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SignalP 4.1 Server

SignalP 4.1 server predicts the presence and location of signal peptide cleavage sites in amino acid sequences from different organisms: Gram-positive prokaryotes, Gram-negative prokaryotes, and eukaryotes. The method incorporates a prediction of cleavage sites and a signal peptide/non-signal peptide prediction based on a combination of several artificial neural networks.

View the version history of this server. All the previous versions are available on line, for comparison and reference.

New: SignalP has been updated to version 4.1 with two new features:

  • an option to choose a D-score cutoff that reproduces the sensitivity of SignalP 3.0 (this will make the false positive rate slightly higher, but still better than that of SignalP 3.0)
  • a customizable minimum length of the predicted signal peptide (default 10).
Additionally, the documentation has been rewritten. The Instructions page is expanded, the Output format page has been clarified, and there are new Performance and FAQ pages.

FAQ Article abstracts Instructions Output format Performance Data

SUBMISSION

Paste a single amino acid sequence or several sequences in FASTA format into the field below:

Submit a file in FASTA format directly from your local disk:

Organism group (explain)
Eukaryotes
Gram-negative bacteria
Gram-positive bacteria
D-cutoff values (explain)
Default (optimized for correlation)
Sensitive (reproduce SignalP 3.0's sensitivity)
User defined:
D-cutoff for SignalP-noTM networks
D-cutoff for SignalP-TM networks
Graphics output (explain)
No graphics
PNG (inline)
PNG (inline) and EPS (as links)
Output format (explain)
Standard
Short (no graphics)
Long
All - SignalP-noTM and SignalP-TM output (no graphics)
Method (explain)
Input sequences may include TM regions
Input sequences do not include TM regions
Positional limits (explain)
Minimal predicted signal peptide length. Default: 10
N-terminal truncation of input sequence (0 means no truncation).
Default: Truncate sequence to a length of 70 aa

Restrictions:
At most 2,000 sequences and 200,000 amino acids per submission; each sequence not more than 6,000 amino acids.

Confidentiality:
The sequences are kept confidential and will be deleted after processing.


CITATIONS

For publication of results, please cite:

SignalP 4.0: discriminating signal peptides from transmembrane regions
Thomas Nordahl Petersen, Søren Brunak, Gunnar von Heijne & Henrik Nielsen
Nature Methods, 8:785-786, 2011

doi:
10.1038/nmeth.1701
PMID: 21959131
Supplementary materials: nmeth.1701-S1.pdf

Other relevant papers:

  • Original paper (version 1.0):

    Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites.
    Henrik Nielsen, Jacob Engelbrecht, Søren Brunak and Gunnar von Heijne.
    Protein Engineering, 10:1-6, 1997.

    View the abstract.

  • SignalP-HMM (version 2.0):

    Prediction of signal peptides and signal anchors by a hidden Markov model.
    Henrik Nielsen and Anders Krogh.
    Proceedings of the Sixth International Conference on Intelligent Systems for Molecular Biology (ISMB 6),
    AAAI Press, Menlo Park, California, pp. 122-130, 1998.

    View the abstract.

  • Version 3.0:

    Improved prediction of signal peptides: SignalP 3.0.
    Jannick Dyrløv Bendtsen, Henrik Nielsen, Gunnar von Heijne and Søren Brunak.
    J. Mol. Biol., 340:783-795, 2004.

    View the abstract.         Download the full article in PDF.

  • Paper about using SignalP and other protein subcellular localization prediction methods:

    Locating proteins in the cell using TargetP, SignalP, and related tools
    Olof Emanuelsson, Søren Brunak, Gunnar von Heijne, Henrik Nielsen
    Nature Protocols 2:953-971 (2007).

    Access the paper and supplementary materials.


PORTABLE VERSION

Would you prefer to run SignalP at your own site? SignalP 4.1 is available as a stand-alone software package, with the same functionality as the service above. Ready-to-ship packages exist for Mac OS X and the most common UNIX platforms. There is a download page for academic users; other users are requested to contact CBS Software Package Manager at software@cbs.dtu.dk.


GETTING HELP

Scientific problems:        Technical problems: