Words similar to gln
Example sentences for: gln
How can you use “gln” in a sentence? Here are some example sentences to help you improve your vocabulary:
To test this further, we generated an in-frame deletion of this region, as originally intended, that showed normal function [ 20 ] . Another domain critical for EC coupling is Csk35 downstream from Peptide A (Leu720-Gln765).
Based on ligand strength, and the likelihood that occupancy is unambiguous in vivo [ 34 ] , His212 may serve as a ligand for Chl a and Gln197 for Chl b.
However, there are many case reports describing patients with progressive neurodegenerative disorders of unknown etiology, collectively referred to as neuronal intranuclear inclusion disease [ 77 ] . While these may consist mainly of unidentified poly-Gln or poly-Ala disorders, the present study raises the possibility that some forms of this disease may arise through unexpected mechanisms, perhaps involving mutations in Rab24 or other poorly characterized members of the Rab GTPase family that mediate trafficking of misfolded proteins within autophagosomes and lysosomes.
Lhcb6, a minor LHCP, contains Gly instead of Pro at the position analogous to 82 in Lhcb1, thus eliminating the peptide bond carbonyl of Gly as a ligand, but Lhcb6 has a potential ligand for Chl b in Gln83 [ 39 40 ] . These two LHCP sub-species, along with Lhca4 are most affected by the lack of Chl b in vivo [ 5 ] . Lhcb4 (apoprotein of CP29) has Val instead of Pro at 'position 82', and the absence of site a 6 in Lhcb4 may contribute to its drastic reduction in Chl b -less mutants [ 5 8 ] . However, Lhcb2, Lhcb3, Lhca1, Lhca2 and Lhca3 contain the Gly peptide carbonyl as a ligand (each has Pro at 'position 82' [ 40 ] ) but are reduced only slightly, if any, in amount by the lack of Chl b.
Although the formation of intranuclear inclusions has not been observed in previous studies of Ras-related GTPases, it is a common feature of several neurodegenerative disorders where abnormal proteins containing poly-Gln tracts are synthesized as a result of CAG codon expansions [ 52 ] . Examples include Huntington's disease (huntingtin) [ 53 54 ] , spinocerebellar ataxia (SCA) types 1 and 3 (ataxin-1 and ataxin-3) [ 55 56 ] and dentatorubral-pallidoluysian atrophy (atrophin-1) [ 57 ] . These poly-Gln protein aggregates typically contain ubiquitin [ 58 ] and members of the Hsp70 chaperone family [ 59 ] , consistent with a proposed pathway for cellular clearance of toxic misfolded proteins.
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