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Functional and biochemical characterization of cucumber genes encoding two copper ATPases CsHMA5 1 and CsHMA5 2

JBC. 2015; 
Magdalena Migocka‡, Ewelina Posyniak‡, Ewa Maciaszczyk-Dziubinska§, Anna Papierniak‡ and Anna Kosieradzaka‡
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Peptide Synthesis … in rabbit against the keyhole limpet hemocyanin-conjugated peptides ISKDGTDHRSREVC, corresponding to N-terminal amino acids 101–114 of CsHMA5.1 protein and TGSGRYKATIFPEGC, corresponding to N-terminal amino acids 202–215 of CsHMA5.2 protein (GenScript) … Get A Quote

摘要

Plant copper P1B-type ATPases appear to be crucial for maintaining copper homeostasis within plant cells, but until now they have been studied mostly in model plant systems. Here, we present the molecular and biochemical characterization of two cucumber copper ATPases, CsHMA5.1 and CsHMA5.2, indicating a different function for HMA5-like proteins in different plants. When expressed in yeast, CsHMA5.1 and CsHMA5.2 localize to the vacuolar membrane and are activated by monovalent copper or silver ions and cysteine, showing different affinities to Cu+ (Km∼1 or 0.5 μM, respectively) and similar affinity to Ag+ (Km ∼2.5 μM). Both proteins restore the growth of yeast mutants sensitive to copper excess and sil... More

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