reactive sites in cytochrome bd complex from E. coli (1993) (25)
The Structures and Properties of Membrane Lipids (1989) (24)
Complex formation between the uncoupler carbonyl cyanide p-trifluoromethoxyphenylhydrazone (FCCP) and valinomycin in the presence of potassium. (1978) (24)
Characterization of the Semiquinone Radical Stabilized by the Cytochrome aa3-600 Menaquinol Oxidase of Bacillus subtilis* (2010) (24)
Site-directed mutagenesis of residues within helix VI in subunit I of the cytochrome bo3 ubiquinol oxidase from Escherichia coli suggests that tyrosine 288 may be a CuB ligand. (1994) (24)
EPR studies of wild‐type and several mutants of cytochrome c oxidase from Rhodobacter sphaeroides: Glu286 is not a bridging ligand in the cytochrome a 3‐CuB center (1995) (24)
Magnetic-circular-dichroism studies of Escherichia coli cytochrome bo. Identification of high-spin ferric, low-spin ferric and ferryl [Fe(IV)] forms of heme o. (1994) (24)
Conformational transitions and molecular hysteresis of cytochrome c oxidase: Varying the redox state by electronic wiring (2010) (23)
Genetic fusion of subunits I, II, and III of the cytochrome bo ubiquinol oxidase from Escherichia coli results in a fully assembled and active enzyme. (1993) (23)
Resonance Raman studies of Escherichia coli cytochrome bd oxidase. Selective enhancement of the three heme chromophores of the "as-isolated" enzyme and characterization of the cyanide adduct. (1995) (23)
Matrix-assisted laser desorption ionization mass spectrometry of membrane proteins: demonstration of a simple method to determine subunit molecular weights of hydrophobic subunits. (1997) (23)
G204D, a mutation that blocks the proton-conducting D-channel of the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides. (2005) (23)
The unusual redox properties of C-type oxidases. (2016) (23)
Regulation by lipids of cofactor binding to a peripheral membrane enzyme: binding of thiamin pyrophosphate to pyruvate oxidase. (1977) (22)
Activation of C55-isoprenoid alcohol phosphokinase from Staphylococcus aureus. II. Biophysical studies. (1976) (22)
Evidence for Distinct Electron Transfer Processes in Terminal Oxidases from Different Origin by Means of Protein Film Voltammetry (2014) (22)
In vivo assembly of the cytochrome d terminal oxidase complex of Escherichia coli from genes encoding the two subunits expressed on separate plasmids. (1991) (22)
Oxygen reaction and proton uptake in helix VIII mutants of cytochrome bo3. (1995) (22)
Nitrogen and proton ENDOR of cytochrome d, hemin, and metmyoglobin in frozen solutions (1993) (22)
Use of an azido-ubiquinone derivative to identify subunit I as the ubiquinol binding site of the cytochrome d terminal oxidase complex of Escherichia coli. (1986) (22)
Vibrational Characteristics of Mutant and Wild-type Carbon Monoxy Cytochrome c Oxidase: Evidence for a Linear Arrangement of Heme a, a3, and CuB (1994) (22)
Relationships between membrane-bound cytochrome o from Vitreoscilla and that of Escherichia coli. (1988) (21)
Direct Electrochemistry of Cytochrome bo Oxidase at a series of Gold Nanoparticles-Modified Electrodes. (2013) (21)
Structure of the cytochrome aa3-600 heme-copper menaquinol oxidase bound to inhibitor HQNO shows TM0 is part of the quinol binding site (2019) (21)
Mutation of a single residue in the ba3 oxidase specifically impairs protonation of the pump site (2015) (21)
Role of the divalent metal cation in the pyruvate oxidase reaction. (1982) (21)
Tryptophan-136 in subunit II of cytochrome bo3 from Escherichia coli may participate in the binding of ubiquinol. (1998) (21)
Solid-state NMR study of the charge-transfer complex between ubiquinone-8 and disulfide bond generating membrane protein DsbB. (2011) (21)
Arginine 391 in Subunit I of the Cytochrome bd Quinol Oxidase from Escherichia coli Stabilizes the Reduced Form of the Hemes and Is Essential for Quinol Oxidase Activity* (2004) (21)
Blocking the K-pathway still allows rapid one-electron reduction of the binuclear center during the anaerobic reduction of the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides. (2010) (20)
Using matrix-assisted laser desorption ionization mass spectrometry to map the quinol binding site of cytochrome bo3 from Escherichia coli. (1998) (20)
Q-band ENDOR (electron nuclear double resonance) of the high-affinity ubisemiquinone center in cytochrome bo3 from Escherichia coli. (2000) (20)
Abortive assembly of succinate-ubiquinone reductase (Complex II) in a ferrochelatase-deficient mutant of Escherichia coli (2001) (20)
Functional role of Thr-312 and Thr-315 in the proton-transfer pathway in ba3 Cytochrome c oxidase from Thermus thermophilus. (2010) (20)
Kinetic studies of the lipid-activated pyruvate oxidase flavoprotein of Escherichia coli. (1985) (20)
Chromophore-protein-water interactions in the L intermediate of bacteriorhodopsin: FTIR study of the photoreaction of L at 80 K. (1999) (20)
Isoelectric focusing and crossed immunoelectrophoresis of heme proteins in the Escherichia coli cytoplasmic membrane (1982) (20)
Cell-free synthesis of cytochrome bo(3) ubiquinol oxidase in artificial membranes. (2012) (20)
Modeling direct electron transfer to a multi-redox center protein: Cytochrome c oxidase (2010) (20)
2D-SEIRA spectroscopy to highlight conformational changes of the cytochrome c oxidase induced by direct electron transfer. (2011) (19)
Distinct forms of the haem o‐Cu binuclear site of oxidised cytochrome bo from Escherichia coli (1993) (19)
Role of aspartate 132 at the orifice of a proton pathway in cytochrome c oxidase (2013) (19)
Role of quinones in the branch of the Escherichia coli respiratory chain that terminates in cytochrome o (1984) (19)
FTIR study of conformational substates in the CO adduct of cytochrome c oxidase from Rhodobacter sphaeroides. (1996) (19)
Direct evidence for the protonation of aspartate-75, proposed to be at a quinol binding site, upon reduction of cytochrome bo3 from Escherichia coli. (2001) (19)
A Purple Cupredoxin from Nitrosopumilus maritimus Containing a Mononuclear Type 1 Copper Center with an Open Binding Site. (2016) (19)
Some recent contributions of FTIR difference spectroscopy to the study of cytochrome oxidase1 (2003) (19)
Characterization of the PIB-Type ATPases Present in Thermus thermophilus (2012) (19)
Analysis of the topology of the cytochrome d terminal oxidase complex of Escherichia coli by alkaline phosphatase fusions (1991) (18)
Membrane Dynamics and Protein-Lipid Interactions (1989) (18)
Microfluidic flow-flash: method for investigating protein dynamics. (2007) (18)
Similar CO binding sites in bacterial cytochrome bo and mammalian cytochrome c oxidase (1993) (18)
A loop between transmembrane helices IX and X of subunit I of cytochrome c oxidase caps the heme a-heme a3-CuB center. (1994) (18)
The carboxy-terminal insert in the Q-loop is needed for functionality of Escherichia coli cytochrome bd-I. (2020) (18)
Water structural changes in the L and M photocycle intermediates of bacteriorhodopsin as revealed by time-resolved step-scan Fourier transform infrared (FTIR) spectroscopy. (2007) (18)
Location of the Substrate Binding Site of the Cytochrome bo3 Ubiquinol Oxidase from Escherichia coli. (2017) (18)
Characterization of the nitric oxide reductase from Thermus thermophilus (2013) (18)
Type 2 NADH Dehydrogenase Is the Only Point of Entry for Electrons into the Streptococcus agalactiae Respiratory Chain and Is a Potential Drug Target (2018) (17)
Reaction of cytochrome bo3 with oxygen: extra redox center(s) are present in the protein. (1995) (17)
Escherichia coli auxotroph host strains for amino acid-selective isotope labeling of recombinant proteins. (2015) (17)
Spectroscopic characterization of mutants supports the assignment of histidine-419 as the axial ligand of heme o in the binuclear center of the cytochrome bo ubiquinol oxidase from Escherichia coli. (1993) (17)
Exploring by Pulsed EPR the Electronic Structure of Ubisemiquinone Bound at the QH Site of Cytochrome bo3 from Escherichia coli with in Vivo 13C-Labeled Methyl and Methoxy Substituents* (2011) (17)
A quantitative radioimmunological screening method for specific gene products. (1982) (17)
Water molecule rearrangements around Leu93 and Trp182 in the formation of the L intermediate in bacteriorhodopsin's photocycle. (2003) (17)
A conserved glutamic acid in helix VI of cytochrome bo3 influences a key step in oxygen reduction. (1997) (16)
Proton nuclear magnetic resonance studies on bacitracin A and its interaction with zinc ion. (1980) (16)
Proton Dynamics at the Membrane Surface. (2016) (16)
Timing of electron and proton transfer in the ba(3) cytochrome c oxidase from Thermus thermophilus. (2012) (16)
Identification, localization, and function of the thiamin pyrophosphate and flavin adenine dinucleotide dependent pyruvate oxidase in isolated membrane vesicles of Escherichia coli B. (1978) (16)
Review and Hypothesis. New insights into the reaction mechanism of transhydrogenase: Swivelling the dIII component may gate the proton channel (2015) (15)
E. coli map. Physical map locations of genes encoding components of the aerobic respiratory chain of Escherichia coli (1991) (15)
Dissection of hydrogen bond interaction network around an iron-sulfur cluster by site-specific isotope labeling of hyperthermophilic archaeal Rieske-type ferredoxin. (2012) (15)
Cryo-EM structures of Escherichia coli cytochrome bo3 reveal bound phospholipids and ubiquinone-8 in a dynamic substrate binding site (2021) (15)
All the O2 Consumed by Thermus thermophilus Cytochrome ba3 Is Delivered to the Active Site through a Long, Open Hydrophobic Tunnel with Entrances within the Lipid Bilayer. (2016) (15)
Proton uptake and pKa changes in the uncoupled Asn139Cys variant of cytochrome c oxidase. (2013) (15)
Interconversion of fast and slow forms of cytochrome bo from Escherichia coli. (1995) (15)
The orientation of the three haems of the 'in situ' ubiquinol oxidase, cytochrome bd, of Escherichia coli. (1992) (15)
Spectroscopic studies of pyruvate oxidase flavoprotein from Escherichia coli trapped in the lipid-activated form by cross-linking. (1985) (15)
Immunological characterization of an Escherichia coli strain which is lacking cytochrome d (1983) (15)
Optical properties of specific complexes between complementary oligoribonucleotides. (1970) (15)
Studies of the thiamin pyrophosphate binding site of Escherichia coli pyruvate oxidase. Evidence for an essential tryptophan residue. (1980) (15)
Relocation of water molecules between the Schiff base and the Thr46-Asp96 region during light-driven unidirectional proton transport by bacteriorhodopsin: an FTIR study of the N intermediate. (2005) (15)
Resonance Raman study on axial ligands of heme irons in cytochrome bd-type ubiquinol oxidase from Escherichia coli (1995) (15)
X-ray transparent microfluidic platforms for membrane protein crystallization with microseeds. (2018) (15)
Catalase Activity of Cytochrome c Oxidase Assayed with Hydrogen Peroxide-Sensitive Electrode Microsensor (2010) (14)
Water as a Cofactor in the Unidirectional Light-Driven Proton Transfer Steps in Bacteriorhodopsin† (2006) (14)
A Role for Internal Water Molecules in Proton Affinity Changes in the Schiff Base and Asp85 for One‐way Proton Transfer in Bacteriorhodopsin † (2008) (14)
The electron distribution in the “activated” state of cytochrome c oxidase (2018) (14)
Spectroscopic studies on heme d in the visible and infrared. (1986) (14)
Mechanistic Aspects of the Q0 -Site of the bc1 -Complex As Revealed by Mutagenesis Studies, and the Crystallographic Structure (1999) (14)
A positive feedback-based gene circuit to increase the production of a membrane protein (2010) (13)
Volume Changes Associated with CO Photodissociation from Fully Reduced Cytochrome bo3 from Escherichia coli (1998) (13)
Structure changes upon deprotonation of the proton release group in the bacteriorhodopsin photocycle. (2012) (13)
Role of respiratory NADH oxidation in the regulation of Staphylococcus aureus virulence (2020) (13)
Resonance Raman Spectroscopy of the Heme Groups of Cytochrome cbb3 in Rhodobacter sphaeroides (1995) (13)
Critical structural role of R481 in cytochrome c oxidase from Rhodobacter sphaeroides. (2009) (13)
Proton Pump Caught in the Act (1999) (13)
Studies of the flavin adenine dinucleotide binding region in Escherichia coli pyruvate oxidase. (1982) (13)
Identification of heme propionate vibrational modes in the resonance Raman spectra of cytochrome c oxidase. (2009) (12)
Escherichia coli pyruvate oxidase: interaction of a peripheral membrane protein with lipids. (1982) (12)
Observation of a novel transient ferryl complex with reduced CuB in cytochrome c oxidase. (1999) (12)
Purification of the aa3-type cytochrome-c oxidase from Rhodopseudomonas sphaeroides. (1986) (12)
Detergent‐solubilized Escherichia coli cytochrome bo 3 ubiquinol oxidase: a monomeric, not a dimeric complex (1999) (12)
A ligand-exchange mechanism of proton pumping involving tyrosine-422 of subunit I of cytochrome oxidase is ruled out. (1996) (12)
Evolution of the cytochrome bd oxygen reductase superfamily and the function of CydAA’ in Archaea (2021) (12)
Isolation and characterization of a new class of cytochrome d terminal oxidase mutants of Escherichia coli (1991) (12)
Characterization of steady-state activities of cytochrome c oxidase at alkaline pH: mimicking the effect of K-channel mutations in the bovine enzyme. (2005) (12)
A pathogenic mutation in cytochrome c oxidase results in impaired proton pumping while retaining O(2)-reduction activity. (2010) (12)
Immunological analysis of the heme proteins present in aerobically grown Escherichia coli (1984) (12)
Photothermal studies of CO photodissociation from mixed valence Escherichia coli cytochrome bo 3 (2005) (11)
Stoichiometry of proton pumping by the cbb3-type oxygen reductase in whole cells of Rhodobacter capsulatus at pH 7 is about 0.5 H+ per electron (2012) (11)
Critical Role of Water Molecules in Proton Translocation by the Membrane-Bound Transhydrogenase. (2017) (11)
Water-mediated hydrogen-bonded network on the cytoplasmic side of the Schiff base of the L photointermediate of bacteriorhodopsin. (2003) (11)
The Semiquinone at the Qi Site of the bc1 Complex Explored Using HYSCORE Spectroscopy and Specific Isotopic Labeling of Ubiquinone in Rhodobacter sphaeroides via 13C Methionine and Construction of a Methionine Auxotroph (2014) (11)
Cytochrome b558 monitors the steady state redox state of the ubiquinone pool in the aerobic respiratory chain of Escherichia coli. (1987) (11)
Introduction: The Structure and Composition of Biomembranes (1989) (11)
Quasi-elastic light scattering studies on pyruvate oxidase. (1977) (11)
Bacterial denitrifying nitric oxide reductases and aerobic respiratory terminal oxidases use similar delivery pathways for their molecular substrates. (2018) (10)
Studies on the complex formed between bacitracin A and divalent cations. (1983) (10)
Ligand-binding properties and heterogeneity of cytochrome bo from Escherichia coli. (1993) (10)
Site-directed mutagenesis of arginine-114 and tryptophan-129 in the cytochrome b subunit of the bc1 complex of Rhodobacter sphaeroides: two highly conserved residues predicted to be near the cytoplasmic surface of putative transmembrane helices B and C. (1994) (10)
Microcin J25 inhibits ubiquinol oxidase activity of purified cytochrome bd-I from Escherichia coli. (2019) (10)
Functional importance of a pair of conserved glutamic acid residues and of Ca(2+) binding in the cbb(3)-type oxygen reductases from Rhodobacter sphaeroides and Vibrio cholerae. (2012) (10)
Proton pumping by an inactive structural variant of cytochrome c oxidase. (2014) (10)
Protein structure: Proton-pumping oxidases (1996) (9)
Specific ligand enhancement of the affinity of E. coli pyruvate oxidase for dipalmitoyl phosphatidylcholine. (1980) (9)
Alternate pathways for NADH oxidation in Thermus thermophilus using type 2 NADH dehydrogenases (2013) (9)
Cytochromes bd-I and bo3 are essential for the bactericidal effect of microcin J25 on Escherichia coli cells. (2018) (9)
Flash-photolysis of fully reduced and mixed-valence CO-bound Rhodobacter sphaeroides cytochrome c oxidase: heme spectral shifts. (2007) (9)
Functional importance of Glutamate-445 and Glutamate-99 in proton-coupled electron transfer during oxygen reduction by cytochrome bd from Escherichia coli. (2018) (9)
Spectral identification of intermediates generated during the reaction of dioxygen with the wild-type and EQ(I-286) mutant of Rhodobacter sphaeroides cytochrome c oxidase. (2012) (9)
Conformational coupling between the active site and residues within the KC-channel of the Vibrio cholerae cbb3-type (C-family) oxygen reductase (2014) (9)
An EPR spin label study of the quinol oxidase, E. coli cytochrome bo3: a search for redox induced conformational changes. (2007) (9)
Q-Band Electron-Nuclear Double Resonance Reveals Out-of-Plane Hydrogen Bonds Stabilize an Anionic Ubisemiquinone in Cytochrome bo3 from Escherichia coli. (2016) (8)
Studies on the quaternary structure of Escherichia coli pyruvate oxidase. (1980) (8)
Solid-state NMR study of a 41 kDa membrane protein complex DsbA/DsbB. (2013) (8)
Factors determining electron-transfer rates in cytochrome c oxidase: studies of the FQ(I-391) mutant of the Rhodobacter sphaeroides enzyme. (1997) (8)
The two transmembrane helices of CcoP are sufficient for assembly of the cbb3-type heme-copper oxygen reductase from Vibrio cholerae. (2015) (8)
Succinate dehydrogenase in Rhodopseudomonas sphaeroides: subunit composition and immunocross-reactivity with other related bacteria (1985) (8)
Characterization and Structural Principles of Membrane Proteins (1989) (8)
Discovery of Prenyltransferase Inhibitors with In Vitro and In Vivo Antibacterial Activity. (2020) (8)
Ca(2+)-binding site in Rhodobacter sphaeroides cytochrome C oxidase. (2002) (8)
Searching for the low affinity ubiquinone binding site in cytochrome bo3 from Escherichia coli. (2017) (8)
Water rearrangement around the Schiff base in the late K (KL) intermediate of the bacteriorhodopsin photocycle (2004) (8)
Identification of the transcriptional start site of the cyd operon from Escherichia coli. (1993) (7)
Unpaired Electron Spin Density Distribution across Reduced [2Fe-2S] Cluster Ligands by 13Cβ-Cysteine Labeling. (2018) (7)
Single mutations that redirect internal proton transfer in the ba3 oxidase from Thermus thermophilus. (2013) (7)
The reaction of hydrogen peroxide with cytochrome bo from E. coli. (1993) (7)
Identification of an active site cysteine residue in Escherichia coli pyruvate oxidase. (1982) (7)
Prokaryotic models for mitochondrial cytochrome c oxidase. (1993) (7)
Coordinating the structural rearrangements associated with unidirectional proton transfer in the bacteriorhodopsin photocycle induced by deprotonation of the proton-release group: a time-resolved difference FTIR spectroscopic study. (2010) (7)
Structural changes due to the deprotonation of the proton release group in the M-photointermediate of bacteriorhodopsin as revealed by time-resolved FTIR spectroscopy. (2008) (7)
The formate complex of the cytochrome bo quinol oxidase of Escherichia coli exhibits a ‘g = 12’ EPR feature analogous to that of ‘slow’ cytochrome oxidase (1992) (7)
Chemical Shift Assignment of the Transmembrane Helices of DsbB by 3D Magic Angle Spinning NMR (2008) (6)
Nitroxide spin labels as EPR reporters of the relaxation and magnetic properties of the heme–copper site in cytochrome bo3, E. coli (2010) (6)
Kinetics and intermediates of the reaction of fully reduced Escherichia coli bo₃ ubiquinol oxidase with O₂. (2014) (6)
Strong-field and integral spin-ligand complexes of the cytochrome bo quinol oxidase in Escherichia coli membrane preparations. (1994) (6)
Conformational studies of Escherichia coli pyruvate oxidase. (1982) (6)
Examination of the reaction of fully reduced cytochrome oxidase with hydrogen peroxide by flow-flash spectroscopy. (1999) (6)
Cytochrome o(cyoABCDE) andd(cydAB) Oxidase Gene Expression inEscherichia coli IsRegulated byOxygen, pH, andthefnrGeneProduct (1990) (6)
Role of the tightly bound quinone for the oxygen reaction of cytochrome bo3 oxidase from Escherichia coli (2018) (6)
Pores, Channels and Transporters (1989) (6)
Biophysical and biochemical studies of bacterial NADH:quinone oxidoreductase (NDH-1). (1994) (6)
X-ray transparent microfluidic chips for high-throughput screening and optimization of in meso membrane protein crystallization. (2017) (6)
The ubiquinol binding site of cytochrome bo3 from Escherichia coli accommodates menaquinone and stabilizes a functional menasemiquinone. (2019) (5)
The highly conserved methionine of subunit I of the heme‐copper oxidases is not at the heme‐copper dinuclear center: Mutagenesis of M110 in subunit I of cytochrome bo 3‐type ubiquinol oxidase from Escherichia coli (1995) (5)
The Lifetimes of Pharaonis Phoborhodopsin Signaling States Depend on the Rates of Proton Transfers—Effects of Hydrostatic Pressure and Stopped Flow Experiments † (2008) (5)
Studies on the interaction between Escherichia coli pyruvate oxidase and a detergent activator by utilization of the fluorescence probe bis(8-p-toluidino-1-naphthalenesulfonate). (1979) (5)
Mechanism of proton transfer through the KC proton pathway in the Vibrio cholerae cbb3 terminal oxidase. (2018) (5)
Q-Band ENDOR (Electron Nuclear Double Resonance) of the Heme o3 Liganding Environment at the Binuclear Center in Cytochrome bo3 from Escherichia coli (2000) (5)
Plasticity in the High Affinity Menaquinone Binding Site of the Cytochrome aa3-600 Menaquinol Oxidase from Bacillus subtilis. (2015) (5)
Communication between R481 and Cu(B) in cytochrome bo(3) ubiquinol oxidase from Escherichia coli. (2009) (5)
Electrogenic events in chromatophores fromRhodobacter sphaeroides lacking high-potential cytochrome b of thebc1-complex (1992) (5)
Proximity of reactive cysteine residue and flavin in Escherichia coli pyruvate oxidase as estimated by fluorescence energy transfer. (1982) (5)
Time-Resolved Electrometric Study of the F→O Transition in Cytochrome c Oxidase. The Effect of Zn2+ Ions on the Positive Side of the Membrane (2021) (5)
The three-spin intermediate at the O–O cleavage and proton-pumping junction in heme–Cu oxidases (2021) (5)
Role of arginine in the binding of thiamin pyrophosphate to Escherichia coli pyruvate oxidase. (1982) (5)
Escherichia coli amino acid auxotrophic expression host strains for investigating protein structure-function relationships. (2020) (4)
A Third Subunit in Ancestral Cytochrome c-Dependent Nitric Oxide Reductases (2014) (4)
Requirement forTerminal Cytochromes inGeneration ofthe Aerobic Signal forthearc Regulatory System inEscherichia coli: StudyUtilizing Deletions andlacFusions ofcyoandcyd (1990) (4)
Dynamics of the KB Proton Pathway in Cytochrome ba3 from Thermus thermophilus (2017) (4)
Identification of a cytochrome bc1 - aa3 supercomplex in Rhodobacter sphaeroides. (2021) (4)
Flash photolysis of the carbon monoxide compounds of mutant and wild-type cytochrome bo from E. coli. (1993) (4)
Proton NMR study of the heme environment in bacterial quinol oxidases. (2004) (4)
Thermodynamics of carbon monoxide photodissociation from the fully reduced cytochrome aa3 oxidase from Rb. sphaeroides. (2006) (4)
Cytochrome aa3 Oxygen Reductase Utilizes the Tunnel Observed in the Crystal Structures To Deliver O2 for Catalysis. (2018) (4)
Activation volumes for intramolecular electron transfer in Escherichia coli cytochrome bo3 (2002) (4)
Lateral and Transverse Asymmetry in Membranes (1989) (4)
Diversity and evolution of nitric oxide reduction (2021) (3)
Evolution of quinol oxidation within the heme‑copper oxidoreductase superfamily. (2022) (3)
Kinetics of intramolecular electron transfer in cytochrome bo3 from Escherichia coli. (2003) (3)
Product-controlled steady-state kinetics between cytochrome aa(3) from Rhodobacter sphaeroides and equine ferrocytochrome c analyzed by a novel spectrophotometric approach. (2012) (3)
Immunochemical analysis of the membrane‐bound succinate dehydrogenase of Escherichia coli (1982) (3)
Deletion of the gene encoding cytochrome b 562 from Rhodobacter sphaeroides (1994) (3)
The CO Photodissociation and Recombination Dynamics of the W172Y/F282T Ligand Channel Mutant of Rhodobacter sphaeroides aa3 Cytochrome c Oxidase (2016) (3)
Activation of Pyruvate Oxidase and Interaction with Membrane Components (1982) (3)
The state of association of the Na+-translocating reduced nicotinamide adenine dinucleotide:quinone oxidoreductase in detergent solution: an ultracentrifugation study (2004) (3)
Specific inhibition of proton pumping by the T315V mutation in the K channel of cytochrome ba3 from Thermus thermophilus. (2021) (3)
Immunological Analysis oftheHemeProteins Present inAerobically GrownEscherichia coli (1984) (3)
Differential effects of glutamate-286 mutations in the aa(3)-type cytochrome c oxidase from Rhodobacter sphaeroides and the cytochrome bo(3) ubiquinol oxidase from Escherichia coli. (2011) (3)
Energy transfer between the nicotinamide nucleotide transhydrogenase and ATP synthase of Escherichia coli (2021) (3)
The binding of a fluorescent activator 2-(N-decyl)aminonaphthalene-6-sulfonic acid to pyruvate oxidase. (1980) (3)
The KC Channel in the cbb3-Type Respiratory Oxygen Reductase from Rhodobacter capsulatus Is Required for Both Chemical and Pumped Protons (2014) (2)
Characterization and X-ray structure of the NADH-dependent coenzyme A disulfide reductase from Thermus thermophilus. (2019) (2)
The oligomeric state of the Caldivirga maquilingensis type III sulfide:Quinone Oxidoreductase is required for membrane binding. (2019) (2)
Cyclopropylglyoxylate as a mechanistic probe of thiamine pyrophosphate dependent pyruvate-metabolizing enzymes (1987) (2)
Effects of Colicin la on Membrane Functions of Escherichia coli (1975) (2)
Rapid Formation of a Semiquinone Species on Oxidation of Quinol by the Cytochrome bo3 Oxidase from Escherichia coli (1998) (2)
Ligand binding properties of bacterial oxidases in relation to cytochrome-c oxidase. (1992) (2)
The Cell Surface: Receptors, Membrane Recycling and Signal Transduction (1989) (2)
The heme-copper oxidoreductase superfamily: Diversity, evolution and ecology (2012) (2)
CO recombination as a probe of the Fe/Cu binuclear centre of terminal protonmotive oxidases. (1993) (1)
Membrane proteins. Current Opinion in Structural Biology 1993, 3:499-500 (1993) (1)
[Interaction of Escherichia coli cytochrome bd with hydrogen peroxide]. (1995) (1)
PROTEIN-LIPID INTERACTIONSl (1977) (1)
S11.34 The semiquinone at the QH site of the cytochrome bo3 from Escherichia coli (2008) (1)
Chapter 5:Coupling Hydride Transfer to Proton Pumping: the Swiveling Mechanism of Transhydrogenase (2017) (1)
Cytochrome aa 3 oxygen reductase utilizes the tunnel observed in the crystal structures to deliver O 2 for catalysis (2018) (1)
Immunochemical analysis of membrane-bound antigens from Escherichia coli which have succinate dehydrogenase activity (1984) (1)
Prediction of Structure for Cytochrome B from Sequence Data: What Information is Available from Sequence Comparison (1990) (1)
cryo-EM Structure of Alternative Complex III/ AA 3 Cytochrome Oxidase Supercomplex from Flavobacterium Johnsoniae (2018) (1)
Electrogenic events in chromatophores from lacking high-potential cytochrome of the -complex (1992) (1)
Ligand binding and conformational dynamics of the E. coli nicotinamide nucleotide transhydrogenase revealed by hydrogen/deuterium exchange mass spectrometry (2022) (1)
Membrane protein complex DsbB-DsbA structure by joint calculations with solid-state NMR and X-ray experimental data (2011) (1)
The electron transfer pathway of Type-C oxygen reductase from V. cholera (2012) (1)
Reaction of cytochrome bo 3 , with oxygen (1995) (1)
Structures of the intermediates in the catalytic cycle of mitochondrial cytochrome c oxidase. (2022) (1)
Genetics of E. Coli Cytochromes which are Components of the Aerobic Respiratory Chain (1987) (1)
Proposed Structure of Heme d, a Prosthetic Group of Bacterial Terminal Oxidases (Fe-Chelat von (I)). (1986) (1)
C55-Isoprenoid Alcohol Phosphokinase: An Intrinsic Membrane Enzyme (1976) (0)
R. sphaeroides photosythetic reaction center mutant - Residue L223, Ser to Trp - Room Temperature Structure Solved on X-ray Transparent Microfluidic Chip (2017) (0)
2.55-Angstrom Cryo-EM structure of Cytochrome bo3 from Escherichia coli in Native Membrane (2021) (0)
Photoselective discrimination of matrix isolated respiratory enzymes from E. coli by Fourier transform infrared spectroscopy (1992) (0)
The family of proton-pumping heme–copper respiratory oxidases (2010) (0)
Chemical shift assignments of DsbA(C33S)/DsbB by solid-state NMR (2013) (0)
Probing Gas Diffusion Pathways in Cytochrome C Oxidase with Explicit and Implicit Ligand Samplings (2012) (0)
Ubiquinol Binding Site of Cytochrome bo3 from Escherichia coli (2021) (0)
The cytochrome oxidases from P. denitrificans, T. thermophilus, E. coli and bovine heart studied by electrochemistry and FTIR/UV/VIS spectroscopy (1999) (0)
Complex formation between valinomycin and FCCP in the presence of potassium (1978) (0)
Comparative Investigation of O2 Delivery Pathwys in A-Type and B-Type Cytochrome C Oxidases (2013) (0)
Resonance Raman spectroscopy of cytochrome d oxidase (1991) (0)
Correction to The Semiquinone at the Qi Site of the bc1 Complex Explored Using HYSCORE Spectroscopy and Specific Isotopic Labeling of Ubiquinone in Rhodobacter sphaeroides via 13C Methionine and Construction of a Methionine Auxotroph (2015) (0)
Site-directed mutagenesis studies on subunit I of the -type cytochrome oxidase of : a brief review of progress to date (1992) (0)
2I1436 Optimization of expression condition and purification of cbb_3-type cytochrome c oxidase(Heme proteins 2,The 48th Annual Meeting of the Biophysical Society of Japan) (2011) (0)
Cytochrome bd oxidase from Escherichia coli is a quinol peroxidase mechanistically adjusted to protecting the cell from hydrogen peroxide (2014) (0)
S11.8 The coupling of electron and proton transfer in haem copper oxidases as studied by peldor spectroscopy (2008) (0)
Regulation ofExpression oftheCytochrome dTerminal Oxidase in Escherichia coli IsTranscriptional (1988) (0)
E.COLIMAPt Physical MapLocations ofGenesEncoding Components ofthe Aerobic Respiratory ChainofEscherichia coli (1991) (0)
Comparative pH and temperature dependent studies on different types of terminal oxidases by protein film voltammetry (2014) (0)
Proton pumping in cytochrome c oxidase — An explicit gating mechanism based on experimental information, electrostatic considerations and QM calculations (2012) (0)
Erratum: (Biochemistry (September 26, 1995) 34 (12144-12151)) (1996) (0)
Dynamics of Internal water molecules of bacteriorhodopsin : a low temperature FTIR study. (1999) (0)
Electrochemical analysis of cytochrome ba3 from T. thermophilus immobilized on gold nanoparticles (2012) (0)
What a Book on Cell Ultrastructure Should Not Be (1989) (0)
Protein Dynamics Coupled to Electron Transfer in Cytochrome C Oxidase from R. Sphaeroides by Time-Resolved Surface-Enhanced 2D-IR-Absorption Spectroscopy (2012) (0)
Kinetics of the Cytochrome C Oxidase from R. Sphaeroidis Under Turn-Over Conditions by Time-Resolved Surface-Enhanced Infrared Absorption Spectroscopy (SEIRas) (2011) (0)
The Monoheme c Subunit of Respiratory Alternative Complex III Is Not Essential for Electron Transfer to Cytochrome aa3 in Flavobacterium johnsoniae (2021) (0)
Using EPR up close and from afar: Elucidating mechanisms in haem copper oxidases (2010) (0)
Structure of the Alternative Complex III from Flavobacterium johnsoniae in a Supercomplex with Cytochrome c Oxidase (2020) (0)
Structure of Alternative Complex III from Flavobacterium johnsoniae (Wild Type) (2018) (0)
CydX is a subunit of Escherichia coli cytochrome bd terminal oxidase and essential for assembly and stability of the di-heme active site (2014) (0)
A comparative study of low-temperature and time resolved FTIR difference spectra of cytochrome oxidases (1997) (0)
Exploring the Proton Channels of Cytochrome Oxidase (1998) (0)
E.coli pyruvate oxidase: a hysteretic enzyme (1984) (0)
Investigation of the proton pump and exit pathway in cytochrome ba3 from Thermus thermophilus (2012) (0)
Proposed Structure (I) for the Prosthetic Group of the Catalase HPII from Escherichia coli (1989) (0)
Cytochrome bd-II from aerobic respiratory chain of Escherichia coli is a proton-motive force generator (2012) (0)
Time-Resolved Electrometric Study of the F→O Transition in Cytochrome c Oxidase. The Effect of Zn2+ Ions on the Positive Side of the Membrane (2021) (0)
High resolution structure of DsbB C41S by joint calculation with solid-state NMR and X-ray data (2013) (0)
Mechanism of transhydrogenase coupling proton translocation and hydride transfer (2014) (0)
Function of the CcoP (subunit III) in the C-family O2 reductase from Vibrio cholerae (2014) (0)
Water Structural Changes in the L and M Photocycle Intermediates of Bacteriorhodopsin as Revealed by Time-Resolved Step-Scan FTIR Spectroscopy + (2014) (0)
QoxABCD from Staphylococcus aureus can be assembled as either an aa3-type or bo3-type menaquinol oxidase and requires CtaM to function (2016) (0)
The use of mutants to examine the putative proton channels of cytochrome oxidase (1997) (0)
2Q1436 Structural Rearrangement for the Unidirectional Proton Transfer in the Bacteriorhodopsin Photocycle : A Time-resolved FTIR Study(Photobiology: Vision & Photoreception 2,The 48th Annual Meeting of the Biophysical Society of Japan) (2011) (0)
Mechanism of proton transfer through the K C proton pathway in the Vibrio cholerae cbb 3 terminal oxidase dynamics in the (2018) (0)
Direct evidence for Acanthamoeba castellanii alternative oxidase gene function (2012) (0)
WITHDRAWN: Characterization of the supercomplex formed by the alternative complex III and the terminal aa3 oxidase from Flavobacterium johnsoniae isolated in styrene:maleic acid copolymer nanodiscs. (2018) (0)
Respiration in Archaea and Bacteria: Diversity of Prokaryotic Electron Transport Carriers. Davide Zannoni, Advances in Photosynthesis and Respiration (Series Editor, Govindjee), Kluwer Academic Publishers, Dordrecht, The Netherlands, Volume 15, 2004, 350 pp, ISBN 1-4020-2001-5, Price EUR 175.00, USD (2005) (0)
Functionality of Single-Cysteine Mutants in Subunit III of Rhodobacter sphaeroides Cytochrome c Oxidase (2009) (0)
How Electron Transfer Is Linked to Conformational Transitions of Peptide Groups of the Cytochrome C Oxidase, a Study By 2d-Ir Spectro-Electrochemistry (2010) (0)
2PT155 Oxygen consumption activity of cbb_3-type cytochrome c oxidase(The 50th Annual Meeting of the Biophysical Society of Japan) (2012) (0)
Metal center ligation and proton pumping in cytochrome c oxidase (1993) (0)
Catalytic Activity of Cytochrome c Oxidase in a Biomimetic Surface Platform Investigated by Spectro-Electrochemistry (2009) (0)
Referees in 1993 (1993) (0)
2P-265 The lifetimes of pharaonis phoborhodopsin signaling states depend on the rates of proton transfers(The 46th Annual Meeting of the Biophysical Society of Japan) (2008) (0)
Choreography and architecture of the proton-pumping machinery in respiratory oxidases (2014) (0)
The superfamily of heme–copper oxidoreductases: Diversity and mechanism (2014) (0)
THE TISSUE FACTOR-FACTOR VII(a) COMPLEX IN BLOOD COAGULATION BY KE KE DISSERTATION Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biochemistry in the Graduate College of the University of Illinois at Urbana-Champaign, 2013 (2013) (0)
Characterization of the semiquinone radical stabilized by the cytochrome aa3-600 menaquinol oxidase of Bacillus subtilis (2010) (0)
X-ray Structure of the proton-pumping cytochrome aa3-600 menaquinol oxidase from Bacillus subtilis complexed with 3-iodo-N-oxo-2-heptyl-4-hydroxyquinoline (2020) (0)
Final Conference Proceedings Report (2007) (0)
2PT156 Purification of cbb_3-type cytochrome c oxidase(The 50th Annual Meeting of the Biophysical Society of Japan) (2012) (0)
Molecular characterization of the nitric oxide reductase from Thermus thermophilus (2012) (0)
Structure of the Alternative Complex III from Flavobacterium johnsoniae in a Supercomplex with Cytochrome c Oxidase (2021) (0)
Protein kinetics via UV/VIS and FTIR imaging on chip (2005) (0)
Partial Steps of Charge Translocation in the Non-Pumping Mutant N139L of Rhodobacter Sphaeroides Cytochrome C Oxidase with a Blocked D-Channel (2010) (0)
Replacing Arg70 by Histidine in The Cytochrome Aa3‐600 Menaquinol Oxidase from Bacillus Subtilis Changes The Nitrogen Interacting with The Semiquinone Formed at The Qh Site But Does Not Eliminate Catalytic Function (2015) (0)
Water as a Cofactor in the Unidirectional Light‐Driven Proton Transfer Steps in Bacteriorhodopsin † (2006) (0)
TIME-RESOLVED GENERATION OF MEMBRANE POTENTIAL BY BA3 CYTOCHROME C OXIDASE FROM THERMUS THERMOPHILUS COUPLED TO THE SINGLE ELECTRON INJECTION INTO THE OH STATE (2020) (0)
The electron distribution in the “activated” state of cytochrome c oxidase (2018) (0)
Resonance Raman Investigation of the R481 Mutants of Cytochrome c Oxidase from R. sphaeroides (2009) (0)
Spectroscopic Investigation of the Roles of F282 and W172 in the Ligand Pathway of Aa3 Cytochrome C Oxidase from Rhodobacter Sphaeroides (2014) (0)
Studies on E445A mutant cytochrome bd oxidase suggest the sequence of hemes in intraprotein electron transfer needs to be revised (2004) (0)
Microfluidic platforms for (Membrane) protein crystallization (2008) (0)
PNAS Plus Significance Statements (2015) (0)
A comparative study of the proton-translocating activities of cytochrome c oxidase from Rhodopseudomonas spheroides and from bovine heart (1982) (0)
Conformational Transitions Associated with Electrochemically-Induced Redox Processes Through the Cytochrome C Oxidase Followed by Time-Resolved 2d-Surface-Enhanced Infrared Absorption Spectroscopy (tr-2d-Seiras) (2010) (0)
Characterization of monoclonal antibodies directed against pyruvate oxidase from Escherichia coli: modulation of antibody-induced inhibition by enzyme conformation. (1986) (0)
The unusual redox properties of the cytochrome cbb3 oxidases from various organisms and their similarity to NO reductases (2016) (0)
Crystal structure of Thermus thermophilis transhydrogeanse domain II dimer (2014) (0)
Researchfeedback-based gene circuit to increase the production of a membrane protein (2010) (0)
Studies of macromolecular structure using fluorescence energy transfer and circular dichroism. (1971) (0)
Transhydrogenase coupling proton translocation and hydride transfer (2014) (0)
Structure of the alternative complex III in a supercomplex with cytochrome oxidase (2018) (0)
C2/2 Rapid kinetic studies of electron transfer in cytochrome oxidase (2008) (0)
James A. Fee 1941–2012 (2012) (0)
Resolving the mechanism of proton pumping coupled to hydride transfer in E. coli Transhydrogenase (2018) (0)
X-ray Structure of the proton-pumping cytochrome aa3-600 menaquinol oxidase from Bacillus subtilis (2020) (0)
1P248 One-way proton transport in bacteriorhodopsin is modulated by changes in the interaction of the Schiff base with water molecules (2004) (0)
Characterizations of Substrate Delivery Pathways in the Nitric Oxide Reductase (2016) (0)
Crystal structure of Thermus thermophilus transhydrogenase heterotrimeric complex of the Alpha1 subunit dimer with the NADP binding domain (domain III) of the Beta subunit in P2(1) (2014) (0)
Quinol oxidases in the superfamily of heme-copper oxidoreductases and the cryoEM structure of the cytochrome bo3 ubiquinol oxidase from E. coli (2022) (0)
P/21 The proton pumping heme-copper oxidases (2008) (0)
Protein kinetics via spectroscopic imaging on a microfluidic chip (2005) (0)
Davide Zannoni (Editor), Respiration in Archaea and Bacteria: Diversity of Prokaryotic Respiratory Systems. Govindjee (Series Editor) Advances in Photosynthesis and Respiration, 310 pages (2006) (0)
The role of acidic residues at the orifice of a proton pathway in cytochrome c oxidase (2013) (0)
Crystal structure of Thermus thermophilis transhydrogeanse domain II dimer SeMet derivative (2014) (0)
Functional importance of residues predicted to be near the bimetallic center of the heme-copper oxidases— a summary of recent results (1995) (0)
Adaptation of aerobic respiration to low O2 environments (Proceedings of the National Academy of Sciences of the United States of America (2011) 108, 34, (14109-14114) DOI: 10.1073/pnas.1018958108) (2012) (0)
Q-band ENDOR reveals out of plane hydrogen bonds stabilize an anionic ubisemiquinone in cytochrome bo 3 from Escherichia coli (2017) (0)

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