Structure of PDB 2ef5 Chain B Binding Site BS02

Receptor Information
>2ef5 Chain B (length=273) Species: 274 (Thermus thermophilus) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
ERVAVVGVPMDLGVDMGPSALRYARLLEQLEDLGYTVEDLGDVPVSLAYL
EEIRAAALVLKERLAALPEGVFPIVLGGDHSLSMGSVAGAARGRRVGVVW
VDAHADFNTPETSSGNVHGMPLAVLSGLGHPRLTEVFRAVDPKDVVLVGV
RSLDPGEKRLLKEAGVRVYTMHEVDRLGVARIAEEVLKHLQGLPLHVSLD
ADVLDPTLAPGVGTPVPGGLTYREAHLLMEILAESGRVQSLDLVEVNPIL
DERNRTAEMLVGLALSLLGKRIF
Ligand information
Ligand IDMN
InChIInChI=1S/Mn/q+2
InChIKeyWAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341[Mn++]
FormulaMn
NameMANGANESE (II) ION
ChEMBL
DrugBankDB06757
ZINC
PDB chain2ef5 Chain B Residue 1602 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2ef5 Crystal structure of the arginase from thermus thermophilus
Resolution2.0 Å
Binding residue
(original residue number in PDB)
H97 D119 D123 D218
Binding residue
(residue number reindexed from 1)
H80 D102 D106 D200
Annotation score1
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
PDBsum2ef5
PubMed
UniProtQ5SI78

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