Protein | Synonyms | Taxonomy |
L-serine dehydratase/L-threonine deaminase | SDH; EC 4.3.1.17; L-serine deaminase; L-threonine dehydratase; TDH; 4.3.1.19 | Homo sapiens (human) |
Serine dehydratase-like | L-serine deaminase; L-serine dehydratase/L-threonine deaminase; L-threonine dehydratase; TDH; 4.3.1.19; Serine dehydratase 2; SDH 2; 4.3.1.17 | Homo sapiens (human) |
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial | AKB ligase; EC 2.3.1.29; Aminoacetone synthase; Glycine acetyltransferase | Homo sapiens (human) |
2-iminobutanoate/2-iminopropanoate deaminase | EC 3.5.99.10; 14.5 kDa translational inhibitor protein; hp14.5; p14.5; Heat-responsive protein 12; Reactive intermediate imine deaminase A homolog; Translation inhibitor L-PSP ribonuclease; UK114 antigen homolog | Homo sapiens (human) |
Inactive L-threonine 3-dehydrogenase, mitochondrial | Short chain dehydrogenase/reductase family 14E member 1 pseudogene | Homo sapiens (human) |
Compound | Description |
hydronium ion | |
NADH | |
ammonium hydroxide | The hydroxy salt of ammonium ion. It is formed when AMMONIA reacts with water molecules in solution. |
Water | A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) |
nad | A coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. It is found widely in nature and is involved in numerous enzymatic reactions in which it serves as an electron carrier by being alternately oxidized (NAD+) and reduced (NADH). (Dorland, 27th ed) |
adenosine triphosphate | An adenine nucleotide containing three phosphate groups esterified to the sugar moiety. In addition to its crucial roles in metabolism adenosine triphosphate is a neurotransmitter. |
alpha-ketobutyric acid | RN given refers to parent cpd; structure |
Coenzyme A | |
Acetyl Coenzyme A | Acetyl CoA participates in the biosynthesis of fatty acids and sterols, in the oxidation of fatty acids and in the metabolism of many amino acids. It also acts as a biological acetylating agent. |