|
161
|
420
|
5scdA |
Structure of liver pyruvate kinase in complex with anthraquinone derivative 58 |
|
93
|
323
|
7vraA |
The crystal structure of egfr t790m/c797s with the inhibitor hc5476 |
|
97
|
323
|
7vreA |
The crystal structure of egfr t790m/c797s with the inhibitor hcd2892 |
|
101
|
350
|
7u31A |
Crystal structure of human gsk3b in complex with g5 |
|
106
|
350
|
7u33A |
Crystal structure of human gsk3b in complex with arn9133 |
|
102
|
350
|
7u36A |
Crystal structure of human gsk3b in complex with arn1484 |
|
97
|
348
|
7u2zA |
Crystal structure of human gsk3b in complex with g12 |
|
266
|
939
|
7r9yA |
Structure of pik3ca with covalent inhibitor 22 |
|
268
|
939
|
7r9vA |
Structure of pik3ca with covalent inhibitor 19 |
|
57
|
214
|
7sanA |
Crystal structure of human hypoxanthine guanine phosphoribzosyltransferase in complex with (4s,7s)-7-hydroxy-4-((guanin-9-yl)methyl)-2,5-dioxaheptan-1,7-diphosphonate |
|
87
|
266
|
7n4rA |
Bruton's tyrosine kinase in complex with compound 21 |
|
85
|
268
|
7l5pA |
Crystal structure of the covalently bonded complex of rilzabrutinib with btk |
|
85
|
265
|
7n4sA |
Bruton's tyrosine kinase in complex with compound 65 |
|
87
|
267
|
7n4qA |
Bruton's tyrosine kinase in complex with compound 45 |
|
91
|
270
|
7l5oA |
Crystal structure of the noncovalently bonded complex of rilzabrutinib with btk |
|
87
|
304
|
5sb2A |
Ddr1, 3-chloro-n-[(1r,2s)-2-phenylcyclopropyl]-5-(1h-pyrrolo[2,3-b]pyridin-5-yloxymethyl)benzamide, 1.600a, p212121, rfree=23.2% |
|
92
|
307
|
5saxA |
Ddr1, 2-[3-(2-pyridin-3-ylethynyl)phenyl]-n-[3-(trifluoromethyl)phenyl]acetamide, 1.902a, second p212121 form, rfree=25.4%, second form |
|
94
|
299
|
5sawA |
Ddr1, 2-[3-(2-pyridin-3-ylethynyl)phenyl]-n-[3-(trifluoromethyl)phenyl]acetamide, 1.601a, p212121, rfree=22.6% |
|
89
|
303
|
5sauA |
Ddr1, 3-[2-(6-aminopyridin-3-yl)ethynyl]-n-[3-(trifluoromethyl)phenyl]benzamide, 1.800a, p212121, rfree=23.1% |
|
89
|
304
|
5sb1A |
Ddr1, 4-chloro-n-[(3s,4r)-4-phenylpyrrolidin-3-yl]-3-(1h-pyrrolo[2,3-b]pyridin-5-yloxymethyl)benzamide, 1.530a, p212121, rfree=21.4% |
|
89
|
300
|
5sayA |
Ddr1, n-[2-[3-(2-aminopyrimidin-5-yl)oxyphenyl]ethyl]-3-(trifluoromethoxy)benzamide, 2.190a, p1211, rfree=27.7% |
|
99
|
302
|
5savA |
Ddr1, n-[2-[3-(2-aminopyrimidin-5-yl)oxyphenyl]ethyl]-3-(trifluoromethoxy)benzamide, 1.760a, p212121, rfree=23.5% |
|
96
|
305
|
5sazA |
Ddr1, 3-chloro-n-[4-chloro-3-(1h-pyrrolo[2,3-b]pyridin-5-ylcarbamoyl)phenyl]-4-(2-hydroxyethylamino)benzamide, 1.802a, p212121, rfree=22.2% |
|
90
|
304
|
5sb0A |
Ddr1, n-[[2-(2-pyridin-3-yloxyethyl)cyclohexyl]methyl]-3-(trifluoromethoxy)benzamide, 1.970a, p212121, rfree=25.6% |
|
318
|
1060
|
8tduA |
Stx-478, a mutant-selective, allosteric inhibitor bound to pi3kalpha |
|
137
|
416
|
8esmA |
Human triacylglycerol synthesizing enzyme dgat1 in complex with t863 inhibitor |
|
76
|
259
|
8tduB |
Stx-478, a mutant-selective, allosteric inhibitor bound to pi3kalpha |
|
107
|
425
|
8fe8B |
Crystal structure of hiv-1 rt in complex with the non-nucleoside inhibitor 18b1 |
|
153
|
556
|
8fe8A |
Crystal structure of hiv-1 rt in complex with the non-nucleoside inhibitor 18b1 |
|
97
|
325
|
8f1zA |
Egfr kinase in complex with bayer #33 |
|
82
|
307
|
8f1wA |
Egfr(t790m/v948r) kinase in complex with poziotinib |
|
83
|
324
|
8f1yA |
Egfr kinase in complex with poziotinib |
|
93
|
322
|
8f1hA |
Egfr kinase in complex with tas6417 (cln-081) |
|
93
|
323
|
8f1xA |
Egfr kinase in complex with mobocertinib (tak-788) |
|
69
|
308
|
8emeA |
Egfr(t790m/v948r) in complex with znl-0056 |
|
119
|
310
|
7yolA |
Crystal structure of tetra mutant (d67e, a68p, l98i, a301s) of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide of serine acetyltransferase from haemophilus influenzae at 2.4 a |
|
111
|
303
|
7yoiA |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.14 a |
|
111
|
302
|
7yomA |
Crystal structure of tetra mutant (d67e,a68p,l98i,a301s) of o-acetylserine sulfhydrylase from salmonella typhimurium in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.8 a |
|
0
|
8
|
7yomB |
Crystal structure of tetra mutant (d67e,a68p,l98i,a301s) of o-acetylserine sulfhydrylase from salmonella typhimurium in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.8 a |
|
0
|
8
|
7yoiB |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.14 a |
|
1
|
7
|
7yohP |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of haemophilus influenzae at 2.5 a |
|
110
|
303
|
7yodA |
Crystal structure of a68p single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of salmonella typhimurium at 2.1 a |
|
103
|
308
|
7yohA |
Crystal structure of i88l single mutant of o-acetylserine sulfhydrylase from haemophilus influenzae in complex with high-affinity inhibitory peptide from serine acetyltransferase of haemophilus influenzae at 2.5 a |
|
76
|
272
|
8dd5A |
Crystal structure of kat6a in complex with inhibitor ctx-648 (pf-9363) |
|
88
|
271
|
8fd9A |
Structure of btk kinase domain with the second-generation inhibitor acalabrutinib |
|
77
|
265
|
8ff0A |
Structure of btk kinase domain with the second-generation inhibitor tirabrutinib |
|
112
|
355
|
8elcA |
Human jnk2 bound to covalent inhibitor yl2056 |
|
135
|
416
|
8etmA |
Human triacylglycerol synthesizing enzyme dgat1 in complex with dgat1in1 inhibitor |
|
295
|
840
|
8fjcA |
Structure of the catalytic domain of streptococcus mutans gtfb complexed to acarbose in tetragonal space group p4322 |
|
144
|
555
|
8ffxA |
Crystal structure of hiv-1 reverse transcriptase in complex with non-nucleoside inhibitor 19980 |
