Structure of PDB 7e51 Chain F Binding Site BS02
Receptor Information
>7e51 Chain F (length=423) Species:
1773
(Mycobacterium tuberculosis) [
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MPIIEQVRAREILDSRGNPTVEVEVALIDGTFARAAVPSGASTGEHEAVE
LRDGGDRYGGKGVQKAVQAVLDEIGPAVIGLNADDQRLVDQALVDLDGTP
DKSRLGGNAILGVSLAVAKAAADSAELPLFRYVGGPNAHILPVPMMNILN
GGAHADTAVDIQEFMVAPIGAPSFVEALRWGAEVYHALKSVLKKEGLSTG
LGDEGGFAPDVAGTTAALDLISRAIESAGLRPGADVALALDAAATEFFTD
GTGYVFEGTTRTADQMTEFYAGLLGAYPLVSIEDPLSEDDWDGWAALTAS
IGDRVQIVGDDIFVTNPERLEEGIERGVANALLVKVNQIGTLTETLDAVT
LAHHGGYRTMISHRSGETEDTMIADLAVAIGSGQIKTGAPARSERVAKYN
QLLRIEEALGDAARYAGDLAFPR
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
7e51 Chain F Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
7e51
Structural snapshots of Mycobacterium tuberculosis enolase reveal dual mode of 2PG binding and its implication in enzyme catalysis.
Resolution
3.23 Å
Binding residue
(original residue number in PDB)
D241 E283 D310
Binding residue
(residue number reindexed from 1)
D241 E283 D310
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.2.1.11
: phosphopyruvate hydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004634
phosphopyruvate hydratase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0006096
glycolytic process
Cellular Component
GO:0000015
phosphopyruvate hydratase complex
GO:0005576
extracellular region
GO:0005737
cytoplasm
GO:0005886
plasma membrane
GO:0009274
peptidoglycan-based cell wall
GO:0009986
cell surface
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7e51
,
PDBe:7e51
,
PDBj:7e51
PDBsum
7e51
PubMed
37860976
UniProt
P9WNL1
|ENO_MYCTU Enolase (Gene Name=eno)
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