Species

KNApSAcK Entry

Organism name Convolvulus subhirsutus
Genus Convolvulus
Family Convolvulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Convolvulus
Linked NCBI taxonomy ID 4122
Linked level genus

Family

Family in NCBI taxonomy Convolvulaceae
ID 4118

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

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
C00002287 External link 512 Convolamine
CHEMBL1514821
CHEMBL1907009
5 / 2 / 3 No. 1355 No. 1
C00002298 External link 512 Phyllalbine
CHEMBL1375175
CHEMBL1555308
CHEMBL2165592
9 / 10 / 8 No. 1355 No. 1

Human Protein / Gene in interactions

9 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002287 C00002298 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002287 C00002298 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002287 C00002298 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002287 C00002298 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002287 C00002298 0 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002298 1 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002298 0 / 0
O75496 Geminin Unclassified protein C00002298 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002298 7 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (10)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#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

KEGG DISEASE (8)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)