Structure of PDB 6gs2 Chain B Binding Site BS02
Receptor Information
>6gs2 Chain B (length=389) Species:
158879
(Staphylococcus aureus subsp. aureus N315) [
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DVLRKLAEQVDDIVFISGTNGKTTTSNLIGHTLKANNIQIIHNNEGANMA
AGITSAFIMQSTPKTKIAVIEIDEGSIPRVLKEVTPSMMVFTNFFRDGEI
DIMVNNIAETISNKGIKLLLNADDPFVSRLKIASDTIVYYGMKAHAHEFE
QSNESRYCPNCGRLLQYDYIHYNQIGHYHCQCGFKREQAKYEISSFDVAP
FLYLNINDEKYDMKIAGDFNAYNALAAYTVLRELGLNEQTIKNGFETYTS
DNGRMQYFKKERKEAMINLAKNPAGMNASLSVGEQLEGEKVYVISLNDNA
ADGRDTSWIYDADFEKLSKQQIEAIIVTGTRAEELQLRLKLAEVEVPIIV
ERDIYKATAKTMDYKGFTVAIPNYTSLAPMLEQLNRSFE
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
6gs2 Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6gs2
Structural basis of cell wall peptidoglycan amidation by the GatD/MurT complex of Staphylococcus aureus.
Resolution
2.04 Å
Binding residue
(original residue number in PDB)
H189 D262
Binding residue
(residue number reindexed from 1)
H147 D218
Annotation score
1
Enzymatic activity
Enzyme Commision number
6.3.5.13
: lipid II isoglutaminyl synthase (glutamine-hydrolyzing).
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0008270
zinc ion binding
GO:0016874
ligase activity
GO:0016879
ligase activity, forming carbon-nitrogen bonds
GO:0016881
acid-amino acid ligase activity
GO:0046872
metal ion binding
GO:0140282
carbon-nitrogen ligase activity on lipid II
Biological Process
GO:0008360
regulation of cell shape
GO:0009058
biosynthetic process
GO:0009252
peptidoglycan biosynthetic process
GO:0071555
cell wall organization
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6gs2
,
PDBe:6gs2
,
PDBj:6gs2
PDBsum
6gs2
PubMed
30154570
UniProt
A0A0H3JUU7
|MURT_STAAN Lipid II isoglutaminyl synthase (glutamine-hydrolyzing) subunit MurT (Gene Name=murT)
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