DC Field | Value | Language |
---|---|---|
dc.contributor.author | 박순희 | ko |
dc.contributor.author | 박찬규 | ko |
dc.date.accessioned | 2013-02-25T00:35:05Z | - |
dc.date.available | 2013-02-25T00:35:05Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1991 | - |
dc.identifier.citation | 한국생화학학회지, v.24, pp.207 - 214 | - |
dc.identifier.issn | 0368-4881 | - |
dc.identifier.uri | http://hdl.handle.net/10203/58439 | - |
dc.description.abstract | To understand the mechanism of protein export in general and to identify conponent(s) of export machinery utilized by ribose-binding protein, we examined the effects of three prlA suppressors on the export of an export-defective mutant rbsB103. We also studied the requirement(s) of SecY protein and leader peptidase on the export of wide-type ribose-binding protein. The export defect of rbsB103 mutation was not suppressed by three prlA alleles tested. However, SecY protein appears to affect for the export of wide-type ribose-binding protein. Wild-type precursor ribose-binding protein was not processed by purified leader peptidase(lep product) in vitro. | - |
dc.language | English | - |
dc.publisher | Korean Society for Medical Biochemistry and Molecular Biology | - |
dc.title | Effects of export machineries on the export of ribose-binding protein | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.citation.volume | 24 | - |
dc.citation.beginningpage | 207 | - |
dc.citation.endingpage | 214 | - |
dc.citation.publicationname | 한국생화학학회지 | - |
dc.contributor.localauthor | 박찬규 | - |
dc.contributor.nonIdAuthor | 박순희 | - |
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