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Related Concept Videos

Multi-pass Transmembrane Proteins and β-barrels01:09

Multi-pass Transmembrane Proteins and β-barrels

In multi-pass transmembrane proteins, the polypeptide chain crosses the membrane more than once. The transmembrane polypeptide chain either forms an α-helix or β-strand structure. α-Helix containing multi-pass transmembrane proteins are ubiquitous, whereas β-strand containing ones are mainly found in gram-negative bacteria, mitochondria, and chloroplasts.
α-Helix containing multi-pass transmembrane proteins
Multi-pass transmembrane proteins such as G-protein-linked receptors (GPCRs) and...
Single-pass Transmembrane Proteins01:25

Single-pass Transmembrane Proteins

Integral membrane proteins are tightly associated with the cell membrane and play a crucial role in cell communication, signaling, adhesion, and transport of the molecules. Some integral membrane proteins are present only in the membrane monolayer. For example, the enzyme fatty acid amide hydrolase is present in the cytoplasmic side of the membrane monolayer. In contrast, another type of integral membrane protein, also known as a transmembrane protein, spans across the membrane. Transmembrane...
Insertion of Single-pass Transmembrane Proteins in the RER01:26

Insertion of Single-pass Transmembrane Proteins in the RER

Integral membrane proteins are proteins adhered to the lipid bilayer of a cell organelle or membrane. They can be of two types: transmembrane integral proteins that span the lipid bilayer and monotopic proteins that are attached to either side of the membrane but do not pass through it.
Integral transmembrane proteins possess transmembrane and extra membrane domains. The transmembrane domains are primarily made of 20-25 hydrophobic amino acids arranged in a helical secondary confirmation. These...
Insertion of Multi-pass Transmembrane Proteins in the RER01:29

Insertion of Multi-pass Transmembrane Proteins in the RER

The rough ER membrane synthesizes, assembles, and embeds transmembrane proteins in diverse topologies. These proteins function as transporters or channels and can remain in the ER membrane or are sent to the Golgi complex, lysosome, and cell membrane.
The multipass transmembrane proteins are the type IV integral membrane proteins with multiple topogenic sequences determining their spatial arrangement in the ER membrane. Nearly all multipass proteins lack a cleavable signal sequence and use...
Protein Diffusion in the Membrane01:24

Protein Diffusion in the Membrane

Proteins show rotational as well as lateral diffusion across the membrane. The lateral diffusion of proteins was confirmed through the cell fusion experiment where mouse and human cells were fused, resulting in hybrid cells. When the human and mouse cells fused, the specific membrane proteins on human and mouse cells were marked with the red and green-fluorescent markers, respectively. Initially, the red and green fluorescence was located on the respective hemisphere of the cell. As time...
Membrane Asymmetry Regulating Transporters01:19

Membrane Asymmetry Regulating Transporters

Enzymes like flippase, floppase, and scramblase transfer phospholipids from one layer to another in the membrane, thereby affecting membrane asymmetry.
Flippase
Eukaryotic flippases are type-IV P-type ATPases or P4-ATPases belonging to P-type ATPase family proteins that are membrane-bound pumps involved in the ATP-mediated transport of ions and molecules across the membrane. Flippases flip specific phospholipids from the outer to the inner leaflet of a membrane. All P4-ATPases have one...

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Related Experiment Video

Updated: May 31, 2026

A Protocol for Computer-Based Protein Structure and Function Prediction
16:41

A Protocol for Computer-Based Protein Structure and Function Prediction

Published on: November 3, 2011

SOMRuler: a novel interpretable transmembrane helices predictor.

Dongjun Yu1, Hongbin Shen, Jingyu Yang

  • 1School of Computer Science and Technology, Nanjing University of Science and Technology, Nanjing, China. njyudj@mail.njust.edu.cn

IEEE Transactions on Nanobioscience
|July 12, 2011
PubMed
Summary
This summary is machine-generated.

SOMRuler, a novel transmembrane helix (TMH) predictor, offers high accuracy and interpretability in membrane protein structure prediction. It uses a self-organizing map to learn helix distribution, generating reliable fuzzy rules for enhanced bioinformatics applications.

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Transmembrane Domain Oligomerization Propensity determined by ToxR Assay
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Last Updated: May 31, 2026

A Protocol for Computer-Based Protein Structure and Function Prediction
16:41

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Published on: November 3, 2011

Transmembrane Domain Oligomerization Propensity determined by ToxR Assay
06:45

Transmembrane Domain Oligomerization Propensity determined by ToxR Assay

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Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
05:08

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins

Published on: July 8, 2025

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Structural Biology

Background:

  • Transmembrane helix (TMH) identification is crucial for membrane protein structure prediction.
  • Current TMH predictors often lack interpretability, functioning as "black boxes".

Purpose of the Study:

  • To introduce SOMRuler, a novel TMH predictor that combines high accuracy with excellent interpretability.
  • To develop a method for extracting human-interpretable fuzzy rules from learned knowledge.

Main Methods:

  • Utilized a self-organizing map (SOM) to learn helix distribution patterns from training data.
  • Extracted fuzzy rules from the SOM's codebook vectors, reducing computational burden and enhancing reliability.
  • Analyzed the validity of extracted fuzzy rules both qualitatively and quantitatively.

Main Results:

  • SOMRuler demonstrated high prediction accuracy, outperforming most existing popular TMH predictors on a benchmark dataset.
  • The method successfully generated interpretable fuzzy rules from learned helix distribution knowledge.
  • The extracted fuzzy rules were shown to be reliable and computationally efficient.

Conclusions:

  • SOMRuler provides an interpretable yet accurate approach to TMH identification in membrane protein structure prediction.
  • The method's flexibility makes it suitable for diverse bioinformatics problems.
  • SOMRuler enhances the understanding of TMH prediction by providing transparent, rule-based insights.