|
62
|
187
|
3voxA |
X-ray crystal structure of wild type hrtr in the apo form |
|
98
|
309
|
3vrnA |
Crystal structure of the tyrosine kinase binding domain of cbl-c |
|
98
|
251
|
3vt4A |
Crystal structures of rat vdr-lbd with r270l mutation |
|
103
|
271
|
3vn2A |
Crystal structure of ppargamma complexed with telmisartan |
|
23
|
73
|
3vrlC |
Crystal structure of bmj4 p24 capsid protein in complex with a10f9 fab |
|
134
|
334
|
3vjbA |
Crystal structure of the human squalene synthase |
|
93
|
251
|
3vt9A |
Crystal structures of rat vdr-lbd with w282r mutation |
|
90
|
322
|
3vjnA |
Crystal structure of the mutated egfr kinase domain (g719s/t790m) in complex with amppnp. |
|
54
|
139
|
3vouA |
The crystal structure of nak-navsulp chimera channel |
|
38
|
247
|
3vutA |
Crystal structures of non-phosphorylated map2k4 |
|
95
|
251
|
3vt5A |
Crystal structures of rat vdr-lbd with r270l mutation |
|
40
|
136
|
3vodA |
Crystal structure of mutant marr c80s from e.coli |
|
28
|
89
|
3vk0A |
Crystal structure of hypothetical transcription factor nhtf from neisseria |
|
70
|
184
|
3vw1A |
Crystal strucuture of the crystal violet-bound form of ramr (transcriptional regurator of tetr family) from salmonella typhimurium |
|
75
|
264
|
3vqxA |
Crystal structure of the catalytic domain of pyrrolysyl-trna synthetase in triclinic crystal form |
|
97
|
250
|
3vrwA |
Vdr ligand binding domain in complex with 22s-butyl-2-methylidene-26,27-dimethyl-19,24-dinor-1alpha,25-dihydroxyvitamin d3 |
|
16
|
84
|
3v9rB |
Crystal structure of saccharomyces cerevisiae mhf complex |
|
104
|
305
|
3vrrA |
Crystal structure of the tyrosine kinase binding domain of cbl-c (pl mutant) in complex with phospho-egfr peptide |
|
102
|
307
|
3vntA |
Crystal structure of the kinase domain of human vegfr2 with a [1,3]thiazolo[5,4-b]pyridine derivative |
|
61
|
174
|
3vrdA |
Crystal structure of flavocytochrome c from thermochromatium tepidum |
|
230
|
714
|
3vllA |
Crystal structure analysis of the ser305ala variant of katg from haloarcula marismortui complexes with inhibitor sha |
|
19
|
80
|
3vymA |
Dimeric hydrogenobacter thermophilus cytochrome c552 |
|
133
|
334
|
3vjcA |
Crystal structure of the human squalene synthase in complex with zaragozic acid a |
|
82
|
229
|
3vmtA |
Crystal structure of staphylococcus aureus membrane-bound transglycosylase in complex with a lipid ii analog |
|
71
|
291
|
3vn9A |
Rifined crystal structure of non-phosphorylated map2k6 in a putative auto-inhibition state |
|
85
|
267
|
3vqvA |
Crystal structure of the catalytic domain of pyrrolysyl-trna synthetase in complex with amppnp (re-refined) |
|
139
|
407
|
3vooA |
Cytochrome p450sp alpha (cyp152b1) mutant a245e |
|
52
|
219
|
3vp7A |
Crystal structure of the beta-alpha repeated, autophagy-specific (bara) domain of vps30/atg6 |
|
250
|
714
|
3vlhA |
Crystal structure analysis of the arg409leu variants of katg from haloarcula marismortui |
|
113
|
284
|
3vjeA |
Crystal structure of the y248a mutant of c(30) carotenoid dehydrosqualene synthase from staphylococcus aureus in complex with zaragozic acid a |
|
147
|
335
|
3vj9A |
Crystal structure of the human squalene synthase |
|
113
|
347
|
3vqhA |
Bromine sad partially resolves multiple binding modes for pka inhibitor h-89 |
|
125
|
286
|
3vpnA |
Crystal structure of human ribonucleotide reductase subunit m2 (hrrm2) mutant |
|
84
|
292
|
3v5qA |
Discovery of a selective trk inhibitor with efficacy in rodent cancer tumor models |
|
103
|
309
|
3vrpA |
Crystal structure of the tyrosine kinase binding domain of cbl-c in complex with phospho-egfr peptide |
|
96
|
251
|
3vt8A |
Crystal structures of rat vdr-lbd with w282r mutation |
|
57
|
249
|
3vrbB |
Mitochondrial rhodoquinol-fumarate reductase from the parasitic nematode ascaris suum with the specific inhibitor flutolanil and substrate fumarate |
|
192
|
587
|
3vr6A |
Crystal structure of amp-pnp bound enterococcus hirae v1-atpase [bv1] |
|
42
|
152
|
3vygB |
Crystal structure of thiocyanate hydrolase mutant r136w |
|
90
|
323
|
3vjoA |
Crystal structure of the wild-type egfr kinase domain in complex with amppnp. |
|
57
|
141
|
3vreA |
The crystal structure of hemoglobin from woolly mammoth in the deoxy form |
|
122
|
447
|
3vryA |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 4-amino-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-7-yl-cyclopentane |
|
71
|
280
|
3vquA |
Crystal structure of human mps1 catalytic domain in complex with 4-[(4-amino-5-cyano-6-ethoxypyridin-2- yl)amino]benzamide |
|
93
|
249
|
3vrtA |
Vdr ligand binding domain in complex with 2-mehylidene-19,25,26,27-tetranor-1alpha,24-dihydroxyvitamind3 |
|
94
|
251
|
3vtdA |
Crystal structure of rat vitamin d receptor bound to a partial agonist 26-adamantyl-23-yne-19-norvitammin d adtk4 |
|
135
|
407
|
3vtjA |
Cytochrome p450sp alpha (cyp152b1) mutant a245h |
|
58
|
146
|
3vreB |
The crystal structure of hemoglobin from woolly mammoth in the deoxy form |
|
83
|
229
|
3vmqA |
Crystal structure of staphylococcus aureus membrane-bound transglycosylase: apoenzyme |
|
123
|
447
|
3vs3A |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 7-[trans-4-(4-methylpiperazin-1-yl)cyclohexyl]-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine |
|
73
|
184
|
3vvzA |
Crystal strucuture of the rhodamine 6g-bound form of ramr (transcriptional regurator of tetr family) from salmonella typhimurium |
