Species

KNApSAcK Entry

Organism name Securigera cretica
Genus Securigera
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Fabaceae
Linked NCBI taxonomy ID 3803
Linked level family

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 (2)

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
C00000297 External link 512 Psoralen
CHEMBL164660
D005363
12 / 6 / 6 0 / 5 No. 1282 No. 25
C00002463 External link 512 Daphnoretin
CHEMBL508494
C035316
14 / 11 / 10 No. 1906 No. 25

Human Protein / Gene in interactions

23 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000297 C00002463 3 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000297 C00002463 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000297 C00002463 0 / 1
P56817 Beta-secretase 1 A1A C00000297 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000297 0 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002463 1 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00000297 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002463 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000297 0 / 0
O75496 Geminin Unclassified protein C00002463 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000297 0 / 0
P20813 Cytochrome P450 2B6 Cytochrome P450 2B6 C00000297 1 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000297 1 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002463 2 / 2
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00000297 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000297 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002463 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002463 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002463 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002463 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00002463 0 / 0
P06746 DNA polymerase beta Enzyme C00002463 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002463 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#614546 Efavirenz, poor metabolism of P20813
#600274 Frontotemporal dementia; ftd P10636
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (12)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00000297
D002280 Carcinoma, Basal Cell C00000297
D017484 Dermatitis, Phototoxic C00000297
D056486 Drug-Induced Liver Injury C00000297
D011565 Psoriasis C00000297