Structure of PDB 3a6f Chain C Binding Site BS01
Receptor Information
>3a6f Chain C (length=257) Species:
303
(Pseudomonas putida) [
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KSVFVGELTWKEYEARVAAGDCVLMLPVGALEQHGHHMCMNVDVLLPTAV
CKRVAERIGALVMPGLQYGYKSQQKSGGGNHFPGTTSLDGATLTGTVQDI
IRELARHGARRLVLMNGHYENSMFIVEGIDLALRELRYAGIQDFKVVVLS
YWDFVKDPAVIQQLYPEGFLGFDIEHGGVFETSLMLALYPDLVDLDRVVD
HPPATFPPYDVFPVDPARTPAPGTLSSAKTASREKGELILEVCVQGIADA
IREEFPP
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
3a6f Chain C Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
3a6f
Substitution of Glu122 by glutamine revealed the function of the second water molecule as a proton donor in the binuclear metal enzyme creatininase
Resolution
1.78 Å
Binding residue
(original residue number in PDB)
E34 D45 H120
Binding residue
(residue number reindexed from 1)
E32 D43 H118
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E34 H36 D45 H120 E122 H178 E183
Catalytic site (residue number reindexed from 1)
E32 H34 D43 H118 E120 H176 E181
Enzyme Commision number
3.5.2.10
: creatininase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0016811
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
GO:0030145
manganese ion binding
GO:0046872
metal ion binding
GO:0047789
creatininase activity
Biological Process
GO:0006601
creatine biosynthetic process
GO:0006602
creatinine catabolic process
GO:0009231
riboflavin biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3a6f
,
PDBe:3a6f
,
PDBj:3a6f
PDBsum
3a6f
PubMed
20043918
UniProt
P83772
|CRNA_PSEPU Creatinine amidohydrolase (Gene Name=crnA)
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