Sauropus androgynus
Species
KNApSAcK Entry
| Organism name | Sauropus androgynus |
|---|---|
| Genus | Sauropus |
| Family | Phyllanthaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Sauropus androgynus |
|---|---|
| Linked NCBI taxonomy ID | 283133 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Phyllanthaceae |
|---|---|
| ID | 233880 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | rosids |
|---|---|
| ID | 71275 |
Metabolite list (3)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00000723
|
Liriodendrin
/ Acanthoside D / (+)-Syringaresinol di-O-beta-glucopyranoside |
CHEMBL446836
CHEMBL505393 |
2 / 2 / 2 | No. 152 |
|
|||
|
C00032855
|
Corchoionoside C
/ (+)-Corchoionoside C |
CHEMBL444196
CHEMBL482383 CHEMBL520291 CHEMBL465921 |
No. 225 |
|
||||
|
C00019679
|
Guanosine
/ 9-beta-D-Ribofuranosylguanine |
CHEMBL278434
CHEMBL375655 CHEMBL240933 CHEMBL607672 CHEMBL2021379 CHEMBL2093064 |
D006151
|
5 / 4 / 4 | 3 / 0 | No. 1761 |
|
Human Protein / Gene in interactions
7 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P23526 | Adenosylhomocysteinase | Enzyme | C00019679 | 1 / 1 |
| P00492 | Hypoxanthine-guanine phosphoribosyltransferase | Enzyme | C00019679 | 2 / 1 |
| P04183 | Thymidine kinase, cytosolic | Enzyme | C00019679 | 0 / 1 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00000723 | 2 / 2 |
| O75496 | Geminin | Unclassified protein | C00000723 | 0 / 0 |
| O00142 | Thymidine kinase 2, mitochondrial | Enzyme | C00019679 | 1 / 1 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00019679 | 0 / 0 |
3 Gene in CTD interactions
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 5594 | MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk | mitogen-activated protein kinase 1 (EC:2.7.11.24) |
C00019679
|
| 5595 | MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK | mitogen-activated protein kinase 3 (EC:2.7.11.24) |
C00019679
|
| 55315 | SLC29A3, ENT3, HCLAP, HJCD, PHID | solute carrier family 29 (equilibrative nucleoside transporter), member 3 |
C00019679
|
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (6)
| OMIM | preferred title | UniProt |
|---|---|---|
| #613752 | Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency |
P23526
|
| #300323 | Kelley-seegmiller syndrome |
P00492
|
| #300322 | Lesch-nyhan syndrome; lns |
P00492
|
| #609560 | Mitochondrial dna depletion syndrome 2 (myopathic type); mtdps2 |
O00142
|
| #257200 | Niemann-pick disease, type a |
P17405
|
| #607616 | Niemann-pick disease, type b |
P17405
|
KEGG DISEASE (6)
| KEGG | name | UniProt |
|---|---|---|
| H00469 | Mitochondrial DNA depletion syndrome (MDS) |
O00142
(related)
|
| H00194 | Lesch-Nyhan syndrome |
P00492
(related)
|
| H00005 | Chronic lymphocytic leukemia (CLL) |
P04183
(marker)
|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
| H00184 | Hypermethioninemia |
P23526
(related)
|