Bayesian model for the classification of GPCR agonists and antagonists

Inhee Choi, Hanjo Kim, Jihoon Jung, Ky Youb Nam, Sung Eun Yoo, Nam Sook Kang, Kyoung Tai No

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


G-protein coupled receptors (GPCRs) are involved in a wide variety of physiological processes and are known to be targets for nearly 50% of drugs. The various functions of GPCRs are affected by their cognate ligands which are mainly classified as agonists and antagonists. The purpose of this study is to develop a Bayesian classification model, that can predict a compound as either human GPCR agonist or antagonist. Total 6627 compounds experimentally determined as either GPCR agonists or antagonists covering all the classes of GPCRs were gathered to comprise the dataset. This model distinguishes GPCR agonists from GPCR antagonists by using chemical fingerprint, FCFP-6. The model revealed distinctive structural characteristics between agonistic and antagonistic compounds: in general, 1) GPCR agonists were flexible and had aliphatic amines, and 2) GPCR antagonists had planar groups and aromatic amines. This model showed very good discriminative ability in general, with pretty good discriminant statistics for the training set (accuracy: 90.1%) and a good predictive ability for the test set (accuracy: 89.2%). Also, receiver operating characteristic (ROC) plot showed the area under the curve (AUC) to be 0.957, and Matthew's Correlation Coefficient (MCC) value was 0.803. The quality of our model suggests that it could aid to classify the compounds as either GPCR agonists or antagonists, especially in the early stages of the drug discovery process.

Original languageEnglish
Pages (from-to)2163-2169
Number of pages7
JournalBulletin of the Korean Chemical Society
Issue number8
Publication statusPublished - 2010 Aug 20

All Science Journal Classification (ASJC) codes

  • Chemistry(all)


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