|
137
|
391
|
7s4cA |
Crystal structure of inhibitor-bound galactokinase |
|
144
|
404
|
7rniB |
Discovery of an anion-dependent farnesyltransferase inhibitor from a phenotypic screen |
|
124
|
391
|
7s49A |
Crystal structure of inhibitor-bound galactokinase |
|
122
|
315
|
7rniA |
Discovery of an anion-dependent farnesyltransferase inhibitor from a phenotypic screen |
|
148
|
404
|
7rn5B |
Discovery of an anion-dependent farnesyltransferase inhibitor from a phenotypic screen |
|
124
|
313
|
7rn5A |
Discovery of an anion-dependent farnesyltransferase inhibitor from a phenotypic screen |
|
88
|
272
|
7jyqA |
Jak2 jh2 in complex with jak020 |
|
80
|
270
|
7jyoA |
Jak2 jh2 in complex with jak064 |
|
97
|
291
|
7jxxA |
Structure of ttbk1 kinase domain in complex with compound 3 |
|
99
|
290
|
7jxyA |
Structure of ttbk1 kinase domain in complex with compound 18 |
|
54
|
186
|
7lunA |
Human parp14 (artd8), catalytic fragment in complex with rbn011980 |
|
134
|
381
|
7kdbA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 35 |
|
134
|
382
|
7kccA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor ag-270 |
|
137
|
380
|
7kceA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 2 |
|
133
|
381
|
7kdaA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 34 |
|
134
|
382
|
7kcfA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor agi-24512 |
|
123
|
404
|
6xddA |
Crystal structure of ire1 in complex with g-3053 |
|
51
|
187
|
7l9yA |
Human parp14 (artd8), catalytic fragment in complex with rbn012042 |
|
108
|
425
|
7kwuB |
Crystal structure of hiv-1 rt in complex with 16c (k07-15) |
|
159
|
556
|
7kwuA |
Crystal structure of hiv-1 rt in complex with 16c (k07-15) |
|
55
|
211
|
7cajA |
Crystal structure of setdb1 tudor domain in complexed with compound 2. |
|
263
|
949
|
7kkeA |
Phosphoinositide 3-kinase gamma bound to a thiazole inhibitor |
|
50
|
189
|
6we2A |
Human parp14 (artd8), catalytic fragment in complex with rbn012759 |
|
162
|
625
|
7m05A |
Cryoem structure of prmt5 bound to covalent pbm-site inhibitor brd-6988 |
|
48
|
306
|
7m05B |
Cryoem structure of prmt5 bound to covalent pbm-site inhibitor brd-6988 |
|
100
|
356
|
7kskA |
Thiophenyl-pyrazolourea derivatives as potent, brian penetrant, orally bioavailable, and isoform-selective jnk3 inhibitors |
|
130
|
380
|
7l1aA |
Human methionine adenosyltransferase 2a bound to methylthioadenosine and inhibitor, di-imido triphosphate (pnpnp) |
|
105
|
356
|
7ksiA |
Thiophenyl-pyrazolourea derivatives as potent, brian penetrant, orally bioavailable, and isoform-selective jnk3 inhibitors |
|
79
|
273
|
6l17A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
41
|
158
|
7kdoA |
Crystal structure of escherichia coli hppk in complex with bisubstrate inhibitor hp-73 |
|
41
|
158
|
7kdrA |
Crystal structure of escherichia coli hppk in complex with bisubstrate inhibitor hp-75 |
|
86
|
269
|
6xjkA |
Jak2 jh2 in complex with jak067 |
|
105
|
336
|
6wl6A |
Cocomplex structure of deoxyhypusine synthase with inhibitor 6-[(2r)-1-amino-4-methylpentan-2-yl]-3-(pyridin-3-yl)-4h,5h,6h,7h-thieno[2,3-c]pyridin-7-one |
|
109
|
336
|
6wkzA |
Cocomplex structure of deoxyhypusine synthase with inhibitor 6-[(1r)-2-amino-1-phenylethyl]-3-(pyridin-3-yl)-4h,5h,6h,7h-thieno[2,3-c]pyridin-7-one |
|
80
|
273
|
6l11A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
83
|
273
|
6l12A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
77
|
273
|
6l13A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
79
|
273
|
6l15A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
79
|
273
|
6l16A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
80
|
273
|
6l14A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
79
|
275
|
6wiwA |
C-src bound to atp-competitive inhibitor i14 |
|
42
|
150
|
6wfgA |
Crystal structure of human naa50 in complex with an inhibitor (compound 3) identified using dna encoded library technology |
|
42
|
151
|
6wfnA |
Crystal structure of human naa50 in complex with accoa and an inhibitor (compound 4a) identified using dna encoded library technology |
|
40
|
153
|
6wfoA |
Crystal structure of human naa50 in complex with accoa and an inhibitor (compound 4b) identified using dna encoded library technology |
|
42
|
150
|
6wf3A |
Crystal structure of human naa50 in complex with a cofactor derived inhibitor (compound 1) |
|
38
|
165
|
6wf5A |
Crystal structure of human naa50 in complex with a truncated cofactor derived inhibitor (compound 2) |
|
83
|
348
|
6vkqA |
Crystal structure of human parp-1 cat domain bound to inhibitor eb-47 |
|
92
|
348
|
6vkoA |
Crystal structure of human parp-1 cat domain bound to inhibitor uktt15 |
|
106
|
350
|
6vkkA |
Crystal structure of human parp-1 cat domain bound to inhibitor rucaparib |
|
83
|
288
|
6w8lA |
Crystal structure of jak1 kinase with compound 10 |
