Structure of PDB 6mfm Chain A Binding Site BS02
Receptor Information
>6mfm Chain A (length=304) Species:
470
(Acinetobacter baumannii) [
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AEFSIIDQYFNRQSHPDVALGIGDDSALITPPPNQQLVICADTLVAGRHF
PLETSPHAIGWKSVAVNLSDIAAMGAKPHSILLAISLPQVDHEWLEGFSQ
GIYDCCNQFGVALIGGDTTQGPHLTITVTAMGWIETGKAVLRSGAKVGDY
VCVSGQIGDAAYGLQHLGHSLQQRLDYPTPRCKLGEELKGLASSMIDVSD
GLAQDLGHILKASKVGARLILEKLPVDPVLQQIEEQQRWQYALAGGDDYE
LCFTITPQNYEKLLQKQLDVKITMIGQIVEQTKLTFEHLGSDYPLQIHGY
QHFA
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
6mfm Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6mfm
Crystal structures of thiamine monophosphate kinase from Acinetobacter baumannii in complex with substrates and products.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
D43 D71
Binding residue
(residue number reindexed from 1)
D42 D70
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.4.16
: thiamine-phosphate kinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005524
ATP binding
GO:0009030
thiamine-phosphate kinase activity
GO:0016301
kinase activity
GO:0046872
metal ion binding
Biological Process
GO:0009228
thiamine biosynthetic process
GO:0009229
thiamine diphosphate biosynthetic process
GO:0016310
phosphorylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:6mfm
,
PDBe:6mfm
,
PDBj:6mfm
PDBsum
6mfm
PubMed
30867460
UniProt
A0A0D5YC82
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