Structure of PDB 3icr Chain B Binding Site BS02
Receptor Information
>3icr Chain B (length=554) Species:
198094
(Bacillus anthracis str. Ames) [
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GSRKIVVVGGVAGGASVAARLRRLSEEDEIIMVERGEYISFANCGLPYYI
GGVITERQKLLVQTVERMSKRFNLDIRVLSEVVKINKEEKTITIKNVTTN
ETYNEAYDVLILSPGAKPIVPSIPGIEEAKALFTLRNVPDTDRIKAYIDE
KKPRHATVIGGGFIGVEMVENLRERGIEVTLVEMANQVMPPIDYEMAAYV
HEHMKNHDVELVFEDGVDALEENGAVVRLKSGSVIQTDMLILAIGVQPES
SLAKGAGLALGVRGTIKVNEKFQTSDPHIYAIGDAIEVKDFVTETETMIP
LAWPANRQGRMLADIIHGHTDSLYKGTLGTSVAKVFDLTVATTGLNEKIL
KRLNIPYEVVHVQANSHAGYYPNATPVLIKLIFNKDSGKIYGAQTLGRDG
VDKRMDVIATAIKANLTVLDLPDLELSYAPPYSSAKDPVNMVGYAASNIV
DGFVDTVQWHEIDRIVENGGYLIDVREPNELKQGMIKGSINIPLDELRDR
LEEVPVDKDIYITCQLGMRGYVAARMLMEKGYKVKNVDGGFKLYGTVLPE
RIVY
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
3icr Chain B Residue 555 [
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Receptor-Ligand Complex Structure
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PDB
3icr
Crystal structure and catalytic properties of Bacillus anthracis CoADR-RHD: implications for flavin-linked sulfur trafficking.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
G9 V11 A12 G13 E34 R35 N43 C44 V82 S113 P114 G115 L135 R136 G283 D284 P300 L301 A302 A305
Binding residue
(residue number reindexed from 1)
G9 V11 A12 G13 E34 R35 N43 C44 V82 S113 P114 G115 L135 R136 G283 D284 P300 L301 A302 A305
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
A12 I39 N43 C44 N306 S427 F453 V454
Catalytic site (residue number reindexed from 1)
A12 I39 N43 C44 N306 S427 F453 V454
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003756
protein disulfide isomerase activity
GO:0016491
oxidoreductase activity
GO:0050451
CoA-disulfide reductase (NADPH) activity
GO:0050660
flavin adenine dinucleotide binding
GO:0050661
NADP binding
View graph for
Molecular Function
External links
PDB
RCSB:3icr
,
PDBe:3icr
,
PDBj:3icr
PDBsum
3icr
PubMed
19725515
UniProt
A0A6L7H7X4
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