1ms6: Difference between revisions
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'''Dipeptide Nitrile Inhibitor Bound to Cathepsin S.'''<br /> | '''Dipeptide Nitrile Inhibitor Bound to Cathepsin S.'''<br /> | ||
==Overview== | ==Overview== | ||
The specificity of the immune response relies on processing of foreign | The specificity of the immune response relies on processing of foreign proteins and presentation of antigenic peptides at the cell surface. Inhibition of antigen presentation, and the subsequent activation of T-cells, should, in theory, modulate the immune response. The cysteine protease Cathepsin S performs a fundamental step in antigen presentation and therefore represents an attractive target for inhibition. Herein, we report a series of potent and reversible Cathepsin S inhibitors based on dipeptide nitriles. These inhibitors show nanomolar inhibition of the target enzyme as well as cellular potency in a human B cell line. The first X-ray crystal structure of a reversible inhibitor cocrystallized with Cathepsin S is also reported. | ||
==About this Structure== | ==About this Structure== | ||
1MS6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with BLN as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Cathepsin_S Cathepsin S], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.22.27 3.4.22.27] Full crystallographic information is available from [http:// | 1MS6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=BLN:'>BLN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Cathepsin_S Cathepsin S], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.22.27 3.4.22.27] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MS6 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Bekkali, Y.]] | [[Category: Bekkali, Y.]] | ||
[[Category: Brown, M | [[Category: Brown, M L.]] | ||
[[Category: Crane, K.]] | [[Category: Crane, K.]] | ||
[[Category: Cywin, C | [[Category: Cywin, C L.]] | ||
[[Category: Davidson, W.]] | [[Category: Davidson, W.]] | ||
[[Category: DeTuri, M.]] | [[Category: DeTuri, M.]] | ||
[[Category: Emmanuel, M | [[Category: Emmanuel, M J.]] | ||
[[Category: Freeman, D | [[Category: Freeman, D M.]] | ||
[[Category: Frye, L | [[Category: Frye, L L.]] | ||
[[Category: Giradot, M.]] | [[Category: Giradot, M.]] | ||
[[Category: Grygon, C | [[Category: Grygon, C A.]] | ||
[[Category: Hao, M | [[Category: Hao, M H.]] | ||
[[Category: Hopkins, J | [[Category: Hopkins, J L.]] | ||
[[Category: Hrapchak, M.]] | [[Category: Hrapchak, M.]] | ||
[[Category: Labadia, M | [[Category: Labadia, M E.]] | ||
[[Category: McNeil, D.]] | [[Category: McNeil, D.]] | ||
[[Category: Morwick, T.]] | [[Category: Morwick, T.]] | ||
[[Category: Pav, S.]] | [[Category: Pav, S.]] | ||
[[Category: Spero, D | [[Category: Spero, D M.]] | ||
[[Category: Thomson, D | [[Category: Thomson, D S.]] | ||
[[Category: Wang, Y.]] | [[Category: Wang, Y.]] | ||
[[Category: Ward, Y | [[Category: Ward, Y D.]] | ||
[[Category: White, D.]] | [[Category: White, D.]] | ||
[[Category: Zindell, R.]] | [[Category: Zindell, R.]] | ||
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[[Category: protease]] | [[Category: protease]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:58:32 2008'' |
Revision as of 14:58, 21 February 2008
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Dipeptide Nitrile Inhibitor Bound to Cathepsin S.
OverviewOverview
The specificity of the immune response relies on processing of foreign proteins and presentation of antigenic peptides at the cell surface. Inhibition of antigen presentation, and the subsequent activation of T-cells, should, in theory, modulate the immune response. The cysteine protease Cathepsin S performs a fundamental step in antigen presentation and therefore represents an attractive target for inhibition. Herein, we report a series of potent and reversible Cathepsin S inhibitors based on dipeptide nitriles. These inhibitors show nanomolar inhibition of the target enzyme as well as cellular potency in a human B cell line. The first X-ray crystal structure of a reversible inhibitor cocrystallized with Cathepsin S is also reported.
About this StructureAbout this Structure
1MS6 is a Single protein structure of sequence from Homo sapiens with as ligand. Active as Cathepsin S, with EC number 3.4.22.27 Full crystallographic information is available from OCA.
ReferenceReference
Design and synthesis of dipeptide nitriles as reversible and potent Cathepsin S inhibitors., Ward YD, Thomson DS, Frye LL, Cywin CL, Morwick T, Emmanuel MJ, Zindell R, McNeil D, Bekkali Y, Girardot M, Hrapchak M, DeTuri M, Crane K, White D, Pav S, Wang Y, Hao MH, Grygon CA, Labadia ME, Freeman DM, Davidson W, Hopkins JL, Brown ML, Spero DM, J Med Chem. 2002 Dec 5;45(25):5471-82. PMID:12459015
Page seeded by OCA on Thu Feb 21 13:58:32 2008
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCA- Pages with broken file links
- Cathepsin S
- Homo sapiens
- Single protein
- Bekkali, Y.
- Brown, M L.
- Crane, K.
- Cywin, C L.
- Davidson, W.
- DeTuri, M.
- Emmanuel, M J.
- Freeman, D M.
- Frye, L L.
- Giradot, M.
- Grygon, C A.
- Hao, M H.
- Hopkins, J L.
- Hrapchak, M.
- Labadia, M E.
- McNeil, D.
- Morwick, T.
- Pav, S.
- Spero, D M.
- Thomson, D S.
- Wang, Y.
- Ward, Y D.
- White, D.
- Zindell, R.
- BLN
- Cathepsin
- Hydrolase
- Protease