Pair-wise alignment quality versus sequence identity (Vogt et al., JMB 249, 816-831,1995)

Slides:



Advertisements
Similar presentations
Introduction to bioinformatics Lecture 9 Multiple sequence alignment (3)
Advertisements

1-month Practical Course Genome Analysis (Integrative Bioinformatics & Genomics) Lecture 5: Multiple sequence alignment (2) Centre for Integrative Bioinformatics.
Multiple Alignment Anders Gorm Pedersen Molecular Evolution Group
Structure Prediction (I): Secondary structure Structure Prediction (I): Secondary structure DNA/Protein structure-function analysis and prediction Lecture.
Bioinformatics as an integrative science Jaap Heringa Faculty of Sciences Faculty of Earth and Life Sciences Integrative Bioinformatics Institute VU (IBIVU)
Structural bioinformatics
Sequence analysis course Lecture 8 Sequence databank searching 1.
Sequence analysis lecture 6 Sequence analysis course Lecture 6 Multiple sequence alignment 2 of 3 Multiple alignment methods.
Sequence analysis course Lecture 7 Multiple sequence alignment 3 of 3 Optimizing progressive multiple alignment methods.
Multiple Sequence Alignment Algorithms in Computational Biology Spring 2006 Most of the slides were created by Dan Geiger and Ydo Wexler and edited by.
1-month Practical Course Genome Analysis Lecture 5: Multiple Sequence Alignment Centre for Integrative Bioinformatics VU (IBIVU) Vrije Universiteit Amsterdam.
Multiple alignment June 29, 2007 Learning objectives- Review sequence alignment answer and answer questions you may have. Understand how the E value may.
What you should know by now Concepts: Pairwise alignment Global, semi-global and local alignment Dynamic programming Sequence similarity (Sum-of-Pairs)
C E N T R F O R I N T E G R A T I V E B I O I N F O R M A T I C S V U E Master Course Sequence Alignment Lecture 10 Database searching Issues (1)
C E N T R F O R I N T E G R A T I V E B I O I N F O R M A T I C S V U E Lecture 6 – 07/01/08 Multiple sequence alignment 2 Sequence analysis 2007 Optimizing.
Multiple sequence alignments and motif discovery Tutorial 5.
Multiple sequence alignment
SnapDRAGON: protein 3D prediction-based DOMAINATION: based on PSI-BLAST Two methods to predict domain boundary sequence positions from sequence information.
Multiple Sequence Alignments
1-month Practical Course Genome Analysis Lecture 5: Multiple Sequence Alignment Centre for Integrative Bioinformatics VU (IBIVU) Vrije Universiteit Amsterdam.
CECS Introduction to Bioinformatics University of Louisville Spring 2003 Dr. Eric Rouchka Lecture 3: Multiple Sequence Alignment Eric C. Rouchka,
C E N T R F O R I N T E G R A T I V E B I O I N F O R M A T I C S V U E Lecture 6 – 16/11/06 Multiple sequence alignment 1 Sequence analysis 2006 Multiple.
Introduction to Bioinformatics From Pairwise to Multiple Alignment.
Chapter 5 Multiple Sequence Alignment.
Multiple Sequence Alignment CSC391/691 Bioinformatics Spring 2004 Fetrow/Burg/Miller (Slides by J. Burg)
Multiple sequence alignment
Biology 4900 Biocomputing.
Multiple Sequence Alignment
Multiple Sequence Alignment May 12, 2009 Announcements Quiz #2 return (average 30) Hand in homework #7 Learning objectives-Understand ClustalW Homework#8-Due.
Protein Sequence Alignment and Database Searching.
Bioinformatics For MNW 2 nd Year Jaap Heringa FEW/FALW Integrative Bioinformatics Institute VU (IBIVU)
Pairwise Sequence Alignment. The most important class of bioinformatics tools – pairwise alignment of DNA and protein seqs. alignment 1alignment 2 Seq.
Sequence Based Analysis Tutorial NIH Proteomics Workshop Lai-Su Yeh, Ph.D. Protein Information Resource at Georgetown University Medical Center.
Multiple Sequence Alignments Craig A. Struble, Ph.D. Department of Mathematics, Statistics, and Computer Science Marquette University.
Bioinformatics Multiple Alignment. Overview Introduction Multiple Alignments Global multiple alignment –Introduction –Scoring –Algorithms.
Multiple alignment: Feng- Doolittle algorithm. Why multiple alignments? Alignment of more than two sequences Usually gives better information about conserved.
Sequence Alignment Only things that are homologous should be compared in a phylogenetic analysis Homologous – sharing a common ancestor This is true for.
That have been aligned so that homologous residues are arranged in columns as much as possible. The sequences have different lengths, which means that.
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight.
Multiple sequence alignment
MUSCLE An Attractive MSA Application. Overview Some background on the MUSCLE software. The innovations and improvements of MUSCLE. The MUSCLE algorithm.
Multiple Alignment and Phylogenetic Trees Csc 487/687 Computing for Bioinformatics.
1 Protein Structure Prediction (Lecture for CS397-CXZ Algorithms in Bioinformatics) April 23, 2004 ChengXiang Zhai Department of Computer Science University.
COT 6930 HPC and Bioinformatics Multiple Sequence Alignment Xingquan Zhu Dept. of Computer Science and Engineering.
Techniques for Protein Sequence Alignment and Database Searching (part2) G P S Raghava Scientist & Head Bioinformatics Centre, Institute of Microbial Technology,
Medical Natural Sciences Year 2: Introduction to Bioinformatics Lecture 9: Multiple sequence alignment (III) Centre for Integrative Bioinformatics VU.
Exercises Pairwise alignment Homology search (BLAST) Multiple alignment (CLUSTAL W) Iterative Profile Search: Profile Search –Pfam –Prosite –PSI-BLAST.
Doug Raiford Lesson 5.  Dynamic programming methods  Needleman-Wunsch (global alignment)  Smith-Waterman (local alignment)  BLAST Fixed: best Linear:
Swiss Institute of Bioinformatics Institut Suisse de Bioinformatique LF Multiple alignments, PATTERNS, PSI-BLAST.
MGM workshop. 19 Oct 2010 Some frequently-used Bioinformatics Tools Konstantinos Mavrommatis Prokaryotic Superprogram.
1 Multiple Sequence Alignment(MSA). 2 Multiple Alignment Number of sequences >2 Global alignment Seek an alignment that maximizes score.
Introduction to bioinformatics Lecture 7 Multiple sequence alignment (1)
V diagonal lines give equivalent residues ILS TRIVHVNSILPSTN V I L S T R I V I L P E F S T Sequence A Sequence B Dot Plots, Path Matrices, Score Matrices.
V diagonal lines give equivalent residues ILS TRIVHVNSILPSTN V I L S T R I V I L P E F S T Sequence A Sequence B Dot Plots, Path Matrices, Score Matrices.
Multiple Sequence Alignment (cont.) (Lecture for CS397-CXZ Algorithms in Bioinformatics) Feb. 13, 2004 ChengXiang Zhai Department of Computer Science University.
Multiple Sequence Alignment Dr. Urmila Kulkarni-Kale Bioinformatics Centre University of Pune
Pairwise alignment Now we know how to do it: How do we get a multiple alignment (three or more sequences)? Multiple alignment: much greater combinatorial.
Multiple sequence alignment (msa)
Common Motifs in Kinases and Phosphatases that Share a Substrate
Introduction to bioinformatics 2008 Lecture 8
Multiple Sequence Alignment
Introduction to bioinformatics 2007 Lecture 10
Sequence Based Analysis Tutorial
Multiple sequence alignment Why?
1-month Practical Course
Homology modelling by distance geometry
Introduction to bioinformatics 2007 Lecture 9
Introduction to bioinformatics lecture 9
Introduction to bioinformatics Lecture 8
Presentation transcript:

Pair-wise alignment quality versus sequence identity (Vogt et al., JMB 249, ,1995)

Heuristics Profile pre-processing Secondary structure-guided alignment Globalised local alignment Matrix extension Objective: try to avoid (early) errors Strategies for progressive alignment optimisation

Clustal, ClustalW, ClustalX Neighbour Joining (NJ) algorithm (Saitou and Nei, 1984) to construct guide tree. Sequence blocks are represented by profiles Individual sequences are additionally weighted according to the branch lengths in the NJ tree. Further carefully crafted heuristics include: –(i) local gap penalties –(ii) automatic selection of the amino acid substitution matrix –(iii) automatic gap penalty adjustment –(iv) mechanism to delay alignment of sequences that appear to be distant at the time they are considered. CLUSTAL (W/X) does not allow iteration (Hogeweg and Hesper, 1984; Corpet, 1988, Gotoh, 1996; Heringa, 1999, 2002)

VHLTPEEKSAVTALWGKVNVDE VGGEALGRLLVVYPWTQRFFE SFGDLSTPDAVMGNPKVKAHG KKVLGAFSDGLAHLDNLKGTFA TLSELHCDKLHVDPENFRLLGN VLVCVLAHHFGKEFTPPVQAAY QKVVAGVANALAHKYH PRIMARY STRUCTURE (amino acid sequence) QUATERNARY STRUCTURE (oligomers) SECONDARY STRUCTURE (helices, strands) TERTIARY STRUCTURE (fold) Protein structure hierarchical levels

Flavodoxin fold: (Helix-beta-helix)

Flavodoxin-cheY NJ tree

1fx1 -PKALIVYGSTTGNTEYTAETIARQLANAG-Y-EVDSRDAASVEAGGLFEGFDLVLLGCSTWGDDSIE------LQDDFIPLFD-SLEETGAQGRK FLAV_DESVH MPKALIVYGSTTGNTEYTAETIARELADAG-Y-EVDSRDAASVEAGGLFEGFDLVLLGCSTWGDDSIE------LQDDFIPLFD-SLEETGAQGRK FLAV_DESGI MPKALIVYGSTTGNTEGVAEAIAKTLNSEG-M-ETTVVNVADVTAPGLAEGYDVVLLGCSTWGDDEIE------LQEDFVPLYE-DLDRAGLKDKK FLAV_DESSA MSKSLIVYGSTTGNTETAAEYVAEAFENKE-I-DVELKNVTDVSVADLGNGYDIVLFGCSTWGEEEIE------LQDDFIPLYD-SLENADLKGKK FLAV_DESDE MSKVLIVFGSSTGNTESIAQKLEELIAAGG-H-EVTLLNAADASAENLADGYDAVLFGCSAWGMEDLE------MQDDFLSLFE-EFNRFGLAGRK FLAV_CLOAB -MKISILYSSKTGKTERVAKLIEEGVKRSGNI-EVKTMNLDAVDKKFLQE-SEGIIFGTPTYYAN ISWEMKKWID-ESSEFNLEGKL FLAV_MEGEL --MVEIVYWSGTGNTEAMANEIEAAVKAAG-A-DVESVRFEDTNVDDVAS-KDVILLGCPAMGSE--E------LEDSVVEPFF-TDLAPKLKGKK 4fxn ---MKIVYWSGTGNTEKMAELIAKGIIESG-K-DVNTINVSDVNIDELLN-EDILILGCSAMGDE--V------LEESEFEPFI-EEISTKISGKK FLAV_ANASP SKKIGLFYGTQTGKTESVAEIIRDEFGNDVVT----LHDVSQAEVTDLND-YQYLIIGCPTWNIGELQ---SD-----WEGLYS-ELDDVDFNGKL FLAV_AZOVI -AKIGLFFGSNTGKTRKVAKSIKKRFDDETMSD---ALNVNRVSAEDFAQ-YQFLILGTPTLGEGELPGLSSDCENESWEEFLP-KIEGLDFSGKT 2fcr --KIGIFFSTSTGNTTEVADFIGKTLGAKADAP---IDVDDVTDPQALKD-YDLLFLGAPTWNTGADTERSGT----SWDEFLYDKLPEVDMKDLP FLAV_ENTAG MATIGIFFGSDTGQTRKVAKLIHQKLDGIADAP---LDVRRATREQFLS--YPVLLLGTPTLGDGELPGVEAGSQYDSWQEFTN-TLSEADLTGKT FLAV_ECOLI -AITGIFFGSDTGNTENIAKMIQKQLGKDVAD----VHDIAKSSKEDLEA-YDILLLGIPTWYYGEAQ-CD WDDFFP-TLEEIDFNGKL 3chy --ADKELKFLVVDDFSTMRRIVRNLLKELG----FNNVEEAEDGVDALN------KLQAGGYGFV--I------SDWNMPNMDG-LELLKTIR :.. : 1fx1 VACFGCGDSSYEYF--CGAVDAIEEKLKNLGAEIVQDG LRIDGDPRAARDDIVGWAHDVRGAI FLAV_DESVH VACFGCGDSSYEYF--CGAVDAIEEKLKNLGAEIVQDG LRIDGDPRAARDDIVGWAHDVRGAI FLAV_DESGI VGVFGCGDSSYTYF--CGAVDVIEKKAEELGATLVASS LKIDGEPDSAE--VLDWAREVLARV FLAV_DESSA VSVFGCGDSDYTYF--CGAVDAIEEKLEKMGAVVIGDS LKIDGDPERDE--IVSWGSGIADKI FLAV_DESDE VAAFASGDQEYEHF--CGAVPAIEERAKELGATIIAEG LKMEGDASNDPEAVASFAEDVLKQL FLAV_CLOAB GAAFSTANSIAGGS--DIALLTILNHLMVKGMLVYSGGVA----FGKPKTHLGYVHINEIQENEDENARIFGERIANKVKQIF FLAV_MEGEL VGLFGSYGWGSGE-----WMDAWKQRTEDTGATVIGTA IVN-EMPDNAPECKE-LGEAAAKA fxn VALFGSYGWGDGK-----WMRDFEERMNGYGCVVVETP LIVQNEPDEAEQDCIEFGKKIANI FLAV_ANASP VAYFGTGDQIGYADNFQDAIGILEEKISQRGGKTVGYWSTDGYDFNDSKALR-NGKFVGLALDEDNQSDLTDDRIKSWVAQLKSEFGL FLAV_AZOVI VALFGLGDQVGYPENYLDALGELYSFFKDRGAKIVGSWSTDGYEFESSEAVV-DGKFVGLALDLDNQSGKTDERVAAWLAQIAPEFGLSL---- 2fcr VAIFGLGDAEGYPDNFCDAIEEIHDCFAKQGAKPVGFSNPDDYDYEESKSVR-DGKFLGLPLDMVNDQIPMEKRVAGWVEAVVSETGV FLAV_ENTAG VALFGLGDQLNYSKNFVSAMRILYDLVIARGACVVGNWPREGYKFSFSAALLENNEFVGLPLDQENQYDLTEERIDSWLEKLKPAVL FLAV_ECOLI VALFGCGDQEDYAEYFCDALGTIRDIIEPRGATIVGHWPTAGYHFEASKGLADDDHFVGLAIDEDRQPELTAERVEKWVKQISEELHLDEILNA 3chy AD--GAMSALPVL-----MVTAEAKKENIIAAAQAGAS GYV-VKPFTAATLEEKLNKIFEKLGM :.. ClustalW Flavodoxin-cheY

Pre-profile generation Score 1-2 Score 1-3 Score 4-5 ACD..YACD..Y ACD..YACD..Y Pre-profiles Pre-alignments ACD..YACD..Y Cut-off

Flavodoxin-cheY: Pre-processing (cut-off  1500) 1fx1 -PKALIVYGSTTGNT-EYTAETIARQLANAG-YEVDSRDAASVEAGGLFEGFDLVLLGCSTWGDDSI------ELQDDFIPLF-DSLEETGAQGRKVACF FLAV_DESDE MSKVLIVFGSSTGNT-ESIaQKLEELIAAGG-HEVTLLNAADASAENLADGYDAVLFgCSAWGMEDL------EMQDDFLSLF-EEFNRFGLAGRKVAAf FLAV_DESVH MPKALIVYGSTTGNT-EYTaETIARELADAG-YEVDSRDAASVEAGGLFEGFDLVLLgCSTWGDDSI------ELQDDFIPLF-DSLEETGAQGRKVACf FLAV_DESSA MSKSLIVYGSTTGNT-ETAaEYVAEAFENKE-IDVELKNVTDVSVADLGNGYDIVLFgCSTWGEEEI------ELQDDFIPLY-DSLENADLKGKKVSVf FLAV_DESGI MPKALIVYGSTTGNT-EGVaEAIAKTLNSEG-METTVVNVADVTAPGLAEGYDVVLLgCSTWGDDEI------ELQEDFVPLY-EDLDRAGLKDKKVGVf 2fcr --KIGIFFSTSTGNT-TEVADFIGKTLGA---KADAPIDVDDVTDPQALKDYDLLFLGAPTWNTG----ADTERSGTSWDEFLYDKLPEVDMKDLPVAIF FLAV_AZOVI -AKIGLFFGSNTGKT-RKVaKSIKKRFDDET-MSDA-LNVNRVS-AEDFAQYQFLILgTPTLGEGELPGLSSDCENESWEEFL-PKIEGLDFSGKTVALf FLAV_ENTAG MATIGIFFGSDTGQT-RKVaKLIHQKLDG---IADAPLDVRRAT-REQFLSYPVLLLgTPTLGDGELPGVEAGSQYDSWQEFT-NTLSEADLTGKTVALf FLAV_ANASP SKKIGLFYGTQTGKT-ESVaEIIRDEFGN---DVVTLHDVSQAE-VTDLNDYQYLIIgCPTWNIGEL QSDWEGLY-SELDDVDFNGKLVAYf FLAV_ECOLI -AITGIFFGSDTGNT-ENIaKMIQKQLGK---DVADVHDIAKSS-KEDLEAYDILLLgIPTWYYGE AQCDWDDFF-PTLEEIDFNGKLVALf 4fxn -MK--IVYWSGTGNT-EKMAELIAKGIIESG-KDVNTINVSDVNIDELL-NEDILILGCSAMGDEVL EESEFEPFI-EEIS-TKISGKKVALF FLAV_MEGEL MVE--IVYWSGTGNT-EAMaNEIEAAVKAAG-ADVESVRFEDTNVDDVA-SKDVILLgCPAMGSEEL EDSVVEPFF-TDLA-PKLKGKKVGLf FLAV_CLOAB -MKISILYSSKTGKT-ERVaKLIEEGVKRSGNIEVKTMNLDAVD-KKFLQESEGIIFgTPTYYAN ISWEMKKWI-DESSEFNLEGKLGAAf 3chy ADKELKFLVVDDFSTMRRIVRNLLKELGFN--NVEEAEDGVDALNKLQAGGYGFVI---SDWNMPNM DGLELL-KTIRADGAMSALPVLM T 1fx1 GCGDS-SY-EYFCGA-VDAIEEKLKNLGAEIVQD GLRIDGD--PRAARDDIVGWAHDVRGAI FLAV_DESDE ASGDQ-EY-EHFCGA-VPAIEERAKELgATIIAE GLKMEGD--ASNDPEAVASfAEDVLKQL FLAV_DESVH GCGDS-SY-EYFCGA-VDAIEEKLKNLgAEIVQD GLRIDGD--PRAARDDIVGwAHDVRGAI FLAV_DESSA GCGDS-DY-TYFCGA-VDAIEEKLEKMgAVVIGD SLKIDGD--PE--RDEIVSwGSGIADKI FLAV_DESGI GCGDS-SY-TYFCGA-VDVIEKKAEELgATLVAS SLKIDGE--PD--SAEVLDwAREVLARV fcr GLGDAEGYPDNFCDA-IEEIHDCFAKQGAKPVGFSNPDDYDYEESKS-VRDGKFLGLPLDMVNDQIPMEKRVAGWVEAVVSETGV FLAV_AZOVI GLGDQVGYPENYLDA-LGELYSFFKDRgAKIVGSWSTDGYEFESSEA-VVDGKFVGLALDLDNQSGKTDERVAAwLAQIAPEFGLS--L-- FLAV_ENTAG GLGDQLNYSKNFVSA-MRILYDLVIARgACVVGNWPREGYKFSFSAALLENNEFVGLPLDQENQYDLTEERIDSwLEKLKPAV-L FLAV_ANASP GTGDQIGYADNFQDA-IGILEEKISQRgGKTVGYWSTDGYDFNDSKA-LRNGKFVGLALDEDNQSDLTDDRIKSwVAQLKSEFGL FLAV_ECOLI GCGDQEDYAEYFCDA-LGTIRDIIEPRgATIVGHWPTAGYHFEASKGLADDDHFVGLAIDEDRQPELTAERVEKwVKQISEELHLDEILNA 4fxn G-----SY-GWGDGKWMRDFEERMNGYGCVVVET PLIVQNE--PDEAEQDCIEFGKKIANI FLAV_MEGEL G-----SY-GWGSGEWMDAWKQRTEDTgATVIGT AIVNEM--PDNA-PECKElGEAAAKA FLAV_CLOAB STANSIAGGSDIA---LLTILNHLMVKgMLVYSG----GVAFGKPKTHLGYVHINEIQENEDENARIfGERiANkVKQIF chy VTAEAKK--ENIIAA AQAGAS GYVV-----KPFTAATLEEKLNKIFEKLGM G

Using structural information 10 years SS prediction method development: Accuracy ± 5% 10 years MSA method development: Accuracy can be ± 40% Amino acid patterns Secondary structure patterns Super-secondary structure patterns Alternate matrices with associated gap penalties according to region

How to combine ss and aa info Dynamic programming search matrix Amino acid substitution matrices MDAGSTVILCFV HHHCCCEEEEEE MDAASTILCGSMDAASTILCGS HHHHCCEEECCHHHHCCEEECC C H E H C E Default

In terms of scoring… So how would you score a profile using this extra information? –Same formula as in lecture 6, but you can use sec. struct. specific substitution scores in various combinations. Where does it fit in? –Very important: structure is always more conserved than sequence so it can help with the insertion(or not) of gaps.

Sequences to be aligned Predict secondary structure HHHHCCEEECCCEEECCHH HHHCCCCEECCCEEHHH HHHHHHHHHHHHHCCCEEEE CCCCCCEECCCEEEECCHH HHHHHCCEEEECCCEECCC Align sequences using secondary structure Secondary structure Multiple alignment

Using predicted secondary structure 1fx1 -PK-ALIVYGSTTGNTEYTAETIARQLANAG-YEVDSRDAASVEAGGLFEGFDLVLLGCSTWGDDSI------ELQDDFIPLFDS-LEETGAQGRKVACF e eeee b ssshhhhhhhhhhhhhhttt eeeee stt tttttt seeee b ee sss ee ttthhhhtt ttss tt eeeee FLAV_DESVH MPK-ALIVYGSTTGNTEYTaETIARELADAG-YEVDSRDAASVEAGGLFEGFDLVLLgCSTWGDDSI------ELQDDFIPLFDS-LEETGAQGRKVACf e eeeeee hhhhhhhhhhhhhhh eeeeee eeeeee hhhhhh eeeee FLAV_DESGI MPK-ALIVYGSTTGNTEGVaEAIAKTLNSEG-METTVVNVADVTAPGLAEGYDVVLLgCSTWGDDEI------ELQEDFVPLYED-LDRAGLKDKKVGVf e eeeeee hhhhhhhhhhhhhh eeeeee hhhhhh eeeeeee hhhhhh eeeeee FLAV_DESSA MSK-SLIVYGSTTGNTETAaEYVAEAFENKE-IDVELKNVTDVSVADLGNGYDIVLFgCSTWGEEEI------ELQDDFIPLYDS-LENADLKGKKVSVf eeeeee hhhhhhhhhhhhhh eeeee eeeee hhhhhhh h eeeee FLAV_DESDE MSK-VLIVFGSSTGNTESIaQKLEELIAAGG-HEVTLLNAADASAENLADGYDAVLFgCSAWGMEDL------EMQDDFLSLFEE-FNRFGLAGRKVAAf eeee hhhhhhhhhhhhhh eeeee hhhhhhhhhhheeeee hhhhhhh hh eeeee 2fcr --K-IGIFFSTSTGNTTEVADFIGKTLGAK---ADAPIDVDDVTDPQALKDYDLLFLGAPTWNTGAD----TERSGTSWDEFLYDKLPEVDMKDLPVAIF eeeee ssshhhhhhhhhhhhhggg b eeggg s gggggg seeeeeee stt s s s sthhhhhhhtggg tt eeeee FLAV_ANASP SKK-IGLFYGTQTGKTESVaEIIRDEFGND--VVTL-HDVSQAE-VTDLNDYQYLIIgCPTWNIGEL QSDWEGLYSE-LDDVDFNGKLVAYf eeeee hhhhhhhhhhhh eee hhh hhhhhhheeeeee hhhhhhhhh eeeeee FLAV_ECOLI -AI-TGIFFGSDTGNTENIaKMIQKQLGKD--VADV-HDIAKSS-KEDLEAYDILLLgIPTWYYGEA QCDWDDFFPT-LEEIDFNGKLVALf eee hhhhhhhhhhhh eee hhh hhhhhhheeeee hhhhh eeeeee FLAV_AZOVI -AK-IGLFFGSNTGKTRKVaKSIKKRFDDET-MSDA-LNVNRVS-AEDFAQYQFLILgTPTLGEGELPGLSSDCENESWEEFLPK-IEGLDFSGKTVALf eee hhhhhhhhhhhhh hhh hhhhhhheeeee hhhhhhhhh eeeeee FLAV_ENTAG MAT-IGIFFGSDTGQTRKVaKLIHQKLDG---IADAPLDVRRAT-REQFLSYPVLLLgTPTLGDGELPGVEAGSQYDSWQEFTNT-LSEADLTGKTVALf eeee hhhhhhhhhhhh hhh hhhhhhheeeee hhhhh eeeee 4fxn ----MKIVYWSGTGNTEKMAELIAKGIIESG-KDVNTINVSDVNIDELLNE-DILILGCSAMGDEVL------E-ESEFEPFIEE-IST-KISGKKVALF eeeee ssshhhhhhhhhhhhhhhtt eeeettt sttttt seeeeee btttb ttthhhhhhh hst t tt eeeee FLAV_MEGEL M---VEIVYWSGTGNTEAMaNEIEAAVKAAG-ADVESVRFEDTNVDDVASK-DVILLgCPAMGSEEL------E-DSVVEPFFTD-LAP-KLKGKKVGLf hhhhhhhhhhhhhh eeeee hhhhhhhh eeeee eeeee FLAV_CLOAB M-K-ISILYSSKTGKTERVaKLIEEGVKRSGNIEVKTMNL-DAVDKKFLQESEGIIFgTPTY-YANI SWEMKKWIDE-SSEFNLEGKLGAAf eee hhhhhhhhhhhhhh eeeeee hhhhhhhhhh eeee hhhhhhhhh eeeee 3chy ADKELKFLVVDDFSTMRRIVRNLLKELGFNN-VEEAEDGV-DALNKLQAGGYGFVISD---WNMPNM DGLELLKTIRADGAMSALPVLMV tt eeee s hhhhhhhhhhhhhht eeeesshh hhhhhhhh eeeee s sss hhhhhhhhhh ttttt eeee 1fx1 GCGDS-SY-EYFCGAVDAIEEKLKNLGAEIVQD GLRIDGD--PRAARDDIVGWAHDVRGAI eee s ss sstthhhhhhhhhhhttt ee s eeees gggghhhhhhhhhhhhhh FLAV_DESVH GCGDS-SY-EYFCGAVDAIEEKLKNLgAEIVQD GLRIDGD--PRAARDDIVGwAHDVRGAI eee hhhhhhhhhhhh eeeee eeeee hhhhhhhhhhhhhh FLAV_DESGI GCGDS-SY-TYFCGAVDVIEKKAEELgATLVAS SLKIDGE--P--DSAEVLDwAREVLARV eee hhhhhhhhhhhh eeeee hhhhhhhhhhh FLAV_DESSA GCGDS-DY-TYFCGAVDAIEEKLEKMgAVVIGD SLKIDGD--P--ERDEIVSwGSGIADKI hhhhhhhhhhhh eeeee e eee FLAV_DESDE ASGDQ-EY-EHFCGAVPAIEERAKELgATIIAE GLKMEGD--ASNDPEAVASfAEDVLKQL e hhhhhhhhhhhhhh eeeee ee hhhhhhhhhhh 2fcr GLGDAEGYPDNFCDAIEEIHDCFAKQGAKPVGFSNPDDYDYEESKSVRD-GKFLGLPLDMVNDQIPMEKRVAGWVEAVVSETGV eee ttt ttsttthhhhhhhhhhhtt eee b gggs s tteet teesseeeettt ss hhhhhhhhhhhhhhhht FLAV_ANASP GTGDQIGYADNFQDAIGILEEKISQRgGKTVGYWSTDGYDFNDSKALR-NGKFVGLALDEDNQSDLTDDRIKSwVAQLKSEFGL hhhhhhhhhhhhhh eeee hhhhhhhhhhhhhhhh FLAV_ECOLI GCGDQEDYAEYFCDALGTIRDIIEPRgATIVGHWPTAGYHFEASKGLADDDHFVGLAIDEDRQPELTAERVEKwVKQISEELHLDEILNA hhhhhhhhhhhhhh eeee hhhhhhhhhhhhhhhhhh FLAV_AZOVI GLGDQVGYPENYLDALGELYSFFKDRgAKIVGSWSTDGYEFESSEAVVD-GKFVGLALDLDNQSGKTDERVAAwLAQIAPEFGLS--L-- e hhhhhhhhhhhhhh eeeee hhhhhhhhhhh FLAV_ENTAG GLGDQLNYSKNFVSAMRILYDLVIARgACVVGNWPREGYKFSFSAALLENNEFVGLPLDQENQYDLTEERIDSwLEKLKPAV-L hhhhhhhhhhhhhhh eeee hhhhhhh hhhhhhhhhhhh 4fxn G-----SYGWGDGKWMRDFEERMNGYGCVVVET PLIVQNE--PDEAEQDCIEFGKKIANI e eesss shhhhhhhhhhhhtt ee s eeees ggghhhhhhhhhhhht FLAV_MEGEL G-----SYGWGSGEWMDAWKQRTEDTgATVIGT AIVNEM--PDNAPE-CKElGEAAAKA hhhhhhhhhhh eeeee eeee h hhhhhhhh FLAV_CLOAB STANSIA-GGSDIALLTILNHLMVK-gMLVYSG----GVAFGKPKTHLG-----YVHINEI--QENEDENARIfGERiANkV--KQIF-- hhhhhhhhhhhhhh eeeee hhhh hhh hhhhhhhhhhhh h 3chy TAEAKKENIIAAAQAGASGY VVK----P-FTAATLEEKLNKIFEKLGM ess hhhhhhhhhtt see ees s hhhhhhhhhhhhhhht G

T-COFFEE Integrating different pair-wise alignment techniques (NW, SW,..) Combining different multiple alignment methods (consensus multiple alignment) Combining sequence alignment methods with structural alignment techniques Plug in user knowledge

Search matrix extension

The T-coffee effect Direct alignment Other sequences Here you see that although a direst alignment might choose one path, using information from the other sequences (T-COFFEE) finds an alternate and usually better one

but..... T-COFFEE (V1.23) multiple sequence alignment Flavodoxin-cheY 1fx1 ----PKALIVYGSTTGNTEYTAETIARQLANAG-YEVDSRDAASVE-AGGLFEGFDLVLLGCSTWGDDSIE------LQDDFIPL-FDSLEETGAQGRK----- FLAV_DESVH ---MPKALIVYGSTTGNTEYTAETIARELADAG-YEVDSRDAASVE-AGGLFEGFDLVLLGCSTWGDDSIE------LQDDFIPL-FDSLEETGAQGRK----- FLAV_DESGI ---MPKALIVYGSTTGNTEGVAEAIAKTLNSEG-METTVVNVADVT-APGLAEGYDVVLLGCSTWGDDEIE------LQEDFVPL-YEDLDRAGLKDKK----- FLAV_DESSA ---MSKSLIVYGSTTGNTETAAEYVAEAFENKE-IDVELKNVTDVS-VADLGNGYDIVLFGCSTWGEEEIE------LQDDFIPL-YDSLENADLKGKK----- FLAV_DESDE ---MSKVLIVFGSSTGNTESIAQKLEELIAAGG-HEVTLLNAADAS-AENLADGYDAVLFGCSAWGMEDLE------MQDDFLSL-FEEFNRFGLAGRK fxn MKIVYWSGTGNTEKMAELIAKGIIESG-KDVNTINVSDVN-IDELL-NEDILILGCSAMGDEVLE ESEFEPF-IEEIS-TKISGKK----- FLAV_MEGEL -----MVEIVYWSGTGNTEAMANEIEAAVKAAG-ADVESVRFEDTN-VDDVA-SKDVILLGCPAMGSEELE DSVVEPF-FTDLA-PKLKGKK----- FLAV_CLOAB ----MKISILYSSKTGKTERVAKLIEEGVKRSGNIEVKTMNLDAVD-KKFLQ-ESEGIIFGTPTYYAN ISWEMKKW-IDESSEFNLEGKL fcr -----KIGIFFSTSTGNTTEVADFIGKTLGAKA---DAPIDVDDVTDPQAL-KDYDLLFLGAPTWNTGA----DTERSGTSWDEFLYDKLPEVDMKDLP----- FLAV_ENTAG ---MATIGIFFGSDTGQTRKVAKLIHQKLDGIA---DAPLDVRRAT-REQF-LSYPVLLLGTPTLGDGELPGVEAGSQYDSWQEF-TNTLSEADLTGKT----- FLAV_ANASP ---SKKIGLFYGTQTGKTESVAEIIRDEFGNDV---VTLHDVSQAE-VTDL-NDYQYLIIGCPTWNIGEL QSDWEGL-YSELDDVDFNGKL----- FLAV_AZOVI ----AKIGLFFGSNTGKTRKVAKSIKKRFDDET-M-SDALNVNRVS-AEDF-AQYQFLILGTPTLGEGELPGLSSDCENESWEEF-LPKIEGLDFSGKT----- FLAV_ECOLI ----AITGIFFGSDTGNTENIAKMIQKQLGKDV---ADVHDIAKSS-KEDL-EAYDILLLGIPTWYYGEA QCDWDDF-FPTLEEIDFNGKL chy ADKELKFLVVD--DFSTMRRIVRNLLKELGFN-NVE-EAEDGVDALNKLQ-AGGYGFVISDWNMPNMDGLE LLKTIRADGAMSALPVLMV :... :. :: 1fx VACFGCGDSS--YEYFCGA-VDAIEEKLKNLGAEIVQDG LRIDGDPRAA--RDDIVGWAHDVRGAI FLAV_DESVH VACFGCGDSS--YEYFCGA-VDAIEEKLKNLGAEIVQDG LRIDGDPRAA--RDDIVGWAHDVRGAI FLAV_DESGI VGVFGCGDSS--YTYFCGA-VDVIEKKAEELGATLVASS LKIDGEPDSA----EVLDWAREVLARV FLAV_DESSA VSVFGCGDSD--YTYFCGA-VDAIEEKLEKMGAVVIGDS LKIDGDPE----RDEIVSWGSGIADKI FLAV_DESDE VAAFASGDQE--YEHFCGA-VPAIEERAKELGATIIAEG LKMEGDASND--PEAVASFAEDVLKQL fxn VALFGS------YGWGDGKWMRDFEERMNGYGCVVVETP LIVQNEPD--EAEQDCIEFGKKIANI FLAV_MEGEL VGLFGS------YGWGSGEWMDAWKQRTEDTGATVIGTA IV--NEMP--DNAPECKELGEAAAKA FLAV_CLOAB GAAFSTANSI--AGGSDIA-LLTILNHLMVKGMLVY----SGGVAFGKPKTHLGYVHINEIQENEDENARIFGERIANKVKQIF fcr VAIFGLGDAEGYPDNFCDA-IEEIHDCFAKQGAKPVGFSNPDDYDYEESKSVRDG-KFLGLPLDMVNDQIPMEKRVAGWVEAVVSETGV FLAV_ENTAG VALFGLGDQLNYSKNFVSA-MRILYDLVIARGACVVGNWPREGYKFSFSAALLENNEFVGLPLDQENQYDLTEERIDSWLEKLKPAVL FLAV_ANASP VAYFGTGDQIGYADNFQDA-IGILEEKISQRGGKTVGYWSTDGYDFNDSKALRNG-KFVGLALDEDNQSDLTDDRIKSWVAQLKSEFGL FLAV_AZOVI VALFGLGDQVGYPENYLDA-LGELYSFFKDRGAKIVGSWSTDGYEFESSEAVVDG-KFVGLALDLDNQSGKTDERVAAWLAQIAPEFGLSL---- FLAV_ECOLI VALFGCGDQEDYAEYFCDA-LGTIRDIIEPRGATIVGHWPTAGYHFEASKGLADDDHFVGLAIDEDRQPELTAERVEKWVKQISEELHLDEILNA 3chy TAEAKKENIIAAAQAGASGYVVKPFT---AATLEEKLNKIFEKLGM

Multiple alignment methods Multi-dimensional dynamic programming Progressive alignment Iterative alignment FROM HERE ON REFER TO THE PRALINE PAPER FOR HELP See further reading section online

Iteration fates Convergence Limit cycle Divergence

Iterative schemes Do an alignment Learn from it Do it better next time round HOW???? Consistency iteration Pre-profile update iteration Improved secondary structure iteration

Consistency scoring Ala131 A131 L133 C126 A131 5

Consistency iteration Pre-profiles Multiple alignment positionalconsistencyscores

Pre-profile update iteration Pre-profiles Multiple alignment

Is the initial ss prediction good enough? 3chy-AA SEQUENCE|| AA |ADKELKFLVVDDFSTMRRIVRNLLKELGFNNVEEAEDGVDALNKLQAGGYGFVISDWNMP| 3chy-AA SEQUENCE|| AA |NMDGLELLKTIRADGAMSALPVLMVTAEAKKENIIAAAQAGASGYVVKPFTAATLEEKLNKIFEKLGM| 3chy-ITERATION-0|| PHD | EEEEEEE HHHHHHHHHHHHHHHHH E HHHHHHHHHH HHHEEE | 3chy-ITERATION-0|| PHD | HHHHHHEEEEEE HHHHHHHHHHHHHHHHH HHHHHHHHHHHHHH | 3chy-ITERATION-1|| PHD | EEEEEEEE HHHHHHHHHHHHHHH HHHHHHHH EEEEEE | 3chy-ITERATION-1|| PHD | HHHHHHEEEEEE HHH HHHHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-2|| PHD | EEEEEEEE HHHHHHHHHHHHHH HHHHHHHHH EEEEEE | 3chy-ITERATION-2|| PHD | HHHHHHEEEEEE HHHHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-3|| PHD | EEEEEEEE HHHHHHHHHHHHHH EEE HHHHHH EEEEE | 3chy-ITERATION-3|| PHD | HHHHHHHHHHHH HHHHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-4|| PHD | EEEEEEEE HHHHHHHHHHHHHH HHHHHHH EEEEE | 3chy-ITERATION-4|| PHD | HHHHH EEEEE HHHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-5|| PHD | EEEEEEEE HHHHHHHHHHHHHH EEE HHHHHH EEEEE | 3chy-ITERATION-5|| PHD | HHHHHHHH EEEEE HHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-6|| PHD | EEEEEEEE HHHHHHHHHHHHHH HHHHHHHH EEEEEE | 3chy-ITERATION-6|| PHD | HHHHHHHH EEEEE HHHHHHHHHHHHHHHH EEEE HHHHHHHHHHHHHH | 3chy-ITERATION-7|| PHD | EEEEEEEE HHHHHHHHHHHHHH EEE HHHHHH EEEEE | 3chy-ITERATION-7|| PHD | HHHHHHHH EEEEEE HHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-8|| PHD | EEEEEEEE HHHHHHHHHHHHHH HHHHHHH EEEEEE | 3chy-ITERATION-8|| PHD | HHHHHHHH EEEEE HHHHHHHHHHHHHHHH EEE HHHHHHHHHHHHHH | 3chy-ITERATION-9|| PHD | EEEEEEEE HHHHHHHHHHHHHH HHHHHHHHHH EEEEE | 3chy-ITERATION-9|| PHD | HHHHHHHH EEEEE HHHHHHHHHHHHHHH EEEE HHHHHHHHHHHHHH |

Sequences to be aligned Align using secondary structure Predict secondary structure HHHHCCEEECCCEEECCHH HHHCCCCEECCCEEHHH HHHHHHHHHHHHHCCCEEEE CCCCCCEECCCEEEECCHH HHHHHCCEEEECCCEECCC Secondary structure Multiple alignment HHHHHCCEEEECCCEECCC Single SequenceMA-based

So what do we do??? A single shot for a good alignment without thinking: MUSCLE, T-Coffee (maybe POA) If you want to experiment with making alignments for a given sequence set: PRALINE –Profile pre-processing –Iteration –Secondary structure-induced alignment –Globalised local alignment There is no single method that always generates the best alignment Therefore best is to use more than one method: e.g. include Dialign2 (local)

Summary Weighting schemes simulating simultaneous multiple alignment –Profile pre-processing (global/local) –Matrix extension (well balanced scheme) Using additional information –secondary structure driven alignment Schemes strike balance between speed and sensitivity