Structure of PDB 1g4t Chain B Binding Site BS01
Receptor Information
>1g4t Chain B (length=227) Species:
1423
(Bacillus subtilis) [
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HHGIRMTRISREMMKELLSVYFIMGSNNTKADPVTVVQKALKGGATLYQF
REKGGDALTGEARIKFAEKAQAACREAGVPFIVNDDVELALNLKADGIHI
GQEDANAKEVRAAIGDMILGVSAHTMSEVKQAEEDGADYVGLGPIYPTET
KKDTRAVQGVSLIEAVRRQGISIPIVGIGGITIDNAAPVIQAGADGVSMI
SAISQAEDPESAARKFREEIQTYKTGR
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
1g4t Chain B Residue 2006 [
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Receptor-Ligand Complex Structure
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PDB
1g4t
Structural characterization of the enzyme-substrate, enzyme-intermediate, and enzyme-product complexes of thiamin phosphate synthase.
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
D1093 D1112
Binding residue
(residue number reindexed from 1)
D85 D104
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R1059 S1130 K1159
Catalytic site (residue number reindexed from 1)
R51 S122 K151
Enzyme Commision number
2.5.1.3
: thiamine phosphate synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004789
thiamine-phosphate diphosphorylase activity
GO:0016740
transferase activity
GO:0046872
metal ion binding
Biological Process
GO:0009228
thiamine biosynthetic process
GO:0009229
thiamine diphosphate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1g4t
,
PDBe:1g4t
,
PDBj:1g4t
PDBsum
1g4t
PubMed
11513589
UniProt
P39594
|THIE_BACSU Thiamine-phosphate synthase (Gene Name=thiE)
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