PXD043707-1

PXD043707 is an original dataset announced via ProteomeXchange.

Title	KAT7 modification in response to DNA damage LC-MS/MS analysis
Description	To identify the acylation modification site of KAT7 in response to DNA damage, we treated HCT116 cells with etoposide, extracted proteins and purified KAT7 protein with KAT-specific antibodies for mass spectrometry analysis.This mass spectrometry identified the level of acylation modification of KAT7 in response to DNA damage in HCT116 cell line.
HostingRepository	PRIDE
AnnounceDate	2024-12-12
AnnouncementXML	Submission_2024-12-12_04:57:24.074.xml
DigitalObjectIdentifier
ReviewLevel	Peer-reviewed dataset
DatasetOrigin	Original dataset
RepositorySupport	Unsupported dataset by repository
PrimarySubmitter	萌 王
SpeciesList	scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationList	monomethylated residue; acetylated residue
Instrument	LTQ Orbitrap Velos Pro; LTQ Orbitrap Elite

Revision	Datetime	Status	ChangeLog Entry
0	2023-07-12 02:58:35	ID requested
⏵ 1	2024-12-12 04:57:24	announced

Dataset with its publication pending

submitter keyword: KAT7 acetylation crotonylation

Yang Yang
contact affiliation	Department of Biochemistry and Biophysics, School of Basic Medical Sciences, Peking University Health Science Center, #38 Xueyuan Road, Beijing 100191, China
contact email	yangsh@bjmu.edu.cn
lab head
萌 王
contact affiliation	Peking university
contact email	2011210027@bjmu.edu.cn
dataset submitter

Dataset FTP location NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/12/PXD043707

PRIDE project URI

• PRIDE
  1. PXD043707
     1. Label: PRIDE project
     2. Name: KAT7 modification in response to DNA damage LC-MS/MS analysis