Structure of PDB 3pzl Chain C Binding Site BS02
Receptor Information
>3pzl Chain C (length=290) Species:
273116
(Thermoplasma volcanium GSS1) [
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ASELRSIFSLKKIADAVNGYEEAKYVVFGIPFDNTSSYRRGSKYAPDSIR
GAYVNLESYEYSYGIDLLASGMADLGDMEESEDVEYVIDTVESVVSAVMS
DGKIPIMLGGEHSITVGAVRALPKDVDLVIVDAHSDFRSSYMGNKYNHAC
VTRRALDLLGEGRITSIGIRSVSREEFEDPDFRKVSFISSFDVKKNGIDK
YIEEVDRKSRRVYISVDMDGIDPAYAPAVGTPEPFGLADTDVRRLIERLS
YKAVGFDIVEFSPLYDNGNTSMLAAKLLQVFIASREKYYK
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
3pzl Chain C Residue 315 [
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Receptor-Ligand Complex Structure
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PDB
3pzl
The crystal structure of agmatine ureohydrolase of Thermoplasma volcanium
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
H124 D144 D148 D229
Binding residue
(residue number reindexed from 1)
H112 D132 D136 D217
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H124 D144 H146 D148 H160 D229 D231 E272
Catalytic site (residue number reindexed from 1)
H112 D132 H134 D136 H148 D217 D219 E260
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
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
Biological Process
GO:0033389
putrescine biosynthetic process from arginine, using agmatinase
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3pzl
,
PDBe:3pzl
,
PDBj:3pzl
PDBsum
3pzl
PubMed
UniProt
Q97BB8
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