1ibc

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[[Image:1ibc.gif|left|200px]]
[[Image:1ibc.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1ibc |SIZE=350|CAPTION= <scene name='initialview01'>1ibc</scene>, resolution 2.73&Aring;
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The line below this paragraph, containing "STRUCTURE_1ibc", creates the "Structure Box" on the page.
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|SITE= <scene name='pdbsite=S1:Inhibitor+Binding+Sub-Site+S1'>S1</scene>, <scene name='pdbsite=S2:Inhibitor+Binding+Sub-Site+S2'>S2</scene>, <scene name='pdbsite=S3:Inhibitor+Binding+Sub-Site+S3'>S3</scene> and <scene name='pdbsite=S4:Inhibitor+Binding+Sub-Site+S4'>S4</scene>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=ACE:ACETYL+GROUP'>ACE</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Caspase-1 Caspase-1], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.22.36 3.4.22.36] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1ibc| PDB=1ibc | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ibc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ibc OCA], [http://www.ebi.ac.uk/pdbsum/1ibc PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ibc RCSB]</span>
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}}
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'''CRYSTAL STRUCTURE OF INHIBITED INTERLEUKIN-1BETA CONVERTING ENZYME'''
'''CRYSTAL STRUCTURE OF INHIBITED INTERLEUKIN-1BETA CONVERTING ENZYME'''
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[[Category: Becker, J W.]]
[[Category: Becker, J W.]]
[[Category: Rotonda, J.]]
[[Category: Rotonda, J.]]
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[[Category: caspase-1]]
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[[Category: Caspase-1]]
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[[Category: complex (hydrolase/peptide)]]
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[[Category: Cysteine protease]]
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[[Category: cysteine protease]]
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[[Category: Ice]]
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[[Category: ice]]
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[[Category: Interleukin-1beta converting enzyme]]
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[[Category: interleukin-1beta converting enzyme]]
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[[Category: Protease]]
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[[Category: protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 19:48:11 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:17:19 2008''
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Revision as of 16:48, 2 May 2008

Template:STRUCTURE 1ibc

CRYSTAL STRUCTURE OF INHIBITED INTERLEUKIN-1BETA CONVERTING ENZYME


Overview

BACKGROUND: Interleukin-1beta converting enzyme (ICE/caspase-1) is the protease responsible for interleukin-1beta (IL-1beta) production in monocytes. It was the first member of a new cysteine protease family to be identified. Members of this family have functions in both inflammation and apoptosis. RESULTS: A novel method for identifying protease specificity, employing a positional-scanning substrate library, was used to determine the amino-acid preferences of ICE. Using this method, the complete specificity of a protease can be mapped in the time required to perform one assay. The results indicate that the optimal tetrapeptide recognition sequence for ICE is WEHD, not YVAD, as previously believed, and this led to the synthesis of an unusually potent aldehyde inhibitor, Ac-WEHD-CHO (Ki = 56 pM). The structural basis for this potent inhibition was determined by X-ray crystallography. CONCLUSIONS: The results presented in this study establish a positional-scanning library as a powerful tool for rapidly and accurately assessing protease specificity. The preferred sequence for ICE (WEHD) differs significantly from that found in human pro-interleukin-1beta (YVHD), which suggests that this protease may have additional endogenous substrates, consistent with evidence linking it to apoptosis and IL-1alpha production.

About this Structure

1IBC is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

A combinatorial approach for determining protease specificities: application to interleukin-1beta converting enzyme (ICE)., Rano TA, Timkey T, Peterson EP, Rotonda J, Nicholson DW, Becker JW, Chapman KT, Thornberry NA, Chem Biol. 1997 Feb;4(2):149-55. PMID:9190289 Page seeded by OCA on Fri May 2 19:48:11 2008

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