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general structure of the TACC genes and proteins is depicted in Fig. 4. The main conserved feature of the TACC family, the TACC domain, is located at the carboxy terminus of the protein. In the case of the C. elegans TAC protein, this structure comprises the majority of the protein and is encoded by two of the three exons of the gene. In the higher organisms, D. melanogaster, and the deuterostomes C. intestinalis to human, this feature is also encoded by the final exons of the gene (five in D. melanogaster, seven in the deuterostome genes). Outside of the TACC domain, however, TACC family members show relatively little homology. It is interesting that each TACC gene contains one large exon, which shows considerable variability between TACC orthologues, and constitutes the main difference between the TACC3 genes in the vertebrates (see below). In deuterostomes, this exon contains the SDP repeat (or in the case of the murine TACC3's, a rodent-specific 24 amino acid repeat), which is responsible for the binding of the SWI/SNF chromatin remodeling complex component GAS41 [15,16]."}

    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T5393","span":{"begin":34,"end":39},"obj":"SO_EXT:0000704"},{"id":"T5394","span":{"begin":44,"end":52},"obj":"CHEBI_PR_EXT:protein"},{"id":"T5395","span":{"begin":85,"end":94},"obj":"SO_EXT:biological_conservation_process_or_quality"},{"id":"T5396","span":{"begin":132,"end":138},"obj":"SO_EXT:0000417"},{"id":"T5397","span":{"begin":158,"end":174},"obj":"CHEBI_SO_EXT:C_terminus_or_C_terminal_region"},{"id":"T5398","span":{"begin":182,"end":189},"obj":"CHEBI_PR_EXT:protein"},{"id":"T5399","span":{"begin":210,"end":220},"obj":"NCBITaxon:6239"},{"id":"T5400","span":{"begin":225,"end":232},"obj":"CHEBI_PR_EXT:protein"},{"id":"T5401","span":{"begin":279,"end":286},"obj":"CHEBI_PR_EXT:protein"},{"id":"T5402","span":{"begin":294,"end":301},"obj":"SO_EXT:sequence_coding_function"},{"id":"T5403","span":{"begin":322,"end":327},"obj":"SO_EXT:0000147"},{"id":"T5404","span":{"begin":335,"end":339},"obj":"SO_EXT:0000704"},{"id":"T5405","span":{"begin":355,"end":364},"obj":"NCBITaxon:1"},{"id":"T5406","span":{"begin":366,"end":381},"obj":"NCBITaxon:7227"},{"id":"T5407","span":{"begin":391,"end":404},"obj":"NCBITaxon:33511"},{"id":"T5408","span":{"begin":405,"end":420},"obj":"NCBITaxon:7719"},{"id":"T5409","span":{"begin":424,"end":429},"obj":"NCBITaxon:9606"},{"id":"T5410","span":{"begin":452,"end":459},"obj":"SO_EXT:sequence_coding_function"},{"id":"T5411","span":{"begin":473,"end":478},"obj":"SO_EXT:0000147"},{"id":"T5412","span":{"begin":486,"end":490},"obj":"SO_EXT:0000704"},{"id":"T5413","span":{"begin":500,"end":515},"obj":"NCBITaxon:7227"},{"id":"T5414","span":{"begin":530,"end":542},"obj":"NCBITaxon:33511"},{"id":"T5415","span":{"begin":543,"end":548},"obj":"SO_EXT:0000704"},{"id":"T5416","span":{"begin":571,"end":577},"obj":"SO_EXT:0000417"},{"id":"T5417","span":{"begin":631,"end":639},"obj":"SO:0000857"},{"id":"T5418","span":{"begin":674,"end":678},"obj":"SO_EXT:0000704"},{"id":"T5419","span":{"begin":698,"end":702},"obj":"SO_EXT:0000147"},{"id":"T5420","span":{"begin":754,"end":765},"obj":"SO_EXT:0000855"},{"id":"T5421","span":{"begin":815,"end":820},"obj":"PR_EXT:000016008"},{"id":"T5422","span":{"begin":821,"end":826},"obj":"SO_EXT:0000704"},{"id":"T5423","span":{"begin":834,"end":845},"obj":"NCBITaxon:7742"},{"id":"T5424","span":{"begin":862,"end":875},"obj":"NCBITaxon:33511"},{"id":"T5425","span":{"begin":882,"end":886},"obj":"SO_EXT:0000147"},{"id":"T5426","span":{"begin":904,"end":910},"obj":"SO_EXT:sequence_repeat_unit_or_region"},{"id":"T5427","span":{"begin":934,"end":940},"obj":"NCBITaxon:39107"},{"id":"T5428","span":{"begin":941,"end":948},"obj":"PR_EXT:000016008"},{"id":"T5429","span":{"begin":952,"end":958},"obj":"NCBITaxon:9989"},{"id":"T5430","span":{"begin":971,"end":981},"obj":"CHEBI_SO_EXT:amino_acid"},{"id":"T5431","span":{"begin":982,"end":988},"obj":"SO_EXT:sequence_repeat_unit_or_region"},{"id":"T5432","span":{"begin":1020,"end":1027},"obj":"CHEMINF_GO_EXT:chemical_binding_or_bond_formation"},{"id":"T5433","span":{"begin":1035,"end":1071},"obj":"GO:0016514"},{"id":"T5434","span":{"begin":1043,"end":1063},"obj":"GO:0006338"},{"id":"T5435","span":{"begin":1082,"end":1087},"obj":"PR_EXT:000017527"}],"text":"The general structure of the TACC genes and proteins is depicted in Fig. 4. The main conserved feature of the TACC family, the TACC domain, is located at the carboxy terminus of the protein. In the case of the C. elegans TAC protein, this structure comprises the majority of the protein and is encoded by two of the three exons of the gene. In the higher organisms, D. melanogaster, and the deuterostomes C. intestinalis to human, this feature is also encoded by the final exons of the gene (five in D. melanogaster, seven in the deuterostome genes). Outside of the TACC domain, however, TACC family members show relatively little homology. It is interesting that each TACC gene contains one large exon, which shows considerable variability between TACC orthologues, and constitutes the main difference between the TACC3 genes in the vertebrates (see below). In deuterostomes, this exon contains the SDP repeat (or in the case of the murine TACC3's, a rodent-specific 24 amino acid repeat), which is responsible for the binding of the SWI/SNF chromatin remodeling complex component GAS41 [15,16]."}

    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T5291","span":{"begin":34,"end":39},"obj":"SO:0000704"},{"id":"T5292","span":{"begin":132,"end":138},"obj":"SO:0000417"},{"id":"T5293","span":{"begin":210,"end":220},"obj":"NCBITaxon:6239"},{"id":"T5294","span":{"begin":322,"end":327},"obj":"SO:0000147"},{"id":"T5295","span":{"begin":335,"end":339},"obj":"SO:0000704"},{"id":"T5296","span":{"begin":355,"end":364},"obj":"NCBITaxon:1"},{"id":"T5297","span":{"begin":366,"end":381},"obj":"NCBITaxon:7227"},{"id":"T5298","span":{"begin":391,"end":404},"obj":"NCBITaxon:33511"},{"id":"T5299","span":{"begin":405,"end":420},"obj":"NCBITaxon:7719"},{"id":"T5300","span":{"begin":424,"end":429},"obj":"NCBITaxon:9606"},{"id":"T5301","span":{"begin":473,"end":478},"obj":"SO:0000147"},{"id":"T5302","span":{"begin":486,"end":490},"obj":"SO:0000704"},{"id":"T5303","span":{"begin":500,"end":515},"obj":"NCBITaxon:7227"},{"id":"T5304","span":{"begin":530,"end":542},"obj":"NCBITaxon:33511"},{"id":"T5305","span":{"begin":543,"end":548},"obj":"SO:0000704"},{"id":"T5306","span":{"begin":571,"end":577},"obj":"SO:0000417"},{"id":"T5307","span":{"begin":631,"end":639},"obj":"SO:0000857"},{"id":"T5308","span":{"begin":674,"end":678},"obj":"SO:0000704"},{"id":"T5309","span":{"begin":698,"end":702},"obj":"SO:0000147"},{"id":"T5310","span":{"begin":754,"end":765},"obj":"SO:0000855"},{"id":"T5311","span":{"begin":815,"end":820},"obj":"PR:000016008"},{"id":"T5312","span":{"begin":821,"end":826},"obj":"SO:0000704"},{"id":"T5313","span":{"begin":834,"end":845},"obj":"NCBITaxon:7742"},{"id":"T5314","span":{"begin":862,"end":875},"obj":"NCBITaxon:33511"},{"id":"T5315","span":{"begin":882,"end":886},"obj":"SO:0000147"},{"id":"T5316","span":{"begin":934,"end":940},"obj":"NCBITaxon:39107"},{"id":"T5317","span":{"begin":941,"end":948},"obj":"PR:000016008"},{"id":"T5318","span":{"begin":952,"end":958},"obj":"NCBITaxon:9989"},{"id":"T5319","span":{"begin":1035,"end":1071},"obj":"GO:0016514"},{"id":"T5320","span":{"begin":1043,"end":1063},"obj":"GO:0006338"},{"id":"T5321","span":{"begin":1082,"end":1087},"obj":"PR:000017527"}],"text":"The general structure of the TACC genes and proteins is depicted in Fig. 4. The main conserved feature of the TACC family, the TACC domain, is located at the carboxy terminus of the protein. In the case of the C. elegans TAC protein, this structure comprises the majority of the protein and is encoded by two of the three exons of the gene. In the higher organisms, D. melanogaster, and the deuterostomes C. intestinalis to human, this feature is also encoded by the final exons of the gene (five in D. melanogaster, seven in the deuterostome genes). Outside of the TACC domain, however, TACC family members show relatively little homology. It is interesting that each TACC gene contains one large exon, which shows considerable variability between TACC orthologues, and constitutes the main difference between the TACC3 genes in the vertebrates (see below). In deuterostomes, this exon contains the SDP repeat (or in the case of the murine TACC3's, a rodent-specific 24 amino acid repeat), which is responsible for the binding of the SWI/SNF chromatin remodeling complex component GAS41 [15,16]."}

    2_test

    {"project":"2_test","denotations":[{"id":"15207008-11903063-9666005","span":{"begin":1089,"end":1091},"obj":"11903063"},{"id":"15207008-11756182-9666006","span":{"begin":1092,"end":1094},"obj":"11756182"}],"text":"The general structure of the TACC genes and proteins is depicted in Fig. 4. The main conserved feature of the TACC family, the TACC domain, is located at the carboxy terminus of the protein. In the case of the C. elegans TAC protein, this structure comprises the majority of the protein and is encoded by two of the three exons of the gene. In the higher organisms, D. melanogaster, and the deuterostomes C. intestinalis to human, this feature is also encoded by the final exons of the gene (five in D. melanogaster, seven in the deuterostome genes). Outside of the TACC domain, however, TACC family members show relatively little homology. It is interesting that each TACC gene contains one large exon, which shows considerable variability between TACC orthologues, and constitutes the main difference between the TACC3 genes in the vertebrates (see below). In deuterostomes, this exon contains the SDP repeat (or in the case of the murine TACC3's, a rodent-specific 24 amino acid repeat), which is responsible for the binding of the SWI/SNF chromatin remodeling complex component GAS41 [15,16]."}