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1 ve, compact form at pH 5.2 in the presence of 0.1 M Mg(2+), was solved by molecular replacement using the model of cowpea
2 omain and a C-terminal catalytic domain joined by a linker, was solved by molecular replacement methods using independent
3 allosteric yeast Saccharomyces cerevisiae chorismate mutase was solved by molecular replacement at a resolution of 2.8 an
4 P2(1)2(1)2(1); the structure of the complex with Mg(2+)*OSB was solved by molecular replacement in space group P2(1)2(1)2
7 bstrate analogue S-(2-oxo)pentadecyl-CoA, and its structure was solved by molecular replacement at 1.4 A resolution.
11 -1 bound to the MMP-10cd at 1.9 A resolution; the structure was solved by molecular replacement and refined with an R-fac
16 s fluorescens kynureninase were obtained, and the structure was solved by molecular replacement using the CsdB coordinate
22 in the active calcium-bound state at 2.03 A resolution that was solved by molecular replacement in the space group P6(5)
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