| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-80 |
Sentence |
denotes |
Recognition of oligosaccharide substrates by N-acetyl-glucosaminyltransferase-V. |
| T1 |
0-80 |
Sentence |
denotes |
Recognition of oligosaccharide substrates by N-acetyl-glucosaminyltransferase-V. |
| TextSentencer_T2 |
81-387 |
Sentence |
denotes |
Six analogs of the trisaccharide 8-methoxycarbonyloctyl 6-O-[2-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-alpha-D-mannopyrano syl] -beta-D-mannopyranoside (3), a previously reported acceptor for N-acetylglucosaminyltransferase-V (GnT-V) have been chemically synthesized and evaluated as GnT-V acceptors. |
| T2 |
81-387 |
Sentence |
denotes |
Six analogs of the trisaccharide 8-methoxycarbonyloctyl 6-O-[2-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-alpha-D-mannopyrano syl] -beta-D-mannopyranoside (3), a previously reported acceptor for N-acetylglucosaminyltransferase-V (GnT-V) have been chemically synthesized and evaluated as GnT-V acceptors. |
| TextSentencer_T3 |
388-653 |
Sentence |
denotes |
Replacement of the beta-D-man rho-O(CH2)8COOMe "reducing end" of 3 by beta-D-Glc rho-O(CH2)7 CH3 gave octyl 6-O-[2-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl]-alpha-D- mannopyranosyl)-beta-D-glucopyranoside (5) whose activity was indistinguishable from that of 3. |
| T3 |
388-653 |
Sentence |
denotes |
Replacement of the beta-D-man rho-O(CH2)8COOMe "reducing end" of 3 by beta-D-Glc rho-O(CH2)7 CH3 gave octyl 6-O-[2-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl]-alpha-D- mannopyranosyl)-beta-D-glucopyranoside (5) whose activity was indistinguishable from that of 3. |
| TextSentencer_T4 |
654-812 |
Sentence |
denotes |
Removal of the 4-OH group of the beta-D-Glc residue in 5 had little effect on the activity, while the corresponding 4-O-methyl derivative was twice as active. |
| T4 |
654-812 |
Sentence |
denotes |
Removal of the 4-OH group of the beta-D-Glc residue in 5 had little effect on the activity, while the corresponding 4-O-methyl derivative was twice as active. |
| TextSentencer_T5 |
813-1024 |
Sentence |
denotes |
Replacement of the C-6 pro-R hydrogen of the same residue by a methyl group gave the L-glycero-D-gluco derivative 8, whereas replacement of the corresponding pro-S hydrogen gave the D-glycero-D-gluco compound 9. |
| T5 |
813-1024 |
Sentence |
denotes |
Replacement of the C-6 pro-R hydrogen of the same residue by a methyl group gave the L-glycero-D-gluco derivative 8, whereas replacement of the corresponding pro-S hydrogen gave the D-glycero-D-gluco compound 9. |
| TextSentencer_T6 |
1025-1284 |
Sentence |
denotes |
Trisaccharide 8, whose rotameric distribution about the C-5-C-6 bond is sterically biased towards the gg conformation was less than half as active as 5 as a GnT-V acceptor, whereas 9, which is biased towards the gt conformation, was more than twice as active. |
| T6 |
1025-1284 |
Sentence |
denotes |
Trisaccharide 8, whose rotameric distribution about the C-5-C-6 bond is sterically biased towards the gg conformation was less than half as active as 5 as a GnT-V acceptor, whereas 9, which is biased towards the gt conformation, was more than twice as active. |
| TextSentencer_T7 |
1285-1379 |
Sentence |
denotes |
These results provide evidence for the conformational control of oligosaccharide biosynthesis. |
| T7 |
1285-1379 |
Sentence |
denotes |
These results provide evidence for the conformational control of oligosaccharide biosynthesis. |
