| 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)
|