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TitleFeasibility and physiological relevance of designing highly potent aminopeptidase-sparing leukotriene A4 hydrolase inhibitors.
Journal, issue, pagesSci Rep, Vol. 7, Page 13591-13591, Year 2017
Publish dateOct 4, 2017 (structure data deposition date)
AuthorsNumao, 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 linksSci Rep / PubMed:29051536
MethodsX-ray diffraction
Resolution1.84 - 2.24 Å
Structure data

PDB-6enb:
LTA4 hydrolase (E297Q) mutant in complex with Pro-Gly-Pro peptide
Method: X-RAY DIFFRACTION / Resolution: 1.84 Å

PDB-6enc:
LTA4 hydrolase in complex with Compound11
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

PDB-6end:
LTA4 hydrolase in complex with Compound15
Method: X-RAY DIFFRACTION / Resolution: 2.24 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-ACT:
ACETATE ION

ChemComp-YB:
YTTERBIUM (III) ION

ChemComp-IMD:
IMIDAZOLE

ChemComp-HOH:
WATER

ChemComp-BGW:
1-[[4-(1,3-benzothiazol-2-yloxy)phenyl]methyl]piperidine-4-carboxylic acid

ChemComp-BGK:
4-([1,3]thiazolo[4,5-b]pyridin-2-yloxy)benzaldehyde

Source
  • homo sapiens (human)
KeywordsHYDROLASE / LTA4H / Substrate / inhibitor

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