Structure of PDB 3mmr Chain A Binding Site BS01
Receptor Information
>3mmr Chain A (length=308) Species:
36329
(Plasmodium falciparum 3D7) [
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KNVSIIGSPLAAGQPLGGVQLACDDLRKLGLHNVIDVLGWKYEDIGNIDN
CYYDNIRNIKEIGIFSKNLFDTMSNELRKKNFVLNIGGDHGVAFSSILSS
LQMYQNLRVIWIDAHGDINIPETSPSGNYHGMTLAHTLGLFKKKVPYFEW
SENLTYLKPENTAIIGIRDIDAYEKIILKKCNINYYTIFDIEKNGIYNTI
CTALEKIDPNSNCPIHISLDIDSVDNVFAPGTGTVAKGGLNYREINLLMK
ILAETKRVVSMDLVEYNPSLDEVDKKVHGDSLPILDNATKTGKLCLELIA
RVLGYDIV
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
3mmr Chain A Residue 412 [
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Receptor-Ligand Complex Structure
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PDB
3mmr
Crystal structure of arginase from Plasmodium falciparum and implications for L-arginine depletion in malarial infection .
Resolution
2.14 Å
Binding residue
(original residue number in PDB)
H193 D216 D220 D323
Binding residue
(residue number reindexed from 1)
H90 D113 D117 D220
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H193 D216 H218 D220 H233 D323 D325 E368
Catalytic site (residue number reindexed from 1)
H90 D113 H115 D117 H130 D220 D222 E265
Enzyme Commision number
3.5.3.1
: arginase.
Gene Ontology
Molecular Function
GO:0004053
arginase activity
GO:0016787
hydrolase activity
GO:0030145
manganese ion binding
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0000050
urea cycle
GO:0006525
arginine metabolic process
GO:0019547
arginine catabolic process to ornithine
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3mmr
,
PDBe:3mmr
,
PDBj:3mmr
PDBsum
3mmr
PubMed
20527960
UniProt
Q8I384
|ARGI_PLAF7 Arginase (Gene Name=ARG)
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