Literature DB >> 11917145

Aromatic-aromatic interactions in and around alpha-helices.

Rajasri Bhattacharyya1, Uttamkumar Samanta, Pinak Chakrabarti.   

Abstract

To understand the role of aromatic-aromatic interactions in imparting specificity to the folding process, the geometries of four aromatic residues with different sequence spacing, located in alpha-helices or five residues from helical ends, interacting with each other have been elucidated. The geometry is found to depend on the sequence difference. Specific interactions (C-H...pi and N-H...pi) which result from this geometry may cause a given pair of residues (such as Phe-His) with a particular sequence difference to occur more than expected. The most conspicuous residue in an aromatic pair in the context of helix stability is His, which is found at the last (C1) position or the two positions (Ncap and Ccap) immediately flanking the helix. An alpha-helix and a contiguous 3(10)-helix or two helices separated by a non-helical residue can have interacting aromatic pairs, the geometry of interaction and the relative orientation between the helices being rather fixed. Short helices can also have interacting residues from either side.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11917145     DOI: 10.1093/protein/15.2.91

Source DB:  PubMed          Journal:  Protein Eng        ISSN: 0269-2139


  12 in total

Review 1.  Implications of aromatic-aromatic interactions: From protein structures to peptide models.

Authors:  Kamlesh Madhusudan Makwana; Radhakrishnan Mahalakshmi
Journal:  Protein Sci       Date:  2015-10-07       Impact factor: 6.725

2.  Molecular dynamics simulations of highly crowded amino acid solutions: comparisons of eight different force field combinations with experiment and with each other.

Authors:  Casey T Andrews; Adrian H Elcock
Journal:  J Chem Theory Comput       Date:  2013-10-08       Impact factor: 6.006

3.  Structure-based stabilization of insulin as a therapeutic protein assembly via enhanced aromatic-aromatic interactions.

Authors:  Nischay K Rege; Nalinda P Wickramasinghe; Alisar N Tustan; Nelson F B Phillips; Vivien C Yee; Faramarz Ismail-Beigi; Michael A Weiss
Journal:  J Biol Chem       Date:  2018-06-07       Impact factor: 5.157

4.  Substituent effect of the stacking interaction between carbon monoxide and benzene.

Authors:  Qiang Zhao
Journal:  J Mol Model       Date:  2018-05-25       Impact factor: 1.810

5.  patcHwork: a user-friendly pH sensitivity analysis web server for protein sequences and structures.

Authors:  Mirko Schmitz; Anne Schultze; Raimonds Vanags; Karsten Voigt; Barbara Di Ventura; Mehmet Ali Öztürk
Journal:  Nucleic Acids Res       Date:  2022-04-19       Impact factor: 19.160

6.  The role of weakly polar and H-bonding interactions in the stabilization of the conformers of FGG, WGG, and YGG: an aqueous phase computational study.

Authors:  József Csontos; Richard F Murphy; Sándor Lovas
Journal:  Biopolymers       Date:  2008-11       Impact factor: 2.505

7.  The Role of Aromatic-Aromatic Interactions in Strand-Strand Stabilization of β-Sheets.

Authors:  Ivan L Budyak; Anastasia Zhuravleva; Lila M Gierasch
Journal:  J Mol Biol       Date:  2013-06-28       Impact factor: 5.469

8.  Carbonic anhydrase modification for carbon management.

Authors:  Anand Giri; Deepak Pant
Journal:  Environ Sci Pollut Res Int       Date:  2019-12-03       Impact factor: 4.223

9.  Synthesis, solid state self-assembly driven by antiparallel π⋯π stacking and {⋯H-C-C-F}2 dimer synthons, and in vitro acetyl cholinesterase inhibition activity of phenoxy pendant isatins.

Authors:  Saba Mehreen; Aman Ullah; Humaira Nadeem; Necmi Dege; Muhammad Moazzam Naseer
Journal:  RSC Adv       Date:  2022-01-12       Impact factor: 3.361

10.  Absolute Configuration and Conformation of (-)-R-t-Butylphenylphosphinoamidate: Chiroptical Spectroscopy and X-ray Analysis.

Authors:  Ana G Petrovic; Prasad L Polavarapu; Andrzej Łopusiński; Dorota Krasowska; Wanda Wieczorek; Małgorzata Szyrej; Jarosław Błaszczyk; Józef Drabowicz
Journal:  J Org Chem       Date:  2020-08-19       Impact factor: 4.354

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.