Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Membrane binding by MinD involves insertion of hydrophobic residues within the C-terminal amphipathic helix into the bilayer.

Journal of bacteriology - 1 Aug 2003

Zhou Huaijin, Lutkenhaus Joe

Abstract excerpt

MinD binds to phospholipid vesicles in the presence of ATP and is released by MinE, which stimulates the MinD ATPase. Membrane binding requires a short conserved C-terminal region, which has the potential to form an amphipathic helix. This finding has led to a model in which the binding of ATP re...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenosine Triphosphatases
Share to Escherichia coli Proteins
Share to Fluorescence Polarization

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hydrophobic and Hydrophilic Interactions

Share to Lipid Bilayers

Share to Microscopy, Electron

Share to Software

Share to Tryptophan

Source

Open in PubMed Open full text

Identifiers

PMID: 12867440
DOI: 10.1128/JB.185.15.4326-4335.2003
PMCID: PMC165746

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12867440-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Membrane binding by MinD involves insertion of hydrophobic residues within the C-terminal amphipathic helix into the bilayer.PMID 12867440Read ↗

Direct MinE-membrane interaction contributes to the proper localization of MinDE in E. coli.Semantic proximity Read ↗

MinE conformational dynamics regulate membrane binding, MinD interaction, and Min oscillation.Semantic proximity Read ↗

The N terminus of MinD contains determinants which affect its dynamic localization and enzymatic activity.Semantic proximity Read ↗

A conserved polar region in the cell division site determinant MinD is required for responding to MinE-induced oscillation but not for localization within coiled arrays.Semantic proximity Read ↗

The switch I and II regions of MinD are required for binding and activating MinC.Semantic proximity Read ↗

Mapping the MinE site involved in interaction with the MinD division site selection protein of Escherichia coli.Semantic proximity Read ↗

The C-terminal transmembrane domain of human phospholipid scramblase 1 is essential for the protein flip-flop activity and Ca²⁺-binding.Semantic proximity Read ↗

Large-scale modulation of reconstituted Min protein patterns and gradients by defined mutations in MinE's membrane targeting sequence.Semantic proximity Read ↗

Activation of TMEM16F by inner gate charged mutations and possible lipid/ion permeation mechanisms.Semantic proximity Read ↗

Transmembrane helix M6 in sarco(endo)plasmic reticulum Ca(2+)-ATPase forms a functional interaction site with phospholamban. Evidence for physical interactions at other sites.Semantic proximity Read ↗

Membrane redistribution of the Escherichia coli MinD protein induced by MinE.Semantic proximity Read ↗

Role of tryptophan residues in interfacial binding of phosphatidylinositol-specific phospholipase C.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.