Structure of PDB 3nip Chain F Binding Site BS01
Receptor Information
>3nip Chain F (length=316) Species:
208964
(Pseudomonas aeruginosa PAO1) [
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NDHPQPLDAAEIPRFAGIPTFMRLPAFTDPAALQVGLIGVPWDGGTTNRA
GARHGPREVRNLSSLMRKVHHVSRIAPYDLVRVGDLGDAPVNPIDLLDSL
RRIEGFYRQVHAAGTLPLSVGGDHLVTLPIFRALGRERPLGMVHFDAHSD
TNDRYFGDNPYTHGTPFRRAIEEGLLDPLRTVQIGIRGSVYSPDDDAFAR
ECGIRVIHMEEFVELGVEATLAEARRVVGAGPTYVSFDVDVLDPAFAPGT
GTPEIGGMTSLQAQQLVRGLRGLDLVGADVVEVSPPFDVGGATALVGATM
MFELLCLLAESAARSA
Ligand information
Ligand ID
16D
InChI
InChI=1S/C6H16N2/c7-5-3-1-2-4-6-8/h1-8H2
InChIKey
NAQMVNRVTILPCV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(CCCN)CCN
ACDLabs 10.04
CACTVS 3.341
NCCCCCCN
Formula
C6 H16 N2
Name
HEXANE-1,6-DIAMINE;
1,6-DIAMINOHEXANE
ChEMBL
CHEMBL303004
DrugBank
DB03260
ZINC
ZINC000001543408
PDB chain
3nip Chain D Residue 327 [
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Receptor-Ligand Complex Structure
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PDB
3nip
Crystal structures of Pseudomonas aeruginosa guanidinobutyrase and guanidinopropionase, members of the ureohydrolase superfamily
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
A294 L297 V298
Binding residue
(residue number reindexed from 1)
A292 L295 V296
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H126 D148 H150 D152 H165 D240 D242 E284
Catalytic site (residue number reindexed from 1)
H124 D146 H148 D150 H163 D238 D240 E282
Enzyme Commision number
3.5.3.17
: guanidinopropionase.
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:0047972
guanidinopropionase activity
Biological Process
GO:0033389
putrescine biosynthetic process from arginine, using agmatinase
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3nip
,
PDBe:3nip
,
PDBj:3nip
PDBsum
3nip
PubMed
21600989
UniProt
Q9I6K2
|GPUA_PSEAE Guanidinopropionase (Gene Name=gpuA)
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