PCIDB

Abuta pahni (Martius) Krukoff & Barneby

Species

KNApSAcK Entry

Organism name Abuta pahni (Martius) Krukoff & Barneby
Genus Abuta
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Abuta
Linked NCBI taxonomy ID 341012
Linked level genus

Family

Family in NCBI taxonomy Menispermaceae
ID 3455

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

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
C00025606 External link 512 Daurisoline
/ (-)-Daurisoline
/ (R,R)-Daurisoline
CHEMBL2216904
C023968
1 / 2 / 2 No. 89 No. 4
C00025652 External link 512 d-Coclaurine
/ Sanjoinine K
/ (R)-Coclaurine
/ (+)-Coclaurine
/ (+)-R-Coclaurine
CHEMBL256448
CHEMBL453291
CHEMBL446211
8 / 17 / 10 No. 253 No. 4
C00025272 External link 512 Stepharine
/ (+)-Stepharine
CHEMBL463957
CHEMBL1975436
C009320
No. 688
C00026064 External link 512 Thalifoline
CHEMBL1813177
No. 2199

Human Protein / Gene in interactions

9 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14618 Pyruvate kinase PKM Enzyme C00025652 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00025606 2 / 2
P04062 Glucosylceramidase Enzyme C00025652 6 / 4
O75496 Geminin Unclassified protein C00025652 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00025652 7 / 3
P10636 Microtubule-associated protein tau Unclassified protein C00025652 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00025652 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00025652 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00025652 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#600274 Frontotemporal dementia; ftd P10636
#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
#613688 Long qt syndrome 2; lqt2 Q12809
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#609620 Short qt syndrome 1; sqt1 Q12809
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (12)

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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)