- Open Access
iDrug: a web-accessible and interactive drug discovery and design platform
© Wang et al.; licensee Chemistry Central Ltd. 2014
- Received: 20 March 2014
- Accepted: 12 May 2014
- Published: 23 May 2014
The progress in computer-aided drug design (CADD) approaches over the past decades accelerated the early-stage pharmaceutical research. Many powerful standalone tools for CADD have been developed in academia. As programs are developed by various research groups, a consistent user-friendly online graphical working environment, combining computational techniques such as pharmacophore mapping, similarity calculation, scoring, and target identification is needed.
We presented a versatile, user-friendly, and efficient online tool for computer-aided drug design based on pharmacophore and 3D molecular similarity searching. The web interface enables binding sites detection, virtual screening hits identification, and drug targets prediction in an interactive manner through a seamless interface to all adapted packages (e.g., Cavity, PocketV.2, PharmMapper, SHAFTS). Several commercially available compound databases for hit identification and a well-annotated pharmacophore database for drug targets prediction were integrated in iDrug as well. The web interface provides tools for real-time molecular building/editing, converting, displaying, and analyzing. All the customized configurations of the functional modules can be accessed through featured session files provided, which can be saved to the local disk and uploaded to resume or update the history work.
iDrug is easy to use, and provides a novel, fast and reliable tool for conducting drug design experiments. By using iDrug, various molecular design processing tasks can be submitted and visualized simply in one browser without installing locally any standalone modeling softwares. iDrug is accessible free of charge at http://lilab.ecust.edu.cn/idrug.
- Online drug design platform
- Cavity detection
- Pharmacophore search
- 3D similarity calculation
- Target prediction
Computer-aided drug design (CADD) is a widely used term that represents computational tools and sources for the storage, management, analysis and modeling of compounds . Benefiting from the dramatic increase of biomacromolecular and small molecular information, CADD techniques are used at various stages of a drug-discovery project, from target identification and validation to lead discovery and optimization, even extending to preclinical trials .
A huge body of CADD software has been developed over the years in many different research groups [3–11]. However, most molecular design packages, with single client interface and powerful algorithms, may require separate license keys to be purchased individually. In addition, due to the complexity and diversity of molecular design procedures, sometimes even trained computational chemists can not perfectly excel in what they are computing . In parallel, the open source and easily accessible software, which provides a great opportunity to perform research in CADD, has often encountered two main problems when being used by medicinal chemists . First, in many instances the authors of CADD software pay more attention to scientific details rather than the usability of software, thus making it rarely associated with the graphical user interface and difficult to use for non-expert experimentalists. Second, individual program usually requires a specific input structure and produces a specific output format, making users incapable of combining different programs.
The striking growth of web technologies provides an alternative strategy to offer the possibility of accessing and running computational chemistry tools directly on the web with a simplified user interface. The major advantages of these web-based solutions are that users can submit models and data to the online servers without regularly downloading and updating the data collections and tools to their local disks. An increasing number of web applications for performing molecular modeling and processing are also available for end users [14–17]. However, these tools are always not able to integrate various molecular design programs and enormous data collections to meet the systematic operations of users to achieve the best results . Besides, even if some initiatives combining different computational programs exists, e.g. for e-LEA3D , Sanjeevini , only focused on structure-based drug design such as molecular docking and de novo drug design which rely on the knowledge of the given structure of the target macromolecule.
List of computational techniques supported by i Drug
Free for academia
Detect and score potential binding sites of a protein
Derive pharmacophore models based on a given receptor of complex structure
Pharmacophore mapping (online web service)
3D similarity calculation
Molecular conformation generation
Python wrapper for the OpenBabel cheminformatics toolkit
Implementation and interface
Chemical and drug target database
Data source of i Drug
Number of entities
NCI Open Database
Cavity detection and structure-based pharmacophore modeling
Identification of protein cavities is of fundamental importance for structure-based pharmacophore derivation. iDrug applies Cavity to detect the potential binding sites on the surface of a given protein structure, and rank them according to the corresponding druggability scores on the basis of geometric shape, hydrogen bonding, and hydrophobic effects. By comparison of the success rate for the first-ranked prediction tested on the PDBBind dataset, Cavity outperformed four popularly used binding sites detection approaches (LIGSITEcsc, Q-sitefinder, SURFNET, and PASS), indicating its accurate prediction of relatively small binding sites on the surface of a protein [8, 33]. Li et al. customized LigBuilder 2.0 to generate and fit the shape of the Cyclophilin A (CypA) binding site and finally obtained two highly potent inhibitors with nanomolar inhibitory potencies (2.59 nM and 1.52 nM) . A receptor-based pharmacophore modeling program Pocket v.2 was used to extract pharmacophore features within cavities . In this approach, hotspot analysis and grid-based scoring were used to identify essential pharmacophore features. As suggested by case study results, Pocket v.2 can yield consistent pharmacophore models for proteins with minor conformational changes upon binding of different ligands, indicating the robustness of the approach. Lai et al. proposed a novel strategy that combined receptor-based common pharmacophores with molecular docking. Three compounds were identified through this strategy to inhibit LTA4H-h and hnps-PLA2 simultaneously .
Normally, iDrug requires a protein 3D structure or a known PDB accession code as input to derive pharmacophore models. All binding sites along with the extracted pharmacophore features will be displayed and ranked by the druggability scores. A small molecular 3D structure in the corresponding binding poses conformation can also be uploaded as the reference to specify the position of the binding site and generate the pharmacophore features representing the corresponding interaction mode. It takes averagely 1–3 minutes for binding sites detection, and the potential binding sites can be interactively viewed and downloaded in PDB files for off-line analysis, which includes the binding pocket surface, the residues around the site, and key features of the pharmacophore model derived from the site.
Pharmacophore mapping and virtual screening
For pharmacophore-based screening, iDrug employs a pharmacophore mapping method called PharmMapper based on feature triplet hashing and searching algorithm . Liu et al. discovered two potent IGF-1R kinase inhibitors via hierarchical strategy based virtual screening (pharmacophore screening and docking), which efficiently reduced the number of “nonhits” passed to docking stage and consequently reduced the computational cost .
The query pharmacophore model can be derived from the potential binding sites detected previously or user customized ones. iDrug allows interactive editing of the features of the pharmacophore query like feature type, positions, and size of the tolerance spheres. Pharmacophore searching is performed against the available or user uploaded databases. The hit compounds are compiled into the table with the corresponding original weblinks whereas applicable, and ranked by the fit values with the query. The superimposed mode of the molecules onto the pharmacophore query along with the corresponding binding site can be interactively visualized in Jmol applet.
iDrug uses the reverse pharmacophore mapping procedure to predict potential drug targets. Qian et al. discovered a novel series of acenaphtho[1,2-b]pyrrole derivatives as potent FGFR1 inhibitors by using this in silico targets screening approach . The results were subsequently validated by enzyme-linked immunosorbent assay. The platform takes a single drug-like molecule or natural product chemical structure as an input and automatically perceives all chemotype features of the query molecule. Users are allowed to modify the perceived pharmacophore model and search the pharmacophore target database with it. The results can also be filtered in terms of both the number of returned results and the properties of the algorithm. Since the geometric matching alignment and scoring method uses rigid conformations, multiple conformers of each query molecule must be generated. In-house program Cyndi [38, 39], which uses a multi-objective evolution algorithm method for conformer searching, was chosen by default to generate multiple conformation. Additionally, the minimum number of each pharmacophore feature type and a fit score cutoff can be specified to discard those target pharmacophore models, of which the corresponding values are less than the threshold. On average, the total time consumed by the complete screening and scoring protocol ranges from 1-2 h depending on the flexibility of the input molecule and filter parameters assigned by the user.
Upon completion of the computations, the results of the hit target pharmacophore models are demonstrated in the form of a ranked list. Each row contains the protein ID, which is a hyperlink points to the PDB website , the target name, the fit values between the small molecule and the pharmacophores, and a unique orientation of a conformation of the query along with the 3D structure information of the target visualized by the Jmol applet. Detailed annotations of the hit targets are presented in a pop-up window when the cursor moves over the corresponding PDB codes. Alternatively, a downloadable zip file containing the aligned pose with the corresponding pharmacophore model and the complete targets information in CSV format is accessible for each returned match.
For the implementation of ligand-based searching, iDrug adopts an efficient 3D similarity calculation method SHAFTS, which is designed to integrate the strength of pharmacophore matching and volumetric overlay approaches . Hits are determined by a hybrid similarity score cut-off and alignment poses of compounds will be generated by enumerating all potential pharmacophore feature triplets matches. Liu et al. discovered sixteen compounds with IC50 < 20 μM, three of which showed low micromolar inhibitory activities against p90 ribosomal S6 protein kinase 2 (RSK2) and exhibited selectivity across a panel of related kinases using SHAFTS . By adopting the same strategy, Xu et al. reported a novel pteridin-7(8H)-one epidermal growth factor receptor (EGFR) inhibitor scaffold with potent and selective inhibitory activity against both wild-type and T790M/L858R mutant EGFRs. The most remarkable agent showed highly inhibitory activity against the growth of gefitinib-resistant H1975 cells, making it a potential lead for further development of EGFR kinase-related anticancer drugs . The results suggests that SHAFTS is an efficient and powerful tool in scaffold hopping and hit identification endeavors. Moreover, Shen et al. used the evodiamine derivative as a probe to search MDL/Symyx Drug Data Report (MDDR)  with ChemMapper. The fourth ranked protein, topoisomerase II (Top2), was a well-known antitumor target. Relaxation assay proved that the analogs of the natural product are potent inhibitor against Top2, with stronger activity than the well-known Top2α inhibitor etoposide .
A chemical structure (sketched online or uploaded in multiple chemical structure file formats) is accepted as the query to perform similarity searching. It takes hours to days per search depending on the complexity of the query molecule and the size of the library.
The outputs are generated as a list of compounds sorted by similarity scores to the query and can be downloaded in a mol2 file. The superimposed pose of each hit with the query can be visualized interactively in Jmol applet along with the molecular surface representation and perceived pharmacophore features by SHAFTS.
Case 1: pharmacophore-based virtual screening
AUC value and EF values at 0.5, 1, 2 and 5% for CDK2 inhibitor pharmacophore-based virtual screening
Case 2: target prediction
Retrieval of 11 targets of 4OH-Tamoxifen by i Drug
Estradiol 17β-hydroxysteroid dehydrogenase 1
Glutathione S-transferase A1
Prostaglandin G/H synthase 2
Liver carboxylesterase 1
Protein kinase C theta type
Alcohol dehydrogenase E chain
Case 3: molecular 3D similarity-based screening
The crystal ligand structure of epidermal growth factor receptor (EGFR, PDB:2RGP) was searched via iDrug. The screening library was created using the DUD-E data sets including 542 active compounds and 35,050 decoy compounds for a baseline enrichment of 1.5%. A multiconformer library was generated using Cyndi with the default settings (up to 200 conformers per a compound), resulting in a library of 2,735,015 conformations.
AUC value and EF values at 0.5, 1, 2 and 5% for EGFR inhibitor similarity virtual screening
Compound data sets
Datasets from four different public sources were used. A set of over 3 million compounds extracted from ZINC  and NCI  were used for both pharmacophore and 3D similarity based virtual screening. Cyndi  was used to generate a maximum of 50 low-energy conformations for each compound. The MUV data sets are based on bioactivity data. MUV consists of 17 targets, each with 30 actives and 15000 decopys . In this study we reproduced the evaluation of Sanders et al and derived pharmacophore queries from the crystal structure of CDK2 (PDB:1AQ1). The DUD-E was originally designed for benchmarking of docking methods . A subset was later extracted for the use in 3D similarity-based virutal screening experiments. The DUD-E contains 102 targets with 22886 clustered ligands drawn from ChEMBL, each with 50 property-matched decoys drawn from ZINC. In this study EGFR with 542 actives were used. Besides, for the user uploaded target compounds, multi conformations (at most 100) would be generated online with Cyndi prior to virtual screening if the ‘Generate Conformers’ is toggled on.
Target pharmacophore databases
The target protein structures co-complexed with small molecules were selected from DrugBank, BindingDB, PDBBind, and PDTD databases. All the small ligands with molecular weight lower than 100, such as solvents, buffers and metal cations, and all the cofactors with molecular weight over 600, such as CoAs, polypeptides and nucleic acids were regarded. For the proteins existing as homopolymers, only one monomer was reserved for analysis. For the proteins determined by NMR with multiple structure models, only the first model was selected for pharmacophore generation. LigandScout  was used in the process of pharmacophore model derivation. As a result, a database with 7302 pharmacophore models were generated and stored in iDrug. This database has been used in our previous publications .
We presented iDrug, a versatile web server for both pharmacophore- and similarity-based virtual screening and target identification to facilitate computational drug discovery. The interface is easy-to-use and can be accessed by user customized sessions to free them from installing standalone softwares. iDrug provides ready-to-access compounds and pharmacophore target databases for virtual screening and target identification. Various applications like binding site identification, structure-based pharmacophore derivation, conformational sampling, pharmacophore searching, and 3D similarity calculation are integrated as individual modules. It enables interactive editing and refinement of pharmacophore hypothesis as well as flexible customization of the parameters. The featured job management system ensures the user privacy and project tracking through a session-based mechanism.
This work was supported by the 863 Hi-Tech Program of China (grant 2012AA020308), the National Natural Science Foundation of China (grants 81230090, 81222046 and 81230076), the Shanghai Committee of Science and Technology (grant 12401900801), and the National S&T Major Project of China (Grants 2013ZX09507004). Honglin Li is also sponsored by Shanghai Rising-Star Tracking Program (grant 13QH1401100) and Fok Ying Tung Education Foundation (141035).
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