Species

KNApSAcK Entry

Organism name Dorstenia gigas
Genus Dorstenia
Family Moraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Dorstenia
Linked NCBI taxonomy ID 106722
Linked level genus

Family

Family in NCBI taxonomy Moraceae
ID 3487

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (9)

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
C00002453 External link 512 Byakangelicin
/ (+)-Byakangelicin
CHEMBL508648
C434685
5 / 2 / 0 No. 579 No. 25
C00036625 External link 512 6-Methoxy-5-(3-methyl-2,3-dihydroxybutyl)-angelicin
No. 579 No. 25
C00036590 External link 512 5,8-Dimethoxy-3-(3-methyl-2,3-dihydroxybutyl)-psoralen
/ (-)-5,8-Dimethoxy-3-(3-methyl-2,3-dihydroxybutyl)-psoralen
No. 579 No. 25
C00036599 External link 512 5-Methoxy-8-(1,1-dimethyl-2,3-dihydroxypropyl)-psoralen
/ (+)-5-Methoxy-8-(1,1-dimethyl-2,3-dihydroxypropyl)-psoralen
No. 579 No. 25
C00032846 External link 512 Cnidilin
/ Knidilin
/ Isophellopterin
CHEMBL1934194
1 / 0 / 0 No. 606 No. 25
C00030532 External link 512 Isoimperatorin
CHEMBL448060
C055542
8 / 13 / 11 3 / 1 No. 606 No. 25
C00037872 External link 512 Swietenocoumarin B
No. 606 No. 25
C00037065 External link 512 Dorstegin
No. 750 No. 25
C00037165 External link 512 Furopinnarin
No. 3930 No. 25

Human Protein / Gene in interactions

12 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P56817 Beta-secretase 1 A1A C00002453 C00030532 C00032846 0 / 0
P22303 Acetylcholinesterase Hydrolase C00030532 1 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002453 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00030532 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002453 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00030532 0 / 0
P02545 Prelamin-A/C Unclassified protein C00030532 11 / 10
Q9UNA4 DNA polymerase iota Enzyme C00030532 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002453 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00030532 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002453 1 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00030532 1 / 1

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00030532
2939 GSTA2, GST2, GSTA2-2, GTA2, GTH2 glutathione S-transferase alpha 2 (EC:2.5.1.18) C00030532
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00030532

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#275210 Restrictive dermopathy, lethal P02545
#112100 Yt blood group antigen P22303

KEGG DISEASE (11)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00030532