1xmi
From Proteopedia
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[[Image:1xmi.png|left|200px]] | [[Image:1xmi.png|left|200px]] | ||
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{{ABSTRACT_PUBMED_15528182}} | {{ABSTRACT_PUBMED_15528182}} | ||
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- | ==Disease== | ||
- | Known disease associated with this structure: Congenital bilateral absence of vas deferens OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421 602421]], Cystic fibrosis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421 602421]], Sweat chloride elevation without CF OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421 602421]], Hypertrypsinemia, neonatal OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421 602421]], Pancreatitis, idiopathic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421 602421]] | ||
==About this Structure== | ==About this Structure== | ||
- | + | [[1xmi]] is a 5 chain structure of [[ABC transporter]] with 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=1XMI OCA]. | |
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+ | ==See Also== | ||
+ | *[[ABC transporter]] | ||
==Reference== | ==Reference== | ||
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[[Category: Cystic fibrosis]] | [[Category: Cystic fibrosis]] | ||
[[Category: F508a]] | [[Category: F508a]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Membrane protein]] | ||
[[Category: Nbd1 domain]] | [[Category: Nbd1 domain]] | ||
[[Category: Nucleotide-binding domain 1]] | [[Category: Nucleotide-binding domain 1]] | ||
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- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 16:13:39 2009'' |
Revision as of 19:30, 26 December 2010
Contents |
Crystal structure of human F508A NBD1 domain with ATP
Template:ABSTRACT PUBMED 15528182
About this Structure
1xmi is a 5 chain structure of ABC transporter with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Lewis HA, Zhao X, Wang C, Sauder JM, Rooney I, Noland BW, Lorimer D, Kearins MC, Conners K, Condon B, Maloney PC, Guggino WB, Hunt JF, Emtage S. Impact of the deltaF508 mutation in first nucleotide-binding domain of human cystic fibrosis transmembrane conductance regulator on domain folding and structure. J Biol Chem. 2005 Jan 14;280(2):1346-53. Epub 2004 Nov 3. PMID:15528182 doi:10.1074/jbc.M410968200
Categories: Channel-conductance-controlling ATPase | Homo sapiens | Condon, B. | Conners, K. | Emtage, S. | GenomiX, Structural. | Guggino, W B. | Hunt, J F. | Kearins, M C. | Lewis, H A. | Lorimer, D. | Maloney, P C. | Noland, B W. | Rooney, I. | Sauder, J M. | Wang, C. | Zhao, X. | Cftr | Cystic fibrosis | F508a | Hydrolase | Membrane protein | Nbd1 domain | Nucleotide-binding domain 1