PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 22555879-0 2012 Copper chaperone antioxidant protein1 is essential for copper homeostasis. Copper 55-61 homolog of anti-oxidant 1 Arabidopsis thaliana 17-37 22899077-1 2012 In a previous study, we demonstrated that Arabidopsis Antioxidant Protein1 (ATX1) plays an essential role in copper (Cu) homeostasis, conferring tolerance to both excess and subclinically deficient Cu. Copper 109-115 homolog of anti-oxidant 1 Arabidopsis thaliana 54-74 22899077-1 2012 In a previous study, we demonstrated that Arabidopsis Antioxidant Protein1 (ATX1) plays an essential role in copper (Cu) homeostasis, conferring tolerance to both excess and subclinically deficient Cu. Copper 109-115 homolog of anti-oxidant 1 Arabidopsis thaliana 76-80 22899077-1 2012 In a previous study, we demonstrated that Arabidopsis Antioxidant Protein1 (ATX1) plays an essential role in copper (Cu) homeostasis, conferring tolerance to both excess and subclinically deficient Cu. Copper 117-119 homolog of anti-oxidant 1 Arabidopsis thaliana 54-74 22899077-1 2012 In a previous study, we demonstrated that Arabidopsis Antioxidant Protein1 (ATX1) plays an essential role in copper (Cu) homeostasis, conferring tolerance to both excess and subclinically deficient Cu. Copper 117-119 homolog of anti-oxidant 1 Arabidopsis thaliana 76-80 22899077-2 2012 The Cu-binding motif MXCXXC was required for the physiological function of ATX1. Copper 4-6 homolog of anti-oxidant 1 Arabidopsis thaliana 75-79 22899077-3 2012 In this study, we found that overexpression of ATX1 resulted in hypersensitivity to severe Cu deficiency despite enhancing tolerance to subclinical Cu deficiency. Copper 91-93 homolog of anti-oxidant 1 Arabidopsis thaliana 47-51 28388654-0 2017 Triplin, a small molecule, reveals copper ion transport in ethylene signaling from ATX1 to RAN1. Copper 35-41 homolog of anti-oxidant 1 Arabidopsis thaliana 83-87 28388654-11 2017 Our study provided genetic evidence for the first time that, copper ions necessary for ethylene receptor biogenesis and signaling are transported from ATX1 to RAN1. Copper 61-67 homolog of anti-oxidant 1 Arabidopsis thaliana 151-155 22555879-7 2012 The shoot and root growth of atx1 and cchatx1 but not cch was specifically hypersensitive to excess Cu but not excess iron, zinc, or cadmium. Copper 100-102 homolog of anti-oxidant 1 Arabidopsis thaliana 29-33 22555879-8 2012 The activities of antioxidant enzymes in atx1 and cchatx1 were markedly regulated in response to excess Cu, which confirms the phenotype of Cu hypersensitivity. Copper 104-106 homolog of anti-oxidant 1 Arabidopsis thaliana 41-45 22555879-8 2012 The activities of antioxidant enzymes in atx1 and cchatx1 were markedly regulated in response to excess Cu, which confirms the phenotype of Cu hypersensitivity. Copper 140-142 homolog of anti-oxidant 1 Arabidopsis thaliana 41-45 22555879-10 2012 Overexpression of ATX1 not only enhanced Cu tolerance and accumulation in excess Cu conditions but also tolerance to Cu deficiency. Copper 41-43 homolog of anti-oxidant 1 Arabidopsis thaliana 18-22 22555879-10 2012 Overexpression of ATX1 not only enhanced Cu tolerance and accumulation in excess Cu conditions but also tolerance to Cu deficiency. Copper 81-83 homolog of anti-oxidant 1 Arabidopsis thaliana 18-22 22555879-11 2012 In addition, the Cu-binding motif MXCXXC of ATX1 was required for these physiological functions. Copper 17-19 homolog of anti-oxidant 1 Arabidopsis thaliana 44-48 22555879-13 2012 In this study, we demonstrate that ATX1 plays an essential role in Cu homeostasis in conferring tolerance to excess Cu and Cu deficiency. Copper 67-69 homolog of anti-oxidant 1 Arabidopsis thaliana 35-39 32031640-1 2020 The copper chaperone ATX1 has been investigated previously in the herbaceous plants Arabidopsis and rice. Copper 4-10 homolog of anti-oxidant 1 Arabidopsis thaliana 21-25 32031640-2 2020 However, the molecular mechanisms of ATX1 underlying copper transport and functional characteristics in the woody plant Populus are poorly understood. Copper 53-59 homolog of anti-oxidant 1 Arabidopsis thaliana 37-41 17223078-0 2007 Higher plants possess two different types of ATX1-like copper chaperones. Copper 55-61 homolog of anti-oxidant 1 Arabidopsis thaliana 45-49 17223078-7 2007 We propose that higher plants express two types of ATX1-like Cu chaperones: the ATX1-type with a predominant function in Cu delivery to P-type ATPases, and the CCH-type with additional CTD-mediated plant-specific functions. Copper 61-63 homolog of anti-oxidant 1 Arabidopsis thaliana 51-55 17223078-7 2007 We propose that higher plants express two types of ATX1-like Cu chaperones: the ATX1-type with a predominant function in Cu delivery to P-type ATPases, and the CCH-type with additional CTD-mediated plant-specific functions. Copper 61-63 homolog of anti-oxidant 1 Arabidopsis thaliana 80-84 16126858-4 2005 The ATX1-like and C-terminal domains contain putative copper-binding motifs. Copper 54-60 homolog of anti-oxidant 1 Arabidopsis thaliana 4-8 16126858-10 2005 This result indicates that the ATX1-like domain is essential for the copper chaperone function of AtCCS in planta. Copper 69-75 homolog of anti-oxidant 1 Arabidopsis thaliana 31-35 15180901-1 2004 BACKGROUND: Arabidopsis thaliana copper metallochaperone CCH is a functional homologue of yeast antioxidant ATX1, involved in cytosolic copper transport. Copper 33-39 homolog of anti-oxidant 1 Arabidopsis thaliana 108-112 15180901-1 2004 BACKGROUND: Arabidopsis thaliana copper metallochaperone CCH is a functional homologue of yeast antioxidant ATX1, involved in cytosolic copper transport. Copper 136-142 homolog of anti-oxidant 1 Arabidopsis thaliana 108-112