Disease:Chromosomal aberrations involving NCOA2 may be a cause of acute myeloid leukemias. Inversion inv (8) (p11;q13) generates the MYST3-NCOA2 oncogene , which consists of the N-terminus part of MYST3/MOZ and the C-terminus part of NCOA2/TIF2. MYST3-NCOA2 binds to CREBBP and disrupts its function in transcription activation. ,Domain:Contains 2 C-terminal transcription activation domains (AD1 and AD2) that can function independently. ,Domain:Contains four Leu-Xaa-Xaa-Leu-Leu (LXXLL) motifs. The LXXLL motifs are essential for the association with nuclear receptors and are , at least in part , functionally redundant. ,Domain:The LLXXLXXXL motif is involved in transcriptional coactivation and CREBBP/CBP binding. ,Function:Transcriptional coactivator for steroid receptors and nuclear receptors. Coactivator of the steroid binding domain (AF-2) but not of the modulating N-terminal domain (AF-1) . Required with NCOA1 to control energy balance between white and brown adipose tissues. ,PTM:Phosphorylated upon DNA damage , probably by ATM or ATR. ,similarity:Belongs to the SRC/p160 nuclear receptor coactivator family. ,similarity:Contains 1 basic helix-loop-helix (bHLH) domain. ,similarity:Contains 1 PAS (PER-ARNT-SIM) domain. ,subunit:Present in a complex containing CARM1 and EP300/P300 , and interacts with CARM1 and NR3C2 (By similarity) . Present in a complex containing NCOA3 , IKKA , IKKB , IKBKG and CREBBP. Interacts (via C-terminus) with CREBBP. Interacts with HIF1A , NCOA1 , APEX and NR3C1. Interacts with CASP8AP2 and TTLL5/STAMP. Interacts with ESR1 , RARA and RXRA. ,
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