Species

KNApSAcK Entry

Organism name Phyllanthus brasiliensis
Genus Phyllanthus
Family Phyllanthaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Phyllanthaceae
Linked NCBI taxonomy ID 233880
Linked level family

Family

Family in NCBI taxonomy Phyllanthaceae
ID 233880

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (1)

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
C00011910 External link 512 Phyllanthoside
CHEMBL510962
CHEMBL1722641
C014754
6 / 11 / 4 No. 2124

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00011910 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00011910 2 / 0
O75496 Geminin Unclassified protein C00011910 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00011910 7 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00011910 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00011910 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114500 Colorectal cancer; crc P84022
#137800 Glioma susceptibility 1; glm1 O75874
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (4)

KEGG name UniProt
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)