Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
32
pubmed:dateCreated
2010-8-2
pubmed:abstractText
Classical arabinogalactan proteins partially defined by type II O-Hyp-linked arabinogalactans (Hyp-AGs) are structural components of the plant extracellular matrix. Recently we described the structure of a small Hyp-AG putatively based on repetitive trigalactosyl subunits and suggested that AGs are less complex and varied than generally supposed. Here we describe three additional AGs with similar subunits. The Hyp-AGs were isolated from two different arabinogalactan protein fusion glycoproteins expressed in tobacco cells; that is, a 22-residue Hyp-AG and a 20-residue Hyp-AG, both isolated from interferon alpha2b-(Ser-Hyp)(20), and a 14-residue Hyp-AG isolated from (Ala-Hyp)(51)-green fluorescent protein. We used NMR spectroscopy to establish the molecular structure of these Hyp-AGs, which share common features: (i) a galactan main chain composed of two 1-->3 beta-linked trigalactosyl blocks linked by a beta-1-->6 bond; (ii) bifurcated side chains with Ara, Rha, GlcUA, and a Gal 6-linked to Gal-1 and Gal-2 of the main-chain trigalactosyl repeats; (iii) a common side chain structure composed of up to six residues, the largest consisting of an alpha-L-Araf-(1-->5)-alpha-L-Araf-(1-->3)-alpha-L-Araf-(1-->3- unit and an alpha-L-Rhap-(1-->4)-beta-D-GlcUAp-(1-->6)-unit, both linked to Gal. The conformational ensemble obtained by using nuclear Overhauser effect data in structure calculations revealed a galactan main chain with a reverse turn involving the beta-1-->6 link between the trigalactosyl blocks, yielding a moderately compact structure stabilized by H-bonds.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-10611282, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-10653785, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-10903497, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-11393510, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-11543565, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-11554470, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-12182702, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-12805588, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-12857818, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-14724279, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-15235117, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-15377216, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-15574842, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-15818563, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-16411951, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-16657818, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-16659963, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-16665859, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-16668765, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-17201686, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-17328066, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-17849372, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-18256186, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-18367218, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-2469683, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-8148875, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-8520220, http://linkedlifedata.com/resource/pubmed/commentcorrection/20489210-8548791
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1083-351X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
6
pubmed:volume
285
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
24575-83
pubmed:dateRevised
2011-8-25
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Plant O-hydroxyproline arabinogalactans are composed of repeating trigalactosyl subunits with short bifurcated side chains.
pubmed:affiliation
Department of Chemistry and Biochemistry, Biochemistry Research Facility, Ohio University, Athens, Ohio 45701, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural