Structure of PDB 6alp Chain A Binding Site BS01
Receptor Information
>6alp Chain A (length=338) Species:
1960
(Streptomyces vinaceus) [
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VRPWSEFRLTPAEAAAAAALAARCAQRYDETDGPEFLLDAPVIAHELPRR
LRTFMARARLDAWPHALVVRGNPVDDAALGSTPVHWRTARTPGSRPLSFL
LMLYAGLLGDVFGWATQQDGRVVTDVLPIKGGEHTLVSSSSRQELGWHTE
DAFSPYRADYVGLLSLRNPDGVATTLAGVPLDDLDERTLDVLFQERFLIR
PDDSHLQVNNSTAQQGRVEFEGIAQAADRPEPVAILTGHRAAPHLRVDGD
FSAPAEGDEEAAAALGTLRKLIDASLYELVLDQGDVAFIDNRRAVHGRRA
FQPRYDGRDRWLKRINITRDLHRSRKAWAGDSRVLGQR
Ligand information
Ligand ID
FE2
InChI
InChI=1S/Fe/q+2
InChIKey
CWYNVVGOOAEACU-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Fe+2]
CACTVS 3.341
[Fe++]
Formula
Fe
Name
FE (II) ION
ChEMBL
DrugBank
DB14510
ZINC
PDB chain
6alp Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6alp
Visualizing the Reaction Cycle in an Iron(II)- and 2-(Oxo)-glutarate-Dependent Hydroxylase.
Resolution
1.99 Å
Binding residue
(original residue number in PDB)
H168 E170 H316
Binding residue
(residue number reindexed from 1)
H148 E150 H296
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.14.11.41
: L-arginine hydroxylase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0016491
oxidoreductase activity
GO:0016706
2-oxoglutarate-dependent dioxygenase activity
GO:0046872
metal ion binding
GO:0102525
2-oxoglutarate, L-arginine oxygenase (succinate-forming) activity
Biological Process
GO:0017000
antibiotic biosynthetic process
Cellular Component
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6alp
,
PDBe:6alp
,
PDBj:6alp
PDBsum
6alp
PubMed
28823155
UniProt
Q6WZB0
|ARGHX_STRVI Alpha-ketoglutarate-dependent L-arginine hydroxylase (Gene Name=vioC)
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