| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-135 |
Sentence |
denotes |
Vesicular-integral membrane protein, VIP36, recognizes high-mannose type glycans containing alpha1-->2 mannosyl residues in MDCK cells. |
| T1 |
0-135 |
Sentence |
denotes |
Vesicular-integral membrane protein, VIP36, recognizes high-mannose type glycans containing alpha1-->2 mannosyl residues in MDCK cells. |
| T1 |
0-135 |
Sentence |
denotes |
Vesicular-integral membrane protein, VIP36, recognizes high-mannose type glycans containing alpha1-->2 mannosyl residues in MDCK cells. |
| TextSentencer_T2 |
136-418 |
Sentence |
denotes |
The 36 kDa vesicular-integral membrane protein, VIP36, has been originally isolated from MDCK cells as a component of glycolipid-enriched detergent-insoluble complexes containing apical marker proteins, and its luminal domain shows homology to leguminous plant lectins and ERGIC-53. |
| T2 |
136-418 |
Sentence |
denotes |
The 36 kDa vesicular-integral membrane protein, VIP36, has been originally isolated from MDCK cells as a component of glycolipid-enriched detergent-insoluble complexes containing apical marker proteins, and its luminal domain shows homology to leguminous plant lectins and ERGIC-53. |
| T2 |
136-418 |
Sentence |
denotes |
The 36 kDa vesicular-integral membrane protein, VIP36, has been originally isolated from MDCK cells as a component of glycolipid-enriched detergent-insoluble complexes containing apical marker proteins, and its luminal domain shows homology to leguminous plant lectins and ERGIC-53. |
| TextSentencer_T3 |
419-632 |
Sentence |
denotes |
As the first step to identify the functional role of VIP36, the carbohydrate binding specificity of VIP36 was investigated using a fusion protein of glutathione- S -transferase and luminal domain of VIP36 (Vip36). |
| T3 |
419-632 |
Sentence |
denotes |
As the first step to identify the functional role of VIP36, the carbohydrate binding specificity of VIP36 was investigated using a fusion protein of glutathione- S -transferase and luminal domain of VIP36 (Vip36). |
| T3 |
419-632 |
Sentence |
denotes |
As the first step to identify the functional role of VIP36, the carbohydrate binding specificity of VIP36 was investigated using a fusion protein of glutathione- S -transferase and luminal domain of VIP36 (Vip36). |
| TextSentencer_T4 |
633-768 |
Sentence |
denotes |
It was found that VIP36 recognizes high-mannose type glycans containing alpha1-->2 Man residues and alpha-amino substituted asparagine. |
| T4 |
633-768 |
Sentence |
denotes |
It was found that VIP36 recognizes high-mannose type glycans containing alpha1-->2 Man residues and alpha-amino substituted asparagine. |
| T4 |
633-768 |
Sentence |
denotes |
It was found that VIP36 recognizes high-mannose type glycans containing alpha1-->2 Man residues and alpha-amino substituted asparagine. |
| TextSentencer_T5 |
769-896 |
Sentence |
denotes |
The binding of Vip36 to high-mannose type glycans was independent of Ca(2+)and theoptimal condition was pH 6.0 at 37 degrees C. |
| T5 |
769-896 |
Sentence |
denotes |
The binding of Vip36 to high-mannose type glycans was independent of Ca(2+)and theoptimal condition was pH 6.0 at 37 degrees C. |
| T5 |
769-977 |
Sentence |
denotes |
The binding of Vip36 to high-mannose type glycans was independent of Ca(2+)and theoptimal condition was pH 6.0 at 37 degrees C. The concentration at which half inhibition of the binding by Man(7-9).GlcNAc(2). |
| TextSentencer_T6 |
897-977 |
Sentence |
denotes |
The concentration at which half inhibition of the binding by Man(7-9).GlcNAc(2). |
| T6 |
897-977 |
Sentence |
denotes |
The concentration at which half inhibition of the binding by Man(7-9).GlcNAc(2). |
| TextSentencer_T7 |
978-983 |
Sentence |
denotes |
N Ac. |
| T7 |
978-983 |
Sentence |
denotes |
N Ac. |
| T6 |
978-1207 |
Sentence |
denotes |
N Ac. Asn occurred was 1.0 x 10(-9)M. The association constant between Man(7-9).GlcNAc(2)in porcine thyroglobulin and immobilized Vip36 was 2.1 x 10(8)M(-1)as determined by means of a biosensor based on surface plasmon resonance. |
| TextSentencer_T8 |
984-1015 |
Sentence |
denotes |
Asn occurred was 1.0 x 10(-9)M. |
| T8 |
984-1015 |
Sentence |
denotes |
Asn occurred was 1.0 x 10(-9)M. |
| TextSentencer_T9 |
1016-1207 |
Sentence |
denotes |
The association constant between Man(7-9).GlcNAc(2)in porcine thyroglobulin and immobilized Vip36 was 2.1 x 10(8)M(-1)as determined by means of a biosensor based on surface plasmon resonance. |
| T9 |
1016-1207 |
Sentence |
denotes |
The association constant between Man(7-9).GlcNAc(2)in porcine thyroglobulin and immobilized Vip36 was 2.1 x 10(8)M(-1)as determined by means of a biosensor based on surface plasmon resonance. |
| TextSentencer_T10 |
1208-1374 |
Sentence |
denotes |
These results indicate that VIP36 functions as an intracellular lectin recognizing glycoproteins which possess high-mannose type glycans, (Manalpha1-->2)(2-4).Man(5). |
| T7 |
1208-1374 |
Sentence |
denotes |
These results indicate that VIP36 functions as an intracellular lectin recognizing glycoproteins which possess high-mannose type glycans, (Manalpha1-->2)(2-4).Man(5). |
| T10 |
1208-1374 |
Sentence |
denotes |
These results indicate that VIP36 functions as an intracellular lectin recognizing glycoproteins which possess high-mannose type glycans, (Manalpha1-->2)(2-4).Man(5). |
| TextSentencer_T11 |
1375-1385 |
Sentence |
denotes |
GlcNAc(2). |
| T8 |
1375-1385 |
Sentence |
denotes |
GlcNAc(2). |
| T11 |
1375-1385 |
Sentence |
denotes |
GlcNAc(2). |