Process View
The chemical reactions and pathways involving any amino acid that requires pyruvate for its synthesis, e.g. alanine.
In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "pyruvate family amino acid metabolic process"
Name | Description | Probability | Func Analog Organism | |
---|---|---|---|---|
ALDOB | aldolase B, fructose-bisphosphate | 0.998 | ||
MASP2 | mannan-binding lectin serine peptidase 2 | 0.249 | ||
CYP2E1 | cytochrome P450, family 2, subfamily E, polypeptide 1 | 0.209 | ||
HNF4A | hepatocyte nuclear factor 4, alpha | 0.107 | ||
HAAO | 3-hydroxyanthranilate 3,4-dioxygenase | 0.073 | ||
PHGDH | phosphoglycerate dehydrogenase | 0.032 | ||
ALDH1L1 | aldehyde dehydrogenase 1 family, member L1 | 0.027 | ||
GCGR | glucagon receptor | 0.027 | ||
IGFALS | insulin-like growth factor binding protein, acid labile subunit | 0.025 | ||
CYP2A6 | cytochrome P450, family 2, subfamily A, polypeptide 6 | 0.020 | ||
CYP1A2 | cytochrome P450, family 1, subfamily A, polypeptide 2 | 0.017 | ||
SLC22A7 | solute carrier family 22 (organic anion transporter), member 7 | 0.017 | ||
C8G | complement component 8, gamma polypeptide | 0.015 | ||
CYP2C9 | cytochrome P450, family 2, subfamily C, polypeptide 9 | 0.015 | ||
SLC28A1 | solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 | 0.014 | ||
SLC22A1 | solute carrier family 22 (organic cation transporter), member 1 | 0.013 | ||
BBS1 | Bardet-Biedl syndrome 1 | 0.013 | ||
CYP3A43 | cytochrome P450, family 3, subfamily A, polypeptide 43 | 0.012 | ||
NR1I3 | nuclear receptor subfamily 1, group I, member 3 | 0.012 | ||
PCK2 | phosphoenolpyruvate carboxykinase 2 (mitochondrial) | 0.011 | ||
MAT1A | methionine adenosyltransferase I, alpha | 0.010 | ||
ADH6 | alcohol dehydrogenase 6 (class V) | 0.010 | ||
EIF4EBP1 | eukaryotic translation initiation factor 4E binding protein 1 | 0.010 | ||
AGXT | alanine-glyoxylate aminotransferase | 0.010 |