Table 1.

¹H-¹H distances determined from trNOEs for the acceptor in the presence of GnT-V.^a

O-Octyl	Glc	Man'	GlcNAc”	Distance(Å)
CH2-1b	H1	---	---	3.0
CH2-1a	H1	---	---	3.0
CH2-2	H1	---	---	3.5
---	H5 - H6(S)	---	---	2.2
---	H1 - H6(S)	---	---	3.3
---	H6(S)	H1'	---	2.5
---	H6(S)	H2'	---	2.9
---	H4	H3'	---	3.0
---	H5	H1'	---	3.5
---	H4	H1'	---	3.9
---	H6(S)	---	H1”	3.0
---	H6(S)	---	NAc	3.6
---	---	H4' - H6'(S)	---	2.9
---	---	H2'	H1”	2.6
---	---	H1'	H1”	2.7
---	---	H2'	H5”	3.5
---	---	H1'	NAc	3.5
---	---	H3'	H1”	3.6
---	---	H6'(S)	NAc	3.6
---	---	H2'	H4”	3.7
---	---	H1'	H5”	4.1
---	---	H2'	NAc	4.8
---	---	H4'	NAc	4.9
---	---	---	H5” - H6”(R)	2.5
---	---	---	H5” - H6”(S)	2.5
---	---	---	H4” - H6”(S)	3.1
---	---	---	H2” - NAc	4.0
---	---	---	H1” - NAc	4.5
---	---	---	H3” - NAc	4.8

^aOnly intermolecular and sugar methylene proton NOEs were included to simplify the table. Intramolecular NOEs were used as reference values to calculate the tabulated NOE values.