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A homologue (also spelled as homolog) is a compound belonging to a homologous series. [1] Compounds within a homologous series typically have a fixed set of functional groups that gives them similar chemical and physical properties. (For example, the series of primary straight-chained alcohols has a hydroxyl at the end of the carbon chain ...
A homologous series is a group of compounds that differ by a constant unit, generally a methylene (−CH 2 −) group. The reactants undergo a homologation when the number of a repeated structural unit in the molecules is increased. The most common homologation reactions increase the number of methylene (−CH 2 −) units in saturated chain ...
Sequences are either homologous or not. [3] This involves that the term "percent homology" is a misnomer. [4] As with morphological and anatomical structures, sequence similarity might occur because of convergent evolution, or, as with shorter sequences, by chance, meaning
Homologous series, a series of organic compounds having different quantities of a repeated unit; Homologous temperature, the temperature of a material as a fraction of its absolute melting point; Homologation reaction, a chemical reaction which produces the next logical member of a homologous series
Owen codified 3 main criteria for determining if features were homologous: position, development, and composition. In 1859, Charles Darwin explained homologous structures as meaning that the organisms concerned shared a body plan from a common ancestor, and that taxa were branches of a single tree of life. [2] [7] [3]
Studying topological features such as these led to the notion of the cycles that represent homology classes (the elements of homology groups). For example, the two embedded circles in a figure-eight shape provide examples of one-dimensional cycles, or 1-cycles, and the 2-torus T 2 {\displaystyle T^{2}} and 2-sphere S 2 {\displaystyle S^{2 ...
Homology model of the DHRS7B protein created with Swiss-model and rendered with PyMOL. Homology modeling, also known as comparative modeling of protein, refers to constructing an atomic-resolution model of the "target" protein from its amino acid sequence and an experimental three-dimensional structure of a related homologous protein (the "template").
"The molecular weight of Sulculus myoglobin is 41kD, 2.5 times larger than other myoglobins." Moreover, its amino acid sequence has no homology with other invertebrate myoglobins or with hemoglobins, but is 35% homologous with human indoleamine dioxygenase (IDO), a vertebrate tryptophan-degrading enzyme. It does not share similar function with IDO.