paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | DISCUSSION | 1 | 52 | [
"B22",
"B51",
"B52",
"B22"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | It is well accepted that L1 element expression is a necessary driver for insertion of Alu and presumably SVA elements (22,51), as well as processed pseudogenes (52). | [
"22",
"51",
"52",
"22"
] | 165 | 37,516 | 1 | false | It is well accepted that L1 element expression is a necessary driver for insertion of Alu and presumably SVA elements, as well as processed pseudogenes. | [
"22,51",
"52"
] | It is well accepted that L1 element expression is a necessary driver for insertion of Alu and presumably SVA elements, as well as processed pseudogenes. | true | true | true | true | true | 6,425 |
1 | DISCUSSION | 1 | 22 | [
"B22",
"B51",
"B52",
"B22"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | More importantly, only expression of the ORF2 of L1 is required to drive Alu mobilization (22). | [
"22",
"51",
"52",
"22"
] | 95 | 37,517 | 1 | false | More importantly, only expression of the ORF2 of L1 is required to drive Alu mobilization. | [
"22"
] | More importantly, only expression of the ORF2 of L1 is required to drive Alu mobilization. | true | true | true | true | true | 6,425 |
1 | DISCUSSION | 1 | 22 | [
"B22",
"B51",
"B52",
"B22"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | Thus, tissues that make spliced forms of L1 RNA but not the FL L1 transcripts may make functional ORF2 and cause mutations by driving Alu retrotransposition. | [
"22",
"51",
"52",
"22"
] | 157 | 37,518 | 0 | false | Thus, tissues that make spliced forms of L1 RNA but not the FL L1 transcripts may make functional ORF2 and cause mutations by driving Alu retrotransposition. | [] | Thus, tissues that make spliced forms of L1 RNA but not the FL L1 transcripts may make functional ORF2 and cause mutations by driving Alu retrotransposition. | true | true | true | true | true | 6,425 |
2 | DISCUSSION | 1 | 23 | [
"B23",
"B2",
"B2",
"B53"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | There are almost twice as many Alu inserts as L1 integrants that have been characterized as causing disease [reviewed in ref. | [
"23",
"2",
"2",
"53"
] | 125 | 37,519 | 0 | false | There are almost twice as many Alu inserts as L1 integrants that have been characterized as causing disease [reviewed in ref. | [] | There are almost twice as many Alu inserts as L1 integrants that have been characterized as causing disease [reviewed in ref. | true | true | true | true | true | 6,426 |
2 | DISCUSSION | 1 | 2 | [
"B23",
"B2",
"B2",
"B53"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | In addition, there are twice as many total Alu elements as L1 copies in the human genome (2). | [
"23",
"2",
"2",
"53"
] | 93 | 37,520 | 1 | false | In addition, there are twice as many total Alu elements as L1 copies in the human genome. | [
"2"
] | In addition, there are twice as many total Alu elements as L1 copies in the human genome. | true | true | true | true | true | 6,426 |
2 | DISCUSSION | 1 | 23 | [
"B23",
"B2",
"B2",
"B53"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | Even though differential post-integration selection against L1 and Alu inserts and a bias in detection of the disease causing integration events can certainly account for some of the disparity in their accumulation rate, it is also possible that the relative paucity of the full-length L1 mRNA in testis and expression o... | [
"23",
"2",
"2",
"53"
] | 452 | 37,521 | 0 | false | Even though differential post-integration selection against L1 and Alu inserts and a bias in detection of the disease causing integration events can certainly account for some of the disparity in their accumulation rate, it is also possible that the relative paucity of the full-length L1 mRNA in testis and expression o... | [] | Even though differential post-integration selection against L1 and Alu inserts and a bias in detection of the disease causing integration events can certainly account for some of the disparity in their accumulation rate, it is also possible that the relative paucity of the full-length L1 mRNA in testis and expression o... | true | true | true | true | true | 6,426 |
2 | DISCUSSION | 1 | 2 | [
"B23",
"B2",
"B2",
"B53"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | Thus, the presence of the SpORF2 products in germ line may contribute to the higher copy number of Alu elements in the genome (2) and their higher contribution to disease (53) relative to L1 inserts. | [
"23",
"2",
"2",
"53"
] | 199 | 37,522 | 1 | false | Thus, the presence of the SpORF2 products in germ line may contribute to the higher copy number of Alu elements in the genome and their higher contribution to disease relative to L1 inserts. | [
"2",
"53"
] | Thus, the presence of the SpORF2 products in germ line may contribute to the higher copy number of Alu elements in the genome and their higher contribution to disease relative to L1 inserts. | true | true | true | true | true | 6,426 |
3 | DISCUSSION | 1 | 54 | [
"B54",
"B55",
"B56",
"B57",
"B58 B59 B60"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | Methylation and promoter strength were originally thought to be the only major regulatory mechanisms restricting L1 activity (54,55). | [
"54",
"55",
"56",
"57",
"58β60"
] | 133 | 37,523 | 0 | false | Methylation and promoter strength were originally thought to be the only major regulatory mechanisms restricting L1 activity. | [
"54,55"
] | Methylation and promoter strength were originally thought to be the only major regulatory mechanisms restricting L1 activity. | true | true | true | true | true | 6,427 |
3 | DISCUSSION | 1 | 56 | [
"B54",
"B55",
"B56",
"B57",
"B58 B59 B60"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | Recently cellular factors, such as the APOBEC3 gene family and the nuclear excision repair endonuclease complex ERCC1/XPF (56) and the potential of RNAi (57), were shown to negatively modulate L1 retrotransposition (58β60). | [
"54",
"55",
"56",
"57",
"58β60"
] | 223 | 37,524 | 1 | false | Recently cellular factors, such as the APOBEC3 gene family and the nuclear excision repair endonuclease complex ERCC1/XPF and the potential of RNAi, were shown to negatively modulate L1 retrotransposition. | [
"56",
"57",
"58β60"
] | Recently cellular factors, such as the APOBEC3 gene family and the nuclear excision repair endonuclease complex ERCC1/XPF and the potential of RNAi, were shown to negatively modulate L1 retrotransposition. | true | true | true | true | true | 6,427 |
3 | DISCUSSION | 1 | 54 | [
"B54",
"B55",
"B56",
"B57",
"B58 B59 B60"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | Even though transcriptional activity of the L1 promoter is almost certainly a crucial step in ensuring endogenous L1 expression, our data demonstrate that it is not the only mechanism controlling production of the retrotranspositionally active L1 mRNA. | [
"54",
"55",
"56",
"57",
"58β60"
] | 252 | 37,525 | 0 | false | Even though transcriptional activity of the L1 promoter is almost certainly a crucial step in ensuring endogenous L1 expression, our data demonstrate that it is not the only mechanism controlling production of the retrotranspositionally active L1 mRNA. | [] | Even though transcriptional activity of the L1 promoter is almost certainly a crucial step in ensuring endogenous L1 expression, our data demonstrate that it is not the only mechanism controlling production of the retrotranspositionally active L1 mRNA. | true | true | true | true | true | 6,427 |
3 | DISCUSSION | 1 | 54 | [
"B54",
"B55",
"B56",
"B57",
"B58 B59 B60"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | Although polyadenylation and splicing were previously shown to limit expression of L1 elements, this is the first demonstration that differential processing of endogenous L1 mRNA can account for considerable differences in the relative abundance of the full-length L1 transcript. | [
"54",
"55",
"56",
"57",
"58β60"
] | 279 | 37,526 | 0 | false | Although polyadenylation and splicing were previously shown to limit expression of L1 elements, this is the first demonstration that differential processing of endogenous L1 mRNA can account for considerable differences in the relative abundance of the full-length L1 transcript. | [] | Although polyadenylation and splicing were previously shown to limit expression of L1 elements, this is the first demonstration that differential processing of endogenous L1 mRNA can account for considerable differences in the relative abundance of the full-length L1 transcript. | true | true | true | true | true | 6,427 |
3 | DISCUSSION | 1 | 54 | [
"B54",
"B55",
"B56",
"B57",
"B58 B59 B60"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | Our studies demonstrate that in most tissues and cell lines, post-transcriptional regulation of L1 RNA is a major factor in controlling L1 expression (Figures 1 and 2). | [
"54",
"55",
"56",
"57",
"58β60"
] | 168 | 37,527 | 0 | false | Our studies demonstrate that in most tissues and cell lines, post-transcriptional regulation of L1 RNA is a major factor in controlling L1 expression (Figures 1 and 2). | [] | Our studies demonstrate that in most tissues and cell lines, post-transcriptional regulation of L1 RNA is a major factor in controlling L1 expression (Figures 1 and 2). | true | true | true | true | true | 6,427 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | In addition to the mobilization of itself and its parasites, L1 activity also produces DNA DSBs (25β27). | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 104 | 37,528 | 1 | false | In addition to the mobilization of itself and its parasites, L1 activity also produces DNA DSBs. | [
"25β27"
] | In addition to the mobilization of itself and its parasites, L1 activity also produces DNA DSBs. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Consistent with the previous reports of DNA damage induced by either the wt L1 of ORF2 alone in cancer cells (27), we demonstrate that expression of the SpORF2 splice product in normal human fibroblasts leads to detectable DNA damage. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 234 | 37,529 | 1 | false | Consistent with the previous reports of DNA damage induced by either the wt L1 of ORF2 alone in cancer cells, we demonstrate that expression of the SpORF2 splice product in normal human fibroblasts leads to detectable DNA damage. | [
"27"
] | Consistent with the previous reports of DNA damage induced by either the wt L1 of ORF2 alone in cancer cells, we demonstrate that expression of the SpORF2 splice product in normal human fibroblasts leads to detectable DNA damage. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | This observation suggests that even very low levels of the L1 ORF2 activity in somatic tissues generated from either the full-length L1 or the SpORF2 splice product may contribute to the gradual accumulation of DNA damage during the lifespan of an individual. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 259 | 37,530 | 0 | false | This observation suggests that even very low levels of the L1 ORF2 activity in somatic tissues generated from either the full-length L1 or the SpORF2 splice product may contribute to the gradual accumulation of DNA damage during the lifespan of an individual. | [] | This observation suggests that even very low levels of the L1 ORF2 activity in somatic tissues generated from either the full-length L1 or the SpORF2 splice product may contribute to the gradual accumulation of DNA damage during the lifespan of an individual. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | This damage can be in the form of de novo integration events of retroelements that can alter gene architecture and expression (14,61,62), point mutations resulting from the error-prone repair of ORF2-induced DNA lesions, or recombination events triggered by the ORF2 nicking activity [reviewed in ref. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 301 | 37,531 | 0 | false | This damage can be in the form of de novo integration events of retroelements that can alter gene architecture and expression, point mutations resulting from the error-prone repair of ORF2-induced DNA lesions, or recombination events triggered by the ORF2 nicking activity [reviewed in ref. | [
"14,61,62"
] | This damage can be in the form of de novo integration events of retroelements that can alter gene architecture and expression, point mutations resulting from the error-prone repair of ORF2-induced DNA lesions, or recombination events triggered by the ORF2 nicking activity [reviewed in ref. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 22 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Furthermore, the ability of L1 elements to produce the SpORF2 splice product means that even retrotranspositionaly incompetent L1 elements that maintain intact ORF2 can generate DNA damage (27,36) and mobilize Alu elements (22). | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 228 | 37,532 | 1 | false | Furthermore, the ability of L1 elements to produce the SpORF2 splice product means that even retrotranspositionaly incompetent L1 elements that maintain intact ORF2 can generate DNA damage and mobilize Alu elements. | [
"27,36",
"22"
] | Furthermore, the ability of L1 elements to produce the SpORF2 splice product means that even retrotranspositionaly incompetent L1 elements that maintain intact ORF2 can generate DNA damage and mobilize Alu elements. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | As summarized in Figure 8 cells, such as adult stem cells, which predominantly produce the SpORF2 transcript are likely to endure little damage associated with the full-length L1 mRNA. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 184 | 37,533 | 0 | false | As summarized in Figure 8 cells, such as adult stem cells, which predominantly produce the SpORF2 transcript are likely to endure little damage associated with the full-length L1 mRNA. | [] | As summarized in Figure 8 cells, such as adult stem cells, which predominantly produce the SpORF2 transcript are likely to endure little damage associated with the full-length L1 mRNA. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | While prostate, esophagus, ovaries and a number of other cell types that produce both the full-length and the SpORF2 mRNAs are possibly exposed to the full arsenal of the L1-related genomic instability. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 202 | 37,534 | 0 | false | While prostate, esophagus, ovaries and a number of other cell types that produce both the full-length and the SpORF2 mRNAs are possibly exposed to the full arsenal of the L1-related genomic instability. | [] | While prostate, esophagus, ovaries and a number of other cell types that produce both the full-length and the SpORF2 mRNAs are possibly exposed to the full arsenal of the L1-related genomic instability. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Thus, L1 elements may potentially contribute, in a way similar to ROS, to both the organismal aging process as well as to a number of age-related diseases potentially in a tissue-specific manner. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 195 | 37,535 | 0 | false | Thus, L1 elements may potentially contribute, in a way similar to ROS, to both the organismal aging process as well as to a number of age-related diseases potentially in a tissue-specific manner. | [] | Thus, L1 elements may potentially contribute, in a way similar to ROS, to both the organismal aging process as well as to a number of age-related diseases potentially in a tissue-specific manner. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | It is even possible that overproduction of L1 elements in cells still expressing p53 (25) could lead to cell death that may serve as a defense mechanism against L1 activity promoting genomic instability that has a potential to contribute to malignant transformation. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 266 | 37,536 | 1 | false | It is even possible that overproduction of L1 elements in cells still expressing p53 could lead to cell death that may serve as a defense mechanism against L1 activity promoting genomic instability that has a potential to contribute to malignant transformation. | [
"25"
] | It is even possible that overproduction of L1 elements in cells still expressing p53 could lead to cell death that may serve as a defense mechanism against L1 activity promoting genomic instability that has a potential to contribute to malignant transformation. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 64β66 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | There is also potential for increased L1-related damage with age because of decreased DNA repair response in aging mammalian cells (64β66) or age-associated hypomethylation of genomic DNA (67). | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 193 | 37,537 | 1 | false | There is also potential for increased L1-related damage with age because of decreased DNA repair response in aging mammalian cells or age-associated hypomethylation of genomic DNA. | [
"64β66",
"67"
] | There is also potential for increased L1-related damage with age because of decreased DNA repair response in aging mammalian cells or age-associated hypomethylation of genomic DNA. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Figure 8.A summary of the biologically relevant L1-related mRNA products and their respective impact on the host genome. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 120 | 37,538 | 0 | false | Figure 8.A summary of the biologically relevant L1-related mRNA products and their respective impact on the host genome. | [] | Figure 8.A summary of the biologically relevant L1-related mRNA products and their respective impact on the host genome. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Transcription of the functional L1 locus results in the production of either the full-length mRNA (FL1mRNA), the splice ORF2 mRNA (SpORF2mRNA) or both. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 151 | 37,539 | 0 | false | Transcription of the functional L1 locus results in the production of either the full-length mRNA (FL1mRNA), the splice ORF2 mRNA (SpORF2mRNA) or both. | [] | Transcription of the functional L1 locus results in the production of either the full-length mRNA (FL1mRNA), the splice ORF2 mRNA or both. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | FL1mRNA protein products can mobilize L1, Alu, and SVA elements, while SpORF2mRNA only produces ORF2 protein and as a result can only assist Alu retrotransposition. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 164 | 37,540 | 0 | false | FL1mRNA protein products can mobilize L1, Alu, and SVA elements, while SpORF2mRNA only produces ORF2 protein and as a result can only assist Alu retrotransposition. | [] | FL1mRNA protein products can mobilize L1, Alu, and SVA elements, while SpORF2mRNA only produces ORF2 protein and as a result can only assist Alu retrotransposition. | true | true | true | true | true | 6,428 |
4 | DISCUSSION | 1 | 25β27 | [
"B25 B26 B27",
"B27",
"B14",
"B61",
"B62",
"B63",
"B27",
"B36",
"B22",
"B25",
"B64 B65 B66",
"B67"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Expression of either L1 mRNA can generate ORF2, which leads to introduction of DNA DSBs potentially resulting in accumulation of mutations in the cellular genome. | [
"25β27",
"27",
"14",
"61",
"62",
"63",
"27",
"36",
"22",
"25",
"64β66",
"67"
] | 162 | 37,541 | 0 | false | Expression of either L1 mRNA can generate ORF2, which leads to introduction of DNA DSBs potentially resulting in accumulation of mutations in the cellular genome. | [] | Expression of either L1 mRNA can generate ORF2, which leads to introduction of DNA DSBs potentially resulting in accumulation of mutations in the cellular genome. | true | true | true | true | true | 6,428 |
5 | DISCUSSION | 0 | null | null | 20,215,437 | null | A summary of the biologically relevant L1-related mRNA products and their respective impact on the host genome. | null | 111 | 37,542 | 0 | false | null | null | A summary of the biologically relevant L1-related mRNA products and their respective impact on the host genome. | true | true | true | true | true | 6,429 |
5 | DISCUSSION | 0 | null | null | 20,215,437 | null | Transcription of the functional L1 locus results in the production of either the full-length mRNA (FL1mRNA), the splice ORF2 mRNA (SpORF2mRNA) or both. | null | 151 | 37,543 | 0 | false | null | null | Transcription of the functional L1 locus results in the production of either the full-length mRNA (FL1mRNA), the splice ORF2 mRNA (SpORF2mRNA) or both. | true | true | true | true | true | 6,429 |
5 | DISCUSSION | 0 | null | null | 20,215,437 | null | FL1mRNA protein products can mobilize L1, Alu, and SVA elements, while SpORF2mRNA only produces ORF2 protein and as a result can only assist Alu retrotransposition. | null | 164 | 37,544 | 0 | false | null | null | FL1mRNA protein products can mobilize L1, Alu, and SVA elements, while SpORF2mRNA only produces ORF2 protein and as a result can only assist Alu retrotransposition. | true | true | true | true | true | 6,429 |
5 | DISCUSSION | 0 | null | null | 20,215,437 | null | Expression of either L1 mRNA can generate ORF2, which leads to introduction of DNA DSBs potentially resulting in accumulation of mutations in the cellular genome. | null | 162 | 37,545 | 0 | false | null | null | Expression of either L1 mRNA can generate ORF2, which leads to introduction of DNA DSBs potentially resulting in accumulation of mutations in the cellular genome. | true | true | true | true | true | 6,429 |
6 | DISCUSSION | 1 | 68 | [
"B68"
] | 20,215,437 | pmid-16618923 | Overall, our data suggest that L1-induced damage to cells is not confined to germ line and it is likely not limited to fully active elements. | [
"68"
] | 141 | 37,546 | 0 | false | Overall, our data suggest that L1-induced damage to cells is not confined to germ line and it is likely not limited to fully active elements. | [] | Overall, our data suggest that L1-induced damage to cells is not confined to germ line and it is likely not limited to fully active elements. | true | true | true | true | true | 6,430 |
6 | DISCUSSION | 1 | 68 | [
"B68"
] | 20,215,437 | pmid-16618923 | In addition, there is a potential for the tissue-specific variation in the L1-associated damage depending on the spectrum of the L1-related molecules supported by individual cell types. | [
"68"
] | 185 | 37,547 | 0 | false | In addition, there is a potential for the tissue-specific variation in the L1-associated damage depending on the spectrum of the L1-related molecules supported by individual cell types. | [] | In addition, there is a potential for the tissue-specific variation in the L1-associated damage depending on the spectrum of the L1-related molecules supported by individual cell types. | true | true | true | true | true | 6,430 |
6 | DISCUSSION | 1 | 68 | [
"B68"
] | 20,215,437 | pmid-16618923 | Our observations combined with the reported variation of the combined L1 activity in the population (68) create the need to reevaluate the potential impact of many of the full-length L1 elements present in the human genome on the human health. | [
"68"
] | 243 | 37,548 | 1 | false | Our observations combined with the reported variation of the combined L1 activity in the population create the need to reevaluate the potential impact of many of the full-length L1 elements present in the human genome on the human health. | [
"68"
] | Our observations combined with the reported variation of the combined L1 activity in the population create the need to reevaluate the potential impact of many of the full-length L1 elements present in the human genome on the human health. | true | true | true | true | true | 6,430 |
6 | DISCUSSION | 1 | 68 | [
"B68"
] | 20,215,437 | pmid-16618923 | Further studies providing a more comprehensive analysis of potential variation in somatic L1 expression among individuals in population will be helpful in ascertaining the impact of these elements on human health. | [
"68"
] | 213 | 37,549 | 0 | false | Further studies providing a more comprehensive analysis of potential variation in somatic L1 expression among individuals in population will be helpful in ascertaining the impact of these elements on human health. | [] | Further studies providing a more comprehensive analysis of potential variation in somatic L1 expression among individuals in population will be helpful in ascertaining the impact of these elements on human health. | true | true | true | true | true | 6,430 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B2"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | Attaching the correct amino acid to its cognate tRNA is an essential step in maintaining the fidelity of protein synthesis. | [
"1",
"2",
"2"
] | 123 | 37,550 | 0 | false | Attaching the correct amino acid to its cognate tRNA is an essential step in maintaining the fidelity of protein synthesis. | [] | Attaching the correct amino acid to its cognate tRNA is an essential step in maintaining the fidelity of protein synthesis. | true | true | true | true | true | 6,431 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B2"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | A group of enzymes, the aminoacyl-tRNA synthetases (aaRSs), pair amino acids with their cognate tRNA; each aaRS is specific for one amino acid:tRNA pair (1). | [
"1",
"2",
"2"
] | 157 | 37,551 | 1 | false | A group of enzymes, the aminoacyl-tRNA synthetases (aaRSs), pair amino acids with their cognate tRNA; each aaRS is specific for one amino acid:tRNA pair. | [
"1"
] | A group of enzymes, the aminoacyl-tRNA synthetases (aaRSs), pair amino acids with their cognate tRNA; each aaRS is specific for one amino acid:tRNA pair. | true | true | true | true | true | 6,431 |
0 | INTRODUCTION | 1 | 2 | [
"B1",
"B2",
"B2"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | However, glutaminyl-tRNA synthetase (GlnRS) is absent in all known archaea and most bacteria, while asparaginyl-tRNA synthetase (AsnRS) is absent in most prokaryotes (2). | [
"1",
"2",
"2"
] | 170 | 37,552 | 1 | false | However, glutaminyl-tRNA synthetase (GlnRS) is absent in all known archaea and most bacteria, while asparaginyl-tRNA synthetase (AsnRS) is absent in most prokaryotes. | [
"2"
] | However, glutaminyl-tRNA synthetase (GlnRS) is absent in all known archaea and most bacteria, while asparaginyl-tRNA synthetase (AsnRS) is absent in most prokaryotes. | true | true | true | true | true | 6,431 |
0 | INTRODUCTION | 1 | 2 | [
"B1",
"B2",
"B2"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | In these organisms, Gln-tRNAGln and/or Asn-tRNAAsn are formed by a tRNA-dependent amino acid transformation process catalyzed by amidotransferase (AdT) enzymes (2). | [
"1",
"2",
"2"
] | 164 | 37,553 | 1 | false | In these organisms, Gln-tRNAGln and/or Asn-tRNAAsn are formed by a tRNA-dependent amino acid transformation process catalyzed by amidotransferase (AdT) enzymes. | [
"2"
] | In these organisms, Gln-tRNAGln and/or Asn-tRNAAsn are formed by a tRNA-dependent amino acid transformation process catalyzed by amidotransferase (AdT) enzymes. | true | true | true | true | true | 6,431 |
1 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5",
"B6",
"B7",
"B2",
"B8",
"B9"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | For Gln-tRNA synthesis ND-GluRS forms Glu-tRNAGln (3) which is then converted to Gln-tRNAGln by a glutamyl-tRNAGln amidotransferase (Glu-AdT) (4). | [
"3",
"4",
"5",
"6",
"7",
"2",
"8",
"9"
] | 146 | 37,554 | 1 | false | For Gln-tRNA synthesis ND-GluRS forms Glu-tRNAGln which is then converted to Gln-tRNAGln by a glutamyl-tRNAGln amidotransferase (Glu-AdT). | [
"3",
"4"
] | For Gln-tRNA synthesis ND-GluRS forms Glu-tRNAGln which is then converted to Gln-tRNAGln by a glutamyl-tRNAGln amidotransferase (Glu-AdT). | true | true | true | true | true | 6,432 |
1 | INTRODUCTION | 1 | 5 | [
"B3",
"B4",
"B5",
"B6",
"B7",
"B2",
"B8",
"B9"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | In a similar manner, Asn-tRNAAsn is formed by the sequential action of ND-AspRS (5) and aspartyl-tRNAAsn amidotransferase (Asp-AdT) (6,7). | [
"3",
"4",
"5",
"6",
"7",
"2",
"8",
"9"
] | 138 | 37,555 | 1 | false | In a similar manner, Asn-tRNAAsn is formed by the sequential action of ND-AspRS and aspartyl-tRNAAsn amidotransferase (Asp-AdT). | [
"5",
"6,7"
] | In a similar manner, Asn-tRNAAsn is formed by the sequential action of ND-AspRS and aspartyl-tRNAAsn amidotransferase (Asp-AdT). | true | true | true | true | true | 6,432 |
1 | INTRODUCTION | 1 | 2 | [
"B3",
"B4",
"B5",
"B6",
"B7",
"B2",
"B8",
"B9"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | In bacteria, the heterotrimeric AdT GatCAB can function for tRNA-dependent synthesis of Gln and Asn (2). | [
"3",
"4",
"5",
"6",
"7",
"2",
"8",
"9"
] | 104 | 37,556 | 1 | false | In bacteria, the heterotrimeric AdT GatCAB can function for tRNA-dependent synthesis of Gln and Asn. | [
"2"
] | In bacteria, the heterotrimeric AdT GatCAB can function for tRNA-dependent synthesis of Gln and Asn. | true | true | true | true | true | 6,432 |
1 | INTRODUCTION | 1 | 8 | [
"B3",
"B4",
"B5",
"B6",
"B7",
"B2",
"B8",
"B9"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | In archaea, however, GatCAB is used solely for Asn-tRNAAsn formation (8), while the archaeal-specific heterodimeric enzyme, GatDE, serves as the Glu-AdT (9). | [
"3",
"4",
"5",
"6",
"7",
"2",
"8",
"9"
] | 157 | 37,557 | 1 | false | In archaea, however, GatCAB is used solely for Asn-tRNAAsn formation, while the archaeal-specific heterodimeric enzyme, GatDE, serves as the Glu-AdT. | [
"8",
"9"
] | In archaea, however, GatCAB is used solely for Asn-tRNAAsn formation, while the archaeal-specific heterodimeric enzyme, GatDE, serves as the Glu-AdT. | true | true | true | true | true | 6,432 |
2 | INTRODUCTION | 1 | 10 | [
"B10",
"B11",
"B12",
"B13",
"B13",
"B13",
"B14",
"B13"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | In the 80s, the existence of complexes of AdTs and ND-aaRSs was proposed (10); these complexes would allow substrate channeling (11) of the misacylated tRNA from the aaRS to the AdT. | [
"10",
"11",
"12",
"13",
"13",
"13",
"14",
"13"
] | 182 | 37,558 | 1 | false | In the 80s, the existence of complexes of AdTs and ND-aaRSs was proposed ; these complexes would allow substrate channeling of the misacylated tRNA from the aaRS to the AdT. | [
"10",
"11"
] | In the 80s, the existence of complexes of AdTs and ND-aaRSs was proposed ; these complexes would allow substrate channeling of the misacylated tRNA from the aaRS to the AdT. | true | true | true | true | true | 6,433 |
2 | INTRODUCTION | 1 | 12 | [
"B10",
"B11",
"B12",
"B13",
"B13",
"B13",
"B14",
"B13"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | While a number of complexes between aaRSs and other proteins have been reported (12), it was only recently shown that a complex exists between ND-AspRS and GatCAB, the transamidosome (13). | [
"10",
"11",
"12",
"13",
"13",
"13",
"14",
"13"
] | 188 | 37,559 | 1 | false | While a number of complexes between aaRSs and other proteins have been reported, it was only recently shown that a complex exists between ND-AspRS and GatCAB, the transamidosome. | [
"12",
"13"
] | While a number of complexes between aaRSs and other proteins have been reported, it was only recently shown that a complex exists between ND-AspRS and GatCAB, the transamidosome. | true | true | true | true | true | 6,433 |
2 | INTRODUCTION | 1 | 13 | [
"B10",
"B11",
"B12",
"B13",
"B13",
"B13",
"B14",
"B13"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | The interaction of these two proteins requires the presence of tRNAAsn and the complex is stable over the course of Asn-tRNA biosynthesis (13), protecting Asn-tRNAAsn from deacylation (13,14) and Asp-tRNAAsn from being recognized by elongation factor EF-Tu (13). | [
"10",
"11",
"12",
"13",
"13",
"13",
"14",
"13"
] | 262 | 37,560 | 2 | true | The interaction of these two proteins requires the presence of tRNAAsn and the complex is stable over the course of Asn-tRNA biosynthesis, protecting Asn-tRNAAsn from deacylation and Asp-tRNAAsn from being recognized by elongation factor EF-Tu. | [
"13",
"13,14",
"13"
] | The interaction of these two proteins requires the presence of tRNAAsn and the complex is stable over the course of Asn-tRNA biosynthesis, protecting Asn-tRNAAsn from deacylation and Asp-tRNAAsn from being recognized by elongation factor EF-Tu. | true | true | true | true | true | 6,433 |
3 | INTRODUCTION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B17"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | Similar complexes have been proposed for ND-GluRSs and AdTs (10,13,15,16). | [
"10",
"13",
"15",
"16",
"17"
] | 74 | 37,561 | 0 | false | Similar complexes have been proposed for ND-GluRSs and AdTs. | [
"10,13,15,16"
] | Similar complexes have been proposed for ND-GluRSs and AdTs. | true | true | true | true | true | 6,434 |
3 | INTRODUCTION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B17"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | We report on such a complex between GatDE and ND-GluRS from the archaeon Methanothermobacter thermautotrophicus. | [
"10",
"13",
"15",
"16",
"17"
] | 112 | 37,562 | 0 | false | We report on such a complex between GatDE and ND-GluRS from the archaeon Methanothermobacter thermautotrophicus. | [] | We report on such a complex between GatDE and ND-GluRS from the archaeon Methanothermobacter thermautotrophicus. | true | true | true | true | true | 6,434 |
3 | INTRODUCTION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B17"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | This archaeal-specific transamidosome (ND-GluRS:GatDE) does not require tRNA to assemble, and specifically synthesizes Gln-tRNAGln. | [
"10",
"13",
"15",
"16",
"17"
] | 131 | 37,563 | 0 | false | This archaeal-specific transamidosome (ND-GluRS:GatDE) does not require tRNA to assemble, and specifically synthesizes Gln-tRNAGln. | [] | This archaeal-specific transamidosome (ND-GluRS:GatDE) does not require tRNA to assemble, and specifically synthesizes Gln-tRNAGln. | true | true | true | true | true | 6,434 |
3 | INTRODUCTION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B17"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | Rather than protecting Gln-tRNAGln from deacylation, the binding of GatDE with ND-GluRS sequesters the aaRS for Gln-tRNAGln formation. | [
"10",
"13",
"15",
"16",
"17"
] | 134 | 37,564 | 0 | false | Rather than protecting Gln-tRNAGln from deacylation, the binding of GatDE with ND-GluRS sequesters the aaRS for Gln-tRNAGln formation. | [] | Rather than protecting Gln-tRNAGln from deacylation, the binding of GatDE with ND-GluRS sequesters the aaRS for Gln-tRNAGln formation. | true | true | true | true | true | 6,434 |
3 | INTRODUCTION | 1 | 17 | [
"B10",
"B13",
"B15",
"B16",
"B17"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | The differences between the two transamidosomes may be a consequence of ND-GluRS being a class I aaRS and ND-AspRS belonging to the class II family (17). | [
"10",
"13",
"15",
"16",
"17"
] | 153 | 37,565 | 1 | false | The differences between the two transamidosomes may be a consequence of ND-GluRS being a class I aaRS and ND-AspRS belonging to the class II family. | [
"17"
] | The differences between the two transamidosomes may be a consequence of ND-GluRS being a class I aaRS and ND-AspRS belonging to the class II family. | true | true | true | true | true | 6,434 |
0 | DISCUSSION | 1 | 13 | [
"B13",
"B27"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | The T. thermophilus transamidosome (ND-AspRS:tRNAAsn:GatCAB) is a ribonucleoprotein (RNP) due to the fact the association of the two proteins is tRNA-dependent (13). | [
"13",
"27"
] | 165 | 37,566 | 1 | false | The T. thermophilus transamidosome (ND-AspRS:tRNAAsn:GatCAB) is a ribonucleoprotein (RNP) due to the fact the association of the two proteins is tRNA-dependent. | [
"13"
] | The T. thermophilus transamidosome (ND-AspRS:tRNAAsn:GatCAB) is a ribonucleoprotein (RNP) due to the fact the association of the two proteins is tRNA-dependent. | true | true | true | true | true | 6,435 |
0 | DISCUSSION | 1 | 27 | [
"B13",
"B27"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | The archaeal-specific transamidosome (ND-GluRS:GatDE), however, is not an RNP as tRNA is not essential for the two enzymes to bind one another, making the ND-GluRS:GatDE complex similar in this respect to the O-phosphoseryl-tRNA synthetase (SepRS):SepCysS complex for Cys-tRNACys formation in methanogenic archaea (27). | [
"13",
"27"
] | 319 | 37,567 | 1 | false | The archaeal-specific transamidosome (ND-GluRS:GatDE), however, is not an RNP as tRNA is not essential for the two enzymes to bind one another, making the ND-GluRS:GatDE complex similar in this respect to the O-phosphoseryl-tRNA synthetase (SepRS):SepCysS complex for Cys-tRNACys formation in methanogenic archaea. | [
"27"
] | The archaeal-specific transamidosome (ND-GluRS:GatDE), however, is not an RNP as tRNA is not essential for the two enzymes to bind one another, making the ND-GluRS:GatDE complex similar in this respect to the O-phosphoseryl-tRNA synthetase (SepRS):SepCysS complex for Cys-tRNACys formation in methanogenic archaea. | true | true | true | true | true | 6,435 |
0 | DISCUSSION | 1 | 13 | [
"B13",
"B27"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-18252769|pmid-17964262|pmid-18425141 | Given the differences between the ND-GluRS:GatDE complex and the T. thermophilus complex, we suggest that a transamidosome is a complex between a ND-aaRS and an AdT in the process of amide aa-tRNA formation. | [
"13",
"27"
] | 207 | 37,568 | 0 | false | Given the differences between the ND-GluRS:GatDE complex and the T. thermophilus complex, we suggest that a transamidosome is a complex between a ND-aaRS and an AdT in the process of amide aa-tRNA formation. | [] | Given the differences between the ND-GluRS:GatDE complex and the T. thermophilus complex, we suggest that a transamidosome is a complex between a ND-aaRS and an AdT in the process of amide aa-tRNA formation. | true | true | true | true | true | 6,435 |
1 | DISCUSSION | 1 | 9 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | GatDE and ND-GluRS associating in an RNA-independent manner may be due to an insertion domain found in GatE but not in its paralog GatB (9,25,28). | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 146 | 37,569 | 0 | false | GatDE and ND-GluRS associating in an RNA-independent manner may be due to an insertion domain found in GatE but not in its paralog GatB. | [
"9,25,28"
] | GatDE and ND-GluRS associating in an RNA-independent manner may be due to an insertion domain found in GatE but not in its paralog GatB. | true | true | true | true | true | 6,436 |
1 | DISCUSSION | 1 | 25 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | The insertion and catalytic domains of GatE form a concave pocket (25) that structural modeling predicts could accommodate ND-GluRS (15), increasing the surface for the AdT to bind the aaRS with. | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 195 | 37,570 | 1 | false | The insertion and catalytic domains of GatE form a concave pocket that structural modeling predicts could accommodate ND-GluRS, increasing the surface for the AdT to bind the aaRS with. | [
"25",
"15"
] | The insertion and catalytic domains of GatE form a concave pocket that structural modeling predicts could accommodate ND-GluRS, increasing the surface for the AdT to bind the aaRS with. | true | true | true | true | true | 6,436 |
1 | DISCUSSION | 1 | 9 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | The tRNA-independent association maybe further aided by the fact that ND-GluRS is a class I aaRS | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 96 | 37,571 | 0 | false | The tRNA-independent association maybe further aided by the fact that ND-GluRS is a class I aaRS | [] | The tRNA-independent association maybe further aided by the fact that ND-GluRS is a class I aaRS | true | true | false | true | false | 6,436 |
1 | DISCUSSION | 1 | 9 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | whereas ND-AspRS is a class II aaRS. | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 36 | 37,572 | 0 | false | whereas ND-AspRS is a class II aaRS. | [] | whereas ND-AspRS is a class II aaRS. | false | true | true | true | false | 6,436 |
1 | DISCUSSION | 1 | 9 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | Class I aaRSs like AdTs bind to the minor groove of the tRNA acceptor stem whereas class II aaRSs bind to the major groove (13,15,17). | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 134 | 37,573 | 0 | false | Class I aaRSs like AdTs bind to the minor groove of the tRNA acceptor stem whereas class II aaRSs bind to the major groove. | [
"13,15,17"
] | Class I aaRSs like AdTs bind to the minor groove of the tRNA acceptor stem whereas class II aaRSs bind to the major groove. | true | true | true | true | true | 6,436 |
1 | DISCUSSION | 1 | 15 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | Consequently, GatDE and ND-GluRS both bind to the same side of tRNAGln (15) while GatCAB and ND-AspRS likely recognize opposite sides of tRNAAsn (13). | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 150 | 37,574 | 1 | false | Consequently, GatDE and ND-GluRS both bind to the same side of tRNAGln while GatCAB and ND-AspRS likely recognize opposite sides of tRNAAsn. | [
"15",
"13"
] | Consequently, GatDE and ND-GluRS both bind to the same side of tRNAGln while GatCAB and ND-AspRS likely recognize opposite sides of tRNAAsn. | true | true | true | true | true | 6,436 |
1 | DISCUSSION | 1 | 13 | [
"B9",
"B25",
"B28",
"B25",
"B15",
"B13",
"B15",
"B17",
"B15",
"B13",
"B13"
] | 20,457,752 | pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127|pmid-9789000|pmid-18252769|pmid-18291416|pmid-10993083|pmid-10993083|pmid-16216574|pmid-18279892|pmid-16216574|pmid-16809540|pmid-17964262|pmid-16809540|pmid-9204708|pmid-16809540|pmid-17964262|pmid-17964262 | Thus, while GatDE and ND-GluRS can associate together, possibly enhanced by the GatE specific insertion domain, and recognize tRNAGln, ND-AspRS and GatCAB can only make minimal contact with one another and still specifically bind tRNAAsn preventing them from associating without tRNA (13). | [
"9",
"25",
"28",
"25",
"15",
"13",
"15",
"17",
"15",
"13",
"13"
] | 289 | 37,575 | 1 | false | Thus, while GatDE and ND-GluRS can associate together, possibly enhanced by the GatE specific insertion domain, and recognize tRNAGln, ND-AspRS and GatCAB can only make minimal contact with one another and still specifically bind tRNAAsn preventing them from associating without tRNA. | [
"13"
] | Thus, while GatDE and ND-GluRS can associate together, possibly enhanced by the GatE specific insertion domain, and recognize tRNAGln, ND-AspRS and GatCAB can only make minimal contact with one another and still specifically bind tRNAAsn preventing them from associating without tRNA. | true | true | true | true | true | 6,436 |
2 | DISCUSSION | 1 | 13 | [
"B13",
"B13",
"B13",
"B13",
"B14",
"B14",
"B27"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | Besides not requiring tRNA to form, the archaeal-specific ND-GluRS:GatDE transamidosome also differs from the ND-AspRS:tRNAAsn:GatCAB complex following aminoacylation and transamidation. | [
"13",
"13",
"13",
"13",
"14",
"14",
"27"
] | 186 | 37,576 | 0 | false | Besides not requiring tRNA to form, the archaeal-specific ND-GluRS:GatDE transamidosome also differs from the ND-AspRS:tRNAAsn:GatCAB complex following aminoacylation and transamidation. | [] | Besides not requiring tRNA to form, the archaeal-specific ND-GluRS:GatDE transamidosome also differs from the ND-AspRS:tRNAAsn:GatCAB complex following aminoacylation and transamidation. | true | true | true | true | true | 6,437 |
2 | DISCUSSION | 1 | 13 | [
"B13",
"B13",
"B13",
"B13",
"B14",
"B14",
"B27"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | The transamidosome for Asn-tRNAAsn synthesis is stable through product formation (13), leading to (i) an increase in ND-AspRS activity (13), (ii) product release becoming rate-limiting (13), (iii) protection of Asp-tRNAAsn and especially Asn-tRNAAsn from deacylation (13,14) and (iv) an enhancement of the KM of GatCAB f... | [
"13",
"13",
"13",
"13",
"14",
"14",
"27"
] | 340 | 37,577 | 3 | true | The transamidosome for Asn-tRNAAsn synthesis is stable through product formation, leading to (i) an increase in ND-AspRS activity, (ii) product release becoming rate-limiting, (iii) protection of Asp-tRNAAsn and especially Asn-tRNAAsn from deacylation and (iv) an enhancement of the KM of GatCAB for Asp-tRNAAsn. | [
"13",
"13",
"13",
"13,14",
"14"
] | The transamidosome for Asn-tRNAAsn synthesis is stable through product formation, leading to (i) an increase in ND-AspRS activity, (ii) product release becoming rate-limiting, (iii) protection of Asp-tRNAAsn and especially Asn-tRNAAsn from deacylation and (iv) an enhancement of the KM of GatCAB for Asp-tRNAAsn. | true | true | true | true | true | 6,437 |
2 | DISCUSSION | 1 | 27 | [
"B13",
"B13",
"B13",
"B13",
"B14",
"B14",
"B27"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | Similar results were found with the SepRS:SepCysS:tRNACys complex which is also stable after aminoacylation (27). | [
"13",
"13",
"13",
"13",
"14",
"14",
"27"
] | 113 | 37,578 | 1 | false | Similar results were found with the SepRS:SepCysS:tRNACys complex which is also stable after aminoacylation. | [
"27"
] | Similar results were found with the SepRS:SepCysS:tRNACys complex which is also stable after aminoacylation. | true | true | true | true | true | 6,437 |
2 | DISCUSSION | 1 | 13 | [
"B13",
"B13",
"B13",
"B13",
"B14",
"B14",
"B27"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | However the archaeal-specific transamidosome, did not protect Glu-tRNAGln nor Gln-tRNAGln from deacylation and does not affect the kinetics of either ND-GluRS or GatDE. | [
"13",
"13",
"13",
"13",
"14",
"14",
"27"
] | 168 | 37,579 | 0 | false | However the archaeal-specific transamidosome, did not protect Glu-tRNAGln nor Gln-tRNAGln from deacylation and does not affect the kinetics of either ND-GluRS or GatDE. | [] | However the archaeal-specific transamidosome, did not protect Glu-tRNAGln nor Gln-tRNAGln from deacylation and does not affect the kinetics of either ND-GluRS or GatDE. | true | true | true | true | true | 6,437 |
2 | DISCUSSION | 1 | 13 | [
"B13",
"B13",
"B13",
"B13",
"B14",
"B14",
"B27"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | Taken all together, this suggests that the ND-GluRS:GatDE complex is not stable through Gln-tRNAGln formation. | [
"13",
"13",
"13",
"13",
"14",
"14",
"27"
] | 110 | 37,580 | 0 | false | Taken all together, this suggests that the ND-GluRS:GatDE complex is not stable through Gln-tRNAGln formation. | [] | Taken all together, this suggests that the ND-GluRS:GatDE complex is not stable through Gln-tRNAGln formation. | true | true | true | true | true | 6,437 |
2 | DISCUSSION | 1 | 13 | [
"B13",
"B13",
"B13",
"B13",
"B14",
"B14",
"B27"
] | 20,457,752 | pmid-3340166|pmid-3775377|pmid-18522650|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17964262|pmid-17929881|pmid-17929881|pmid-18425141 | In agreement we did not detect ND-GluRS:GatDE bound to Gln-tRNAGln in our gel filtration studies. | [
"13",
"13",
"13",
"13",
"14",
"14",
"27"
] | 97 | 37,581 | 0 | false | In agreement we did not detect ND-GluRS:GatDE bound to Gln-tRNAGln in our gel filtration studies. | [] | In agreement we did not detect ND-GluRS:GatDE bound to Gln-tRNAGln in our gel filtration studies. | true | true | true | true | true | 6,437 |
3 | DISCUSSION | 1 | 14 | [
"B14"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | The kinetic and deacylation data also suggest the archaeal-specific complex is not stable after aminoacylation. | [
"14"
] | 111 | 37,582 | 0 | false | The kinetic and deacylation data also suggest the archaeal-specific complex is not stable after aminoacylation. | [] | The kinetic and deacylation data also suggest the archaeal-specific complex is not stable after aminoacylation. | true | true | true | true | true | 6,438 |
3 | DISCUSSION | 1 | 14 | [
"B14"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | GatDE protects Glu-tRNAGln from deacylation whereas the addition of ND-GluRS actually increases the deacylation rate of the aa-tRNA species, possibly due to the aaRS favoring tRNAGln over Glx-tRNAGln species. | [
"14"
] | 208 | 37,583 | 0 | false | GatDE protects Glu-tRNAGln from deacylation whereas the addition of ND-GluRS actually increases the deacylation rate of the aa-tRNA species, possibly due to the aaRS favoring tRNAGln over Glx-tRNAGln species. | [] | GatDE protects Glu-tRNAGln from deacylation whereas the addition of ND-GluRS actually increases the deacylation rate of the aa-tRNA species, possibly due to the aaRS favoring tRNAGln over Glx-tRNAGln species. | true | true | true | true | true | 6,438 |
3 | DISCUSSION | 1 | 14 | [
"B14"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | This deacylation is probably not significant in vivo due to the presence of GatDE and EF-1Ξ±. | [
"14"
] | 92 | 37,584 | 0 | false | This deacylation is probably not significant in vivo due to the presence of GatDE and EF-1Ξ±. | [] | This deacylation is probably not significant in vivo due to the presence of GatDE and EF-1Ξ±. | true | true | true | true | true | 6,438 |
3 | DISCUSSION | 1 | 14 | [
"B14"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | Also, unlike ND-AspRS and GatCAB (14), the presence of ND-GluRS does not decrease the KM of GatDE for its mischarged substrate (Glu-tRNAGln). | [
"14"
] | 141 | 37,585 | 1 | false | Also, unlike ND-AspRS and GatCAB, the presence of ND-GluRS does not decrease the KM of GatDE for its mischarged substrate (Glu-tRNAGln). | [
"14"
] | Also, unlike ND-AspRS and GatCAB, the presence of ND-GluRS does not decrease the KM of GatDE for its mischarged substrate (Glu-tRNAGln). | true | true | true | true | true | 6,438 |
3 | DISCUSSION | 1 | 14 | [
"B14"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-9204708|pmid-17929881 | Thus, GatDE may remain bound to Glu-tRNAGln while ND-GluRS dissociates after aminoacylation. | [
"14"
] | 92 | 37,586 | 0 | false | Thus, GatDE may remain bound to Glu-tRNAGln while ND-GluRS dissociates after aminoacylation. | [] | Thus, GatDE may remain bound to Glu-tRNAGln while ND-GluRS dissociates after aminoacylation. | true | true | true | true | true | 6,438 |
4 | DISCUSSION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B13",
"B16"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-17964262|pmid-19906721 | Such a scenario would fit the structural modeling of the transamidosomes (10,13,15,16). | [
"10",
"13",
"15",
"16",
"13",
"16"
] | 87 | 37,587 | 0 | false | Such a scenario would fit the structural modeling of the transamidosomes. | [
"10,13,15,16"
] | Such a scenario would fit the structural modeling of the transamidosomes. | true | true | true | true | true | 6,439 |
4 | DISCUSSION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B13",
"B16"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-17964262|pmid-19906721 | While ND-GluRS and GatDE both binding to the tRNAGln minor groove may allow the enzymes to associate without the tRNA present, such an orientation of the proteins would hinder the movement of 3β² aminoacylated end of the tRNA acceptor stem from the aminoacylation active site of the ND-aaRS to the catalytic pocket of the... | [
"10",
"13",
"15",
"16",
"13",
"16"
] | 375 | 37,588 | 0 | false | While ND-GluRS and GatDE both binding to the tRNAGln minor groove may allow the enzymes to associate without the tRNA present, such an orientation of the proteins would hinder the movement of 3β² aminoacylated end of the tRNA acceptor stem from the aminoacylation active site of the ND-aaRS to the catalytic pocket of the... | [] | While ND-GluRS and GatDE both binding to the tRNAGln minor groove may allow the enzymes to associate without the tRNA present, such an orientation of the proteins would hinder the movement of 3β² aminoacylated end of the tRNA acceptor stem from the aminoacylation active site of the ND-aaRS to the catalytic pocket of the... | true | true | true | true | true | 6,439 |
4 | DISCUSSION | 1 | 13 | [
"B10",
"B13",
"B15",
"B16",
"B13",
"B16"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-17964262|pmid-19906721 | In the case of ND-AspRS and GatCAB, the fact they bind to opposite sides of the tRNA enables the 3β²-end of acceptor stem to easily flip from the aminoacylation site in the aaRS to the transamidation site of the AdT (13). | [
"10",
"13",
"15",
"16",
"13",
"16"
] | 220 | 37,589 | 1 | false | In the case of ND-AspRS and GatCAB, the fact they bind to opposite sides of the tRNA enables the 3β²-end of acceptor stem to easily flip from the aminoacylation site in the aaRS to the transamidation site of the AdT. | [
"13"
] | In the case of ND-AspRS and GatCAB, the fact they bind to opposite sides of the tRNA enables the 3β²-end of acceptor stem to easily flip from the aminoacylation site in the aaRS to the transamidation site of the AdT. | true | true | true | true | true | 6,439 |
4 | DISCUSSION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B13",
"B16"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-17964262|pmid-19906721 | ND-GluRS dissociating from the complex after aminoacylation would eliminate the steric hindrance and allow the 3β² glutamylated end of tRNAGln to bind in the catalytic pocket of GatE for transamidation. | [
"10",
"13",
"15",
"16",
"13",
"16"
] | 201 | 37,590 | 0 | false | ND-GluRS dissociating from the complex after aminoacylation would eliminate the steric hindrance and allow the 3β² glutamylated end of tRNAGln to bind in the catalytic pocket of GatE for transamidation. | [] | ND-GluRS dissociating from the complex after aminoacylation would eliminate the steric hindrance and allow the 3β² glutamylated end of tRNAGln to bind in the catalytic pocket of GatE for transamidation. | true | true | true | true | true | 6,439 |
4 | DISCUSSION | 1 | 16 | [
"B10",
"B13",
"B15",
"B16",
"B13",
"B16"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-17964262|pmid-19906721 | The putative bacterial ND-GluRS:GatCAB complex may behave in a similar manner as it is expected that GatCAB binds tRNA like GatDE (16). | [
"10",
"13",
"15",
"16",
"13",
"16"
] | 135 | 37,591 | 1 | false | The putative bacterial ND-GluRS:GatCAB complex may behave in a similar manner as it is expected that GatCAB binds tRNA like GatDE. | [
"16"
] | The putative bacterial ND-GluRS:GatCAB complex may behave in a similar manner as it is expected that GatCAB binds tRNA like GatDE. | true | true | true | true | true | 6,439 |
4 | DISCUSSION | 1 | 10 | [
"B10",
"B13",
"B15",
"B16",
"B13",
"B16"
] | 20,457,752 | pmid-3340166|pmid-17964262|pmid-16809540|pmid-19906721|pmid-17964262|pmid-19906721 | However, given GatB lacks the insertion domain found in GatE, the association of ND-GluRS with GatCAB may require tRNAGln. | [
"10",
"13",
"15",
"16",
"13",
"16"
] | 122 | 37,592 | 0 | false | However, given GatB lacks the insertion domain found in GatE, the association of ND-GluRS with GatCAB may require tRNAGln. | [] | However, given GatB lacks the insertion domain found in GatE, the association of ND-GluRS with GatCAB may require tRNAGln. | true | true | true | true | true | 6,439 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Given the above, we propose the following model for RNA-dependent biosynthesis of Gln in archaea (Figure 6). | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 108 | 37,593 | 0 | false | Given the above, we propose the following model for RNA-dependent biosynthesis of Gln in archaea. | [
"Figure 6"
] | Given the above, we propose the following model for RNA-dependent biosynthesis of Gln in archaea. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | First, GatDE and ND-GluRS associate with the aaRS binding in the concave pocket formed by the GatE-specific insertion domain. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 125 | 37,594 | 0 | false | First, GatDE and ND-GluRS associate with the aaRS binding in the concave pocket formed by the GatE-specific insertion domain. | [] | First, GatDE and ND-GluRS associate with the aaRS binding in the concave pocket formed by the GatE-specific insertion domain. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Next, the ND-GluRS:GatDE complex recognizes tRNAGln with the 3β²-end of the acceptor stem in the active site of the aaRS, while GatDE makes contact with the D-loop of the tRNA to distinguish tRNAGln from tRNAGlu (15). | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 216 | 37,595 | 1 | false | Next, the ND-GluRS:GatDE complex recognizes tRNAGln with the 3β²-end of the acceptor stem in the active site of the aaRS, while GatDE makes contact with the D-loop of the tRNA to distinguish tRNAGln from tRNAGlu. | [
"15"
] | Next, the ND-GluRS:GatDE complex recognizes tRNAGln with the 3β²-end of the acceptor stem in the active site of the aaRS, while GatDE makes contact with the D-loop of the tRNA to distinguish tRNAGln from tRNAGlu. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Alternatively, ND-GluRS could first find tRNAGln followed by GatDE binding. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 75 | 37,596 | 0 | false | Alternatively, ND-GluRS could first find tRNAGln followed by GatDE binding. | [] | Alternatively, ND-GluRS could first find tRNAGln followed by GatDE binding. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Following aminoacylation, ND-GluRS dissociates from the complex allowing the 3β² glutamylated end of tRNAGln to flip into the GatE catalytic pocket. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 147 | 37,597 | 0 | false | Following aminoacylation, ND-GluRS dissociates from the complex allowing the 3β² glutamylated end of tRNAGln to flip into the GatE catalytic pocket. | [] | Following aminoacylation, ND-GluRS dissociates from the complex allowing the 3β² glutamylated end of tRNAGln to flip into the GatE catalytic pocket. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | GatDE recognition of the A1-U72 (15) may properly position the glutamyl-moiety for transamidation as well as serve as a final proofreading step to ensure the enzyme does not transamidate Glu-tRNAGlu. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 199 | 37,598 | 1 | false | GatDE recognition of the A1-U72 may properly position the glutamyl-moiety for transamidation as well as serve as a final proofreading step to ensure the enzyme does not transamidate Glu-tRNAGlu. | [
"15"
] | GatDE recognition of the A1-U72 may properly position the glutamyl-moiety for transamidation as well as serve as a final proofreading step to ensure the enzyme does not transamidate Glu-tRNAGlu. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Binding of Glu-tRNAGln is expected to trigger conformational changes in GatDE to enable the AdT to liberate ammonia from free Asn or Gln to use in amidating the mischarged tRNA species (19,25). | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 193 | 37,599 | 0 | false | Binding of Glu-tRNAGln is expected to trigger conformational changes in GatDE to enable the AdT to liberate ammonia from free Asn or Gln to use in amidating the mischarged tRNA species. | [
"19,25"
] | Binding of Glu-tRNAGln is expected to trigger conformational changes in GatDE to enable the AdT to liberate ammonia from free Asn or Gln to use in amidating the mischarged tRNA species. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | After transamidation, GatDE releases Gln-tRNAGln to be used in protein synthesis and the AdT is free to bind ND-GluRS and start the cycle again. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 144 | 37,600 | 0 | false | After transamidation, GatDE releases Gln-tRNAGln to be used in protein synthesis and the AdT is free to bind ND-GluRS and start the cycle again. | [] | After transamidation, GatDE releases Gln-tRNAGln to be used in protein synthesis and the AdT is free to bind ND-GluRS and start the cycle again. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Alternatively, GatDE could also remain unbound to transamidate any free Glu-tRNAGln in the cell. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 96 | 37,601 | 0 | false | Alternatively, GatDE could also remain unbound to transamidate any free Glu-tRNAGln in the cell. | [] | Alternatively, GatDE could also remain unbound to transamidate any free Glu-tRNAGln in the cell. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Figure 6.Cycle of RNA-dependent biosynthesis of Gln in Archaea. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 63 | 37,602 | 0 | false | Figure 6.Cycle of RNA-dependent biosynthesis of Gln in Archaea. | [] | Figure 6.Cycle of RNA-dependent biosynthesis of Gln in Archaea. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 1 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (1) GatDE (orange) associates with ND-GluRS (lime). | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 51 | 37,603 | 1 | false | GatDE (orange) associates with ND-GluRS (lime). | [
"1"
] | GatDE (orange) associates with ND-GluRS (lime). | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 2 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (2) ND-GluRS:GatDE binary complex binds tRNAGln (silver-blue) to form the ternary complex. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 90 | 37,604 | 1 | false | ND-GluRS:GatDE binary complex binds tRNAGln (silver-blue) to form the ternary complex. | [
"2"
] | ND-GluRS:GatDE binary complex binds tRNAGln (silver-blue) to form the ternary complex. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | In the transamidosome (ND-GluRS:GatDE:tRNAGln), ND-GluRS glutamylates tRNAGln. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 78 | 37,605 | 0 | false | In the transamidosome (ND-GluRS:GatDE:tRNAGln), ND-GluRS glutamylates tRNAGln. | [] | In the transamidosome (ND-GluRS:GatDE:tRNAGln), ND-GluRS glutamylates tRNAGln. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 4 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (4) ND-GluRS dissociates from the complex allowing the 3β² CCA-end of the tRNA to flip into the GatDE kinase active site. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 120 | 37,606 | 1 | false | ND-GluRS dissociates from the complex allowing the 3β² CCA-end of the tRNA to flip into the GatDE kinase active site. | [
"4"
] | ND-GluRS dissociates from the complex allowing the 3β² CCA-end of the tRNA to flip into the GatDE kinase active site. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 5 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (5) GatDE transamidates the tRNA-bound Glu to Gln. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 50 | 37,607 | 1 | false | GatDE transamidates the tRNA-bound Glu to Gln. | [
"5"
] | GatDE transamidates the tRNA-bound Glu to Gln. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 6 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (6) Gln-tRNAGln is released from GatDE. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 39 | 37,608 | 1 | false | Gln-tRNAGln is released from GatDE. | [
"6"
] | Gln-tRNAGln is released from GatDE. | true | true | true | true | true | 6,440 |
5 | DISCUSSION | 1 | 15 | [
"B15",
"B15",
"B19",
"B25",
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-16809540|pmid-16809540|pmid-15611111|pmid-16216574|pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | For clarity only one GatDE monomer is shown. | [
"15",
"15",
"19",
"25",
"1",
"2",
"3",
"4",
"5",
"6"
] | 44 | 37,609 | 0 | false | For clarity only one GatDE monomer is shown. | [] | For clarity only one GatDE monomer is shown. | true | true | true | true | true | 6,440 |
6 | DISCUSSION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | Cycle of RNA-dependent biosynthesis of Gln in Archaea. | [
"1",
"2",
"3",
"4",
"5",
"6"
] | 54 | 37,610 | 0 | false | Cycle of RNA-dependent biosynthesis of Gln in Archaea. | [] | Cycle of RNA-dependent biosynthesis of Gln in Archaea. | true | true | true | true | true | 6,441 |
6 | DISCUSSION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (1) GatDE (orange) associates with ND-GluRS (lime). | [
"1",
"2",
"3",
"4",
"5",
"6"
] | 51 | 37,611 | 1 | false | GatDE (orange) associates with ND-GluRS (lime). | [
"1"
] | GatDE (orange) associates with ND-GluRS (lime). | true | true | true | true | true | 6,441 |
6 | DISCUSSION | 1 | 2 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (2) ND-GluRS:GatDE binary complex binds tRNAGln (silver-blue) to form the ternary complex. | [
"1",
"2",
"3",
"4",
"5",
"6"
] | 90 | 37,612 | 1 | false | ND-GluRS:GatDE binary complex binds tRNAGln (silver-blue) to form the ternary complex. | [
"2"
] | ND-GluRS:GatDE binary complex binds tRNAGln (silver-blue) to form the ternary complex. | true | true | true | true | true | 6,441 |
6 | DISCUSSION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | In the transamidosome (ND-GluRS:GatDE:tRNAGln), ND-GluRS glutamylates tRNAGln. | [
"1",
"2",
"3",
"4",
"5",
"6"
] | 78 | 37,613 | 0 | false | In the transamidosome (ND-GluRS:GatDE:tRNAGln), ND-GluRS glutamylates tRNAGln. | [] | In the transamidosome (ND-GluRS:GatDE:tRNAGln), ND-GluRS glutamylates tRNAGln. | true | true | true | true | true | 6,441 |
6 | DISCUSSION | 1 | 4 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (4) ND-GluRS dissociates from the complex allowing the 3β² CCA-end of the tRNA to flip into the GatDE kinase active site. | [
"1",
"2",
"3",
"4",
"5",
"6"
] | 120 | 37,614 | 1 | false | ND-GluRS dissociates from the complex allowing the 3β² CCA-end of the tRNA to flip into the GatDE kinase active site. | [
"4"
] | ND-GluRS dissociates from the complex allowing the 3β² CCA-end of the tRNA to flip into the GatDE kinase active site. | true | true | true | true | true | 6,441 |
6 | DISCUSSION | 1 | 5 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6"
] | 20,457,752 | pmid-10966471|pmid-18252769|pmid-3079749|pmid-4972364|pmid-9220965|pmid-8757127 | (5) GatDE transamidates the tRNA-bound Glu to Gln. | [
"1",
"2",
"3",
"4",
"5",
"6"
] | 50 | 37,615 | 1 | false | GatDE transamidates the tRNA-bound Glu to Gln. | [
"5"
] | GatDE transamidates the tRNA-bound Glu to Gln. | true | true | true | true | true | 6,441 |
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