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Manual The Molecular Chaperones Interaction Networks in Protein Folding and Degradation

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FOLDING AND AGGREGATION

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CHAPERONES AND MISFOLDED PROTEINS

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Walid A. Houry

New Titles. Pick and Choose. Literature Updates. For Members. For Librarians. RSS Feeds. Chemistry World. Education in Chemistry. Open Access. Historical Collection. You do not have JavaScript enabled. Please enable JavaScript to access the full features of the site or access our non-JavaScript page. Issue 2, Previous Article Next Article. From the journal: Molecular Omics. You have access to this article. Please wait while we load your content Something went wrong.

One of the major products of this research field has been the identification of putative PPI drug targets within the chaperone network, which might be used to change chaperone "decisions" and rebalance proteostasis. The snippet could not be located in the article text. This may be because the snippet appears in a figure legend, contains special characters or spans different sections of the article. Acc Chem Res.

Bibliographic Information

Author manuscript; available in PMC Apr PMID: Abrams , and Jason E. Corresponding author. Correspondence: Jason E. Gestwicki, Ph. Copyright notice. The publisher's final edited version of this article is available at Acc Chem Res. See other articles in PMC that cite the published article. Graphical Abstract. Open in a separate window. Introduction to the Chaperone Network. Figure 1.

Protein folding in the cell | SALAHUDDIN | Journal of Biochemistry and Molecular Biology Research

The physical interactions of the major chaperone families. Heat shock protein 70 Hsp Figure 2. Putting It All Together.

Other Hsp70 Interactions in Prokaryotes. Hsp90 Co-Chaperones. Figure 3. PPIs with Hsp Small Heat Shock Proteins. Figure 4. PPIs of the sHsps. Oligomeric Interactions of the sHsps. Hetero-oligomerization of sHsps. Client Interactions with sHsps. Connections with Other Chaperones: Because sHsps lack enzymatic activity, they must coordinate with other chaperone families to engage in complex functions.

Cellular Context. Chemical Biology to Drug Discovery.

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Biographical Information Rebecca Freilich received her B. Nature , , — J Biol Chem , , — Biochemistry , 54 , — ACS chemical biology , 5 , — Nat Struct Biol , 8 , — Curr Pharm Des , 19 , — Exp Biol Med Maywood , , — Cell reports , 11 , — Biochemistry , 49 , — Cell reports , 1 , — Frontiers in bioengineering and biotechnology , 3 , Analyst , DOI Anal Chem , 85 , — ACS Chem Biol , 8 , — Science , , — PLoS Biol , 12 , e J Mol Biol , , — Cell Stress Chaperones , 22 , — Nat Struct Mol Biol , 18 , — Nat Rev Mol Cell Biol , 11 , — Mol Cell , 69 , — e ACS chemical biology , 7 , — PLoS genetics , 13 , e Frontiers in molecular biosciences , 2 , Nat Struct Mol Biol , 25 , 90— Nat Struct Mol Biol , 25 , 83— Cell , , — Mol Cell , 17 , — Cell chemical biology , 23 , — Structure , 20 , — Trends Biochem Sci , 28 , — Biochemistry , 52 , — EMBO Rep , 2 , — J Med Chem , 53 , — Curr Top Med Chem , 16 , — Biol Psychiatry , 74 , — Nature chemical biology , 9 , — Cancer Res , 74 , — Annual review of pharmacology and toxicology , 55 , — Nat Struct Mol Biol , 19 , — Nature reviews , 5 , — Journal of proteomics , 75 , — Cell , 90 , 65— Mol Cell , 11 , — Eur J Biochem , , 1—8.

Ann N Y Acad Sci , , — Adv Cancer Res , , 51— Biochim Biophys Acta , , —