Structure of PDB 6vp5 Chain D Binding Site BS01
Receptor Information
>6vp5 Chain D (length=331) Species:
319
(Pseudomonas savastanoi pv. phaseolicola) [
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NLQTFELPTEVTGCAADISLGRALIQAWQKDGIFQIKTDSEQDRKTQEAM
AASKQFCKEPLTFKSSCVSDLTYSGYVASGEEVTAGKPDFPEIFTVCKDL
SVGDQRVKAGWPCHGPVPWPNNTYQKSMKTFMEELGLAGERLLKLTALGF
ELPINTFTDLTRDGWHHMRVLRFPPQTSTLSRGIGAHTEYGLLVIAAQDD
VGGLYIRPPVEGEKRNRNWLPGESSAGMFEHDEPWTFVTPTPGVWTVFPG
DILQFMTGGQLLSTPHKVKLNTRERFACAYFHEPNFEASAYPLFEPANER
IHYGEHFTNMFMRCYPDRITTQRINKENRLA
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
6vp5 Chain D Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6vp5
An Iron(IV)-Oxo Intermediate Initiating l-Arginine Oxidation but Not Ethylene Production by the 2-Oxoglutarate-Dependent Oxygenase, Ethylene-Forming Enzyme.
Resolution
1.97 Å
Binding residue
(original residue number in PDB)
H189 E191 H268
Binding residue
(residue number reindexed from 1)
H187 E189 H266
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.13.12.19
: 2-oxoglutarate dioxygenase (ethylene-forming).
1.14.20.7
: 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate- forming).
Gene Ontology
Molecular Function
GO:0016706
2-oxoglutarate-dependent dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
GO:0102276
2-oxoglutarate oxygenase/decarboxylase (ethylene-forming) activity
Biological Process
GO:0009693
ethylene biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6vp5
,
PDBe:6vp5
,
PDBj:6vp5
PDBsum
6vp5
PubMed
33522811
UniProt
P32021
|EFE_PSESH 2-oxoglutarate-dependent ethylene/succinate-forming enzyme (Gene Name=efe)
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