Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-90 |
Sentence |
denotes |
NMR and molecular modeling reveal key structural features of synthetic nodulation factors. |
TextSentencer_T2 |
91-248 |
Sentence |
denotes |
Nod factors are lipochitoligosaccharides originally produced by the soil bacteria Rhizobia that are involved in the symbiotic process with leguminous plants. |
TextSentencer_T3 |
249-426 |
Sentence |
denotes |
Some synthetic analogs of the Nod factors present a strong biological activity, and the conformational behavior of these molecules is of interest for structure/function studies. |
TextSentencer_T4 |
427-634 |
Sentence |
denotes |
Nod factor analogs containing an insertion of a phenyl group in the acyl chain at the oligosaccharidic non-reducing end were previously synthesized (Grenouillat N, Vauzeilles B, Bono J-J, Samain E, Beau J-M. |
TextSentencer_T5 |
635-640 |
Sentence |
denotes |
2004. |
TextSentencer_T6 |
641-749 |
Sentence |
denotes |
Simple synthesis of nodulation-factor analogues exhibiting high affinity towards a specific binding protein. |
TextSentencer_T7 |
750-773 |
Sentence |
denotes |
Angew Chem Int Ed Engl. |
TextSentencer_T8 |
774-783 |
Sentence |
denotes |
43:4644). |
TextSentencer_T9 |
784-937 |
Sentence |
denotes |
Conformational studies of natural compounds and synthetic analogs have been performed combining molecular dynamics simulations in explicit water and NMR. |
TextSentencer_T10 |
938-1160 |
Sentence |
denotes |
Data revealed that the glycosidic head group can adopt only restricted conformations, whereas chemical modifications of the lipid chains, highly flexible in a water environment, influence the global shape of the molecules. |
TextSentencer_T11 |
1161-1311 |
Sentence |
denotes |
Collected structural data could be used in the future to rationalize and understand their biological activity and affinity toward a putative receptor. |
T1 |
0-90 |
Sentence |
denotes |
NMR and molecular modeling reveal key structural features of synthetic nodulation factors. |
T2 |
91-248 |
Sentence |
denotes |
Nod factors are lipochitoligosaccharides originally produced by the soil bacteria Rhizobia that are involved in the symbiotic process with leguminous plants. |
T3 |
249-426 |
Sentence |
denotes |
Some synthetic analogs of the Nod factors present a strong biological activity, and the conformational behavior of these molecules is of interest for structure/function studies. |
T4 |
427-640 |
Sentence |
denotes |
Nod factor analogs containing an insertion of a phenyl group in the acyl chain at the oligosaccharidic non-reducing end were previously synthesized (Grenouillat N, Vauzeilles B, Bono J-J, Samain E, Beau J-M. 2004. |
T5 |
641-749 |
Sentence |
denotes |
Simple synthesis of nodulation-factor analogues exhibiting high affinity towards a specific binding protein. |
T6 |
750-783 |
Sentence |
denotes |
Angew Chem Int Ed Engl. 43:4644). |
T7 |
784-937 |
Sentence |
denotes |
Conformational studies of natural compounds and synthetic analogs have been performed combining molecular dynamics simulations in explicit water and NMR. |
T8 |
938-1160 |
Sentence |
denotes |
Data revealed that the glycosidic head group can adopt only restricted conformations, whereas chemical modifications of the lipid chains, highly flexible in a water environment, influence the global shape of the molecules. |
T9 |
1161-1311 |
Sentence |
denotes |
Collected structural data could be used in the future to rationalize and understand their biological activity and affinity toward a putative receptor. |
T1 |
0-90 |
Sentence |
denotes |
NMR and molecular modeling reveal key structural features of synthetic nodulation factors. |
T2 |
91-248 |
Sentence |
denotes |
Nod factors are lipochitoligosaccharides originally produced by the soil bacteria Rhizobia that are involved in the symbiotic process with leguminous plants. |
T3 |
249-426 |
Sentence |
denotes |
Some synthetic analogs of the Nod factors present a strong biological activity, and the conformational behavior of these molecules is of interest for structure/function studies. |
T4 |
427-634 |
Sentence |
denotes |
Nod factor analogs containing an insertion of a phenyl group in the acyl chain at the oligosaccharidic non-reducing end were previously synthesized (Grenouillat N, Vauzeilles B, Bono J-J, Samain E, Beau J-M. |
T5 |
635-640 |
Sentence |
denotes |
2004. |
T6 |
641-749 |
Sentence |
denotes |
Simple synthesis of nodulation-factor analogues exhibiting high affinity towards a specific binding protein. |
T7 |
750-773 |
Sentence |
denotes |
Angew Chem Int Ed Engl. |
T8 |
774-783 |
Sentence |
denotes |
43:4644). |
T9 |
784-937 |
Sentence |
denotes |
Conformational studies of natural compounds and synthetic analogs have been performed combining molecular dynamics simulations in explicit water and NMR. |
T10 |
938-1160 |
Sentence |
denotes |
Data revealed that the glycosidic head group can adopt only restricted conformations, whereas chemical modifications of the lipid chains, highly flexible in a water environment, influence the global shape of the molecules. |
T11 |
1161-1311 |
Sentence |
denotes |
Collected structural data could be used in the future to rationalize and understand their biological activity and affinity toward a putative receptor. |