protein structure obtaining 3-d structure obtaining 3-d structure (nmr)

Protein Structure

Obtaining 3-D structure

Obtaining 3-D structure (NMR)

Obtaining 3-D structure (Bioinformatics)

3-D structure (dynamics / computation)

Subdomain Rearrangement in HIV-1 Reverse Transcriptase

Protein Databases

UniProt is the universal protein database, a central repository of protein data created by combining Swiss-Prot, TrEMBL and PIR. This makes it the world's most comprehensive resource on protein information.The Protein Information Resource (PIR), located at Georgetown University Medical Center (GUMC), is an integrated public bioinformatics resource to support genomic and proteomic research, and scientific studies. Swiss-Prot is a curated biological database of protein sequences from different species created in 1986 by Amos Bairoch during his PhD and developed by the Swiss Institute of Bioinformatics and the European Bioinformatics Institute. Pfam is a large collection of multiple sequence alignments and hidden Markov models covering many common protein domains and families. PDBNCBIhttp://proteome.nih.gov/links.html

PubMed – Protein Databases

The Protein database contains sequence data from the translated coding regions from DNA sequences in GenBank, EMBL, and DDBJ as well as protein sequences submitted to Protein Information Resource (PIR), SWISS-PROT, Protein Research Foundation (PRF), and Protein Data Bank (PDB) (sequences from solved structures).

The Structure database or Molecular Modeling Database (MMDB) contains experimental data from crystallographic and NMR structure determinations. The data for MMDB are obtained from the Protein Data Bank (PDB). The NCBI has cross-linked structural data to bibliographic information, to the sequence databases, and to the NCBI taxonomy. Use Cn3D, the NCBI 3D structure viewer, for easy interactive visualization of molecular structures from Entrez.

Tutorial: http://www.pdb.org/pdbstatic/tutorials/tutorial.html

Example – PDBhttp://www.pdb.org Only proteins with known structures are included.

Protein Visualization Softwares• Cn3d• RasMol• TOPS• Chime

• DSSP• Molscript• Ribbons• MSMS• Surfnet• …

PubMed Structure Database

PubMed Structure Database

Protein Structure Classification - SCOP

• Structure Classification Of Proteins database • http://scop.mrc-lmb.cam.ac.uk/scop/

• Hierarchical Clustering• Family – clear evolutionarily relationship• Superfamily – probable common evolutionary origin• Fold – major structural similarity

• Boundaries between levels are more or less subjective

• Conservative evolutionary classification leads to many new divisions at the family and superfamily levels, therefore it is recommended to first focus on higher levels in the classification tree.

Protein Structure Classification - SCOP

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Protein Structure Classification - SCOP

Class Number of foldsNumber of superfamilies

Number of families

All alpha proteins 218 376 608

All beta proteins 144 290 560

Alpha and beta proteins ()

136 222 629

Alpha and beta proteins ()

279 409 717

Multi-domain proteins 46 46 61

Membrane and cell surface proteins

47 88 99

Small proteins 75 108 171

Total 945 1539 2845

Scop Classification StatisticsSCOP: Structural Classification of Proteins. 1.69 release

25973 PDB Entries (1 Oct 2004). 70859 Domains. 1 Literature Reference(excluding nucleic acids and theoretical models)

Protein Structure Classification - SCOP

Protein Structure Classification - SCOP

Protein Structure Classification - SCOP

Protein Structure Classification - SCOP

Protein Structure Classification - SCOP

Protein Structure Classification - CATH

• CATH Protein Structure Classification• http://www.cathdb.info/latest/index.html

• CATH is a hierarchical classification of protein domain structures, which clusters proteins at four major levels, Class(C), Architecture(A), Topology(T) and Homologous superfamily (H).

• Class, derived from secondary structure content, is assigned for more than 90% of protein structures automatically.

• Architecture, which describes the gross orientation of secondary structures, independent of connectivities, is currently assigned manually.

• The topology level clusters structures into fold groups according to their topological connections and numbers of secondary structures.

• The homologous superfamilies cluster proteins with highly similar structures and functions. The assignments of structures to fold groups and homologous superfamilies are made by sequence and structure comparisons.

Protein Structure Classification - CATH

CATH vs. SCOP

Secondary Structure PredictionAGADIR - An algorithm to predict the helical content of peptides APSSP - Advanced Protein Secondary Structure Prediction Server GOR - Garnier et al, 1996 HNN - Hierarchical Neural Network method (Guermeur, 1997) Jpred - A consensus method for protein secondary structure prediction at University of Dundee JUFO - Protein secondary structure prediction from sequence (neural network) nnPredict - University of California at San Francisco (UCSF) Porter - University College Dublin PredictProtein - PHDsec, PHDacc, PHDhtm, PHDtopology, PHDthreader, MaxHom, EvalSec from Columbia University Prof - Cascaded Multiple Classifiers for Secondary Structure Prediction PSA - BioMolecular Engineering Research Center (BMERC) / Boston PSIpred - Various protein structure prediction methods at Brunel University SOPMA - Geourjon and Deléage, 1995 SSpro - Secondary structure prediction using bidirectional recurrent neural networks at University of California DLP - Domain linker prediction at RIKEN

http://us.expasy.org/tools/#secondary

Secondary Structure Prediction - HNN

• >gi|78099986|sp|P0ABK2|CYDB_ECOLI Cytochrome d ubiquinol oxidase subunit 2 (Cytochrome d ubiquinol oxidase subunit II) (Cytochrome bd-I oxidase subunit II) MIDYEVLRFIWWLLVGVLLIGFAVTDGFDMGVGMLTRFLGRNDTERRIMINSIAPHWDGNQVWLITAGGA LFAAWPMVYAAAFSGFYVAMILVLASLFFRPVGFDYRSKIEETRWRNMWDWGIFIGSFVPPLVIGVAFGN LLQGVPFNVDEYLRLYYTGNFFQLLNPFGLLAGVVSVGMIITQGATYLQMRTVGELHLRTRATAQVAALV TLVCFALAGVWVMYGIDGYVVKSTMDHYAASNPLNKEVVREAGAWLVNFNNTPILWAIPALGVVLPLLTI LTARMDKAAWAFVFSSLTLACIILTAGIAMFPFVMPSSTMMNASLTMWDATSSQLTLNVMTWVAVVLVPIILLY

TAWCYWKMFGRITKEDIERNTHSLY

• http://npsa-pbil.ibcp.fr/cgi-bin/secpred_hnn.pl

Secondary Structure Prediction - HNN

10 20 30 40 50 60 70 | | | | | | | MIDYEVLRFIWWLLVGVLLIGFAVTDGFDMGVGMLTRFLGRNDTERRIMINSIAPHWDGNQVWLITAGGA ccchhhhhhhhhhhhhhheeeeehccchhcchhhhhheecccccceeeeeeccccccccceeeeeeccch LFAAWPMVYAAAFSGFYVAMILVLASLFFRPVGFDYRSKIEETRWRNMWDWGIFIGSFVPPLVIGVAFGN hhhhhhhhhhhhhhhhhhhhhhhhhhhhhcccccccccchhhhhhhhhhcceeehccchccheehhhhhc LLQGVPFNVDEYLRLYYTGNFFQLLNPFGLLAGVVSVGMIITQGATYLQMRTVGELHLRTRATAQVAALV hhcccccchhhhheeeeccchhhhhcchceccceeeeeeeeeccchhhhhhhchhhhhhchhhhhhhhhh TLVCFALAGVWVMYGIDGYVVKSTMDHYAASNPLNKEVVREAGAWLVNFNNTPILWAIPALGVVLPLLTI hhhhhhccceeeeeeccceeeeeccccccccccchhhhhhhhhhhheeccccceeeeccchhhhhhhhhh LTARMDKAAWAFVFSSLTLACIILTAGIAMFPFVMPSSTMMNASLTMWDATSSQLTLNVMTWVAVVLVPI hhhhhhhhhhhhhhhhhhhhhhhhhcchhhcccccccchhhccccchhcccchhhhhhhhhhhhhhhhhh ILLYTAWCYWKMFGRITKEDIERNTHSLY hhhhhhhhhhhhhhhcchhhhhhhccccc

Sequence length : 379 HNN : Alpha helix (Hh) : 209 is 55.15% 310 helix (Gg) : 0 is 0.00% Pi helix (Ii) : 0 is 0.00% Beta bridge (Bb) : 0 is 0.00% Extended strand (Ee) : 55 is 14.51% Beta turn (Tt) : 0 is 0.00% Bend region (Ss) : 0 is 0.00% Random coil (Cc) : 115 is 30.34% Ambigous states (?) : 0 is 0.00% Other states : 0 is 0.00%

Secondary Structure Prediction - HNN

Motifs Readily Identified from Sequence

• Zinc Finger - order and spacing of a pattern for cysteine and histidine.

• Leucine zippers – two antiparallel alpha helices held together by interactions between hybrophobic leucine residues at every seventh position in each helix.

• Coiled coils – 2-3 helices coiled around each other in a left-handed supercoil (3.5 residue/turn instead of 3.6 – 7/two turns); first and fourth are always hydrophobic, others hydrophilic; 5-10 heptads.

• Transmembrane-spanning proteins – alpha helices comprising amino acids with hydrophobic side chains, typically 20-30 residues.

Topology PredictionPSORT - Prediction of protein subcellular localization TargetP - Prediction of subcellular location DAS - Prediction of transmembrane regions in prokaryotes using the Dense Alignment Surface method (Stockholm University) HMMTOP - Prediction of transmembrane helices and topology of proteins (Hungarian Academy of Sciences) PredictProtein - Prediction of transmembrane helix location and topology (Columbia University) SOSUI - Prediction of transmembrane regions (Nagoya University, Japan) TMAP - Transmembrane detection based on multiple sequence alignment (Karolinska Institut; Sweden) TMHMM - Prediction of transmembrane helices in proteins (CBS; Denmark) TMpred - Prediction of transmembrane regions and protein orientation (EMBnet-CH) TopPred - Topology prediction of membrane proteins (France)

http://us.expasy.org/tools

Tertiary Structure PredictionComparative modeling

SWISS-MODEL - An automated knowledge-based protein modelling server 3Djigsaw - Three-dimensional models for proteins based on homologues of known structure CPHmodels - Automated neural-network based protein modelling server ESyPred3D - Automated homology modeling program using neural networks Geno3d - Automatic modeling of protein three-dimensional structure SDSC1 - Protein Structure Homology Modeling Server

Threading 3D-PSSM - Protein fold recognition using 1D and 3D sequence profiles coupled with secondary structure information (Foldfit) Fugue - Sequence-structure homology recognition HHpred - Protein homology detection and structure prediction by HMM-HMM comparison Libellula - Neural network approach to evaluate fold recognition results LOOPP - Sequence to sequence, sequence to structure, and structure to structure alignment SAM-T02 - HMM-based Protein Structure Prediction Threader - Protein fold recognition ProSup - Protein structure superimposition SWEET - Constructing 3D models of saccharides from their sequences

Ab initio HMMSTR/Rosetta - Prediction of protein structure from sequence

http://us.expasy.org/tools

Tertiary Structure PredictionComparative modeling

3Djigsaw - Three-dimensional models for proteins based on homologues of known structure

Contreras-Moreira,B., Bates,P.A. (2002) Domain Fishing: a first step in protein comparative modelling. Bioinformatics 18: 1141-1142.

Tertiary Structure PredictionThreading

3D-PSSM - Protein fold recognition using 1D and 3D sequence profiles coupled with secondary structure information (Foldfit) Fugue - Sequence-structure homology recognition HHpred - Protein homology detection and structure prediction by HMM-HMM comparison Libellula - Neural network approach to evaluate fold recognition results LOOPP - Sequence to sequence, sequence to structure, and structure to structure alignment SAM-T02 - HMM-based Protein Structure Prediction Threader - Protein fold recognition ProSup - Protein structure superimposition SWEET - Constructing 3D models of saccharides from their sequences

Tertiary Structure PredictionThreading

The term threading was first coined by Jones, Taylor and Thornton in 1992, and originally referred specifically to the use of a full 3-D structure atomic representation of the protein template in fold recognition. Today, the terms threading and fold recognition are frequently (though somewhat incorrectly) used interchangeably.

The basic idea is that the target sequence (the protein sequence for which the structure is being predicted) is threaded through the backbone structures of a collection of template proteins (known as the fold library) and a “goodness of fit” score calculated for each sequence-structure alignment. This goodness of fit is often derived in terms of an empirical energy function, based on statistics derived from known protein structures, but many other scoring functions have been proposed and tried over the years.

Threading methods share some of the characteristics of both comparative modelling methods (the sequence alignment aspect) and ab initio prediction methods (predicting structure based on identifying low-energy conformations of the target protein).

http://en.wikipedia.org/wiki/Threading_%28protein_sequence%29

Tertiary Structure Prediction

Ab initio (de novo)

• From scratch – using physical property instead of known structures

• Mimic folding process – minimize certain energy function, stochastic modeling (e.g., simulated annealing)

• Computationally expensive – requires large clusters, large machines (e.g., IBM BlueGene) or distributed computing, currently only work for small peptides

• Big potential in the future – understand the dynamics, accuracy, and applications in drug development

Tertiary Structure PredictionAb initio (de novo)

Prediction Scoring with RosettaRosetta uses a scoring function to judge different conformations. The process consists of making 'moves' (changing the bond angles of a particular group of amino acids) and then scoring the new conformation.

The Rosetta score is a weighted sum of component scores, where each component score is judging a different aspect of protein structure.

Environment score: Here, hydrophobic residues as represented as orange stars, so the left conformation is good (all the hydrophobics together) while the rightmost conformation is bad (with the hydrophobic amino acids not touching).

Pair-score: Two conformations of a polypeptide are shown, one (top) where the chain is folded back on itself bringing two cysteins together (yellow+yellow = possible disulphide bond) and forming a salt-bridge (blue+red = opposites attract). The conformation at bottom does not make these pairings and the pair-score would, thus, favor the top conformation.

http://www.grid.org/projects/hpf/howitworks_scoring.htm

Evaluation - CASPCASP - Critical Assessment of Techniques for Protein Structure

Prediction, is a community-wide experiment (though it is commonly referred to as a competition) for protein structure prediction taking place every two years since 1994. (http://predictioncenter.org/)

The main goal of CASP is to obtain an in-depth and objective assessment of our current abilities and inabilities in the area of protein structure prediction. To this end, participants will predict as much as possible about a set of soon to be known structures. These will be true predictions, not ‘post-dictions’ made on already known structures. CASP7 will particularly address the following questions:

1. Are the models produced similar to the corresponding experimental structure?

2. Is the mapping of the target sequence onto the proposed structure (i.e. the alignment) correct?

3. Have similar structures that a model can be based on been identified? 4. Are comparative models more accurate than can be obtained by simply

copying the best template? 5. Has there been progress from the earlier CASPs? 6. What methods are most effective? 7. Where can future effort be most productively focused?

Evaluation - CASPEvaluation of the results is carried out in the following prediction categories:• tertiary structure prediction (all CASPs) • secondary structure prediction (dropped after CASP5) • prediction of structure complexes (CASP2 only; a separate experiment -

CAPRI - carries on this subject) • residue-residue contact prediction (starting CASP4) • disordered regions prediction (starting CASP5) • domain boundary prediction (starting CASP6) • function prediction (starting CASP6) • model quality assessment (starting CASP7) • model refinement (starting CASP7)

Tertiary structure prediction category was further subdivided into• homology modelling • fold recognition (also called protein threading; Note, this is incorrect as

threading is a method) • de novo structure prediction Now referred to as 'New Fold' as many

methods apply evaluation, or scoring, functions that are biased by knowledge of native protein structures, such an example would be an artificial neural network.

Evaluation - CASPNumber of human expert groups registered 207

Number of prediction servers registered 98

Number of targets released 104

Targets canceled 4

Valid targets 100

Refinement targets 9

Prediction formatNumber of groups

contributingNumber of models designated as 1

Total number of models

3D coordinates 180 12393 48339

Alignments to PDB structures

15 966 3896

Residue-residue contacts

17 1473 1561

Structural domains assignments

27 2258 2515

Disordered regions 19 1801 1801

Function prediction 22 1317 1930

Quality assessment 29 2326 3228

Model refinement 26 136 447

All 255 (unique) 22670 63717

Proteomics

The term proteome was coined by Mark Wilkins in 1995 and is used to describe the entire complement of proteins in a given biological organism or system at a given time, i.e. the protein products of the genome. The term has been applied to several different types of biological systems. A cellular proteome is the collection of proteins found in a particular cell type under a particular set of environmental conditions such as exposure to hormone stimulation.

Proteomics vs. Genomics

The proteome is larger than the genome, especially in eukaryotes, in the sense that there are more proteins than genes. This is due to alternative Splicing_(genetics) splicing of genes and post-translational modifications like glycosylation or phosphorylation.

The proteome has at least two levels of complexity lacking in the genome. When the genome is defined by the sequence of nucleotides, the proteome cannot be limited to the sum of the sequences of the proteins present. Knowledge of the proteome requires knowledge of (1) the structure of the proteins in the proteome and (2) the functional interaction between the proteins.

Proteomics Techniques – 2D Gel

Proteomics, the study of the proteome, has largely been practiced through the separation of proteins by two dimensional gel electrophoresis. In the first dimension, the proteins are separated by isoelectric focusing, which resolves proteins on the basis of charge. In the second dimension, proteins are separated by molecular weight using SDS-PAGE. The gel is dyed with Coomassie Blue or silver to visualize the proteins. Spots on the gel are proteins that have migrated to specific locations.

Matching is a big issue

Proteomics Techniques – Mass Spec

Peptide mass fingerprinting identifies a protein by cleaving it into short peptides and then deduces the protein's identity by matching the observed peptide masses against a sequence database. Tandem mass spectrometry, on the other hand, can get sequence information from individual peptides by isolating them, colliding them with a nonreactive gas, and then cataloging the fragment ions produced.

Proteomics Techniques – Mass Spec

Proteomics Techniques – Mass Spec

Proteomics Techniques – Microarray

Measures mRNA level, no change in mRNA does not necessarily mean no change in protein expression and function due to effects of posttranslational modulation.