2bbt | pdb_00002bbt
From Proteopedia
Human deltaF508 NBD1 with two solublizing mutations.
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| 2bbt, resolution 2.300Å | |||||||||||||
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| Ligands: | MG and ATP | ||||||||||||
| Gene: | CFTR, ABCC7 (Homo sapiens) | ||||||||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||||||||
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
2BBT is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Sun Mar 23 14:43:37 2008
