Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김철근 | - |
dc.date.accessioned | 2019-08-12T06:47:31Z | - |
dc.date.available | 2019-08-12T06:47:31Z | - |
dc.date.issued | 2019-03 | - |
dc.identifier.citation | Journal of the Korean Magnetic Resonance Society, v. 23, NO 1, Page. 20-25 | en_US |
dc.identifier.issn | 1226-6531 | - |
dc.identifier.uri | http://koreascience.or.kr/article/JAKO201912761598908.page | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/108492 | - |
dc.description.abstract | The transcription factor CP2c has been recently validated as an oncogenic protein that can serve as a promising target for anticancer therapy. We have recently documented that a recombinant protein corresponding to the putative DNA-binding region (residues 63-244) of CP2c adopted two different conformers, one of which is dominated by zinc binding. However, in the present study, a longer construct encompassing residues 63-302 appeared to form a single structural domain. This domain could be considered to adopt a functionally relevant fold, as the known specific binding of a dodecapeptide to this protein was evident. Hence, the residues 63-302 region rather than 63-244 can be regarded as a natively folded structural domain of CP2c. In addition, it was confirmed that zinc ions can bind to this putative DNA-binding domain of CP2c, which resulted in reduced stability of the protein. In this context, it is suggested that the mode of action of CP2c would resemble that of tumor suppressor p53. | en_US |
dc.description.sponsorship | This study was supported by the National Research Foundation (NRF) (grant no. 2016R1A2B4009700). The use of NMR and CD machines was supported by the Korea Basic Science Institute (Ochang, Korea) under the R&D program (project No. D38700) supervised by the Ministry of Science and ICT. | en_US |
dc.language.iso | en | en_US |
dc.publisher | 한국자기공명학회 | en_US |
dc.subject | CP2c | en_US |
dc.subject | DNA-binding domain | en_US |
dc.subject | NMR | en_US |
dc.subject | p53 | en_US |
dc.subject | structural domain | en_US |
dc.subject | zinc binding | en_US |
dc.title | Structural characterization of the putative DNA-binding domain of CP2c and its relevance to zinc binding | en_US |
dc.type | Article | en_US |
dc.relation.no | 1 | - |
dc.relation.volume | 23 | - |
dc.identifier.doi | 10.6564/JKMRS.2019.23.1.020 | - |
dc.relation.page | 20-25 | - |
dc.relation.journal | Journal of the Korean Magnetic Resonance Society | - |
dc.contributor.googleauthor | Ryu, Ki-Sung | - |
dc.contributor.googleauthor | Jo, Ku-Sung | - |
dc.contributor.googleauthor | Kim, Na-Young | - |
dc.contributor.googleauthor | Jeon, Eun-Jae | - |
dc.contributor.googleauthor | Park, Sung Jean | - |
dc.contributor.googleauthor | Kim, Hyun-Hwi | - |
dc.contributor.googleauthor | Kim, Eun-Hee | - |
dc.contributor.googleauthor | Kim, Chan-Gil | - |
dc.contributor.googleauthor | Kim, Chul Geun | - |
dc.contributor.googleauthor | Won, Hyung-Sik | - |
dc.relation.code | 2019034995 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF NATURAL SCIENCES[S] | - |
dc.sector.department | DEPARTMENT OF LIFE SCIENCE | - |
dc.identifier.pid | cgkim | - |
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