Structure of PDB 8fuo Chain B Binding Site BS02

Receptor Information
>8fuo Chain B (length=365) Species: 1219028 (Rhodococcus wratislaviensis NBRC 100605) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
TLPAPSVTTGIVDADIHPVPQDGALEPYLDDRWKKHIREYGVRTTTGLQF
ISEYPQMYGGAMRADAWPESGYPGSDRELLRTQLLDKHNIQLGVLQCLAP
GGQTLNPAGQALNQELAAALCRATNDWQLEHLVYPDPRMRAAIPVTFETP
DYAVAEIERVGADPGVVAVLGTSKTLEPLGSRKYWPIYEASVAQNLPIQF
HLSQGGGHANTGTGWTSYHTEYHTGHVQSFQSQLLSLVLSGTFDRFPTLK
VMFVEGNVAHFAPLIQRMDYTWETLRGELPDLQRKPSEYIRDHIWASTQP
IDEPEKPEHLAELLEEFCGDNVVFATDYPHFDFDDPETAFPRSFPVDLRD
KILRGNGMRFFGVTN
Ligand information
Ligand IDFE
InChIInChI=1S/Fe/q+3
InChIKeyVTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
FormulaFe
NameFE (III) ION
ChEMBL
DrugBankDB13949
ZINC
PDB chain8fuo Chain B Residue 403 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB8fuo Enzymatic Hydroxylation of Aliphatic C-H Bonds by a Mn/Fe Cofactor.
Resolution2.43 Å
Binding residue
(original residue number in PDB)
D25 H27 H211 E265 D337
Binding residue
(residue number reindexed from 1)
D15 H17 H201 E255 D327
Annotation score4
Enzymatic activity
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0016787 hydrolase activity
GO:0016829 lyase activity
GO:0016831 carboxy-lyase activity
GO:0046872 metal ion binding
Biological Process
GO:0019748 secondary metabolic process
Cellular Component
GO:0005737 cytoplasm

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:8fuo, PDBe:8fuo, PDBj:8fuo
PDBsum8fuo
PubMed37471626
UniProtA0A402C2Q3

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