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Fold Recognition Ole Lund, Assistant professor, CBS
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OL Fold recognition Find template for modeling – 1st step in comparative modeling Can be used to predict function
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OL Template identification Search with sequence – Blast against proteins with known structure – Psi-Blast against all proteins – Fold recognition methods Use biological information Functional annotation in databases Active site/motifs
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OL Blast derivatives: PDB-BLAST Procedure 1. Build sequence profile by iterative PSI-BLAST search against a sequence database 2. Use profile to search database of proteins with known structure Advantage – Makes sure hid to protein with known structure is not hidden behind a lot of hits to other proteins
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OL BLAST derivatives: Transitive BLAST Procedure 1. Find homologues to query (your) sequence 2. Find homologues to these homologues 3. Etc. – Can be implemented with e.g. BLAST or PSI- BLAST Also known as Intermediate Sequence Search (ISS)
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OL CASP – Critical Assessment of Structure Predictions – Every second year – Sequences from about-to-be-solved-structures are given to groups who submit their predictions before the structure is published – Modelers make prediction – Meeting in Asilomar where correct answers are revealed
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OL Target difficulty CM: Comparative (homology) modeling CM/FR: not PSI-BLAST (but ISS) findable FR(H): Homologous fold recognition FR(A): Analogous fold recognition NF/FR: Partly New fold NF: New Fold (used to be called Ab Initio - from first principles- prediction)
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OL CASP5 overview
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OL Successful fold recognition groups at CASP5 3D-Jury (Leszek Rychlewski) 3D-CAM (Krzysztof Ginalski) Template recombination (Paul Bates) HMAP (Barry Honig) PROSPECT (Ying Xu) ATOME (Gilles Labesse)
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OL 3D-Jury (Rychlewski) Inspired by Ab initio modeling methods – Average of frequently obtained low energy structures is often closer to the native structure than the lowest energy structure Find most abundant high scoring models 1. Use output from a set of servers 2. Superimpose all pairs of structures 3. Similarity score S ij = # of C pairs within 3.5Å (if #>40;else S ij =0) 4. 3D-Jury score = i S ij /(N+1) Similar methods developed by A Elofsson (Pcons) and D Fischer (3D shotgun) Rychlewski.doc
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OL 3D-CAM (Krzysztof Ginalski) 3D-Consensus Alignment Method – Structural alignment for all members of fold from FSSP – Conservation of specific residues and contacts responsible for maintaining tertiary structure critical for substrate binding and/or catalysis – Find homologues with iterative PSI-BLAST – Align with ClustalW – identify conserved residues – Structural integrity of alignments – Manual realignment – Fold recognition for homologues – Modelling – Verification Visually Computationally (Verify3D, ProsaII, WHAT_CHECK) Ginalski.doc
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OL Paul A Bates - In Silico Recombination of Templates, Alignments and Models Problems – Models rarely better than templates – Manual intervention have marginal effect Possible solution – Recombination of models Abstract
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OL Paul A Bates – Modelling Procedure Define domains Make models (FAMS/Pmodeller/EsyPred3D) – Manual inspection/correction of alignments – Alignment of annotated residues (PFAM) – Preferably use alignment with >2 bits/aa Select pair of models – Superimpose – Crossover or mutate (average coordinates) Select best proportion – Contact pair potentials – Solvation energies (calculated from solvent accessible area) Convergence – Minimization and final refinements Abstract
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OL Barry Honig Sequence&structure profile-profile based alignment – Database of template profiles Multiple structure alignment Sequence based profiles Position specific gap penalties derived from secondary structure Calibration to estimate statistical significance – Query profile Sequence based profile Predicted secondary structure (consensus between PSI- PRED,PHD,JNET) Abstract
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OL Ying Xu PROSPECT: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 4. alignment gap penalties. Abstract
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OL Gilles Labesse Meta Server – 3D-PSSM, PDB-BLAST, FUGUE, GenTHREADER, SAM-T99, JPRED-2 Tool for Incremental Threading optimization (T.I.T.O.) Consensus ranking Abstract
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OL LiveBench The Live Bench Project is a continuous benchmarking program. Every week sequences of newly released PDB proteins are being submitted to participating fold recognition servers. The results are collected and continuous evaluated using automated model assessment programs. A summary of the results is produced after several months of data collection. The servers must delay the updating of their structural template libraries by one week to participate.
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OL Meta Server
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OL Meta Server http://bioinfo.pl/meta/target.pl?id=7296
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OL Score # correct # wrong
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OL Best servers? FFA3 3DS5 INBG SHUM 3DPS 3DS3 FUG3 SHGU FUG2 PCO2 PRO2 MGTH SFPP PMO3
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OL Links to fold recognition servers Databases of links – http://bioinfo.pl/meta/servers.html http://bioinfo.pl/meta/servers.html – http://mmtsb.scripps.edu/cgi-bin/renderrelres?protmodel http://mmtsb.scripps.edu/cgi-bin/renderrelres?protmodel Meta server – http://bioinfo.pl/meta/ (Example: http://bioinfo.pl/meta/target.pl?id=7296 ) http://bioinfo.pl/meta/http://bioinfo.pl/meta/target.pl?id=7296 3DPSSM – good graphical output – http://www.sbg.bio.ic.ac.uk/servers/3dpssm/ http://www.sbg.bio.ic.ac.uk/servers/3dpssm/ GenTHREADER – http://bioinf.cs.ucl.ac.uk/psipred/ http://bioinf.cs.ucl.ac.uk/psipred/ FUGUE2 – http://www-cryst.bioc.cam.ac.uk/~fugue/prfsearch.html http://www-cryst.bioc.cam.ac.uk/~fugue/prfsearch.html SAM – http://www.cse.ucsc.edu/research/compbio/HMM-apps/T99-query.html http://www.cse.ucsc.edu/research/compbio/HMM-apps/T99-query.html FOLD – http://fold.doe-mbi.ucla.edu/ http://fold.doe-mbi.ucla.edu/ FFAS/PDBBLAST – http://bioinformatics.burnham-inst.org/ http://bioinformatics.burnham-inst.org/
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