Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Pleosporaceae 6

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (5)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00016655 External link 512 Radicinin
/ Stemphylone
CHEMBL1894884
CHEMBL1994984
10 / 6 / 7
C00034923 External link 512 4-Epiradicinol
/ (-)-4-Epiradicinol
C00049695 External link 512 3-Epiradicinol
C00049696 External link 512 3-Methoxy-3-epiradicinol
/ (-)-3-Methoxy-3-epiradicinol
C00049742 External link 512 Radicinol

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00016655 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00016655 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00016655 2 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00016655 2 / 0
O75496 Geminin Unclassified protein C00016655 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00016655 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00016655 1 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00016655 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00016655 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00016655 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (7)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)