| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-188 |
Sentence |
denotes |
Cloning and functional expression of the human GlcNAc-1-P transferase, the enzyme for the committed step of the dolichol cycle, by heterologous complementation in Saccharomyces cerevisiae. |
| T1 |
0-188 |
Sentence |
denotes |
Cloning and functional expression of the human GlcNAc-1-P transferase, the enzyme for the committed step of the dolichol cycle, by heterologous complementation in Saccharomyces cerevisiae. |
| T1 |
0-188 |
Sentence |
denotes |
Cloning and functional expression of the human GlcNAc-1-P transferase, the enzyme for the committed step of the dolichol cycle, by heterologous complementation in Saccharomyces cerevisiae. |
| TextSentencer_T2 |
189-322 |
Sentence |
denotes |
The gene for the human dolichol cycle GlcNAc-1-P transferase (ALG7/GPT) was cloned by screening a human lung fibroblast cDNA library. |
| T2 |
189-322 |
Sentence |
denotes |
The gene for the human dolichol cycle GlcNAc-1-P transferase (ALG7/GPT) was cloned by screening a human lung fibroblast cDNA library. |
| T2 |
189-322 |
Sentence |
denotes |
The gene for the human dolichol cycle GlcNAc-1-P transferase (ALG7/GPT) was cloned by screening a human lung fibroblast cDNA library. |
| TextSentencer_T3 |
323-514 |
Sentence |
denotes |
The library was constructed in a Saccharomyces cerevisiae expression vector, and the positive clone was identified by complementation of the conditional lethal S.cerevisiae strain YPH-A7-GAL. |
| T3 |
323-514 |
Sentence |
denotes |
The library was constructed in a Saccharomyces cerevisiae expression vector, and the positive clone was identified by complementation of the conditional lethal S.cerevisiae strain YPH-A7-GAL. |
| T3 |
323-514 |
Sentence |
denotes |
The library was constructed in a Saccharomyces cerevisiae expression vector, and the positive clone was identified by complementation of the conditional lethal S.cerevisiae strain YPH-A7-GAL. |
| TextSentencer_T4 |
515-639 |
Sentence |
denotes |
This strain was constructed by replacing the endogenous promoter of the GPT-gene by the stringently regulated GAL1-promoter. |
| T4 |
515-639 |
Sentence |
denotes |
This strain was constructed by replacing the endogenous promoter of the GPT-gene by the stringently regulated GAL1-promoter. |
| T4 |
515-639 |
Sentence |
denotes |
This strain was constructed by replacing the endogenous promoter of the GPT-gene by the stringently regulated GAL1-promoter. |
| TextSentencer_T5 |
640-718 |
Sentence |
denotes |
This construct allows to specifically suppress the endogenous enzyme activity. |
| T5 |
640-718 |
Sentence |
denotes |
This construct allows to specifically suppress the endogenous enzyme activity. |
| T5 |
640-718 |
Sentence |
denotes |
This construct allows to specifically suppress the endogenous enzyme activity. |
| TextSentencer_T6 |
719-901 |
Sentence |
denotes |
The insert of the positive clone displayed an open reading frame of 1200 nucleotides, coding for a putative protein of 400 amino acids with a calculated molecular weight of 44.7 kDa. |
| T6 |
719-901 |
Sentence |
denotes |
The insert of the positive clone displayed an open reading frame of 1200 nucleotides, coding for a putative protein of 400 amino acids with a calculated molecular weight of 44.7 kDa. |
| T6 |
719-901 |
Sentence |
denotes |
The insert of the positive clone displayed an open reading frame of 1200 nucleotides, coding for a putative protein of 400 amino acids with a calculated molecular weight of 44.7 kDa. |
| TextSentencer_T7 |
902-1088 |
Sentence |
denotes |
The deduced protein sequence shows a homology of over 90% when compared with other mammalian GPT sequences, thus resembling the close phylogenetic relationship between mammalian species. |
| T7 |
902-1088 |
Sentence |
denotes |
The deduced protein sequence shows a homology of over 90% when compared with other mammalian GPT sequences, thus resembling the close phylogenetic relationship between mammalian species. |
| T7 |
902-1088 |
Sentence |
denotes |
The deduced protein sequence shows a homology of over 90% when compared with other mammalian GPT sequences, thus resembling the close phylogenetic relationship between mammalian species. |
| TextSentencer_T8 |
1089-1259 |
Sentence |
denotes |
This homology however decreases to 40-50% when compared to more distantly related organisms such as S.cerevisiae , Schizosaccharomyces pombe , or Leishmania amazonensis . |
| T8 |
1089-1259 |
Sentence |
denotes |
This homology however decreases to 40-50% when compared to more distantly related organisms such as S.cerevisiae , Schizosaccharomyces pombe , or Leishmania amazonensis . |
| T8 |
1089-1259 |
Sentence |
denotes |
This homology however decreases to 40-50% when compared to more distantly related organisms such as S.cerevisiae , Schizosaccharomyces pombe , or Leishmania amazonensis . |
| TextSentencer_T9 |
1260-1395 |
Sentence |
denotes |
Biochemical characterization of the recombinant protein showed that it is functionally expressed in the S.cerevisiae strain YPH-A7-GAL. |
| T9 |
1260-1395 |
Sentence |
denotes |
Biochemical characterization of the recombinant protein showed that it is functionally expressed in the S.cerevisiae strain YPH-A7-GAL. |
| T9 |
1260-1395 |
Sentence |
denotes |
Biochemical characterization of the recombinant protein showed that it is functionally expressed in the S.cerevisiae strain YPH-A7-GAL. |
| TextSentencer_T10 |
1396-1613 |
Sentence |
denotes |
GlcNAc- and GlcNAc2-PP-Dolichol biosynthesis could be shown with isolated S.cerevisiae membranes from cells harboring the recombinant plasmid and grown on glucose thus suppressing transcription of the endogenous gene. |
| T10 |
1396-1613 |
Sentence |
denotes |
GlcNAc- and GlcNAc2-PP-Dolichol biosynthesis could be shown with isolated S.cerevisiae membranes from cells harboring the recombinant plasmid and grown on glucose thus suppressing transcription of the endogenous gene. |
| T10 |
1396-1613 |
Sentence |
denotes |
GlcNAc- and GlcNAc2-PP-Dolichol biosynthesis could be shown with isolated S.cerevisiae membranes from cells harboring the recombinant plasmid and grown on glucose thus suppressing transcription of the endogenous gene. |
| TextSentencer_T11 |
1614-1698 |
Sentence |
denotes |
Synthesis could be stimulated by dolicholphosphate and was inhibited by tunicamycin. |
| T11 |
1614-1698 |
Sentence |
denotes |
Synthesis could be stimulated by dolicholphosphate and was inhibited by tunicamycin. |
| T11 |
1614-1698 |
Sentence |
denotes |
Synthesis could be stimulated by dolicholphosphate and was inhibited by tunicamycin. |
| TextSentencer_T12 |
1699-1940 |
Sentence |
denotes |
These results show that we have cloned the human GlcNAc-1-P transferase by heterologous complementation in S. cerevisiae, a strategy that may be useful for the cloning and characterization of glycosyltransferases from a variety of organisms. |
| T12 |
1699-1940 |
Sentence |
denotes |
These results show that we have cloned the human GlcNAc-1-P transferase by heterologous complementation in S. cerevisiae, a strategy that may be useful for the cloning and characterization of glycosyltransferases from a variety of organisms. |
| T12 |
1699-1940 |
Sentence |
denotes |
These results show that we have cloned the human GlcNAc-1-P transferase by heterologous complementation in S. cerevisiae, a strategy that may be useful for the cloning and characterization of glycosyltransferases from a variety of organisms. |