Abstract
Cell adhesion molecules play a crucial role in fundamental biological processes via regulating cell–cell interactions. Nerve injury induced protein1 (Ninjurin1) is a novel adhesion protein that has no significant homology with other known cell adhesion molecules. Here we present the assignment of an 81 aa construct for human Ninjurin1 Extracellular N-Terminal (ENT) domain, which comprises the critical adhesion domain.
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Acknowledgments
This study was supported by the National Research Foundation of Korea (NRF) grant funded by Korean government (MEST) (Grant number 20110001207). This study was also supported by a grant of the Korea Healthcare technology R&D Project, Ministry for Health, Welfare & Family Affairs, Republic of Korea. (Grant number:A092006). This work was supported in part by 2011 BK21 project for Medicine, Dentistry, and Pharmacy. We thank Korea Basic Science Institute (KBSI) and National Center for Inter-University Research Facilities (NCIRF) for using their NMR machines.
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Lee, IG., Jang, SB., Kim, JH. et al. 1H, 13C and 15N chemical shift assignments of Ninjurin1 Extracellular N-terminal Domain. Biomol NMR Assign 7, 159–162 (2013). https://doi.org/10.1007/s12104-012-9400-3
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DOI: https://doi.org/10.1007/s12104-012-9400-3