Towards the Understanding of the Folding of Methylene Units in the Glutamine Residue

✍ Scribed by Carlos Alemán; M. Cristina Vega; Eloísa Navarro; Dr. Jordi Puiggalí

• Book ID: 105360571
• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 518 KB
• Volume: 2
• Category: Article
• ISSN: 1075-2617
• DOI: 10.1002/psc.75

✦ Synopsis

The conformational preferences of the methylenic sequence in the side chain of the glutamine residue were investigated by ab initio and semi-empirical quantum mechanical calculations and examination of both the Brookhaven Protein Databank and Cambridge Structural Data Base. The results were analysed on the basis of our previous findings about the folding of methylene groups in aliphatic segments. Both energy calculations and the crystallographic structure of small peptides indicate that methylene units of the glutamine residue tend to fold in a gauche conformation. In contrast, such groups usually adopt an all-trans conformation in proteins due basically to the entropic and solvent contributions. These results have been demonstrated by computing the entropic correction to the free energy and evaluating the solvent effects through SCRF calculations.