Dissection of a β-barrel motif leads to a functional dimer: The case of the intestinal fatty acid binding protein
Author:
Publisher
Wiley
Subject
Molecular Biology,Biochemistry
Reference41 articles.
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1. Application of target repositioning and in silico screening to exploit fatty acid binding proteins (FABPs) from Echinococcus multilocularis as possible drug targets;Journal of Computer-Aided Molecular Design;2020-10-17
2. Structural coalescence underlies the aggregation propensity of a β-barrel protein motif;PLOS ONE;2017-02-10
3. Intervening in the β-barrel structure of lipid binding proteins: Consequences on folding, ligand-binding and aggregation propensity;Prostaglandins, Leukotrienes and Essential Fatty Acids;2015-02
4. Toward a common aggregation mechanism for a β-barrel protein family: Insights derived from a stable dimeric species;Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics;2014-09
5. Truncation of a β-Barrel Scaffold Dissociates Intrinsic Stability from Its Propensity to Aggregation;Biophysical Journal;2012-11
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