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    • https://espanol.libretexts.org/Quimica/Libro%3A_Qu%C3%ADmica_Org%C3%A1nica_con_%C3%A9nfasis_Biol%C3%B3gico_(Soderberg)/09%3A_Reacciones_de_sustitucion_nucleofilica%2C_parte_II/9.2%3A_Digesti%C3%B3n_de_carbohidrato_mediante_glicosidasas_-_una_reacci%C3%B3n_SN1
      In the retaining reaction, however, the bottom side aspartate (Asp 2 ) acts as a nucleophile instead of as a base (step 2 below) , attacking the electrophilic carbon directly and forming what is refer...In the retaining reaction, however, the bottom side aspartate (Asp 2 ) acts as a nucleophile instead of as a base (step 2 below) , attacking the electrophilic carbon directly and forming what is referred to as a covalent intermediate (the enzyme is covalently attached to the terminal glucose molecule via the aspartate residue).

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