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2bbt

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|PDB= 2bbt |SIZE=350|CAPTION= <scene name='initialview01'>2bbt</scene>, resolution 2.300&Aring;
|PDB= 2bbt |SIZE=350|CAPTION= <scene name='initialview01'>2bbt</scene>, resolution 2.300&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene> and <scene name='pdbligand=ATP:ADENOSINE-5'-TRIPHOSPHATE'>ATP</scene>
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|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene> and <scene name='pdbligand=ATP:ADENOSINE-5&#39;-TRIPHOSPHATE'>ATP</scene>
|ACTIVITY=
|ACTIVITY=
|GENE= CFTR, ABCC7 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= CFTR, ABCC7 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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[[Category: atp binding cassette]]
[[Category: atp binding cassette]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:59:51 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 23 14:43:37 2008''

Revision as of 12:43, 23 March 2008

Image:2bbt.gif


PDB ID 2bbt

Drag the structure with the mouse to rotate
, resolution 2.300Å
Ligands: and
Gene: CFTR, ABCC7 (Homo sapiens)
Coordinates: save as pdb, mmCIF, xml



Human deltaF508 NBD1 with two solublizing mutations.


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

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