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TB Mobile: Appifying Data on Antituberculosis Molecule
                       Targets



 Sean Ekins1, 2 , Alex M. Clark3, Malabika Sarker4, Carolyn Talcott4,
                            Barry A. Bunin2

     Collaborative Drug Discovery, 1633 Bayshore Highway, Suite 342, Burlingame, CA 94010, USA.
     1

       2
        Collaborations in Chemistry, 5616 Hilltop Needmore Road, Fuquay-Varina, NC 27526, USA.
      3
       Molecular Materials Informatics, 1900 St. Jacques #302, Montreal Quebec, Canada H3J 2S1
                4
                 SRI International, 333 Ravenswood Avenue, Menlo Park, CA 94025, USA.

                                                 .
TB facts

    Tuberculosis Kills 1.6-1.7m/yr (~1 every 8 seconds)
    1/3rd of worlds population infected!!!!

    Multi drug resistance in 4.3% of cases
    Extensively drug resistant increasing incidence
    No new drugs in over 40 yrs until Bedaquiline
    Drug-drug interactions and Co-morbidity with HIV

    Increase in HTS phenotypic screening
    1000’s of hits no idea of target

    Use of computational methods with TB is rare

    Ekins et al,
    Trends in Microbiology
    19: 65-74, 2011
~ 20 public datasets for TB
Including Novartis data on TB hits
>300,000 cpds

Patents, Papers Annotated by CDD

Open to browse by anyone

 http://www.collaborativedrug.
 com/register
Fitting into the drug discovery
                  process




Ekins et al,
Trends in
Microbiology
19: 65-74, 2011
Predicting the target/s for small molecules




                  Pathway analysis
                  Binding site similarity to Mtb proteins
                  Docking
                  Bayesian Models - ligand similarity
Dataset Curation: TB molecules and target information
  database connects molecule, gene, pathway and literature
Multi-step process

1.Identification of essential in vivo enzymes of Mtb involved intensive literature
mining and manual curation, to extract all the genes essential for Mtb growth in
vivo across species.

2.Homolog information was collated from other studies.

3.Collection of metabolic pathway information involved using TBDB.

4.Identifying molecules and drugs with known or predicted targets involved
searching the CDD databases for manually curated data. The structures and
data were exported for combination with the other data.

5.All data were combined with URL links to literature and TBDB and deposited in
the CDD database.

Over 700 molecules in dataset
                                Sarker et al., Pharm Res 2012, 29, 2115-2127.
TB molecules and target information database connects
       molecule, gene, pathway and literature
Why not create an App for TB?




                                         Exposure to huge audience
                                          with “smart phones”
                                         Make science more
                                          accessible = >communication
                                         Hardware is powerful
                                         Mobile – take a phone into
                                          field and do science more
                                          readily than a laptop
Williams et al DDT 16:928-939, 2011      Bite size chunk of program
TB content in Open Drug Discovery Teams (ODDT)




Sharing information and molecules openly – useful experience for
developing TB Mobile
                                       Mol Inform. 2012 Aug;31(8):585-597
TB Mobile layout on iPhone and Android




    iPhone                  Android
TB Mobile Molecule Detail and Links




iPhone                 Android
TB Mobile Similarity Searching in the app




  iPhone                   Android
TB Mobile – Filtering and Sharing Functions




 Each molecule can be copied to the clipboard then
 opened with other apps (e.g. MMDS, MolPrime,
 MolSync, ChemSpider, and from these exported via
 Twitter or email) or shared via Dropbox.
TB Mobile – Filtering and Sharing Functions




Data can also be filtered by target name, pathway name,
essentiality and human ortholog
Process used to evaluate TB Mobile

   Draw structures either in app or paste from
    other apps e.g. MMDS
   TB Mobile ranks content
   Take a screenshot of results
   Compare to published data
   Annotate results, tabulate
Results for pyridomycin on iPad
14 First line drugs active against Mtb evaluated in
 TB Mobile app and the top 3 molecules shown




     Confirms all in TB Mobile and retrieved
May suggest additional potential targets for known drugs
Pyrazinamide - activated to pyrazinoic acid may have
several targets e.g. FAS I and others
Molecules active against Mtb evaluated in TB Mobile app

 to illustrate a workflow we have curated an additional set
 of 20 molecules published since 2009 that have activity
 against Mtb and were identified by HTS or other methods
Molecules active against Mtb evaluated in TB Mobile app
Using TB Mobile app with
     recent GSK TB hits

Ballel et al.,
Fueling Open-Source drug discovery: 177 small-
molecule leads against tuberculosis
ChemMedChem 2013.


11 hits from GSK may be targeting a limited
array of targets.

TB Mobile biased towards those with larger
numbers of molecules.

GSK353069A looks like a dhfr inhibitor.

No experimental verification of these predictions

Compound availability is however unclear.
TB Mobile – poster on




                        http://goo.gl/UTTH0
TB Mobile – Is on iTunes and Google play
                    and it is FREE




http://goo.gl/vPOKS



                              http://goo.gl/iDJFR
TB mobile – find out more at www.scimobileapps.com




                 http://goo.gl/Goa4e
TB Mobile – Is on the Pistoia Alliance App Catalog




                     Connectivity with other apps from
                     Molecular Materials Informatics
Paper published




http://goo.gl/7fGFW
What next ?

   Update with more data
   Add a weighting or scoring function to account
    for heavily populated targets
   Expand beyond the similarity measure
   Add algorithms to predict activity

   Could we appify data for other diseases/ targets
Benefits of creating TB Mobile

   Exposure of CDD content from collaboration with
    SRI
   More visibility for brand in new places
   Experiment in small database with focus on
    content delivery
   A functional app to reach scientists that may not
    have cheminformatics or bioinformatics training
Acknowledgments

   2R42AI088893-02 “Identification of novel therapeutics for tuberculosis
    combining cheminformatics, diverse databases and logic based pathway
    analysis” from the National Institute of Allergy And Infectious Diseases. (PI:
    S. Ekins)

   The CDD TB has been developed thanks to funding from the Bill and
    Melinda Gates Foundation (Grant#49852 “Collaborative drug discovery for
    TB through a novel database of SAR data optimized to promote data
    archiving and sharing”).
You can find me @...                                               CDD Booth 205
PAPER ID: 13433
PAPER TITLE: “Dispensing processes profoundly impact biological assays and computational and
statistical analyses”
April 8th 8.35am Room 349

PAPER ID: 14750
PAPER TITLE: “Enhancing High Throughput Screening For Mycobacterium tuberculosis Drug Discovery
Using Bayesian Models”
April 9th 1.30pm Room 353
PAPER ID: 21524

PAPER TITLE: “Navigating between patents, papers, abstracts and databases using public sources and
tools”
April 9th 3.50pm Room 350
PAPER ID: 13358

PAPER TITLE: “TB Mobile: Appifying Data on Anti-tuberculosis Molecule Targets”
April 10th 8.30am Room 357

PAPER ID: 13382
PAPER TITLE: “Challenges and recommendations for obtaining chemical structures of industry-provided
repurposing candidates”
April 10th 10.20am Room 350

PAPER ID: 13438
PAPER TITLE: “Dual-event machine learning models to accelerate drug discovery”
April 10th 3.05 pm Room 350

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TB Mobile: Appifying data on antituberculosis molecule targets

  • 1. TB Mobile: Appifying Data on Antituberculosis Molecule Targets Sean Ekins1, 2 , Alex M. Clark3, Malabika Sarker4, Carolyn Talcott4, Barry A. Bunin2 Collaborative Drug Discovery, 1633 Bayshore Highway, Suite 342, Burlingame, CA 94010, USA. 1 2 Collaborations in Chemistry, 5616 Hilltop Needmore Road, Fuquay-Varina, NC 27526, USA. 3 Molecular Materials Informatics, 1900 St. Jacques #302, Montreal Quebec, Canada H3J 2S1 4 SRI International, 333 Ravenswood Avenue, Menlo Park, CA 94025, USA. .
  • 2. TB facts  Tuberculosis Kills 1.6-1.7m/yr (~1 every 8 seconds)  1/3rd of worlds population infected!!!!  Multi drug resistance in 4.3% of cases  Extensively drug resistant increasing incidence  No new drugs in over 40 yrs until Bedaquiline  Drug-drug interactions and Co-morbidity with HIV  Increase in HTS phenotypic screening  1000’s of hits no idea of target  Use of computational methods with TB is rare Ekins et al, Trends in Microbiology 19: 65-74, 2011
  • 3. ~ 20 public datasets for TB Including Novartis data on TB hits >300,000 cpds Patents, Papers Annotated by CDD Open to browse by anyone http://www.collaborativedrug. com/register
  • 4. Fitting into the drug discovery process Ekins et al, Trends in Microbiology 19: 65-74, 2011
  • 5. Predicting the target/s for small molecules Pathway analysis Binding site similarity to Mtb proteins Docking Bayesian Models - ligand similarity
  • 6. Dataset Curation: TB molecules and target information database connects molecule, gene, pathway and literature Multi-step process 1.Identification of essential in vivo enzymes of Mtb involved intensive literature mining and manual curation, to extract all the genes essential for Mtb growth in vivo across species. 2.Homolog information was collated from other studies. 3.Collection of metabolic pathway information involved using TBDB. 4.Identifying molecules and drugs with known or predicted targets involved searching the CDD databases for manually curated data. The structures and data were exported for combination with the other data. 5.All data were combined with URL links to literature and TBDB and deposited in the CDD database. Over 700 molecules in dataset Sarker et al., Pharm Res 2012, 29, 2115-2127.
  • 7. TB molecules and target information database connects molecule, gene, pathway and literature
  • 8. Why not create an App for TB?  Exposure to huge audience with “smart phones”  Make science more accessible = >communication  Hardware is powerful  Mobile – take a phone into field and do science more readily than a laptop Williams et al DDT 16:928-939, 2011  Bite size chunk of program
  • 9. TB content in Open Drug Discovery Teams (ODDT) Sharing information and molecules openly – useful experience for developing TB Mobile Mol Inform. 2012 Aug;31(8):585-597
  • 10. TB Mobile layout on iPhone and Android iPhone Android
  • 11. TB Mobile Molecule Detail and Links iPhone Android
  • 12. TB Mobile Similarity Searching in the app iPhone Android
  • 13. TB Mobile – Filtering and Sharing Functions Each molecule can be copied to the clipboard then opened with other apps (e.g. MMDS, MolPrime, MolSync, ChemSpider, and from these exported via Twitter or email) or shared via Dropbox.
  • 14. TB Mobile – Filtering and Sharing Functions Data can also be filtered by target name, pathway name, essentiality and human ortholog
  • 15. Process used to evaluate TB Mobile  Draw structures either in app or paste from other apps e.g. MMDS  TB Mobile ranks content  Take a screenshot of results  Compare to published data  Annotate results, tabulate
  • 17. 14 First line drugs active against Mtb evaluated in TB Mobile app and the top 3 molecules shown Confirms all in TB Mobile and retrieved
  • 18. May suggest additional potential targets for known drugs Pyrazinamide - activated to pyrazinoic acid may have several targets e.g. FAS I and others
  • 19. Molecules active against Mtb evaluated in TB Mobile app to illustrate a workflow we have curated an additional set of 20 molecules published since 2009 that have activity against Mtb and were identified by HTS or other methods
  • 20. Molecules active against Mtb evaluated in TB Mobile app
  • 21. Using TB Mobile app with recent GSK TB hits Ballel et al., Fueling Open-Source drug discovery: 177 small- molecule leads against tuberculosis ChemMedChem 2013. 11 hits from GSK may be targeting a limited array of targets. TB Mobile biased towards those with larger numbers of molecules. GSK353069A looks like a dhfr inhibitor. No experimental verification of these predictions Compound availability is however unclear.
  • 22. TB Mobile – poster on http://goo.gl/UTTH0
  • 23. TB Mobile – Is on iTunes and Google play and it is FREE http://goo.gl/vPOKS http://goo.gl/iDJFR
  • 24. TB mobile – find out more at www.scimobileapps.com http://goo.gl/Goa4e
  • 25. TB Mobile – Is on the Pistoia Alliance App Catalog Connectivity with other apps from Molecular Materials Informatics
  • 27. What next ?  Update with more data  Add a weighting or scoring function to account for heavily populated targets  Expand beyond the similarity measure  Add algorithms to predict activity  Could we appify data for other diseases/ targets
  • 28. Benefits of creating TB Mobile  Exposure of CDD content from collaboration with SRI  More visibility for brand in new places  Experiment in small database with focus on content delivery  A functional app to reach scientists that may not have cheminformatics or bioinformatics training
  • 29. Acknowledgments  2R42AI088893-02 “Identification of novel therapeutics for tuberculosis combining cheminformatics, diverse databases and logic based pathway analysis” from the National Institute of Allergy And Infectious Diseases. (PI: S. Ekins)  The CDD TB has been developed thanks to funding from the Bill and Melinda Gates Foundation (Grant#49852 “Collaborative drug discovery for TB through a novel database of SAR data optimized to promote data archiving and sharing”).
  • 30. You can find me @... CDD Booth 205 PAPER ID: 13433 PAPER TITLE: “Dispensing processes profoundly impact biological assays and computational and statistical analyses” April 8th 8.35am Room 349 PAPER ID: 14750 PAPER TITLE: “Enhancing High Throughput Screening For Mycobacterium tuberculosis Drug Discovery Using Bayesian Models” April 9th 1.30pm Room 353 PAPER ID: 21524 PAPER TITLE: “Navigating between patents, papers, abstracts and databases using public sources and tools” April 9th 3.50pm Room 350 PAPER ID: 13358 PAPER TITLE: “TB Mobile: Appifying Data on Anti-tuberculosis Molecule Targets” April 10th 8.30am Room 357 PAPER ID: 13382 PAPER TITLE: “Challenges and recommendations for obtaining chemical structures of industry-provided repurposing candidates” April 10th 10.20am Room 350 PAPER ID: 13438 PAPER TITLE: “Dual-event machine learning models to accelerate drug discovery” April 10th 3.05 pm Room 350