Citation: Pg. Wang et al., Screening combinatorial libraries for optimal enzyme substrates by mass spectrometry, RAP C MASS, 15(14), 2001, pp. 1166-1171
Authors:
Wei, YM
Yi, T
Huntington, KM
Chaudhury, C
Pei, DH
Citation: Ym. Wei et al., Identification of a potent peptide deformylase inhibitor from a rationallydesigned combinatorial library, J COMB CHEM, 2(6), 2000, pp. 650-657
Authors:
Liao, H
Yuan, CH
Su, MI
Yongkiettrakul, S
Qin, DY
Li, HY
Byeon, IJL
Pei, DH
Tsai, MD
Citation: H. Liao et al., Structure of the FHA1 domain of yeast Rad53 and identification of binding sites for both FHA1 and its target protein Rad9, J MOL BIOL, 304(5), 2000, pp. 941-951
Citation: Kd. Beebe et al., Determination of the binding specificity of the SH2 domains of protein tyrosine phosphatase SHP-1 through the screening of a combinatorial phosphotyrosyl peptide library, BIOCHEM, 39(43), 2000, pp. 13251-13260
Citation: Ptr. Rajagopalan et al., Characterization of cobalt(II)-substituted peptide deformylase: Function of the metal ion and the catalytic residue Glu-133, BIOCHEM, 39(4), 2000, pp. 779-790
Authors:
Huntington, KM
Bienvenue, DL
Wei, YM
Bennett, B
Holz, RC
Pei, DH
Citation: Km. Huntington et al., Slow-binding inhibition of the aminopeptidase from Aeromonas proteolytica by peptide thiols: Synthesis and spectroscopic characterization, BIOCHEM, 38(47), 1999, pp. 15587-15596
Authors:
Hu, YJ
Wei, YM
Zhou, Y
Rajagopalan, PTR
Pei, DH
Citation: Yj. Hu et al., Determination of substrate specificity for peptide deformylase through thescreening of a combinatorial peptide library, BIOCHEM, 38(2), 1999, pp. 643-650
Authors:
Arabaci, G
Guo, XC
Beebe, KD
Coggeshall, KM
Pei, DH
Citation: G. Arabaci et al., alpha-Haloacetophenone derivatives as photoreversible covalent inhibitors of protein tyrosine phosphatases, J AM CHEM S, 121(21), 1999, pp. 5085-5086