Structure of PDB 6vsh Chain A Binding Site BS01
Receptor Information
>6vsh Chain A (length=332) Species:
40324
(Stenotrophomonas maltophilia) [
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ATFVRNAWYVAALPEELSEKPLGRTILDTPLALYRQPDGVVAALLDICPH
RFAPLSDGILVNGHLQCPYHGLEFDGGGQCVHNPHGNGARPASLNVRSFP
VVERDALIWIWPGDPALADPGAIPDFGCRVDPAYRTVGGYGHVDCNYKLL
VDNLMDLGHAQYVHRALEREVIVGDGEIQALMKIPGGTPSVLMAKFLRGA
NTPVDAWNDIRWNKVSAMLNFIAVAPEGTPKEQSIHSRGTHILTPETEAS
CHYFFGSSRNFGIDDPEMDGVLRSWQAQALVKEDKVVVEAIERRRAYVEA
NGIRPAMLSCDEAAVRVSREIEKLEQLEAARL
Ligand information
Ligand ID
FES
InChI
InChI=1S/2Fe.2S
InChIKey
NIXDOXVAJZFRNF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
[Fe]1S[Fe]S1
CACTVS 3.341
OpenEye OEToolkits 1.5.0
S1[Fe]S[Fe]1
Formula
Fe2 S2
Name
FE2/S2 (INORGANIC) CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
6vsh Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6vsh
Dicamba monooxygenase: structural insights into a dynamic Rieske oxygenase that catalyzes an exocyclic monooxygenation.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
C49 H51 R52 C68 Y70 H71 L73
Binding residue
(residue number reindexed from 1)
C48 H50 R51 C67 Y69 H70 L72
Annotation score
3
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:6vsh
,
PDBe:6vsh
,
PDBj:6vsh
PDBsum
6vsh
PubMed
19616009
UniProt
Q5S3I3
|DDMC_STEMA Dicamba O-demethylase, oxygenase component (Gene Name=ddmC)
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