Structure of PDB 3ey4 Chain B Binding Site BS01
Receptor Information
>3ey4 Chain B (length=255) Species:
9606
(Homo sapiens) [
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FRPEMLQGKKVIVTGASKGIGREMAYHLAKMGAHVVVTARSKETLQKVVS
HCLELGAASAHYIAGTMEDMTFAEQFVAQAGKLMGGLDMLILNHITNTSL
NLFHDDIHHVRKSMEVNFLSYVVLTVAALPMLKQSNGSIVVVSSLAGKVA
YPMVAAYSASKFALDGFFSSIRKEYSVSRVNVSITLCVLGLIDTETAMKA
VSGIVHMQAAPKEECALEIIKGGALRQEEVYYDSSLWTTLLIRNPSRKIL
EFLYS
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/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/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
3ey4 Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
3ey4
Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11-hydroxysteroid dehydrogenase type 1 (11-HSD1) inhibitors: Reducing pregnane X receptor (PXR) activity and exploring activity in a monkey pharmacodynamic model
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
G41 S43 K44 G45 A65 R66 S67 M93 N119 I121 N123 S170 Y183 K187 L215 G216 L217 I218 T220 T222
Binding residue
(residue number reindexed from 1)
G15 S17 K18 G19 A39 R40 S41 M67 N93 I95 N97 S144 Y157 K161 L189 G190 L191 I192 T194 T196
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S170 Y183 K187
Catalytic site (residue number reindexed from 1)
S144 Y157 K161
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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Biological Process
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Cellular Component
External links
PDB
RCSB:3ey4
,
PDBe:3ey4
,
PDBj:3ey4
PDBsum
3ey4
PubMed
UniProt
P28845
|DHI1_HUMAN 11-beta-hydroxysteroid dehydrogenase 1 (Gene Name=HSD11B1)
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