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	<id>https://eln.excellgen.com/index.php?action=history&amp;feed=atom&amp;title=Restriction_Enzymes</id>
	<title>Restriction Enzymes - Revision history</title>
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	<updated>2026-10-19T16:38:25Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=Restriction_Enzymes&amp;diff=16104&amp;oldid=prev</id>
		<title>Paul.xu at 14:06, 20 June 2017</title>
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		<updated>2017-06-20T14:06:02Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;PD . . . D/EXK motif&lt;br /&gt;
 PD-(D/E)XK superfamily of Mg2+-dependent nucleases&lt;br /&gt;
type II restriction enzymes (REases) (reviews: [1, 2]) and later found in diverse enzymes involved in DNA replication, repair, and recombination, including phage λ exonuclease [3], bacterial enzymes exerting ssDNA nicking in the context of methyl-directed and very-short-patch DNA repair: MutH [4] and Vsr [5], Tn7 transposase TnsA [6], archaeal Holliday junction resolvases (AHJRs) Hjc/Hje [7, 8, 9], phage T7 endonuclease I [10], the XPF/Rad1/Mus81 family of nucleases that cleaves branched structures generated during DNA repair, replication, and recombination [11], and RecB nuclease &lt;br /&gt;
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 PD and D/EXK, are not invariant, and can be separated (‘…’) by anywhere from 4 (BcnI) to 51 (SgrAI) amino acids. Compounding matters, in some enzymes, the D/E or K residues, are recruited from other parts of the protein (e.g. EcoRII (310); BspD6I (311)).&lt;br /&gt;
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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081073/&lt;br /&gt;
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[ftp://ftp.neb.com/pub/rebase ftp://ftp.neb.com/pub/rebase]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
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