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Prediction of protein function Lars Juhl Jensen EMBL Heidelberg
Overview ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Why do we need to predict function?
What do we mean by function? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Descriptions of protein function ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Molecular function ,[object Object],[object Object],[object Object]
Biological process ,[object Object],[object Object],[object Object]
Cellular component ,[object Object],[object Object],[object Object]
Homology-based transfer of annotation Lars Juhl Jensen EMBL Heidelberg
Detection of homologs ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Sequence similarity, sequence homology, and functional homology ,[object Object],[object Object],[object Object],[object Object]
Orthologs vs. paralogs
Functional consequences of gene duplication ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
1–to–1 orthology ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
1–to–many orthology ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Many–to–many orthology ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Detection of orthologs ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Construction of gene trees ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Reciprocal matches ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Orthologous groups ,[object Object],[object Object],[object Object]
Definition of orthologous groups
 
 
COGs, KOGs, and NOGs ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
Clustering based on similarity ,[object Object],[object Object],[object Object],[object Object],[object Object]
 
Meta-servers ,[object Object],[object Object],[object Object]
Function prediction from protein domains Lars Juhl Jensen EMBL Heidelberg
When homology searches fail ,[object Object],[object Object],[object Object]
Protein domains ,[object Object],[object Object],[object Object],[object Object]
 
 
 
 
 
 
 
 
Which domain resource should I use? ,[object Object],[object Object],[object Object],[object Object]
Predicting globular domains and intrinsically disordered regions ,[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
 
 
 
 
Summary ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Acknowledgments ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Prediction of functional motifs from sequence Lars Juhl Jensen EMBL Heidelberg
Proteins – more than just globular domains ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Insulin Receptor Substrate 1
Databases of functional motifs ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
 
 
Prediction of ELMs ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
 
 
Construction of data sets ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Machine learning ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
Kinase-specific prediction of phosphorylation sites (NetPhosK) ,[object Object],[object Object],[object Object],[object Object]
Prediction of signal peptides from sequence (SignalP) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Machine learning can help identify errors in curated databases ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Signal peptide or propeptide
Signal peptide or propeptide Propeptide cleavage Signal peptide cleavage
Wrong start codon
Use of short linear motifs for function prediction ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Feature-based prediction of protein function Lars Juhl Jensen EMBL Heidelberg
Function prediction from post translational modifications ,[object Object],[object Object],[object Object]
The concept of ProtFun
 
Function prediction on the human prion sequence ############## ProtFun 1.1 predictions ############## >PRIO_HUMAN # Functional category  Prob  Odds Amino_acid_biosynthesis  0.020  0.909 Biosynthesis_of_cofactors  0.032  0.444 Cell_envelope  0.146  2.393 Cellular_processes  0.053  0.726 Central_intermediary_metabolism  0.130  2.063 Energy_metabolism  0.029  0.322 Fatty_acid_metabolism  0.017  1.308 Purines_and_pyrimidines  0.528  2.173 Regulatory_functions  0.013  0.081 Replication_and_transcription  0.020  0.075 Translation  0.035  0.795 Transport_and_binding  => 0.831  2.027 # Enzyme/nonenzyme  Prob  Odds Enzyme  0.250  0.873 Nonenzyme  => 0.750  1.051 # Enzyme class  Prob  Odds Oxidoreductase (EC 1.-.-.-)  0.070  0.336 Transferase  (EC 2.-.-.-)  0.031  0.090 Hydrolase  (EC 3.-.-.-)  0.057  0.180 Isomerase  (EC 4.-.-.-)  0.020  0.426 Ligase  (EC 5.-.-.-)  0.010  0.313 Lyase  (EC 6.-.-.-)  0.017  0.334
ProtFun data sets ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Prediction performance on cellular role categories
Prediction performance on enzyme categories
Predictive performance on Gene Ontology categories
Non-classical secretion ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
SecretomeP data sets ,[object Object],[object Object],[object Object],[object Object],[object Object]
Secreted proteins are typically small
ROC plot for SecretomeP
Similar properties of classically and non-classically secreted proteins
 
A look into the black box ,[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
 
SecretomeP feature usage
ProtFun performance for other organisms ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Mapping category performances onto input features
Performance contribution of sequence derived features ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Evolution conserves protein features and function ,[object Object],[object Object],[object Object]
Conclusions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Acknowledgments ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Prediction of functional interaction networks Lars Juhl Jensen EMBL Heidelberg
What is an interaction? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The use of interaction networks for function prediction ,[object Object],[object Object],[object Object]
 
 
Functional interaction networks
Evidence types ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Phylogenetic profiles
 
 
 
Cell Cellulosomes Cellulose
Formalizing the phylogenetic profile method Align all proteins against all Calculate best-hit profile Join similar species by PCA Calculate PC profile distances Calibrate against KEGG maps
Gene neighborhood
Gene neighborhood Identify runs of adjacent genes with the same direction Score each gene pair based on intergenic distances Calibrate against KEGG maps Infer associations in other species
Gene fusion
Gene fusion Find in  A  genes that match a the same gene in  B Exclude overlapping alignments Calibrate against KEGG  maps Calculate all-against-all pairwise alignments
Calibration of quality scores ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Data integration
Protein-protein interaction databases ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Physical protein interactions Make binary representation of complexes Yeast two-hybrid data sets are inherently binary Calculate score from number of (co-)occurrences Calculate score from non-shared partners Calibrate against KEGG maps Infer associations in other species Combine evidence from experiments
Binary representations of purification data
Topology based quality scores ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Mining microarray expression databases Re-normalize arrays by modern method to remove biases Build expression matrix Combine similar arrays by PCA Construct predictor by Gaussian kernel density estimation Calibrate against KEGG maps Infer associations in other species
Databases of curated knowledge ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Co-occurrence in the scientific texts Associate abstracts with species Identify gene names in title/abstract Count (co-)occurrences of genes Test significance of associations Calibrate against KEGG maps Infer associations in other species
Databases used for text mining ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],Natural Language Processing
Multiple types of interactions
Transfer of evidence ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
Evidence transfer based on “fuzzy orthology” ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],? Source species Target species
The power of cross-species transfer and evidence integration
The power of cross-species transfer and evidence integration
The power of cross-species transfer and evidence integration
The power of cross-species transfer and evidence integration
The power of cross-species transfer and evidence integration
The power of cross-species transfer and evidence integration
The big challenge
Prediction of “mode of action”
Summary ,[object Object],[object Object],[object Object],[object Object],[object Object]
Acknowledgments ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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