2pzg
From Proteopedia
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caption="2pzg, resolution 1.800Å" /> | caption="2pzg, resolution 1.800Å" /> | ||
'''Minimal human CFTR first nucleotide binding domain as a monomer'''<br /> | '''Minimal human CFTR first nucleotide binding domain as a monomer'''<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 18:34:31 2008'' |
Revision as of 16:34, 21 February 2008
|
Minimal human CFTR first nucleotide binding domain as a monomer
Disease
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 Structure
2PZG 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 18:34:31 2008
Categories: Homo sapiens | Single protein | Atwell, S. | Conners, K. | Emtage, S. | Gheyi, T. | Glenn, N R. | Hendle, J. | Lewis, H A. | Lu, F. | Rodgers, L A. | Romero, R. | Sauder, J M. | Smith, D. | Tien, H. | Wasserman, S R. | Zhao, X. | ATP | GOL | MG | Abc transporter | Cftr | Hydrolase | Nbd
