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http://purl.uniprot.org/citations/1718985http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1718985http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1718985http://www.w3.org/2000/01/rdf-schema#comment"cDNAs encoding human and mouse microtubule-associated protein 4 (MAP 4) were isolated. MAP 4 is encoded by a single gene. Multiple MAP 4 mRNAs are transcribed that are differentially expressed among mouse tissues. Open reading frames for the human and mouse MAP 4 clones indicate three distinct regions consisting of related sequences with different motifs. Approximately 30% of the protein is tandem related repeats of approximately 14 amino acids. Another region contains clusters of serine and proline. Four 18-mer repeats characteristic of the microtubule-binding domains of MAP 2 and tau are located at the carboxyl-terminal portion of MAP 4. Amino acid sequence analysis revealed that human and mouse MAP 4 are homologs of the bovine 190-kDa MAP/MAP U (Aizawa, H., Emori, Y., Murofushi, H., Kawasakai, H., Sakai, H., and Suzuki, K. (1990) J. Biol. Chem. 265, 13849-13855). Mouse and human MAP 4 and the bovine 190-kDa MAP are approximately 75% similar, indicating that these proteins are all members of the same class. Domains with extremely high conservation (greater than or equal to 88%) are: 1) the extreme amino terminus; 2) a proline-rich region between the KDM and S,P domains; 3) the microtubule-binding domain; and 4) the extreme carboxyl terminus."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.org/dc/terms/identifier"doi:10.1016/s0021-9258(18)54720-7"xsd:string
http://purl.uniprot.org/citations/1718985http://purl.org/dc/terms/identifier"doi:10.1016/s0021-9258(18)54720-7"xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/author"Tenbarge K.M."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/author"Tenbarge K.M."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/author"West R.R."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/author"West R.R."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/author"Olmsted J.B."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/author"Olmsted J.B."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/date"1991"xsd:gYear
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/date"1991"xsd:gYear
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/pages"21886-21896"xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/pages"21886-21896"xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/title"A model for microtubule-associated protein 4 structure. Domains defined by comparisons of human, mouse, and bovine sequences."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/title"A model for microtubule-associated protein 4 structure. Domains defined by comparisons of human, mouse, and bovine sequences."xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/volume"266"xsd:string
http://purl.uniprot.org/citations/1718985http://purl.uniprot.org/core/volume"266"xsd:string
http://purl.uniprot.org/citations/1718985http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/1718985
http://purl.uniprot.org/citations/1718985http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/1718985
http://purl.uniprot.org/citations/1718985http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/1718985
http://purl.uniprot.org/citations/1718985http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/1718985