EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
4.2.1.150 | additional information | generation of Cdyl transgenic mice by microinjection of a Cdyl construct into the pro-nuclei of fertilized oocytes, derived from intercross of C57BL/6 3 CBA F1 mice | Mus musculus |
EC Number | KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
4.2.1.150 | additional information | - |
additional information | steady-state kinetics of the CDYL-catalyzed hydratation reaction compared to mitochondrial metabolic enzyme enoyl-CoA hydratase (ECH, EC 4.2.1.17) as a positive control | Homo sapiens |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
4.2.1.150 | mitochondrion | - |
Homo sapiens | 5739 | - |
4.2.1.150 | mitochondrion | - |
Mus musculus | 5739 | - |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.2.1.150 | crotonyl-CoA + H2O | Homo sapiens | - |
3-hydroxybutyryl-CoA | - |
r | |
4.2.1.150 | crotonyl-CoA + H2O | Mus musculus | - |
3-hydroxybutyryl-CoA | - |
r | |
4.2.1.150 | crotonyl-CoA + H2O | Mus musculus C57BL/6 | - |
3-hydroxybutyryl-CoA | - |
r |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
4.2.1.150 | Homo sapiens | Q9Y232 | - |
- |
4.2.1.150 | Mus musculus | Q9WTK2 | - |
- |
4.2.1.150 | Mus musculus C57BL/6 | Q9WTK2 | - |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
4.2.1.150 | HeLa cell | - |
Homo sapiens | - |
4.2.1.150 | spermatid | - |
Homo sapiens | - |
4.2.1.150 | spermatid | - |
Mus musculus | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.2.1.150 | crotonyl-CoA + H2O | - |
Homo sapiens | 3-hydroxybutyryl-CoA | - |
r | |
4.2.1.150 | crotonyl-CoA + H2O | - |
Mus musculus | 3-hydroxybutyryl-CoA | - |
r | |
4.2.1.150 | crotonyl-CoA + H2O | - |
Mus musculus C57BL/6 | 3-hydroxybutyryl-CoA | - |
r |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
4.2.1.150 | CDYL | - |
Homo sapiens |
4.2.1.150 | CDYL | - |
Mus musculus |
4.2.1.150 | chromodomain Y-like protein | - |
Homo sapiens |
4.2.1.150 | chromodomain Y-like protein | - |
Mus musculus |
4.2.1.150 | crotonyl-CoA hydratase | - |
Homo sapiens |
4.2.1.150 | crotonyl-CoA hydratase | - |
Mus musculus |
4.2.1.150 | More | cf. EC 4.2.1.17 | Homo sapiens |
4.2.1.150 | More | cf. EC 4.2.1.17 | Mus musculus |
EC Number | General Information | Comment | Organism |
---|---|---|---|
4.2.1.150 | evolution | the C-terminal CoAP domain of the CDY family proteins including CDYL has a three-dimensional structure closely resembling enoyl-CoA hydratase, which catalyzes the hydratation of 2-trans-enoyl-CoA into beta-hydroxyacyl-CoA in mitochondria during beta-oxidation of fatty acids | Homo sapiens |
4.2.1.150 | evolution | the C-terminal CoAP domain of the CDY family proteins including CDYL has a three-dimensional structure closely resembling enoyl-CoA hydratase, which catalyzes the hydratation of 2-trans-enoyl-CoA into beta-hydroxyacyl-CoA in mitochondria during beta-oxidation of fatty acids | Mus musculus |
4.2.1.150 | malfunction | Cdyl knockout mice are embryonically lethal or died shortly after birth with significantly reduced levels of histone Kcr in elongating spermatids from Cdyl transgenic mice compared to that from wild-type mice, although the level of histone acetylation is comparable | Mus musculus |
4.2.1.150 | malfunction | the levels of total histone Kcr and H2BK12cr on the promoter of known CDYL target genes BDNF, NEUROD1, SCG10, and MYT1 increase significantly in CDYL-KO HeLa cells, whereas the regional level of H3K27me3 in these cells decreases, expression patterns, overview | Homo sapiens |
4.2.1.150 | additional information | both the chromodomain and CoAP domain of CDYL are required for its negative regulation of histone Kcr | Homo sapiens |
4.2.1.150 | additional information | both the chromodomain and CoAP domain of CDYL are required for its negative regulation of histone Kcr | Mus musculus |
4.2.1.150 | physiological function | the chromodomain Y-like protein CDYL acts as a crotonyl-CoA hydratase to negatively regulate histone crotonylation. The chromodomain Y-like transcription corepressor CDYL negatively regulates histone Kcr by acting as a crotonyl-CoA hydratase to convert crotonyl-CoA to beta-hydroxybutyryl-CoA. This activity is intrinsically linked to the transcription repression function of CDYL and is implemented in reactivation of sex chromosome-linked genes and histone replacement during spermatogenesis. The negative regulation of histone Kcr by CDYL is intrinsically linked to its transcription repression activity and functionally implemented in the reactivation of sex chromosome-linked genes in round spermatids and genome-wide histone replacement in elongating spermatids | Mus musculus |
4.2.1.150 | physiological function | the chromodomain Y-like protein CDYL acts as a crotonyl-CoA hydratase to negatively regulate histone crotonylation. The chromodomain Y-like transcription corepressor CDYL negatively regulates histone Kcr by acting as a crotonyl-CoA hydratase to convert crotonyl-CoA to beta-hydroxybutyryl-CoA. This activity is intrinsically linked to the transcription repression function of CDYL and is implemented in reactivation of sex chromosome-linked genes and histone replacement during spermatogenesis. The negative regulation of histone Kcr by CDYL is intrinsically linked to its transcription repression activity and functionally implemented in the reactivation of sex chromosome-linked genes in round spermatids and genome-wide histone replacement in elongating spermatids. Cdyl regulates the expression of sex chromosome-linked escaped genes in postmeiotic spermatogenic cells by mainly influencing histone Kcr on the gene promoters. The enzyme is important in the physiology of male reproduction and the mechanism of the spermatogenic failure in AZFc (azoospermia factor c)-deleted infertile men | Homo sapiens |