Metabolite

KNApSAcK Entry

id C00000797
Name PT / Phosphinothricin
CAS RN 35597-44-5
Standard InChI InChI=1S/C5H12NO4P/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10)
Standard InChI (Main Layer) InChI=1S/C5H12NO4P/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10)

Cluster

Phytochemical cluster
KCF-S cluster No. 4761

Link

ChEMBL

By standard InChI CHEMBL450298
By standard InChI Main Layer CHEMBL145114 CHEMBL450298

KEGG

By LinkDB C05042

CTD

By CAS RN

Species

Summary

Plant class

class name count

Family

family name count
Streptomycetaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Streptomyces hygroscopicus 1912 Streptomycetaceae Bacteria

Human Protein / Gene in interaction

5 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q14416 Metabotropic glutamate receptor 2 Metabotropic glutamate receptor CHEMBL145114 CHEMBL896253 (1)
0 / 0
Q13255 Metabotropic glutamate receptor 1 Metabotropic glutamate receptor CHEMBL145114 CHEMBL896251 (1)
1 / 0
Q14832 Metabotropic glutamate receptor 3 Metabotropic glutamate receptor CHEMBL145114 CHEMBL896254 (1)
0 / 0
P41594 Metabotropic glutamate receptor 5 Metabotropic glutamate receptor CHEMBL145114 CHEMBL896252 (1)
0 / 0
P15104 Glutamine synthetase Enzyme CHEMBL145114 CHEMBL684445 (1) CHEMBL684446 (1)
CHEMBL684447 (1) CHEMBL684578 (1)
CHEMBL684579 (1) CHEMBL688456 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (2)

OMIM preferred title UniProt
#610015 Glutamine deficiency, congenital P15104
#614831 Spinocerebellar ataxia, autosomal recessive 13; scar13 Q13255

KEGG DISEASE (1)

KEGG disease name UniProt
H00923 Congenital systemic glutamine deficiency (CSGD) P15104 (related)