|
39
|
122
|
4qjfB |
X-ray crystal structure of thermocuccus kodakarensis rna polymerase rpp4/rpo7 (rpof/rpoe) complex |
|
57
|
205
|
4ettA |
Crystal structure of rabbit ryanodine receptor 1 mutant e2764k |
|
45
|
110
|
4f6gA |
Aquomet structure of his100trp cerebratulus lacteus mini-hemoglobin |
|
117
|
354
|
4fa9A |
Crystal structure of wt maug in complex with pre-methylamine dehydrogenase aged 30 days |
|
83
|
226
|
4q59A |
Crystal structure of plectin 1a actin-binding domain |
|
93
|
290
|
4f0iA |
Crystal structure of apo trka |
|
121
|
354
|
4fa4A |
Crystal structure of wt maug in complex with pre-methylamine dehydrogenase aged 10 days |
|
35
|
91
|
4ewiA |
Crystal structure of the nlrp4 pyrin domain |
|
88
|
299
|
4f63A |
Crystal structure of human fibroblast growth factor receptor 1 kinase domain in complex with compound 1 |
|
344
|
1102
|
4ddwA |
Thermotoga maritima reverse gyrase, c-centered orthorhombic form |
|
86
|
342
|
4f1iA |
Crystal structure of semet tdp2 from caenorhabditis elegans |
|
24
|
134
|
5gahJ |
Rnc in complex with srp with detached ng domain |
|
65
|
162
|
4f0tA |
X-ray crystal structure of phycocyanin from synechocystis sp. pcc 6803 |
|
61
|
380
|
4qiwC |
Crystal structure of euryarchaeal rna polymerase from thermococcus kodakarensis |
|
91
|
290
|
4f08A |
Discovery and optimization of c-2 methyl imidazo-pyrrolopyridines as potent and orally bioavailable jak1 inhibitors with selectivity over jak2 |
|
84
|
273
|
4f4pA |
Syk in complex with ligand lasw836 |
|
110
|
316
|
4qj3A |
Structure of a fragment of human phospholipase c-beta3 delta472-559, in complex with galphaq |
|
34
|
78
|
4f8dA |
Crystal structure of an r46a mutant of the restriction-modification controller protein c.esp1396i (monoclinic form) |
|
159
|
535
|
4hstB |
Crystal structure of a double mutant of a class iii engineered cephalosporin acylase |
|
44
|
110
|
4f68A |
Oxy structure of tyr11phe/gln44leu/thr48val/ala55trp cerebratulus lacteus mini-hemoglobin |
|
123
|
294
|
4evfA |
Crystal structure of apo alpha-1 giardin |
|
45
|
110
|
4f6bA |
Aquomet structure of his100phe cerebratulus lacteus mini-hemoglobin |
|
82
|
287
|
4hviA |
Jak3 kinase domain in complex with 2-cyclopropyl-5h-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((r)-1-methyl-2-oxo-2-piperidin-1-yl-ethyl)-amide |
|
143
|
345
|
4ezdA |
Crystal structure of the ut-b urea transporter from bos taurus bound to selenourea |
|
97
|
290
|
4qmqA |
Mst3 in complex with cp-673451 |
|
113
|
284
|
4f6xA |
Crystal structure of dehydrosqualene synthase (crtm) from s. aureus complexed with bph-1112 |
|
137
|
338
|
4htzA |
Crystal structure of pde2 catalytic domain in space group p1 |
|
26
|
83
|
4f44A |
Neurotrophin p75ntr intracellular domain |
|
164
|
431
|
4f6rB |
Tubulin:stathmin-like domain complex |
|
10
|
63
|
4qiwN |
Crystal structure of euryarchaeal rna polymerase from thermococcus kodakarensis |
|
120
|
294
|
4evhA |
Crystal structure of calcium-bound alpha-1 giardin |
|
46
|
110
|
4f6fA |
Carbonmonoxy structure of his100phe cerebratulus lacteus mini-hemoglobin |
|
71
|
274
|
4pp7A |
Highly potent and selective 3-n-methylquinazoline-4(3h)-one based inhibitors of b-rafv600e kinase |
|
108
|
386
|
4eutA |
Structure of bx-795 complexed with unphosphorylated human tbk1 kinase-uld domain |
|
69
|
201
|
4f71A |
Crystal structure of had family enzyme bt-2542 (target efi-501088) from bacteroides thetaiotaomicron, wild-type protein, complex with magnesium and inorganic phosphate |
|
25
|
90
|
4ereA |
Crystal structure of mdm2 (17-111) in complex with compound 23 |
|
75
|
276
|
4f1oA |
Crystal structure of the l1180t mutant roco4 kinase domain from d. discoideum bound to appcp |
|
100
|
266
|
4f6sB |
Crystal structure of human cdk8/cycc in complex with compound 7 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]urea) |
|
48
|
129
|
4qy9A |
X-ray structure of the adduct between hen egg white lysozyme and auoxo3, a cytotoxic gold(iii) compound |
|
30
|
118
|
4f0aA |
Crystal structure of xwnt8 in complex with the cysteine-rich domain of frizzled 8 |
|
87
|
302
|
4f65A |
Crystal structure of human fibroblast growth factor receptor 1 kinase domain in complex with compound 8 |
|
97
|
268
|
4f7jB |
Crystal structure of human cdk8/cycc in complex with compound 3 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-(2-hydroxyethyl)urea) |
|
80
|
217
|
4ex7A |
Crystal structure of the alnumycin p phosphatase in complex with free phosphate |
|
117
|
348
|
4f9wA |
Human p38alpha mapk in complex with a novel and selective small molecule inhibitor |
|
26
|
92
|
4qocA |
Crystal structure of compound 16 bound to mdm2(17-111), {(3r,5r,6s)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-[(1s)-1-cyclopropyl-2-(pyrrolidin-1-ylsulfonyl)ethyl]-3-methyl-2-oxopiperidin-3-yl}acetic acid |
|
99
|
267
|
4f7sB |
Crystal structure of human cdk8/cycc in the dmg-in conformation |
|
247
|
583
|
4f5uA |
Crystal structure of equine serum albumin at 2.04 resolution |
|
102
|
338
|
4er5A |
Crystal structure of human dot1l in complex with 2 molecules of epz004777 |
|
69
|
270
|
4f52A |
Structure of a glomulin-rbx1-cul1 complex |
|
45
|
110
|
4f6jA |
Carbonmonoxy structure of his100trp cerebratulus lacteus mini-hemoglobin |
