| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-100 |
Sentence |
denotes |
Human ZG16p recognizes pathogenic fungi through non-self polyvalent mannose in the digestive system. |
| T1 |
0-100 |
Sentence |
denotes |
Human ZG16p recognizes pathogenic fungi through non-self polyvalent mannose in the digestive system. |
| T1 |
0-100 |
Sentence |
denotes |
Human ZG16p recognizes pathogenic fungi through non-self polyvalent mannose in the digestive system. |
| TextSentencer_T2 |
101-245 |
Sentence |
denotes |
Human zymogen granule protein 16 (ZG16p) contains a Jacalin-like lectin domain, although its glycan-binding properties are not fully understood. |
| T2 |
101-245 |
Sentence |
denotes |
Human zymogen granule protein 16 (ZG16p) contains a Jacalin-like lectin domain, although its glycan-binding properties are not fully understood. |
| T2 |
101-245 |
Sentence |
denotes |
Human zymogen granule protein 16 (ZG16p) contains a Jacalin-like lectin domain, although its glycan-binding properties are not fully understood. |
| TextSentencer_T3 |
246-352 |
Sentence |
denotes |
Here, we screened the glycan-binding specificity of ZG16p by recently developed glycoconjugate microarray. |
| T3 |
246-352 |
Sentence |
denotes |
Here, we screened the glycan-binding specificity of ZG16p by recently developed glycoconjugate microarray. |
| T3 |
246-352 |
Sentence |
denotes |
Here, we screened the glycan-binding specificity of ZG16p by recently developed glycoconjugate microarray. |
| TextSentencer_T4 |
353-453 |
Sentence |
denotes |
ZG16p appeared to exhibit selective binding to α- and β-linked mannose-polyacrylamide-biotin probes. |
| T4 |
353-453 |
Sentence |
denotes |
ZG16p appeared to exhibit selective binding to α- and β-linked mannose-polyacrylamide-biotin probes. |
| T4 |
353-453 |
Sentence |
denotes |
ZG16p appeared to exhibit selective binding to α- and β-linked mannose-polyacrylamide-biotin probes. |
| TextSentencer_T5 |
454-677 |
Sentence |
denotes |
In more quantitative analysis using frontal affinity chromatography, dissociation constants to two types of polyvalent mannose, i.e. high-density mannose and yeast mannan, were determined to be 1.3 and 1.7 µM, respectively. |
| T5 |
454-677 |
Sentence |
denotes |
In more quantitative analysis using frontal affinity chromatography, dissociation constants to two types of polyvalent mannose, i.e. high-density mannose and yeast mannan, were determined to be 1.3 and 1.7 µM, respectively. |
| T5 |
454-677 |
Sentence |
denotes |
In more quantitative analysis using frontal affinity chromatography, dissociation constants to two types of polyvalent mannose, i.e. high-density mannose and yeast mannan, were determined to be 1.3 and 1.7 µM, respectively. |
| TextSentencer_T6 |
678-853 |
Sentence |
denotes |
Mutation of the evolutionarily conserved amino acid Asp151, which is involved in sugar binding among the Jacalin-related lectins (JRLs), abolished binding activity to mannose. |
| T6 |
678-853 |
Sentence |
denotes |
Mutation of the evolutionarily conserved amino acid Asp151, which is involved in sugar binding among the Jacalin-related lectins (JRLs), abolished binding activity to mannose. |
| T6 |
678-853 |
Sentence |
denotes |
Mutation of the evolutionarily conserved amino acid Asp151, which is involved in sugar binding among the Jacalin-related lectins (JRLs), abolished binding activity to mannose. |
| TextSentencer_T7 |
854-1090 |
Sentence |
denotes |
By immunohistochemical staining, ZG16p was specifically detected in mucus-secreting cells of the digestive system such as serosanguineous acinar cells of the parotid gland, acinar cells of the pancreas and goblet cells of the intestine. |
| T7 |
854-1090 |
Sentence |
denotes |
By immunohistochemical staining, ZG16p was specifically detected in mucus-secreting cells of the digestive system such as serosanguineous acinar cells of the parotid gland, acinar cells of the pancreas and goblet cells of the intestine. |
| T7 |
854-1090 |
Sentence |
denotes |
By immunohistochemical staining, ZG16p was specifically detected in mucus-secreting cells of the digestive system such as serosanguineous acinar cells of the parotid gland, acinar cells of the pancreas and goblet cells of the intestine. |
| TextSentencer_T8 |
1091-1215 |
Sentence |
denotes |
Finally, we showed that ZG16p recognizes pathogenic Candida and Malassezia species in a polyvalent mannose-dependent manner. |
| T8 |
1091-1215 |
Sentence |
denotes |
Finally, we showed that ZG16p recognizes pathogenic Candida and Malassezia species in a polyvalent mannose-dependent manner. |
| T8 |
1091-1215 |
Sentence |
denotes |
Finally, we showed that ZG16p recognizes pathogenic Candida and Malassezia species in a polyvalent mannose-dependent manner. |
| TextSentencer_T9 |
1216-1376 |
Sentence |
denotes |
We propose that ZG16p is a novel member of mannose-specific JRLs, which recognizes pathogenic fungi through non-self polyvalent mannose in the digestive system. |
| T9 |
1216-1376 |
Sentence |
denotes |
We propose that ZG16p is a novel member of mannose-specific JRLs, which recognizes pathogenic fungi through non-self polyvalent mannose in the digestive system. |
| T9 |
1216-1376 |
Sentence |
denotes |
We propose that ZG16p is a novel member of mannose-specific JRLs, which recognizes pathogenic fungi through non-self polyvalent mannose in the digestive system. |