Organism name | Astragalus spp. |
---|---|
Genus | Astragalus |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Astragalus |
---|---|
Linked NCBI taxonomy ID | 20400 |
Linked level | genus |
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 |
---|---|---|---|---|---|---|---|---|
C00010161
![]() |
7,2'-Dihydroxy-3',4'-dimethoxyisoflavone 7-O-glucoside
|
No. 2 | No. 15 |
![]() |
||||
C00005134
![]() |
Kaempferol 3-xyloside
|
CHEMBL518420
CHEMBL477730 |
No. 2 | 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 |
![]() |
C00009715
![]() |
(+-)-Mucronulatol
/ 7,3'-Dihydroxy-2',4'-dimethoxyisoflavan |
CHEMBL253474
CHEMBL478971 CHEMBL1087024 |
5 / 1 / 0 | No. 73 | No. 15 |
![]() |
||
C00002075
![]() |
Swainsonine
/ (-)-Swainsonine |
CHEMBL63139
CHEMBL292716 CHEMBL302300 CHEMBL65098 CHEMBL371197 |
D017026
|
4 / 2 / 4 | No. 677 | No. 2 |
![]() |
|
C00002050
![]() |
Lentiginosine
|
CHEMBL63254
|
C063984
|
No. 677 | No. 2 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UNA4 | DNA polymerase iota | Enzyme | C00005138 C00009715 | 0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00009715 | 0 / 0 |
P43403 | Tyrosine-protein kinase ZAP-70 | Syk | C00002075 | 1 / 2 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005138 | 0 / 0 |
O43561 | Linker for activation of T-cells family member 1 | Unclassified protein | C00002075 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00009715 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00005138 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00009715 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00005138 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005138 | 0 / 0 |
P14679 | Tyrosinase | Oxidoreductase | C00005138 | 4 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00005138 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00005138 | 1 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005138 | 0 / 0 |
P06239 | Tyrosine-protein kinase Lck | Src | C00002075 | 0 / 1 |
O00754 | Lysosomal alpha-mannosidase | Enzyme | C00002075 | 1 / 2 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00009715 | 1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00005138 | 0 / 3 |
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
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#248500 | Mannosidosis, alpha b, lysosomal; mansa |
O00754
|
#269840 | Selective t-cell defect; stcd |
P43403
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00139 | alpha-Mannosidosis |
O00754
(related)
|
H00422 | Glycoproteinoses |
O00754
(related)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00093 | Combined immunodeficiencies (CIDs) |
P06239
(related)
P43403 (related) |
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
P43403
(marker)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|