1nx3: Difference between revisions
New page: left|200px<br /><applet load="1nx3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nx3, resolution 2.45Å" /> '''Calpain Domain VI in... |
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[[Image:1nx3.jpg|left|200px]]<br /><applet load="1nx3" size=" | [[Image:1nx3.jpg|left|200px]]<br /><applet load="1nx3" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1nx3, resolution 2.45Å" /> | caption="1nx3, resolution 2.45Å" /> | ||
'''Calpain Domain VI in Complex with the Inhibitor PD150606'''<br /> | '''Calpain Domain VI in Complex with the Inhibitor PD150606'''<br /> | ||
==Overview== | ==Overview== | ||
The Ca(2+)-dependent cysteine protease calpain along with its endogenous | The Ca(2+)-dependent cysteine protease calpain along with its endogenous inhibitor calpastatin is widely distributed. The interactions between calpain and calpastatin have been studied to better understand the nature of calpain inhibition by calpastatin, which can aid the design of small molecule inhibitors to calpain. Here we present the crystal structure of a complex between a calpastatin peptide and the calcium-binding domain VI of calpain. DIC19 is a 19 residue peptide, which corresponds to one of the three interacting domains of calpastatin, which is known to interact with domain VI of calpain. We present two crystal structures of DIC19 bound to domain VI of calpain, determined by molecular replacement methods to 2.5A and 2.2A resolution. In the process of crystallizing the inhibitor complex, a new native crystal form was identified which had the homodimer 2-fold axis along a crystallographic axis as opposed to the previously observed dimer in the asymmetric unit. The crystal structures of the native domain VI and its inhibitor PD150606 (3-(4-iodophenyl)-2-mercapto-(Z)-2-propenoic acid) complex were determined with the help of molecular replacement methods to 2.0A and 2.3A resolution, respectively. In addition, we built a homology model for the complex between domain IV and DIA19 peptide of calpastatin. Finally, we present a model for the calpastatin-inhibited calpain. | ||
==About this Structure== | ==About this Structure== | ||
1NX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with CA and ISA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Hydrolase Hydrolase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.22.52 and 3.4.22.53 3.4.22.52 and 3.4.22.53] Full crystallographic information is available from [http:// | 1NX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=ISA:'>ISA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Hydrolase Hydrolase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.22.52 and 3.4.22.53 3.4.22.52 and 3.4.22.53] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NX3 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Sus scrofa]] | [[Category: Sus scrofa]] | ||
[[Category: Chattopadhyay, D.]] | [[Category: Chattopadhyay, D.]] | ||
[[Category: Deivanayagam, C | [[Category: Deivanayagam, C C.S.]] | ||
[[Category: Lin, G | [[Category: Lin, G D.]] | ||
[[Category: Maki, M.]] | [[Category: Maki, M.]] | ||
[[Category: Moore, D.]] | [[Category: Moore, D.]] | ||
[[Category: Narayana, S | [[Category: Narayana, S V.L.]] | ||
[[Category: Todd, B.]] | [[Category: Todd, B.]] | ||
[[Category: Wang, K | [[Category: Wang, K K.W.]] | ||
[[Category: CA]] | [[Category: CA]] | ||
[[Category: ISA]] | [[Category: ISA]] | ||
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[[Category: hydrolase]] | [[Category: hydrolase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:11:04 2008'' |