Structure of PDB 6vst Chain B Binding Site BS01
Receptor Information
>6vst Chain B (length=318) Species:
3880
(Medicago truncatula) [
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SPALLEKAQNRVIDAALTFIRERAKFKGELMRSLGGVAATSSLLGVPLGH
HSSFHEGSAFAPPRIREAIWCDSTNSTTEEGKNLRDPRVITNVGDVPIEE
IRDCGVDDKRLANVISESVKLVMDEDPLRPLVLGGDHSISFPVVRAVSEK
LGGAVDILHFDAHPDLYHDFEGNYYSHASPFARIMEGGYARRLVQVGIRS
ITNDVREQVKKYGVETHEMRTLSRDRPILENLKLGEGVKGVYVSIDVDSL
DPSIAPGVSHHEPGGLLFRDILNILQNLQGDIVGGDVVEYNPQRDTYDGI
TALVAAKLVRELAAKMSK
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
6vst Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6vst
The Neighboring Subunit Is Engaged to Stabilize the Substrate in the Active Site of Plant Arginases.
Resolution
2.12 Å
Binding residue
(original residue number in PDB)
D181 H183 D266 D268
Binding residue
(residue number reindexed from 1)
D161 H163 D246 D248
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.3.1
: arginase.
3.5.3.11
: agmatinase.
Gene Ontology
Molecular Function
GO:0004053
arginase 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:0000050
urea cycle
GO:0006525
arginine metabolic process
GO:0009446
putrescine biosynthetic process
GO:0019547
arginine catabolic process to ornithine
GO:0033388
putrescine biosynthetic process from arginine
GO:0033389
putrescine biosynthetic process from arginine, using agmatinase
GO:0034214
protein hexamerization
Cellular Component
GO:0005739
mitochondrion
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6vst
,
PDBe:6vst
,
PDBj:6vst
PDBsum
6vst
PubMed
32754173
UniProt
G7JFU5
|ARGI_MEDTR Arginase, mitochondrial (Gene Name=ARGAH)
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