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Compartments in the eukaryotic cell. Protein targeting/localization signals. Signal peptide Mitochondrial targeting peptide Chloroplast targeting peptide LPxTG sorting signal Peroxisomal targeting signal (PTS2) Signal anchor Nuclear localization signal ER/Golgi retention signal
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Protein targeting/localization signals • Signal peptide • Mitochondrial targeting peptide • Chloroplast targeting peptide • LPxTG sorting signal • Peroxisomal targeting signal (PTS2) • Signal anchor • Nuclear localization signal • ER/Golgi retention signal • Peroxisomal targeting signal (PTS1) • Transmembrane helices Cleaved Uncleaved
Prokaryotic signal peptide logos Gram-negative bacteria Gram-positive bacteria
Positive and negative training data: secreted versus cytoplasmic and nuclear sequences 130 YGIW_ECOLI MAKFAAVIAVMALCSAPVMAAEQGGFSGPSATQSQAGGFQGPNGSVTTVESAKSLRDDTWVTLRGNIVERISDDLYVFKD 80 ASGTINVDIDHKRWNGVTVTPKDTVEIQGEVDKDWNSVEIDVKQIRKVNP 160 SSSSSSSSSSSSSSSSSSSSCMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMM 80 MMMMMMMMMMMMMMMMMMM------------------------------- 160 184 PMFA_PROMI MKLSKIALAAALVFGINSVATAENETPAPKVSSTKGEIQLKGEIVNSACGLAASSSPVIVDFSEIPTSALANLQKAGNIK 80 KDIELQDCDTTVAKTATVSYTPSVVNAVNKDLASFVSGNASGAGIGLMDAGSKAVKWNTATTPVQLINGVSKIPFVAYVQ 160 AESADAKVTPGEFQAVINFQVDYQ 240 SSSSSSSSSSSSSSSSSSSSSSCMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMM 80 MMMMMMMMMMMMMMMMMMM------------------------------------------------------------- 160 ------------------------ 324 CYSB_KLEAE MKLQQLRYIVEVVNHNLNVSSTAEGLYTSQPGISKQVRMLEDELGIQIFARSGKHLTQVTPAGQEIIRIAREVLSKVDAI 80 KSVAGEHTWPDKGSLYVATTHTQARYALPGVIKGFIERYPRVSLHMHQGSPTQIAEAVSKGNADFAIATEALHLYDDLVM 160 LPCYHWNRSIVVTPEHPLATKASVSIEELAQYPLVTYTFGFTGRSELDTAFNRAGLTPRIVFTATDADVIKTYVRLGLGV 240 GVIASMAVDPVSDPDLVKLDANGIFSHSTTKIGFRRSTFLRSYMYDFIQRFAPHLTRDVVDTAVALRSNEDIEAMFKDIK 320 LPEK 400 MMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMM 80 MMMMMMMMMMMMMMMMMMM------------------------------------------------------------- 160 -------------------------------------------------------------------------------- 240 -------------------------------------------------------------------------------- 320 ---- 400 157 SBMC_ECOLI MNYEIKQEEKRTVAGFHLVGPWEQTVKKGFEQLMMWVDSKNIVPKEWVAVYYDNPDETPAEKLRCDTVVTVPGYFTLPEN 80 SEGVILTEITGGQYAVAVARVVGDDFAKPWYQFFNSLLQDSAYEMLPKPCFEVYLNNGAEDGYWDIEMYVAVQPKHH 160 MMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMMM 80 MMMMMMMMMMMMMMMMMMM---------------------------------------------------------- 160
Data partitioning for training and test Training Test Remove highly similar sequences from data set, where cleavage site Information reliably can be transferred by alignment. A redundancy reduced data set can be used to make, say five-fold cross-validation. The training set may ideally contain equal amounts of sequences with negative and positive examples.
Sliding window Sequence: MAKFAAVIAVMALCSAPVMAAEQGGFSGPSATQSQAGGFQGPNGSVTTVES ... Window size here is 9 (example) Window 1: MAKFAAVIA Window 2: AKFAAVIAV Window 3: KFAAVIAVM Window 4: FAAVIAVMA ... Window 10: VMALCSAPV ... For signal peptide prediction typically the first 70 aa of positive and negative sequenes are used.
Symmetric and asymmetric neural network window sizes • SignalP uses two different networks for signal peptide prediction: • Cleavage site prediction network (C-score) • Signal peptide vs. non-signal peptide discrimination • network (S-score) • An asymmetric window is used for cleavage site prediction (more information are found upstream of the cleavage site (see logo)) • A symmetric window is used for discrimination between signal peptide windows and mature protein windows
Performance calculation tp: true positive tn: true negative fp: false positive fn: false negative
Optimization of window sizes Optimization of window sizes for SignalP version 3.0
NN window sizes for SignalP 3.0 Window sizes used in the final method An asymmetric window is best for the cleavage site prediction, whereas symmetric windows is best for discrimination.
SignalP 3.0 architecture In addition to sequence input, composition (entire sequence) and position of the sliding window was used in the neural network of SignalP 3.0
Data set From SWISS-PROT rel. 40.0 Highly curated Cleaned for spurious residues at pos. -1 Length and composition improves the performance significantly Length improves both discrimination and cleavage performance Composition improves discrimination D-score Average of mean-S score and Y-max score Better discrimination What is new in SignalP version 3.0!
Some of the manually curated databases contain obvious errors that can be eliminated General ``SIGNAL´´ errors Signal peptide include propeptide Wrong signal peptide cleavage site The secreted protein is processed by proteases Wrong start codon used Signal peptide of different class, ie. TAT or bacteriocin (prokaryote) Database annotation errors
Signal peptide or propeptide Signal peptide cleavage Propeptide cleavage
Performance of three different SignalP versions SignalP1 paper now has more than 3300 citations, SignalP3 more than 1,200.
Exons and introns: discontinous protein coding regions in eukaryotes
Two ways to solve the problem Predict splice sites (GT-donor and AG-acceptor) or Predict coding versus non-coding (at least in non-UTRs)
C C TGGACCGGGTGA 0.12 0.11 0.10
C TGGACCGGGTGA C 0.12 0.11 0.10 0.14
TGGACCGGGTGA C G 0.12 0.11 0.10 0.14 0.23
1 HUMA1ATP TACATCTTCTTTAAAGGTAAGGTTGCTCAACCA 1 HUMA1ATP CCTGAAGCTCTCCAAGGTGAGATCACCCTGACG 1 HUMACCYBA CCACACCCGCCGCCAGGTAAGCCCGGCCAGCCG 1 HUMACCYBA CGAGAAGATGACCCAGGTGAGTGGCCCGCTACC 1 HUMACTGA GCGCCCCAGACACCAGGTGAGTGGATGGCGCCG 1 HUMACTGA AGAGAAGATGACTCAGGTGAGGCTCGGCCGACG 1 HUMACTGA CACCATGAAGATCAAGGTGAGTCGAGGGGTTGG 1 HUMADAG TCTTATACTATGGCAGGTAAGTCCATACAGAAG 1 HUMALPHA CGTGGCTCTGTCCAAGGTAAGTGCTGGGCTACC 1 HUMALPI CCTGGCTCTGTCCAAGGTAAGGGCTGGGCCACC 1 HUMALPPD TGTGGCTCTGTCCAAGGTAAGTGCTGGGCTACC 1 HUMAPRTA CCTGGAGTACGGGAAGGTAAGAGGGCTGGGGTG 1 HUMCAPG GAAGGCTGCCTTCAAGGTAAGGCATGGGCATTG 1 HUMCFVII GGAGTGTCCATGGCAGGTAAGGCTTCCCCTGGC 1 HUMCP21OH CACCTTGGGCTGCAAGGTGAGAGGCTGATCTCG 1 HUMCP21OHC CACCTTGGGCTGCAAGGTGAGAGGCTGATCTCG 1 HUMCS1 GTGGCAATGGCTCCAGGTAAGCGCCCCTAAAAT 1 HUMCSFGMA AATGTTTGACCTCCAGGTAAGATGCTTCTCTCT 1 HUMCSPB AAAGACTTCCTTTAAGGTAAGACTATGCACCTG 1 HUMCSFGMA AATGTTTGACCTCCAGGTAAGATGCTTCTCTCT 1 HUMCSPB AAAGACTTCCTTTAAGGTAAGACTATGCACCTG 1 HUMCYC1A GCTACGGACACCTCAGGTGAGCGCTGGGCCGGG ... 2 HUMA1ATP CCTGGGACAGTGAATCGTAAGTATGCCTTTCAC 2 HUMA1ATP AAAATGAAGACAGAAGGTGATTCCCCAACCTGA 2 HUMA1GLY2 CGCCACCCTGGACCGGGTGAGTGCCTGGGCTAG 2 HUMA1GLY2 GAGAGTACCAGACCCGGTGAGAGCCCCCATTCC 2 HUMA1GLY2 ACCGTCTCCAGATACGGTGAGGGCCAGCCCTCA 2 HUMA1GLY2 GGGCTGTCTTTCTATGGTAGGCATGCTTAGCAG 2 HUMA1GLY2 CACCGACTGGAAAAAGGTAAACGCAAGGGATTG 2 HUMACCYBA GCGCCCCAGGCACCAGGTAGGGGAGCTGGCTGG 2 HUMACCYBA CAGCCTTCCTTCCTGGGTGAGTGGAGACTGTCT 2 HUMACCYBA CACAATGAAGATCAAGGTGGGTGTCTTTCCTGC 2 HUMACTGA TCGCGTTTCTCTGCCGGTGAGCGCCCCGCCCCG 2 HUMADAG CTTCGACAAGCCCAAAGTGAGCGCGCGCGGGGG 2 HUMADAG TGTCCAGGCCTACCAGGTGGGTCCTGTGAGAAG 2 HUMADAG CGAAGTAGTAAAAGAGGTGAGGGCCTGGGCTGG ... 11 HUMCS1 AACGCAACAGAAATCCGTGAGTGGATGCCGTCT 11 HUMGHN AACACAACAGAAATCCGTGAGTGGATGCCTTCT 52 HUMHSP90B CTCTAATGCTTCTGATGTAGGTGCTCTGGTTTC 80 HUMMETIF1 ACCTCCTGCAAGAAGAGTGAGTGTGAGGCCATC 112 HUMHSP90B ATACCAGAGTATCTCAGTGAGTATCTCCTTGGC 113 HUMHST GCGGACACCCGCGACAGTGAGTGGCGCGGCCAG 113 HUMLACTA GACATCTCCTGTGACAGTGAGTAGCCCCTATAA 151 HUMKAL2 ATCGAACCAGAGGAGTGTACGCCTGGGCCAGAT 157 HUMCS1 CACCTACCAGGAGTTTGTAAGTTCTTGGGGAAT 157 HUMGHN CACCTACCAGGAGTTTGTAAGCTCTTGGGGAAT 164 HUMALPHA CAACATGGACATTGATGTGCGACCCCCGGGCCA 622 HUMCFVII CTGATCGCGGTGCTGGGTGGGTACCACTCTCCC 636 HUMADAG CCTGGAACCAGGCTGAGTGAGTGATGGGCCTGG 895 HUMAPOCIB TCCAGCAAGGATTCAGGTTGTTGAGTGCTTGGG 970 HUMALPHA CGGGCCAAGAAAGCAGGTGGAGCTGGGGCCCGG 2114 HUMAPRTA ATCGACTACATCGCAGGCGAGTGCCAGTGGCCG