Evidence map›Paper›PMID 23113706›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2013

Determining protein structures from NOESY distance constraints by semidefinite programming.

Babak Alipanahi, Nathan Krislock, Ali Ghodsi, Henry Wolkowicz, Logan Donaldson, Ming Li

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Babak AlipanahiDavid R. Cheriton School of Computer Science, University of Waterloo, Waterloo, Ontario, Canada.
Nathan Krislock
Ali Ghodsi
Henry Wolkowicz
Logan Donaldson
Ming Li

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contemporary practical methods for protein nuclear magnetic resonance (NMR) structure determination use molecular dynamics coupled with a simulated annealing schedule. The objective of these methods is to minimize the error of deviating from the nuclear overhauser effect (NOE) distance constraints. However, the corresponding objective function is highly nonconvex and, consequently, difficult to optimize. Euclidean distance matrix (EDM) methods based on semidefinite programming (SDP) provide a natural framework for these problems. However, the high complexity of SDP solvers and the often noisy distance constraints provide major challenges to this approach. The main contribution of this article is a new SDP formulation for the EDM approach that overcomes these two difficulties. We model the protein as a set of intersecting two- and three-dimensional cliques. Then, we adapt and extend a technique called semidefinite facial reduction to reduce the SDP problem size to approximately one quarter of the size of the original problem. The reduced SDP problem can be solved approximately 100 times faster, and it is also more resistant to numerical problems from erroneous and inexact distance bounds.

Indexed as

AlgorithmsSoftwareDatabases, ProteinGlycineMagnetic Resonance SpectroscopyProteinsProtein Structure, SecondaryGlycineProteins

Identifiers

PMID23113706
PMCPMC3619149

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Registered trials

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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.