Species

KNApSAcK Entry

Organism name Trillium spp.
Genus Trillium
Family Trilliaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Trillium
Linked NCBI taxonomy ID 49674
Linked level genus

Family

Family in NCBI taxonomy Melanthiaceae
ID 50362

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Liliopsida
ID 4447

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
C00003575 External link 512 Dioscin
CHEMBL507001
CHEMBL2036081
CHEMBL2036082
C019357
0 / 2 No. 17 No. 11
C00003576 External link 512 Diosgenin
CHEMBL412437
CHEMBL1551855
CHEMBL1553328
D004144
6 / 10 / 7 15 / 2 No. 171 No. 11

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00003576 3 / 0
P40763 Signal transducer and activator of transcription 3 Transcription Factor C00003576 1 / 2
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00003576 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003576 0 / 1
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00003576 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00003576 4 / 3

15 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00003576
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00003576
597 BCL2A1, ACC-1, ACC-2, BCL2L5, BFL1, GRS, HBPA1 BCL2-related protein A1 C00003576
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00003576
329 BIRC2, API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 baculoviral IAP repeat containing 2 C00003576
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00003576
8837 CFLAR, CASH, CASP8AP1, CLARP, Casper, FLAME, FLAME-1, FLAME1, FLIP, I-FLICE, MRIT, c-FLIP, c-FLIPL, c-FLIPR, c-FLIPS CASP8 and FADD-like apoptosis regulator C00003576
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00003576
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00003576
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00003576
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00003576
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00003576
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00003576
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00003576
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00003576

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (10)

OMIM preferred title UniProt
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#600274 Frontotemporal dementia; ftd P10636
#143500 Gilbert syndrome P22309
P22310
#147060 Hyper-ige recurrent infection syndrome, autosomal dominant P40763
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (7)

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)
H00208 Hyperbilirubinemia P22309 (related)
H00016 Oral cancer P40763 (related)
H00107 Other well-defined immunodeficiency syndromes P40763 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00003575
D009336 Necrosis C00003575
D002779 Cholestasis C00003576
D006949 Hyperlipidemias C00003576