Species

KNApSAcK Entry

Organism name Trididemnum solidum
Genus Trididemnum
Family Didemnidae
Kingdom Animalia

NCBI taxonomy

Entry

Linked NCBI taxonomy name Trididemnum solidum
Linked NCBI taxonomy ID 1079459
Linked level species

Family

Family in NCBI taxonomy Didemnidae
ID 107393

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Metazoa
ID 33208

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
C00044711 External link 512 Didemnin B
CHEMBL405852
CHEMBL407121
CHEMBL262897
CHEMBL386301
CHEMBL1966062
CHEMBL1971194
CHEMBL2304286
7 / 11 / 7 No. 1729

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00044711 1 / 1
O75496 Geminin Unclassified protein C00044711 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00044711 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00044711 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00044711 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00044711 1 / 0
Q06710 Paired box protein Pax-8 Unclassified protein C00044711 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#137800 Glioma susceptibility 1; glm1 O75874
#218700 Hypothyroidism, congenital, nongoitrous, 2; chng2 Q06710
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (7)

KEGG name UniProt
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00032 Thyroid cancer Q06710 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) Q06710 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)