Structure of PDB 3gl0 Chain B Binding Site BS02
Receptor Information
>3gl0 Chain B (length=334) Species:
40324
(Stenotrophomonas maltophilia) [
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ATFVRNAWYVAALPEELSEKPLGRTILDTPLALYRQPDGVVAALLDICPH
RFAPLSDGILVNGHLQCPYHGLEFDGGGQCVHNPHGNGARPASLNVRSFP
VVERDALIWIWPGDPALADPGAIPDFGCRVDPAYRTVGGYGHVDCNYKLL
VDNLMDLGHAQYVHRANAQTDAFDRLEREVIVGDGEIQALMKIPGGTPSV
LMAKFPVDAWNDIRWNKVSAMLNFIAVAPEGTPKEQSIHSRGTHILTPET
EASCHYFFGSSRNFGIDDPEMDGVLRSWQAQALVKEDKVVVEAIERRRAY
VEANGIRPAMLSCDEAAVRVSREIEKLEQLEAAR
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
3gl0 Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3gl0
Crystal structure of dicamba monooxygenase: a Rieske nonheme oxygenase that catalyzes oxidative demethylation.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
H160 H165 D294
Binding residue
(residue number reindexed from 1)
H159 H164 D287
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.14.15.-
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0016491
oxidoreductase activity
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0046872
metal ion binding
GO:0051537
2 iron, 2 sulfur cluster binding
Biological Process
GO:0009056
catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3gl0
,
PDBe:3gl0
,
PDBj:3gl0
PDBsum
3gl0
PubMed
19616011
UniProt
Q5S3I3
|DDMC_STEMA Dicamba O-demethylase, oxygenase component (Gene Name=ddmC)
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