2op3 | pdb_00002op3

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

Template:STRUCTURE 2op3

File:2op3.png

The structure of cathepsin S with a novel 2-arylphenoxyacetaldehyde inhibitor derived by the Substrate Activity Screening (SAS) method

Template:ABSTRACT PUBMED 17469812

About this Structure

2OP3 is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Inagaki H, Tsuruoka H, Hornsby M, Lesley SA, Spraggon G, Ellman JA. Characterization and optimization of selective, nonpeptidic inhibitors of cathepsin S with an unprecedented binding mode. J Med Chem. 2007 May 31;50(11):2693-9. Epub 2007 May 1. PMID:17469812 doi:https://dx.doi.org/10.1021/jm070111+

Page seeded by OCA on Tue Feb 17 18:57:57 2009

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OCA

[1] Inagaki H, Tsuruoka H, Hornsby M, Lesley SA, Spraggon G, Ellman JA. Characterization and optimization of selective, nonpeptidic inhibitors of cathepsin S with an unprecedented binding mode. J Med Chem. 2007 May 31;50(11):2693-9. Epub 2007 May 1. PMID:17469812 doi:https://dx.doi.org/10.1021/jm070111+

2op3 | pdb_00002op3

The structure of cathepsin S with a novel 2-arylphenoxyacetaldehyde inhibitor derived by the Substrate Activity Screening (SAS) method

About this Structure

Reference

Proteopedia Page Contributors and Editors (what is this?)

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