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. 2013 Oct 18;42(1):3–19. doi: 10.1093/nar/gkt990

Table 2.

Nomenclature of Type II restriction enzymes

Subtype Features of restriction enzymesa Examples
Type IIP Palindromic recognition sequence; recognized by both homodimeric and monomeric enzymes; cleavage occurs symmetrically, usually within the recognition sequence Prototypes EcoRI & EcoRV
Type IIA Asymmetric recognition sequence FokI
Type IIB Cleavage on both sides of the recognition sequence BcgI
Type IIC Single, combination R-M polypeptide HaeIV
Type IIE Two sequences required for cleavage, one serving as allosteric effector EcoRII, Sau3AI
Type IIF Two sequences required for cleavage, concerted reaction by homotetramer SfiI
Type IIG Requires AdoMet cofactor for both R-M Eco57I
Type IIH Separate M and S subunits; MTase organization similar to Type I systems BcgI
Type IIM Require methylated recognition sequence; Type IIP or Type IIA DpnI
Type IIS Asymmetric recognition sequence; cleavage at fixed positions usually outside recognition sequence FokI
Type IIT Heterodimeric restriction enzyme. Bpu10I, BslI
Putatives All subtypes
Control Control proteins of Type II restriction enzymes C.BamHI, C.PvuII

The characteristics of the orthodox Type IIP enzymes originally distinguished this group of enzymes from the Type I and III R-M systems. Type IIP is the largest group, owing to its valuable role in molecular science and its commercial value, but the current classification and growing number of R-M systems (putatively) identified, makes it clear that Type II enzymes are highly diverse and the boundaries with the other types are beginning to blur; see also Figure 3 and text for details.

aThese classifications reflect enzyme properties and activities, and not their evolutionary relationships. The classifications are not exclusive, and one enzyme can often belong several classes. Thus BcgI, for example, is Type IIA, B, C, G and H (see text for details).