2hh5

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[[Image:2hh5.png|left|200px]]
[[Image:2hh5.png|left|200px]]
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==About this Structure==
==About this Structure==
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2HH5 is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2HH5 OCA].
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[[2hh5]] is a 2 chain structure of [[Cathepsin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2HH5 OCA].
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==See Also==
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*[[Cathepsin]]
==Reference==
==Reference==
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[[Category: Arylaminoethyl-amide]]
[[Category: Arylaminoethyl-amide]]
[[Category: Cathepsin s]]
[[Category: Cathepsin s]]
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[[Category: Hydrolase]]
[[Category: Inhibition]]
[[Category: Inhibition]]
[[Category: Noncovalent]]
[[Category: Noncovalent]]
[[Category: Zinc]]
[[Category: Zinc]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 15:39:51 2009''
 

Revision as of 08:22, 26 December 2010

Template:STRUCTURE 2hh5

Contents

Crystal Structure of Cathepsin S in complex with a Zinc mediated non-covalent arylaminoethyl amide

Template:ABSTRACT PUBMED 16876402

About this Structure

2hh5 is a 2 chain structure of Cathepsin with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Tully DC, Liu H, Chatterjee AK, Alper PB, Epple R, Williams JA, Roberts MJ, Woodmansee DH, Masick BT, Tumanut C, Li J, Spraggon G, Hornsby M, Chang J, Tuntland T, Hollenbeck T, Gordon P, Harris JL, Karanewsky DS. Synthesis and SAR of arylaminoethyl amides as noncovalent inhibitors of cathepsin S: P3 cyclic ethers. Bioorg Med Chem Lett. 2006 Oct 1;16(19):5112-7. Epub 2006 Jul 28. PMID:16876402 doi:http://dx.doi.org/10.1016/j.bmcl.2006.07.033
  • Tully DC, Liu H, Alper PB, Chatterjee AK, Epple R, Roberts MJ, Williams JA, Nguyen KT, Woodmansee DH, Tumanut C, Li J, Spraggon G, Chang J, Tuntland T, Harris JL, Karanewsky DS. Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: heterocyclic P3. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1975-80. Epub 2006 Jan 30. PMID:16446091 doi:http://dx.doi.org/10.1016/j.bmcl.2005.12.095

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