| 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)
|