|
89
|
304
|
4bdgA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
271
|
727
|
3zwaA |
Crystal structure of rat peroxisomal multifunctional enzyme type 1 (rpmfe1) complexed with 3s-hydroxy-hexanoyl-coa |
|
106
|
294
|
3zmcA |
Native structure of farnesyl pyrophosphate synthase from pseudomonas aeruginosa pa01, with bound substrate molecule geranyl pyrophosphate. |
|
77
|
284
|
4a07A |
Human pdk1 kinase domain in complex with allosteric activator ps171 bound to the pif-pocket |
|
77
|
188
|
4aiaA |
The structural basis of 3-methyladenine recognition by 3- methyladenine dna glycosylase i (tag) from staphylococcus aureus |
|
77
|
277
|
4a4xA |
Nek2-ede bound to cct248662 |
|
80
|
290
|
4a4oA |
Crystal structure of polo-like kinase 1 in complex with a 2-(2-amino- pyrimidin-4-yl)-1,5,6,7-tetrahydro-pyrrolopyridin-4-one inhibitor |
|
74
|
277
|
4afeA |
Nek2 bound to hybrid compound 21 |
|
106
|
347
|
3zsiA |
X-ray structure of p38alpha bound to vx-745 |
|
102
|
275
|
4a4vA |
Ligand binding domain of human ppar gamma in complex with amorfrutin 2 |
|
182
|
499
|
4a79A |
Crystal structure of human monoamine oxidase b (mao b) in complex with pioglitazone |
|
113
|
295
|
3zouA |
Native structure of farnesyl pyrophosphate synthase from pseudomonas aeruginosa pa01, with bound fragment spb02696, and substrate geranyl pyrophosphate. |
|
65
|
200
|
4ap9A |
Crystal structure of phosphoserine phosphatase from t. onnurineus in complex with ndsb-201 |
|
111
|
349
|
3zshA |
X-ray structure of p38alpha bound to scio-469 |
|
27
|
79
|
4a3vB |
Yeast regulatory particle proteasome assembly chaperone hsm3 in complex with rpt1 c-terminal fragment |
|
94
|
339
|
4ae9A |
Structure and function of the human sperm-specific isoform of protein kinase a (pka) catalytic subunit c alpha 2 |
|
96
|
292
|
4appA |
Crystal structure of the human p21-activated kinase 4 in complex with (s)-n-(5-(3-benzyl-1-methylpiperazine-4-carbonyl)-6,6-dimethyl-1,4,5, 6-tetrahydropyrrolo(3,4-c)pyrazol-3-yl)-3-phenoxybenzamide |
|
64
|
162
|
3zrjA |
Complex of clpv n-domain with vipb peptide |
|
228
|
666
|
3zn0A |
Lsd1-corest in complex with prsfaa peptide |
|
113
|
328
|
4anmA |
Complex of ck2 with a cdc7 inhibitor |
|
149
|
303
|
3zx6A |
Structure of hamp(af1503)-tsr fusion - hamp (a291v) mutant |
|
100
|
339
|
4ae6A |
Structure and function of the human sperm-specific isoform of protein kinase a (pka) catalytic subunit calpha 2 |
|
49
|
143
|
4aomA |
Mtip and myoa complex |
|
72
|
270
|
3zxtA |
Dimeric structure of dapk-1 catalytic domain in complex with amppcp- mg |
|
16
|
73
|
4aaiA |
Thermostable protein from hyperthermophilic virus ssv-rh |
|
78
|
277
|
4agwA |
Discovery of a small molecule type ii inhibitor of wild-type and gatekeeper mutants of bcr-abl, pdgfralpha, kit, and src kinases |
|
269
|
766
|
3zedA |
X-ray structure of the birnavirus vp1-vp3 complex |
|
119
|
347
|
4arlA |
Structure of the inactive pesticin d207a mutant |
|
96
|
308
|
4anlA |
Structure of g1269a mutant anaplastic lymphoma kinase |
|
41
|
111
|
3zrwA |
The structure of the dimeric hamp-dhp fusion a291v mutant |
|
13
|
58
|
3zvqB |
Crystal structure of proteolyzed lysozyme |
|
94
|
307
|
4aaaA |
Crystal structure of the human cdkl2 kinase domain |
|
180
|
499
|
4a7aA |
Crystal structure of human monoamine oxidase b (mao b) in complex with rosiglitazone |
|
87
|
282
|
4an3A |
Crystal structures of human mek1 with carboxamide-based allosteric inhibitor xl518 (gdc-0973), or related analogs. |
|
145
|
414
|
4apyA |
Ethylene glycol-bound form of p450 cyp125a3 from mycobacterium smegmatis |
|
145
|
382
|
3zpxA |
Ustilago maydis lipase um03410, short form without flap |
|
224
|
637
|
3ziuA |
Crystal structure of mycoplasma mobile leucyl-trna synthetase with leu-ams in the active site |
|
98
|
350
|
4accA |
Gsk3b in complex with inhibitor |
|
54
|
184
|
4a0yA |
Structure of the global transcription regulator fapr from staphylococcus aureus |
|
21
|
80
|
3zoxA |
Crystal structure of n64del mutant of nitrosomonas europaea cytochrome c552 (monoclinic space group) |
|
90
|
282
|
4an2A |
Crystal structures of human mek1 with carboxamide-based allosteric inhibitor xl518 (gdc-0973), or related analogs. |
|
136
|
396
|
3zpiA |
Pikc d50n mutant in p21 space group |
|
53
|
184
|
4a0xA |
Structure of the global transcription regulator fapr from staphylococcus aureus |
|
103
|
348
|
3zrmA |
Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors |
|
250
|
710
|
3wnuA |
The crystal structure of catalase-peroxidase, katg, from synechococcus pcc7942 |
|
103
|
250
|
3zraA |
Structural basis for agonism and antagonism for a set of chemically related progesterone receptor modulators |
|
89
|
324
|
4aaoA |
Maca-h93g |
|
95
|
350
|
4achA |
Gsk3b in complex with inhibitor |
|
104
|
309
|
4anpA |
Crystal structure of human phenylalanine hydroxylase in complex with a pharmacological chaperone |
|
46
|
108
|
3zrvA |
The high resolution structure of a dimeric hamp-dhp fusion displays asymmetry - a291f mutant |
