Structure of PDB 3fa4 Chain G Binding Site BS01
Receptor Information
>3fa4 Chain G (length=284) Species:
5061
(Aspergillus niger) [
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PMVTAATSLRRALENPDSFIVAPGVYDGLSARVALSAGFDALYMTGAGTA
ASVHGQADLGICTLNDMRANAEMISNISPSTPVIADADTGYGGPIMVART
TEQYSRSGVAAFHIEDQVQTGKILVDTDTYVTRIRAAVQARQRIGSDIVV
IARTDSLQTHGYEESVARLRAARDAGADVGFLEGITSREMARQVIQDLAG
WPLLLNMVEHGATPSISAAEAKEMGFRIIIFPFAALGPAVAAMREAMEKL
KRDGIPGLDKEMTPQMLFRVCGLDESMKVDAQAG
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3fa4 Chain G Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
3fa4
Structure and function of 2,3-dimethylmalate lyase, a PEP mutase/isocitrate lyase superfamily member.
Resolution
2.18 Å
Binding residue
(original residue number in PDB)
D87 D89
Binding residue
(residue number reindexed from 1)
D86 D88
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y44 T46 G47 A48 D59 D87 D89 H114 E116 R161 E191 N214 T221 S223
Catalytic site (residue number reindexed from 1)
Y43 T45 G46 A47 D58 D86 D88 H113 E115 R153 E183 N206 T213 S215
Enzyme Commision number
4.1.3.30
: methylisocitrate lyase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016787
hydrolase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:3fa4
,
PDBe:3fa4
,
PDBj:3fa4
PDBsum
3fa4
PubMed
19133276
UniProt
Q2L887
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