PXD007100

PXD007100 is an original dataset announced via ProteomeXchange.

Title	Phosphoproteomic analysis of the X-ray induced DNA damage response in dividing cells from wild type and atm mutants using LC-MSMS
Description	Rapid and effective DNA damage responses are required for plant growth and maintenance of active meristems under conditions of genotoxic stress. Here, analysis of the post-translational signalling network in mitotically dividing cells revealed a wide network of highly dynamic changes in the phosphoprotein profile of genotoxin treated cells, mediated in part by the ATAXIA TELANGIECTASIA MUTATED (ATM) protein kinase
HostingRepository	PRIDE
AnnounceDate	2019-08-19
AnnouncementXML	Submission_2019-08-19_00:54:55.xml
DigitalObjectIdentifier	https://dx.doi.org/10.6019/PXD007100
ReviewLevel	Peer-reviewed dataset
DatasetOrigin	Original dataset
RepositorySupport	Supported dataset by repository
PrimarySubmitter	Chris West
SpeciesList	scientific name: Arabidopsis thaliana (Mouse-ear cress); NCBI TaxID: 3702;
ModificationList	phosphorylated residue; monohydroxylated residue; iodoacetamide derivatized residue
Instrument	LTQ Orbitrap Elite

Revision	Datetime	Status	ChangeLog Entry
0	2017-07-21 06:30:16	ID requested
⏵ 1	2019-08-19 00:54:56	announced

Waterworth WM, Wilson M, Wang D, Nuhse T, Warward S, Selley J, West CE, Phosphoproteomic analysis reveals plant DNA damage signalling pathways with a functional role for histone H2AX phosphorylation in plant growth under genotoxic stress. Plant J, 100(5):1007-1021(2019) [pubmed]

curator keyword: Biological

submitter keyword: Arabidopsis thaliana, DNA damage response, ATM, LC-MSMS

Chris West
contact affiliation	Faculty of Biological Science University of Leeds UK
contact email	c.e.west@leeds.ac.uk
lab head
Chris West
contact affiliation	University of Leeds
contact email	c.e.west@leeds.ac.uk
dataset submitter

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PRIDE project URI

• PRIDE
  1. PXD007100
     1. Label: PRIDE project
     2. Name: Phosphoproteomic analysis of the X-ray induced DNA damage response in dividing cells from wild type and atm mutants using LC-MSMS