KMT5A

KMT5A
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKMT5A, PR-Set7, SET07, SET8, SETD8, lysine methyltransferase 5A, PR/SET07
External IDsOMIM: 607240; MGI: 1915206; HomoloGene: 41372; GeneCards: KMT5A; OMA:KMT5A - orthologs
EC number2.1.1.354
Orthologs
SpeciesHumanMouse
Entrez

387893

67956

Ensembl

ENSG00000183955

ENSMUSG00000049327

UniProt

Q9NQR1

Q2YDW7

RefSeq (mRNA)

NM_030241
NM_001310723
NM_001310725
NM_001310727

RefSeq (protein)
Location (UCSC)Chr 12: 123.38 – 123.41 MbChr 5: 124.58 – 124.6 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

N-lysine methyltransferase KMT5A is an enzyme that in humans is encoded by the KMT5A gene. 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