Structure of PDB 3nio Chain D Binding Site BS02
Receptor Information
>3nio Chain D (length=316) Species:
208964
(Pseudomonas aeruginosa PAO1) [
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NLHQPLGGNEMPRFGGIATMMRLPHVQSPAELDALDAAFVGVPLDIGTSL
RSGTRFGPREIRAESVMIRPYNMATGAAPFDSLNVADIGDVAINTFNLLE
AVRIIEQEYDRILGHGILPLTLGGDHTITLPILRAIKKKHGKVGLVHVDA
HADVNDHMFGEKIAHGTTFRRAVEEDLLDCDRVVQIGLRAQGYTAEDFNW
SRKQGFRVVQAEECWHKSLEPLMAEVREKVGGGPVYLSFDIDGIDPAWAP
GTGTPEIGGLTTIQAMEIIRGCQGLDLIGCDLVEVSPPYDTTGNTSLLGA
NLLYEMLCVLPGVVRR
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
3nio Chain D Residue 1608 [
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Receptor-Ligand Complex Structure
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PDB
3nio
Crystal structures of Pseudomonas aeruginosa guanidinobutyrase and guanidinopropionase, members of the ureohydrolase superfamily
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D152 H154 D243 D245
Binding residue
(residue number reindexed from 1)
D149 H151 D240 D242
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H129 D152 H154 D156 H168 D243 D245 E287
Catalytic site (residue number reindexed from 1)
H126 D149 H151 D153 H165 D240 D242 E284
Enzyme Commision number
3.5.3.7
: guanidinobutyrase.
Gene Ontology
Molecular Function
GO:0008783
agmatinase activity
GO:0016787
hydrolase activity
GO:0016813
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines
GO:0046872
metal ion binding
GO:0047971
guanidinobutyrase activity
Biological Process
GO:0006527
arginine catabolic process
GO:0033389
putrescine biosynthetic process from arginine, using agmatinase
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3nio
,
PDBe:3nio
,
PDBj:3nio
PDBsum
3nio
PubMed
21600989
UniProt
Q9I3S3
|GBUA_PSEAE Guanidinobutyrase (Gene Name=gbuA)
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