Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
3 S-adenosyl-L-methionine + a [histone H3]-L-lysine36 | Mus musculus | overall reaction | 3 S-adenosyl-L-homocysteine + a [histone H3]-N6,N6,N6-trimethyl-L-lysine36 | - |
? | |
S-adenosyl-L-methionine + a [histone H3]-L-lysine36 | Mus musculus | - |
S-adenosyl-L-homocysteine + a [histone H3]-N6-methyl-L-lysine36 | - |
? | |
S-adenosyl-L-methionine + a [histone H3]-N6,N6-dimethyl-L-lysine36 | Mus musculus | - |
S-adenosyl-L-homocysteine + a [histone H3]-N6,N6,N6-trimethyl-L-lysine36 | - |
? | |
S-adenosyl-L-methionine + a [histone H3]-N6-methyl-L-lysine36 | Mus musculus | - |
S-adenosyl-L-homocysteine + a [histone H3]-N6,N6-dimethyl-L-lysine36 | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Mus musculus | Q8BVE8 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
embryo | - |
Mus musculus | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
3 S-adenosyl-L-methionine + a [histone H3]-L-lysine36 | overall reaction | Mus musculus | 3 S-adenosyl-L-homocysteine + a [histone H3]-N6,N6,N6-trimethyl-L-lysine36 | - |
? | |
S-adenosyl-L-methionine + a [histone H3]-L-lysine36 | - |
Mus musculus | S-adenosyl-L-homocysteine + a [histone H3]-N6-methyl-L-lysine36 | - |
? | |
S-adenosyl-L-methionine + a [histone H3]-N6,N6-dimethyl-L-lysine36 | - |
Mus musculus | S-adenosyl-L-homocysteine + a [histone H3]-N6,N6,N6-trimethyl-L-lysine36 | - |
? | |
S-adenosyl-L-methionine + a [histone H3]-N6-methyl-L-lysine36 | - |
Mus musculus | S-adenosyl-L-homocysteine + a [histone H3]-N6,N6-dimethyl-L-lysine36 | - |
? |
Synonyms | Comment | Organism |
---|---|---|
H3K36 trimethyltransferase | - |
Mus musculus |
Whsc1 | - |
Mus musculus |
General Information | Comment | Organism |
---|---|---|
malfunction | enzyme mutations are associated with Wolf-Hirschhorn syndrome, which is characterized by skeletal abnormalities. Enzyme-deficient embryos exhibit defects in ossification in the occipital bone and sternum. Enzyme knockdown in pre-osteoblast cells perturbs histone modification patterns in bone-related genes and leads to defects in bone differentiation | Mus musculus |
physiological function | the enzyme regulates gene expression through Runt-related transcription factor 2, a transcription factor central to bone development, and p300, a histone acetyltransferase, to promote bone differentiation. The enzyme fine-tunes the expression of bone-related genes by acting as a modulator in balancing histone H3 lysine 36 trimethylation and histone acetylation. The enzyme is involved in osteoblast differentiation but not proliferation | Mus musculus |