Secondary structure prediction has been around for almost a quarter of a century. The early methods suffered from a lack of data. Predictions were performed on single sequences rather than families of homologous sequences, and there were relatively few known 3D structures from which to derive parameters. Probably the most famous early methods are those of Chou & Fasman, Garnier, Osguthorbe & Robson (GOR) and Lim. Although the authors originally claimed quite high accuracies (70-80 %), under careful examination, the methods were shown to be only between 56 and 60% accurate (see Kabsch & Sander, 1984 given below). An early problem in secondary structure prediction had been the inclusion of structures used to derive parameters in the set of structures used to assess the accuracy of the method.
Some good references on the subject:
2. INRODUCTION
Primary structure (Amino acid sequence)
↓
Secondary structure (α-helix, β-sheet)
↓
Tertiary structure (Three-dimensional
structure formed by assembly of secondary
structures)
↓
Quaternary structure (Structure formed by
more than one polypeptide chains)
3. Secondary Structure
Defined as the local conformation of protein backbone
Primary Structure —folding— Secondary Structure
a helix and b sheet
Secondary Structure
Regular Secondary
Structure
(a-helices, b-sheets)
Irregular
Secondary
Structure
(Tight turns,
Random coils,
bulges)
4.
5. a helix
•common confirmation.
•spiral structure
•Tightly packed coiled polypeptide
backbone, with extending side chains
•Spontaneous
•stabilized by H-bonding between amide
hydrogens and carbonyl oxygens of peptide
bonds.
•R-groups lie on the exterior of the helix
and perpendicular to its axis.
•complete turn of helix —3.6 aminoacyl
residues with distance 0.54 nm
e.g. the keratins- entirely α-helical
Myoglobin- 80% helical
6. •Glycine and Proline , bulky amino acids,
charged amino acids favor disruption of the
helix.
7. b sheet
•β-sheets are composed of 2 or more different regions of
stretches of at least 5-10 amino acids.
•The folding and alignment of stretches of the polypeptide
backbone aside one another to form β-sheets is stabilized by
H-bonding between amide hydrogens and carbonyl oxygens
•the peptide backbone of the β sheet is highly extended.
•R groups of adjacent residues point in opposite directions.
• β-sheets are either parallel or antiparallel
10. What is secondary
structure prediction?
Given a protein sequence (primary structure)
1st step in prediction of protein structure.
Technique concerned with determination of secondary structure of
given polypeptide by locating the Coils Alpha Helix Beta Strands in
plypeptide
GHWIATRGQLIREAYEDYRHFSSECPFIP
Predict its secondary structure content
(C=Coils H=Alpha Helix E=Beta Strands)
CEEEEECHHHHHHHHHHHCCCHHCCCCCC
11. Why secondary structure
prediction?
o secondary structure —tertiary structure prediction
o Protein function prediction
o Protein classification
o Predicting structural change
o detection and alignment of remote homology between proteins
o on detecting transmembrane regions, solvent-accessibleresidues,
and other important features of molecules
o Detection of hydrophobic region and hydrophilic region
12. Prediction methods
o Statistical method
o Chou-Fasman method, GOR I-IV
o Nearest neighbors
o NNSSP, SSPAL
o Neural network
o PHD, Psi-Pred, J-Pred
o Support vector machine (SVM)
o HMM
13. Chou-Fasman algorithm
Chou and fasman in 1978
It is based on assigning a set of prediction value to amino
acid residue in polypeptide and applying an algorithm to the
conformational parameter and positional frequency.
conformational parameter for each amino acid is calculated
by considering the relative frequency of each 20 amino
acid in proteins
By this C=Coils H=Alpha Helix E=Beta Strands are
determined
Also called preference parameter
14. • A table of prediction value or preference parameter for each
of 20 amino acid in alpha helix ,beta plate and turn
already calculated and standardised.
• To obtain the prediction value the frequency of amino
acids( i) in structure is divided by of all residences in
protein (s)
• i/s
• The resulting structural parameter of
p(alpha),p(beta),p(turn)vary —0.5 to 1.5 for 20 amino acid
15.
16. Window is scanned to find a short sequence of
amino acid that has high probability to form one
type of structure
When 4 out of 6 amino acid have high
probability >1.03 the – alpha helix
3 out of 5 amino acid with probability >1.03-beta
RULES
17. ALGORITHM
o Note preference parameter for 20 aa in peptide
o Scan the window and identify the region where 4 out of
6 contiguous residue have p(alpha helix) >1.00
o Continue scanning in both the direction until the 4
contiguous residue that have an average p(alpha
helix)<1.00,end of helix
o If segment is longer than 5aa and p(alpha helix)>p(beta
sheet )-segment –completely alpha helix
o scan different segment and identify - alpha helix
18. Identify the region where 3 out of 5 aa have the
value of p( beta sheet) >1.00 ,region is predicted
as beta sheet
Continue scanning both the direction until 4
residue that have p( beta sheet) <1.00
End of beta sheet
average p( beta sheet) >105 and p( beta sheet)
>p(alpha helix) than consider complete segment
as b pleated sheet
19. If any region is over lapping than consider it as
alpha helix if average p(alpha helix)>p(beta sheet )
Or beta sheet if p(alpha helix)<p(beta sheet )
To identify turn
P(t)=f(j)f(j+1)f(j+2)f(j+3)
J=residual number
23. GOR METHOD
• GOR(Garnier,Osguthorpe,Robson)1978
• Chou fasman method is based on assumption that each amino
acid individually influence the 2ry structure of sequence
• GOR is based on, amino acid flanking the central amino acid
will influence the 2ry structure
• Consider a peptide central amino acid
side amino acid
• It assume that amino acid up to 8 residue on sides will
influence the 2ry structure of central residue
• 4th version
• 64% accurate
24. ALGORITHUM
•It uses the sliding window of 17 amino acid
•The side amino acid sequence and alignment is determined to
predict secondary structure of central sequence
•Good for helix than sheet because beta sheet has more inter
sequence hydrogen bonding
•36.5% accurate for beta sheet
•input any amino acid sequence
•Output tells about secondary structure
25.
26. NEAREST NEIGHBOUR
METHOD
o Based on ,short homologues sequences of amino acids
have the same secondary structure
o It predicts secondary structure of central homologues
segment by neighbour homologues sequences
o By using structural database find some secondary
structure of sequence which may be homologues to our
target sequence
o Naturally evolved proteins with 35% identical amino acid
sequence will have same secondary structure
o Find some sequence which may match with target
sequence
o Scoring matrix,MSA
30. Neural network
Input signals are summed
and turned into zero or one
3.
J1
J2
J3
J4
Feed-forward multilayer network
Input layer Hidden layer Output layer
neurons
37. Suggested reading:
Chapter 15 in “Current Topics in Computational Molecular
Biology, edited by Tao Jiang, Ying Xu, and Michael Zhang. MIT
Press. 2002.”
Bioinformatics by Cynthia and per jambeck
Bioinformatics by S.C.RASTOGI
Bioinformatics By Andreas
Optional reading:
Review by Burkhard Rost:
http://cubic.bioc.columbia.edu/papers/2003_r
ev_dekker/paper.html
Reference