Structure-based subsite specificity mapping of human cathepsin D using statine-based inhibitors.

Ítems similars

• Exploration of subsite binding specificity of human cathepsin D through kinetics and rule-based molecular modeling.
  per: Scarborough, P. E., et al.
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• Prime region subsite specificity characterization of human cathepsin D: the dominant role of position 128.
  per: Beyer, B. M., et al.
  Publicat: (1998)
• Crystal structures of native and inhibited forms of human cathepsin D: implications for lysosomal targeting and drug design.
  per: Baldwin, E T, et al.
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• Structure-based development of specific inhibitors for individual cathepsins and their medical applications
  per: KATUNUMA, Nobuhiko
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• Design of kallidin-releasing tissue kallikrein inhibitors based on the specificities of the enzyme's binding subsites.
  per: Portaro, F C, et al.
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