Structure of PDB 3gl0 Chain B Binding Site BS03
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
OXY
InChI
InChI=1S/O2/c1-2
InChIKey
MYMOFIZGZYHOMD-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OpenEye OEToolkits 1.5.0
O=O
Formula
O2
Name
OXYGEN MOLECULE
ChEMBL
CHEMBL1234886
DrugBank
DB09140
ZINC
PDB chain
3gl0 Chain B Residue 600 [
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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
Binding residue
(residue number reindexed from 1)
H159 H164
Annotation score
5
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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