1ckw: Difference between revisions

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{{Seed}}
[[Image:1ckw.png|left|200px]]
[[Image:1ckw.png|left|200px]]


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==About this Structure==
==About this Structure==
1CKW is a [[Single protein]] structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CKW OCA].  
[[1ckw]] is a 1 chain structure of [[ABC transporter]]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CKW OCA].  
 
==See Also==
*[[ABC transporter]]


==Reference==
==Reference==
Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the Phe508 region, the most common site of disease-causing DeltaF508 mutation., Massiah MA, Ko YH, Pedersen PL, Mildvan AS, Biochemistry. 1999 Jun 8;38(23):7453-61. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10360942 10360942]
<ref group="xtra">PMID:10360942</ref><references group="xtra"/>
[[Category: Single protein]]
[[Category: Ko, Y H.]]
[[Category: Ko, Y H.]]
[[Category: Massiah, M A.]]
[[Category: Massiah, M A.]]
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[[Category: Pedersen, P L.]]
[[Category: Pedersen, P L.]]
[[Category: Cystic fibrosis]]
[[Category: Cystic fibrosis]]
[[Category: Metal transport]]
[[Category: Nmr]]
[[Category: Nmr]]
[[Category: P25_tfe]]
[[Category: P25_tfe]]
[[Category: Peptide]]
[[Category: Peptide]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jun 30 20:53:21 2008''

Revision as of 02:09, 27 December 2010

File:1ckw.png

Template:STRUCTURE 1ckw

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION

Template:ABSTRACT PUBMED 10360942

About this Structure

1ckw is a 1 chain structure of ABC transporter. Full experimental information is available from OCA.

See Also

Reference

  1. Massiah MA, Ko YH, Pedersen PL, Mildvan AS. Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the Phe508 region, the most common site of disease-causing DeltaF508 mutation. Biochemistry. 1999 Jun 8;38(23):7453-61. PMID:10360942 doi:10.1021/bi9903603

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