Species

KNApSAcK Entry

Organism name Trigonella caerulea
Genus Trigonella
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Trigonella caerulea
Linked NCBI taxonomy ID 200963
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (1)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00001200 External link 512 Pyruvic acid
CHEMBL1162144
D019289
5 / 2 / 2 10 / 4 No. 2782

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O15427 Monocarboxylate transporter 4 Unclassified protein C00001200 0 / 0
Q92959 Solute carrier organic anion transporter family member 2A1 Unclassified protein C00001200 1 / 0
O60669 Monocarboxylate transporter 2 Unclassified protein C00001200 0 / 0
Q05BR4 SLC16A10 protein Unclassified protein C00001200 0 / 0
Q9C0B1 Alpha-ketoglutarate-dependent dioxygenase FTO Unclassified protein C00001200 1 / 2

10 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
31 ACACA, ACAC, ACACAD, ACC, ACC1, ACCA acetyl-CoA carboxylase alpha (EC:6.4.1.2 6.3.4.14) C00001200
1487 CTBP1, BARS C-terminal binding protein 1 C00001200
1488 CTBP2 C-terminal binding protein 2 C00001200
1586 CYP17A1, CPT7, CYP17, P450C17, S17AH cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) C00001200
14103 C00001200
2516 NR5A1, AD4BP, ELP, FTZ1, FTZF1, POF7, SF-1, SF1, SPGF8, SRXY3 nuclear receptor subfamily 5, group A, member 1 C00001200
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001200
23411 SIRT1, SIR2L1 sirtuin 1 C00001200
6566 SLC16A1, HHF7, MCT, MCT1 solute carrier family 16 (monocarboxylate transporter), member 1 C00001200
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00001200

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (2)

OMIM preferred title UniProt
#612938 Growth retardation, developmental delay, coarse facies, and early death; gdfd Q9C0B1
#614441 Hypertrophic osteoarthropathy, primary, autosomal recessive, 2; phoar2 Q92959

KEGG DISEASE (2)

KEGG name UniProt
H00409 Type II diabetes mellitus Q9C0B1 (related)
H00926 Growth retardation, developmental delay, coarse facies, and early death Q9C0B1 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006943 Hyperglycemia C00001200
D028361 Mitochondrial Diseases C00001200
D009135 Muscular Diseases C00001200
D009336 Necrosis C00001200