1pau

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[[Image:1pau.gif|left|200px]]<br />
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[[Image:1pau.gif|left|200px]]<br /><applet load="1pau" size="450" color="white" frame="true" align="right" spinBox="true"
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<applet load="1pau" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1pau, resolution 2.5&Aring;" />
caption="1pau, resolution 2.5&Aring;" />
'''CRYSTAL STRUCTURE OF THE COMPLEX OF APOPAIN WITH THE TETRAPEPTIDE ALDEHYDE INHIBITOR AC-DEVD-CHO'''<br />
'''CRYSTAL STRUCTURE OF THE COMPLEX OF APOPAIN WITH THE TETRAPEPTIDE ALDEHYDE INHIBITOR AC-DEVD-CHO'''<br />
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==About this Structure==
==About this Structure==
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1PAU is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ACE as [http://en.wikipedia.org/wiki/ligand ligand]. The following page contains interesting information on the relation of 1PAU with [[http://pdb.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/pdb56_1.html Caspases]]. Structure known Active Sites: S1, S2, S3 and S4. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PAU OCA].
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1PAU is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ACE as [http://en.wikipedia.org/wiki/ligand ligand]. The following page contains interesting information on the relation of 1PAU with [[http://pdb.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/pdb56_1.html Caspases]]. Known structural/functional Sites: <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>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PAU OCA].
==Reference==
==Reference==
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[[Category: yama]]
[[Category: yama]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:41:43 2007''
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 17:50:57 2007''

Revision as of 15:41, 18 December 2007


1pau, resolution 2.5Å

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CRYSTAL STRUCTURE OF THE COMPLEX OF APOPAIN WITH THE TETRAPEPTIDE ALDEHYDE INHIBITOR AC-DEVD-CHO

Overview

Cysteine proteases related to mammalian interleukin-1 beta converting, enzyme (ICE) and to its Caenorhabditis elegans homologue, CED-3, play a, critical role in the biochemical events that culminate in apoptosis. We, have determined the three-dimensional structure of a complex of the human, CED-3 homologue CPP32/apopain with a potent tetrapeptide-aldehyde, inhibitor. The protein resembles ICE in overall structure, but its S4, subsite is strikingly different in size and chemical composition. These, differences account for the variation in specificity between the ICE- and, CED-3-related proteases and enable the design of specific inhibitors that, can probe the physiological functions of the proteins and disease states, with which they are associated.

About this Structure

1PAU is a Protein complex structure of sequences from Homo sapiens with ACE as ligand. The following page contains interesting information on the relation of 1PAU with [Caspases]. Known structural/functional Sites: , , and . Full crystallographic information is available from OCA.

Reference

The three-dimensional structure of apopain/CPP32, a key mediator of apoptosis., Rotonda J, Nicholson DW, Fazil KM, Gallant M, Gareau Y, Labelle M, Peterson EP, Rasper DM, Ruel R, Vaillancourt JP, Thornberry NA, Becker JW, Nat Struct Biol. 1996 Jul;3(7):619-25. PMID:8673606

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