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HIV-1 integrase is composed of three domains: the N-terminal (residues 1-49), the core domain (residues 50-212) and the C-terminal domain (residues 213-288). The core domain is responsible for the catalytic activity of the enzyme. It contains three acidic residues, the D,D-35-E motif which plays a key role in catalysis. The N-terminal domain includes the conserved HHCC motif, which binds zinc. The C-terminal domain is less well conserved. [http://www.jbc.org/content/276/26/23213/F2.expansion.html]
HIV-1 integrase is composed of three domains: the N-terminal (residues 1-49), the core domain (residues 50-212) and the C-terminal domain (residues 213-288). The core domain is responsible for the catalytic activity of the enzyme. It contains three acidic residues, the D,D-35-E motif which plays a key role in catalysis. The N-terminal domain includes the conserved HHCC motif, which binds zinc. The C-terminal domain is less well conserved. [http://www.jbc.org/content/276/26/23213/F2.expansion.html]
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The complex with the two DNA are displayed on the proteopedia page [[5u1c]].
====Structure and role of the core domain in the integration====
====Structure and role of the core domain in the integration====
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==See also==
==See also==
http://proteopedia.org/wiki/index.php/2b4j :integrase ligated with the cofactor LEDGF/p75
http://proteopedia.org/wiki/index.php/2b4j :integrase ligated with the cofactor LEDGF/p75
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http://proteopedia.org/wiki/index.php/5u1c : integrase complex with the two DNAs
== References ==
== References ==

Revision as of 22:07, 10 January 2019

This Sandbox is Reserved from 06/12/2018, through 30/06/2019 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1480 through Sandbox Reserved 1543.
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3lpt - HIV integrase

3lpt, resolution 2.00Å

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