» Articles » PMID: 15111065

A Combined Transmembrane Topology and Signal Peptide Prediction Method

Overview
Journal J Mol Biol
Publisher Elsevier
Date 2004 Apr 28
PMID 15111065
Citations 1161
Authors
Affiliations
Soon will be listed here.
Abstract

An inherent problem in transmembrane protein topology prediction and signal peptide prediction is the high similarity between the hydrophobic regions of a transmembrane helix and that of a signal peptide, leading to cross-reaction between the two types of predictions. To improve predictions further, it is therefore important to make a predictor that aims to discriminate between the two classes. In addition, topology information can be gained when successfully predicting a signal peptide leading a transmembrane protein since it dictates that the N terminus of the mature protein must be on the non-cytoplasmic side of the membrane. Here, we present Phobius, a combined transmembrane protein topology and signal peptide predictor. The predictor is based on a hidden Markov model (HMM) that models the different sequence regions of a signal peptide and the different regions of a transmembrane protein in a series of interconnected states. Training was done on a newly assembled and curated dataset. Compared to TMHMM and SignalP, errors coming from cross-prediction between transmembrane segments and signal peptides were reduced substantially by Phobius. False classifications of signal peptides were reduced from 26.1% to 3.9% and false classifications of transmembrane helices were reduced from 19.0% to 7.7%. Phobius was applied to the proteomes of Homo sapiens and Escherichia coli. Here we also noted a drastic reduction of false classifications compared to TMHMM/SignalP, suggesting that Phobius is well suited for whole-genome annotation of signal peptides and transmembrane regions. The method is available at as well as at

Citing Articles

Evolutionary genomics reveals variation in structure and genetic content implicated in virulence and lifestyle in the genus Gaeumannomyces.

Hill R, Grey M, Fedi M, Smith D, Canning G, Ward S BMC Genomics. 2025; 26(1):239.

PMID: 40075289 PMC: 11905480. DOI: 10.1186/s12864-025-11432-0.


Hookworm genes encoding intestinal excreted-secreted proteins are transcriptionally upregulated in response to the host's immune system.

Schwarz E, Noon J, Chicca J, Garceau C, Li H, Antoshechkin I bioRxiv. 2025; .

PMID: 39975173 PMC: 11838427. DOI: 10.1101/2025.02.01.636063.


Dispensable genome and segmental duplications drive the genome plasticity in .

Navasca A, Singh J, Rivera-Varas V, Gill U, Secor G, Baldwin T Front Fungal Biol. 2025; 6:1432339.

PMID: 39974207 PMC: 11835900. DOI: 10.3389/ffunb.2025.1432339.


Classification of polyphenol oxidases shows ancient gene duplication leading to two distinct enzyme types.

Meitil I, de O G Silva C, Pedersen A, Agger J iScience. 2025; 28(2):111771.

PMID: 39925425 PMC: 11803259. DOI: 10.1016/j.isci.2025.111771.


Effector proteins of Funneliformis mosseae BR221: unravelling plant-fungal interactions through reference-based transcriptome analysis, in vitro validation, and protein‒protein docking studies.

Vasistha P, Singh P, Srivastava D, Johny L, Shukla S BMC Genomics. 2025; 26(1):42.

PMID: 39819563 PMC: 11736945. DOI: 10.1186/s12864-024-10918-7.