Structure of PDB 2rh4 Chain A Binding Site BS01
Receptor Information
>2rh4 Chain A (length=257) Species:
1902
(Streptomyces coelicolor) [
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DSEVALVTGATSGIGLEIARRLGKEGLRVFVCARGEEGLRTTLKELREAG
VEADGRTCDVRSVPEIEALVAAVVERYGPVDVLVNNAGRPGGGATAELAD
ELWLDVVETNLTGVFRVTKQVLKAGGMLERGTGRIVNIASTGGKQGVVHA
APYSASKHGVVGFTKALGLELARTGITVNAVCPGFVETPMAASVREHYSD
IWEVSTEEAFDRITARVPIGRYVQPSEVAEMVAYLIGPGAAAVTAQALNV
CGGLGNY
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
2rh4 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
2rh4
Inhibition kinetics and emodin cocrystal structure of a type II polyketide ketoreductase
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
G13 T15 S16 G17 I18 A37 R38 G39 C62 D63 V64 N90 G92 S144 Y157 K161 P187 G188 V190 T192 M194
Binding residue
(residue number reindexed from 1)
G9 T11 S12 G13 I14 A33 R34 G35 C58 D59 V60 N86 G88 S140 Y153 K157 P183 G184 V186 T188 M190
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G17 N114 S144 Y157 K161 Y202
Catalytic site (residue number reindexed from 1)
G13 N110 S140 Y153 K157 Y198
Enzyme Commision number
1.3.1.-
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
Biological Process
GO:0008202
steroid metabolic process
GO:0017000
antibiotic biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2rh4
,
PDBe:2rh4
,
PDBj:2rh4
PDBsum
2rh4
PubMed
18205400
UniProt
P16544
|ACT3_STRCO Putative ketoacyl reductase (Gene Name=actIII)
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