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2b1u

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(New page: 200px<br /> <applet load="2b1u" size="450" color="white" frame="true" align="right" spinBox="true" caption="2b1u" /> '''Solution structure of Calmodulin-like Skin ...)
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'''Solution structure of Calmodulin-like Skin Protein C terminal domain'''<br />
'''Solution structure of Calmodulin-like Skin Protein C terminal domain'''<br />
==Overview==
==Overview==
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The structure and dynamics of human calmodulin-like skin protein (CLSP), have been characterized by NMR spectroscopy. The mobility of CLSP has been, found to be different for the N-terminal and C-terminal domains. The, isolated domains were also expressed and analyzed. The structure of the, isolated C-terminal domain is presented. The N-terminal domain is, characterized by four stable helices, which experience large fluctuations., This is shown to be due to mutations in the hydrophobic core. The overall, N-terminal domain behavior is similar both in the full-length protein and, in the isolated domain. By exploiting the capability of Tb3+ bound to CLSP, to induce partial orientation of the molecule in a magnetic field, restricted motion of one domain with respect to the other was proved. By, using NMR, ITC, and ESI-MS, the calcium and magnesium binding properties, were investigated. Finally, CLSP is framed into the evolutionary scheme of, the calmodulin-like family.
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The structure and dynamics of human calmodulin-like skin protein (CLSP) have been characterized by NMR spectroscopy. The mobility of CLSP has been found to be different for the N-terminal and C-terminal domains. The isolated domains were also expressed and analyzed. The structure of the isolated C-terminal domain is presented. The N-terminal domain is characterized by four stable helices, which experience large fluctuations. This is shown to be due to mutations in the hydrophobic core. The overall N-terminal domain behavior is similar both in the full-length protein and in the isolated domain. By exploiting the capability of Tb3+ bound to CLSP to induce partial orientation of the molecule in a magnetic field, restricted motion of one domain with respect to the other was proved. By using NMR, ITC, and ESI-MS, the calcium and magnesium binding properties were investigated. Finally, CLSP is framed into the evolutionary scheme of the calmodulin-like family.
==About this Structure==
==About this Structure==
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2B1U is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2B1U OCA].
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2B1U is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B1U OCA].
==Reference==
==Reference==
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[[Category: Chirivino, E.]]
[[Category: Chirivino, E.]]
[[Category: Luchinat, C.]]
[[Category: Luchinat, C.]]
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[[Category: SPINE, Structural.Proteomics.in.Europe.]]
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[[Category: SPINE, Structural Proteomics in Europe.]]
[[Category: backbone dynamic]]
[[Category: backbone dynamic]]
[[Category: calmodulin-like skin protein]]
[[Category: calmodulin-like skin protein]]
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[[Category: structural proteomics in europe]]
[[Category: structural proteomics in europe]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:57:10 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:33:22 2008''

Revision as of 14:33, 21 February 2008


2b1u

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Solution structure of Calmodulin-like Skin Protein C terminal domain

Overview

The structure and dynamics of human calmodulin-like skin protein (CLSP) have been characterized by NMR spectroscopy. The mobility of CLSP has been found to be different for the N-terminal and C-terminal domains. The isolated domains were also expressed and analyzed. The structure of the isolated C-terminal domain is presented. The N-terminal domain is characterized by four stable helices, which experience large fluctuations. This is shown to be due to mutations in the hydrophobic core. The overall N-terminal domain behavior is similar both in the full-length protein and in the isolated domain. By exploiting the capability of Tb3+ bound to CLSP to induce partial orientation of the molecule in a magnetic field, restricted motion of one domain with respect to the other was proved. By using NMR, ITC, and ESI-MS, the calcium and magnesium binding properties were investigated. Finally, CLSP is framed into the evolutionary scheme of the calmodulin-like family.

About this Structure

2B1U is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

A structural and dynamic characterization of the EF-hand protein CLSP., Babini E, Bertini I, Capozzi F, Chirivino E, Luchinat C, Structure. 2006 Jun;14(6):1029-38. PMID:16765896

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