Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Charles H. Clapp"'
Autor:
Kathleen A. Bishop, Megan Young, Natasha F. Bassett, Yuhan Fu, Thomas Young, Justin Pachuski, Gillian Carter, Charles H. Clapp
Publikováno v:
Bioorganic chemistry. 78
Lipoxygenases catalyze the oxygenation of polyunsaturated fatty acids and their derivatives to produce conjugated diene hydroperoxides. Soybean lipoxygenase-1 (SBLO-1) has been the subject of intensive structural and mechanistic study, but the manner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8861cd14240e228bd0233967a01bc4c
https://pubmed.ncbi.nlm.nih.gov/29573638
https://pubmed.ncbi.nlm.nih.gov/29573638
Autor:
Morgan J. Price, Dillon Hershelman, Patricia A. Plumeri, Peter M. Findeis, Iris Lu, Charles H. Clapp, Yuhan Fu, Fred Karaisz, Kirsten M. Kahler, Natasha F. Bassett
Publikováno v:
Archives of Biochemistry and Biophysics. 674:108082
Plant lipoxygenases oxygenate linoleic acid to produce 13(S)-hydroperoxy-9Z,11E-octadecadienoic acid (13(S)-HPOD) or 9-hydroperoxy-10E,12Z-octadecadienoic acid (9(S)-HPOD). The manner in which these enzymes bind substrates and the mechanisms by which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cfb30a0cac20abb1723dcc2e3f59343
https://doi.org/10.1016/j.abb.2019.108082
https://doi.org/10.1016/j.abb.2019.108082
Autor:
David J. Hinnenkamp, Charles H. Clapp
Publikováno v:
The FASEB Journal. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d275a968240aeb335274eed57334bdb6
https://doi.org/10.1096/fasebj.30.1_supplement.1083.9
https://doi.org/10.1096/fasebj.30.1_supplement.1083.9
Autor:
Natasha F. Bassett, Charles H. Clapp
Publikováno v:
The FASEB Journal. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbbcbf211f0f857ac4033990697d5fb3
https://doi.org/10.1096/fasebj.30.1_supplement.1083.15
https://doi.org/10.1096/fasebj.30.1_supplement.1083.15
Publikováno v:
The FASEB Journal. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::149d954a9fbde9424a5ba16cc7b027ac
https://doi.org/10.1096/fasebj.30.1_supplement.1083.17
https://doi.org/10.1096/fasebj.30.1_supplement.1083.17
Autor:
Danny Muskardin, Charles H. Clapp, Yingmei Yang, Anna Marie Grandizio, Michael Kagey, and Alan Bicker, Douglas Turner
Publikováno v:
Biochemistry. 41:11504-11511
Soybean lipoxygenase-1 is inactivated by micromolar concentrations of the following hydrophobic thiols: 1-octanethiol, 12(S)-mercapto-9(Z)-octadecenoic acid (S-12-HSODE), 12(R)-mercapto-9(Z)-octadecenoic acid (R-12-HSODE), and 12-mercaptooctadecanoic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb5ff968491e9d363ff24a2133954533
https://doi.org/10.1021/bi020229m
https://doi.org/10.1021/bi020229m
Publikováno v:
Biochemistry. 39:2603-2611
Previous work has demonstrated that the ferric form of soybean lipoxygenase-1 will catalyze an elimination reaction on 12-iodo-cis-9-octadecenoic acid (12-IODE) to produce 9, 11-octadecadienoic acid and iodide ion. Elimination is accompanied by irrev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84a7eacbfbadd3e5cc4b21c0400cd93c
https://doi.org/10.1021/bi992487y
https://doi.org/10.1021/bi992487y
Autor:
Rebecca Anne Howell, Charles H. Clapp
Publikováno v:
The FASEB Journal. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939711eedb3d02b353290e30c5cf26b9
https://doi.org/10.1096/fasebj.27.1_supplement.789.14
https://doi.org/10.1096/fasebj.27.1_supplement.789.14
Autor:
Cody L. Johnson, Charles H. Clapp
Publikováno v:
The FASEB Journal. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2199836f6ecb1990e184cfc9d0ce5687
https://doi.org/10.1096/fasebj.27.1_supplement.789.16
https://doi.org/10.1096/fasebj.27.1_supplement.789.16
Publikováno v:
Biochemistry. 34:264-272
The ferric form of soybean lipoxygenase catalyzes an elimination reaction on 12-iodo-cis-9-octadecenoic acid (12-IODE) to produce iodide ions and 9,11-octadecadienoic acid (9, 11-ODA). If excess 13(S)-hydroperoxy-cis-9,trans-11-octadecadienoic acid (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b68636728659fedeec3bb82fb4ef8fe
https://doi.org/10.1021/bi00001a032
https://doi.org/10.1021/bi00001a032