Evidence map›Paper›PMID 23973084›Full record

ArticleMethods in cell biology2013

Using MTBindingSim as a tool for experimental planning and interpretation.

Julia T Philip, Aranda R Duan, Emily O Alberico, Holly V Goodson

Abstract read
In one paragraph

Article in Methods in cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Julia T PhilipDepartment of Chemistry and Biochemistry, Interdisciplinary Center for the Study of Biocomplexity, University of Notre Dame, Notre Dame, Indiana, USA.
Aranda R Duan
Emily O Alberico
Holly V Goodson

Funding

Chemistry-Biochemistry-Biology Training Program at Notre DameT32GM075762 · NIGMS · UNIVERSITY OF NOTRE DAME · PI CHANG, MAYLAND F, MOBASHERY, SHAHRIAR · 2007 to 2021
$3.7M
Interactions between CLIP-170 and tubulinR01GM065420 · NIGMS · UNIVERSITY OF NOTRE DAME · PI GOODSON, HOLLY V · 2003 to 2007
$1.6M
NIGMS NIH HHS R01 GM065420NIGMS NIH HHS T32 GM075762
6 · The paper itself

Abstract

MTBindingSim is a program that enables users to simulate experiments in which proteins or other ligands (e.g., drugs) bind to microtubules or other polymers under various binding models. The purpose of MTBindingSim is to help researchers and students gain an intuitive understanding of binding behavior and design experiments to distinguish between different binding mechanisms. MTBindingSim is open-source, freely available software and can be found at bindingtutor.org/mtbindingsim. This chapter first describes the capabilities of MTBindingSim, including the experimental designs and protein-binding models that it simulates, and then discusses two examples in which MTBindingSim is utilized in an experimental context. In the first, MTBindingSim is used to investigate potential explanations for unusual behavior observed in the binding of the neuronal protein Tau to microtubules, demonstrating that some potential explanations are incompatible with the experimental data. In the second example, MTBindingSim is used to design experiments to examine the question of whether the plus-end tracking protein EB1 binds preferentially to the microtubule seam.

Indexed as

Computer SimulationBinding SitesHumansMicrotubule-Associated ProteinsMicrotubulesPolymersProtein BindingSoftwaretau ProteinsMAPRE1 protein, humanMicrotubule-Associated ProteinsPolymerstau ProteinsBinding ModelComputer SimulationEB1MTBindingSimProtein BindingTau

Identifiers

PMID23973084
PMCPMC6938681

What OpenQuestion holds

Textmetadata
LicenceTDM
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.