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Heavy-chain mutants: Ser(H35)Ala, Val(H37)Leu, Tyr(H91)Phe, Trp(H103)Phe; light-chain mutants: Tyr(L34)Phe, Tyr(L36)Phe, Phe(L98)Tyr, Tyr(L34)Phe/Phe(L98)Tyr.
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Heavy-chain mutants: Ser(H35)Ala, Val(H37)Leu, Tyr(H91)Phe, Trp(H103)Phe; light-chain mutants: Tyr(L34)Phe, Tyr(L36)Phe, Phe(L98)Tyr, Tyr(L34)Phe/Phe(L98)Tyr.
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The glutaric amide group of 1 minimally perturbs the electronic structure of trans-stilbene (4). Thus, we estimate the reduction potential of 1 to be 1.9 V versus the normal hydrogen electrode (NHE) (13), and that of 1* to be about +1.4 V versus NHE. The Trp cation radical reduction potential is estimated to be +1.1 V versus NHE (14).
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We thank S. Ferguson for assistance in Fab preparation and the staff at Advanced Light Source beamline 5.0.1 for their support. We gratefully acknowledge A. Deniz for providing access to his fluorimeter, and S. Mukhopadhyay for assistance with anisotropy measurements as well as helpful discussions. We thank J. Saltiel as well as the reviewers for critically reading the manuscript and providing helpful comments. Coordinates and structure factors for the EP2-25C10-1 complex have been deposited at the Protein Data Bank (PDB) with accession number 2NZR. Supported by NIH grants GM38273 (I.A.W, GM56528 (P.G.S, and DK19038 (H.B.G, and a Skaggs predoctoral fellowship and Jairo H. Arévalo fellowship from The Scripps Research Institute graduate program E.W.D, This is publication 18959-MB from The Scripps Research Institute
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We thank S. Ferguson for assistance in Fab preparation and the staff at Advanced Light Source beamline 5.0.1 for their support. We gratefully acknowledge A. Deniz for providing access to his fluorimeter, and S. Mukhopadhyay for assistance with anisotropy measurements as well as helpful discussions. We thank J. Saltiel as well as the reviewers for critically reading the manuscript and providing helpful comments. Coordinates and structure factors for the EP2-25C10-1 complex have been deposited at the Protein Data Bank (PDB) with accession number 2NZR. Supported by NIH grants GM38273 (I.A.W.), GM56528 (P.G.S.), and DK19038 (H.B.G.) and a Skaggs predoctoral fellowship and Jairo H. Arévalo fellowship from The Scripps Research Institute graduate program (E.W.D.). This is publication 18959-MB from The Scripps Research Institute.
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