Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-115 |
Sentence |
denotes |
Aspartic acid 252 and asparagine 185 are essential for activity of lipid N-acetylglucosaminylphosphate transferase. |
T1 |
0-115 |
Sentence |
denotes |
Aspartic acid 252 and asparagine 185 are essential for activity of lipid N-acetylglucosaminylphosphate transferase. |
T1 |
0-115 |
Sentence |
denotes |
Aspartic acid 252 and asparagine 185 are essential for activity of lipid N-acetylglucosaminylphosphate transferase. |
TextSentencer_T2 |
116-403 |
Sentence |
denotes |
A key step in the assembly of oligosaccharide-lipid intermediates in N-linked glycosylation is the transfer of N-acetylglucosamine 1-phosphate to dolichyl phosphate, catalyzed by the enzyme UDP-N-acetylglucosaminyl:dolichyl phosphate N-acetylglucosaminyl phosphoryl transferase (L-G1PT). |
T2 |
116-403 |
Sentence |
denotes |
A key step in the assembly of oligosaccharide-lipid intermediates in N-linked glycosylation is the transfer of N-acetylglucosamine 1-phosphate to dolichyl phosphate, catalyzed by the enzyme UDP-N-acetylglucosaminyl:dolichyl phosphate N-acetylglucosaminyl phosphoryl transferase (L-G1PT). |
T2 |
116-403 |
Sentence |
denotes |
A key step in the assembly of oligosaccharide-lipid intermediates in N-linked glycosylation is the transfer of N-acetylglucosamine 1-phosphate to dolichyl phosphate, catalyzed by the enzyme UDP-N-acetylglucosaminyl:dolichyl phosphate N-acetylglucosaminyl phosphoryl transferase (L-G1PT). |
TextSentencer_T3 |
404-532 |
Sentence |
denotes |
Comparison of the amino acid sequences of L-G1PT from five diverse species showed 75 amino acids identical in all five proteins. |
T3 |
404-532 |
Sentence |
denotes |
Comparison of the amino acid sequences of L-G1PT from five diverse species showed 75 amino acids identical in all five proteins. |
T3 |
404-532 |
Sentence |
denotes |
Comparison of the amino acid sequences of L-G1PT from five diverse species showed 75 amino acids identical in all five proteins. |
TextSentencer_T4 |
533-734 |
Sentence |
denotes |
Using site-directed mutagenesis, we analyzed the importance of a number of these conserved residues to the enzymatic activity of L-G1PT using a plasmid shuffling procedure in Schizosaccharomyces pombe. |
T4 |
533-734 |
Sentence |
denotes |
Using site-directed mutagenesis, we analyzed the importance of a number of these conserved residues to the enzymatic activity of L-G1PT using a plasmid shuffling procedure in Schizosaccharomyces pombe. |
T4 |
533-734 |
Sentence |
denotes |
Using site-directed mutagenesis, we analyzed the importance of a number of these conserved residues to the enzymatic activity of L-G1PT using a plasmid shuffling procedure in Schizosaccharomyces pombe. |
TextSentencer_T5 |
735-883 |
Sentence |
denotes |
S. pombe cells containing a chromosomal deletion of the essential gpt+ gene are rescued by a plasmid containing the S. pombe gpt open reading frame. |
T5 |
735-883 |
Sentence |
denotes |
S. pombe cells containing a chromosomal deletion of the essential gpt+ gene are rescued by a plasmid containing the S. pombe gpt open reading frame. |
T5 |
735-883 |
Sentence |
denotes |
S. pombe cells containing a chromosomal deletion of the essential gpt+ gene are rescued by a plasmid containing the S. pombe gpt open reading frame. |
TextSentencer_T6 |
884-1066 |
Sentence |
denotes |
Replacement of that plasmid by a plasmid encoding a mutated hamster L-G1PT cDNA sequence indicated that the mutated protein provided sufficient enzyme activity to permit cell growth. |
T6 |
884-1066 |
Sentence |
denotes |
Replacement of that plasmid by a plasmid encoding a mutated hamster L-G1PT cDNA sequence indicated that the mutated protein provided sufficient enzyme activity to permit cell growth. |
T6 |
884-1066 |
Sentence |
denotes |
Replacement of that plasmid by a plasmid encoding a mutated hamster L-G1PT cDNA sequence indicated that the mutated protein provided sufficient enzyme activity to permit cell growth. |
TextSentencer_T7 |
1067-1204 |
Sentence |
denotes |
Mutations of aspartic acid 252 and asparagine 185 did not allow plasmid shuffling, indicating these residues were essential for activity. |
T7 |
1067-1204 |
Sentence |
denotes |
Mutations of aspartic acid 252 and asparagine 185 did not allow plasmid shuffling, indicating these residues were essential for activity. |
T7 |
1067-1204 |
Sentence |
denotes |
Mutations of aspartic acid 252 and asparagine 185 did not allow plasmid shuffling, indicating these residues were essential for activity. |
TextSentencer_T8 |
1205-1336 |
Sentence |
denotes |
A combination of mutations at asparagine 182 and tryptophan 122 did not allow plasmid shuffling, although the single mutations did. |
T8 |
1205-1336 |
Sentence |
denotes |
A combination of mutations at asparagine 182 and tryptophan 122 did not allow plasmid shuffling, although the single mutations did. |
T8 |
1205-1336 |
Sentence |
denotes |
A combination of mutations at asparagine 182 and tryptophan 122 did not allow plasmid shuffling, although the single mutations did. |
TextSentencer_T9 |
1337-1526 |
Sentence |
denotes |
Overexpression of the mutant proteins in S. pombe conferred tunicamycin (TM) resistance, indicating that the mutant proteins had a conformation necessary for binding TM, a substrate analog. |
T9 |
1337-1526 |
Sentence |
denotes |
Overexpression of the mutant proteins in S. pombe conferred tunicamycin (TM) resistance, indicating that the mutant proteins had a conformation necessary for binding TM, a substrate analog. |
T9 |
1337-1526 |
Sentence |
denotes |
Overexpression of the mutant proteins in S. pombe conferred tunicamycin (TM) resistance, indicating that the mutant proteins had a conformation necessary for binding TM, a substrate analog. |
TextSentencer_T10 |
1527-1638 |
Sentence |
denotes |
The mutant proteins were also detected in Western blots and were correctly localized to the membrane fractions. |
T10 |
1527-1638 |
Sentence |
denotes |
The mutant proteins were also detected in Western blots and were correctly localized to the membrane fractions. |
T10 |
1527-1638 |
Sentence |
denotes |
The mutant proteins were also detected in Western blots and were correctly localized to the membrane fractions. |
TextSentencer_T11 |
1639-1795 |
Sentence |
denotes |
However, the overexpressed proteins did not increase the endogenous level of enzymatic activity in these cells, indicating they were enzymatically inactive. |
T11 |
1639-1795 |
Sentence |
denotes |
However, the overexpressed proteins did not increase the endogenous level of enzymatic activity in these cells, indicating they were enzymatically inactive. |
T11 |
1639-1795 |
Sentence |
denotes |
However, the overexpressed proteins did not increase the endogenous level of enzymatic activity in these cells, indicating they were enzymatically inactive. |