Species

KNApSAcK Entry

Organism name Pyracantha fortuneana (MAXIM) LI
Genus Pyracantha
Family Rosaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pyracantha
Linked NCBI taxonomy ID 144561
Linked level genus

Family

Family in NCBI taxonomy Rosaceae
ID 3745

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (11)

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
C00030324 External link 512 Fortuneanoside H
/ (-)-Fortuneanoside H
No. 1 No. 15
C00030318 External link 512 Fortuneanoside A
/ (-)-Fortuneanoside A
No. 2 No. 15
C00030328 External link 512 Fortuneanoside L
/ (-)-Fortuneanoside L
No. 2 No. 15
C00030321 External link 512 Fortuneanoside D
/ (-)-Fortuneanoside D
CHEMBL526100
1 / 4 / 2 No. 122 No. 15
C00030322 External link 512 Fortuneanoside E
/ (-)-Fortuneanoside E
CHEMBL498291
1 / 4 / 2 No. 122 No. 15
C00030320 External link 512 Fortuneanoside C
/ (-)-Fortuneanoside C
CHEMBL497445
1 / 4 / 2 No. 122 No. 15
C00030319 External link 512 Fortuneanoside B
/ (-)-Fortuneanoside B
CHEMBL497444
1 / 4 / 2 No. 122 No. 15
C00030325 External link 512 Fortuneanoside I
/ (-)-Fortuneanoside I
No. 122 No. 15
C00030326 External link 512 Fortuneanoside J
/ (-)-Fortuneanoside J
No. 122 No. 15
C00030327 External link 512 Fortuneanoside K
/ (-)-Fortuneanoside K
No. 122 No. 15
C00030323 External link 512 Fortuneanoside G
/ Fortuneanoside (-)-G
No. 122 No. 15

Human Protein / Gene in interactions

1 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14679 Tyrosinase Oxidoreductase C00030319 C00030320 C00030321 C00030322 4 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679

KEGG DISEASE (2)

KEGG name UniProt
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)