Species

KNApSAcK Entry

Organism name Tedania anhelans
Genus
Family
Kingdom

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
C00026537 External link 512 Norharman
/ Carbazoline
/ beta-Carboline
/ 2-Azacarbazole
/ 2,9-Diazafluorene
CHEMBL275224
C010262
50 / 17 / 8 8 / 1 No. 1889 No. 4

Human Protein / Gene in interactions

50 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00026537 4 / 1
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00026537 0 / 0
O14965 Aurora kinase A Aur C00026537 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00026537 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00026537 0 / 0
Q00535 Cyclin-dependent kinase 5 Cdk5 C00026537 0 / 0
O14920 Inhibitor of nuclear factor kappa-B kinase subunit beta Other serine/threonine protein kinase C00026537 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00026537 0 / 0
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00026537 0 / 0
O75496 Geminin Unclassified protein C00026537 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00026537 0 / 0
O15111 Inhibitor of nuclear factor kappa-B kinase subunit alpha Other serine/threonine protein kinase C00026537 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00026537 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00026537 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00026537 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00026537 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00026537 0 / 0
Q05513 Protein kinase C zeta type Iota C00026537 0 / 0
Q04759 Protein kinase C theta type Delta C00026537 0 / 1
Q02156 Protein kinase C epsilon type Eta C00026537 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00026537 0 / 0
P17252 Protein kinase C alpha type Alpha C00026537 0 / 0
Q05655 Protein kinase C delta type Delta C00026537 0 / 0
P05129 Protein kinase C gamma type Alpha C00026537 1 / 1
P05771 Protein kinase C beta type Alpha C00026537 0 / 0
P24723 Protein kinase C eta type Eta C00026537 1 / 0
P41743 Protein kinase C iota type Iota C00026537 0 / 0
Q15139 Serine/threonine-protein kinase D1 Pkd C00026537 0 / 0
Q9UN88 Gamma-aminobutyric acid receptor subunit theta GABA-A theta C00026537 0 / 0
P28472 Gamma-aminobutyric acid receptor subunit beta-3 GABA-A beta C00026537 1 / 0
P14867 Gamma-aminobutyric acid receptor subunit alpha-1 GABA-A alpha C00026537 1 / 1
P48169 Gamma-aminobutyric acid receptor subunit alpha-4 GABA-A alpha C00026537 0 / 0
O14764 Gamma-aminobutyric acid receptor subunit delta GABA-A delta C00026537 1 / 1
P31644 Gamma-aminobutyric acid receptor subunit alpha-5 GABA-A alpha C00026537 0 / 0
Q99928 Gamma-aminobutyric acid receptor subunit gamma-3 GABA-A gamma C00026537 0 / 0
P78334 Gamma-aminobutyric acid receptor subunit epsilon GABA-A epsilon C00026537 0 / 0
Q8N1C3 Gamma-aminobutyric acid receptor subunit gamma-1 GABA-A gamma C00026537 0 / 0
P34903 Gamma-aminobutyric acid receptor subunit alpha-3 GABA-A alpha C00026537 0 / 0
O00591 Gamma-aminobutyric acid receptor subunit pi GABA-A pi C00026537 0 / 0
P47870 Gamma-aminobutyric acid receptor subunit beta-2 GABA-A beta C00026537 0 / 0
P18507 Gamma-aminobutyric acid receptor subunit gamma-2 GABA-A gamma C00026537 4 / 2
P18505 Gamma-aminobutyric acid receptor subunit beta-1 GABA-A beta C00026537 0 / 0
Q16445 Gamma-aminobutyric acid receptor subunit alpha-6 GABA-A alpha C00026537 0 / 0
P47869 Gamma-aminobutyric acid receptor subunit alpha-2 GABA-A alpha C00026537 1 / 0
P22694 cAMP-dependent protein kinase catalytic subunit beta Pka C00026537 0 / 0
P17612 cAMP-dependent protein kinase catalytic subunit alpha Pka C00026537 0 / 0
P22612 cAMP-dependent protein kinase catalytic subunit gamma Pka C00026537 0 / 0
P68400 Casein kinase II subunit alpha Ck2 C00026537 0 / 0
P19784 Casein kinase II subunit alpha' Ck2 C00026537 0 / 0
P67870 Casein kinase II subunit beta REG serine/threonine protein kinase family C00026537 0 / 0

8 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00026537
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00026537
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00026537
1555 CYP2B6, CPB6, CYP2B, CYP2B7, CYP2B7P, CYPIIB6, EFVM, IIB1, P450 cytochrome P450, family 2, subfamily B, polypeptide 6 (EC:1.14.14.1) C00026537
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00026537
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00026537
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00026537
4129 MAOB monoamine oxidase B (EC:1.4.3.4) C00026537

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#103780 Alcohol dependence P47869
#613630 Cocoon syndrome O15111
#119900 Digital clubbing, isolated congenital P15428
#607208 Dravet syndrome P18507
#607681 Epilepsy, childhood absence, susceptibility to, 2; eca2 P18507
#612269 Epilepsy, childhood absence, susceptibility to, 5; eca5 P28472
#613060 Epilepsy, idiopathic generalized, susceptibility to, 10; eig10 O14764
#611136 Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 P14867
#604233 Generalized epilepsy with febrile seizures plus, type 1; gefsp1 P18507
#611277 Generalized epilepsy with febrile seizures plus, type 3; gefsp3 P18507
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#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
#605361 Spinocerebellar ataxia 14; sca14 P05129
#601367 Stroke, ischemic P24723

KEGG DISEASE (8)

KEGG name UniProt
H00783 Febrile seizures O14764 (related)
P18507 (related)
H00882 Cocoon syndrome O15111 (related)
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
H00808 Idiopathic generalized epilepsies (IGEs) P14867 (related)
P18507 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00408 Type I diabetes mellitus Q04759 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D019970 Cocaine-Related Disorders C00026537