Species

KNApSAcK Entry

Organism name Aspergillus clavatus (NRRL5890)
Genus Aspergillus
Family Trichocomaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aspergillus
Linked NCBI taxonomy ID 5052
Linked level genus

Family

Family in NCBI taxonomy Aspergillaceae
ID 1131492

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (3)

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
C00023553 External link 512 FTC
/ Tryptoquivaline
/ Tryptoquivaline A
/ Tryptoquivaline C'
CHEMBL1399348
C010522
6 / 8 / 4 1 / 0 No. 597
C00023554 External link 512 Tryptoquivalone
/ Tryptoquivaline B
/ Nortryptoquivalone
C010521
No. 597
C00023555 External link 512 FTD
/ Tryptoquivaline D
/ Nortryptoquivaline
/ Norisotryptoquivaline
No. 597

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00023553 0 / 0
Q9Y2T6 G-protein coupled receptor 55 Lysophosphatidylinositol receptor C00023553 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00023553 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00023553 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00023553 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00023553 0 / 0

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
9429 ABCG2, ABC15, ABCP, BCRP, BCRP1, BMDP, CD338, CDw338, EST157481, GOUT1, MRX, MXR, MXR1, UAQTL1 ATP-binding cassette, sub-family G (WHITE), member 2 C00023553

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#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
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (4)

KEGG name UniProt
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)