乙酰化
辅因子
赖氨酸
辅酶A
化学
组蛋白
辅活化剂
立体化学
基质(水族馆)
酰基辅酶A
生物化学
活动站点
酶
P300-CBP转录因子
结合位点
氨基酸
生物
组蛋白乙酰转移酶
还原酶
DNA
基因
转录因子
生态学
作者
Zuzanna Kaczmarska,Esther Ortega,Afsaneh Goudarzi,He Huang,S.‐H. KIM,José Antonio Márquez,Yingming Zhao,Saadi Khochbin,Daniel Panne
标识
DOI:10.1038/nchembio.2217
摘要
Histone acetylation plays an important role in transcriptional activation. Histones are also modified by chemically diverse acylations that are frequently deposited by p300, a transcriptional coactivator that uses a number of different acyl-CoA cofactors. Here we report that while p300 is a robust acetylase, its activity gets weaker with increasing acyl-CoA chain length. Crystal structures of p300 in complex with propionyl-, crotonyl-, or butyryl-CoA show that the aliphatic portions of these cofactors are bound in the lysine substrate-binding tunnel in a conformation that is incompatible with substrate transfer. Lysine substrate binding is predicted to remodel the acyl-CoA ligands into a conformation compatible with acyl-chain transfer. This remodeling requires that the aliphatic portion of acyl-CoA be accommodated in a hydrophobic pocket in the enzymes active site. The size of the pocket and its aliphatic nature exclude long-chain and charged acyl-CoA variants, presumably explaining the cofactor preference for p300.
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