1tw6

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[[Image:1tw6.gif|left|200px]]
[[Image:1tw6.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1tw6 |SIZE=350|CAPTION= <scene name='initialview01'>1tw6</scene>, resolution 1.713&Aring;
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The line below this paragraph, containing "STRUCTURE_1tw6", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=BTB:2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL'>BTB</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=LI:LITHIUM+ION'>LI</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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|GENE= BIRC7 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), DIABLO, SMAC ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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|DOMAIN=
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{{STRUCTURE_1tw6| PDB=1tw6 | SCENE= }}
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|RELATEDENTRY=[[1oxn|1OXN]], [[1oxq|1OXQ]], [[1oy7|1OY7]], [[1nw9|1NW9]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1tw6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1tw6 OCA], [http://www.ebi.ac.uk/pdbsum/1tw6 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1tw6 RCSB]</span>
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'''Structure of an ML-IAP/XIAP chimera bound to a 9mer peptide derived from Smac'''
'''Structure of an ML-IAP/XIAP chimera bound to a 9mer peptide derived from Smac'''
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[[Category: Vucic, D.]]
[[Category: Vucic, D.]]
[[Category: Wallweber, H J.A.]]
[[Category: Wallweber, H J.A.]]
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[[Category: apoptosis inhibition]]
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[[Category: Apoptosis inhibition]]
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[[Category: peptide complex]]
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[[Category: Peptide complex]]
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[[Category: zinc binding]]
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[[Category: Zinc binding]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 10:26:40 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:01:58 2008''
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Revision as of 07:26, 3 May 2008

Template:STRUCTURE 1tw6

Structure of an ML-IAP/XIAP chimera bound to a 9mer peptide derived from Smac


Overview

ML-IAP (melanoma inhibitor of apoptosis) is a potent anti-apoptotic protein that is strongly up-regulated in melanoma and confers protection against a variety of pro-apoptotic stimuli. The mechanism by which ML-IAP regulates apoptosis is unclear, although weak inhibition of caspases 3 and 9 has been reported. Here, the binding to and inhibition of caspase 9 by the single BIR (baculovirus IAP repeat) domain of ML-IAP has been investigated and found to be significantly less potent than the ubiquitously expressed XIAP (X-linked IAP). Engineering of the ML-IAP-BIR domain, based on comparisons with the third BIR domain of XIAP, resulted in a chimeric BIR domain that binds to and inhibits caspase 9 significantly better than either ML-IAP-BIR or XIAP-BIR3. Mutational analysis of the ML-IAP-BIR domain demonstrated that similar enhancements in caspase 9 affinity can be achieved with only three amino acid substitutions. However, none of these modifications affected binding of the ML-IAP-BIR domain to the IAP antagonist Smac (second mitochondrial activator of caspases). ML-IAP-BIR was found to bind mature Smac with low nanomolar affinity, similar to that of XIAP-BIR2-BIR3. Correspondingly, increased expression of ML-IAP results in formation of a ML-IAP-Smac complex and disruption of the endogenous interaction between XIAP and mature Smac. These results suggest that ML-IAP might regulate apoptosis by sequestering Smac and preventing it from antagonizing XIAP-mediated inhibition of caspases, rather than by direct inhibition of caspases.

About this Structure

1TW6 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Engineering ML-IAP to produce an extraordinarily potent caspase 9 inhibitor: implications for Smac-dependent anti-apoptotic activity of ML-IAP., Vucic D, Franklin MC, Wallweber HJ, Das K, Eckelman BP, Shin H, Elliott LO, Kadkhodayan S, Deshayes K, Salvesen GS, Fairbrother WJ, Biochem J. 2005 Jan 1;385(Pt 1):11-20. PMID:15485396 Page seeded by OCA on Sat May 3 10:26:40 2008

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