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-Structure paper
Title | Feasibility and physiological relevance of designing highly potent aminopeptidase-sparing leukotriene A4 hydrolase inhibitors. |
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Journal, issue, pages | Sci Rep, Vol. 7, Page 13591-13591, Year 2017 |
Publish date | Oct 4, 2017 (structure data deposition date) |
Authors | Numao, S. / Hasler, F. / Laguerre, C. / Srinivas, H. / Wack, N. / Jager, P. / Schmid, A. / Osmont, A. / Rothlisberger, P. / Houguenade, J. ...Numao, S. / Hasler, F. / Laguerre, C. / Srinivas, H. / Wack, N. / Jager, P. / Schmid, A. / Osmont, A. / Rothlisberger, P. / Houguenade, J. / Bergsdorf, C. / Dawson, J. / Carte, N. / Hofmann, A. / Markert, C. / Hardaker, L. / Billich, A. / Wolf, R.M. / Penno, C.A. / Bollbuck, B. / Miltz, W. / Rohn, T.A. |
External links | Sci Rep / PubMed:29051536 |
Methods | X-ray diffraction |
Resolution | 1.84 - 2.24 Å |
Structure data | PDB-6enb: PDB-6enc: PDB-6end: |
Chemicals | ChemComp-ZN: ChemComp-ACT: ChemComp-YB: ChemComp-IMD: ChemComp-HOH: ChemComp-BGW: ChemComp-BGK: |
Source |
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Keywords | HYDROLASE / LTA4H / Substrate / inhibitor |