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1aec

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[[Image:1aec.gif|left|200px]]
[[Image:1aec.gif|left|200px]]
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{{Structure
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|PDB= 1aec |SIZE=350|CAPTION= <scene name='initialview01'>1aec</scene>, resolution 1.86&Aring;
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The line below this paragraph, containing "STRUCTURE_1aec", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=E64:N-[N-[1-HYDROXYCARBOXYETHYL-CARBONYL]LEUCYLAMINO-BUTYL]-GUANIDINE'>E64</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/Actinidain Actinidain], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.22.14 3.4.22.14] </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_1aec| PDB=1aec | 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=1aec FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aec OCA], [http://www.ebi.ac.uk/pdbsum/1aec PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1aec RCSB]</span>
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}}
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'''CRYSTAL STRUCTURE OF ACTINIDIN-E-64 COMPLEX+'''
'''CRYSTAL STRUCTURE OF ACTINIDIN-E-64 COMPLEX+'''
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Varughese, K I.]]
[[Category: Varughese, K I.]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 10:09:24 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 18:38:23 2008''
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Revision as of 07:09, 2 May 2008

Template:STRUCTURE 1aec

CRYSTAL STRUCTURE OF ACTINIDIN-E-64 COMPLEX+


Overview

E-64, 1-(L-trans-epoxysuccinylleucylamino)-4-guanidinobutane, is a potent and highly selective irreversible inhibitor of cysteine proteases. The crystal structure of a complex of actinidin and E-64 has been determined at 1.86-A resolution by using the difference Fourier method and refined to an R-factor of 14.5%. The electron density map clearly shows that the C2 atom of the E-64 epoxide ring is covalently bonded to the S atom of the active-site cysteine 25. The charged carboxyl group of E-64 forms four H-bonds with the protein and thus may play an important role in favorably positioning the inhibitor molecule for nucleophilic attack by the active-site thiolate anion. The interaction features between E-64 and actinidin are very similar to those seen in the papain-E-64 complex; however, the amino-4-guanidinobutane group orients differently. The crystals of the actinidin-E-64 complex diffracted much better than the papain-E-64 complex, and consequently the present study provides more precise geometrical information on the binding of the inhibitor. Moreover, this study provides yet another confirmation that the binding of E-64 is at the S subsites and not at the S' subsites as has been previously proposed. The original actinidin structure has been revised using the new cDNA sequence information.

About this Structure

1AEC is a Single protein structure of sequence from Actinidia chinensis. Full crystallographic information is available from OCA.

Reference

Crystal structure of an actinidin-E-64 complex., Varughese KI, Su Y, Cromwell D, Hasnain S, Xuong NH, Biochemistry. 1992 Jun 9;31(22):5172-6. PMID:1606141 Page seeded by OCA on Fri May 2 10:09:24 2008

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