Structure of PDB 5ow7 Chain A Binding Site BS02
Receptor Information
>5ow7 Chain A (length=240) Species:
7955
(Danio rerio) [
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HMLSDEQMQIINSLVEAHHKTYDDSYSDFVRFRPPVRRLSMLPHLADLVS
YSIQKVIGFAKMIPGFRDLTAEDQIALLKSSAIEIIMLRSNQSFSLEDMS
WSCGGPDFKYCINDVTKAGHTLELLEPLVKFQVGLKKLKLHEEEHVLLMA
ICLLSPDRPGVQDHVRIEALQDRLCDVLQAYIRIQHPGGRLLYAKMIQKL
ADLRSLNEEHSKQYRSLSFQPEHSMQLTPLVLEVFGSEVS
Ligand information
Ligand ID
AYK
InChI
InChI=1S/C26H41NO3/c1-17(2)27-24(29)16-26(5,30)23-13-12-22-19(7-6-14-25(22,23)4)9-10-20-15-21(28)11-8-18(20)3/h9-10,17,21-23,28,30H,3,6-8,11-16H2,1-2,4-5H3,(H,27,29)/b19-9+,20-10-/t21-,22-,23-,25-,26-/m0/s1
InChIKey
CSLRSUXCVDRFJS-YDGCZWIRSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(C)NC(=O)C[C@](C)(O)[C@H]1CC[C@H]2/C(CCC[C@]12C)=C/C=C3/C[C@@H](O)CCC3=C
OpenEye OEToolkits 2.0.6
CC(C)NC(=O)CC(C)(C1CCC2C1(CCCC2=CC=C3CC(CCC3=C)O)C)O
CACTVS 3.385
CC(C)NC(=O)C[C](C)(O)[CH]1CC[CH]2C(CCC[C]12C)=CC=C3C[CH](O)CCC3=C
OpenEye OEToolkits 2.0.6
CC(C)NC(=O)C[C@@](C)([C@H]1CC[C@@H]\2[C@@]1(CCC/C2=C\C=C/3\C[C@H](CCC3=C)O)C)O
Formula
C26 H41 N O3
Name
ChEMBL
DrugBank
ZINC
PDB chain
5ow7 Chain A Residue 4000 [
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Receptor-Ligand Complex Structure
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PDB
5ow7
Investigation of 20S-hydroxyvitamin D3 analogs and their 1 alpha-OH derivatives as potent vitamin D receptor agonists with anti-inflammatory activities.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
Y175 V262 S303 S306 W314 C316 H333 H423
Binding residue
(residue number reindexed from 1)
Y22 V49 S90 S93 W101 C103 H120 H210
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0004879
nuclear receptor activity
Biological Process
GO:0006355
regulation of DNA-templated transcription
Cellular Component
GO:0005634
nucleus
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5ow7
,
PDBe:5ow7
,
PDBj:5ow7
PDBsum
5ow7
PubMed
29367669
UniProt
Q9PTN2
|VDRA_DANRE Vitamin D3 receptor A (Gene Name=vdra)
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