PCIDB

Trigonella coerulescens

Family in NCBI taxonomy	Fabaceae
ID	3803

Kingdom (Superkingdom) in NCBI taxonomy	Viridiplantae
ID	33090

Plant class	rosids
ID	71275

KNApSAcK ID	name	ChEMBL link	CTD link	# of proteins in ChEMBL interaction / related OMIM / related KEGG DISEASE	KCF-S cluster	phytochemical cluster
C00005182	Kaempferol 3,7-diglucoside / Kaempferol 3,7-O-beta-D-diglucopyranoside	CHEMBL2206209			No. 1	No. 15
C00003825	3',4',7-Trihydroxyflavone / 7,3',4'-Trihydroxyflavone	CHEMBL301624		4 / 5 / 5	No. 71	No. 15
C00003800	7,4'-Dihydroxyflavone	CHEMBL294878	C085172	17 / 19 / 16	No. 76	No. 15

accession	description	class description	KNApSAcK metabolite in interactions	# of diseases (OMIM / KEGG)
Q16637	Survival motor neuron protein	Unclassified protein	C00003800	4 / 1
Q03181	Peroxisome proliferator-activated receptor delta	NR1C2	C00003800	0 / 0
O95271	Tankyrase-1	Enzyme	C00003825	0 / 0
P05091	Aldehyde dehydrogenase, mitochondrial	Oxidoreductase	C00003800	1 / 1
Q9Y3R4	Sialidase-2	Enzyme	C00003800	0 / 0
P00352	Retinal dehydrogenase 1	Enzyme	C00003800	0 / 0
P09874	Poly [ADP-ribose] polymerase 1	Enzyme	C00003825	0 / 0
P11511	Cytochrome P450 19A1	Cytochrome P450 19A1	C00003800	2 / 2
P37231	Peroxisome proliferator-activated receptor gamma	NR1C3	C00003800	5 / 3
P06280	Alpha-galactosidase A	Enzyme	C00003800	1 / 1
P28482	Mitogen-activated protein kinase 1	Erk	C00003800	0 / 0
Q99714	3-hydroxyacyl-CoA dehydrogenase type-2	Enzyme	C00003800	3 / 3
P15428	15-hydroxyprostaglandin dehydrogenase [NAD(+)]	Enzyme	C00003800	2 / 2
Q9H2K2	Tankyrase-2	Enzyme	C00003825	0 / 0
P08684	Cytochrome P450 3A4	Cytochrome P450 3A4	C00003800	0 / 1
Q07869	Peroxisome proliferator-activated receptor alpha	NR1C1	C00003800	0 / 0
P06239	Tyrosine-protein kinase Lck	Src	C00003800	0 / 1
O14746	Telomerase reverse transcriptase	Enzyme	C00003825	5 / 5
B2RXH2	Lysine-specific demethylase 4E	Enzyme	C00003800	0 / 0
P27338	Amine oxidase [flavin-containing] B	Oxidoreductase	C00003800	0 / 0
P21397	Amine oxidase [flavin-containing] A	Oxidoreductase	C00003800	1 / 1

OMIM	preferred title	UniProt
#300438	17-beta-hydroxysteroid dehydrogenase x deficiency	Q99714
#610251	Alcohol sensitivity, acute	P05091
#609135	Aplastic anemia	O14746
#613546	Aromatase deficiency	P11511
#139300	Aromatase excess syndrome; aexs	P11511
%606641	Body mass index; bmi	P37231
#300615	Brunner syndrome	P21397
#609338	Carotid intimal medial thickness 1	P37231
#119900	Digital clubbing, isolated congenital	P15428
#613989	Dyskeratosis congenita, autosomal dominant, 2; dkca2	O14746
#301500	Fabry disease	P06280
#137800	Glioma susceptibility 1; glm1	P37231
#259100	Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1	P15428
#604367	Lipodystrophy, familial partial, type 3; fpld3	P37231
#615134	Melanoma, cutaneous malignant, susceptibility to, 9; cmm9	O14746
#300705	Mental retardation, x-linked 17; mrx17	Q99714
#300220	Mental retardation, x-linked, syndromic 10; mrxs10	Q99714
#601665	Obesity	P37231
#614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1	O14746
#178500	Pulmonary fibrosis, idiopathic; ipf	O14746
#253300	Spinal muscular atrophy, type i; sma1	Q16637
#253550	Spinal muscular atrophy, type ii; sma2	Q16637
#253400	Spinal muscular atrophy, type iii; sma3	Q16637
#271150	Spinal muscular atrophy, type iv; sma4	Q16637

KEGG	name	UniProt
H00764	Cri du chat syndrome	O14746 (related)
H01132	Aplastic anemia (AA)	O14746 (related)
H01299	Idiopathic pulmonary fibrosis	O14746 (related)
H00022	Bladder cancer	O14746 (marker)
H00024	Prostate cancer	O14746 (marker)
H01071	Acute alcohol sensitivity	P05091 (related)
H00093	Combined immunodeficiencies (CIDs)	P06239 (related)
H00125	Fabry disease	P06280 (related)
H00036	Osteosarcoma	P08684 (marker)
H00599	46,XX disorders of sex development (Disorders related to androgen excess)	P11511 (related)
H00794	Aromatase excess syndrome	P11511 (related)
H00457	Primary hypertrophic osteoarthropathy (PHO)	P15428 (related)
H01246	Isolated congenital nail clubbing (ICNC)	P15428 (related)
H00548	Brunner syndrome	P21397 (related)
H00032	Thyroid cancer	P37231 (related)
H00409	Type II diabetes mellitus	P37231 (related)
H00420	Familial partial lipodystrophy (FPL)	P37231 (related)
H00455	Spinal muscular atrophy (SMA)	Q16637 (related)
H00480	Non-syndromic X-linked mental retardation	Q99714 (related)
H00658	Syndromic X-linked mental retardation	Q99714 (related)
H00925	2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency	Q99714 (related)