Structure of PDB 3ri3 Chain B Binding Site BS02
Receptor Information
>3ri3 Chain B (length=257) Species:
1902
(Streptomyces coelicolor) [
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RGSHMATQDSEVALVTGATSGIGLEIARRLGKEGLRVFVCARGEEGLRTT
LKELREAGVEADGRTCDVRSVPEIEALVAAVVERYGPVDVLVNNAGRLGG
GATAELADELWLDVVETNLTGVFRVTKQVLKAGGMLERGTGRIVNIASTG
GKQGVVHAAPYSASKHGVVGFTKALGLELARTGITVNAVCPGFVETPMAA
SVREHTEEAFDRITARVPIGRYVQPSEVAEMVAYLIGPGAAAVTAQALNV
CGGLGNY
Ligand information
Ligand ID
EMO
InChI
InChI=1S/C15H10O5/c1-6-2-8-12(10(17)3-6)15(20)13-9(14(8)19)4-7(16)5-11(13)18/h2-5,16-18H,1H3
InChIKey
RHMXXJGYXNZAPX-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
Cc1cc2c(c(c1)O)C(=O)c3c(cc(cc3O)O)C2=O
ACDLabs 10.04
O=C2c1c(O)cc(cc1C(=O)c3c2c(O)cc(O)c3)C
CACTVS 3.341
Cc1cc(O)c2C(=O)c3c(O)cc(O)cc3C(=O)c2c1
Formula
C15 H10 O5
Name
3-METHYL-1,6,8-TRIHYDROXYANTHRAQUINONE;
EMODIN
ChEMBL
CHEMBL289277
DrugBank
DB07715
ZINC
ZINC000003824868
PDB chain
3ri3 Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
3ri3
Structural and Biochemical Analyses of Regio- and Stereospecificities Observed in a Type II Polyketide Ketoreductase.
Resolution
2.292 Å
Binding residue
(original residue number in PDB)
V151 V198 L258
Binding residue
(residue number reindexed from 1)
V155 V202 L254
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G17 N114 S144 Y157 K161
Catalytic site (residue number reindexed from 1)
G21 N118 S148 Y161 K165
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:3ri3
,
PDBe:3ri3
,
PDBj:3ri3
PDBsum
3ri3
PubMed
21506596
UniProt
P16544
|ACT3_STRCO Putative ketoacyl reductase (Gene Name=actIII)
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