|
89
|
325
|
7u9aA |
Egfr in complex with a macrocyclic inhibitor |
|
132
|
330
|
7t08A |
Cryptococcus neoformans protein farnesyltransferase in complex with fpp and inhibitor 2q |
|
177
|
518
|
7t08B |
Cryptococcus neoformans protein farnesyltransferase in complex with fpp and inhibitor 2q |
|
76
|
286
|
7vtoA |
The crystal structure of pak1 with the inhibitor gw8510 |
|
149
|
407
|
8e9eB |
Rat protein farnesyltransferase in complex with fpp and inhibitor 2f |
|
127
|
323
|
8e9eA |
Rat protein farnesyltransferase in complex with fpp and inhibitor 2f |
|
77
|
273
|
7shvA |
Crystal structure of braf kinase domain bound to gdc0879 |
|
42
|
152
|
7siaA |
Hiv integrase core domain in complex with inhibitor 2-[2-(2-{3-[(4-{2-[(3-{2-[3-(carboxymethyl)-5-methyl-1-benzofuran-2-yl]ethynyl}phenyl)formamido]ethyl}piperazin-1-yl)methyl]phenyl}ethynyl)-5-methyl-1-benzofuran-3-yl]acetic acid |
|
108
|
352
|
7t1iA |
Crystal structure of cab1 pantothenate kinase from saccharomyces cerevisiae in complex with compound yu385597 |
|
115
|
355
|
7t1gA |
Crystal structure of cab1 pantothenate kinase from saccharomyces cerevisiae in complex with compound yu385595 |
|
115
|
356
|
7t1hA |
Crystal structure of cab1 pantothenate kinase from saccharomyces cerevisiae in complex with compound yu281445 |
|
114
|
400
|
8d23A |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with inhibitor sgt529 |
|
116
|
400
|
8d25A |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with inhibitor sgt530 |
|
113
|
400
|
8d1rA |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with inhibitor sgt520 |
|
92
|
306
|
7wclA |
Crystal structure of fgfr1 kinase domain with pemigatinib |
|
77
|
296
|
7rxoA |
Crystal structure of cdk2 liganded with compound wn333 |
|
58
|
247
|
7ty2A |
Crystal structure of setd2 bound to an indole-based inhibitor |
|
59
|
248
|
7ty3A |
Crystal structure of setd2 bound to an indole-based inhibitor |
|
86
|
287
|
7uyvA |
Crystal structure of jak3 kinase domain in complex with compound 25 |
|
96
|
288
|
7uyrA |
Crystal structure of tyk2 kinase domain in complex with compound 12 |
|
82
|
288
|
7uysA |
Crystal structure of tyk2 kinase domain in complex with compound 16 |
|
88
|
290
|
7uywA |
Crystal structure of jak2 kinase domain in complex with compound 30 |
|
33
|
126
|
7ssbA |
Co-structure of pkg1 regulatory domain with compound 33 |
|
84
|
288
|
7uytA |
Crystal structure of tyk2 kinase domain in complex with compound 25 |
|
85
|
289
|
7uyuA |
Crystal structure of tyk2 kinase domain in complex with compound 30 |
|
160
|
453
|
7urdA |
Human porcn in complex with lgk974 and wnt3a peptide |
|
154
|
453
|
7ureA |
Human porcn in complex with palmitoleoylated wnt3a peptide |
|
194
|
491
|
7urfA |
Human hhat h379c in complex with shh n-terminal peptide |
|
0
|
20
|
7urdB |
Human porcn in complex with lgk974 and wnt3a peptide |
|
20
|
107
|
7uraL |
Human porcn in complex with palmitoleoyl-coa |
|
21
|
107
|
7ureL |
Human porcn in complex with palmitoleoylated wnt3a peptide |
|
92
|
291
|
7up7A |
Crystal structure of c-terminal domain of msk1 in complex with covalently bound with literature rsk2 inhibitor indazole cyanoacrylamide compound 26 (soak) |
|
14
|
117
|
7urfO |
Human hhat h379c in complex with shh n-terminal peptide |
|
27
|
119
|
7urdH |
Human porcn in complex with lgk974 and wnt3a peptide |
|
155
|
453
|
7uraA |
Human porcn in complex with palmitoleoyl-coa |
|
146
|
453
|
7urcA |
Human porcn in complex with lgk974 |
|
24
|
119
|
7uraH |
Human porcn in complex with palmitoleoyl-coa |
|
18
|
111
|
7urfP |
Human hhat h379c in complex with shh n-terminal peptide |
|
1
|
20
|
7ureB |
Human porcn in complex with palmitoleoylated wnt3a peptide |
|
17
|
107
|
7urdL |
Human porcn in complex with lgk974 and wnt3a peptide |
|
22
|
119
|
7ureH |
Human porcn in complex with palmitoleoylated wnt3a peptide |
|
15
|
107
|
7urcL |
Human porcn in complex with lgk974 |
|
20
|
119
|
7urcH |
Human porcn in complex with lgk974 |
|
132
|
380
|
7rxvA |
Human methionine adenosyltransferase 2a bound to methylthioadenosine, malonate (mla) and mgf3 |
|
236
|
948
|
6xrnA |
Crystal structure of human pi3k-gamma in complex with compound 17 |
|
310
|
946
|
7jiuA |
Human pi3kdelta in complex with compound 2f |
|
90
|
270
|
7n5oA |
Fragment-based discovery of a novel bruton's tyrosine kinase inhibitor |
|
89
|
270
|
7n5rA |
Fragment-based discovery of a novel bruton's tyrosine kinase inhibitor |
|
90
|
270
|
7n5yA |
Fragment-based drug design of a novel, covalent bruton's tyrosine kinase inhibitor |
|
90
|
270
|
7n5xA |
Fragment-based discovery of a novel bruton's tyrosine kinase inhibitor |
