Found 7718 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: hydrolase/hydrolase inhibitor

Total Genus Sequence Length pdb Title
41 154 7n03A Crystal structure of mth1 in complex with compound 31
43 155 7n13A Crystal structure of mth1 in complex with compound 32
47 159 7ovyA Crystal structure of a dimeric based inhibitor jg34 in complex with the mmp-12 catalytic domain
94 313 7sgwA Papain-like protease of sars cov-2 in complex with plp_snyder630 inhibitor
98 315 7sgvA Papain-like protease of sars cov-2, c111s mutant, in complex with plp_snyder630 inhibitor
94 313 7sguA Papain-like protease of sars cov-2, c111s mutant, in complex with plp_snyder608 inhibitor
49 236 7n7xAAA Crystal structure of bcx7353(orladeyo) in complex with human plasma kallikrein serine protease domain at 2.1 angstrom resolution
9 53 7md3H The f1 region of apoptolidin-bound saccharomyces cerevisiae atp synthase
127 392 7m7dA Crystal structure of the indoleamine 2,3-dioxygenagse 1 (ido1) complexed with iacs-8968
84 275 7md3G The f1 region of apoptolidin-bound saccharomyces cerevisiae atp synthase
132 469 7md2D The f1 region of ammocidin-bound saccharomyces cerevisiae atp synthase
8 53 7md2H The f1 region of ammocidin-bound saccharomyces cerevisiae atp synthase
139 468 7md3D The f1 region of apoptolidin-bound saccharomyces cerevisiae atp synthase
165 485 7md2A The f1 region of ammocidin-bound saccharomyces cerevisiae atp synthase
152 483 7md3A The f1 region of apoptolidin-bound saccharomyces cerevisiae atp synthase
77 275 7md2G The f1 region of ammocidin-bound saccharomyces cerevisiae atp synthase
56 237 7mboA Factor xia (pichia pastoris; c500s [c122s]) in complex with the inhibitor milvexian (bms-986177), iupac name:(6r,10s)-10-{4-[5-chloro-2-(4-chloro-1h-1,2,3-triazol-1-yl)phenyl]-6- oxopyrimidin-1(6h)-yl}-1-(difluoromethyl)-6-methyl-1,4,7,8,9,10-hexahydro-15,11- (metheno)pyrazolo[4,3-b][1,7]diazacyclotetradecin-5(6h)-one
79 286 7lgsA Structure of egfr_d770_n771insnpg/v948r in complex with covalent inhibitor osimertinib.
84 250 7l5fA Crystal structure of n-(2-oxocyclobutyl) decanamide bound aiia-co
128 317 7k4iA Human arginase 1 in complex with compound 06.
351 970 7k1fA Crystal structure of human insulin degrading enzyme (ide) in complex with compound bdm_88558
352 970 7k1eA Crystal structure of human insulin degrading enzyme (ide) in complex with compound bdm_88646
55 223 7josA Crystal structure of bbki complexed with human kallikrein 4
52 223 7jowE Crystal structure of bbki complexed with human kallikrein 4
32 165 7joeI Crystal structure of bbki complexed with human kallikrein 4
47 169 7ju8A X-ray structure of mmp-13 in complex with 4-(1,2,3-thiadiazol-4-yl)pyridine
57 223 7jodE Crytsal structure of bbki complexed with human kallikrein 4
34 166 7jodI Crytsal structure of bbki complexed with human kallikrein 4
31 164 7jowI Crystal structure of bbki complexed with human kallikrein 4
65 215 7jujA Cruzain bound to gallinamide inhibitor
32 165 7josB Crystal structure of bbki complexed with human kallikrein 4
56 223 7jwxA Crystal structure of trypsin bound o-methyl benzamidine
50 223 7joeE Crystal structure of bbki complexed with human kallikrein 4
84 330 5sapA Endothiapepsin in complex with compound fu58-2
87 330 5sanA Endothiapepsin in complex with compound fu5-4
79 305 7rn1A Crystal structure of the sars-cov-2 (covid-19) main protease in complex with inhibitor jun9-62-2r
85 302 7rn0A Crystal structure of the sars-cov-2 (covid-19) main protease in complex with inhibitor jun9-57-3r
86 330 5sasA Endothiapepsin in complex with compound fu290-2
87 330 5sarA Endothiapepsin in complex with compound fu290-1
86 330 5satA Endothiapepsin in complex with compound fu66-1
87 330 5samA Endothiapepsin in complex with compound fu5-3
85 330 5saoA Endothiapepsin in complex with compound fu58-1
84 330 5salA Endothiapepsin in complex with compound fu5-2
87 330 5saqA Endothiapepsin in complex with compound fu58-3
85 330 5sakA Endothiapepsin in complex with compound fu5-1
147 368 7motA Structure of hdac2 in complex with an inhibitor (compound 9)
146 368 7mosA Structure of hdac2 in complex with a macrocyclic inhibitor (compound 4)
102 390 7myuA Bace-1 in complex with compound #22
110 391 7myiA Bace-1 in complex with compound #6
77 303 7mbiA Structure of sars-cov2 3cl protease covalently bound to peptidomimetic inhibitor