Achievements of Raghava's group

Traditionally small molecules are used as drug; in recent years number of approved drugs based on small molecules is decreasing. Therapeutic peptides are possible alternative to traditional drugs based on small chemical compounds. Despite their tremendous importance in the field of biology and medicine, so far limited efforts has been made in the field of peptide bioinformatics. Raghava’s group developed numerous computational tools for designing therapeutic peptides. Following are major web-servers developed by his group; i) ToxinPred: Prediction of toxicity of peptides and proteins, ii) THPpred: Designing of tumor homing peptide, iii) CellPPD: Prediction of highly effective cell penetrating peptides, iv) AntiCP: Discovering novel anticancer peptides, v) PepStr: Tertiary structure prediction of peptide from their sequence, vi) AntiBP2: Identification of antibacterial peptides and vii) HLP: Predicting half-life of peptides in intestine like environment.

Personalized or Strain specific Medicines In the era of next generation sequencing where sequencing of whole genome of pathogens (bacteria/fungus/virus) and human is affordable; it is important to develop person or strain-specific medicine. Group is in the process of developing in silico tools for personalized medicine, following are major resources developed in last few years: a) HIVcoPred: Prediction HIV-1 coreceptor from its V3-loop sequence; b) CancerDR: Pharmacological profiling of anticancer drugs against large number of cancer cell lines; c) DipCells: Promiscuous inhibitors against pancreatic cancer cell-lines; d) HerceptinR: Herceptin resistance database against various cancer cell-lines with genomic information; e) PCMdb: methylation information about important genes across various pancreatic cell lines and tissues and f) CancerDP: prioritization of anticancer drugs based on genomic information. In addition group have sequenced, assembled and annotate large number of microbial genomes.

Protein Structures Prediction The prediction of structure of a protein is one of major challenge in the field of drug development. His group developed method for predicting secondary structure (regular as well as irregular), super secondary structure (e.g. beta-hairpins, beta-barrels) and tertiary structure (ab initio methods for bioactive peptides). The performance of their best secondary structure prediction method was ranked within the top 5 methods in the world, according to the community wide competitions like CASP, CAFASP and EVA. Following are major servers developed for predicting structure of proteins. AlphaPred: ANN based method for predicting alpha-turn in a protein. APSSP2: Prediction of secondary structure of proteins from their sequence. AR_NHPred: Identification of aromatic-backbone NH interaction in proteins. Betatpred2: Prediction of Beta-turns using multiple sequence alignment. BetaTurns: Predict different types of beta-turns in a protein. BhairPred: ANN and SVM based models for predicting beta hairpins in proteins. CHpredicts: Identification of CH-O, CH-PI interactions in backbone residues. GammaPred: Prediction of gamma-turn containing residues in a protein. SARpred: Predicting real-value of surface accessibility of protein residues. TBBpred: Identification of Transmembrane Beta Barrel regions in a protein.

Molecular Interactions in Biology Molecular interactions play a vital role in the field of biology whether it is protein-protein or protein-peptide or protein-nucleotide interactions. Raghava’s group developed web servers for predicting different type of interactions that includes interaction of proteins with peptide, DNA, RNA and ligand. Following are major web servers developed by his group. ATPint: Identification of ATP binding sites in ATP-binding proteins. GlycoEP: Prediction of C-, N- and O-glycosylation site in eukaryotic proteins. GlycoPP: Prediction of potential N-and O-glycosites in prokaryotic proteins. GTPbinder: Identification of GTP binding residue in protein sequences. NADbinder: Prediction of NAD binding proteins and their interacting residues. Pprint: A method for identification of RNA-interacting residues in a protein. PreMieR: Identification of mannose interacting residues in protein sequences. RNApin: Prediction of protein interacting nucleotides in RNA sequences.VitaPred: Identification of different class of vitamin interacting residues in a protein.

Annotation of Genomes/Proteomes Presently thousands of organisms have been sequenced and databases maintain whole genome sequencing is growing with exponential rate. This has posed a major challenge for bioinformaticians to annotate these genomes for predicting the genes and the repeat regions. The protein sequence databases are also growing exponentially due to progress in sequence techniques. The major problem is functional annotation, as most of the proteins obtained from the genomes do not provide any information about the function of protein. Group is developing in-silico methods for annotating genomes and proteomes. In case of genome annotation, group have developed tools for predicting i) protein coding region in prokaryotic genomes using Fast Fourier Transformation, ii) similarity aided ab Initio method for predicting location and structure of genes in eukaryote genomes, iii) identification of spectral repeats using FFT and iv) genome-wide similarity search using BLAST and FASTA. It is difficult to predict function of a protein directly, thus group developed methods for predicting important class of proteins and proteins reside in specific location of a cell. Following are major web-severs developed for functional annotation of proteins. NRpred: Model for prediction and classification of nuclear receptors. GPCRpred: Prediction of families and superfamilies of GPCR. PSLPred: Prediction of subcellular localization of bacterial proteins. Mitpred: Identification of mitochondrial proteins with high accuracy. HSLpred: Subcellular localization of human proteins. ALGpred: Prediction of allergenic proteins and mapping of IgE epitopes. PseaPred: Proteins secreted by malarial parasite into infected-erythrocyte. RSLPred: SVM based method for subcellular localization of rice proteins. COPid: Composition based identification and classification of proteins. ESLPred2: Subcellular localization of eukaryotic proteins. CyclinPred: A SVM based prediction method to identify novel cyclins. CytoPred: A webserver for prediction and classification of cytokines. TBPred: Subcellular localization of mycobacterial proteins. ProPrint: Protein-protein interaction prediction. Cancer_Pred: Specially trained for predicting the cancer lectins.

Development of Computational Resources for Drug Discovery Open Source Drug Discovery (OSDD) is an initiative with a vision to provide affordable healthcare to the developing world. Its major aims to synergize the power of genomics, computational technologies and facilitate the participation of young and brilliant talent from Universities and industry. Raghava’s group developed and maintain inslico module of OSDD called “Computational Resources for Drug Discovery (CRDD)”. Under CRDD all the resources related to computer-aided drug design(CADD) have been collected and compiled at a single platform. Major initiatives have been taken to bring down the cost of CAAD software by developing open source in the filed of drug discovery. Following are major web-services developed by his group. DrugMint: Prediction, virtual screening and design of Drug-like Molecules. MDRIpred: Identification of inhibitor against drug resistant M. Tuberculosis. KiDoQ: Inhibitiors against dihydrodipicolinate synthase enzyme of mycobacterium. TOXIpred: Prediction of aqueous toxicity of small molecules. MetaPred: Prediction of cytochrome P450 isoform responsible for metabolizing a drug molecule. GDoQ: Prediction of GLMU inhibitors using QSAR and docking approach. ntEGFR: Designing of imidazothiazoles/pyrazolopyrimidines based inhibitors against wild/mutant EGFR. DiPCells: Designing of inhibitors against pancreatic cancer cell lines.

Customized Operating System for Drug Design (OSDDlinux) OSDDlinux is a customized linux operating system for drug discovery that integrates open source software, libraries, workflows and web services in linux for creating environment for drug discovery. First time an attempt has been made to customize linux to provide service to the community working in the field of drug discovery. OSDDlinux may bring down the cost of drug discovery as well as it may increase speed of drug discovery. This open source operating system will allow students, academicians & researchers to contribute towards drug discovery/designing.

Infrastructure for Bioinformatics and IT related Services He is a coordinator of one of the Bioinformatics Centres established by DBT (Department of Biotechnology, India); all over India with the objectives to create infrastructure for information dissemination in the field of biotechnology. Over the years he has provided IT (Information Technology) related services to the scientific community and maintained world-class infrastructure for bioinformatics. A large number of web resources has been developed including creation of bioinformatics resouces at UAMS, USA. Following are major URLs provides the information of resources developed at maintained by his team; i) Institute home page http://webs.iiitd.edu.in/ , ii) Department web page http://webs.iiitd.edu.in/bic/ , iii) Group web page http://webs.iiitd.edu.in/raghava/ , iv) OSDDlinux http://osddlinux.osdd.net/ , v) CRDD web page http://webs.iiitd.edu.in/ , vi) CSIR informatics http://info.csir.res.in/ , vii) UAMS http://bioinformatics.uams.edu/ , viii) OSCADD http://webs.iiitd.edu.in/oscadd/ , ix) Google scholar page http://scholar.google.co.in/citations?user=XK5GUiYAAAAJ , x) Researchgate https://www.researchgate.net/profile/Gajendra_Raghava xi) WikiPedia http://en.wikipedia.org/wiki/Gajendra_Pal_Singh_Raghava