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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

J.P. Tam

Department of Microbiology and Immunology

Vanderbilt University


Tennessee 37232



Name/email consistency: high



  • Department of Microbiology and Immunology, Vanderbilt University, Nashville, Tennessee 37232, USA. 1998 - 2001


  1. Tandem ligation of unprotected peptides through thiaprolyl and cysteinyl bonds in water. Tam, J.P., Yu, Q., Yang, J.L. J. Am. Chem. Soc. (2001) [Pubmed]
  2. Methods and strategies of peptide ligation. Tam, J.P., Xu, J., Eom, K.D. Biopolymers (2001) [Pubmed]
  3. Tandem peptide ligation for synthetic and natural biologicals. Tam, J.P., Yu, Q., Lu, Y.A. Biologicals (2001) [Pubmed]
  4. Design of salt-insensitive glycine-rich antimicrobial peptides with cyclic tricystine structures. Tam, J.P., Lu, Y.A., Yang, J.L. Biochemistry (2000) [Pubmed]
  5. An unusual structural motif of antimicrobial peptides containing end-to-end macrocycle and cystine-knot disulfides. Tam, J.P., Lu, Y.A., Yang, J.L., Chiu, K.W. Proc. Natl. Acad. Sci. U.S.A. (1999) [Pubmed]
  6. Orthogonal ligation strategies for peptide and protein. Tam, J.P., Yu, Q., Miao, Z. Biopolymers (1999) [Pubmed]
  7. A biomimetic strategy in the synthesis and fragmentation of cyclic protein. Tam, J.P., Lu, Y.A. Protein Sci. (1998) [Pubmed]
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