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. 2001 Feb 1;20(3):433–445. doi: 10.1093/emboj/20.3.433

Table III. Mutagenesis of catalytically important residues in GRESAG4.1.

Mutation Specific activity(% wild type) Correlate inmammalian ACs Context inmammalian ACs(Tesmer et al., 1997) Vmax
D906A 0.005 Mg2+ coordination D396 VC1
E943A 0.08 salt bridge to R934 K936 IIC2 (salt bridge to D923; C1–C2 interface) wild type 10-fold decreased (Tang et al., 1995)
K945A 0.1 binds to N1 of adenine K938 IIC2 (salt bridge to D1018 IIC2) wild type (Tang et al., 1995)
D949A 0.008 Mg2+ coordination D440 VC1 <10-fold inactive (Tang et al., 1995)
R1022A 60 γ-phosphate binding R484 VC1 wild type10-fold decreased (Tang et al., 1995)
N1049A 0.03 active site structure,water coordination N1025 IIC2 <10-fold-inactive (Yan et al., 1997)
R1053A 0.1 stabilization of transition state, binds to α- and/orβ-phosphate R1029 IIC2 <10-fold- inactive (Tang et al., 1995; Yan et al., 1997)
E1055A 54 (salt bridge to R1022 inGRESAG4.1) E518 VC1 (salt bridge to R484) wild type (Tang et al., 1995; Dessauer et al., 1997)