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10.1007/s10534-017-0058-2 http://scihub22266oqcxt.onion/10.1007/s10534-017-0058-2 C5684295!5684295 !29063292     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=29063292 &cmd=llinks): Failed to open stream: HTTP request failed! 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The six metal binding domains in human copper transporter, ATP7B: molecular biophysics and disease-causing mutations |pdf=|usr=}}{{29063292 }} gab.com Text The six metal binding domains in human copper transporter, ATP7B: molecular biophysics and disease-causing mutations JO: Biometals http://www.kidney.de/pget.php?&tw=1&pmid=29063292 #FOAvip Wilson Disease (WD) is a hereditary genetic disorder, which coincides with a dysfunctional copper (Cu) metabolism caused by mutations in ATP7B, a membrane-bound P(1B)-type ATPase responsible for Cu export from hepatic cells. The N-terminal part (~ 600 residues) of the multi-domain 1400-residue ATP7B constitutes six metal binding domains (MBDs), each of which can bind a copper ion, interact with other ATP7B domains as well as with different proteins. Although the ATP7B's MBDs have been investigated in vitro and in vivo intensively, it remains unclear how these domains modulate overall structure, dynamics, stability and function of ATP7B. The presence of six MBDs is unique to mammalian ATP7B homologs, and many WD causing missense mutations are found in these domains. Here, we have summarized previously reported in vitro biophysical data on the MBDs of ATP7B and WD point mutations located in these domains. Besides the demonstration of where the research field stands today, this review showcasts the need for further biophysical investigation about the roles of MBDs in ATP7B function. Molecular mechanisms of ATP7B are important not only in the development of new WD treatment but also for other aspects of human physiology where Cu transport plays a role. Twit Text FOAVip The six metal binding domains in human copper transporter, ATP7B: molecular biophysics and disease-causing mutations ????Biometals http://www.kidney.de/pget.php?&tw=1&pmid=29063292 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29063292 #FOAvip English Wikipedia <ref>{{Cite pmid|29063292 }}</ref> The six metal binding domains in human copper transporter, ATP7B: molecular biophysics and disease-causing mutations #MMPMID29063292 Ariöz C ; Li Y ; Wittung-Stafshede P Biometals 2017[Dec]; 30 (6 ): 823-840 PMID29063292 show ga Wilson Disease (WD) is a hereditary genetic disorder, which coincides with a dysfunctional copper (Cu) metabolism caused by mutations in ATP7B, a membrane-bound P(1B)-type ATPase responsible for Cu export from hepatic cells. The N-terminal part (~ 600 residues) of the multi-domain 1400-residue ATP7B constitutes six metal binding domains (MBDs), each of which can bind a copper ion, interact with other ATP7B domains as well as with different proteins. Although the ATP7B's MBDs have been investigated in vitro and in vivo intensively, it remains unclear how these domains modulate overall structure, dynamics, stability and function of ATP7B. The presence of six MBDs is unique to mammalian ATP7B homologs, and many WD causing missense mutations are found in these domains. Here, we have summarized previously reported in vitro biophysical data on the MBDs of ATP7B and WD point mutations located in these domains. Besides the demonstration of where the research field stands today, this review showcasts the need for further biophysical investigation about the roles of MBDs in ATP7B function. Molecular mechanisms of ATP7B are important not only in the development of new WD treatment but also for other aspects of human physiology where Cu transport plays a role. |*Mutation [MESH] |Binding Sites [MESH] |Copper Transport Proteins [MESH] |Copper-Transporting ATPases/*chemistry/genetics/*metabolism [MESH] |Copper/*metabolism [MESH] |Hepatolenticular Degeneration/*genetics [MESH] |Humans [MESH] |Metallochaperones/metabolism [MESH] |Molecular Chaperones [MESH]The six metal binding domains in human copper transporter, ATP7B: mole(epmc).pdf DeepDyve Pubget Overpricing