Year |
Citation |
Score |
2019 |
Hershelman D, Kahler KM, Price MJ, Lu I, Fu Y, Plumeri PA, Karaisz F, Bassett NF, Findeis PM, Clapp CH. Oxygenation reactions catalyzed by the F557V mutant of soybean Lipoxygenase-1: Evidence for two orientations of substrate binding. Archives of Biochemistry and Biophysics. 108082. PMID 31473191 DOI: 10.1016/J.Abb.2019.108082 |
0.381 |
|
2018 |
Clapp CH, Pachuski J, Bassett NF, Bishop KA, Carter G, Young M, Young T, Fu Y. N-linoleoylamino acids as chiral probes of substrate binding by soybean lipoxygenase-1. Bioorganic Chemistry. 78: 170-177. PMID 29573638 DOI: 10.1016/J.Bioorg.2018.03.010 |
0.45 |
|
2011 |
Chohany LE, Bishop KA, Camic H, Sup SJ, Findeis PM, Clapp CH. Cationic substrates of soybean lipoxygenase-1. Bioorganic Chemistry. 39: 94-100. PMID 21257189 DOI: 10.1016/J.Bioorg.2010.12.003 |
0.328 |
|
2007 |
Clapp CH, Pachuski J, Bishop KA, Young MM. N-Linoleyl amino acids as chiral probes for the substrate binding site of soybean lipoxygenase-1 The Faseb Journal. 21. DOI: 10.1096/Fasebj.21.5.A276-D |
0.4 |
|
2006 |
Clapp CH, Strulson M, Rodriguez PC, Lo R, Novak MJ. Oxygenation of monounsaturated fatty acids by soybean lipoxygenase-1: evidence for transient hydroperoxide formation. Biochemistry. 45: 15884-92. PMID 17176111 DOI: 10.1021/Bi0619425 |
0.421 |
|
2002 |
Clapp CH, Grandizio AM, Yang Y, Kagey M, Turner D, Bicker A, Muskardin D. Irreversible inactivation of soybean lipoxygenase-1 by hydrophobic thiols. Biochemistry. 41: 11504-11. PMID 12234194 DOI: 10.1021/Bi020229M |
0.46 |
|
2001 |
Clapp CH, Senchak SE, Stover TJ, Potter TC, Findeis PM, Novak MJ. Soybean lipoxygenase-mediated oxygenation of monounsaturated fatty acids to enones. Journal of the American Chemical Society. 123: 747-8. PMID 11456594 DOI: 10.1021/Ja0032071 |
0.381 |
|
2000 |
Clapp CH, McKown J, Xu H, Grandizio AM, Yang G, Fayer J. The action of soybean lipoxygenase-1 on 12-iodo-cis-9-octadecenoic acid: the importance of C11-H bond breaking. Biochemistry. 39: 2603-11. PMID 10704209 DOI: 10.1021/Bi992487Y |
0.378 |
|
1995 |
Clapp CH, Grandizio AM, McAskill SA, Moser R. Action of soybean lipoxygenase 1 on 12-iodo-cis-9-octadecenoic acid and 12-bromo-cis-9-octadecenoic acid. Biochemistry. 34: 264-72. PMID 7819206 DOI: 10.1021/Bi00001A032 |
0.432 |
|
1989 |
Bergin JD, Clapp CH. Inhibition of aminopeptidase M by alkyl D-cysteinates. Journal of Enzyme Inhibition. 3: 127-31. PMID 2577378 DOI: 10.3109/14756368909030371 |
0.322 |
|
1989 |
Campbell JR, Clapp CH. A new method for the preparation of carboxy-labeled unsaturated fatty acids and its application to linoleic acid Bioorganic Chemistry. 17: 281-286. DOI: 10.1016/0045-2068(89)90030-8 |
0.445 |
|
1988 |
Rotenberg SA, Grandizio AM, Selzer AT, Clapp CH. Inactivation of soybean lipoxygenase 1 by 12-iodo-cis-9-octadecenoic acid. Biochemistry. 27: 8813-8. PMID 3149510 DOI: 10.1021/Bi00424A019 |
0.589 |
|
1988 |
Wiseman JS, Skoog MT, Clapp CH. Activity of soybean lipoxygenase in the absence of lipid hydroperoxide. Biochemistry. 27: 8810-3. PMID 3149509 DOI: 10.1021/Bi00424A018 |
0.364 |
|
1985 |
Clapp CH, Banerjee A, Rotenberg SA. Inhibition of soybean lipoxygenase 1 by N-alkylhydroxylamines. Biochemistry. 24: 1826-30. PMID 2990543 DOI: 10.1021/Bi00329A004 |
0.568 |
|
1976 |
Clapp CH, Satterthwait A, Westheimer FH. Monomeric methyl metaphosphate. II. Electrophilic aromatic substitution Cheminform. 7. DOI: 10.1002/Chin.197605236 |
0.402 |
|
1975 |
Clapp CH, Satterthwait A, Westheimer FH. Monomeric methyl metaphosphate. II. Electrophilic aromatic substitution Journal of the American Chemical Society. 97: 6873-6874. DOI: 10.1021/Ja00856A052 |
0.402 |
|
1975 |
Clapp CH, Satterthwait A, Westheimer FH. Monomeric methyl metaphosphate. II. Electrophilic aromatic substitution [10] Journal of the American Chemical Society. 97: 6873-6874. |
0.509 |
|
1974 |
Clapp CH, Westheimer FH. Monomeric methyl metaphosphate Journal of the American Chemical Society. 96: 6710-6714. DOI: 10.1021/Ja00828A028 |
0.53 |
|
1974 |
CLAPP CH, WESTHEIMER FH. ChemInform Abstract: MONOMERIC METHYL METAPHOSPHATE Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197452341 |
0.532 |
|
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