|
78
|
271
|
3vbyA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
142
|
335
|
3v66A |
Human squalene synthase in complex with 2-(1-{2-[(4r,6s)-8-chloro-6-(2,3-dimethoxyphenyl)-4h,6h-pyrrolo[1,2-a][4,1]benzoxazepin-4-yl]acetyl}-4-piperidinyl)acetic acid |
|
13
|
40
|
3vejA |
Crystal structure of the get5 carboxyl domain from s. cerevisiae |
|
125
|
325
|
3v1xA |
Crystal structure of 2-methylisoborneol synthase from streptomyces coelicolor a3(2) in complex with mg2+ and 2-fluorogeranyl diphosphate |
|
28
|
88
|
3v9rA |
Crystal structure of saccharomyces cerevisiae mhf complex |
|
70
|
216
|
3v42A |
Crystal structure of renal tumor suppressor protein, folliculin |
|
100
|
322
|
3v8lA |
Crystal structure of staphylococcus aureus biotin protein ligase in complex with biotinyl-5'-amp |
|
93
|
355
|
3vhkA |
Crystal structure of the vegfr2 kinase domain in complex with a back pocket binder |
|
123
|
332
|
3v94A |
Tcrpdec1 catalytic domain in complex with inhibitor wyq16 |
|
31
|
94
|
3vh5T |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form i |
|
24
|
90
|
3uw5A |
Crystal structure of the bir domain of mliap bound to gdc0152 |
|
105
|
357
|
3v6sA |
Discovery of potent and selective covalent inhibitors of jnk |
|
227
|
583
|
3v09A |
Crystal structure of rabbit serum albumin |
|
70
|
164
|
3v57A |
Crystal structure of the b-phycoerythrin from the red algae porphyridium cruentum at ph8 |
|
98
|
249
|
3v49A |
Structure of ar lbd with activator peptide and sarm inhibitor 1 |
|
123
|
395
|
3v8sA |
Human rho-associated protein kinase 1 (rock 1) in complex with indazole derivative (compound 18) |
|
89
|
242
|
3v3qA |
Crystal structure of human nur77 ligand-binding domain in complex with ethyl 2-[2,3,4 trimethoxy-6(1-octanoyl)phenyl]acetate |
|
42
|
98
|
3vh6A |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form ii |
|
42
|
120
|
3v2lA |
Structure of anopheles gambiae odorant binding protein 20 bound to polyethylene glycol |
|
70
|
264
|
3v8tA |
Crystal structure of interleukin-2 inducible t-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 477 |
|
24
|
84
|
3vbgA |
Structure of hdm2 with dimer inducing indolyl hydantoin ro-2443 |
|
205
|
639
|
3v5wA |
Human g protein-coupled receptor kinase 2 in complex with soluble gbetagamma subunits and paroxetine |
|
27
|
73
|
3vh6W |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form ii |
|
102
|
267
|
3vi8A |
Human ppar alpha ligand binding domain in complex with a synthetic agonist aphm13 |
|
29
|
87
|
3v3bA |
Structure of the stapled p53 peptide bound to mdm2 |
|
283
|
1066
|
3tw7A |
Structure of rhizobium etli pyruvate carboxylase t882a crystallized without acetyl coenzyme-a |
|
101
|
255
|
3vhwA |
Crystal structure of the human vitamin d receptor ligand binding domain complexed with 4-mp |
|
95
|
351
|
3v00A |
Studies of a constitutively active g-alpha subunit provide insights into the mechanism of g protein activation. |
|
69
|
177
|
3v58B |
Crystal structure of the b-phycoerythrin from the red algae porphyridium cruentum at ph5 |
|
84
|
273
|
3vf8A |
Crystal structure of spleen tyrosine kinase syk catalytic domain with pyrazolylbenzimidazole inhibitor 416 |
|
59
|
152
|
3v2vA |
Nitrite bound chlorin substituted myoglobin- method 1 |
|
46
|
136
|
3vb2A |
Crystal structure of the reduced form of marr from e.coli |
|
85
|
297
|
3vgoA |
Crystal structure of the n-terminal fragment of cbl-b |
|
102
|
357
|
3v6rA |
Discovery of potent and selective covalent inhibitors of jnk |
|
104
|
271
|
3v9yA |
Crystal structure of the ppargamma-lbd complexed with a cercosporamide derivative modulator |
|
144
|
335
|
3vj8A |
Crystal structure of the human squalene synthase |
|
96
|
292
|
3uzpA |
Crystal structure of ck1d with pf670462 from p21 crystal form |
|
42
|
100
|
3vh5A |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form i |
|
192
|
595
|
3v6qA |
Crystal structure of the complex of bovine lactoperoxidase with carbon monoxide at 2.0 a resolution |
|
83
|
289
|
3vfdA |
Human spastin aaa domain |
|
75
|
262
|
3v5lA |
Crystal structure of interleukin-2 inducible t-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 542 |
|
79
|
272
|
3vf9A |
Crystal structure of spleen tyrosine kinase syk catalytic domain with thienopyrazolylindole inhibitor 027 |
|
71
|
190
|
5hbuA |
Structure of the e. coli nucleoid occlusion protein slma bound to dna and the c-terminal tail of the cytoskeletal cell division protein ftsz |
|
157
|
566
|
3utoA |
Twitchin kinase region from c.elegans (fn31-nl-kin-crd-ig26) |
|
148
|
465
|
3v5tA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1299 |
|
134
|
410
|
3v8fA |
Crystal structure of crosslinked gltph v216c-m385c mutant |
|
266
|
735
|
3ut2A |
Crystal structure of fungal magkatg2 |
|
97
|
357
|
3v3vA |
Structural and functional analysis of quercetagetin, a natural jnk1 inhibitor |
|
59
|
151
|
3vauA |
Myoglobin nitrite structure: nitriheme modified |
|
31
|
97
|
3vh6T |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form ii |
