| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-115 |
Sentence |
denotes |
Characterization of a putative 3-deoxy-D-manno-2-octulosonic acid (Kdo) transferase gene from Arabidopsis thaliana. |
| T1 |
0-115 |
Sentence |
denotes |
Characterization of a putative 3-deoxy-D-manno-2-octulosonic acid (Kdo) transferase gene from Arabidopsis thaliana. |
| T1 |
0-115 |
Sentence |
denotes |
Characterization of a putative 3-deoxy-D-manno-2-octulosonic acid (Kdo) transferase gene from Arabidopsis thaliana. |
| TextSentencer_T2 |
116-268 |
Sentence |
denotes |
The structures of the pectic polysaccharide rhamnogalacturonan II (RG-II) pectin constituent are remarkably evolutionary conserved in all plant species. |
| T2 |
116-268 |
Sentence |
denotes |
The structures of the pectic polysaccharide rhamnogalacturonan II (RG-II) pectin constituent are remarkably evolutionary conserved in all plant species. |
| T2 |
116-268 |
Sentence |
denotes |
The structures of the pectic polysaccharide rhamnogalacturonan II (RG-II) pectin constituent are remarkably evolutionary conserved in all plant species. |
| TextSentencer_T3 |
269-330 |
Sentence |
denotes |
At least 12 different glycosyl residues are present in RG-II. |
| T3 |
269-330 |
Sentence |
denotes |
At least 12 different glycosyl residues are present in RG-II. |
| T3 |
269-330 |
Sentence |
denotes |
At least 12 different glycosyl residues are present in RG-II. |
| TextSentencer_T4 |
331-514 |
Sentence |
denotes |
Among them is the seldom eight-carbon sugar 3-deoxy-d-manno-octulosonic acid (Kdo) whose biosynthetic pathway has been shown to be conserved between plants and Gram-negative bacteria. |
| T4 |
331-514 |
Sentence |
denotes |
Among them is the seldom eight-carbon sugar 3-deoxy-d-manno-octulosonic acid (Kdo) whose biosynthetic pathway has been shown to be conserved between plants and Gram-negative bacteria. |
| T4 |
331-514 |
Sentence |
denotes |
Among them is the seldom eight-carbon sugar 3-deoxy-d-manno-octulosonic acid (Kdo) whose biosynthetic pathway has been shown to be conserved between plants and Gram-negative bacteria. |
| TextSentencer_T5 |
515-788 |
Sentence |
denotes |
Kdo is formed in the cytosol by the condensation of phosphoenol pyruvate with d-arabinose-5-P and then activated by coupling to cytidine monophosphate (CMP) prior to its incorporation in the Golgi apparatus by a Kdo transferase (KDTA) into the nascent polysaccharide RG-II. |
| T5 |
515-788 |
Sentence |
denotes |
Kdo is formed in the cytosol by the condensation of phosphoenol pyruvate with d-arabinose-5-P and then activated by coupling to cytidine monophosphate (CMP) prior to its incorporation in the Golgi apparatus by a Kdo transferase (KDTA) into the nascent polysaccharide RG-II. |
| T5 |
515-788 |
Sentence |
denotes |
Kdo is formed in the cytosol by the condensation of phosphoenol pyruvate with d-arabinose-5-P and then activated by coupling to cytidine monophosphate (CMP) prior to its incorporation in the Golgi apparatus by a Kdo transferase (KDTA) into the nascent polysaccharide RG-II. |
| TextSentencer_T6 |
789-962 |
Sentence |
denotes |
To gain new insight into RG-II biosynthesis and function, we isolated and characterized null mutants for the unique putative KDTA (AtKDTA) encoded in the Arabidopsis genome. |
| T6 |
789-962 |
Sentence |
denotes |
To gain new insight into RG-II biosynthesis and function, we isolated and characterized null mutants for the unique putative KDTA (AtKDTA) encoded in the Arabidopsis genome. |
| T6 |
789-962 |
Sentence |
denotes |
To gain new insight into RG-II biosynthesis and function, we isolated and characterized null mutants for the unique putative KDTA (AtKDTA) encoded in the Arabidopsis genome. |
| TextSentencer_T7 |
963-1159 |
Sentence |
denotes |
We provide evidence that, in contrast to mutants affecting the RG-II biosynthesis, the extinction of the AtKDTA gene expression does not result in any developmental phenotype in the AtkdtA plants. |
| T7 |
963-1159 |
Sentence |
denotes |
We provide evidence that, in contrast to mutants affecting the RG-II biosynthesis, the extinction of the AtKDTA gene expression does not result in any developmental phenotype in the AtkdtA plants. |
| T7 |
963-1159 |
Sentence |
denotes |
We provide evidence that, in contrast to mutants affecting the RG-II biosynthesis, the extinction of the AtKDTA gene expression does not result in any developmental phenotype in the AtkdtA plants. |
| TextSentencer_T8 |
1160-1297 |
Sentence |
denotes |
Furthermore, the structure of RG-II from the null mutants was not altered and contained wild-type amount of Rha-alpha(1-5)Kdo side chain. |
| T8 |
1160-1297 |
Sentence |
denotes |
Furthermore, the structure of RG-II from the null mutants was not altered and contained wild-type amount of Rha-alpha(1-5)Kdo side chain. |
| T8 |
1160-1297 |
Sentence |
denotes |
Furthermore, the structure of RG-II from the null mutants was not altered and contained wild-type amount of Rha-alpha(1-5)Kdo side chain. |
| TextSentencer_T9 |
1298-1442 |
Sentence |
denotes |
The cellular localization of AtKDTA was investigated by using laser scanning confocal imaging of the protein fused to green fluorescent protein. |
| T9 |
1298-1442 |
Sentence |
denotes |
The cellular localization of AtKDTA was investigated by using laser scanning confocal imaging of the protein fused to green fluorescent protein. |
| T9 |
1298-1442 |
Sentence |
denotes |
The cellular localization of AtKDTA was investigated by using laser scanning confocal imaging of the protein fused to green fluorescent protein. |
| TextSentencer_T10 |
1443-1557 |
Sentence |
denotes |
In agreement with its cellular prediction, the fusion protein was demonstrated to be targeted to the mitochondria. |
| T10 |
1443-1557 |
Sentence |
denotes |
In agreement with its cellular prediction, the fusion protein was demonstrated to be targeted to the mitochondria. |
| T10 |
1443-1557 |
Sentence |
denotes |
In agreement with its cellular prediction, the fusion protein was demonstrated to be targeted to the mitochondria. |
| TextSentencer_T11 |
1558-1827 |
Sentence |
denotes |
These data, together with data deduced from sequence analyses of higher plant genomes, suggest that AtKDTA encodes a putative KDTA involved in the synthesis of a mitochondrial not yet identified lipid A-like molecule rather than in the synthesis of the cell wall RG-II. |
| T11 |
1558-1827 |
Sentence |
denotes |
These data, together with data deduced from sequence analyses of higher plant genomes, suggest that AtKDTA encodes a putative KDTA involved in the synthesis of a mitochondrial not yet identified lipid A-like molecule rather than in the synthesis of the cell wall RG-II. |
| T11 |
1558-1827 |
Sentence |
denotes |
These data, together with data deduced from sequence analyses of higher plant genomes, suggest that AtKDTA encodes a putative KDTA involved in the synthesis of a mitochondrial not yet identified lipid A-like molecule rather than in the synthesis of the cell wall RG-II. |