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KMT5A
Protein-coding gene in humans From Wikipedia, the free encyclopedia
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N-lysine methyltransferase KMT5A is an enzyme that in humans is encoded by the KMT5A gene.[5][6][7][8] The enzyme is a histone methyltransferase, SET domain-containing and lysine-specific. The enzyme transfers one methyl group to histone H4 lysine residue at position 20. S-Adenosyl methionine (SAM) is both the cofactor and the methyl group donor. The lysine residue is converted to N6-methyllysine residue.

This histone modification is often abbreviated H4K20me1:
- H4 - type of histone
- K - symbol of lysine
- 20 - position of the lysine residue modified
- me - abbreviation for methyl group
- 1 - number of methyl groups transferred
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