Species

KNApSAcK Entry

Organism name Botryllus giganteum
Genus Botryllus
Family Botryllidae
Kingdom Animalia

NCBI taxonomy

Entry

Linked NCBI taxonomy name Botryllus
Linked NCBI taxonomy ID 30300
Linked level genus

Family

Family in NCBI taxonomy Styelidae
ID 7721

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Metazoa
ID 33208

Plant class

Plant class
ID

Metabolite list (2)

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
C00043309 External link 512 Benzylamine
CHEMBL522
C030796
8 / 3 / 2 No. 885
C00002657 External link 512 p-Formylphenol
/ 4-Hydroxybenzaldehyde
/ p-Hydroxybenzaldehyde
CHEMBL14193
C011483
3 / 2 / 2 No. 2076

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002657 1 / 1
P42574 Caspase-3 C14 C00043309 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00043309 1 / 1
P08183 Multidrug resistance protein 1 drug C00043309 1 / 0
P19801 Amiloride-sensitive amine oxidase [copper-containing] Enzyme C00043309 0 / 0
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00002657 0 / 0
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002657 1 / 1
Q16853 Membrane primary amine oxidase Enzyme C00043309 0 / 0
P55210 Caspase-7 C14 C00043309 0 / 0
P07477 Trypsin-1 S1A C00043309 1 / 1
P11086 Phenylethanolamine N-methyltransferase Enzyme C00043309 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#300615 Brunner syndrome P21397
#613163 Gaba-transaminase deficiency P80404
#612244 Inflammatory bowel disease 13; ibd13 P08183
#167800 Pancreatitis, hereditary; pctt P07477
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649

KEGG DISEASE (4)

KEGG name UniProt
H00933 Hereditary pancreatitis P07477 (related)
H00548 Brunner syndrome P21397 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H01257 GABA-transaminase deficiency P80404 (related)