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Structure paper

TitleBinding of Pro-Gly-Pro at the active site of leukotriene A4 hydrolase/aminopeptidase and development of an epoxide hydrolase selective inhibitor.
Journal, issue, pagesProc. Natl. Acad. Sci. USA, Vol. 111, Page 4227-4232, Year 2014
Publish dateJun 4, 2013 (structure data deposition date)
AuthorsStsiapanava, A. / Olsson, U. / Wan, M. / Kleinschmidt, T. / Rutishauser, D. / Zubarev, R.A. / Samuelsson, B. / Rinaldo-Matthis, A. / Haeggstrom, J.Z.
External linksProc. Natl. Acad. Sci. USA / PubMed:24591641
MethodsX-ray diffraction
Resolution1.618 - 1.72 Å
Structure data

PDB-4l2l:
Human Leukotriene A4 Hydrolase complexed with ligand 4-(4-benzylphenyl)thiazol-2-amine
Method: X-RAY DIFFRACTION / Resolution: 1.648 Å

PDB-4mkt:
Human Leukotriene A4 Hydrolase in complex with Pro-Gly-Pro analogue and 4-(4-benzylphenyl)thiazol-2-amine
Method: X-RAY DIFFRACTION / Resolution: 1.618 Å

PDB-4ms6:
Human Leukotriene A4 Hydrolase in complex with Pro-Gly-Pro analogue
Method: X-RAY DIFFRACTION / Resolution: 1.72 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-1V6:
4-(4-benzylphenyl)-1,3-thiazol-2-amine

ChemComp-YB:
YTTERBIUM (III) ION

ChemComp-ACT:
ACETATE ION

ChemComp-HOH:
WATER

ChemComp-28T:
1-{4-oxo-4-[(2S)-pyrrolidin-2-yl]butanoyl}-L-proline

ChemComp-ACY:
ACETIC ACID

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / Metalloprotein / Hydrolase / protease / Zinc binding / HYDROLASE-HYDROLASE INHIBITOR complex / Leukotriene A4 Hydrolase

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