|
81
|
298
|
7ra5A |
Cdk2 in complex with compound 4 |
|
102
|
356
|
7s1nA |
N-aromatic-substituted indazole derivatives as brain penetrant and orally bioavailable jnk3 inhibitors |
|
83
|
271
|
7r60A |
Btk in complex with 18a |
|
86
|
270
|
7r61A |
Btk in complex with 25a |
|
69
|
200
|
7myhA |
Ubiquitin variant ubv.k.2 in complex with ube2k |
|
14
|
71
|
7myfC |
Ubiquitin variant ubv.k.1 in complex with ube2k |
|
14
|
72
|
7myfB |
Ubiquitin variant ubv.k.1 in complex with ube2k |
|
123
|
401
|
7n6qA |
Structure of pppa bound human acat2 |
|
125
|
401
|
7n6rA |
Structure of nevanimibe bound human acat2 |
|
22
|
74
|
7myhB |
Ubiquitin variant ubv.k.2 in complex with ube2k |
|
51
|
196
|
7myfA |
Ubiquitin variant ubv.k.1 in complex with ube2k |
|
44
|
151
|
7ke0A |
Hiv-1 integrase catalytic core domain complexed with allosteric inhibitor stp03-0404 |
|
125
|
361
|
7ea0A |
Crystal structure of human pyruvate dehydrogenase kinase 2 in complex with compound 1 |
|
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 |
|
134
|
382
|
7kcfA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor agi-24512 |
|
133
|
381
|
7kdaA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 34 |
|
137
|
380
|
7kceA |
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 2 |
|
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 |
