The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Helix Signals in Proteins
Abstract
The α helix, first proposed by Pauling and co-workers, is a hallmark of protein structure, and much effort has been directed toward understanding which sequences can form helices. The helix hypothesis, introduced here, provides a tentative answer to this question. The hypothesis states that a necessary condition for helix formation is the presence of residues flanking the helix termini whose side chains can form hydrogen bonds with the initial four-helix > N-H groups and final four-helix > C-O groups; these eight groups would otherwise lack intrahelical partners. This simple hypothesis implies the existence of a stereochemical code in which certain sequences have the hydrogen-bonding capacity to function as helix boundaries and thereby enable the helix to form autonomously. The three-dimensional structure of a protein is a consequence of the genetic code, but the rules relating sequence to structure are still unknown. The ensuing analysis supports the idea that a stereochemical code for the α helix resides in its boundary residues.
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Cites
Kabsch, W., & Sander, C. (1983) · Biopolymers · doi:10.1002/bip.360221211 · Cited by 15,320
Chou, P. Y., & Fasman, G. D. (1974) · Biochemistry · doi:10.1021/bi00699a001 · Cited by 2,172
Cited by
Funnels, pathways, and the energy landscape of protein folding: A synthesis
Bryngelson, J. D., Onuchic, J. N., Socci, N. D., & Wolynes, P. G. (1995) · Proteins: Structure, Function, and Bioinformatics · doi:10.1002/prot.340210302 · Cited by 2,648
“Sequences may need special start or stop residues to form terminal hydrogen bonds gracefully, using sidechains [38, 39].”
BackgroundIce-binding structure and mechanism of an antifreeze protein from winter flounder
Sicheri, F., & Yang, D. S. C. (1995) · Nature · doi:10.1038/375427a0 · Cited by 417
Muñoz, V., & Serrano, L. (1995) · Journal of Molecular Biology · doi:10.1006/jmbi.1994.0024 · Cited by 251
Stabilization of alpha-helical structures in short peptides via end capping
Forood, B., Feliciano, E. J., & Nambiar, K. P. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.3.838 · Cited by 235
RQT complex dissociates ribosomes collided on endogenous RQC substrate SDD1
Matsuo, Y., Tesina, P., Nakajima, S., Mizuno, M., Endo, A., Buschauer, R., Cheng, J., Shounai, O., Ikeuchi, K., Saeki, Y., et al. (2020) · Nature Structural & Molecular Biology · doi:10.1038/s41594-020-0393-9 · Cited by 150
Metadata
- Authors
- Presta, L. G., & Rose, G. D.
- Venue
- Science
- Published
- 1988-06-17
- Volume
- 240
- Issue
- 4859
- Pages
- 1632-1641
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2056770911
- Cited by
- 646
- References
- 2
- FWCI
- 9.66
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.