|
18
|
99
|
7ldyA |
Hiv-1 protease wt (nl4-3) in complex with tmc-126 |
|
80
|
305
|
7mb4A |
Sars-cov-2 main protease (mpro) c145a in complex with cleavage site nsp4/5 (p6-p1) |
|
18
|
99
|
7ma1A |
Hiv-1 protease (i84v) in complex with grl-98065 |
|
18
|
99
|
7m9mA |
Hiv-1 protease wt (nl4-3) in complex with lr3-55 |
|
80
|
302
|
7mb7A |
Sars-cov-2 main protease (mpro) c145a in complex with cleavage site nsp7/8 (p6-p1) |
|
0
|
6
|
7mb7B |
Sars-cov-2 main protease (mpro) c145a in complex with cleavage site nsp7/8 (p6-p1) |
|
18
|
99
|
7maiA |
Hiv-1 protease (i84v) in complex with pu5 (lr4-47) |
|
17
|
99
|
7makA |
Hiv-1 protease (i84v) in complex with pu7 (lr3-67) |
|
17
|
99
|
7le1A |
Hiv-1 protease wt (nl4-3) in complex with umass2 |
|
72
|
220
|
8edeA |
Crystal structure of covalent inhibitor 2-chloro-n'-(n-(4-chlorophenyl)-n-methylglycyl)acetohydrazide bound to ubiquitin c-terminal hydrolase-l1 |
|
96
|
267
|
7x3pA |
Crystal structure of human sirt5 in complex with diazirine inhibitor 9 |
|
49
|
168
|
8jugA |
Crystal structure of human mmp-7 in complex with inhibitor |
|
53
|
169
|
8judA |
Crystal structure of human mmp-7 in complex with inhibitor |
|
48
|
168
|
8jufA |
Crystal structure of human mmp-7 in complex with inhibitor |
|
143
|
407
|
8jubA |
Crystal structure of glutaminase c in complex with compound 27 |
|
134
|
407
|
8jueA |
Crystal structure of glutaminase c in complex with compound 11 |
|
90
|
316
|
8esiA |
Bile salt hydrolase from b. longum with covalent inhibitor bound |
|
85
|
324
|
8esgA |
Bile salt hydrolase b from lactobacillus gasseri with covalent inhibitor bound |
|
86
|
322
|
8eslA |
Bile salt hydrolase from a bacteroidales species with covalent inhibitor bound |
|
76
|
315
|
8eteA |
Bile salt hydrolase from b. longum with covalent inhibitor bound |
|
86
|
324
|
8etfA |
Bile salt hydrolase b from lactobacillus gasseri with covalent inhibitor bound |
|
123
|
360
|
8sdrA |
Crystal structure of pdc-3 beta-lactamase in complex with the boronic acid inhibitor lp-06 |
|
79
|
305
|
8dd6A |
Sars-cov-2 main protease (mpro) h163a mutant in complex with gc376 |
|
118
|
357
|
8fqwA |
Adc-30 in complex with boronic acid transition state inhibitor mb076 |
|
120
|
357
|
8fqoA |
Adc-33 in complex with boronic acid transition state inhibitor mb076 |
|
123
|
355
|
8fqsB |
Adc-212 in complex with boronic acid transition state inhibitor mb076 |
|
125
|
358
|
8fquA |
Adc-219 in complex with boronic acid transition state inhibitor mb076 |
|
121
|
357
|
8fqmA |
Adc-7 in complex with boronic acid transition state inhibitor mb076 |
|
121
|
358
|
8fqqA |
Adc-162 in complex with boronic acid transition state inhibitor mb076 |
|
64
|
194
|
7x8xA |
Structural insights into mycobacterium tuberculosis clpp1p2 inhibition by cediranib: implications for developing antimicrobial agents targeting clp protease |
|
59
|
177
|
7x8xB |
Structural insights into mycobacterium tuberculosis clpp1p2 inhibition by cediranib: implications for developing antimicrobial agents targeting clp protease |
|
57
|
245
|
8f7vA |
Macrocyclic plasmin inhibitor |
|
126
|
320
|
8di4A |
Discovery of mk-8189, a highly potent and selective pde10a inhibitor for the treatment of schizophrenia |
|
17
|
92
|
7usoB |
Crystal structure of caspase-3 with peptide inhibitor acitvkd-cho |
|
17
|
91
|
7uspB |
Crystal structure of caspase-3 with peptide inhibitor acitv(orn)d-cho |
|
51
|
140
|
7uspA |
Crystal structure of caspase-3 with peptide inhibitor acitv(orn)d-cho |
|
51
|
141
|
7usqA |
Crystal structure of caspase-3 with peptide inhibitor acdvpd-cho |
|
18
|
93
|
7usqB |
Crystal structure of caspase-3 with peptide inhibitor acdvpd-cho |
|
50
|
139
|
7usoA |
Crystal structure of caspase-3 with peptide inhibitor acitvkd-cho |
|
93
|
263
|
7u70A |
Crystal structure of ctx-m-14 with compound 2 |
|
95
|
260
|
7u8sA |
Crystal structure of kpc-2 with compound 2 |
|
78
|
229
|
7uoyA |
Ndm1-inhibitor co-structure |
|
75
|
228
|
7up3A |
Ndm1-inhibitor co-structure |
|
82
|
241
|
7uoxA |
Ndm1-inhibitor co-structure |
|
80
|
241
|
7up1A |
Ndm1-inhibitor co-structure |
|
71
|
230
|
7up2A |
Ndm1-inhibitor co-structure |
|
258
|
778
|
8e3jA |
Co-crystal structure of chaetomium glucosidase with compound 4 |
|
267
|
778
|
8e3pA |
Co-crystal structure of chaetomium glucosidase with compound 5 |
|
95
|
315
|
8g62A |
Papain-like protease of sars cov-2 in complex with remodilin ncgc 390004 |
|
107
|
377
|
7tuoA |
Crystal structure analysis of human usp28 complex with a compound |
