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4AHH

R31K - Angiogenin mutants and amyotrophic lateral sclerosis - a biochemical and biological analysis

Summary for 4AHH
Entry DOI10.2210/pdb4ahh/pdb
Related1A4Y 1ANG 1AWZ 1B1E 1B1I 1B1J 1H0D 1H52 1H53 1HBY 1K58 1K59 1K5A 1K5B 1UN3 1UN4 1UN5 2ANG 4AHD 4AHE 4AHF 4AHG 4AHI 4AHJ 4AHK 4AHL 4AHM
DescriptorANGIOGENIN, L(+)-TARTARIC ACID (3 entities in total)
Functional Keywordshydrolase, amyotrophic, lateral sclerosis, neovascularisation
Biological sourceHOMO SAPIENS (HUMAN)
Cellular locationSecreted: P03950
Total number of polymer chains1
Total formula weight14291.11
Authors
Thiyagarajan, N.,Ferguson, R.,Saha, S.,Pham, T.,Subramanian, V.,Acharya, K.R. (deposition date: 2012-02-06, release date: 2012-10-10, Last modification date: 2024-10-16)
Primary citationThiyagarajan, N.,Ferguson, R.,Subramanian, V.,Acharya, K.R.
Structural and Molecular Insights Into the Mechanism of Action of Human Angiogenin-Als Variants in Neurons.
Nat.Commun., 3:1121-, 2012
Cited by
PubMed Abstract: Mutations in angiogenin (ANG), a member of the ribonuclease A superfamily, are associated with amyotrophic lateral sclerosis (ALS; sporadic and familial) and Parkinson's disease. We have previously shown that ANG is expressed in neurons during neuro-ectodermal differentiation, and that it has both neurotrophic and neuroprotective functions. Here we report the atomic resolution structure of native ANG and 11 ANG-ALS variants. We correlate the structural changes to the effects on neuronal survival and the ability to induce stress granules in neuronal cell lines. ANG-ALS variants that affect the structure of the catalytic site and either decrease or increase the RNase activity affect neuronal survival. Neuronal cell lines expressing the ANG-ALS variants also lack the ability to form stress granules. Our structure-function studies on these ANG-ALS variants are the first to provide insights into the cellular and molecular mechanisms underlying their role in ALS.
PubMed: 23047679
DOI: 10.1038/NCOMMS2126
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.498 Å)
Structure validation

226707

數據於2024-10-30公開中

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