Structure of PDB 5mln Chain B Binding Site BS01
Receptor Information
>5mln Chain B (length=238) Species:
5490
(Starmerella magnoliae) [
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TSNALVTGGSRGIGAASAIKLAQEGYNVTLASRSVDKLNEVKAKLPIVQD
GQKHYIWELDLADVEAASSFKGAPLPARSYDVFVSNAGVAAFSPTADHDD
KEWQNLLAVNLSSPIALTKALLKDVSERPVDKPLQIIYISSVAGLHGAAQ
VAVYSASKAGLDGFMRSVAREVGPKGIHVNSINPGYTKTEMTAGIEALPD
LPIKGWIEPEAIADAVLFLAKSKNITGTNIVVDNGLIA
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
5mln Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5mln
One-Pot Biocatalytic Double Oxidation of alpha-Isophorone for the Synthesis of Ketoisophorone
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
G11 S13 R14 G15 I16 S35 R36 S37 L64 N89 A90 G91 I142 S144 Y157 K161 P187 G188 Y189 T190 T192 M194 T195
Binding residue
(residue number reindexed from 1)
G8 S10 R11 G12 I13 S32 R33 S34 L61 N86 A87 G88 I139 S141 Y154 K158 P184 G185 Y186 T187 T189 M191 T192
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G15 S144 Y157
Catalytic site (residue number reindexed from 1)
G12 S141 Y154
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
View graph for
Molecular Function
External links
PDB
RCSB:5mln
,
PDBe:5mln
,
PDBj:5mln
PDBsum
5mln
PubMed
UniProt
B8K244
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