Organism name | Tephrosia obovata |
---|---|
Genus | Tephrosia |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Tephrosia obovata |
---|---|
Linked NCBI taxonomy ID | 185973 |
Linked level | species |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
C00008431
![]() |
Obovatin
|
CHEMBL1689204
|
No. 127 | No. 14 |
![]() |
|||
C00007084
![]() |
Pongachalcone I
|
No. 130 |
![]() |
|||||
C00002580
![]() |
Toxicarol
/ Toxicarin / alpha-Toxicarol |
CHEMBL508992
CHEMBL1488225 |
10 / 9 / 6 | No. 589 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00002580 | 4 / 1 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00002580 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002580 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002580 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00002580 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002580 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002580 | 0 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002580 | 4 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002580 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002580 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|