PXD007845 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | HEK293T LC-MS/MS . |
Description | Leucine plays crucial roles in protein proteolytic autophagy process, but the underlying mechanisms are not fully understood. Here, we combined in vitro reconstitution with comparative proteomics technology to identify the potential regulators for leucine-mediated autophagy pathway. We established a in vitro cell-free systems to mimic the activation of autophagy by monitoring the translocation of readout protein ATG14 to the autophagosome membrane. Based on the system, we further screened the potential regulators involved in the leucine-mediated autophagy pathway using comparative proteomics strategy. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-07 |
AnnouncementXML | Submission_2024-10-07_10:10:23.292.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Guokai Yan |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | iTRAQ8plex-116 reporter+balance reagent acylated residue |
Instrument | TripleTOF 5600 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2017-09-26 02:41:41 | ID requested | |
⏵ 1 | 2024-10-07 10:10:23 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
curator keyword: Biological |
submitter keyword: HEK293T,cell-free system, leucine, iTRAQ |
Contact List
Xianghua Yan |
contact affiliation | College of Animal Sciences & Technology, Huazhong Agricultural University |
contact email | xhyan@mail.hzau.edu.cn |
lab head | |
Guokai Yan |
contact affiliation | College of Animal Sciences & Technology, Huazhong Agricultural University |
contact email | gkyan@webmail.hzau.edu.cn |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD007845
- Label: PRIDE project
- Name: HEK293T LC-MS/MS