Structure of PDB 5d86 Chain A Binding Site BS02
Receptor Information
>5d86 Chain A (length=318) Species:
426430
(Staphylococcus aureus subsp. aureus str. Newman) [
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CHDSLLDSVGQTPMVQLHQLFPKHEVFAKLEYMNPGGSMKDRPAKYIIEH
GIKHGLITENTHLIESTSGNLGIALAMIAKIKGLKLTCVVDPKISPTNLK
IIKSYGANVEMVEEPDAHGGYLMTRIAKVQELLATIDDAYWINQFANELN
WQSHYHGAGTEIVETIKQPIDYFVAPVSTTGSIMGMSRKIKEVHPNAQIV
AVDAKGSVIFGDKPINRELPGIGASRVPEILNRSEINQVIHVDDYQSALG
CRKLIDYEGIFAGGSTGSIIAAIEQLITSIEEGATIVTILPDRGDRYLDL
VYSDTWLEKMKSRQGVKS
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
5d86 Chain A Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
5d86
Deciphering the Substrate Specificity of SbnA, the Enzyme Catalyzing the First Step in Staphyloferrin B Biosynthesis.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
S232 R233
Binding residue
(residue number reindexed from 1)
S225 R226
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K47 S272
Catalytic site (residue number reindexed from 1)
K40 S265
Enzyme Commision number
2.5.1.140
: N-(2-amino-2-carboxyethyl)-L-glutamate synthase.
Gene Ontology
Molecular Function
GO:0004124
cysteine synthase activity
GO:0016740
transferase activity
GO:0016765
transferase activity, transferring alkyl or aryl (other than methyl) groups
Biological Process
GO:0006535
cysteine biosynthetic process from serine
GO:0019344
cysteine 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:5d86
,
PDBe:5d86
,
PDBj:5d86
PDBsum
5d86
PubMed
26794841
UniProt
A6QDA0
|SBNA_STAAE N-(2-amino-2-carboxyethyl)-L-glutamate synthase (Gene Name=sbnA)
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