Structural basis of lysine-acetylated HIV-1 Tat recognition by PCAF bromodomain.

Article Details

Citation

Mujtaba S, He Y, Zeng L, Farooq A, Carlson JE, Ott M, Verdin E, Zhou MM

Structural basis of lysine-acetylated HIV-1 Tat recognition by PCAF bromodomain.

Mol Cell. 2002 Mar;9(3):575-86.

PubMed ID
11931765 [ View in PubMed
]
Abstract

The human immunodeficiency virus type 1 (HIV-1) trans-activator protein Tat stimulates transcription of the integrated HIV-1 genome and promotes viral replication in infected cells. Tat transactivation activity is dependent on lysine acetylation and its association with nuclear histone acetyltransferases p300/CBP (CREB binding protein) and p300/CBP-associated factor (PCAF). Here, we show that the bromodomain of PCAF binds specifically to HIV-1 Tat acetylated at lysine 50 and that this interaction competes effectively against HIV-1 TAR RNA binding to the lysine-acetylated Tat. The three-dimensional solution structure of the PCAF bromodomain in complex with a lysine 50-acetylated Tat peptide together with biochemical analyses provides the structural basis for the specificity of this molecular recognition and reveals insights into the differences in ligand selectivity of bromodomains.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Histone acetyltransferase KAT2BQ92831Details