Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2016 Jul 12;44(19):9231–9244. doi: 10.1093/nar/gkw630

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

PMC Copyright notice

Figure 1. — CAG codon usage in the transcriptome. (A) The CAG glutamine codon is recognised by the single copy SUP70 gene, encoding . The sup70-65 allele defines a variant lacking a base-pairing interaction at the base of the anticodon stem. (B) The sup70-65 mutation causes a pseudohyphal growth phenotype. (C) The CAG frequencies were recorded for all S. cerevisiae ORFs. (D) The cellular abundance of yeast proteins (66) was plotted against the binned proportional content of CAG codons relative to ORF length. (E) For each yeast ORF, the position of the first (5′-most) CAG codon was recorded and plotted against the cellular protein abundance.

Inline graphic — CAG codon usage in the transcriptome. (A) The CAG glutamine codon is recognised by the single copy SUP70 gene, encoding . The sup70-65 allele defines a variant lacking a base-pairing interaction at the base of the anticodon stem. (B) The sup70-65 mutation causes a pseudohyphal growth phenotype. (C) The CAG frequencies were recorded for all S. cerevisiae ORFs. (D) The cellular abundance of yeast proteins (66) was plotted against the binned proportional content of CAG codons relative to ORF length. (E) For each yeast ORF, the position of the first (5′-most) CAG codon was recorded and plotted against the cellular protein abundance.