PubMed:19233847
Annnotations
PMID_GLOBAL
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 665-682 | DiseaseOrPhenotypicFeature | denotes | Angelman syndrome | 0007113 |
T2 | 1288-1303 | DiseaseOrPhenotypicFeature | denotes | cystic fibrosis | 0009061 |
T3 | 1574-1577 | DiseaseOrPhenotypicFeature | denotes | can | 0012833 |
T4 | 1624-1641 | DiseaseOrPhenotypicFeature | denotes | Angelman syndrome | 0007113 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-179 | Sentence | denotes | The ubiquitin ligase E6-AP is induced and recruited to aggresomes in response to proteasome inhibition and may be involved in the ubiquitination of Hsp70-bound misfolded proteins. |
T2 | 180-304 | Sentence | denotes | Cells are equipped with an efficient quality control system to selectively eliminate abnormally folded and damaged proteins. |
T3 | 305-485 | Sentence | denotes | Initially the cell tries to refold the unfolded proteins with the help of molecular chaperones, and failure to refold leads to their degradation by the ubiquitin proteasome system. |
T4 | 486-584 | Sentence | denotes | But how this proteolytic machinery recognizes the abnormally folded proteins is poorly understood. |
T5 | 585-813 | Sentence | denotes | Here, we report that E6-AP, a HECT domain family ubiquitin ligase implicated in Angelman syndrome, interacts with the substrate binding domain of Hsp70/Hsc70 chaperones and promotes the degradation of chaperone bound substrates. |
T6 | 814-997 | Sentence | denotes | The expression of E6-AP was dramatically induced under a variety of stresses, and overexpression of E6-AP was found to protect against endoplasmic reticulum stress-induced cell death. |
T7 | 998-1234 | Sentence | denotes | The inhibition of proteasome function not only increases the expression of E6-AP but also causes its redistribution around microtubule-organizing center, a subcellular structure for the degradation of the cytoplasmic misfolded proteins. |
T8 | 1235-1375 | Sentence | denotes | E6-AP is also recruited to aggresomes containing the cystic fibrosis transmembrane conductance regulator or expanded polyglutamine proteins. |
T9 | 1376-1469 | Sentence | denotes | Finally, we demonstrate that E6-AP ubiquitinates misfolded luciferase that is bound by Hsp70. |
T10 | 1470-1727 | Sentence | denotes | Our results suggest that E6-AP functions as a cellular quality control ubiquitin ligase and, therefore, can be implicated not only in the pathogenesis of Angelman syndrome but also in the biology of neurodegenerative disorders involving protein aggregation. |
DisGeNET
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T0 | 914-919 | gene:7337 | denotes | E6-AP |
T1 | 971-977 | disease:C3825627 | denotes | stress |
T2 | 832-837 | gene:7337 | denotes | E6-AP |
T3 | 971-977 | disease:C3825627 | denotes | stress |
T4 | 1495-1500 | gene:7337 | denotes | E6-AP |
T5 | 1669-1696 | disease:C0524851 | denotes | neurodegenerative disorders |
T6 | 1495-1500 | gene:7337 | denotes | E6-AP |
T7 | 1624-1641 | disease:C0162635 | denotes | Angelman syndrome |
R1 | T0 | T1 | associated_with | E6-AP,stress |
R2 | T2 | T3 | associated_with | E6-AP,stress |
R3 | T4 | T5 | associated_with | E6-AP,neurodegenerative disorders |
R4 | T6 | T7 | associated_with | E6-AP,Angelman syndrome |
bionlp-st-epi-2011-training
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 4-13 | Protein | denotes | ubiquitin |
T2 | 21-26 | Protein | denotes | E6-AP |
T3 | 457-466 | Protein | denotes | ubiquitin |
T4 | 606-611 | Protein | denotes | E6-AP |
T5 | 634-643 | Protein | denotes | ubiquitin |
T6 | 737-742 | Protein | denotes | Hsc70 |
T7 | 832-837 | Protein | denotes | E6-AP |
T8 | 914-919 | Protein | denotes | E6-AP |
T9 | 1073-1078 | Protein | denotes | E6-AP |
T10 | 1235-1240 | Protein | denotes | E6-AP |
T11 | 1288-1339 | Protein | denotes | cystic fibrosis transmembrane conductance regulator |
T12 | 1405-1410 | Protein | denotes | E6-AP |
T13 | 1435-1445 | Protein | denotes | luciferase |
T14 | 1495-1500 | Protein | denotes | E6-AP |
T15 | 1541-1550 | Protein | denotes | ubiquitin |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
19233847-9#25#30#gene7337 | 1495-1500 | gene7337 | denotes | E6-AP |
19233847-9#154#171#diseaseC0162635 | 1624-1641 | diseaseC0162635 | denotes | Angelman syndrome |
19233847-9#199#226#diseaseC0524851 | 1669-1696 | diseaseC0524851 | denotes | neurodegenerative disorders |
25#30#gene7337154#171#diseaseC0162635 | 19233847-9#25#30#gene7337 | 19233847-9#154#171#diseaseC0162635 | associated_with | E6-AP,Angelman syndrome |
25#30#gene7337199#226#diseaseC0524851 | 19233847-9#25#30#gene7337 | 19233847-9#199#226#diseaseC0524851 | associated_with | E6-AP,neurodegenerative disorders |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 665-682 | Disease | denotes | Angelman syndrome | http://purl.obolibrary.org/obo/MONDO_0007113 |
T2 | 1288-1303 | Disease | denotes | cystic fibrosis | http://purl.obolibrary.org/obo/MONDO_0009061 |
T3 | 1624-1641 | Disease | denotes | Angelman syndrome | http://purl.obolibrary.org/obo/MONDO_0007113 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 961-970 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |
T2 | 1121-1132 | Body_part | denotes | microtubule | http://purl.obolibrary.org/obo/GO_0005874 |
T3 | 1203-1214 | Body_part | denotes | cytoplasmic | http://purl.obolibrary.org/obo/GO_0005737 |
T4 | 1304-1317 | Body_part | denotes | transmembrane | http://purl.obolibrary.org/obo/GO_0016020 |