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4NJ8

Crystal structure of the human ANKS3 SAM Domain L52A mutant

Summary for 4NJ8
Entry DOI10.2210/pdb4nj8/pdb
Related4NL9
DescriptorAnkyrin repeat and SAM domain-containing protein 3 (2 entities in total)
Functional Keywordssam domain, protein-protein interaction domain, polymerization domain, structural protein
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight15984.30
Authors
Leettola, C.N.,Cascio, D.,Bowie, J.U. (deposition date: 2013-11-08, release date: 2014-07-16, Last modification date: 2024-02-28)
Primary citationLeettola, C.N.,Knight, M.J.,Cascio, D.,Hoffman, S.,Bowie, J.U.
Characterization of the SAM domain of the PKD-related protein ANKS6 and its interaction with ANKS3.
Bmc Struct.Biol., 14:17-17, 2014
Cited by
PubMed Abstract: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disorder leading to end-stage renal failure in humans. In the PKD/Mhm(cy/+) rat model of ADPKD, the point mutation R823W in the sterile alpha motif (SAM) domain of the protein ANKS6 is responsible for disease. SAM domains are known protein-protein interaction domains, capable of binding each other to form polymers and heterodimers. Despite its physiological importance, little is known about the function of ANKS6 and how the R823W point mutation leads to PKD. Recent work has revealed that ANKS6 interacts with a related protein called ANKS3. Both ANKS6 and ANKS3 have a similar domain structure, with ankyrin repeats at the N-terminus and a SAM domain at the C-terminus.
PubMed: 24998259
DOI: 10.1186/1472-6807-14-17
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.6 Å)
Structure validation

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