PCIDB

Teucridium parvifolium

Species

KNApSAcK Entry

Organism name Teucridium parvifolium
Genus Teucridium
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Teucridium parvifolium
Linked NCBI taxonomy ID 54474
Linked level species

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (4)

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
C00004205 External link 512 Linarin
/ Buddleoflavonoloside
/ Acacetin 7-rutinoside
/ Acacetin 7-O-rutinoside
CHEMBL447738
CHEMBL509502
CHEMBL601333
CHEMBL1357379
C008282
1 / 2 / 2 No. 1 No. 15
C00004240 External link 512 Pectolinarigenin 7-rutinoside
/ Pectolinarigenin 7-O-rutinoside
CHEMBL445978
CHEMBL1515284
C052786
2 / 0 / 0 No. 1 No. 15
C00006229 External link 512 Vicenin 2
/ Apigenin 6,8-di-C-glucoside
CHEMBL1442950
6 / 14 / 8 No. 1 No. 15
C00013638 External link 512 Scutellarein 4'-methyl ether 7-rutinoside
/ 7-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-5,6-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
No. 1 No. 15

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004240 C00006229 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00004205 2 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00006229 7 / 3
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00004240 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00006229 1 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00006229 0 / 0
P04062 Glucosylceramidase Enzyme C00006229 6 / 4
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00006229 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (16)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#119900 Digital clubbing, isolated congenital P15428
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#232300 Glycogen storage disease ii P10253
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#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 (10)

KEGG name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)