Structure of PDB 3d2m Chain A Binding Site BS02
Receptor Information
>3d2m Chain A (length=424) Species:
242231
(Neisseria gonorrhoeae FA 1090) [
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DSFVAHFREAAPYIRQMRGTTLVAGIDGRLLEGGTLNKLAADIGLLSQLG
IRLVLIHGAYHFLDRLAAAQGRTPHYCRGLRVTDETSLGQAQQFAGTVRS
RFEAALCGSSVPLVSGNFLTARPIGVIDGTDMEYAGVIRKTDTAALRFQL
DAGNIVWMPPLGHSYGGKTFNLDMVQAAASVAVSLQAEKLVYLTLSDGIS
RPDGTLAETLSAQEAQSLAEHAASETRRLISSAVAALEGGVHRVQILNGA
ADGSLLQELFTRNGIGTSIAKEAFVSIRQAHSGDIPHIAALIRPLEEQGI
LLHRSREYLENHISEFSILEHDGNLYGCAALKTFAEADCGEIACLAVSPQ
AQDGGYGERLLAHIIDKARGIGISRLFALSTNTGEWFAERGFQTASEDEL
PETRRKDYRSNGRNSHILVRRLHR
Ligand information
Ligand ID
GLU
InChI
InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1
InChIKey
WHUUTDBJXJRKMK-VKHMYHEASA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)C(N)CCC(=O)O
OpenEye OEToolkits 1.7.0
C(CC(=O)O)C(C(=O)O)N
OpenEye OEToolkits 1.7.0
C(CC(=O)O)[C@@H](C(=O)O)N
CACTVS 3.370
N[C@@H](CCC(O)=O)C(O)=O
CACTVS 3.370
N[CH](CCC(O)=O)C(O)=O
Formula
C5 H9 N O4
Name
GLUTAMIC ACID
ChEMBL
CHEMBL575060
DrugBank
DB00142
ZINC
ZINC000001482113
PDB chain
3d2m Chain A Residue 438 [
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Receptor-Ligand Complex Structure
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PDB
3d2m
Mechanism of Allosteric Inhibition of N-Acetyl-L-glutamate Synthase by L-Arginine.
Resolution
2.21 Å
Binding residue
(original residue number in PDB)
L314 R316 A355 C356 L391 R425 S427
Binding residue
(residue number reindexed from 1)
L302 R304 A343 C344 L379 R413 S415
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
I30
Catalytic site (residue number reindexed from 1)
I26
Enzyme Commision number
2.3.1.1
: amino-acid N-acetyltransferase.
Gene Ontology
Molecular Function
GO:0004042
L-glutamate N-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
Biological Process
GO:0006526
L-arginine 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:3d2m
,
PDBe:3d2m
,
PDBj:3d2m
PDBsum
3d2m
PubMed
19095660
UniProt
Q5FAK7
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