Species

KNApSAcK Entry

Organism name Aplysinella rhax
Genus Aplysinella
Family Druinellidae
Kingdom Animalia

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aplysinella rhax
Linked NCBI taxonomy ID 375147
Linked level species

Family

Family in NCBI taxonomy Aplysinellidae
ID 283410

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
C00028862 External link 512 Bisprasin
/ Psammaplin A
CHEMBL83747
C098378
15 / 11 / 5 No. 4998

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q14376 UDP-glucose 4-epimerase Enzyme C00028862 1 / 1
Q13547 Histone deacetylase 1 Hydrolase C00028862 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00028862 5 / 3
P26358 DNA (cytosine-5)-methyltransferase 1 Transferase C00028862 2 / 0
Q96EB6 NAD-dependent protein deacetylase sirtuin-1 Enzyme C00028862 0 / 0
Q9UBN7 Histone deacetylase 6 Hydrolase C00028862 0 / 0
Q9BY41 Histone deacetylase 8 Hydrolase C00028862 2 / 0
Q969S8 Histone deacetylase 10 Hydrolase C00028862 0 / 0
O15379 Histone deacetylase 3 Hydrolase C00028862 0 / 0
P56524 Histone deacetylase 4 Hydrolase C00028862 1 / 1
Q8WUI4 Histone deacetylase 7 Hydrolase C00028862 0 / 0
Q9UQL6 Histone deacetylase 5 Hydrolase C00028862 0 / 0
Q9UKV0 Histone deacetylase 9 Hydrolase C00028862 0 / 0
Q92769 Histone deacetylase 2 Hydrolase C00028862 0 / 0
Q96DB2 Histone deacetylase 11 Hydrolase C00028862 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
%606641 Body mass index; bmi P37231
#600430 Brachydactyly-mental retardation syndrome; bdmr P56524
#609338 Carotid intimal medial thickness 1 P37231
#604121 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant; adcadn P26358
#300882 Cornelia de lange syndrome 5; cdls5 Q9BY41
#230350 Galactose epimerase deficiency Q14376
#137800 Glioma susceptibility 1; glm1 P37231
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#614116 Neuropathy, hereditary sensory, type ie; hsn1e P26358
#601665 Obesity P37231
#309585 Wilson-turner x-linked mental retardation syndrome; wts Q9BY41

KEGG DISEASE (5)

KEGG name UniProt
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00561 Brachydacytly-mental retardation syndrome and Smith-Magenis syndrome P56524 (related)
H00070 Galactosemia Q14376 (related)