2bbs | pdb_00002bbs
From Proteopedia
Human deltaF508 NBD1 with three solubilizing mutations
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| 2bbs, resolution 2.050Å | |||||||||||||
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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
2BBS is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Mar 20 15:59:55 2008
