- Open Access
Identification of novel conserved functional motifs across most Influenza A viral strains
- Mahmoud ElHefnawi†1, 2Email author,
- Osama AlAidi3Email author,
- Nafisa Mohamed2,
- Mona Kamar2,
- Iman El-Azab4,
- Suher Zada2, 5 and
- Rania Siam2, 5
© ElHefnawi et al; licensee BioMed Central Ltd. 2011
- Received: 6 November 2010
- Accepted: 27 January 2011
- Published: 27 January 2011
Influenza A virus poses a continuous threat to global public health. Design of novel universal drugs and vaccine requires a careful analysis of different strains of Influenza A viral genome from diverse hosts and subtypes. We performed a systematic in silico analysis of Influenza A viral segments of all available Influenza A viral strains and subtypes and grouped them based on host, subtype, and years isolated, and through multiple sequence alignments we extrapolated conserved regions, motifs, and accessible regions for functional mapping and annotation.
Across all species and strains 87 highly conserved regions (conservation percentage > = 90%) and 19 functional motifs (conservation percentage = 100%) were found in PB2, PB1, PA, NP, M, and NS segments. The conservation percentage of these segments ranged between 94 - 98% in human strains (the most conserved), 85 - 93% in swine strains (the most variable), and 91 - 94% in avian strains. The most conserved segment was different in each host (PB1 for human strains, NS for avian strains, and M for swine strains). Target accessibility prediction yielded 324 accessible regions, with a single stranded probability > 0.5, of which 78 coincided with conserved regions. Some of the interesting annotations in these regions included sites for protein-protein interactions, the RNA binding groove, and the proton ion channel.
The influenza virus has evolved to adapt to its host through variations in the GC content and conservation percentage of the conserved regions. Nineteen universal conserved functional motifs were discovered, of which some were accessible regions with interesting biological functions. These regions will serve as a foundation for universal drug targets as well as universal vaccine design.
- Nucleocapsid Protein
- Functional Motif
- Accessible Region
- Human Strain
The influenza A virus is a major threat to world health and economy. The polymerase of this RNA virus lacks proof reading activity , which gives rise to considerable viral variability culminating in the 3 different types A, B and C, in addition to many subtypes based on variations in the hemagglutinin (HA) and the neuraminidase (NA) surface proteins . The influenza genome consists of 8 RNA segments and encodes 10 proteins including the internal structural proteins, nucleocapsid protein (NP), and the two matrix proteins (M1 & M2) [3, 4].
The surface proteins neuraminidase (NA) and hemagglutinin (HA) have been studied extensively and the antigenic variations in the these surface glycoproteins are used to subtype influenza A. Additionally, three of the influenza polypeptides are associated with RNA polymerase activity (PA, PB1, PB2). The RNA binding non-structural protein (NS) contributes to viral pathogenicity and plays a central role in the prevention of interferon mediated antiviral response [3, 4].
Genetic reassortment of the Influenza A virus within different hosts (including avian and swine), and antigenic shifts and drifts in the HA and NA proteins, are the cause of widespread pandemics in immunologically unfamiliar populations. These have resulted in serious outbreaks and pandemics, such as those of 1918, 1957, 1968, and 2009 . This change in genetic and antigenic composition, presents an ever-present challenge for the development of influenza vaccines and antiviral medications.
Bioinformatics has played a major role in several aspect of virology research; these include predicting viral RNA structure , the structural and functional analysis of viral proteins , and immunoinformatics to predict epitopes and reverse vaccinology . Such studies have assisted the development of biomarkers for the diagnosis, staging, and prognosis  of viruses (for a review see ). Additionally, computer-aided drug designs have led to the identification and validation of drugs  for many major viruses, such as HIV, influenza and HCV , helping the world face the challenges of such major viral diseases with a huge medical care burden [13, 14]. Molecular modelling studies have in addition provided mechanistic explanations for such questions like drug modes of action, virus-receptor interaction, and virus-host interactions. In these lines of research, conserved regions found in viruses, extrapolated from multiple sequence alignments of different strains, were essential in functional prediction through the identification of epitopes and motifs [15–17].
Several studies have addressed different aspects of the influenza virus, its evolution, structure, and function analysis, to delineate the molecular mechanisms of pathogenicity and continuous resistance to immune response. Several previous studies performed phylogenic analysis and addressed the evolution of one or more Influenza A viral segments . Additionally, methodical analysis of the whole genome has identified co-occurrence of mutation networks and other properties, such as relative codon usage (rscu) and codon usage patterns (cup), as features of Influenza evolution . Motif prediction in the HA influenza genes and proteins has been previously conducted .
Our study is a comprehensive systematic comparative nucleotide genomic analysis that complements prior analyses and utilizes complete influenza viral segments isolated from different hosts such as humans, avians, swine, and a fourth group for all other hosts, that belong to different HA and NA subtypes, and from different geographic regions and years. The main theme of the current study is genome conservation among different strains. This is achieved by the utilization of all available complete segment sequences from the NCBI's Influenza Virus Resource database in order to achieve a reasonable comparative analysis between the main three hosts: human, swine, and avian, to highlight regions that could serve as targets for universal drug and vaccine design. The need for high sequence conservation as a prerequisite of efficient siRNA design for the Influenza A virus has been highlighted previously . The identification of conserved regions in the influenza M gene has been previously reported.
In the current study, meta-analysis of the Influenza A viral genome segments from different hosts, different subtypes, and different geographic regions is performed. Genomic conserved regions across all diverse strains and hosts are extracted by multiple sequence alignments and the conservation percentage is calculated. An analysis of inter- and intra- host strains segmental genomic variability of Influenza A viral segments for human, avian, and swine hosts, and the GC percentage of the segments in the different hosts, is also conducted. Completely conserved genomic functional motifs are identified and analysed through functional annotation. This work will not only provide understanding of the natural selection of the Influenza A virus, but will serve as a foundation for gene therapy, and novel Influenza A universal drug and vaccine design to target highly conserved regions with crucial functions. Moreover, the bioinformatics sequence analysis workflow that is presented and applied could be used for research into the understanding of the evolution of viruses and the design of universal drug targets.
Preprocessing and alignment of Influenza sequences.
Number of sequences downloaded and utilized in this study for each of the influenza viral segments and their conserved regions, the longest conserved region of each segment and the conserved regions with highest conservation percentage are recorded
Number of sequences
Number of conserved regions
Longest conserved region in each segment
Conserved regions with highest conservation percentage
Region 12 (from nt 2165 to 2317)
PB2 - 12: Position 2165 to 2317
Region 2 (from nt 230 to 493)
PB1 - 22: Position 2012 to 2064
Region 7 (from nt 690 to 677)
PA-6: Position 621 to 677
Region 1 (from nt 62 to 161)
NP-13: Position 1447 to 1486
Region 8 (from nt 733 to 1000)
M-6: Position 599 to 663
Region 6 (from nt 492 to 700)
NS-1: Position 59 to 137
Inter- and Intra- host strains conservation and variability analysis of the influenza segments
Our approach in grouping the sequences according to species infected/ host isolated from enabled an analysis of inter- and intra- species conservation and variability. A comparison of the inter- and intra- host alignments of the influenza segments using the Plotcon and Infoalign tools results shows that swine strains are the most variable (similarity plots illustrated in figures 1 and 2). This result was expected, since the swine strains can mix with both avian and human influenza strains. The human strains are the most conserved except in segment PB2, where the avian is more conserved. The conservation percentage of the segments ranged between 94 - 98% in human strains (the most conserved), 91 - 94% in avian strains and 85 - 93% in swine strains (the most variable). On the other hand, intra-segmental comparisons reveal that the PB1 segment is the most conserved in human strains (98.1%), followed by PB2, NP, PA, NS, and finally the M segment. For the avian host strains, the NS and M segments show the most conservation (94.5%), followed by the PB1, NP, PA, and finally the PB2 segment. In the swine strains the M segment shows the most conservation followed by the segments NP, PB2, PA, and finally PB1.
Identification of 87 conserved regions in the influenza genome
The influenza genome segments conservation and GC percentage in the different hosts
Conservation % & GC% in Segments
Identification of functional motifs and annotation of conserved regions and motifs
Evolutionary highly conserved motifs in Influenza A virus
start position (consensus sequence)
End Position (Consensus Sequence)
H5N1 Start Position
H5N1 End Position
Repeated Positions On H5N1
Mapping on Conserved Regions
(2238 - 2243)
(1243 - 1248)
(1246 - 1251)
(1624 - 1629)
(1994 - 1999)
(101 to 106)
( 368- 373)
We found 4 motifs in the PB2 segment; motif 2 (GAAACG) is repeated twice in the H5N1 reference sequence; and motifs 2, 3, and 4 were previously identified as a conserved region involved in RNA packaging . Interestingly, motif 3 also partially overlaps the nuclear localization signal (NLS). In segment PB1, four motifs were found; motif 1 (ATGATG) is repeated five times and motif 3 (GAGATC) is repeated twice on the H5N1 reference sequence. In PA, two motifs were identified that overlap with RNA packaging annotations . Segment M contains six motifs; motif 4 is the longest (CTCACCGTGCCCAGTGA). In segment NS, three motifs were found; and motif 3 (AATGGA) is repeated three times on the H5N1 reference sequence.
Functional annotation of the conserved regions and motifs was also performed by mapping of the regions and motifs on the 3D structure. Structural mapping of these conserved regions on the available influenza domains from PDB revealed many interesting functions, explaining their selection for conservation.
Analysis of many conserved regions in PB2 and PA revealed that they are mostly on the surface and are involved in protein-protein interactions. The same applies to the NP protein. Interestingly, conserved regions 5, 6, and 7 together form the RNA binding groove (ElHefnawi et. al., submitted).
There are three large conserved regions (Cr2, Cr6, Cr9) found on the NS1 protein  (PDB id: 3F5T) that is expressed by segment 8 of the virus genome (represented in figure 4b). They lie mainly on the surface of the protein and may play an important roles in the binding of different molecules and ligands that contribute to the promiscuity of the NS1 in its immune counterattack mechanisms. Clefts found in these conserved regions could bind to different immune system components (Figure 4c). Cr6 contains four functional motifs with sequences of (AGGTAGA, AGGATGTCAA and three motifs of the sequence AATGGA). The immune system interception functions of the NS1 protein are quite similar to those of the NS5A protein of Hepatitis C virus that was shown previously to have different immune system counterattack mechanisms. This is an interesting property of many viruses that deserves further analysis.
Predictions of accessible target regions and mapping to conserved regions
We have also assessed accessible regions and mapped them to conserved regions to infer their potential use as drug targets. Understanding accessible regions is a critical factor; for example, at least half of the siRNA target region needs to be accessible preferentially in the terminal ends. Therefore, the accessibility of the segments was calculated using the SFOLD server. We located 324 regions on six segments and mapped them to conserved regions (Figure 3). In PB2, ten accessible regions mapped to conserved regions, in PB1, 24; in PA, 16; in NP, 14; in M, 7; and in NS, 7. The accessible regions, which overlap with functional motifs, are presented in figure 3 and additional file 9.
This in silico study analyzed Influenza A virus genome segments available in the Influenza A virus resource at NCBI and grouped them according to host, strain, and year to determine conserved regions across all species studied. The higher variability in the influenza sequences isolated from swine host suggests greater hazards in future pandemics. The higher GC percentage of Influenza sequences infecting avian hosts indicates adaptation to the higher host temperature. The evolution of the influenza virus is driven by adaptation mechanisms to its host. Identification of highly-conserved functional motifs and accessible regions of all sequences was obtained. Eighty-seven conserved regions, nineteen functional motifs, and many potentially accessible regions were identified. These data on the Influenza A virus segments were utilized in the optimal design of universal therapeutic small interfering RNA molecules. The complete workflow including the siRNA design and selection figure will be presented in the next publication(ElHefnawi, submitted) and can help in other future drug and vaccine design.
Collection of sequences
Complete sequences for all segments of Influenza A virus were downloaded in groups using the advanced database search at the NCBI's Influenza Virus Resource . We utilized both the entire nucleotide sequences, in addition to coding sequences for single segments encoding the following proteins; segments PB2, PB1, PA, NP, M, NS, HA, and NA. We utilized approximately 30,000 influenza sequences for the eight segments. The number of sequences utilized from each segment is represented in Table 1.
Grouping of sequences
Swine strain sequences
- (B)Avian strain sequences were sub divided into the following groups:
H9 and Mixed strains
H10, H11, H12, H13, H14, H15, H16
- (C)Human strain sequences were divided into the following groups:
H9, H7, H5
H1 strains were further subdivided, based on the year of isolation, into the following two subcategories; H1 strains isolated between 1918 and 2000, and H1 strains isolated between 2001 and 2007.
H3 strains were further subdivided based on year of isolation into the following three subcategories; H3 isolated between 1968 and 1998, between 1999 and 2002, and between 2003 and 2007.
Miscellaneous: all other strains infecting species other than avian, human and swine.
The above categorization of the sequences facilitated the management of the data, allowed the identification of diversity in the sequences based on the host and year isolated, and helped in the determination of conservations amongst strains. This categorization allowed us to conduct comparative mutational analysis in all segments followed by the calculation of conservation percentage. Such subtype classification according to the immunological nature of strains, and identification of the similarity of structural proteins across strains, combined with sub-categorization at the nucleotide level, will facilitate drug design as siRNA data mining.
Alignment and conservation analysis
Multiple Sequence Alignments of whole Influenza segments
The program MUSCLE version 3.6  was used to align primary sequence groups. The resulting aligned sequences were aligned by profile-profile alignment using the same MUSCLE 3.6 program.
First the alignments were performed by aligning strains isolated from the same host, as discussed above, where avian strains were aligned separately from human and swine strains. Second, human and swine strain sequences were aligned, and the resulting file was aligned with the avian sequence file, and then all other host strains. This order was followed because human and swine strains are generally more homologous than avian strains. For similar reasons, the avian strains were added before the other host species. Based on phylogenetic distances, such an order in the alignment sequences enhances conservation finding and facilitates the management of diversity in sequences.
The BIOPERL modules were used for automating the analysis of the alignments using different tools from EMBOSS like GeeCee , Logobar , Infoalign , Cons  and Plotcon . Scripts were written for each of these tools and run under the Biolinux operating environment . These scripts are available upon request. The consensus sequence for each segment was calculated using the Cons tool from EMBOSS  and submitted to Genbank.
Inter- and intra- host genomic conservation analysis
Conservation and variability across the eight IAV segments in the different hosts was studied by plotting the conservation of the alignments using the Plotcon tool from EMBOSS . Additionally, the Infoalign tool from EMBOSS was used to calculate the conservation percentage of the segments in the different hosts in order to study inter-species and intra-host variability  (Table 2). The GC % for each segment was also calculated using the GeeCee tool from EMBOSS as shown in Table 2.
Conserved region identification
Conserved nucleotide regions were extracted using the Bioedit program .
I- Entropy calculation
Mining for conserved sequences among the aligned sequences was performed by determining the entropy of regions with at least 21 nucleotides in length with a maximum of 2 mismatches. Therefore, we defined an area as conserved if 19 identical continuous nucleotides were detected in all strains with an additional 2-nucleotide mismatch (total 21 nucleotides).
Entropy calculation was followed by checking the number of mismatches in each of our identified conserved regions. The conserved regions were mapped to the 8 segments on the influenza virus as illustrated in figure 3 and additional file 7.
Logo bars for all conserved regions were generated using the logo bar tool (additional file 8). The conservation percent of every conserved region was calculated using Infoalign from EMBOSS  and tabulated in additional file 7.
Functional motifs identification and annotation of conserved regions and motifs
One-hundred-percent conserved motifs of a minimum length of 6 bp in all IAV segments were extracted using the BIOEDIT program . The motifs were mapped to the H5N1 reference genome, and to the conserved regions (Table 3). Also, the H5N1 avian flu reference sequence was checked for other occurrences of these motifs. The perfect conservation of these motifs suggests biological significance and a potential role in the Influenza life cycle.
Functional annotation of the conserved regions and functional motifs was performed after mapping them on the PDB 3D protein files of their segments, and using annotations available for these proteins from the PDB SUM server . After downloading the relevant structure files we highlighted the conserved regions on the structure to show their positions and configuration. Then we used the annotation knowledge gained from the PDBsum for linking the regions with their correlated functions. The annotation at the genome level was performed using Rfam in order to search for conserved regions in RNA structures with specific annotations.
Genomic accessibility forRNAi-based therapeutic design
The SFOLD tool was used to calculate the target accessibility of the Influenza segments using the consensus sequence for each segment calculated from the multiple sequence alignment . A region was considered accessible if at least the average single stranded probability using Sfold was greater than 0.5 for 9 consecutive nucleotides. The results are tabulated in additional file 9 and the regions that map to conserved regions are highlighted in figure 3.
This work was partially funded by an American University in Cairo (AUC) Research Grant to RS and a Yousef-Jameel Science and Technology Research Centre (YJ-STRC) at AUC grant to SZ. We acknowledge the effort of the Information Technology Institute intake 30 Bioinformatics track graduate students who helped in the tabulation of the conservation percentages in hosts and segments.
- Li OT, Chan MC, Leung CS, Chan RW, Guan Y, Nicholls JM, Poon LL: Full factorial analysis of mammalian and avian influenza polymerase subunits suggests a role of an efficient polymerase for virus adaptation. PLoS One 2009, 4: e5658. 10.1371/journal.pone.0005658PubMed CentralView ArticlePubMedGoogle Scholar
- Skehel J: An overview of influenza haemagglutinin and neuraminidase. Biologicals 2009, 37: 177-178. 10.1016/j.biologicals.2009.02.012View ArticlePubMedGoogle Scholar
- Ghedin E, Sengamalay NA, Shumway M, Zaborsky J, Feldblyum T, Subbu V, Spiro DJ, Sitz J, Koo H, Bolotov P, et al.: Large-scale sequencing of human influenza reveals the dynamic nature of viral genome evolution. Nature 2005, 437: 1162-1166. 10.1038/nature04239View ArticlePubMedGoogle Scholar
- Garten RJ, Davis CT, Russell CA, Shu B, Lindstrom S, Balish A, Sessions WM, Xu X, Skepner E, Deyde V, et al.: Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humans. Science 2009, 325: 197-201. 10.1126/science.1176225PubMed CentralView ArticlePubMedGoogle Scholar
- Tamuri AU, Dos Reis M, Hay AJ, Goldstein RA: Identifying changes in selective constraints: host shifts in influenza. PLoS Comput Biol 2009, 5: e1000564. 10.1371/journal.pcbi.1000564PubMed CentralView ArticlePubMedGoogle Scholar
- Schroeder SJ: Advances in RNA structure prediction from sequence: new tools for generating hypotheses about viral RNA structure-function relationships. J Virol 2009, 83: 6326-6334. 10.1128/JVI.00251-09PubMed CentralView ArticlePubMedGoogle Scholar
- Elhefnawi MM, Youssif AA, Ghalwash AZ, Behaidy WH: An Integrated Methodology for Mining Promiscuous Proteins: A Case Study of an Integrative Bioinformatics Approach for Hepatitis C Virus Non-structural 5a Protein. Adv Exp Med Biol 680: 299-305. full_textGoogle Scholar
- Sirskyj D, Diaz-Mitoma F, Golshani A, Kumar A, Azizi A: Innovative bioinformatic approaches for developing peptide-based vaccines against hypervariable viruses. Immunol Cell Biol 2011,89(1):81-9. 10.1038/icb.2010.65View ArticlePubMedGoogle Scholar
- ElHefnawi MM, Zada S, El-Azab IA: Prediction of prognostic biomarkers for Interferon-based therapy to Hepatitis C Virus patients: a metaanalysis of the NS5A protein in subtypes 1a, 1b, and 3a. Virol J 7: 130. 10.1186/1743-422X-7-130Google Scholar
- Yan Q: Bioinformatics databases and tools in virology research: an overview. In Silico Biol 2008, 8: 71-85.PubMedGoogle Scholar
- Fischer HP: Towards quantitative biology: integration of biological information to elucidate disease pathways and to guide drug discovery. Biotechnol Annu Rev 2005, 11: 1-68. full_textView ArticlePubMedGoogle Scholar
- Orth AP, Batalov S, Perrone M, Chanda SK: The promise of genomics to identify novel therapeutic targets. Expert Opin Ther Targets 2004, 8: 587-596. 10.1517/14728220.127.116.117View ArticlePubMedGoogle Scholar
- Yin PD, Das D, Mitsuya H: Overcoming HIV drug resistance through rational drug design based on molecular, biochemical, and structural profiles of HIV resistance. Cell Mol Life Sci 2006, 63: 1706-1724. 10.1007/s00018-006-6009-7View ArticlePubMedGoogle Scholar
- Mitrasinovic PM: Advances in the structure-based design of the influenza A neuraminidase inhibitors. Curr Drug Targets 11: 315-326. 10.2174/138945010790711932Google Scholar
- Khan AM, Miotto O, Nascimento EJ, Srinivasan KN, Heiny AT, Zhang GL, Marques ET, Tan TW, Brusic V, Salmon J, August JT: Conservation and variability of dengue virus proteins: implications for vaccine design. PLoS Negl Trop Dis 2008, 2: e272. 10.1371/journal.pntd.0000272PubMed CentralView ArticlePubMedGoogle Scholar
- Ahn I, Son HS: The current trend of avian influenza viruses in bioinformatics research. J Prev Med Public Health 2007, 40: 185-190. 10.3961/jpmph.2007.40.2.185View ArticlePubMedGoogle Scholar
- Gendoo DM, El-Hefnawi MM, Werner M, Siam R: Correlating novel variable and conserved motifs in the Hemagglutinin protein with significant biological functions. Virol J 2008, 5: 91. 10.1186/1743-422X-5-91PubMed CentralView ArticlePubMedGoogle Scholar
- Bush RM, Fitch WM, Bender CA, Cox NJ: Positive selection on the H3 hemagglutinin gene of human influenza virus A. Mol Biol Evol 1999, 16: 1457-1465.View ArticlePubMedGoogle Scholar
- Du X, Wang Z, Wu A, Song L, Cao Y, Hang H, Jiang T: Networks of genomic co-occurrence capture characteristics of human influenza A (H3N2) evolution. Genome Res 2008, 18: 178-187. 10.1101/gr.6969007PubMed CentralView ArticlePubMedGoogle Scholar
- Ge Q, McManus MT, Nguyen T, Shen CH, Sharp PA, Eisen HN, Chen J: RNA interference of influenza virus production by directly targeting mRNA for degradation and indirectly inhibiting all viral RNA transcription. Proc Natl Acad Sci USA 2003, 100: 2718-2723. 10.1073/pnas.0437841100PubMed CentralView ArticlePubMedGoogle Scholar
- Furuse Y, Suzuki A, Kamigaki T, Oshitani H: Evolution of the M gene of the influenza A virus in different host species: large-scale sequence analysis. Virol J 2009, 6: 67. 10.1186/1743-422X-6-67PubMed CentralView ArticlePubMedGoogle Scholar
- Bao Y, Bolotov P, Dernovoy D, Kiryutin B, Zaslavsky L, Tatusova T, Ostell J, Lipman D: The influenza virus resource at the National Center for Biotechnology Information. J Virol 2008, 82: 596-601. 10.1128/JVI.02005-07PubMed CentralView ArticlePubMedGoogle Scholar
- Edgar RC: MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 2004, 32: 1792-1797. 10.1093/nar/gkh340PubMed CentralView ArticlePubMedGoogle Scholar
- Marsh GA, Rabadan R, Levine AJ, Palese P: Highly conserved regions of influenza a virus polymerase gene segments are critical for efficient viral RNA packaging. J Virol 2008, 82: 2295-2304. 10.1128/JVI.02267-07PubMed CentralView ArticlePubMedGoogle Scholar
- Obayashi E, Yoshida H, Kawai F, Shibayama N, Kawaguchi A, Nagata K, Tame JR, Park SY: The structural basis for an essential subunit interaction in influenza virus RNA polymerase. Nature 2008, 454: 1127-1131. 10.1038/nature07225View ArticlePubMedGoogle Scholar
- Schnell JR, Chou JJ: Structure and mechanism of the M2 proton channel of influenza A virus. Nature 2008, 451: 591-595. 10.1038/nature06531PubMed CentralView ArticlePubMedGoogle Scholar
- Bornholdt ZA, Prasad BV: X-ray structure of NS1 from a highly pathogenic H5N1 influenza virus. Nature 2008, 456: 985-988. 10.1038/nature07444PubMed CentralView ArticlePubMedGoogle Scholar
- El Hefnawi MM, El Behaidy WH, Youssif AA, Ghalwash AZ, El Housseiny LA, Zada S: Natural genetic engineering of hepatitis C virus NS5A for immune system counterattack. Ann N Y Acad Sci 2009, 1178: 173-185. 10.1111/j.1749-6632.2009.05003.xView ArticlePubMedGoogle Scholar
- Rice P, Longden I, Bleasby A: EMBOSS: the European Molecular Biology Open Software Suite. Trends Genet 2000, 16: 276-277. 10.1016/S0168-9525(00)02024-2View ArticlePubMedGoogle Scholar
- Perez-Bercoff A, Koch J, Burglin TR: LogoBar: bar graph visualization of protein logos with gaps. Bioinformatics 2006, 22: 112-114. 10.1093/bioinformatics/bti761View ArticlePubMedGoogle Scholar
- Field D, Tiwari B, Booth T, Houten S, Swan D, Bertrand N, Thurston M: Open software for biologists: from famine to feast. Nat Biotechnol 2006, 24: 801-803. 10.1038/nbt0706-801View ArticlePubMedGoogle Scholar
- Hall TA: BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 1999, 41: 95-98.Google Scholar
- Laskowski RA: PDBsum new things. Nucleic Acids Res 2009, 37: D355-359. 10.1093/nar/gkn860PubMed CentralView ArticlePubMedGoogle Scholar
- Ding Y, Chan CY, Lawrence CE: Sfold web server for statistical folding and rational design of nucleic acids. Nucleic Acids Res 2004, 32: W135-141. 10.1093/nar/gkh449PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.