ArticleMethods in molecular biology (Clifton, N.J.)2026
Studying the Protein-Membrane Interaction of a Mycobacterial ABC Transporter Through Coarse-Grained Simulations.
Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Direct interactions with the surrounding lipid bilayer are crucial for regulating the function of membrane transporters. These interactions are essential for controlling the conformational changes that drive the transport cycle. From a pharmacological perspective, understanding these specific interactions is crucial because transporters in pathogenic bacteria serve as key targets for the development of new antibiotics. However, experimentally characterizing the specific and transient nature of protein-lipid interactions at a molecular level remains a significant challenge. Coarse-grained (CG) molecular dynamics (MD) simulations have become a popular computational tool, allowing the exploration of long timescales needed to observe the dynamic interplay between proteins and their membrane environments. In this chapter, we will outline a protocol that includes designing, simulating, and analyzing a CG-MD system, with a focus on characterizing protein-lipid interactions. As an example, the simulation of the Mycobacterium tuberculosis siderophore transporter, IrtAB, will be used to demonstrate how to set up and analyze these complex biomolecular systems.
Indexed as
Identifiers
42681349What Socratic holds
Registered trials
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 Socratic graph.