William T. Wickner
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American biochemist
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William T. Wicknerbiology Degrees
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Molecular Biology
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Biology
William T. Wickner's Degrees
- Bachelors Biochemistry University of California, Berkeley
- PhD Biochemistry Stanford University
Why Is William T. Wickner Influential?
(Suggest an Edit or Addition)According to Wikipedia, William T. Wickner , is an authority on membrane fusion, a fundamental process in all eukaryotic cells. Education Bill Wickner, brother of prion biologist Reed Wickner and Cornell graduate Nancy Wickner Kogan, is a 1967 graduate of Yale University and a 1973 M.D. graduate of Harvard Medical School. At Harvard, he worked with Eugene P. Kennedy.
William T. Wickner'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
- SecA promotes preprotein translocation by undergoing ATP-driven cycles of membrane insertion and deinsertion (1994) (569)
- Sec18p (NSF)-Driven Release of Sec17p (α-SNAP) Can Precede Docking and Fusion of Yeast Vacuoles (1996) (560)
- Multiple mechanisms of protein insertion into and across membranes. (1985) (548)
- The binding cascade of SecB to SecA to SecY E mediates preprotein targeting to the E. coli plasma membrane (1990) (547)
- The ATPase activity of secA is regulated by acidic phospholipids, secY, and the leader and mature domains of precursor proteins (1990) (532)
- The purified E. coli integral membrane protein SecY E is sufficient for reconstitution of SecA-dependent precursor protein translocation (1990) (516)
- A Ypt/Rab effector complex containing the Sec1 homolog Vps33p is required for homotypic vacuole fusion. (2000) (472)
- Homotypic vacuolar fusion mediated by t- and v-SNAREs (1997) (460)
- Δμ H+ and ATP function at different steps of the catalytic cycle of preprotein translocase (1991) (453)
- Protein Translocation Across Biological Membranes (2005) (427)
- The enzymology of protein translocation across the Escherichia coli plasma membrane. (1991) (410)
- SecA protein hydrolyzes ATP and is an essential component of the protein translocation ATPase of Escherichia coli. (1989) (356)
- Defining the functions of trans-SNARE pairs (1998) (340)
- The assembly of proteins into biological membranes: The membrane trigger hypothesis. (1979) (331)
- SecA membrane cycling at SecYEG is driven by distinct ATP binding and hydrolysis events and is regulated by SecD and SecF (1995) (325)
- Distinct catalytic roles of the SecYE, SecG and SecDFyajC subunits of preprotein translocase holoenzyme (1997) (304)
- The GTPase Ypt7p of Saccharomyces cerevisiae is required on both partner vacuoles for the homotypic fusion step of vacuole inheritance. (1995) (276)
- Three pure chaperone proteins of Escherichia coli‐‐SecB, trigger factor and GroEL‐‐form soluble complexes with precursor proteins in vitro. (1989) (269)
- Leader peptidase catalyzes the release of exported proteins from the outer surface of the Escherichia coli plasma membrane. (1985) (269)
- Membrane fusion: five lipids, four SNAREs, three chaperones, two nucleotides, and a Rab, all dancing in a ring on yeast vacuoles. (2010) (265)
- Sequence of the leader peptidase gene of Escherichia coli and the orientation of leader peptidase in the bacterial envelope. (1983) (253)
- A Vacuolar v–t-SNARE Complex, the Predominant Form In Vivo and on Isolated Vacuoles, Is Disassembled and Activated for Docking and Fusion (1998) (253)
- Purification of active HOPS complex reveals its affinities for phosphoinositides and the SNARE Vam7p (2006) (246)
- Docking of Yeast Vacuoles Is Catalyzed by the Ras-like GTPase Ypt7p after Symmetric Priming by Sec18p (NSF) (1997) (239)
- A direct role for the Sec1/Munc18-family protein Vps33 as a template for SNARE assembly (2015) (233)
- Vacuole Fusion at a Ring of Vertex Docking Sites Leaves Membrane Fragments within the Organelle (2002) (220)
- The Docking Stage of Yeast Vacuole Fusion Requires the Transfer of Proteins from a Cis-Snare Complex to a Rab/Ypt Protein (2000) (219)
- The SecDFyajC domain of preprotein translocase controls preprotein movement by regulating SecA membrane cycling (1997) (219)
- Multiple methods of visualizing the yeast vacuole permit evaluation of its morphology and inheritance during the cell cycle (1987) (219)
- Interdependent assembly of specific regulatory lipids and membrane fusion proteins into the vertex ring domain of docked vacuoles (2004) (204)
- Yeast homotypic vacuole fusion: a window on organelle trafficking mechanisms. (2000) (204)
- Trigger factor: a soluble protein that folds pro-OmpA into a membrane-assembly-competent form. (1987) (204)
- Sec18p (NSF)-driven release of Sec17p (alpha-SNAP) can precede docking and fusion of yeast vacuoles. (1996) (202)
- Assembly of proteins into membranes. (1980) (202)
- Purification and characterization of leader (signal) peptidase from Escherichia coli. (1980) (193)
- RNA synthesis initiates in vitro conversion of M13 DNA to its replicative form. (1972) (184)
- The SecA and SecY subunits of translocase are the nearest neighbors of a translocating preprotein, shielding it from phospholipids. (1993) (181)
- Functional reconstitution of bacterial Tat translocation in vitro (2001) (179)
- Organelle Inheritance (1996) (177)
- Effects of two sec genes on protein assembly into the plasma membrane of Escherichia coli. (1985) (173)
- Remodeling of organelle-bound actin is required for yeast vacuole fusion (2002) (172)
- Homotypic vacuole fusion requires Sec17p (yeast alpha‐SNAP) and Sec18p (yeast NSF). (1996) (171)
- Genomic analysis of homotypic vacuole fusion. (2002) (169)
- Yeast vacuoles and membrane fusion pathways (2002) (169)
- Three v-SNAREs and Two t-SNAREs, Present in a Pentameric cis-SNARE Complex on Isolated Vacuoles, Are Essential for Homotypic Fusion (1999) (168)
- G-protein ligands inhibit in vitro reactions of vacuole inheritance (1994) (168)
- Reconstituted membrane fusion requires regulatory lipids, SNAREs and synergistic SNARE chaperones (2008) (167)
- SecA protein, a peripheral protein of the Escherichia coli plasma membrane, is essential for the functional binding and translocation of proOmpA. (1989) (163)
- Biogenesis of the Gram-Negative Bacterial Envelope (1997) (160)
- ProOmpA is stabilized for membrane translocation by either purified E. coli trigger factor or canine signal recognition particle (1988) (152)
- The “trigger factor cycle” includes ribosomes, presecretory proteins, and the plasma membrane (1988) (143)
- HOPS proofreads the trans-SNARE complex for yeast vacuole fusion. (2008) (135)
- Hierarchy of protein assembly at the vertex ring domain for yeast vacuole docking and fusion (2003) (134)
- HOPS Initiates Vacuole Docking by Tethering Membranes before trans-SNARE Complex Assembly (2010) (129)
- Synthesis, assembly into the cytoplasmic membrane, and proteolytic processing of the precursor of coliphage M13 coat protein. (1980) (129)
- SecYEG and SecA Are the Stoichiometric Components of Preprotein Translocase (*) (1995) (123)
- Trigger factor depletion or overproduction causes defective cell division but does not block protein export (1990) (123)
- Translocation can drive the unfolding of a preprotein domain. (1993) (122)
- Initiation of DNA synthesis: synthesis of phiX174 replicative form requires RNA synthesis resistant to rifampicin. (1972) (122)
- Sec17p and HOPS, in distinct SNARE complexes, mediate SNARE complex disruption or assembly for fusion (2005) (121)
- In vitro reactions of vacuole inheritance in Saccharomyces cerevisiae (1992) (120)
- Phosphatidylinositol 4,5-bisphosphate regulates two steps of homotypic vacuole fusion. (2000) (119)
- The isolation of homogeneous leader peptidase from a strain of Escherichia coli which overproduces the enzyme. (1982) (119)
- Procoat, the precursor of M13 coat protein, requires an electrochemical potential for membrane insertion. (1980) (115)
- Rho1p and Cdc42p act after Ypt7p to regulate vacuole docking (2001) (114)
- Vam7p, a vacuolar SNAP‐25 homolog, is required for SNARE complex integrity and vacuole docking and fusion (1998) (114)
- SecY, SecE, and band 1 form the membrane-embedded domain of Escherichia coli preprotein translocase. (1992) (112)
- ProOmpA contains secondary and tertiary structure prior to translocation and is shielded from aggregation by association with SecB protein. (1990) (109)
- Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusion. (1999) (108)
- A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion (2004) (107)
- ProOmpA spontaneously folds in a membrane assembly competent state which trigger factor stabilizes. (1988) (105)
- Isolation of the Escherichia coli leader peptidase gene and effects of leader peptidase overproduction in vivo. (1981) (105)
- SecD and SecF are required for the proton electrochemical gradient stimulation of preprotein translocation. (1994) (105)
- Escherichia coli Preprotein Translocase* (1996) (105)
- Minimal membrane docking requirements revealed by reconstitution of Rab GTPase-dependent membrane fusion from purified components (2009) (105)
- Sequential action of two GTPases to promote vacuole docking and fusion (2000) (102)
- Use of phoA fusions to study the topology of the Escherichia coli inner membrane protein leader peptidase (1989) (101)
- HOPS prevents the disassembly of trans‐SNARE complexes by Sec17p/Sec18p during membrane fusion (2010) (99)
- Mutants of Saccharomyces cerevisiae that block intervacuole vesicular traffic and vacuole division and segregation. (1990) (97)
- Molecular characterization of VAC1, a gene required for vacuole inheritance and vacuole protein sorting. (1992) (96)
- Proteins Needed for Vesicle Budding from the Golgi Complex Are Also Required for the Docking Step of Homotypic Vacuole Fusion (2000) (92)
- Intervacuole exchange in the yeast zygote: a new pathway in organelle communication. (1988) (92)
- M13 procoat and a pre-immunoglobulin share processing specificity but use different membrane receptor mechanisms. (1983) (92)
- Trans-SNARE interactions elicit Ca2+ efflux from the yeast vacuole lumen (2004) (91)
- Diacylglycerol and Its Formation by Phospholipase C Regulate Rab- and SNARE-dependent Yeast Vacuole Fusion* (2004) (89)
- LMA1 Binds to Vacuoles at Sec18p (NSF), Transfers upon ATP Hydrolysis to a t-SNARE (Vam3p) Complex, and Is Released during Fusion (1998) (89)
- Interactions of melittin, a preprotein model, with detergents. (1979) (86)
- Leader peptidase is found in both the inner and outer membranes of Escherichia coli. (1981) (86)
- Mechanisms of membrane assembly: effects of energy poisons on the conversion of soluble M13 coliphage procoat to membrane-bound coat protein. (1980) (84)
- Thioredoxin is required for vacuole inheritance in Saccharomyces cerevisiae (1996) (82)
- Determination of four biochemically distinct, sequential stages during vacuole inheritance in vitro (1994) (81)
- Assays of vacuole fusion resolve the stages of docking, lipid mixing, and content mixing (2007) (81)
- trans-SNARE complex assembly and yeast vacuole membrane fusion (2007) (81)
- Mechanisms of membrane assembly: general lessons from the study of M13 coat protein and Escherichia coli leader peptidase. (1988) (80)
- Excess vacuolar SNAREs drive lysis and Rab bypass fusion (2007) (80)
- The PrlA and PrlG phenotypes are caused by a loosened association among the translocase SecYEG subunits (1999) (79)
- Both an N-terminal 65-kDa domain and a C-terminal 30-kDa domain of SecA cycle into the membrane at SecYEG during translocation. (1997) (79)
- Evaluating the oligomeric state of SecYEG in preprotein translocase (2000) (78)
- Yeast KEX2 protease and mannosyltransferase I are localized to distinct compartments of the secretory pathway (1989) (77)
- The Major Role of the Rab Ypt7p in Vacuole Fusion Is Supporting HOPS Membrane Association*♦ (2009) (76)
- A new form of DNA polymerase 3 and a copolymerase replicate a long, single-stranded primer-template. (1973) (75)
- Membranes linked by trans-SNARE complexes require lipids prone to non-bilayer structure for progression to fusion (2014) (75)
- A Heterodimer of Thioredoxin and IB 2 Cooperates with Sec18p (NSF) to Promote Yeast Vacuole Inheritance (1997) (74)
- The cytoplasmic carboxy terminus of M13 procoat is required for the membrane insertion of its central domain (1986) (73)
- Asymmetric orientation of phage M13 coat protein in Escherichia coli cytoplasmic membranes and in synthetic lipid vesicles. (1976) (72)
- Sec‐dependent membrane protein biogenesis: SecYEG, preprotein hydrophobicity and translocation kinetics control the stop‐transfer function (1998) (72)
- A new role for a SNARE protein as a regulator of the Ypt7/Rab-dependent stage of docking. (2000) (72)
- Conserved residues of the leader peptide are essential for cleavage by leader peptidase. (1985) (71)
- Complex Lipid Requirements for SNARE- and SNARE Chaperone-dependent Membrane Fusion* (2009) (71)
- Bacterial leader peptidase, a membrane protein without a leader peptide, uses the same export pathway as pre-secretory proteins (1984) (71)
- Enolase Activates Homotypic Vacuole Fusion and Protein Transport to the Vacuole in Yeast* (2006) (70)
- A holoenzyme form of deoxyribonucleic acid polymerase III. Isolation and properties. (1974) (70)
- A cascade of multiple proteins and lipids catalyzes membrane fusion (2017) (66)
- The protease‐protected 30 kDa domain of SecA is largely inaccessible to the membrane lipid phase (1997) (63)
- Soluble precursor of an integral membrane protein: synthesis of procoat protein in Escherichia coli infected with bacteriophage M13. (1979) (62)
- Subunit dynamics in Escherichia coli preprotein translocase. (1994) (61)
- The biosynthesis of membrane-bound M13 coat protein. Energetics and assembly intermediates. (1982) (61)
- Proton transfer is rate-limiting for translocation of precursor proteins by the Escherichia coli translocase. (1991) (58)
- Phosphoinositides and SNARE chaperones synergistically assemble and remodel SNARE complexes for membrane fusion (2009) (58)
- How ATP drives proteins across membranes. (1994) (58)
- Asymmetric orientation of a phage coat protein in cytoplasmic membrane of Escherichia coli. (1975) (57)
- A distinct tethering step is vital for vacuole membrane fusion (2014) (57)
- The tethering complex HOPS catalyzes assembly of the soluble SNARE Vam7 into fusogenic trans-SNARE complexes (2013) (56)
- Both hydrophobic domains of M13 procoat are required to initiate membrane insertion. (1986) (54)
- Yeast vacuoles fragment when microtubules are disrupted (1988) (52)
- DNA polymerase 3 star requires ATP to start synthesis on a primed DNA. (1973) (50)
- Protein-lipid interactions. Studies of the M13 coat protein in dimyristoylphosphatidylcholine vesicles using parinaric acid. (1979) (50)
- Leader peptidase of Escherichia coli: critical role of a small domain in membrane assembly. (1987) (49)
- The role of the polar, carboxyl-terminal domain of Escherichia coli leader peptidase in its translocation across the plasma membrane. (1986) (49)
- A lipid-anchored SNARE supports membrane fusion (2011) (48)
- Stringent 3Q·1R Composition of the SNARE 0-Layer Can Be Bypassed for Fusion by Compensatory SNARE Mutation or by Lipid Bilayer Modification* (2007) (47)
- Translational and post-translational cleavage of M13 procoat protein: extracts of both the cytoplasmic and outer membranes of Escherichia coli contain leader peptidase activity. (1979) (47)
- Synthesis of phage M13 coat protein and its assembly into membranes in vitro. (1978) (45)
- The cytoplasmic domain of Escherichia coli leader peptidase is a "translocation poison" sequence. (1988) (45)
- Resolution of organelle docking and fusion kinetics in a cell-free assay. (2004) (45)
- Melittin forms crystals which are suitable for high resolution X-ray structural analysis and which reveal a molecular 2-fold axis of symmetry. (1980) (45)
- Genetic mapping of the Escherichia coli leader (signal) peptidase gene (lep): a new approach for determining the map position of a cloned gene (1983) (45)
- Membrane assembly from purified components. II. Assembly of M13 procoat into liposomes reconstituted with purified leader peptidase (1981) (44)
- Functional reconstitution of ypt7p GTPase and a purified vacuole SNARE complex. (1998) (44)
- Isolation of mutants in M13 coat protein that affect its synthesis, processing, and assembly into phage. (1985) (44)
- Distinct Targeting and Fusion Functions of the PX and SNARE Domains of Yeast Vacuolar Vam7p* (2007) (44)
- Reconstitution of rapid and asymmetric assembly of M13 procoat protein into liposomes which have bacterial leader peptidase. (1983) (43)
- Purified Escherichia coli preprotein translocase catalyzes multiple cycles of precursor protein translocation. (1993) (43)
- Role of hydrophobic forces in membrane protein asymmetry. (1977) (42)
- Recombinant forms of M13 procoat with an OmpA leader sequence or a large carboxy‐terminal extension retain their independence of secY function. (1987) (42)
- Band 1 subunit of Escherichia coli preportein translocase and integral membrane export factor P12 are the same protein. (1994) (41)
- I2B is a small cytosolic protein that participates in vacuole fusion. (1997) (41)
- Sec17 can trigger fusion of trans-SNARE paired membranes without Sec18 (2015) (39)
- Requirements for substrate recognition by bacterial leader peptidase. (1986) (39)
- Endogenous SecA Catalyzes Preprotein Translocation at SecYEG* (1998) (37)
- Sec18p and Vam7p remodel trans‐SNARE complexes to permit a lipid‐anchored R‐SNARE to support yeast vacuole fusion (2007) (37)
- Secretion and membrane assembly. (1989) (35)
- Sec17/Sec18 act twice, enhancing membrane fusion and then disassembling cis-SNARE complexes (2017) (35)
- HOPS catalyzes the interdependent assembly of each vacuolar SNARE into a SNARE complex (2017) (35)
- Solubilization and functional reconstitution of the protein-translocation enzymes of Escherichia coli. (1990) (35)
- The secY protein can act post-translationally to promote bacterial protein export. (1986) (34)
- Membrane assembly: Posttranslational insertion of M13 procoat protein into E. coli membranes and its proteolytic conversion to coat protein in vitro (1981) (33)
- Improved reconstitution of yeast vacuole fusion with physiological SNARE concentrations reveals an asymmetric Rab(GTP) requirement (2016) (33)
- Membrane assembly from purified components. I. Isolated M13 procoat does not require ribosomes or soluble proteins for processing by membranes (1981) (33)
- A truncated form of the Pho80 cyclin redirects the Pho85 kinase to disrupt vacuole inheritance in S. cerevisiae (1995) (32)
- The SecA Subunit of Escherichia coliPreprotein Translocase Is Exposed to the Periplasm (1998) (32)
- Ion Regulation of Homotypic Vacuole Fusion in Saccharomyces cerevisiae* (2005) (31)
- Inhibition of purified Escherichia coli leader peptidase by the leader (signal) peptide of bacteriophage M13 procoat (1987) (31)
- The internal signal sequence of Escherichia coli leader peptidase is necessary, but not sufficient, for its rapid membrane assembly. (1987) (30)
- Phosphorylation of the effector complex HOPS by the vacuolar kinase Yck3p confers Rab nucleotide specificity for vacuole docking and fusion (2012) (30)
- Purification and characterization of leader peptidase from Escherichia coli. (1983) (30)
- Yeast vacuolar HOPS, regulated by its kinase, exploits affinities for acidic lipids and Rab:GTP for membrane binding and to catalyze tethering and fusion (2015) (29)
- Vam10p defines a Sec18p-independent step of priming that allows yeast vacuole tethering (2003) (28)
- Reversible, cooperative reactions of yeast vacuole docking (2006) (28)
- M13 coat protein as a model of membrane assembly (1983) (26)
- The nascent-polypeptide-associated complex: having a "NAC" for fidelity in translocation. (1995) (25)
- HOPS recognizes each SNARE, assembling ternary trans-complexes for rapid fusion upon engagement with the 4th SNARE (2020) (22)
- Procoat, the precursor of M13 coat protein, inserts post-translationally into the membrane of cells infected by wild-type virus (1981) (21)
- The leader region of pre-maltose binding protein binds amphiphiles. A model for self-assembly in protein export. (1985) (21)
- A novel form of RNA polymerase from Escherichia coli. (1974) (21)
- Phosphoinositides Function Asymmetrically for Membrane Fusion, Promoting Tethering and 3Q-SNARE Subcomplex Assembly* (2010) (20)
- The role of the mature domain of proOmpA in the translocation ATPase reaction. (1992) (19)
- Processing of preproteins by liposomes bearing leader peptidase. (1984) (19)
- Bem1p Is a Positive Regulator of the Homotypic Fusion of Yeast Vacuoles* (2006) (18)
- Fusion Proteins and Select Lipids Cooperate as Membrane Receptors for the Soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (SNARE) Vam7p* (2013) (18)
- N-terminal domain of vacuolar SNARE Vam7p promotes trans-SNARE complex assembly (2012) (16)
- Characterization of the internal signal-anchor domain of Escherichia coli leader peptidase. (1988) (16)
- Tethering guides fusion-competent trans-SNARE assembly (2019) (12)
- Fractionation of membrane vesicles from coliphage M13-infected Escherichia coli (1976) (12)
- Sec17/Sec18 can support membrane fusion without help from completion of SNARE zippering (2021) (11)
- Membrane-associated assembly of M13 phage in extracts of virus-infected Escherichia coli. (1977) (11)
- A short region upstream of the yeast vacuolar Qa-SNARE heptad-repeats promotes membrane fusion through enhanced SNARE complex assembly (2017) (10)
- A truncated form of the Pho80 cyclin of Saccharomyces cerevisiae induces expression of a small cytosolic factor which inhibits vacuole inheritance (1996) (9)
- Studies of asymmetric membrane assembly. (1977) (9)
- Organelle inheritance in a test tube: the yeast vacuole (1996) (8)
- Sec17 (α-SNAP) and Sec18 (NSF) restrict membrane fusion to R-SNAREs, Q-SNAREs, and SM proteins from identical compartments (2019) (7)
- Profile of Thomas Südhof, James Rothman, and Randy Schekman, 2013 Nobel Laureates in Physiology or Medicine (2013) (6)
- Bacterial Protein Translocation (1988) (6)
- The purification of M13 procoat, a membrane protein precursor. (1982) (6)
- Chris Raetz, scientist and enduring friend (2011) (5)
- Asymmetric Rab activation of vacuolar HOPS to catalyze SNARE complex assembly (2020) (5)
- Christian Raetz: scientist and friend extraordinaire. (2013) (5)
- Assembly of intermediates for rapid membrane fusion (2017) (4)
- In vitro insertion of leader peptidase into Escherichia coli membrane vesicles (1988) (4)
- THE THREE LIVES OF M13 COAT PROTEIN: A VIRION CAPSID, AN INTEGRAL MEMBRANE PROTEIN, AND A SOLUBLE CYTOPLASMIC PROPROTEIN * (1980) (4)
- Phosphatidylinositol and phosphatidylinositol-3-phosphate activate HOPS to catalyze SNARE assembly, allowing small headgroup lipids to support the terminal steps of membrane fusion (2021) (4)
- Eugene Patrick Kennedy, 1919–2011 (2011) (3)
- Role of M13 Gene 1 Protein in Filamentous Virus Assembly (1980) (3)
- Fusion with wild-type SNARE domains is controlled by juxtamembrane domains, transmembrane anchors, and Sec17 (2022) (3)
- Fusion proteins and select lipids cooperate as membrane receptors for the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) Vam7p. (2013) (3)
- Fusion of tethered membranes can be driven by Sec18/NSF and Sec17/αSNAP without HOPS (2021) (2)
- On the road to translocase. (1995) (2)
- Correction: Membranes linked by trans-SNARE complexes require lipids prone to non-bilayer structure for progression to fusion (2015) (2)
- A Rab prenyl membrane-anchor allows effector recognition to be regulated by guanine nucleotide (2020) (1)
- [4] Molecular genetics of Escherichia coli leader peptidase (1983) (1)
- Analysis of M13 procoat assembly into membranes in vitro. (1983) (1)
- Vacuole Division and Inheritance in Saccharomyces Cerevisiae (1988) (0)
- Initiation of DNA Synthesis: Requires RNA Synthesis Resistant to Rifampicin* Synthesis of 4x174 Replicative Form (dd gene product/dnaB gene product/Ml3 DNA/spermidine) (1979) (0)
- Homotypic Vacuole Fusion Occurs by Sequential Priming, Docking and Fusion Reactions. Priming Frees (0)
- UseofphoAFusions ToStudytheTopology oftheEscherichia coli InnerMembraneProtein Leader Peptidase (1989) (0)
- Author response: Sec17/Sec18 act twice, enhancing membrane fusion and then disassembling cis-SNARE complexes (2017) (0)
- HOPS recognizes each SNARE, assembling ternary trans-complexes for sudden fusion upon engagement with the 4th SNARE (2019) (0)
- Vacuole Inheritance: A New Window on Interorganelle Traffic (1998) (0)
- ProOmpAcontains secondary andtertiary structure prior totranslocation andisshielded fromaggregation by association withSecBprotein (1990) (0)
- Reconstitution of E. Coli Preprotein Translocation using Purified Components (1992) (0)
- Author response: A distinct tethering step is vital for vacuole membrane fusion (2014) (0)
- Molecular genetics of Escherichia coli leader peptidase. (1983) (0)
- E. coli preprotein translocase: A 6 stroke engine with 2 fuels and 2 piston rods (1996) (0)
- Pulse-labeling studies of membrane assembly and protein secretion in intact cells: M13 coat protein. (1983) (0)
- TheGTPaseYpt7pofSaccharomyces cerevisiae is required on bothpartner vacuoles forthehomotypic fusion stepofvacuole inheritance (1995) (0)
- A Reductionist Approach to Understanding Membrane Fusion (2017) (0)
- Studies of the Path of Assembly of Bacteriophage M13 Coat Protein Into the Escherichia coli Cytoplasmic Membrane (1980) (0)
- Author response: HOPS recognizes each SNARE, assembling ternary trans-complexes for rapid fusion upon engagement with the 4th SNARE (2020) (0)
- Mechanisms of membrane assembly : Effects of energy poisons on the conversion of soluble M 13 coliphage procoat to membrane-bound coat protein ( leader peptidase / membrane potential / integral membrane protein / uncoupler-resistant mutants / membrane trigger hypothesis ) (0)
- Sec18 supports membrane fusion by promoting Sec17 membrane association (2022) (0)
- Organelle Inheritance in Budding Yeast (1994) (0)
- PI3P regulates multiple stages of membrane fusion (2023) (0)
- Asymmetric orientation of phage M 13 coat protein in Escherichia coli cytoplasmic membranes and in synthetic lipid vesicles ( virus structure / membrane assembly ) (0)
- Mechanisms of secretion and membrane assembly (1987) (0)
- Membrane Fusion can be Driven by Sec18/NSF, Sec17/αSNAP, and trans-SNARE complex without HOPS (2021) (0)
- Author response: Fusion of tethered membranes can be driven by Sec18/NSF and Sec17/αSNAP without HOPS (2021) (0)
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