2bbt
From Proteopedia
Human deltaF508 NBD1 with two solublizing mutations.
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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 with MG and ATP as ligands. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 21:00:43 2007
