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PDBe Entry: 3cho 
Crystal structure of leukotriene a4 hydrolase in complex with 2-amino-N-[4-(phenylmethoxy)phenyl]-acetamide
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HYDROLASE
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X-RAY DIFFRACTION
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Resolution: 1.8 Å, R-factor: 18.9%, Free R-factor: 22.3%, Spacegroup: P 21 21 21
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22/04/2008, deposition: 10/03/2008, last revision: 24/02/2009
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Thunnissen, M.M.G.M. ; Adler, M. ; Whitlow, M.
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Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase. BIOORG.MED.CHEM. vol:16, pag:4963-4983 (2008) [PubMed ID 18394906 ]
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EPOXIDE HYDROLASE , ALPHA-BETA PROTEIN , LEUKOTRIENE BIOSYNTHESIS , METALLOPROTEASE , Inhibitor complex , Alternative splicing , Cytoplasm , Metal-binding , Multifunctional enzyme , Zinc
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3.3.2.6 ExPASy BRENDA (A)
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Homo sapiens(human) 9606 (A)
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Leukotriene A-4 hydrolase (EC 3.3.2.6) (Leukotriene A(4) hydrolase) (LTA-4 hydrolase) P09960 (A)
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A
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1hs6, 1gw6, 1h19, 1sqm, 3chp, 3chq, 3chr, 3chs, 2vj8
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| A |
Leukotriene A-4 hydrolase |
Protein |
P09960 (LKHA4_HUMAN)
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610 |
100% |
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| A |
ZINC ION |
ZN
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| A |
YTTERBIUM (III) ION |
YB
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| A |
ACETATE ION |
ACT
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| A |
N-[4-(BENZYLOXY)PHENYL]GLYCINAMIDE |
4BG
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