Structure of PDB 4ijv Chain B Binding Site BS01
Receptor Information
>4ijv Chain B (length=281) Species:
9606
(Homo sapiens) [
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MASMTGGQQMGRGSNEEFRPEMLQGKKVIVTGASKGIGREMAYHLAKMGA
HVVVTARSKETLQKVVSHCLELGAASAHYIAGTMEDMTFAEQFVAQAGKL
MGGLDMLILNHITNTSLNLFHDDIHHVRKSMEVNFLSYVVLTVAALPMLK
QSNGSIVVVSSLAGKVAYPMVAAYSASKFALDGFFSSIRKEYSVSRVNVS
ITLCVLGLIDTETAMKAVSGIVHMQAAPKEECALEIIKGGALRQEEVYYD
SSRWTTLLIRNPCRKILEELYSTSYNMDRFI
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
4ijv Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4ijv
Optimization of 1,2,4-Triazolopyridines as Inhibitors of Human 11 beta-Hydroxysteroid Dehydrogenase Type 1 (11 beta-HSD-1).
Resolution
2.35 Å
Binding residue
(original residue number in PDB)
G41 S43 K44 G45 I46 A65 R66 S67 T92 M93 N119 I121 V168 S170 Y183 K187 L215 G216 I218 T220 T222 A223
Binding residue
(residue number reindexed from 1)
G32 S34 K35 G36 I37 A56 R57 S58 T83 M84 N110 I112 V159 S161 Y174 K178 L206 G207 I209 T211 T213 A214
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S170 Y183 K187
Catalytic site (residue number reindexed from 1)
S161 Y174 K178
Enzyme Commision number
1.1.1.146
: 11beta-hydroxysteroid dehydrogenase.
1.1.1.201
: 7beta-hydroxysteroid dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0005496
steroid binding
GO:0016491
oxidoreductase activity
GO:0042803
protein homodimerization activity
GO:0047022
7-beta-hydroxysteroid dehydrogenase (NADP+) activity
GO:0050661
NADP binding
GO:0070524
11-beta-hydroxysteroid dehydrogenase (NADP+) activity
GO:0102196
cortisol dehydrogenase activity
Biological Process
GO:0006706
steroid catabolic process
GO:0008202
steroid metabolic process
GO:0030324
lung development
Cellular Component
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0016020
membrane
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Cellular Component
External links
PDB
RCSB:4ijv
,
PDBe:4ijv
,
PDBj:4ijv
PDBsum
4ijv
PubMed
25050169
UniProt
P28845
|DHI1_HUMAN 11-beta-hydroxysteroid dehydrogenase 1 (Gene Name=HSD11B1)
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