3avs
From Proteopedia
Jump to navigationJump to search
Catalytic fragment of UTX/KDM6A bound with N-oxyalylglycine, and Ni(II)
| ||||||||||||
Structural highlights
DiseaseKDM6A_HUMAN Kabuki syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionKDM6A_HUMAN Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-27'. Plays a central role in regulation of posterior development, by regulating HOX gene expression. Demethylation of 'Lys-27' of histone H3 is concomitant with methylation of 'Lys-4' of histone H3, and regulates the recruitment of the PRC1 complex and monoubiquitination of histone H2A.[1] [2] See AlsoReferences
| ||||||||||||||||||||
This page was last modified 14:02, 13 March 2024.