Structural basis for the N‐degron specificity of ClpS1 from Arabidopsis thaliana. (30th December 2020)
- Record Type:
- Journal Article
- Title:
- Structural basis for the N‐degron specificity of ClpS1 from Arabidopsis thaliana. (30th December 2020)
- Main Title:
- Structural basis for the N‐degron specificity of ClpS1 from Arabidopsis thaliana
- Authors:
- Kim, Leehyeon
Heo, Jiwon
Kwon, Do Hoon
Shin, Jin Seok
Jang, Se Hwan
Park, Zee‐Yong
Song, Hyun Kyu - Abstract:
- Abstract: The N‐degron pathway determines the half‐life of proteins in both prokaryotes and eukaryotes by precisely recognizing the N‐terminal residue (N‐degron) of substrates. ClpS proteins from bacteria bind to substrates containing hydrophobic N‐degrons (Leu, Phe, Tyr, and Trp) and deliver them to the caseinolytic protease system ClpAP. This mechanism is preserved in organelles such as mitochondria and chloroplasts. Bacterial ClpS adaptors bind preferentially to Leu and Phe N‐degrons; however, ClpS1 from Arabidopsis thaliana (AtClpS1) shows a difference in that it binds strongly to Phe and Trp N‐degrons and only weakly to Leu. This difference in behavior cannot be explained without structural information due to the high sequence homology between bacterial and plant ClpS proteins. Here, we report the structure of AtClpS1 at 2.0 Å resolution in the presence of a bound N‐degron. The key determinants for α‐amino group recognition are conserved among all ClpS proteins, but the α3‐helix of eukaryotic AtClpS1 is significantly shortened, and consequently, a loop forming a pocket for the N‐degron is moved slightly outward to enlarge the pocket. In addition, amino acid replacement from Val to Ala causes a reduction in hydrophobic interactions with Leu N‐degron. A combination of the fine‐tuned hydrophobic residues in the pocket and the basic gatekeeper at the entrance of the pocket controls the N‐degron selectivity of the plant ClpS protein. Abstract : PDB Code(s): 7D34 ;
- Is Part Of:
- Protein science. Volume 30:Number 3(2021)
- Journal:
- Protein science
- Issue:
- Volume 30:Number 3(2021)
- Issue Display:
- Volume 30, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 30
- Issue:
- 3
- Issue Sort Value:
- 2021-0030-0003-0000
- Page Start:
- 700
- Page End:
- 708
- Publication Date:
- 2020-12-30
- Subjects:
- ClpS -- complex structure -- N‐degron pathway -- N‐end rule -- plant chloroplast -- type‐2 substrate -- X‐ray crystallography
Proteins -- Periodicals
572.6 - Journal URLs:
- http://www.proteinscience.org/ ↗
http://www3.interscience.wiley.com/journal/121502357/ ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1002/pro.4018 ↗
- Languages:
- English
- ISSNs:
- 0961-8368
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.105500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15883.xml