2pzf: Difference between revisions
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caption="2pzf, resolution 2.000Å" /> | caption="2pzf, resolution 2.000Å" /> | ||
'''Minimal human CFTR first nucleotide binding domain as a head-to-tail dimer with delta F508'''<br /> | '''Minimal human CFTR first nucleotide binding domain as a head-to-tail dimer with delta F508'''<br /> | ||
==Disease== | |||
Known diseases 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]], 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]], Sweat chloride elevation without CF OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421 602421]] | |||
==About this Structure== | ==About this Structure== | ||
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[[Category: Emtage, S.]] | [[Category: Emtage, S.]] | ||
[[Category: Gheyi, T.]] | [[Category: Gheyi, T.]] | ||
[[Category: Glenn, N | [[Category: Glenn, N R.]] | ||
[[Category: Hendle, J.]] | [[Category: Hendle, J.]] | ||
[[Category: Lewis, H | [[Category: Lewis, H A.]] | ||
[[Category: Lu, F.]] | [[Category: Lu, F.]] | ||
[[Category: Rodgers, L | [[Category: Rodgers, L A.]] | ||
[[Category: Romero, R.]] | [[Category: Romero, R.]] | ||
[[Category: Sauder, J | [[Category: Sauder, J M.]] | ||
[[Category: Smith, D.]] | [[Category: Smith, D.]] | ||
[[Category: Tien, H.]] | [[Category: Tien, H.]] | ||
[[Category: Wasserman, S | [[Category: Wasserman, S R.]] | ||
[[Category: Zhao, X.]] | [[Category: Zhao, X.]] | ||
[[Category: ATP]] | [[Category: ATP]] | ||
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[[Category: nbd]] | [[Category: nbd]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:34:28 2008'' | ||
Revision as of 19:34, 21 February 2008
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Minimal human CFTR first nucleotide binding domain as a head-to-tail dimer with delta F508
DiseaseDisease
Known diseases associated with this structure: Congenital bilateral absence of vas deferens OMIM:[602421], Cystic fibrosis OMIM:[602421], Hypertrypsinemia, neonatal OMIM:[602421], Pancreatitis, idiopathic OMIM:[602421], Sweat chloride elevation without CF OMIM:[602421]
About this StructureAbout this Structure
2PZF is a Single protein structure of sequence from Homo sapiens with and as ligands. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Feb 21 18:34:28 2008