Organism name | Lupinus albus L. |
---|---|
Genus | Lupinus |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Lupinus albus |
---|---|
Linked NCBI taxonomy ID | 3870 |
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 |
---|---|---|---|---|---|---|---|---|
C00036495
![]() |
2'-Hydroxygenistein 7,4'-O-diglucoside
|
No. 1 | No. 15 |
![]() |
||||
C00010106
![]() |
Genistein 7,4'-O-diglucoside
/ Genistein 7,4'-di-O-glucoside / Genistein-7,4'-di-O-beta-glucopyranoside |
No. 1 | No. 15 |
![]() |
||||
C00005138
![]() |
Astragalin
/ Kaempferol 3-glucoside / Kaempferol 3-O-beta-D-glucoside / Kaempferol 3-O-beta-D-glucopyranoside |
CHEMBL233930
CHEMBL453290 CHEMBL1572115 |
C001579
|
10 / 6 / 7 | 0 / 1 | No. 2 | No. 15 |
![]() |
C00005137
![]() |
Trifolin
/ Kaempferol 3-O-beta-D-galactopyranoside |
CHEMBL233930
CHEMBL453290 CHEMBL1572115 |
C066407
|
10 / 6 / 7 | 1 / 1 | No. 2 | No. 15 |
![]() |
C00010119
![]() |
Oroboside
/ Orobol 7-O-glucoside |
No. 2 | No. 15 |
![]() |
||||
C00005525
![]() |
Isorhamnetin 3-glucoside
/ Isorhamnetin 3-O-glucoside / Isorhamnetin 3-O-beta-D-glucoside / Isorhamnetin 3-O-beta-D-glucopyranoside |
CHEMBL234316
CHEMBL516621 |
1 / 1 / 0 | No. 2 | No. 15 |
![]() |
||
C00001017
![]() |
Cosmosiin
/ Apigenin 7-glucoside / (-)-Apigenin 7-glucoside / Apigenin 7-O-beta-D-glucopyranoside |
CHEMBL487995
CHEMBL487017 CHEMBL1591566 CHEMBL2165585 |
C057792
|
5 / 6 / 1 | No. 2 | No. 15 |
![]() |
|
C00009453
![]() |
2'-Hydroxygenistein
|
CHEMBL6665
|
8 / 6 / 5 | No. 71 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005137 C00005138 C00009453 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00005137 C00005138 C00009453 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005137 C00005138 C00009453 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00005137 C00005138 C00009453 | 1 / 1 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005137 C00005138 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005137 C00005138 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00005137 C00005138 | 0 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00005137 C00005138 | 0 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00001017 C00009453 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00005137 C00005138 | 1 / 1 |
P14679 | Tyrosinase | Oxidoreductase | C00005137 C00005138 | 4 / 2 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00001017 | 0 / 0 |
Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00001017 | 2 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001017 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00009453 | 1 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00009453 | 4 / 3 |
P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00005525 | 1 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00009453 | 0 / 0 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00001017 | 4 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
5320 | PLA2G2A, MOM1, PLA2, PLA2B, PLA2L, PLA2S, PLAS1, sPLA2 | phospholipase A2, group IIA (platelets, synovial fluid) (EC:3.1.1.4) |
C00005137
|
OMIM | preferred title | UniProt |
---|---|---|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#614490 | Blood group, junior system; jr |
Q9UNQ0
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#614674 | Periodic fever, menstrual cycle-dependent |
P08908
|
#172700 | Pick disease of brain |
P10636
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|