ARD1/YHR013C Literature Guide Help

Other names published for ARD1: NAA10, YHR013C

ARD1 - Strains/Constructs (23)

ReferenceOther Genes Addressed
Foyn H, et al.  (2013) Protein N-terminal acetyltransferases act as N-terminal propionyltransferases in vitro and in vivo. Mol Cell Proteomics 12(1):42-54
Milliman EJ, et al.  (2012) Recruitment of rpd3 to the telomere depends on the protein arginine methyltransferase hmt1. PLoS One 7(8):e44656
Zill OA, et al.  (2012) Evolutionary analysis of heterochromatin protein compatibility by interspecies complementation in Saccharomyces. Genetics 192(3):1001-14
Scott DC, et al.  (2011) N-terminal acetylation acts as an avidity enhancer within an interconnected multiprotein complex. Science 334(6056):674-8
Hwang CS, et al.  (2010) N-terminal acetylation of cellular proteins creates specific degradation signals. Science 327(5968):973-7
Arnesen T, et al.  (2009) Proteomics analyses reveal the evolutionary conservation and divergence of N-terminal acetyltransferases from yeast and humans. Proc Natl Acad Sci U S A 106(20):8157-62
Pezza JA, et al.  (2009) The NatA acetyltransferase couples Sup35 prion complexes to the [PSI+] phenotype. Mol Biol Cell 20(3):1068-80
Polevoda B, et al.  (2009) Properties of Nat4, an Nalpha-acetyltransferase of Saccharomyces cerevisiae that modifies N termini of histones H2A and H4. Mol Cell Biol 29(11):2913-24
Aragon AD, et al.  (2008) Characterization of differentiated quiescent and nonquiescent cells in yeast stationary-phase cultures. Mol Biol Cell 19(3):1271-80
Fiechter V, et al.  (2008) The evolutionary conserved BER1 gene is involved in microtubule stability in yeast. Curr Genet 53(2):107-15
Mozdy AD, et al.  (2008) Multiple yeast genes, including Paf1 complex genes, affect telomere length via telomerase RNA abundance. Mol Cell Biol 28(12):4152-61
Polevoda B, et al.  (2008) Yeast N(alpha)-terminal acetyltransferases are associated with ribosomes. J Cell Biochem 103(2):492-508
Jiang L, et al.  (2007) Global assessment of combinatorial post-translational modification of core histones in yeast using contemporary mass spectrometry. LYS4 trimethylation correlates with degree of acetylation on the same H3 tail. J Biol Chem 282(38):27923-34
Onishi M, et al.  (2007) Role of the Conserved Sir3-BAH Domain in Nucleosome Binding and Silent Chromatin Assembly. Mol Cell 28(6):1015-28
Raue U, et al.  (2007) Association of protein biogenesis factors at the yeast ribosomal tunnel exit is affected by the translational status and nascent polypeptide sequence. J Biol Chem 282(11):7809-16
Connelly JJ, et al.  (2006) Structure and function of the Saccharomyces cerevisiae Sir3 BAH domain. Mol Cell Biol 26(8):3256-65
Gatbonton T, et al.  (2006) Telomere length as a quantitative trait: genome-wide survey and genetic mapping of telomere length-control genes in yeast. PLoS Genet 2(3):e35
Tong AH, et al.  (2004) Global mapping of the yeast genetic interaction network. Science 303(5659):808-13
Gautschi M, et al.  (2003) The yeast N(alpha)-acetyltransferase NatA is quantitatively anchored to the ribosome and interacts with nascent polypeptides. Mol Cell Biol 23(20):7403-14
Arnold RJ, et al.  (1999) The action of N-terminal acetyltransferases on yeast ribosomal proteins. J Biol Chem 274(52):37035-40
Mastrangelo MF, et al.  (1992) Disruption of a silencer domain by a retrotransposon. Genetics 131(3):519-29
Mullen JR, et al.  (1989) Identification and characterization of genes and mutants for an N-terminal acetyltransferase from yeast. EMBO J 8(7):2067-75
Whiteway M and Szostak JW  (1985) The ARD1 gene of yeast functions in the switch between the mitotic cell cycle and alternative developmental pathways. Cell 43(2 Pt 1):483-92