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Socket: a program for identifying and analysing coiled-coil motifs within protein structures.
J Mol Biol. 2001 Apr 13; 307(5):1427-50.JM

Abstract

The coiled coil is arguably the simplest protein-structure motif and probably the most ubiquitous facilitator of protein-protein interactions. Coiled coils comprise two or more alpha-helices that wind around each other to form "supercoils". The hallmark of most coiled coils is a regular sequence pattern known as the heptad repeat. Despite this apparent simplicity and relatedness at the sequence level, coiled coils display a considerable degree of structural diversity: the helices may be arranged parallel or anti-parallel and may form a variety of oligomer states. To aid studies of coiled coils, we developed SOCKET, a computer program to identify these motifs automatically in protein structures. We used SOCKET to gather a set of unambiguous coiled-coil structures from the RCSB Protein Data Bank. Rather than searching for sequence features, the algorithm recognises the characteristic knobs-into-holes side-chain packing of coiled coils; this proved to be straightforward to implement and was able to distinguish coiled coils from the great majority of helix-helix packing arrangements observed in globular domains. SOCKET unambiguously defines coiled-coil helix boundaries, oligomerisation states and helix orientations, and also assigns heptad registers. Structures retrieved from the Protein Data Bank included parallel and anti-parallel variants of two, three and four-stranded coiled coils, one example of a parallel pentamer and a small number of structures that extend the classical description of a coiled coil. We anticipate that our structural database and the associated sequence data that we have gathered will be of use in identifying principles for coiled-coil assembly, prediction and design. To illustrate this we give examples of sequence and structural analyses of the structures that are possible using the new data bases, and we present amino acid profiles for the heptad repeats of different motifs.

Authors+Show Affiliations

Centre for Biomolecular Design and Drug Development, School of Biological Sciences, University of Sussex, Falmer, East Sussex, BN1 9QG, UK.No affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

11292353

Citation

Walshaw, J, and D N. Woolfson. "Socket: a Program for Identifying and Analysing Coiled-coil Motifs Within Protein Structures." Journal of Molecular Biology, vol. 307, no. 5, 2001, pp. 1427-50.
Walshaw J, Woolfson DN. Socket: a program for identifying and analysing coiled-coil motifs within protein structures. J Mol Biol. 2001;307(5):1427-50.
Walshaw, J., & Woolfson, D. N. (2001). Socket: a program for identifying and analysing coiled-coil motifs within protein structures. Journal of Molecular Biology, 307(5), 1427-50.
Walshaw J, Woolfson DN. Socket: a Program for Identifying and Analysing Coiled-coil Motifs Within Protein Structures. J Mol Biol. 2001 Apr 13;307(5):1427-50. PubMed PMID: 11292353.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Socket: a program for identifying and analysing coiled-coil motifs within protein structures. AU - Walshaw,J, AU - Woolfson,D N, PY - 2001/4/9/pubmed PY - 2001/5/22/medline PY - 2001/4/9/entrez SP - 1427 EP - 50 JF - Journal of molecular biology JO - J Mol Biol VL - 307 IS - 5 N2 - The coiled coil is arguably the simplest protein-structure motif and probably the most ubiquitous facilitator of protein-protein interactions. Coiled coils comprise two or more alpha-helices that wind around each other to form "supercoils". The hallmark of most coiled coils is a regular sequence pattern known as the heptad repeat. Despite this apparent simplicity and relatedness at the sequence level, coiled coils display a considerable degree of structural diversity: the helices may be arranged parallel or anti-parallel and may form a variety of oligomer states. To aid studies of coiled coils, we developed SOCKET, a computer program to identify these motifs automatically in protein structures. We used SOCKET to gather a set of unambiguous coiled-coil structures from the RCSB Protein Data Bank. Rather than searching for sequence features, the algorithm recognises the characteristic knobs-into-holes side-chain packing of coiled coils; this proved to be straightforward to implement and was able to distinguish coiled coils from the great majority of helix-helix packing arrangements observed in globular domains. SOCKET unambiguously defines coiled-coil helix boundaries, oligomerisation states and helix orientations, and also assigns heptad registers. Structures retrieved from the Protein Data Bank included parallel and anti-parallel variants of two, three and four-stranded coiled coils, one example of a parallel pentamer and a small number of structures that extend the classical description of a coiled coil. We anticipate that our structural database and the associated sequence data that we have gathered will be of use in identifying principles for coiled-coil assembly, prediction and design. To illustrate this we give examples of sequence and structural analyses of the structures that are possible using the new data bases, and we present amino acid profiles for the heptad repeats of different motifs. SN - 0022-2836 UR - https://www.unboundmedicine.com/medline/citation/11292353/Socket:_a_program_for_identifying_and_analysing_coiled_coil_motifs_within_protein_structures_ DB - PRIME DP - Unbound Medicine ER -