Protein Structure Prediction: Homology Modeling & Threading/Fold Recognition D. Mohanty NII, New Delhi.

Protein Structure Prediction:Homology Modeling

&Threading/Fold Recognition

D. Mohanty

NII, New Delhi

Experimental Methods for Structure Determination

Computational Approaches for Protein Structure Prediction

•Methods based on laws of physical chemistry

Ab initio folding using Molecular Mechanics

Forcefield

•Knowledge-based Methods Homology Modelling

Fold Recognition or Threading

Interactions between atoms in a protein

Schematic depiction of the free energy surface of a protein

Energy MinimizationMolecular Dynamics Monte Carlo Simulations

Computational tools for exploringenergy surface & locating minimas

Structure Prediction Flowchart

http://www.bmm.icnet.uk/people/rob/CCP11BBS/flowchart2.html

Homology Modelling

Homology (or Comparative) modelling involves, building a 3D model for a protein of unknown structure (the target) on the basis of sequence similarity to proteins of known structure (the templates).

Necessary requirements for homology modeling:•Sequence similarity between the target and the template

must be detectable.

•Substantially correct alignment between the target

sequence and template must be calculated.

Homology or comparative modelling is Possible because:•The 3D structures of the proteins in a family are more conserved than their sequences. Therefore, if similarity between two proteins is detectable at the sequence level,structural similarity can usually be assumed.•Small changes in protein sequence usually results in small changes in 3D structure.

But large changes in protein sequence can also result in small changes in its 3D structure i.e. Proteins with non-detectable sequence similarity can have similar structures.

Steps in ComparativeProtein StructureModelling

Target

Template

TargetTemplate

Simple sequence-sequence alignment using BLAST does not give alignment over the entire length.

Sidechain Modelling

Rotamer Library

Loop Modelling

Model Validation

•Ramachandran Plot for backbone dihedrals

•Packing & Accessibility of amino acids

Threading or Fold Recognition

•Proteins often adopt similar folds despite no significant sequence or functional similarity.

•For many proteins there will be suitable template structures in PDB.

•Unfortunately, lack of sequence similarity will mean that many of these are undetected by sequence-only comparison done in homology modelling.

Goal of Fold Recognition or Threading

•Fold recognition methods attempt to detect the fold thatis compatible with a particular query sequence.

•Unlike sequence-only comparison, these methods takeadvantage of the extra information made available by3D structure.

•In effect, fold prediction methods turn the protein folding problem on its head: rather than predicting howa sequence will fold, they predict how well a fold will fit a sequence.

47%

17%

5%

There are many examples of proteins exhibiting high structural similarity but less than 15% sequence identity.

Classical sequence alignment fails to detect homologybelow 25-30% sequence identity.

One needs sequence comparison methods which take intoaccount structural environment of amino acids.

Alternate approach is Threading or Fold Recognition, where sequence is compared directly to structure.

Compatibility of a sequence with a given fold

A practical approach for fold recognition

•Although fold prediction methods are not 100% accurate, the methods are still very useful.

•Run many different methods on many sequences from your homologous protein family. After all these runs, one can build up aconsensus picture of the likely fold.

•Remember that a correct fold may not be at the top of the list, but it is likely to be in the top 10 scoring folds.

•Think about the function of your protein, and look into the functionof the predicted folds.

•Don’t trust the alignments, rather use them as starting points.

Applications of comparative modeling. The potential uses of a comparative model depend on its accuracy. This in turn depends significantly on the sequence identity between the target and the template structure on which the model was based.