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

. 2020 Jun 19;11:3145. doi: 10.1038/s41467-020-16784-7

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

© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Fig. 1 — A diverse array of MS datasets for H. volcanii has been compiled for the initial reanalysis by the ArcPP. For each dataset, strains (separated by comma), cellular fractions (Mem, membrane; Cyt, cytosol; SN, culture supernatant, TCE, total cell extract), growth conditions (stat, stationary; exp, exponential growth phase), enzyme(s) used for protein digestion, and fractionation methods on peptide (SCX, strong cation exchange chromatography; high pH, high pH reversed-phase chromatography) or protein level (gel, SDS-PAGE; CsCl, CsCl gradient) with the number of fractions indicated in parentheses, quantification methods (iTRAQ, isobaric tags for relative and absolute quantitation; SILAC, stable isotope labeling with amino acids in cell culture; SWATH, sequential window acquisition of all theoretical fragment ion spectra), instruments employed, corresponding PRIDE IDs with references and the sum of all spectra are noted. Experiments were performed by five different laboratories. For more details see Supplementary Tables 2-4 and Supplementary Data 1-2. Source data are provided as a Source data file.