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-Structure paper
Title | Potent, selective and orally bioavailable leucine-rich repeat kinase 2 (LRRK2) inhibitors. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 26, Page 2631-2635, Year 2016 |
Publish date | Feb 18, 2016 (structure data deposition date) |
Authors | Greshock, T.J. / Sanders, J.M. / Drolet, R.E. / Rajapakse, H.A. / Chang, R.K. / Kim, B. / Rada, V.L. / Tiscia, H.E. / Su, H. / Lai, M.T. ...Greshock, T.J. / Sanders, J.M. / Drolet, R.E. / Rajapakse, H.A. / Chang, R.K. / Kim, B. / Rada, V.L. / Tiscia, H.E. / Su, H. / Lai, M.T. / Sur, S.M. / Sanchez, R.I. / Bilodeau, M.T. / Renger, J.J. / Kern, J.T. / McCauley, J.A. |
External links | Bioorg. Med. Chem. Lett. / PubMed:27106707 |
Methods | X-ray diffraction |
Resolution | 2.33 Å |
Structure data | PDB-5i8a: |
Chemicals | ChemComp-69C: ChemComp-CL: ChemComp-ACT: ChemComp-HOH: |
Source |
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Keywords | TRANSFERASE/TRANSFERASE INHIBITOR / kinase / inhibitor / active site / TRANSFERASE-TRANSFERASE INHIBITOR complex |