Structure of PDB 2ef5 Chain B Binding Site BS02
Receptor Information
>2ef5 Chain B (length=273) Species:
274
(Thermus thermophilus) [
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ERVAVVGVPMDLGVDMGPSALRYARLLEQLEDLGYTVEDLGDVPVSLAYL
EEIRAAALVLKERLAALPEGVFPIVLGGDHSLSMGSVAGAARGRRVGVVW
VDAHADFNTPETSSGNVHGMPLAVLSGLGHPRLTEVFRAVDPKDVVLVGV
RSLDPGEKRLLKEAGVRVYTMHEVDRLGVARIAEEVLKHLQGLPLHVSLD
ADVLDPTLAPGVGTPVPGGLTYREAHLLMEILAESGRVQSLDLVEVNPIL
DERNRTAEMLVGLALSLLGKRIF
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
2ef5 Chain B Residue 1602 [
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Receptor-Ligand Complex Structure
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PDB
2ef5
Crystal structure of the arginase from thermus thermophilus
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
H97 D119 D123 D218
Binding residue
(residue number reindexed from 1)
H80 D102 D106 D200
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H97 D119 H121 D123 H136 D218 D220 E263
Catalytic site (residue number reindexed from 1)
H80 D102 H104 D106 H118 D200 D202 E245
Enzyme Commision number
3.5.3.1
: arginase.
Gene Ontology
Molecular Function
GO:0004053
arginase activity
GO:0016787
hydrolase activity
GO:0016813
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines
GO:0030145
manganese ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006525
arginine metabolic process
GO:0019547
arginine catabolic process to ornithine
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2ef5
,
PDBe:2ef5
,
PDBj:2ef5
PDBsum
2ef5
PubMed
UniProt
Q5SI78
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