Evidence map›Paper›PMID 21366353›Full record

ArticleJournal of proteome research2011

Correlation between protein function and ligand binding profiles.

Matthew D Shortridge, Michael Bokemper, Jennifer C Copeland, Jaime L Stark, Robert Powers

Abstract read
In one paragraph

Article in Journal of proteome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Matthew D ShortridgeDepartment of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588-0304, United States.
Michael Bokemper
Jennifer C Copeland
Jaime L Stark
Robert Powers

Funding

EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015468 · NCRR · UNIVERSITY OF NEBRASKA LINCOLN · PI PAUL, PREM S · 2000 to 2000
$2.0M
Revealing Functions for Newly Discovered Proteins by FAST-NMRR21AI081154 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI POWERS, ROBERT · 2009 to 2010
$376k
NCRR NIH HHS C06 RR015468NCRR NIH HHS RR015468-01NIAID NIH HHS R21 AI081154NIAID NIH HHS R21AI081154
6 · The paper itself

Abstract

We report that proteins with the same function bind the same set of small molecules from a standardized chemical library. This observation led to a quantifiable and rapidly adaptable method for protein functional analysis using experimentally derived ligand binding profiles. Ligand binding is measured using a high-throughput NMR ligand affinity screen with a structurally diverse chemical library. The method was demonstrated using a set of 19 proteins with a range of functions. A statistically significant similarity in ligand binding profiles was only observed between the two functionally identical albumins and between the five functionally similar amylases. This new approach is independent of sequence, structure, or evolutionary information and, therefore, extends our ability to analyze and functionally annotate novel genes.

Indexed as

LigandsProtein BindingAmylasesHumansMagnetic Resonance SpectroscopyMolecular Sequence AnnotationProteinsProteomicsSerum AlbuminAmylasesLigandsProteinsSerum Albumin

Identifiers

PMID21366353
PMCPMC3090486

What OpenQuestion holds

Textmetadata
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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.