Structure of PDB 1m3u Chain F Binding Site BS01
Receptor Information
>1m3u Chain F (length=262) Species:
562
(Escherichia coli) [
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PTTISLLQKYKQEKKRFATITAYDYSFAKLFADEGLNVMLVGDSLGMTVQ
GHDSTLPVTVADIAYHTAAVRRGAPNCLLLADLPFMAYATPEQAFENAAT
VMRAGANMVKIEGGEWLVETVQMLTERAVPVCGHLGLTPQSVNIFGGYKV
QGRGDEAGDQLLSDALALEAAGAQLLVLECVPVELAKRITEALAIPVIGI
GAGNVTDGQILVMHDAFGITGGHIPKFAKNFLAETGDIRAAVRQYMAEVE
SGVYPGEEHSFH
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
1m3u Chain F Residue 266 [
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Receptor-Ligand Complex Structure
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PDB
1m3u
Structure of E. coli Ketopantoate Hydroxymethyl Transferase Complexed with Ketopantoate and Mg(2+), Solved by Locating 160 Selenomethionine Sites.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D45 D84
Binding residue
(residue number reindexed from 1)
D43 D82
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.1.2.11
: 3-methyl-2-oxobutanoate hydroxymethyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003864
3-methyl-2-oxobutanoate hydroxymethyltransferase activity
GO:0016740
transferase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0015940
pantothenate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1m3u
,
PDBe:1m3u
,
PDBj:1m3u
PDBsum
1m3u
PubMed
12906829
UniProt
P31057
|PANB_ECOLI 3-methyl-2-oxobutanoate hydroxymethyltransferase (Gene Name=panB)
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