(Q24307723)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

Crystal structure of human wildtype and S581L-mutant glycyl-tRNA synthetase, an enzyme underlying distal spinal muscular atrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

main subject

crystal structure

0 references

spinal muscular atrophy

1 reference

inferred from title

Glycyl-tRNA synthetase 1

1 reference

protein dimerization activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

muscular atrophy

1 reference

Distal hereditary motor neuropathies

inferred from title

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Jingshan Ren

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Louise E Bird

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Kevin Talbot

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

Paul A James

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

David K Stammers

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

language of work or name

English

0 references

publication date

29 May 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

volume

581

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

issue

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

page(s)

2959-2964

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17544401%20AND%20SRC:MED&resulttype=core&format=json

Glycyl-tRNA synthetase from Thermus thermophilus--wide structural divergence with other prokaryotic glycyl-tRNA synthetases and functional inter-relation with prokaryotic and eukaryotic glycylation systems

31 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Evolution of different oligomeric glycyl-tRNA synthetases

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Improved methods for building protein models in electron density maps and the location of errors in these models

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Interaction between human tRNA synthetases involves repeated sequence elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Partition of tRNA synthetases into two classes based on mutually exclusive sets of sequence motifs

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

SCOP database in 2004: refinements integrate structure and sequence family data

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Crystal structure and deletion analysis show that the accessory subunit of mammalian DNA polymerase gamma, Pol gamma B, functions as a homodimer

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

The structure of threonyl-tRNA synthetase-tRNA(Thr) complex enlightens its repressor activity and reveals an essential zinc ion in the active site

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Glycyl-tRNA synthetase uses a negatively charged pit for specific recognition and activation of glycine

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Crystallization and preliminary X-ray analysis of a native human tRNA synthetase whose allelic variants are associated with Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

3'-Azido-3'-deoxythymidine drug resistance mutations in HIV-1 reverse transcriptase can induce long range conformational changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Structural insights into the evolution of an antibody combining site

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Crystal structure of a eukaryote/archaeon-like protyl-tRNA synthetase and its complex with tRNAPro(CGG)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Thermodynamic characterization of the binding of nucleotides to glycyl-tRNA synthetase

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Long-range intramolecular signaling in a tRNA synthetase complex revealed by pre-steady-state kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Glycyl-tRNA synthetase from baker's yeast. Interconversion between active and inactive forms of the enzyme.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

7 January 2021

inferred from DOI database lookup

Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.05.046

7 January 2021