ATP5G3 Polyclonal Antibody, 100ul In vitro Transcription It is a ligand for

It is a ligand for the NKG2-D type II integral membrane protein receptor

Although this gene has been reported to map to chromosome 17 in the Smith-Magenis syndrome region| the best alignments for this gene are to chromosome 16

A germline mutation of VHL is the basis of familial inheritance of VHL syndrome

The coiled-coil motif is involved in homodimerization| the Sec7 domain contains guanine-nucleotide exchange protein (GEP) activity| and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes

Mutation in this gene

ATP5G3 Polyclonal Antibody, 100ul In vitro Transcription It is a ligand forATP5G3 (ATP synthase, H+ transporting, mitochondrial Fo complex subunit C3) encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi subunit complexes: the soluble catalytic core, F1, and the membrane spanning component, Fo, comprising the proton channel.