1psn: Difference between revisions

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[[Image:1psn.gif|left|200px]]
[[Image:1psn.gif|left|200px]]


{{Structure
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Pepsin_A Pepsin A], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.1 3.4.23.1] </span>
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1psn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1psn OCA], [http://www.ebi.ac.uk/pdbsum/1psn PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1psn RCSB]</span>
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'''THE CRYSTAL STRUCTURE OF HUMAN PEPSIN AND ITS COMPLEX WITH PEPSTATIN'''
'''THE CRYSTAL STRUCTURE OF HUMAN PEPSIN AND ITS COMPLEX WITH PEPSTATIN'''
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[[Category: Mosimann, S C.]]
[[Category: Mosimann, S C.]]
[[Category: Tarasova, N.]]
[[Category: Tarasova, N.]]
[[Category: hydrolase (acid proteinase)]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 05:26:27 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:04:03 2008''

Revision as of 05:26, 3 May 2008

File:1psn.gif

Template:STRUCTURE 1psn

THE CRYSTAL STRUCTURE OF HUMAN PEPSIN AND ITS COMPLEX WITH PEPSTATIN


OverviewOverview

The three-dimensional crystal structure of human pepsin and that of its complex with pepstatin have been solved by X-ray crystallographic methods. The native pepsin structure has been refined with data collected to 2.2 A resolution to an R-factor of 19.7%. The pepsin:pepstatin structure has been refined with data to 2.0 A resolution to an R-factor of 18.5%. The hydrogen bonding interactions and the conformation adopted by pepstatin are very similar to those found in complexes of pepstatin with other aspartic proteinases. The enzyme undergoes a conformational change upon inhibitor binding to enclose the inhibitor more tightly. The analysis of the binding sites indicates that they form an extended tube without distinct binding pockets. By comparing the residues on the binding surface with those of the other human aspartic proteinases, it has been possible to rationalize some of the experimental data concerning the different specificities. At the S1 site, valine at position 120 in renin instead of isoleucine, as in the other enzymes, allows for binding of larger hydrophobic residues. The possibility of multiple conformations for the P2 residue makes the analysis of the S2 site difficult. However, it is possible to see that the specific interactions that renin makes with histidine at P2 would not be possible in the case of the other enzymes. At the S3 site, the smaller volume that is accessible in pepsin compared to the other enzymes is consistent with its preference for smaller residues at the P3 position.

About this StructureAbout this Structure

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

ReferenceReference

Crystal structure of human pepsin and its complex with pepstatin., Fujinaga M, Chernaia MM, Tarasova NI, Mosimann SC, James MN, Protein Sci. 1995 May;4(5):960-72. PMID:7663352 Page seeded by OCA on Sat May 3 05:26:27 2008

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