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Mol Gen Genet. 1995 Mar 20;246(6):723-8
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Protein Sci. 1995 Aug;4(8):1618-32
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J Biol Chem. 1997 Feb 28;272(9):5571-8
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Genes Cells. 1996 Oct;1(10):923-42
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Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4289-94
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Curr Opin Genet Dev. 1997 Apr;7(2):182-91
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GCN5-related histone N-acetyltransferases belong to a diverse superfamily that includes the yeast SPT10 protein.
Trends Biochem Sci. 1997 May;22(5):154-5
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Genes Dev. 1997 Jul 1;11(13):1640-50
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Cell. 1997 Aug 8;90(3):569-80
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Genetics. 1997 Oct;147(2):451-65
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Mol Cell Biol. 1997 Nov;17(11):6212-22
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Trends Genet. 1997 Nov;13(11):427-9
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Mol Cell Biol. 1997 Jun;17(6):3220-8
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Genes Dev. 1996 Apr 15;10(8):905-20
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Structure/functional properties of the yeast dual regulator protein NGG1 that are required for glucose repression.
J Biol Chem. 1996 Apr 19;271(16):9298-306
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Structural and functional analysis of yeast putative adaptors. Evidence for an adaptor complex in vivo.
J Biol Chem. 1996 Mar 1;271(9):5237-45
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Repression domain of the yeast global repressor Tup1 interacts directly with histones H3 and H4.
Genes Dev. 1996 May 15;10(10):1247-59
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ADA5/SPT20 links the ADA and SPT genes, which are involved in yeast transcription.
Mol Cell Biol. 1996 Jun;16(6):3197-205
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SPT20/ADA5 encodes a novel protein functionally related to the TATA-binding protein and important for transcription in Saccharomyces cerevisiae.
Mol Cell Biol. 1996 Jun;16(6):3206-13
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Active barnase variants with completely random hydrophobic cores.
Proc Natl Acad Sci U S A. 1996 May 28;93(11):5590-4
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Structure and critical residues at the active site of spermidine/spermine-N1-acetyltransferase.
Biochem J. 1996 Jun 15;316 ( Pt 3):697-701
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Transcriptional activation by yeast PDR1p is inhibited by its association with NGG1p/ADA3p.
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Special HATs for special occasions: linking histone acetylation to chromatin assembly and gene activation.
Curr Opin Genet Dev. 1996 Apr;6(2):176-84
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Cell. 1996 Jul 12;86(1):13-9
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A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A.
Nature. 1996 Jul 25;382(6589):319-24
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Efficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation pattern.
Mol Cell Biol. 1996 Aug;16(8):4349-56
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RGFGIGS is an amino acid sequence required for acetyl coenzyme A binding and activity of human spermidine/spermine N1acetyltransferase.
J Biol Chem. 1996 Aug 2;271(31):18920-4
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Yeast SAS silencing genes and human genes associated with AML and HIV-1 Tat interactions are homologous with acetyltransferases.
Nat Genet. 1996 Sep;14(1):42-9
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Transcription-linked acetylation by Gcn5p of histones H3 and H4 at specific lysines.
Nature. 1996 Sep 19;383(6597):269-72
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Searching databases of conserved sequence regions by aligning protein multiple-alignments.
Nucleic Acids Res. 1996 Oct 1;24(19):3836-45
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Remodeling chromatin structures for transcription: what happens to the histones?
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The transcriptional coactivators p300 and CBP are histone acetyltransferases.
Cell. 1996 Nov 29;87(5):953-9
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ADR1 activation domains contact the histone acetyltransferase GCN5 and the core transcriptional factor TFIIB.
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The CBP co-activator is a histone acetyltransferase.
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Mol Cell Biol. 1997 Jan;17(1):519-27
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The TAF(II)250 subunit of TFIID has histone acetyltransferase activity.
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Improved shuttle vectors for cloning and high-level Cu(2+)-mediated expression of foreign genes in yeast.
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MAK3 encodes an N-acetyltransferase whose modification of the L-A gag NH2 terminus is necessary for virus particle assembly.
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