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The X-linked lethal Ogden syndrome was the first reported human genetic disorder associated with a mutation in an N-terminal acetyltransferase gene. The affected males harbour a Ser37Pro mutation in the gene encoding hNaa10, the catalytic subunit of NatA, themajor human NAT. In order to understand t...
ORGANISM(S): Homo sapiens (Human) 
2016-04-12 | PXD001282 | Pride
Naa10 is a Nα-terminal acetyltransferase that, in a complex with its auxiliary subunit Naa15, co-translationally acetylates the α-amino group of newly synthetized proteins as they emerge from the ribosome. Roughly 40-50% of the human proteome is acetylated by Naa10, rendering this an enzyme with one...
ORGANISM(S): Saccharomyces cerevisiae 
2016-09-07 | GSE86466 | GEO
Gene expression microarrays accompanying "Proteomic and genomic characterization of a yeast model for Ogden syndrome" by Doerfel et al 2016 in press at Yeast. Naa10 is a Na-terminal acetyltransferase that, in a complex with its auxiliary subunit Naa15, co-translationally acetylates the a-amino group...
ORGANISM(S): Saccharomyces cerevisiae 
2016-09-03 | GSE86358 | GEO
Naa10 is a N-terminal acetyltransferase that, in a complex with its auxiliary subunit Naa15, co-translationally acetylates the -amino group of newly synthetized proteins as they emerge from the ribosome. Roughly 40-50% of the human proteome is acetylated by Naa10, rendering this an enzyme with one o...
ORGANISM(S): Saccharomyces cerevisiae (Baker's yeast) 
2016-09-28 | PXD004923 | Pride
Abstract: N-terminal acetylation (Nt-acetylation) occurs on the majority of eukaryotic proteins and is catalysed by N-terminal acetyltransferases (NATs). Nt- acetylation is increasingly recognized as a vital modification with functional implications ranging from protein degradation to protein locali...
ORGANISM(S): Saccharomyces cerevisiae (Baker's yeast) 
2014-01-29 | PXD000316 | Pride
Proteomic and genomic characterization of a yeast model for Ogden syndrome [RNA-seq and Ribo-seq]
Proteomic and genomic characterization of a yeast model for Ogden syndrome [microarray]
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