Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Asokan Anbanandam"'
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0209726 (2019)
The lanthanides (Ln3+), or rare earth elements, have proven to be useful tools for biomolecular NMR, X-ray crystallographic, and fluorescence analyses due to their unique 4f orbitals. However, their utility in biological applications has been limited
Externí odkaz:
https://doaj.org/article/82038a31b60a42d09778c77ad77dcf51
Autor:
Li Zheng, Sylvie Chenavas, Fabien Kieken, Andrew Trease, Sarah Brownell, Asokan Anbanandam, Paul L. Sorgen, Gaelle Spagnol
Publikováno v:
Biomolecules, Vol 10, Iss 10, p 1452 (2020)
The autosomal-dominant pleiotropic disorder called oculodentodigital dysplasia (ODDD) is caused by mutations in the gap junction protein Cx43. Of the 73 mutations identified to date, over one-third are localized in the cytoplasmic loop (Cx43CL) domai
Externí odkaz:
https://doaj.org/article/dd07bdbc63064969b5961f51ed306e92
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91760 (2014)
ChxR is an atypical two-component signal transduction response regulator (RR) of the OmpR/PhoB subfamily encoded by the obligate intracellular bacterial pathogen Chlamydia trachomatis. Despite structural homology within both receiver and effector dom
Externí odkaz:
https://doaj.org/article/bf6bdaea5c6e4a56a9cd21adf9095bfb
Autor:
Malissa Fenton, Wade Borcherds, Lihong Chen, Asokan Anbanandam, Jiandong Chen, Gary Daughdrill
Publikováno v:
SSRN Electronic Journal.
Autor:
Teruna J. Siahaan, Ahmed Alaofi, Vivitri Dewi Prasasty, Asokan Anbanandam, Elinaz Farokhi, Krzysztof Kuczera
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 35:92-104
The goal of this work is to probe the interaction between cyclic cHAVc3 peptide and the EC1 domain of human E-cadherin protein. Cyclic cHAVc3 peptide (cyclo(1,6)Ac-CSHAVC-NH2) binds to the EC1 domain as shown by chemical shift perturbations in the 2D
Autor:
Sylvie Chenavas, Fabien Kieken, Sarah Brownell, Paul L. Sorgen, Asokan Anbanandam, Andrew J. Trease, Li Zheng, Gaelle Spagnol
Publikováno v:
Biomolecules
Volume 10
Issue 10
Biomolecules, Vol 10, Iss 1452, p 1452 (2020)
Volume 10
Issue 10
Biomolecules, Vol 10, Iss 1452, p 1452 (2020)
The autosomal-dominant pleiotropic disorder called oculodentodigital dysplasia (ODDD) is caused by mutations in the gap junction protein Cx43. Of the 73 mutations identified to date, over one-third are localized in the cytoplasmic loop (Cx43CL) domai
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 3, p e0209726 (2019)
PLoS ONE, Vol 14, Iss 3, p e0209726 (2019)
The lanthanides (Ln3+), or rare earth elements, have proven to be useful tools for biomolecular NMR, X-ray crystallographic, and fluorescence analyses due to their unique 4f orbitals. However, their utility in biological applications has been limited
Autor:
Ragul Gowthaman, Sven A. Miller, Anuradha Roy, Steven A. Rogers, Jittasak Khowsathit, David K. Johnson, Lan Lan, Asokan Anbanandam, Nan Bai, John Karanicolas, Liang Xu, Chunjing Liu, Jeffrey Aubé
Publikováno v:
Journal of Medicinal Chemistry. 59:4152-4170
Protein-protein interactions represent an exciting and challenging target class for therapeutic intervention using small molecules. Protein interaction sites are often devoid of the deep surface pockets presented by "traditional" drug targets, and cr
Autor:
Mary Elizabeth Krause, Asokan Anbanandam, Vivitri Dewi Prasasty, Teruna J. Siahaan, Jennifer S. Laurence, Usman Sumo Friend Tambunan
Publikováno v:
Biomolecular NMR Assignments. 9:31-35
The Extracellular 1 (EC1) domain of E-cadherin has been shown to be important for cadherin-cadherin homophilic interactions. Cadherins are responsible for calcium-mediated cell-cell adhesion located at the adherens junction of the biological barriers
Autor:
Yunjeong Kim, Asokan Anbanandam, Kyeong-Ok Chang, Om Prakash, Daisuke Takahashi, Xiaolan Yao, Yasuaki Hiromasa
Publikováno v:
Protein Science. 22:347-357
Norovirus protease is an essential enzyme for proteolytic maturation of norovirus nonstructural proteins and has been implicated as a potential target for antiviral drug development. Although X-ray structural studies of the protease give us wealth of