Structure of PDB 8ful Chain E Binding Site BS01

Receptor Information
>8ful Chain E (length=350) Species: 1219028 (Rhodococcus wratislaviensis NBRC 100605) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
VPAVVDCDVHAVLPSPHSLIPYLDEYWADQLVAQLAPTYEPNYHPRGSAI
AQHSDASVDENGRAATTAENLVKDVFADGFTDFAVVNCLYGVQQIHQPRR
EMAHARALNHWIANEWLDKDDRLRASIVVPQGSPRAAAEEIDFWSGDKRF
VQVLLLGQSELLYGREINWPIWEAAEAAGLPVTLHIGGVFRQAPTSVGWP
ASHLEWYVGQQSNIEAQLNSIISEGILQKFPKTKILLSELGFNWLPPFMW
KFDKLWKSYRPDIPWVQESPLELIREHVRVTTSPSDGAEEAGRLDSIVDR
LGSDRMLVYSSDYPHKHHSGPRDIENGTHSPELLDRIYRRNAFDLYNLVV
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 chain8ful Chain E Residue 401 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB8ful Enzymatic Hydroxylation of Aliphatic C-H Bonds by a Mn/Fe Cofactor.
Resolution2.29 Å
Binding residue
(original residue number in PDB)
D36 H38 H213 E267 D340
Binding residue
(residue number reindexed from 1)
D8 H10 H185 E239 D312
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

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:8ful, PDBe:8ful, PDBj:8ful
PDBsum8ful
PubMed37471626
UniProtA0A402C2V4

[Back to BioLiP]