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@ARTICLE{Grela:141082,
author = {Grela, P. and Gajda, M. J. and Armache, J. P. and Beckmann,
R. and Krokowski, D. and Svergun, D. I. and Grankowski, N.
and Tchorzewski, M. and DESY},
title = {{S}olution structure of natively assembled yeast ribosomal
stalk determined by {S}mall {A}ngle {X}-ray {S}cattering},
journal = {Biochemical journal},
volume = {444},
number = {2},
issn = {0006-2936},
address = {London},
publisher = {Portland Press},
reportid = {PHPPUBDB-24926},
pages = {205 - 209},
year = {2012},
note = {ISSN 1470-8728 not unique: **2 hits**.},
abstract = {The ribosomal stalk of the 60S subunit has been shown to
play a crucial role in all steps of protein synthesis, but
its structure and exact molecular function remain an
unanswered question. In the present study, we show the
low-resolution models of the solution structure of the yeast
ribosomal stalk, composed of five proteins, P0-(P1-P2)(2).
The model of the pentameric stalk complex determined by
small-angle X-ray scattering reveals an elongated shape with
a maximum length of 13 nm. The model displays three distinct
lobes, which may correspond to the individual P1-P2
heterodimers anchored to the C-terminal domain of the P0
protein.},
keywords = {Protein Binding: physiology / Protein Multimerization /
Protein Structure, Tertiary / Ribosomal Proteins: chemistry
/ Saccharomyces cerevisiae: chemistry / Saccharomyces
cerevisiae Proteins: chemistry / Scattering, Small Angle /
X-Ray Diffraction: methods / RPP0 protein, S cerevisiae (NLM
Chemicals) / Ribosomal Proteins (NLM Chemicals) /
Saccharomyces cerevisiae Proteins (NLM Chemicals) /
ribosomal protein P0 (NLM Chemicals)},
cin = {EMBL(-2012)},
ddc = {540},
cid = {$I:(DE-H253)EMBL_-2012_-20130307$},
pnm = {DORIS Beamline D1.2 (POF2-54G13)},
pid = {G:(DE-H253)POF2-D1.2-20130405},
experiment = {EXP:(DE-H253)D-D1.2-20150101},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22458705},
UT = {WOS:000304643200006},
doi = {10.1042/BJ20120115},
url = {https://bib-pubdb1.desy.de/record/141082},
}