Structural basis for conformational switching and GTP loading of the large G protein atlastin (Q24310183)

identical protein binding

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Holger Sondermann

7

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author name string

Laura J Byrnes

1

0 references

Avtar Singh

2

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Kylan Szeto

3

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Nicole M Benvin

4

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John P O'Donnell

5

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Warren R Zipfel

A pseudoatomic model of the dynamin polymer identifies a hydrolysis-dependent powerstroke

6

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language of work or name

English

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publication date

6 February 2013

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published in

The EMBO Journal

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volume

32

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issue

3

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page(s)

369-84

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cites work

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Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

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A class of dynamin-like GTPases involved in the generation of the tubular ER network

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Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

19 March 2017

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Structure of myxovirus resistance protein a reveals intra- and intermolecular domain interactions required for the antiviral function

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The crystal structure of dynamin

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Crystal structure of nucleotide-free dynamin

19 March 2017

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Structures of the atlastin GTPase provide insight into homotypic fusion of endoplasmic reticulum membranes

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Structural basis for the nucleotide-dependent dimerization of the large G protein atlastin-1/SPG3A

19 March 2017

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G domain dimerization controls dynamin's assembly-stimulated GTPase activity

19 March 2017

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Structure of human guanylate-binding protein 1 representing a unique class of GTP-binding proteins

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Identification of residues in the human guanylate-binding protein 1 critical for nucleotide binding and cooperative GTP hydrolysis

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Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

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Lipid interaction of the C terminus and association of the transmembrane segments facilitate atlastin-mediated homotypic endoplasmic reticulum fusion

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An intramolecular salt bridge drives the soluble domain of GTP-bound atlastin into the postfusion conformation

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GTP-dependent packing of a three-helix bundle is required for atlastin-mediated fusion

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Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain.

27 September 2017

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Differential curvature sensing and generating activities of dynamin isoforms provide opportunities for tissue-specific regulation.

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Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin

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GTPase cycle of dynamin is coupled to membrane squeeze and release, leading to spontaneous fission

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Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis

27 September 2017

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Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

27 September 2017

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27 September 2017

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Dynamin self-assembly stimulates its GTPase activity

27 September 2017

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27 September 2017

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Processing of X-ray diffraction data collected in oscillation mode

30 May 2018

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Real-time visualization of dynamin-catalyzed membrane fission and vesicle release

21 January 2018

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In Arabidopsis, the spatial and dynamic organization of the endoplasmic reticulum and Golgi apparatus is influenced by the integrity of the C-terminal domain of RHD3, a non-essential GTPase

21 January 2018

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

21 January 2018

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A bacterial dynamin-like protein

21 January 2018

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Nucleotide-dependent conformational changes in dynamin: evidence for a mechanochemical molecular spring

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/23334294

12 December 2020

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23334294

12 December 2020

Hereditary spastic paraplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23334294

12 December 2020

The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features

1 reference

https://pubmed.ncbi.nlm.nih.gov/23334294

12 December 2020

Identifiers

DOI

10.1038/EMBOJ.2012.353

1 reference

release_e4eajonpo5advgfwxm5fccupwy

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/e4eajonpo5advgfwxm5fccupwy

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

PubMed publication ID

23334294

1 reference