1xf9

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[[Image:1xf9.gif|left|200px]]
[[Image:1xf9.gif|left|200px]]
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{{Structure
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|PDB= 1xf9 |SIZE=350|CAPTION= <scene name='initialview01'>1xf9</scene>, resolution 2.70&Aring;
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The line below this paragraph, containing "STRUCTURE_1xf9", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=ACY:ACETIC+ACID'>ACY</scene>, <scene name='pdbligand=ATP:ADENOSINE-5&#39;-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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or leave the SCENE parameter empty for the default display.
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|GENE= Cftr, Abcc7 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 Mus musculus])
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|DOMAIN=
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{{STRUCTURE_1xf9| PDB=1xf9 | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1xf9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1xf9 OCA], [http://www.ebi.ac.uk/pdbsum/1xf9 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1xf9 RCSB]</span>
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'''Structure of NBD1 from murine CFTR- F508S mutant'''
'''Structure of NBD1 from murine CFTR- F508S mutant'''
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[[Category: Thibodeau, P H.]]
[[Category: Thibodeau, P H.]]
[[Category: Thomas, P J.]]
[[Category: Thomas, P J.]]
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[[Category: abc transporter]]
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[[Category: Abc transporter]]
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[[Category: atp]]
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[[Category: Atp]]
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[[Category: cystic fibrosis]]
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[[Category: Cystic fibrosis]]
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[[Category: nucleotide-binding domain]]
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[[Category: Nucleotide-binding domain]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 14:57:12 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:48:48 2008''
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Revision as of 11:57, 3 May 2008

Template:STRUCTURE 1xf9

Structure of NBD1 from murine CFTR- F508S mutant


Overview

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR), an integral membrane protein, cause cystic fibrosis (CF). The most common CF-causing mutant, deletion of Phe508, fails to properly fold. To elucidate the role Phe508 plays in the folding of CFTR, missense mutations at this position were generated. Only one missense mutation had a pronounced effect on the stability and folding of the isolated domain in vitro. In contrast, many substitutions, including those of charged and bulky residues, disrupted folding of full-length CFTR in cells. Structures of two mutant nucleotide-binding domains (NBDs) reveal only local alterations of the surface near position 508. These results suggest that the peptide backbone plays a role in the proper folding of the domain, whereas the side chain plays a role in defining a surface of NBD1 that potentially interacts with other domains during the maturation of intact CFTR.

About this Structure

1XF9 is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.

Reference

Side chain and backbone contributions of Phe508 to CFTR folding., Thibodeau PH, Brautigam CA, Machius M, Thomas PJ, Nat Struct Mol Biol. 2005 Jan;12(1):10-6. Epub 2004 Dec 26. PMID:15619636 Page seeded by OCA on Sat May 3 14:57:12 2008

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