Structure of PDB 3vmt Chain A Binding Site BS03
Receptor Information
>3vmt Chain A (length=222) Species:
158878
(Staphylococcus aureus subsp. aureus Mu50) [
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RILLKILLTILIIIALFIGIMYFLSTRDNVDELRKIENKSSFVSADNMPE
YVKGAFISMEDERFYNHHGFDLKGTTRALFSTGGSTITQQVVKNYFYDND
RSFTRKVKELFVAHRVEKQYNKNEILSFYLNNIYFGDNQYTLEGAANHYF
GTTVNKNSTTMSHITVLQSAILASKVNAPSVYNINNMSENFTQRVSTNLE
KMKQQNYINETQYQQAMSQLNR
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
3vmt Chain A Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
3vmt
Crystal structure of Staphylococcus aureus transglycosylase in complex with a lipid II analog and elucidation of peptidoglycan synthesis mechanism
Resolution
2.299 Å
Binding residue
(original residue number in PDB)
D111 T115 Q136
Binding residue
(residue number reindexed from 1)
D71 T75 Q89
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E100 G131 S132 Q136
Catalytic site (residue number reindexed from 1)
E60 G84 S85 Q89
Enzyme Commision number
2.4.99.28
: peptidoglycan glycosyltransferase.
Gene Ontology
Molecular Function
GO:0008658
penicillin binding
GO:0008955
peptidoglycan glycosyltransferase activity
GO:0016757
glycosyltransferase activity
Biological Process
GO:0008360
regulation of cell shape
GO:0009252
peptidoglycan biosynthetic process
GO:0046677
response to antibiotic
GO:0071555
cell wall organization
Cellular Component
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3vmt
,
PDBe:3vmt
,
PDBj:3vmt
PDBsum
3vmt
PubMed
22493270
UniProt
Q99T05
|MGT_STAAM Monofunctional glycosyltransferase (Gene Name=mgt)
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