|
78
|
221
|
7k3dA |
The structure of ntmt1 in complex with compound dc1-13 |
|
47
|
152
|
6wc8A |
Hiv integrase core domain in complex with inhibitor 2-(5-(3-fluorophenyl)-2-(2-(thiophen-2-yl)ethynyl)-1- benzofuran-3-yl)ethanoic acid |
|
89
|
289
|
7m0kA |
Hpk1 in complex with compound 1 |
|
41
|
150
|
6we7A |
Hiv integrase core domain in complex with inhibitor 3-methyl-2-{5-methyl-2-[2-(thiophen-2-yl)ethynyl]-1- benzofuran-3-yl}butanoic acid |
|
96
|
293
|
7m0mA |
Hpk1 in complex with compound 1 |
|
52
|
189
|
6we3A |
Human parp14 (artd8), catalytic fragment in complex with compound 3 |
|
49
|
186
|
6we4A |
Human parp14 (artd8), catalytic fragment in complex with compound 2 |
|
90
|
288
|
7botA |
Human sirt2 in complex with myristoyl thiourea inhibitor, no.23 |
|
95
|
288
|
7bosA |
Human sirt2 in complex with myristoyl thiourea inhibitor, no.13 |
|
255
|
944
|
7jx0A |
Nvs-pi3-4 bound to the pi3kg catalytic subunit p110 gamma |
|
269
|
947
|
7jwzA |
Ipi-549 bound to the pi3kg catalytic subunit p110 gamma |
|
105
|
343
|
7ljeA |
Discovery of spirohydantoins as selective, orally bioavailable inhibitors of p300/cbp histone acetyltransferases |
|
41
|
150
|
6w42A |
Hiv integrase core domain in complex with inhibitor 2-(5-methyl-2-(2-(thiophen-2-yl)ethynyl)-1-benzofuran-3-yl)acetic acid |
|
91
|
288
|
7l25A |
Hpk1 in complex with compound 18 |
|
42
|
148
|
6w0uA |
Hiv integrase core domain in complex with inhibitor 2-(2-ethynyl-5-methyl-1-benzofuran-3-yl)acetic acid |
|
106
|
322
|
6vxuA |
Structure of human vaccinia-related kinase 1 (vrk1) bound to ach471 |
|
41
|
151
|
6vx2A |
Hiv integrase core domain in complex with inhibitor (5-methyl-1-benzofuran-3-yl)acetic acid |
|
89
|
326
|
6wadA |
Crystal structure of human protein arginine n-methyltransferase 6 (prmt6) in complex with mt2739 inhibitor |
|
92
|
296
|
6lxyA |
Irak4 in complex with inhibitor |
|
228
|
592
|
7k41A |
Bacterial o-glcnacase (oga) with compound |
|
462
|
1454
|
6w2jA |
Cps1 bound to allosteric inhibitor h3b-374 |
|
83
|
295
|
7c2wA |
Crystal structure of irak4 kinase in complex with a small molecule inhibitor |
|
302
|
1013
|
7jisA |
Human pi3kdelta in complex with compound 2f |
|
101
|
297
|
7c2vA |
Crystal structure of irak4 kinase in complex with the inhibitor ca-4948 |
|
67
|
273
|
7bucA |
Crystal structure of ehmt2 set domain in complex with compound 13 |
|
97
|
300
|
7ju6A |
Structure of ret protein tyrosine kinase in complex with selpercatinib |
|
80
|
169
|
7jisB |
Human pi3kdelta in complex with compound 2f |
|
139
|
402
|
7jx9A |
The crystal structure of human ornithine aminotransferase with an intermediate bound during inactivation by (1s,3s)-3-amino-4-(hexafluoropropan-2-ylidenyl)-cyclopentane-1-carboxylic acid. |
|
72
|
298
|
7kacA |
Crystal structure of hpk1 (map4k1) kinase in complex with 5-{[4-{[(1s)-2-hydroxy-1-phenylethyl]amino}-5-(1,3,4-oxadiazol-2-yl)pyrimidin-2-yl]amino}-3,3-dimethyl-2-benzofuran-1(3h)-one |
|
98
|
314
|
7ju5A |
Structure of ret protein tyrosine kinase in complex with pralsetinib |
|
72
|
198
|
6w8hA |
H-pgds complexed with inhibitor 1y |
|
127
|
402
|
6w3kA |
Structure of unphosphorylated human ire1 bound to g-9807 |
|
97
|
305
|
6vglA |
Jak2 jh1 in complex with ruxolitinib |
|
84
|
267
|
6vxqA |
Bruton's tyrosine kinase in complex with compound 5 |
|
91
|
267
|
6w06A |
Bruton's tyrosine kinase in complex with compound 6 |
|
205
|
562
|
6w4gA |
Hepatitis c virus polymerase ns5b with ro inhibitor for sar studies |
|
87
|
266
|
6w07A |
Bruton's tyrosine kinase in complex with compound 1 |
|
81
|
279
|
6umwA |
Crystal structure of hephb1 bound with chlortetracycline |
|
88
|
343
|
7juyC |
Crystal structure of ksr1:mek1 in complex with amp-pnp, and allosteric mek inhibitor cobimetinib |
|
75
|
281
|
7juwB |
Crystal structure of ksr1:mek1 in complex with amp-pnp |
|
76
|
281
|
7juyB |
Crystal structure of ksr1:mek1 in complex with amp-pnp, and allosteric mek inhibitor cobimetinib |
|
126
|
362
|
5qtgA |
T. brucei fpps in complex with cid 126782062 |
|
127
|
363
|
5qt7A |
T. brucei fpps in complex with cid 66669982 |
|
92
|
323
|
6ludA |
Crystal structure of egfr(l858r/t790m/c797s) in complex with osimertinib |
|
129
|
362
|
5qtkA |
T. brucei fpps in complex with cid 69539 |
|
129
|
363
|
5qt9A |
T. brucei fpps in complex with cid 23155989 |
|
124
|
363
|
5qt8A |
T. brucei fpps in complex with cas 34105-16-3 |
|
133
|
362
|
5qthA |
T. brucei fpps in complex with cid 2799882 |
|
120
|
363
|
5qt4A |
T. brucei fpps in complex with cid 3599333 |
|
131
|
363
|
5qtbA |
T. brucei fpps in complex with cid 303798 |
