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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
2000-12-8
pubmed:abstractText
The recombinant transmembrane protein type XIII collagen is shown to reside on the plasma membrane of insect cells in a 'type II' orientation. Expressions of deletion constructs showed that sequences important for the association of three alpha1(XIII) chains reside in their N- rather than C-terminal portion. In particular, a deletion of residues 63-83 immediately adjacent to the transmembrane domain abolished the formation of disulfide-bonded trimers. The results imply that nucleation of the type XIII collagen triple helix occurs at the N-terminal region and that triple helix formation proceeds from the N- to the C-terminus, in opposite orientation to that of the fibrillar collagens. Interestingly, a sequence homologous to the deleted residues was found at the same plasma membrane-adjacent location in other collagenous transmembrane proteins, suggesting that it may be a conserved association domain. The type XIII collagen was secreted into insect cell medium in low amounts, but this secretion was markedly enhanced when the cytosolic portion was lacking. The cleavage occurred in the non-collagenous NC1 domain after four arginines and was inhibited by a furin protease inhibitor.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-10429945, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-10504453, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-10713152, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-10722741, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-1447209, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-1447210, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-1651913, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-1698771, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-1894651, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-2111957, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-2768343, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-3015601, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-3547403, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-3722183, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-4326447, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-6273419, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7297567, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7398630, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7577848, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7722465, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7754035, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7819326, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-7867067, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-8246446, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-8473327, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-8662631, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9052743, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9118952, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9353231, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9362484, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9371801, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9468508, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9503366, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9524357, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9588004, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9599222, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9624150, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9736768, http://linkedlifedata.com/resource/pubmed/commentcorrection/11013208-9894811
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0261-4189
pubmed:author
pubmed:issnType
Print
pubmed:day
2
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5051-9
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11013208-Amino Acid Sequence, pubmed-meshheading:11013208-Animals, pubmed-meshheading:11013208-Cell Line, pubmed-meshheading:11013208-Cell Membrane, pubmed-meshheading:11013208-Collagen, pubmed-meshheading:11013208-Conserved Sequence, pubmed-meshheading:11013208-Disulfides, pubmed-meshheading:11013208-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:11013208-Fluorescent Antibody Technique, pubmed-meshheading:11013208-Furin, pubmed-meshheading:11013208-Insects, pubmed-meshheading:11013208-Membrane Proteins, pubmed-meshheading:11013208-Microscopy, Immunoelectron, pubmed-meshheading:11013208-Molecular Sequence Data, pubmed-meshheading:11013208-Protease Inhibitors, pubmed-meshheading:11013208-Protein Structure, Quaternary, pubmed-meshheading:11013208-Protein Structure, Tertiary, pubmed-meshheading:11013208-Sequence Alignment, pubmed-meshheading:11013208-Sequence Analysis, Protein, pubmed-meshheading:11013208-Subtilisins
pubmed:year
2000
pubmed:articleTitle
A short sequence in the N-terminal region is required for the trimerization of type XIII collagen and is conserved in other collagenous transmembrane proteins.
pubmed:affiliation
Collagen Research Unit, Biocenter and Department of Medical Biochemistry, University of Oulu, FIN-90220 Oulu, Finland.
pubmed:publicationType
Journal Article
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