|
94
|
303
|
4hw7A |
Crystal structure of fms kinase domain with a small molecular inhibitor, plx647-ome |
|
123
|
348
|
4qteA |
Structure of erk2 in complex with vtx-11e, 4-{2-[(2-chloro-4-fluorophenyl)amino]-5-methylpyrimidin-4-yl}-n-[(1s)-1-(3-chlorophenyl)-2-hydroxyethyl]-1h-pyrrole-2-carboxamide |
|
59
|
141
|
4f4oA |
Structure of the haptoglobin-haemoglobin complex |
|
158
|
492
|
4f3eA |
Crystal structure of thermus thermophilus hb8 casa |
|
107
|
349
|
4ewqA |
Human p38 alpha mapk in complex with a pyridazine based inhibitor |
|
90
|
260
|
4f47A |
The structure of enoyl-coa hydratase echa19 from mycobacterium marinum |
|
23
|
98
|
4hv0A |
Structure and function of avtr, a novel transcriptional regulator from a hyperthermophilic archaeal lipothrixvirus |
|
100
|
350
|
4eyjA |
Mapk13 complex with inhibitor |
|
98
|
267
|
4f6uB |
Crystal structure of human cdk8/cycc in complex with compound 5 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-[3-(morpholin-4-yl)propyl]urea) |
|
65
|
291
|
4ez5A |
Cdk6 (monomeric) in complex with inhibitor |
|
121
|
354
|
4favA |
Crystal structure of wt maug in complex with pre-methylamine dehydrogenase aged 50 days |
|
91
|
290
|
4f09A |
Discovery and optimization of c-2 methyl imidazo-pyrrolopyridines as potent and orally bioavailable jak1 inhibitors with selectivity over jak2 |
|
112
|
349
|
4f9yA |
Human p38 alpha mapk in complex with a novel and selective small molecule inhibitor |
|
104
|
361
|
4f6uA |
Crystal structure of human cdk8/cycc in complex with compound 5 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-[3-(morpholin-4-yl)propyl]urea) |
|
91
|
291
|
4pmpA |
The structure of trka kinase bound to the inhibitor 1-cyclopropyl-1-[3-(1,3-thiazol-2-yl)benzyl]-3-[4-(trifluoromethoxy)phenyl]urea |
|
152
|
535
|
4hsrB |
Crystal structure of a class iii engineered cephalosporin acylase |
|
62
|
197
|
4qnqA |
Crystal structure analysis of full-length bcl-xl in complex with the inhibitor abt-263 |
|
58
|
155
|
4f0zB |
Crystal structure of calcineurin in complex with the calcineurin-inhibiting domain of the african swine fever virus protein a238l |
|
100
|
356
|
4f9bA |
Human cdc7 kinase in complex with dbf4 and pha767491 |
|
236
|
583
|
4f5tA |
Crystal structure of equine serum albumin |
|
77
|
302
|
4ez7A |
Cdk2 in complex with staurosporine and 2 molecules of 8-anilino-1-naphthalene sulfonic acid |
|
17
|
61
|
4f2lA |
Structure of a regulatory domain of ampk |
|
156
|
437
|
4f6rA |
Tubulin:stathmin-like domain complex |
|
81
|
219
|
4ex6A |
Crystal structure of the alnumycin p phosphatase alnb |
|
62
|
161
|
4f0uB |
X-ray crystal structure of allophycocyanin from synechococcus elongatus pcc 7942 |
|
117
|
350
|
4fa2A |
Human p38 alpha mitogen-activated kinase in complex with sb239063 |
|
23
|
134
|
5gagJ |
Rnc in complex with srp-sr in the closed state |
|
42
|
119
|
4f7fA |
Structure of anopheles gambiae odorant binding protein 20 |
|
67
|
161
|
4po5B |
Crystal structure of allophycocyanin b from synechocystis pcc 6803 |
|
157
|
524
|
4pknA |
Crystal structure of the football-shaped groel-groes2-(adpbefx)14 complex containing substrate rubisco |
|
132
|
560
|
4eq5A |
Dna ligase from the archaeon thermococcus sibiricus |
|
83
|
315
|
4exmA |
The crystal structure of an engineered phage lysin containing the binding domain of pesticin and the killing domain of t4-lysozyme |
|
103
|
359
|
4f7sA |
Crystal structure of human cdk8/cycc in the dmg-in conformation |
|
295
|
784
|
4e7zA |
Myosin vi (md) pre-powerstroke state, p21 crystal form |
|
295
|
908
|
4e36A |
Crystal structure of the human endoplasmic reticulum aminopeptidase 2 variant n392k |
|
58
|
150
|
4hw3A |
Discovery of potent mcl-1 inhibitors using fragment-based methods and structure-based design |
|
87
|
284
|
4qmnA |
Mst3 in complex with bosutinib |
|
67
|
213
|
4ev0A |
Crystal structure of thermus thermophilus catabolite activator protein |
|
83
|
287
|
4hvdA |
Jak3 kinase domain in complex with 2-cyclopropyl-5h-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((s)-1,2,2-trimethyl-propyl)-amide |
|
73
|
239
|
4f3qA |
Structure of a yebc family protein (cbu_1566) from coxiella burnetii |
|
91
|
361
|
4f7lA |
Crystal structure of human cdk8/cycc in complex with compound 2 (tert-butyl [3-({[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]carbamoyl}amino)propyl]carbamate) |
|
119
|
354
|
4fa5A |
Crystal structure of wt maug in complex with pre-methylamine dehydrogenase aged 20 days |
|
35
|
95
|
4qnhB |
Calcium-calmodulin (t79d) complexed with the calmodulin binding domain from a small conductance potassium channel sk2-a |
|
93
|
266
|
4f70B |
Crystal structure of human cdk8/cycc in complex with compound 4 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-[2-(morpholin-4-yl)ethyl]urea) |
|
119
|
354
|
4fa1A |
Crystal structure of wt maug in complex with pre-methylamine dehydrogenase aged 130 days. |
|
78
|
275
|
4ewhA |
Co-crystal structure of ack1 with inhibitor |
|
100
|
356
|
4f9aA |
Human cdc7 kinase in complex with dbf4 and nucleotide |
|
93
|
328
|
4er3A |
Crystal structure of human dot1l in complex with inhibitor epz004777 |
|
67
|
201
|
4f72A |
Crystal structure of had family enzyme bt-2542 (target efi-501088) from bacteroides thetaiotaomicron, asp12ala mutant, complex with magnesium and inorganic phosphate |
|
124
|
371
|
4eziA |
Crystal structure of a putative hydrolase (lpg1103) from legionella pneumophila subsp. pneumophila str. philadelphia 1 at 1.15 a resolution |
