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'''Pseudo amino acid composition''', or '''PseAA composition''', or '''Chou's PseAAC''',
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<ref name=SX2>{{cite journal | doi= 10.4236/jbise.2013.64054 |last1=Lin |first1=Sheng-Xiang |last2= Lapointe |first2= Jacques|title= Theoretical and experimental biology in one —A symposium in honour of Professor Kuo-Chen Chou’s 50th anniversary and Professor Richard Giegé’s 40th anniversary of their scientific careers|year=2013 |volume=6 |pages=435–442 |journal=JBiSE}}</ref>
was originally introduced by Kuo-Chen Chou in 2001 to represent [[protein]] samples for improving [[protein subcellular localization prediction]] and [[membrane protein]] type prediction.<ref name="chou1">{{cite journal | author = Chou KC | title = Prediction of protein cellular attributes using pseudo-amino acid composition | journal = Proteins | volume = 43 | issue = 3 | pages = 246–55 |date=May 2001 | pmid = 11288174 | doi = 10.1002/prot.1035| url = | issn = }}</ref>
 
== Background ==
To predict the [[subcellular localization]] of proteins and other attributes based on their sequence, two kinds of models are generally used to represent protein samples: (1) the sequential model, and (2) the non-sequential model or discrete model.
 
The most typical sequential representation for a protein sample is its entire [[amino acid]] (AA) sequence, which can contain its most complete information. This is an obvious advantage of the sequential model. To get the desired results, the sequence-similarity-search-based tools are usually utilized to conduct the prediction. However, this kind of approach fails when a query protein does not have significant homology to the known protein(s). Thus, various discrete models were proposed which do not rely on sequence-order.
 
The simplest discrete model is using the amino acid composition (AAC) to represent protein samples, formulated as follows. Given a protein sequence '''P'''  with <math> L </math> amino acid residues, i.e.,
* <math> \mathbf{P}={\begin{bmatrix} \mathrm{R}_1 \mathrm{R}_2 \mathrm{R}_3 \mathrm{R}_4 \mathrm{R}_5 \mathrm{R}_6 \mathrm{R}_7 \cdots \mathrm{R}_L\end{bmatrix}}  \qquad  \text{(1)} </math>
 
where R<sub>1</sub> represents the 1st residue of the protein '''P''', R<sub>2</sub> the 2nd residue, and so forth, according to the amino acic composition (AAC) model, the protein '''P''' of '''Eq.1''' can be expressed by
* <math> \mathbf{P}={\begin{bmatrix} f_1 & f_2 & \cdots & f_{20} \end{bmatrix}}^{\mathbf{T}}  \qquad  \text{(2)} </math>
 
where <math>\, f_u \, (u=1, 2, \cdots, 20) </math>  are the normalized occurrence frequencies of the 20 native amino acids in '''P''', and '''T''' the transposing operator. Accordingly, the amino acid composition of a protein can be easily derived once the [[protein sequencing]] information is known.
 
Owing to its simplicity, the amino acid composition (AAC) model was widely used in many earlier statistical methods for predicting protein attributes. However, all the sequence-order information is lost. This is its main shortcoming.
 
== Concept ==
 
To avoid completely losing the sequence-order information, the concept of PseAA ('''pse'''udo '''a'''mino '''a'''cid) composition was proposed.<ref name=chou1/> In contrast with the conventional amino acid composition that contains 20 components with each reflecting the occurrence frequency for one of the 20 native amino acids in a protein, the PseAA composition contains a set of greater than 20 discrete factors, where the first 20 represent the components of its conventional AA composition while the additional factors incorporate some sequence-order information via various modes.
 
The additional factors are a series of rank-different correlation factors along a protein chain, but they can also be any combinations of other factors so long as they can reflect some sorts of sequence-order effects one way or the other. Therefore, the essence of PseAA composition is that on one hand it covers the AA composition, but on the other hand it contains the information beyond the AA composition and hence can better reflect the feature of a protein sequence through a discrete model.
 
Meanwhile, various modes to formulate the PseAA composition have also been developed, as summarized in a review.<ref name="chou2">{{cite journal | last = Chou K-C | first1 = Kuo-Chen|title=Pseudo amino acid composition and its applications in bioinformatics, proteomics and system biology. | journal=Current Proteomics | volume = 6 | pages = 262–274 | year = 2009 | doi = 10.2174/157016409789973707 | issue = 4}}</ref>
 
== Algorithm ==
[[File:Chou's PseAAC illustration.jpg|thumb|500px|right|'''Figure 1'''. A schematic drawing to show (a) the 1st-tier, (b) the 2nd-tier, and (3) the 3rd-tier sequence-order-correlation mode along a protein sequence, where  R<sub>1</sub> represents the amino acid residue at the sequence position 1,  R<sub>2</sub> at position 2, and so forth (cf. '''Eq.1'''), and the coupling factors <math>J_{i,j} </math> are given by '''Eq.6'''. Panel (a) reflects the correlation mode between all the most contiguous residues, panel (b) that between all the 2nd most contiguous residues, and panel (c) that between all the 3rd most contiguous residues.]]
 
According to the PseAA composition model, the protein '''P''' of '''Eq.1''' can be formulated as
 
* <math> \mathbf{P}={\begin{bmatrix} p_1, \, p_2, \,  \ldots,\, p_{20}, \, p_{20+1}, \, \ldots, \, p_{20+\lambda} \end{bmatrix}}^{\mathbf{T}},  \,\,\, (\lambda < L )  \qquad  \text{(3)} </math>
 
where the (<math>20+\lambda</math>) components are given by
 
* <math> p_u =  \begin{cases}
\dfrac {f_u} {\sum_{i=1}^{20}f_i \, + \, w\sum_{k=1}^{\lambda} \tau_k},  &  (1 \le u \le 20)
\\[10pt]
\dfrac {w \tau_{u-20}} {\sum_{i=1}^{20} f_i \, + \, w\sum_{k=1}^{\lambda} \tau_k}, & (20+1 \le u \le 20+\lambda)
\end{cases}
\qquad  \text{(4)}
</math>
 
where <math>w</math> is the weight factor, and <math>\tau_k</math> the <math>k</math>-th tier correlation factor that reflects the sequence order correlation between all the <math>k</math>-th most contiguous residues as formulated by
* <math>
\tau_k = \frac {1}{L-k} \sum_{i=1}^{L-k} \, \mathrm{J}_{i, i+k},  \,\,\,  (k <  L)
\qquad  \text{(5)} </math>
 
with
* <math>
\mathrm{J}_{i, i+k} = \frac{1}{\Gamma} \sum_{q=1}^{\Gamma} \left[\Phi_{q}\left(\mathrm{R}_{i+k}\right) - \Phi_{q}\left(\mathrm{R}_{i}\right ) \right]^2
\qquad    \text{(6)}
</math>
 
where <math>\Phi_{q}\left(\mathrm{R}_{i}\right)</math> is the <math>{q}</math>-th function of the amino acid <math>\mathrm{R}_i \,</math>, and <math>\Gamma\,</math> the total number of the functions considered. For example, in the original paper by Chou,<ref name=chou1/> <math>\Phi_{1}\left(\mathrm{R}_{i}\right)</math>, <math>\Psi_{2}\left(\mathrm{R}_{i}\right)</math> and <math>\Psi_{3}\left(\mathrm{R}_{i}\right)</math> are respectively the hydrophobicity value, hydrophilicity value, and side chain mass of amino acid <math>\mathrm{R}_i \,</math>;  while <math> \Phi_{1}\left(\mathrm{R}_{i+1}\right)</math>, <math>\Phi_{2}\left(\mathrm{R}_{i+1}\right)</math> and <math>\Phi_{3}\left(\mathrm{R}_{i+1}\right)</math> the corresponding values for the amino acid <math>\mathrm{R}_{i+1} \,</math>. Therefore, the total number of functions considered there is <math>\Gamma =3 \, </math>.  It can be seen from '''Eq.3''' that the first 20 components, i.e. <math>p_1, \, p_2, \,  \cdots,\, p_{20} </math> are associated with the conventional AA composition of protein, while the remaining components <math>p_{20+1}, \, \cdots, \, p_{20+\lambda} </math> are the  correlation factors that reflect the 1st tier, 2nd tier, , and the <math>\lambda \,</math>-th tier sequence order correlation patterns ('''Figure 1''').  
It is through these additional <math>\lambda \,</math> factors that some important sequence-order effects are incorporated.
 
<math>\lambda \,</math> in '''Eq.3''' is a parameter of integer and that choosing a different integer for <math>\lambda \,</math> will lead to a dimension-different PseAA composition.<ref name="pmid17698024">{{cite journal | author = Chou KC, Shen HB | title = Recent progress in protein subcellular location prediction | journal = Anal. Biochem. | volume = 370 | issue = 1 | pages = 1–16 |date=November 2007 | pmid = 17698024 | doi = 10.1016/j.ab.2007.07.006 | url = | issn = }}</ref>
 
Using '''Eq.6''' is just one of the modes for deriving the correlation factors or PseAA components. The others, such as the physicochemical distance mode<ref name="pmid11097861">{{cite journal | author = Chou KC | title = Prediction of protein subcellular locations by incorporating quasi-sequence-order effect | journal = Biochem. Biophys. Res. Commun. | volume = 278 | issue = 2 | pages = 477–83 |date=November 2000 | pmid = 11097861 | doi = 10.1006/bbrc.2000.3815 | url = | issn = }}</ref> and amphiphilic pattern mode,<ref name="pmid15308540">{{cite journal | author = Chou KC | title = Using amphiphilic pseudo amino acid composition to predict enzyme subfamily classes | journal = Bioinformatics | volume = 21 | issue = 1 | pages = 10–9 |date=January 2005 | pmid = 15308540 | doi = 10.1093/bioinformatics/bth466 | url = | issn = }}</ref> can also be used to derive different types of PseAA composition, as summarized in a review paper.<ref name=chou2/>
 
== Applications ==
 
Since '''PseAA composition''' was introduced, it has been widely used to predict various attributes of proteins, such as structural classes of proteins,<ref name="pmid21106461">{{cite journal | author = Sahu SS, Panda G | title = A novel feature representation method based on Chou's pseudo amino acid composition for protein structural class prediction | journal = Comput Biol Chem | volume = 34 | issue = 5-6 | pages = 320–7 |date=December 2010 | pmid = 21106461 | doi = 10.1016/j.compbiolchem.2010.09.002 }}</ref><ref name="pmid16920060">{{cite journal | author = Chen C, Zhou X, Tian Y, Zou X, Cai P | title = Predicting protein structural class with pseudo-amino acid composition and support vector machine fusion network | journal = Anal. Biochem. | volume = 357 | issue = 1 | pages = 116–21 |date=October 2006 | pmid = 16920060 | doi = 10.1016/j.ab.2006.07.022  }}</ref> enzyme family classes and subfamily classes,<ref name="pmid17628605">{{cite journal | author = Zhou XB, Chen C, Li ZC, Zou XY | title = Using Chou's amphiphilic pseudo-amino acid composition and support vector machine for prediction of enzyme subfamily classes | journal = J. Theor. Biol. | volume = 248 | issue = 3 | pages = 546–51 |date=October 2007 | pmid = 17628605 | doi = 10.1016/j.jtbi.2007.06.001  }}</ref>  GABA(A) receptor proteins,<ref name="pmid21536049">{{cite journal | author = Mohabatkar H, Mohammad Beigi M, Esmaeili A | title = Prediction of GABA(A) receptor proteins using the concept of Chou's pseudo-amino acid composition and support vector machine | journal = J. Theor. Biol. | volume = 281 | issue = 1 | pages = 18–23 |date=July 2011 | pmid = 21536049 | doi = 10.1016/j.jtbi.2011.04.017 }}</ref>  protein folding rates,<ref name="pmid21328402">{{cite journal | author = Guo J, Rao N, Liu G, Yang Y, Wang G | title = Predicting protein folding rates using the concept of Chou's pseudo amino acid composition | journal = J Comput Chem | volume = 32 | issue = 8 | pages = 1612–7 |date=June 2011 | pmid = 21328402 | doi = 10.1002/jcc.21740 }}</ref> cyclin proteins,<ref name="pmid20450487">{{cite journal | author = Mohabatkar H | title = Prediction of cyclin proteins using Chou's pseudo amino acid composition | journal = Protein Pept. Lett. | volume = 17 | issue = 10 | pages = 1207–14 |date=October 2010 | pmid = 20450487 | doi = }}</ref> supersecondary structure,<ref name="pmid20652881">{{cite journal | author = Zou D, He Z, He J, Xia Y | title = Supersecondary structure prediction using Chou's pseudo amino acid composition | journal = J Comput Chem | volume = 32 | issue = 2 | pages = 271–8 |date=January 2011 | pmid = 20652881 | doi = 10.1002/jcc.21616 }}</ref> subcellular location of proteins,<ref name="pmid18074191">{{cite journal | author = Zhang SW, Zhang YL, Yang HF, Zhao CH, Pan Q | title = Using the concept of Chou's pseudo amino acid composition to predict protein subcellular localization: an approach by incorporating evolutionary information and von Neumann entropies | journal = Amino Acids | volume = 34 | issue = 4 | pages = 565–72 |date=May 2008 | pmid = 18074191 | doi = 10.1007/s00726-007-0010-9  }}</ref><ref name="pmid22750634">{{cite journal | author = Mei, S. | title = Predicting plant protein subcellular multi-localization by Chou's PseAAC formulation based multi-label homolog knowledge transfer learning | journal = Journal of Theoretical Biology| volume = 310 | pages = 80–87 |date=June 2012 | pmid = 22750634 | doi = 10.1016/j.jtbi.2012.06.028}}</ref> subnuclear location of proteins,<ref name="Mundra_2007">{{cite journal | author = Mundra P, Kumar M, Kumar KK, Jayaraman VK,  Kulkarni BD|title=Using pseudo amino acid composition to predict protein subnuclear localization: Approached with PSSM|journal=Pattern Recognition Letters |date=October 2007 | volume = 28 | issue = 13 | pages = 1610–1615 | doi = 10.1016/j.patrec.2007.04.001}}</ref> apoptosis protein subcellular localization,<ref name="pmid17572445">{{cite journal | author = Chen YL, Li QZ | title = Prediction of apoptosis protein subcellular location using improved hybrid approach and pseudo-amino acid composition | journal = J. Theor. Biol. | volume = 248 | issue = 2 | pages = 377–81 |date=September 2007 | pmid = 17572445 | doi = 10.1016/j.jtbi.2007.05.019  }}</ref> submitochondria localization,<ref name="pmid18175047">{{cite journal | author = Nanni L, Lumini A | title = Genetic programming for creating Chou's pseudo amino acid based features for submitochondria localization | journal = Amino Acids | volume = 34 | issue = 4 | pages = 653–60 |date=May 2008 | pmid = 18175047 | doi = 10.1007/s00726-007-0018-1  }}</ref> protein quaternary structure,<ref name="pmid18427713">{{cite journal | author = Zhang SW, Chen W, Yang F, Pan Q | title = Using Chou's pseudo amino acid composition to predict protein quaternary structure: a sequence-segmented PseAAC approach | journal = Amino Acids | volume = 35 | issue = 3 | pages = 591–8 |date=October 2008 | pmid = 18427713 | doi = 10.1007/s00726-008-0086-x  }}</ref><ref name="pmid22990717">{{cite journal | author = Sun, X. Y., Shi, S. P., Qiu, J. D., Suo, S. B., Huang, S. Y. & Liang, R. P. | title = Identifying protein quaternary structural attributes by incorporating physicochemical properties into the general form of Chou's PseAAC via discrete wavelet transform | journal = Molecular BioSystems| volume = 8 | pages = 3178–84 | year = 2012  | pmid = 22990717 | doi = 10.1039/c2mb25280e}}</ref> bacterial secreted proteins,<ref name="pmid21860064">{{cite journal | author = Nanni, L., Lumini, A., Gupta, D. & Garg, A.| title = Identifying Bacterial Virulent Proteins by Fusing a Set of Classifiers Based on Variants of Chou's Pseudo Amino Acid Composition and on Evolutionary Information| journal = IEEE/ACM Trans Comput Biol Bioinform| volume = 9 | pages = 467–475 |date=August 2012 | pmid = 21860064 | doi = 10.1109/TCBB.2011.117| url = }}</ref> conotoxin superfamily and family classification,<ref name="pmid16890961">{{cite journal | author = Mondal S, Bhavna R, Mohan Babu R, Ramakumar S | title = Pseudo amino acid composition and multi-class support vector machines approach for conotoxin superfamily classification | journal = J. Theor. Biol. | volume = 243 | issue = 2 | pages = 252–60 |date=November 2006 | pmid = 16890961 | doi = 10.1016/j.jtbi.2006.06.014  }}</ref> protease types,<ref name="pmid16456852">{{cite journal | author = Zhou GP, Cai YD | title = Predicting protease types by hybridizing gene ontology and pseudo amino acid composition | journal = Proteins | volume = 63 | issue = 3 | pages = 681–4 |date=May 2006 | pmid = 16456852 | doi = 10.1002/prot.20898  }}</ref> [[G protein-coupled receptor|GPCR]] types,<ref name="pmid19364489">{{cite journal | author = Qiu JD, Huang JH, Liang RP, Lu XQ | title = Prediction of G-protein-coupled receptor classes based on the concept of Chou's pseudo amino acid composition: an approach from discrete wavelet transform | journal = Anal. Biochem. | volume = 390 | issue = 1 | pages = 68–73 |date=July 2009 | pmid = 19364489 | doi = 10.1016/j.ab.2009.04.009  }}</ref><ref name="pmid122316312">{{cite journal | author = Zia Ur, R. & Khan, A. | title = Identifying GPCRs and their Types with Chou's Pseudo Amino Acid Composition: An Approach from Multi-scale Energy Representation and Position Specific Scoring Matrix| journal = Protein & Peptide Letters. | volume = 19  | pages = 890–903 | year = 2012 | pmid = 22316312  }}</ref> human papillomaviruses,
<ref name="pmid19961864">{{cite journal | author = Esmaeili M, Mohabatkar H, Mohsenzadeh S | title = Using the concept of Chou's pseudo amino acid composition for risk type prediction of human papillomaviruses | journal = J. Theor. Biol. | volume = 263 | issue = 2 | pages = 203–9 |date=March 2010 | pmid = 19961864 | doi = 10.1016/j.jtbi.2009.11.016}}</ref>  outer membrane proteins,<ref name="pmid122185508">{{cite journal | author = Hayat, M. & Khan, A. | title = Discriminating Outer Membrane Proteins with Fuzzy K-Nearest Neighbor Algorithms Based on the General Form of Chou's PseAAC | journal = Protein & Peptide Letters| volume = 19 | pages = 411–421 |date=April 2012 | pmid = 22185508 }}</ref>  membrane protein types,<ref name="pmid 23137835 ">{{cite journal | author = Chen, Y. K. & Li, K. B.| title = Predicting membrane protein types by incorporating protein topology, domains, signal peptides, and physicochemical properties into the general form of Chou's pseudo amino acid composition  | journal = Journal of Theoretical Biology | volume = 318 | pages = 1–12 | year = 2012  | pmid = 23137835 | doi = 10.1016/j.jtbi.2012.10.033}}</ref> protein secondary structural contents,<ref name="pmid19149669">{{cite journal | author = Chen C, Chen L, Zou X, Cai P | title = Prediction of protein secondary structure content by using the concept of Chou's pseudo amino acid composition and support vector machine | journal = Protein Pept. Lett. | volume = 16 | issue = 1 | pages = 27–31 | year = 2009 | pmid = 19149669 | doi = 10.2174/092986609787049420 }}</ref> metalloproteinase family <ref name="pmid22143437">{{cite journal | author = Mohammad Beigi, M., Behjati, M. & Mohabatkar, H.| title = Prediction of metalloproteinase family based on the concept of Chou's pseudo amino acid composition using a machine learning approach | journal = Journal of Structural and Functional Genomics| volume = 12 | pages = 191–197 | year = 2011 | pmid = 22143437 | doi = 10.1007/s10969-011-9120-4}}</ref>  subcellular localization of mycobacterial proteins,<ref name="pmid18782071">{{cite journal | author = Lin H, Ding H, Guo FB, Zhang AY, Huang J | title = Predicting subcellular localization of mycobacterial proteins by using Chou's pseudo amino acid composition | journal = Protein Pept. Lett. | volume = 15 | issue = 7 | pages = 739–44 | year = 2008 | pmid = 18782071 | doi = 10.2174/092986608785133681 }}</ref> antibacterial peptides <ref name="pmid22894156">{{cite journal | author = Khosravian, M., Faramarzi, F. K., Beigi, M. M., Behbahani, M. & Mohabatkar, H| title = Predicting Antibacterial Peptides by the Concept of Chou's Pseudo-amino Acid Composition and Machine Learning Methods | journal = Protein Pept. Lett. | volume = 20 | pages = 180–186 | year = 2013 | pmid = 22894156 }}</ref>  lipase types,<ref name="pmid19075826">{{cite journal | author = Zhang GY, Li HC, Gao JQ, Fang BS | title = Predicting lipase types by improved Chou's pseudo-amino acid composition | journal = Protein Pept. Lett. | volume = 15 | issue = 10 | pages = 1132–7 | year = 2008 | pmid = 19075826 | doi = 10.2174/092986608786071184 }}</ref> allergenic proteins <ref name="pmid22931491">{{cite journal | author = Mohabatkar, H., Beigi, M. M., Abdolahi, K. & Mohsenzadeh, S. | title = Prediction of allergenic proteins by means of the concept of Chou's pseudo amino acid composition and a machine learning approach| journal = Medicinal Chemistry| volume = 9 | pages = 133–137 | year = 2013 | pmid = 22931491 }}</ref>  DNA-binding proteins,<ref name="pmid17624492">{{cite journal | author = Fang Y, Guo Y, Feng Y, Li M | title = Predicting DNA-binding proteins: approached from Chou's pseudo amino acid composition and other specific sequence features | journal = Amino Acids | volume = 34 | issue = 1 | pages = 103–9 |date=January 2008 | pmid = 17624492 | doi = 10.1007/s00726-007-0568-2  }}</ref>  essential proteins,<ref name="pmid23276224">{{cite journal | author = Sarangi, A. N., Lohani, M. & Aggarwal, R.| title = Prediction of Essential Proteins in Prokaryotes by Incorporating Various Physico-chemical Features into the General form of Chou's Pseudo Amino Acid Composition | journal = Protein Pept. Lett. | volume = 20 | pages = 781–795 | year = 2013 | pmid = 23276224 }}</ref> cell wall lytic enzymes,<ref name="pmid19356130">{{cite journal | author = Ding H, Luo L, Lin H | title = Prediction of cell wall lytic enzymes using Chou's amphiphilic pseudo amino acid composition | journal = Protein Pept. Lett. | volume = 16 | issue = 4 | pages = 351–5 | year = 2009 | pmid = 19356130 | doi = 10.2174/092986609787848045 }}</ref>  cofactors of oxidoreductases,<ref name="pmid18471832">{{cite journal | author = Zhang GY, Fang BS | title = Predicting the cofactors of oxidoreductases based on amino acid composition distribution and Chou's amphiphilic pseudo-amino acid composition | journal = J. Theor. Biol. | volume = 253 | issue = 2 | pages = 310–5 |date=July 2008 | pmid = 18471832 | doi = 10.1016/j.jtbi.2008.03.015  }}</ref>  among many other protein attributes and protein-related features (see, e.g., the review paper by Gonzalez-Diaz et al.<ref name="pmid18297652">{{cite journal | author = González-Díaz H, González-Díaz Y, Santana L, Ubeira FM, Uriarte E | title = Proteomics, networks and connectivity indices | journal = Proteomics | volume = 8 | issue = 4 | pages = 750–78 |date=February 2008 | pmid = 18297652 | doi = 10.1002/pmic.200700638 }}</ref> as well as the relevant references cited therein).
 
Ever since the concept of PseAA composition was introduced, it has been widely utilized to predict various protein attributes.  It has also been used to incorporate the [[protein domain]] or FunD (functional domain) information and GO ([[gene ontology]]) information for improving the prediction quality for the subcellular localization of proteins.<ref name="pmid18274516">{{cite journal | author = Chou KC, Shen HB | title = Cell-PLoc: a package of Web servers for predicting subcellular localization of proteins in various organisms | journal = Nat Protoc | volume = 3 | issue = 2 | pages = 153–62 | year = 2008 | pmid = 18274516 | doi = 10.1038/nprot.2007.494 | url = http://chou.med.harvard.edu/bioinf/Cell-PLoc/ | issn = }}</ref> as well as their other attributes.
 
Meanwhile, the concept of PseAA composition has also stimulated the generation of  pseudo-folding topological indices and pseudo-folding lattice network.<ref name="pmid19296677">{{cite journal | author = Agüero-Chapin G, Varona-Santos J, de la Riva GA, Antunes A, González-Vlla T, Uriarte E, González-Díaz H | title = Alignment-free prediction of polygalacturonases with pseudofolding topological indices: experimental isolation from Coffea arabica and prediction of a new sequence | journal = J. Proteome Res. | volume = 8 | issue = 4 | pages = 2122–8 |date=April 2009 | pmid = 19296677 | doi = 10.1021/pr800867y  }}</ref><ref name="pmid18992259">{{cite journal | author = Perez-Bello A, Munteanu CR, Ubeira FM, De Magalhães AL, Uriarte E, González-Díaz H | title = Alignment-free prediction of mycobacterial DNA promoters based on pseudo-folding lattice network or star-graph topological indices | journal = J. Theor. Biol. | volume = 256 | issue = 3 | pages = 458–66 |date=February 2009 | pmid = 18992259 | doi = 10.1016/j.jtbi.2008.09.035  }}</ref><ref name="pmid19578942">{{cite journal | author = González-Díaz H, Dea-Ayuela MA, Pérez-Montoto LG, Prado-Prado FJ, Agüero-Chapín G, Bolas-Fernández F, Vazquez-Padrón RI, Ubeira FM | title = QSAR for RNases and theoretic-experimental study of molecular diversity on peptide mass fingerprints of a new Leishmania infantum protein | journal = Mol. Divers. | volume = 14 | issue = 2 | pages = 349–69 |date=May 2010 | pmid = 19578942 | doi = 10.1007/s11030-009-9178-0  }}</ref>
 
Recently, two open accessible tools were established to generate various modes of Chou’s pseudo amino acid composition.<ref name="pmid22459120">{{cite journal | author = Du, P., Wang, X., Xu, C. & Gao, Y.  | title
= PseAAC-Builder: A cross-platform stand-alone program for generating various special Chou's pseudo-amino acid compositions| journal = Analytical Biochemistry | volume = 425 | pages = 117–9|date=March 2012 | pmid = 22459120 | doi = 10.1016/j.ab.2012.03.015}}</ref><ref name="pmid23426256">{{cite journal | author = Cao, D. S., Xu, Q. S. & Liang, Y. Z. | title = propy: a tool to generate various modes of Chou's PseAAC| journal = Bioinformatics | volume = 29 | pages = 960–962|date=April 2013 | pmid = 23426256 | doi = 10.1093/bioinformatics/btt072}}</ref>
 
== References ==
{{Reflist|colwidth=30em}}
 
== External links ==
* [http://chou.med.harvard.edu/bioinf/PseAAC/ PseAAC web server]<ref name="pmid17976365">{{cite journal | author = Shen HB, Chou KC | title = PseAAC: a flexible web server for generating various kinds of protein pseudo amino acid composition | journal = Anal. Biochem. | volume = 373 | issue = 2 | pages = 386–8 |date=February 2008 | pmid = 17976365 | doi = 10.1016/j.ab.2007.10.012 | url = | issn = }}</ref>
{{Reflist}}
 
[[Category:Amino acids]]
[[Category:Bioinformatics algorithms]]

Latest revision as of 12:42, 6 July 2014

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