1axa

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==About this Structure==
==About this Structure==
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[[1axa]] is a 2 chain structure of [[Virus protease]] with sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AXA OCA].
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[[1axa]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AXA OCA].
==See Also==
==See Also==

Revision as of 10:23, 20 October 2012

Template:STRUCTURE 1axa

Contents

ACTIVE-SITE MOBILITY IN HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 PROTEASE AS DEMONSTRATED BY CRYSTAL STRUCTURE OF A28S MUTANT

Template:ABSTRACT PUBMED 9521105

About this Structure

1axa is a 2 chain structure with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  • Hong L, Hartsuck JA, Foundling S, Ermolieff J, Tang J. Active-site mobility in human immunodeficiency virus, type 1, protease as demonstrated by crystal structure of A28S mutant. Protein Sci. 1998 Feb;7(2):300-5. PMID:9521105
  • Bannwarth L, Rose T, Dufau L, Vanderesse R, Dumond J, Jamart-Gregoire B, Pannecouque C, De Clercq E, Reboud-Ravaux M. Dimer disruption and monomer sequestration by alkyl tripeptides are successful strategies for inhibiting wild-type and multidrug-resistant mutated HIV-1 proteases. Biochemistry. 2009 Jan 20;48(2):379-87. PMID:19105629 doi:10.1021/bi801422u

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