|
95
|
310
|
3vrqA |
Crystal structure of the tyrosine kinase binding domain of cbl-c (pl mutant) |
|
78
|
185
|
3vp5A |
X-ray crystal structure of wild type hrtr in the holo form |
|
99
|
252
|
3vjsA |
Vitamin d receptor complex with a carborane compound |
|
106
|
447
|
3vs7A |
Crystal structure of hck complexed with a pyrazolo-pyrimidine inhibitor 1-cyclopentyl-3-(1h-pyrrolo[2,3-b]pyridin-5-yl)-1h-pyrazolo[3,4-d]pyrimidin-4-amine |
|
57
|
141
|
3vrgA |
The crystal structure of hemoglobin from woolly mammoth in the met form |
|
100
|
251
|
3vtcA |
Crystal structure of rat vitamin d receptor bound to a partial agonist 26-adamantyl-23-yne-19-norvitammin d adtk3 |
|
181
|
500
|
3vu8A |
Metionyl-trna synthetase from thermus thermophilus complexed with methionyl-adenylate analogue |
|
95
|
274
|
3vjiA |
Human ppar gamma ligand binding domain in complex with jkpl53 |
|
66
|
229
|
3vmrA |
Crystal structure of staphylococcus aureus membrane-bound transglycosylase in complex with moenomycin |
|
116
|
447
|
3vs5A |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 7-(1-methylpiperidin-4-yl)-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine |
|
109
|
447
|
3vs0A |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor n-[4-(4-amino-7-cyclopentyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzamide |
|
110
|
447
|
3vs4A |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 5-(4-phenoxyphenyl)-7-(tetrahydro-2h-pyran-4-yl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine |
|
106
|
260
|
3vhvA |
Mineralocorticoid receptor ligand-binding domain with non-steroidal antagonist |
|
76
|
271
|
3vqiA |
Crystal structure of kluyveromyces marxianus atg5 |
|
95
|
358
|
3vulA |
Crystal structure of a cysteine-deficient mutant m1 in map kinase jnk1 |
|
42
|
136
|
3voeA |
Crystal structure of wild type marr (apo form) from e.coli |
|
183
|
588
|
3vr4A |
Crystal structure of enterococcus hirae v1-atpase [ev1] |
|
250
|
714
|
3vlkA |
Crystal structure analysis of the ser305ala variant of katg from haloarcula marismortui |
|
48
|
148
|
3vncA |
Crystal structure of tip-alpha n25 from helicobacter pylori in its natural dimeric form |
|
98
|
251
|
3vt6A |
Crystal structure of rat vdr-lbd with 2-substituted-16-ene-22-thia-1alpha,25-dihydroxy-26,27-dimethyl-19-norvitamin d3 |
|
104
|
358
|
3vukA |
Crystal structure of a cysteine-deficient mutant m5 in map kinase jnk1 |
|
117
|
447
|
3vrzA |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 1-[4-(4-amino-7-cyclopentyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]-3-benzylurea |
|
108
|
358
|
3vuhA |
Crystal structure of a cysteine-deficient mutant m3 in map kinase jnk1 |
|
96
|
274
|
3vjhA |
Human ppar gamma ligand binding domain in complex with jkpl35 |
|
99
|
250
|
3vrvA |
Vdr ligand binding domain in complex with 2-methylidene-26,27-dimethyl-19,24-dinor-1alpha,25-dihydroxyvitamin d3 |
|
229
|
700
|
3vlmA |
Crystal structure analysis of the met244ala variant of katg from haloarcula marismortui |
|
81
|
202
|
3vibA |
Structural basis for multidrug recognition and antimicrobial resistance by mtrr, an efflux pump regulator from neisseria gonorrhoeae |
|
99
|
251
|
3vruA |
Vdr ligand binding domain in complex with 2-methylidene-19,24-dinor-1alpha,25-dihydroxy vitamind3 |
|
100
|
308
|
3vroA |
Crystal structure of the tyrosine kinase binding domain of cbl-c in complex with phospho-src peptide |
|
51
|
151
|
3v4gA |
1.60 angstrom resolution crystal structure of an arginine repressor from vibrio vulnificus cmcp6 |
|
57
|
249
|
3vr8B |
Mitochondrial rhodoquinol-fumarate reductase from the parasitic nematode ascaris suum |
|
100
|
272
|
3vsoA |
Human ppar gamma ligand binding domain in complex with a gamma selective agonist mekt21 |
|
41
|
129
|
3vnwA |
Crystal structure of cytochrome c552 from thermus thermophilus at ph 5.44 |
|
59
|
146
|
3vrfB |
The crystal structure of hemoglobin from woolly mammoth in the carbonmonoxy forms |
|
98
|
251
|
3vtbA |
Crystal structure of rat vitamin d receptor bound to a partial agonist 25-adamantyl-23-yne-19-norvitammin d adtk1 |
|
103
|
261
|
3vt3A |
Crystal structures of rat vdr-lbd with r270l mutation |
|
71
|
189
|
3vprA |
Crystal structure of a tetr family transcriptional regulator pfmr from thermus thermophilus hb8 |
|
185
|
586
|
3vr2A |
Crystal structure of nucleotide-free a3b3 complex from enterococcus hirae v-atpase [ea3b3] |
|
53
|
155
|
3vwoA |
Crystal structure of peptidoglycan hydrolase mutant from sphingomonas sp. a1 |
|
103
|
274
|
3vspA |
Human ppar gamma ligand binding domain in complex with a gamma selective agonist mekt28 |
|
112
|
447
|
3vs1A |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 1-[4-(4-amino-7-cyclopentyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]-3-phenylurea |
|
122
|
284
|
3vjdA |
Crystal structure of the y248a mutant of c(30) carotenoid dehydrosqualene synthase from staphylococcus aureus |
|
50
|
249
|
3vraB |
Mitochondrial rhodoquinol-fumarate reductase from the parasitic nematode ascaris suum with the specific inhibitor atpenin a5 |
|
251
|
714
|
3vljA |
Crystal structure analysis of the cyanide arg409leu variant complexes with o-dianisidine in katg from haloarcula marismortui |
|
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 |
|
57
|
141
|
3vreA |
The crystal structure of hemoglobin from woolly mammoth in the deoxy form |
|
90
|
323
|
3vjoA |
Crystal structure of the wild-type egfr kinase domain in complex with amppnp. |
|
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 |
