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PEP-FOLD: an updated de novo structure prediction server for both linear and disulfide bonded cyclic peptides.


ABSTRACT: In the context of the renewed interest of peptides as therapeutics, it is important to have an on-line resource for 3D structure prediction of peptides with well-defined structures in aqueous solution. We present an updated version of PEP-FOLD allowing the treatment of both linear and disulphide bonded cyclic peptides with 9-36 amino acids. The server makes possible to define disulphide bonds and any residue-residue proximity under the guidance of the biologists. Using a benchmark of 34 cyclic peptides with one, two and three disulphide bonds, the best PEP-FOLD models deviate by an average RMS of 2.75?Å from the full NMR structures. Using a benchmark of 37 linear peptides, PEP-FOLD locates lowest-energy conformations deviating by 3?Å RMS from the NMR rigid cores. The evolution of PEP-FOLD comes as a new on-line service to supersede the previous server. The server is available at: http://bioserv.rpbs.univ-paris-diderot.fr/PEP-FOLD.

SUBMITTER: Thevenet P 

PROVIDER: S-EPMC3394260 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

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PEP-FOLD: an updated de novo structure prediction server for both linear and disulfide bonded cyclic peptides.

Thévenet Pierre P   Shen Yimin Y   Maupetit Julien J   Guyon Frédéric F   Derreumaux Philippe P   Tufféry Pierre P  

Nucleic acids research 20120511 Web Server issue


In the context of the renewed interest of peptides as therapeutics, it is important to have an on-line resource for 3D structure prediction of peptides with well-defined structures in aqueous solution. We present an updated version of PEP-FOLD allowing the treatment of both linear and disulphide bonded cyclic peptides with 9-36 amino acids. The server makes possible to define disulphide bonds and any residue-residue proximity under the guidance of the biologists. Using a benchmark of 34 cyclic p  ...[more]

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