about
P184
Rotating with the brakes on and other unresolved features of the vacuolar ATPaseThe cellular response to vascular endothelial growth factors requires co-ordinated signal transduction, trafficking and proteolysisFlexibility within the rotor and stators of the vacuolar H+-ATPaseExpression, purification and secondary structure analysis of Saccharomyces cerevisiae vacuolar membrane H+-ATPase subunit F (Vma7p).Cryo-electron microscopy of the vacuolar ATPase motor reveals its mechanical and regulatory complexitySubunit positioning and stator filament stiffness in regulation and power transmission in the V1 motor of the Manduca sexta V-ATPase.PA1b inhibitor binding to subunits c and e of the vacuolar ATPase reveals its insecticidal mechanismStructure and function of the vacuolar H+-ATPase: moving from low-resolution models to high-resolution structures.Structural divergence of the rotary ATPases.Vascular endothelial growth factors: multitasking functionality in metabolism, health and disease.Extracellular and Luminal pH Regulation by Vacuolar H+-ATPase Isoform Expression and Targeting to the Plasma Membrane and Endosomes.VEGFR2 Trafficking, Signaling and Proteolysis is Regulated by the Ubiquitin Isopeptidase USP8.An expanded and flexible form of the vacuolar ATPase membrane sector.VEGF-A isoforms program differential VEGFR2 signal transduction, trafficking and proteolysis.Structure of the vacuolar H+-ATPase rotary motor reveals new mechanistic insightsUbiquitination of basal VEGFR2 regulates signal transduction and endothelial function.Interaction of spin-labeled inhibitors of the vacuolar H+-ATPase with the transmembrane Vo-sector.Interaction of inhibitors of the vacuolar H(+)-ATPase with the transmembrane Vo-sector.A site-directed cross-linking approach to the characterization of subunit E-subunit G contacts in the vacuolar H+-ATPase stator.Incorporation of transmembrane peptides from the vacuolar H(+)-ATPase in phospholipid membranes: spin-label electron paramagnetic resonance and polarized infrared spectroscopy.Concanamycin and indolyl pentadieneamide inhibitors of the vacuolar H+-ATPase bind with high affinity to the purified proteolipid subunit of the membrane domain.Motivations for donating blood and reasons why people lapse or never donate in Leeds, England: a 2001 questionnaire-based survey.Defined sites of interaction between subunits E (Vma4p), C (Vma5p), and G (Vma10p) within the stator structure of the vacuolar H+-ATPase.Receptor Tyrosine Kinase Ubiquitination and De-Ubiquitination in Signal Transduction and Receptor Trafficking.New biophysical probes for structure-activity analyses of vacuolar-H+ -ATPase enzymes.Identification of lipid-accessible sites on the nephrops 16-kDa proteolipid incorporated into a hybrid vacuolar H(+)-ATPase: site-directed labeling with N-(1-Pyrenyl)cyclohexylcarbodiimide and fluorescence quenching analysis.Helical interactions and membrane disposition of the 16-kDa proteolipid subunit of the vacuolar H(+)-ATPase analyzed by cysteine replacement mutagenesis.Cyanobacterial thylakoid membrane proteins are reversibly phosphorylated under plastoquinone-reducing conditions in vitro.Modification of a glnB-like gene product by photosynthetic electron transport in the cyanobacterium Synechococcus 6301.Structure and localization of an essential transmembrane segment of the proton translocation channel of yeast H+-V-ATPaseRemuneration for blood donation and attitudes towards blood donation and receipt in Leeds
P50
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P50
description
hulumtues
@sq
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Michael A. Harrison
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P6366
P106
P1153
7401595128
P185
P21
P31
P496
0000-0002-7826-7472
P6178
01206556310.38
P6366
2129865978