2014
DOI: 10.1016/j.bbrc.2014.01.119
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Guanine nucleotide-binding protein subunit beta-2-like 1, a new Annexin A7 interacting protein

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Cited by 13 publications
(10 citation statements)
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“…These results indicated that ANXA7 could promote proliferation, and increase migration and invasion in mouse hepatocarcinoma cell line. The downregulating ANXA7 in the gene level by RNAi technique has been confirmed by our previous studies [4][5][6][7]9]. In this study, we showed a decreased expression of ANXA7 by using anti-ANXA7 antibody in the protein level.…”
Section: Discussionsupporting
confidence: 90%
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“…These results indicated that ANXA7 could promote proliferation, and increase migration and invasion in mouse hepatocarcinoma cell line. The downregulating ANXA7 in the gene level by RNAi technique has been confirmed by our previous studies [4][5][6][7]9]. In this study, we showed a decreased expression of ANXA7 by using anti-ANXA7 antibody in the protein level.…”
Section: Discussionsupporting
confidence: 90%
“…Our previous studies have also indicated that 33 genes, such as ANXA7, Sorcin, Gelsolin showed different expressions in both gene and protein levels in Hca-F and Hca-P cell lines [2][3][4][5][6][7][8][9].…”
Section: Introductionmentioning
confidence: 99%
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“…For 12 example, Annexin A7 formed a complex with RACK1 in mouse 13 hepatocarcinoma cells. RACK1-Annexin A7 complex had a positive 14 effects on potentials of metastasis [1]. Furthermore, Annexin A7 15 binded the binder of Arl two (BART) in pancreatic cancer cells.…”
mentioning
confidence: 99%
“…This appears to occur via a nucleotide-binding domain located in the N-terminus of nucleotide-sensitive annexins [ 46 ]. While the molecular details still remain sparse, the interaction may occur directly [ 48 ] or in the case of AnxA7, via bona fide nucleotide-binding proteins such as guanine nucleotide-binding protein subunit beta-2-like 1 (also known as the receptor for activated C kinase 1 (RACK1)) [ 49 ]. Earlier studies on the interaction of AnxA6 with nucleotides suggested the existence of two AnxA6 domains within residues 293-301 and 641-649 that potentially bind the phosphate groups of GTP [ 48 ].…”
Section: Molecular Characteristics and Anxa6-mediated Functionsmentioning
confidence: 99%