Structure of PDB 2bty Chain B Binding Site BS02

Receptor Information
>2bty Chain B (length=282) Species: 2336 (Thermotoga maritima) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MRIDTVNVLLEALPYIKEFYGKTFVIKFGGSAMKQENAKKAFIQDIILLK
YTGIKPIIVHGGGPAISQMMKDLGIEPVFKNGHRVTDEKTMEIVEMVLVG
KINKEIVMNLNLHGGRAVGICGKDSKLIVAEKETKHGDIGYVGKVKKVNP
EILHALIENDYIPVIAPVGIGEDGHSYNINADTAAAEIAKSLMAEKLILL
TDVDGVLKDGKLISTLTPDEAEELIRDGTVTGGMIPKVECAVSAVRGGVG
AVHIINGGLEHAILLEIFSRKGIGTMIKELEG
Ligand information
Ligand IDNLG
InChIInChI=1S/C7H11NO5/c1-4(9)8-5(7(12)13)2-3-6(10)11/h5H,2-3H2,1H3,(H,8,9)(H,10,11)(H,12,13)/t5-/m0/s1
InChIKeyRFMMMVDNIPUKGG-YFKPBYRVSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04O=C(NC(C(=O)O)CCC(=O)O)C
OpenEye OEToolkits 1.5.0CC(=O)N[C@@H](CCC(=O)O)C(=O)O
CACTVS 3.341CC(=O)N[C@@H](CCC(O)=O)C(O)=O
CACTVS 3.341CC(=O)N[CH](CCC(O)=O)C(O)=O
OpenEye OEToolkits 1.5.0CC(=O)NC(CCC(=O)O)C(=O)O
FormulaC7 H11 N O5
NameN-ACETYL-L-GLUTAMATE
ChEMBLCHEMBL1234751
DrugBankDB04075
ZINCZINC000001532704
PDB chain2bty Chain B Residue 1284 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB2bty Structural Bases of Feed-Back Control of Arginine Biosynthesis, Revealed by the Structure of Two Hexameric N-Acetylglutamate Kinases, from Thermotoga Maritima and Pseudomonas Aeruginosa
Resolution2.75 Å
Binding residue
(original residue number in PDB)
K27 G29 G30 G61 N180 D182
Binding residue
(residue number reindexed from 1)
K27 G29 G30 G61 N180 D182
Annotation score3
Enzymatic activity
Catalytic site (original residue number in PDB) K27 G30 G63 D182 K237
Catalytic site (residue number reindexed from 1) K27 G30 G63 D182 K237
Enzyme Commision number 2.7.2.8: acetylglutamate kinase.
Gene Ontology
Molecular Function
GO:0003991 acetylglutamate kinase activity
GO:0005524 ATP binding
GO:0016301 kinase activity
Biological Process
GO:0006526 L-arginine biosynthetic process
GO:0016310 phosphorylation
GO:0042450 arginine biosynthetic process via ornithine
Cellular Component
GO:0005737 cytoplasm

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:2bty, PDBe:2bty, PDBj:2bty
PDBsum2bty
PubMed16376937
UniProtQ9X2A4|ARGB_THEMA Acetylglutamate kinase (Gene Name=argB)

[Back to BioLiP]