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CA2 — VDAC2

Text-mined interactions from Literome

Báthori et al., J Biol Chem 2006 : Ca2+ dependent control of the permeability properties of the mitochondrial outer membrane and voltage dependent anion-selective channel ( VDAC ) ... Recognizing that the bilayer studies had been commonly conducted at supraphysiological [Ca2+ ] and [ K+ ], we determined the effect of Ca2+ on VDAC activity
Deniaud et al., Oncogene 2008 (Calcium Signaling) : The specificity of this apoptosis pathway was validated in cells using a panel of pharmacological agents that chelate Ca2+ ( BAPTA-AM ) or inhibit inositol-1,4,5-trisphosphate receptor ( IP(3)R; 2-aminoethoxydiphenyl borate ), voltage dependent anion channel ( VDAC) (4,4'-diisothiocyanatostilbene-2,2'-disulfonate, NADH ), the permeability transition pore ( cyclosporin A and bongkrekic acid ), caspases ( z-VAD-fmk ) and protein synthesis ( cycloheximide )