Species

KNApSAcK Entry

Organism name Curvularia sp. AB 2090A-11 (NRRL 22559)
Genus Curvularia
Family Pleosporaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Curvularia
Linked NCBI taxonomy ID 5502
Linked level genus

Family

Family in NCBI taxonomy Pleosporaceae
ID 28556

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

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
C00016655 External link 512 Radicinin
/ Stemphylone
CHEMBL1894884
CHEMBL1994984
10 / 6 / 7 No. 2439

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)