Evidence map›Paper›PMID 8618859›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

How are close residues of protein structures distributed in primary sequence?

L Brocchieri, S Karlin

Open access · greenAbstract readComparative Study
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Structural bioinformatics analysis of free cysteines in protein environments.Journal of the Taiwan Institute of Chemical Engineers · 2009
    Article
  3. Measures of residue density in protein structures.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  4. Atom density in protein structures.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  5. Clusters of charged residues in protein three-dimensional structures.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  6. The folding mechanism of larger model proteins: role of native structure.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

L BrocchieriDepartment of Mathematics, Stanford University, CA 94305-2125, USA.
S Karlin
Stanford University · US

Funding

THEORY &APPLIED STUDIES IN EVOLUTIONARY GENETICSR01GM010452 · NIGMS · STANFORD UNIVERSITY · PI KARLIN, SAMUEL · 1985 to 2006
$2.1M
MOLECULAR SEQUENCE DATAR01HG000335 · NHGRI · STANFORD UNIVERSITY · PI KARLIN, SAMUEL · 1990 to 2001
$449k
NHGRI NIH HHS 5R01HG00335-07NIGMS NIH HHS 2R01GM10452-31
6 · The paper itself

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.

Indexed as

Amino Acid SequenceProtein ConformationProtein Structure, SecondaryMacromolecular SubstancesMolecular Sequence DataProteinsSolventsMacromolecular SubstancesProteinsSolvents

Identifiers

PMID8618859
PMCPMC40311
OpenAlexW2001504699

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.