Structure of PDB 4q3p Chain D Binding Site BS01
Receptor Information
>4q3p Chain D (length=332) Species:
6183
(Schistosoma mansoni) [
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KLLYTSANFLGIPTNRGQPKIGTYQGPELIRKSNFFQLVAEDGIQLTDCG
DIIPVELNEAEDPQRFGMKWSRSFSLTTLRIAERVEELMKSTPLVIVGGD
HSMATGTILGHAEAKPDLCVLWIDAHGDINTPLNSASGNMHGMPLSFLVK
ELQDQIPWLDDFEGIKPCLNASNIAYIGLRDLDAHETHDIRKHGIAYFTM
LDVDRMGIEAVIKEALLAVNPRLEKAIHLSFDIDALDPLVAPSTGTAVPG
GLTLREGLRICEEVSATGKLSVVELAELNPLLGSQEDVLKTQSSAVHILR
ACLGHCRSGHLPFKVRNLTDQGIMSRAAHMQT
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
4q3p Chain D Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
4q3p
Crystal Structure of Schistosoma mansoni Arginase, a Potential Drug Target for the Treatment of Schistosomiasis.
Resolution
2.501 Å
Binding residue
(original residue number in PDB)
H131 D154 D158 D262
Binding residue
(residue number reindexed from 1)
H101 D124 D128 D232
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H131 D154 H156 D158 H171 D262 D264 E307
Catalytic site (residue number reindexed from 1)
H101 D124 H126 D128 H141 D232 D234 E277
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:0000050
urea cycle
GO:0006525
arginine metabolic process
GO:0019547
arginine catabolic process to ornithine
Cellular Component
GO:0005634
nucleus
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:4q3p
,
PDBe:4q3p
,
PDBj:4q3p
PDBsum
4q3p
PubMed
25007099
UniProt
Q6WVP6
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