Structural basis for catalytic and inhibitory mechanisms of human prostaglandin reductase PTGR2Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor bindingCrystal structures of human glutaminyl cyclase, an enzyme responsible for protein N-terminal pyroglutamate formation.Homodimeric hexaprenyl pyrophosphate synthase from the thermoacidophilic crenarchaeon Sulfolobus solfataricus displays asymmetric subunit structures.Structure of a heterotetrameric geranyl pyrophosphate synthase from mint (Mentha piperita) reveals intersubunit regulationMechanism of action and inhibition of dehydrosqualene synthaseA cholesterol biosynthesis inhibitor blocks Staphylococcus aureus virulenceStructural and functional roles of glycosylation in fungal laccase from Lentinus spThe hexameric structures of human heat shock protein 90Determinants of the inhibition of a Taiwan habu venom metalloproteinase by its endogenous inhibitors revealed by X-ray crystallography and synthetic inhibitor analoguesThe 1.35 A structure of cadmium-substituted TM-3, a snake-venom metalloproteinase from Taiwan habu: elucidation of a TNFalpha-converting enzyme-like active-site structure with a distorted octahedral geometry of cadmiumCrystal structure of actinomycin D bound to the CTG triplet repeat sequences linked to neurological diseasesThe Refined Crystal Structure of an Eel Pout Type III Antifreeze Protein RD1 at 0.62-Å Resolution Reveals Structural Microheterogeneity of Protein and SolvationCrystal structure of yeast cytosine deaminase. Insights into enzyme mechanism and evolutionCatalytic mechanism revealed by the crystal structure of undecaprenyl pyrophosphate synthase in complex with sulfate, magnesium, and tritonCrystal Structure of the Hyperthermophilic Archaeal DNA-Binding Protein Sso10b2 at a Resolution of 1.85 AngstromsCrystal structure of a platelet-agglutinating factor isolated from the venom of Taiwan habu (Trimeresurus mucrosquamatus)Crystal structure of octaprenyl pyrophosphate synthase from hyperthermophilic Thermotoga maritima and mechanism of product chain length determinationThe functional role of the binuclear metal center in D-aminoacylase: one-metal activation and second-metal attenuationEnzyme-substrate interactions revealed by the crystal structures of the archaeal Sulfolobus PTP-fold phosphatase and its phosphopeptide complexesCrystal structure of the left-handed archaeal RadA helical filament: identification of a functional motif for controlling quaternary structures and enzymatic functions of RecA family proteinsBisphosphonates target multiple sites in both cis- and trans-prenyltransferasesThe crystal structure of XC1258 from Xanthomonas campestris: a putative procaryotic Nit protein with an arsenic adduct in the active siteStructural and Functional Analyses of Five Conserved Positively Charged Residues in the L1 and N-Terminal DNA Binding Motifs of Archaeal RadA ProteinStructural basis of mercury- and zinc-conjugated complexes as SARS-CoV 3C-like protease inhibitorsA conserved hydrogen-bond network in the catalytic centre of animal glutaminyl cyclases is critical for catalysisCrystal structure of IcaR, a repressor of the TetR family implicated in biofilm formation in Staphylococcus epidermidisStructure-Based Inhibitors Exhibit Differential Activities againstHelicobacter pyloriandEscherichia coliUndecaprenyl Pyrophosphate SynthasesStructures of a potent phenylalkyl bisphosphonate inhibitor bound to farnesyl and geranylgeranyl diphosphate synthasesCrystal structure of the C-terminal domain of a flagellar hook-capping protein from Xanthomonas campestrisInhibition of Geranylgeranyl Diphosphate Synthase by Bisphosphonates: A Crystallographic and Computational Investigation †Cysteine S-Nitrosylation Protects Protein-tyrosine Phosphatase 1B against Oxidation-induced Permanent InactivationThe first crystal structure of gluconolactonase important in the glucose secondary metabolic pathwaysCrystal structure of RecX: a potent regulatory protein of RecA from Xanthomonas campestrisWhite spot syndrome virus protein ICP11: A histone-binding DNA mimic that disrupts nucleosome assemblyXC1028 from Xanthomonas campestris adopts a PilZ domain-like structure without a c-di-GMP switchStructural Basis of Inhibition Specificities of 3C and 3C-like Proteases by Zinc-coordinating and Peptidomimetic CompoundsThree New Structures of Left-Handed RadA Helical Filaments: Structural Flexibility of N-Terminal Domain Is Critical for Recombinase ActivityLipophilic Bisphosphonates as Dual Farnesyl/Geranylgeranyl Diphosphate Synthase Inhibitors: An X-ray and NMR InvestigationStructure, assembly, and mechanism of a PLP-dependent dodecameric L-aspartate beta-decarboxylase
P50
Q24313365-CED0CFE6-01C4-4F7F-B6E3-2908875B08DCQ24338927-15CBE491-3091-40BE-AD73-8AB8C66CF427Q24532111-2A70A177-4A94-415D-B321-83E6F0EFB20CQ24535031-EFF2635C-4563-451A-B3FC-E9C8E7548A07Q24614031-3E7A6DEC-EF62-4803-B9D8-86064952BFA0Q24628816-8AD162C7-A329-4D49-8DED-0DA22D72EEC3Q24650591-E909DEA1-B470-42B2-BFCD-4850C2CF8718Q27311374-E2B8615D-1C8D-47FB-B5D3-B0B7F8DC4BC6Q27340111-10CC15B3-96EF-4550-A4C1-73367123B2E2Q27639192-72D4C0A6-2341-49A2-BBFF-C2380443ACA1Q27639199-EF2D9EBB-FD5E-4365-9B8B-AEAC08F648EEQ27639967-92147A2B-4BE2-480A-83CA-82444B12513CQ27640357-254A1ED9-613B-4DC8-88F1-55CD33AE62D3Q27640699-33CA781A-2874-4710-8020-4AF7AEC54A4CQ27641294-74B0A9B3-B8E6-4CE7-B501-39A38EA609F1Q27641584-257B978D-5501-4031-B4FA-B8213F4A9818Q27642529-B094F5FD-A509-4BCC-8F35-DCC93E7A9BF6Q27642538-D94C2E16-4985-4863-9C07-9EBFCEF66348Q27643008-B9FE4F8D-7670-471D-B5ED-AF22B8F79755Q27643332-2F1DC4A4-BBE7-4E13-BA6A-B76688C6F076Q27643938-747866A0-AE53-4D7E-9314-7E3AC771A1E8Q27645000-E4956494-97D2-4DBA-A878-4F26891C4AF6Q27646808-8C5BC0F1-9E6F-4338-93FC-CF0E3F7AE2F6Q27648064-D2B33B33-3CA9-4A73-8BD9-4C723FB8C115Q27648952-5D65B860-8A52-492A-9DDC-CF147459EEDAQ27649277-A826A008-D879-484F-8469-D7B793229824Q27649569-11196EB8-5799-4AC3-ABE6-6BC42A1D6009Q27650204-E5E144A5-6468-434F-A608-374161A9FA74Q27650471-C3F80E9B-5D80-4A75-B346-1DC0CF9CC0D3Q27651027-0A23625F-328A-4A19-867A-88BCFA916609Q27652214-4698D762-F883-47D7-AE01-F01DB04A44BBQ27652444-06C5C6F4-3A7F-45AF-B543-B27F32BEEBE7Q27652481-17519789-EF70-4D68-9BFC-A4114ED881ADQ27652872-57631AF2-998E-49EB-8315-A0C5A6227705Q27653182-33A029A0-A74B-4B1B-B0DE-B202ED06B271Q27653355-D918B1B0-DCC9-40BF-A913-A06A02FA8AF9Q27653428-88FD02D6-C95B-449A-89D5-41CAD7518F0AQ27654195-2EAB953A-DFE2-4E00-AB95-E062CA710FEFQ27654261-A439010F-4246-4CC3-86DB-37E98C51F31BQ27654766-A3910013-ED92-40C9-BB29-E53421D15DD8
P50
description
Taiwanese biochemist (born 1945)
@en
farmacoloog
@nl
name
Andrew H.-J. Wang
@ast
Andrew H.-J. Wang
@en
Andrew H.-J. Wang
@es
王惠鈞
@zh
type
label
Andrew H.-J. Wang
@ast
Andrew H.-J. Wang
@en
Andrew H.-J. Wang
@es
王惠鈞
@zh
altLabel
Andrew Wang
@en
Wang AH
@en
Wang Hui-jun
@en
Wáng Huìjūn
@en
prefLabel
Andrew H.-J. Wang
@ast
Andrew H.-J. Wang
@en
Andrew H.-J. Wang
@es
王惠鈞
@zh
P166
P21
P27
P31
P4012
P569
1945-11-29T00:00:00Z