Structure of PDB 4ie3 Chain B Binding Site BS02
Receptor Information
>4ie3 Chain B (length=306) Species:
9606
(Homo sapiens) [
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HSVAVIGAPFSQGQKRKGVEHGPAAIREAGLMKRLSSLGCHLKDFGDLSF
TPVPKDDLYNNLIVNPRSVGLANQELAEVVSRAVSDGYSCVTLGGDHSLA
IGTISGHARHCPDLCVVWVDAHADINTPLTTSSGNLHGQPVSFLLRELQD
KVPQLPGFSWIKPCISSASIVYIGLRDVDPPEHFILKNYDIQYFSMRDID
RLGIQKVMERTFDLLIGKRQRPIHLSFDIDAFDPTLAPATGTPVVGGLTY
REGMYIAEEIHNTGLLSALDLVEVNPQLATSEEEAKTTANLAVDVIASSF
GQTREG
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
4ie3 Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4ie3
2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors.
Resolution
2.3522 Å
Binding residue
(original residue number in PDB)
D143 H145 D251 D253
Binding residue
(residue number reindexed from 1)
D120 H122 D228 D230
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H120 D143 H145 D147 H160 D251 D253 E296
Catalytic site (residue number reindexed from 1)
H97 D120 H122 D124 H137 D228 D230 E273
Enzyme Commision number
3.5.3.1
: arginase.
Gene Ontology
Molecular Function
GO:0004053
arginase activity
GO:0016813
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines
GO:0046872
metal ion binding
Biological Process
GO:0006525
arginine metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:4ie3
,
PDBe:4ie3
,
PDBj:4ie3
PDBsum
4ie3
PubMed
23453840
UniProt
P78540
|ARGI2_HUMAN Arginase-2, mitochondrial (Gene Name=ARG2)
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