Structure of PDB 3pxw Chain B Binding Site BS01
Receptor Information
>3pxw Chain B (length=355) Species:
318586
(Paracoccus denitrificans PD1222) [
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ADDALAALGAQLFVDPALSRNATQSCATCHDPARAFTDPREGKAGLAVSV
GDDGQSHGDRNTPTLGYAALVPAFHRDANGKYKGGQFWDGRADDLKQQAG
QPMLNPVEMAMPDRAAVAARLRDDPAYRTGFEALFGKGVLDDPERAFDAA
AEALAAYQATGEFSPFDSKYDRVMRGEEKFTPLEEFGYTVFITWNCRLCH
MQRKQGVAERETFTNFEYHNIGLPVNETAREASGLGADHVDHGLLARPGI
EDPAQSGRFKVPSLRNVAVTGPYMHNGVFTDLRTAILFYNKYTSRRPEAK
INPETGAPWGEPEVARNLSLAELQSGLMLDDGRVDALVAFLETLTDRRYE
PLLEE
Ligand information
Ligand ID
NO
InChI
InChI=1S/HNO/c1-2/h1H
InChIKey
ODUCDPQEXGNKDN-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
OpenEye OEToolkits 2.0.7
[N]=O
Formula
N O
Name
NITRIC OXIDE;
Nitrogen monoxide
ChEMBL
CHEMBL1234765
DrugBank
ZINC
PDB chain
3pxw Chain B Residue 375 [
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Receptor-Ligand Complex Structure
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PDB
3pxw
Crystal Structures of CO and NO Adducts of MauG in Complex with Pre-Methylamine Dehydrogenase: Implications for the Mechanism of Dioxygen Activation.
Resolution
2.11 Å
Binding residue
(original residue number in PDB)
P107 E113
Binding residue
(residue number reindexed from 1)
P102 E108
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E113
Catalytic site (residue number reindexed from 1)
E108
Enzyme Commision number
1.-.-.-
Gene Ontology
Molecular Function
GO:0004130
cytochrome-c peroxidase activity
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:3pxw
,
PDBe:3pxw
,
PDBj:3pxw
PDBsum
3pxw
PubMed
21355604
UniProt
Q51658
|MAUG_PARDP Methylamine utilization protein MauG (Gene Name=mauG)
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