Species

KNApSAcK Entry

Organism name Osmunda asiatica
Genus Osmunda
Family Osmundaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Osmunda
Linked NCBI taxonomy ID 3283
Linked level genus

Family

Family in NCBI taxonomy Osmundaceae
ID 3282

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Euphyllophyta
ID 78536

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
C00005135 External link 512 Asiaticalin
CHEMBL233930
CHEMBL453290
CHEMBL1572115
10 / 6 / 7 No. 2 No. 15

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 C00005135 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00005135 0 / 0
P07237 Protein disulfide-isomerase Enzyme C00005135 0 / 0
P15121 Aldose reductase Enzyme C00005135 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00005135 1 / 1
P14679 Tyrosinase Oxidoreductase C00005135 4 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00005135 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00005135 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005135 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00005135 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#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)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)