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C. elegans daf-6 Encodes a Patched-Related Protein
C. elegans daf-6 Encodes a Patched-Related Protein

... that these vacuoles contained matrix material. Consistent with this observation, EM cross-sections of daf6(e1377) animals revealed that amphid cilia resided within a sheath cell pocket containing material similar in electron density to matrix material (Figure 1O). These findings are also consistent ...
Chapter-Translation (Prokaryotes)
Chapter-Translation (Prokaryotes)

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Protein Engineering in the Development of
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... The aggregation or assembly of two or more domains into a coiled-coil bundle is reversible with changes in pH, temperature, and ionic strength. The conditions under which assembly occurs are dependent on the primary sequence. The reversible assembly makes the leucine zipper domain ideal to serve as ...
Alpha Diagnostic Intl Inc., 6203 Woodlake Center Dr, San Antonio
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... (LRR)), the domain is an arc-shaped α–β-repeat structure that is also found in many protein-binding contexts, including the extracellular-binding domain of certain surface receptors11,12. In most cases, FBLs also seem to involve substrate phosphorylation for their interaction, but this does not seem ...
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Leukaemia Section t(3;7)(q26;q21) Atlas of Genetics and Cytogenetics in Oncology and Haematology
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... in AML with t(3;12) translocation. EVI1 is also involved in other translocations such as t(2;3)(p13;q26), t(2;3)(q23;q26), t(3;17)(q26;q22) and t(3;13)(q26;q13-14). Other studies have reported abnormal expression of EVI1 in MDS and AML without 3q26 structural abnormalities, suggesting that inappropr ...
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... p27Kip1 are stabilized, and this process commits a cell to senescence (11). Finding out whether Tax and Cdc20 physically interact could help verify this theory. Point mutations of Tax have been assayed for comparison against wildtype activity (11). The phenotypes suggested that the growth arrest bin ...
PDF
PDF

... response to GA and include mutants with alterations in both GA perception and GA signal transduction. Hence, GA-insensitive mutants display a similar dwarf phenotype to GA-deficient mutants, except that they fail to respond to exogenous GA. By contrast, mutants with constitutively active GA response ...
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... They add the specific amino acid to the correct tRNA in an ATP dependent charging reaction Each enzyme recognises a specific amino acid and its cognate tRNA, but does not only use the anti-codon for the specificity of this reaction There are 20 amino acids, 24-60 tRNAs and generally approximately th ...
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Characterization and expression of an mRNA encoding a wound

... peptide protects the exposed fracture surface from pathogenic invasion. Some expression is also apparent in nonzone cells and, whilst no cell separation takes place in this tissue, the process of explant generation may provide a sufficient wound signal to promote transcription of the TAB7 gene in th ...
conference on multiple hereditary exostoses abstract
conference on multiple hereditary exostoses abstract

... multiple EXT mutations have been described. A review of the literature documented 82 and 39 different mutations in the EXT1 and EXT2 genes respectively. Twenty of the EXT1 mutations and 4 of the EXT2 mutations were identified in more than one family. The EXT1 gene mutations include 45 frameshift, 14 ...
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Protein moonlighting



Protein moonlighting (or gene sharing) is a phenomenon by which a protein can perform more than one function. Ancestral moonlighting proteins originally possessed a single function but through evolution, acquired additional functions. Many proteins that moonlight are enzymes; others are receptors, ion channels or chaperones. The most common primary function of moonlighting proteins is enzymatic catalysis, but these enzymes have acquired secondary non-enzymatic roles. Some examples of functions of moonlighting proteins secondary to catalysis include signal transduction, transcriptional regulation, apoptosis, motility, and structural.Protein moonlighting may occur widely in nature. Protein moonlighting through gene sharing differs from the use of a single gene to generate different proteins by alternative RNA splicing, DNA rearrangement, or post-translational processing. It is also different from multifunctionality of the protein, in which the protein has multiple domains, each serving a different function. Protein moonlighting by gene sharing means that a gene may acquire and maintain a second function without gene duplication and without loss of the primary function. Such genes are under two or more entirely different selective constraints.Various techniques have been used to reveal moonlighting functions in proteins. The detection of a protein in unexpected locations within cells, cell types, or tissues may suggest that a protein has a moonlighting function. Furthermore, sequence or structure homology of a protein may be used to infer both primary function as well as secondary moonlighting functions of a protein.The most well-studied examples of gene sharing are crystallins. These proteins, when expressed at low levels in many tissues function as enzymes, but when expressed at high levels in eye tissue, become densely packed and thus form lenses. While the recognition of gene sharing is relatively recent—the term was coined in 1988, after crystallins in chickens and ducks were found to be identical to separately identified enzymes—recent studies have found many examples throughout the living world. Joram Piatigorsky has suggested that many or all proteins exhibit gene sharing to some extent, and that gene sharing is a key aspect of molecular evolution. The genes encoding crystallins must maintain sequences for catalytic function and transparency maintenance function.Inappropriate moonlighting is a contributing factor in some genetic diseases, and moonlighting provides a possible mechanism by which bacteria may become resistant to antibiotics.
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