|
84
|
299
|
9zj1A |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor nn-iv-169 |
|
87
|
299
|
9zj3A |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor amj-ii-72 |
|
83
|
307
|
9zjcA |
Crystal structure of mers 3cl protease in complex with inhibitor ikr-i-52 |
|
82
|
306
|
9zj8A |
Crystal structure of mers 3cl protease in complex with inhibitor amj-ii-72 |
|
91
|
305
|
9zzhA |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor csd-v-169 |
|
83
|
299
|
9zj2A |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor amj-ii-122 |
|
83
|
302
|
9zj6A |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor psr-i-162 |
|
88
|
306
|
9zj5A |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor ikr-i-52 |
|
82
|
304
|
9zj4A |
Crystal structure of sars-cov-2 3cl protease in complex with inhibitor ikr-i-45 |
|
83
|
305
|
9zjbA |
Crystal structure of mers 3cl protease in complex with inhibitor ikr-i-46 |
|
153
|
576
|
9ohnA |
Cryo-em structure of human p97/vcp bound to inhibitor gnd-135 |
|
152
|
427
|
10akA |
Crystal structure of human wrn helicase with compound 4 |
|
147
|
421
|
10ajA |
Crystal structure of human wrn helicase with compound 1 |
|
77
|
301
|
10dvA |
Room temperature x-ray structure of sars cov-2 main protease intermediate precursor with ensitrelvir (esv) |
|
86
|
332
|
9uf9A |
Crystal structure of pepstatin a bound to rhodotorula mucilaginosa aspartic protease rmuap1 |
|
77
|
240
|
9nizA |
Fphi, staphylococcus aureus fluorophosphonate-binding serine hydrolases i, in complex with carbamoyl fluoride compound 18 |
|
79
|
240
|
9nixA |
Fphi, staphylococcus aureus fluorophosphonate-binding serine hydrolases i, in complex with carbamoyl fluoride compound 21 |
|
203
|
707
|
9q62A |
Human prolyl endopeptidase (prep) - complex with kt-2-108 |
|
202
|
707
|
9q6jA |
Human prolyl endopeptidase (prep) - complex with kt-2-126 |
|
201
|
706
|
9q5yA |
Human prolyl endopeptidase (prep) - complex with yx45 |
|
206
|
708
|
9q5zA |
Human prolyl endopeptidase (prep) - complex with kt-1-147 |
|
204
|
707
|
9q6lA |
Human prolyl endopeptidase (prep) - complex with kt-2-197 |
|
202
|
707
|
9q66A |
Human prolyl endopeptidase (prep) - complex with jp-4-1-7 |
|
211
|
709
|
9q5xA |
Human prolyl endopeptidase (prep) - complex with kt-2-74 |
|
210
|
707
|
9q6kA |
Human prolyl endopeptidase (prep) - complex with jp-2-1-7 |
|
232
|
707
|
9q6xA |
Human prolyl endopeptidase (prep) - complex with kt-2-186 |
|
198
|
706
|
9q65B |
Human prolyl endopeptidase (prep) - complex with kt-2-75 |
|
230
|
707
|
9q64A |
Human prolyl endopeptidase (prep) - complex with kt-2-59 |
|
202
|
707
|
9xykA |
Human prolyl endopeptidase (prep) - complex with jp-7-1-7 |
|
154
|
472
|
9md7A |
Hip1 complex with inhibitor #1 (hip1-1) via ser228 |
|
165
|
478
|
9md8A |
Hip1 complex with inhibitor #2 (hip1-2) via ser228 |
|
63
|
169
|
9nznA |
Crystal structure of kirsten rat sarcoma g12c complexed with gdp and covalently bound to an adduct of (2s)-1-{4-[(7p)-7-(8-ethynyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-{[(2r,4r,7as)-2-fluorotetrahydro-1h-pyrrolizin-7a(5h)-yl]methoxy}pyrido[4,3-d]pyrimidin-4-yl]piperazin-1-yl}-2-fluoro-3-(1, |
|
60
|
169
|
9nzmA |
Crystal structure of kirsten rat sarcoma g12c complexed with gmppnp and covalently bound to an adduct of {(2s)-4-[7-(8-chloronaphthalen-1-yl)-2-{[(2s)-1-methylpyrrolidin-2-yl]methoxy}-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-yl]-1-[(2z)-2-fluoro-3-(pyridin-2-yl)prop-2-enoyl]piperazin-2-yl}acetonit |
|
131
|
664
|
9dpzA |
Potent inhibition of the protein arginine deiminases (pad1-4) by targeting a ca2+ dependent allosteric binding site |
|
130
|
664
|
9dopA |
Inhibiting peptidylarginine deiminases (pad1-4) by targeting a ca2+ dependent allosteric binding site |
|
91
|
308
|
9cybA |
Sars-cov-2 plpro in complex with inhibitor wehi-p1 |
|
86
|
307
|
9cycA |
Sars-cov-2 plpro in complex with inhibitor wehi-p2 |
|
90
|
308
|
9cykA |
Sars-cov-2 plpro in complex with inhibitor wehi-p24 |
|
82
|
309
|
9cydA |
Sars-cov-2 plpro in complex with inhibitor wehi-p4 |
|
58
|
241
|
8g1vA |
Crystal structure matriptase (c731s) in complex with inhibitor mm1132-2 |
|
117
|
659
|
8wciP |
Cryo-em structure of the inhibitor-bound vo complex from enterococcus hirae |
|
69
|
156
|
8wciA |
Cryo-em structure of the inhibitor-bound vo complex from enterococcus hirae |
|
83
|
305
|
8wz0A |
Sars-cov-2 3clpro bound to covalent inhibitor |
|
18
|
99
|
9obiA |
Room temperature x-ray structure of hiv-1 protease in complex with inhibitor grl-075-24a |
|
87
|
301
|
9mvqA |
Crystal structure of sars-cov-2 main protease (mpro) variant q192t in complex with inhibitor avi-4303 |
|
86
|
305
|
9mvmA |
Crystal structure of sars-cov-2 main protease (mpro)in complex with inhibitor avi-3318 |
|
77
|
305
|
9mvpA |
Crystal structure of sars-cov-2 main protease (mpro)in complex with inhibitor avi-4516 |
|
51
|
163
|
9ct8C |
Tricomplex of compound 2, kras g12d, and cypa |
|
63
|
170
|
9ctbA |
Tri-complex of zoldonrasib (rmc-9805), kras g12d, and cypa |
|
63
|
170
|
9ct8A |
Tricomplex of compound 2, kras g12d, and cypa |
