Abstract

Open PHACTS is a pre-competitive project to answer scientific questions developed recently by the pharmaceutical industry. Having high quality biological interaction information in the Open PHACTS Discovery Platform is needed to answer multiple pathway related questions. To address this, updated WikiPathways data has been added to the platform. This data includes information about biological interactions, such as stimulation and inhibition. The platform's Application Programming Interface (API) was extended with appropriate calls to reference these interactions. These new methods of the Open PHACTS API are available now.

Highlights

  • Targeting proteins to ideally restore normal biological processes is a common starting point in drug discovery[1]

  • The importance and need of providing access to interaction information for real-world research questions was outlined in a recent Open PHACTS paper[8]

  • The Open PHACTS project was born out of the desire to integrate pharmacological data from multiple pre-competitive sources to efficiently address scientific questions that cannot be answered with single data sources[8]

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Summary

Introduction

Targeting proteins to ideally restore normal biological processes is a common starting point in drug discovery[1]. The Open PHACTS project was born out of the desire to integrate pharmacological data from multiple pre-competitive sources to efficiently address scientific questions that cannot be answered with single data sources[8]. It integrates data using linked data approaches[3] from chemical and biological sources such as ChEBI, ChEMBL, UniProt, and WikiPathways[6]. The OPDP did not previously include calls to access specific up- and downstream interaction effects This information is needed for questions related to drug repositioning and repurposing. We describe how to identify alternative targets in the same cellular pathway using OPDP against the WikiPathways data

Methods
Schreiber SL
Full Text
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