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| [[Image:1ppg.gif|left|200px]] | | {{Seed}} |
| | [[Image:1ppg.png|left|200px]] |
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| {{STRUCTURE_1ppg| PDB=1ppg | SCENE= }} | | {{STRUCTURE_1ppg| PDB=1ppg | SCENE= }} |
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| '''THE REFINED 2.3 ANGSTROMS CRYSTAL STRUCTURE OF HUMAN LEUKOCYTE ELASTASE IN A COMPLEX WITH A VALINE CHLOROMETHYL KETONE INHIBITOR'''
| | ===THE REFINED 2.3 ANGSTROMS CRYSTAL STRUCTURE OF HUMAN LEUKOCYTE ELASTASE IN A COMPLEX WITH A VALINE CHLOROMETHYL KETONE INHIBITOR=== |
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| ==Overview==
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| The stoichiometric complex formed between human leukocyte elastase and a synthetic MeO-Suc-Ala-Ala-Pro-Val chloromethyl ketone inhibitor was co-crystallized and its X-ray structure determined, using Patterson search methods. Its structure has been crystallographically refined to a final R value of 0.145 (8.0 and 2.3 A). The enzyme structure is very similar to that recently observed in a complex formed with the ovomucoid third domain from turkey [(1986) EMBO J. 5,2453-2458]. The rms deviation of all alpha-carbon atoms is 0.32 A. The peptidic inhibitor is bound in a similar overall conformation as the ovomucoid binding segment. Covalent bonds are formed between Val-P1 of the inhibitor and His-57 NE2 and Ser-195 OG of the enzyme. The carbonyl carbon is tetrahedrally deformed to a hemiketal. The valine side chain is arranged in the S1 pocket in the g-conformation. | | The line below this paragraph, {{ABSTRACT_PUBMED_3391280}}, adds the Publication Abstract to the page |
| | (as it appears on PubMed at http://www.pubmed.gov), where 3391280 is the PubMed ID number. |
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| | {{ABSTRACT_PUBMED_3391280}} |
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| ==About this Structure== | | ==About this Structure== |
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| [[Category: Bode, W.]] | | [[Category: Bode, W.]] |
| [[Category: Wei, A-Z.]] | | [[Category: Wei, A-Z.]] |
| ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 05:20:17 2008'' | | |
| | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 22:49:16 2008'' |