Structure of PDB 4r82 Chain B Binding Site BS04
Receptor Information
>4r82 Chain B (length=165) Species:
1908
(Streptomyces globisporus) [
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AELVDPKDRVQLRRVFGDFPTGVTVVTVGGSEPRGMTANSFTSVSLSPPL
VLICVGKDAVMHQRLTALPTFAVSVLEAGQEKAARHFADHSVDQFDTVDW
VLGEESGAPLIAGAVAHLECAIHRLYEGGDHTIFLGEVITATRWPAREGM
LFSGGRFRRFAPDAD
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
4r82 Chain B Residue 207 [
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Receptor-Ligand Complex Structure
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PDB
4r82
Crystal Structures of SgcE6 and SgcC, the Two-Component Monooxygenase That Catalyzes Hydroxylation of a Carrier Protein-Tethered Substrate during the Biosynthesis of the Enediyne Antitumor Antibiotic C-1027 in Streptomyces globisporus.
Resolution
1.659 Å
Binding residue
(original residue number in PDB)
M44 T45 A46 N47 S48 C62 V63 A67 A96 F164
Binding residue
(residue number reindexed from 1)
M36 T37 A38 N39 S40 C54 V55 A59 A88 F152
Annotation score
3
Enzymatic activity
Enzyme Commision number
1.5.1.37
: FAD reductase (NADH).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0016646
oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor
GO:0042602
riboflavin reductase (NADPH) activity
Biological Process
GO:0006208
pyrimidine nucleobase catabolic process
GO:0017000
antibiotic biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:4r82
,
PDBe:4r82
,
PDBj:4r82
PDBsum
4r82
PubMed
27560143
UniProt
Q8GME2
|SGCE6_STRGL NADH-dependent FAD reductase (Gene Name=sgcE6)
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