Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Didemnidae 3
Aglajidae 1

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
C00034540 External link 512 Homodolastatin 16
C00034565 External link 512 Kulokekahilide 1
C00043955 External link 512 Tamandarin A
/ (-)-Tamandarin A
CHEMBL216937
C00043956 External link 512 Tamandarin B
/ (-)-Tamandarin B
C00044711 External link 512 Didemnin B
CHEMBL405852
CHEMBL407121
CHEMBL262897
CHEMBL386301
CHEMBL1966062
CHEMBL1971194
CHEMBL2304286
7 / 11 / 7

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)