ArticleProceedings of the National Academy of Sciences of the United States of America1995
How are close residues of protein structures distributed in primary sequence?
Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed, 32 citations in OpenAlex.
- Article
- Structural bioinformatics analysis of free cysteines in protein environments.Journal of the Taiwan Institute of Chemical Engineers · 2009Article
- Measures of residue density in protein structures.Proceedings of the National Academy of Sciences of the United States of America · 1999Article
- Atom density in protein structures.Proceedings of the National Academy of Sciences of the United States of America · 1999Article
- Clusters of charged residues in protein three-dimensional structures.Proceedings of the National Academy of Sciences of the United States of America · 1996Article
- The folding mechanism of larger model proteins: role of native structure.Proceedings of the National Academy of Sciences of the United States of America · 1996Article
- Evolutionary conservation of RecA genes in relation to protein structure and function.Journal of bacteriology · 1996Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
Structurally neighboring residues are categorized according to their separation in the primary sequence as proximal (1-4 positions apart) and otherwise distal, which in turn is divided into near (5-20 positions), far (21-50 positions), very far ( > 50 positions), and interchain (from different chains of the same structure). These categories describe the linear distance histogram (LDH) for three-dimensional neighboring residue types. Among the main results are the following: (i) nearest-neighbor hydrophobic residues tend to be increasingly distally separated in the linear sequence, thus most often connecting distinct secondary structure units. (ii) The LDHs of oppositely charged nearest-neighbors emphasize proximal positions with a subsidiary maximum for very far positions. (iii) Cysteine-cysteine structural interactions rarely involve proximal positions. (iv) The greatest numbers of interchain specific nearest-neighbors in protein structures are composed of oppositely charged residues. (v) The largest fraction of side-chain neighboring residues from beta-strands involves near positions, emphasizing associations between consecutive strands. (vi) Exposed residue pairs are predominantly located in proximal linear positions, while buried residue pairs principally correspond to far or very far distal positions. The results are principally invariant to protein sizes, amino acid usages, linear distance normalizations, and over- and underrepresentations among nearest-neighbor types. Interpretations and hypotheses concerning the LDHs, particularly those of hydrophobic and charged pairings, are discussed with respect to protein stability and functionality. The pronounced occurrence of oppositely charged interchain contacts is consistent with many observations on protein complexes where multichain stabilization is facilitated by electrostatic interactions.
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