Chemoproteomics Reveals USP5 (Ubiquitin Carboxyl-Terminal Hydrolase 5) as Promising Target of the Marine Polyketide Gracilioether A.

Publication Year: 2024

DOI:
10.3390/md22010041

PMCID:
PMC10817451

PMID:
38248666

Journal Information

Full Title: Mar Drugs

Abbreviation: Mar Drugs

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Pharmacology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"gel bands were then excised from the gel and submitted to trypsin digestion for the next bottom-up nano-esi-uplc-ms/ms analysis (data available via proteomexchange with identifier pxd048098).; the mass spectrometry proteomics data have been deposited to the proteomexchange consortium via the pride [ ] partner repository with the data set identifier pxd048098.; supplementary materials the following supporting information can be downloaded at: https://www mdpi com/article/10 3390/md22010041/s1 figure s1: list of transitions of usp5 tryptic peptides selected for the analysis of the lip experiment; figure s2: usp5 peptides identified with the lip experiment involved in binding with gea; figure s3: binding mode of hhy (in violet) superimposed to its pose (in green) in the crystal structure of usp5 (pdb code: 6dxt); figure s4: uncropped image displaying the gel related to one of the darts experiments; figure s5: uncropped image of the western blot confirmation of darts experiments; figure s6: darts data for usp5; figure s7: peak area of peptide transition analyzed in the t-lip experiments; figure s8: plot of the ru values obtained through spr analysis in function of gea concentrations [ 16 19 20 21 22 ]."

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"Conflicts of Interest The authors declare no conflicts of interest."

Evidence found in paper:

"This research was funded by the University of Salerno (FARB 2021) ORSA215145 project, and by Ministero dell’Università e della Ricerca (MUR)—PRIN2022 project, “2022RCTY7M, BiTMaP: Coupling the power of bioinformatics and experimental tools for accelerating the production, structural elucidation, and target identification of marine natural products” and PRIN2022-PNRR project, “P2022CKMPW, TACSI Driver: a multitasks platform to guide the Target identification, Assessment of the binding, Collection of natural products from waste, Synthesis of derivatives, and In vitro/In vivo polypharmacological profile evaluation of bioactive compounds”."

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Last Updated: Aug 05, 2025