From owner-bionews@hgmp.mrc.ac.uk Mon Dec 18 20:58:01 2000 Return-Path: Received: by mercury.hgmp.mrc.ac.uk (Postfix, from userid 110) id A500A17B1D; Mon, 18 Dec 2000 20:57:54 +0000 (GMT) Received: by mercury.hgmp.mrc.ac.uk (Postfix, from userid 6022) id 0C13717BEF; Mon, 18 Dec 2000 20:57:50 +0000 (GMT) Received: by mercury.hgmp.mrc.ac.uk (Postfix, from userid 6024) id 6DF9E17B5A; Fri, 15 Dec 2000 23:44:25 +0000 (GMT) Received: from sws1.ctd.ornl.gov (sws1.ctd.ornl.gov [128.219.128.109]) by mercury.hgmp.mrc.ac.uk (Postfix) with SMTP id AD662415DA for ; Fri, 15 Dec 2000 23:44:18 +0000 (GMT) Received: (qmail 22036 invoked by uid 12); 15 Dec 2000 23:44:14 -0000 To: bionet-announce@net.bio.net From: Dong Xu Newsgroups: bionet.announce Subject: Version 1.0 of PROSPECT Organization: Oak Ridge National Lab, Oak Ridge, TN Message-ID: <3A3AACCD.80207F55@ornl.gov> Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Mailer: Mozilla 4.72 [en] (X11; U; SunOS 5.6 sun4u) X-Accept-Language: en Date: Mon, 18 Dec 2000 20:57:50 +0000 (GMT) Sender: owner-bionews@hgmp.mrc.ac.uk Precedence: bulk Announcement: Version 1.0 of PROSPECT ===================================== The Computational Protein Structure Group of Oak Ridge National Laboratory would like to announce the release of PROSPECT Version 1.0. PROSPECT (PROtein Structure Prediction and Evaluation Computer Toolkit) is a threading-based protein structure prediction system. PROSPECT is particularly designed to recognize structural folds whose sequence have no significant homology to the target sequence. For detailed information about PROSPECT, please check http://compbio.ornl.gov/structure/prospect/ PROSPECT has a number of unique features -- * The system guarantees to find the globally-optimal alignments for a given energy function with any combination of the following terms: (1) mutation energy (including position-specific score matrix derived from multiple-sequence alignments), (2) singleton energy (including matching scores to the predicted secondary structures), (3) pairwise contact potential (distance dependent or independent), and (4) alignment gap penalties. * The system allows users to easily incorporate biological knowledge and constraints into the threading process to find optimal alignments under the specified constraints, which may include: - specified disulfide bonds - specified active sites - specified secondary structures - specified NOE restraints in NMR - specified gaps with no gap penalties * The system provides a prediction confidence assessment for each prediction based on a neural-net method and an evaluation of compactness of the predicted structure. * A Web-based interface is available to browse the threading alignments and 3D structures. PROSPECT is free of charge to academic users. Please contact the authors (Ying Xu at xyn@ornl.gov or Dong Xu at xud@ornl.gov) about the download information. For commercial users, please contact the authors for licensing information. .