pathway Info Card

Membrane Docking

Information about Membrane Docking: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Membrane Docking

Most recent studies have shown that Membrane Docking shares some biological mechanisms with acrosome-reaction, autophagy, cell-activation, cell-adhesion, diapedesis, endocytosis, exocytosis, lipid-binding, localization, membrane-fusion, prenylation, protein-import, regulation-of-protein-phosphorylation, secretion, secretory-pathway, snare-complex-assembly, t-cell-activation, transport, vesicle-docking, vesicle-fusion.

Among the many pathways, these few ones have gauged particular interests from scientists studying Membrane Docking, and have been seen in publications frequently: acrosome-reaction, autophagy, cell-activation, cell-adhesion, diapedesis, endocytosis, exocytosis, lipid-binding, localization, membrane-fusion, prenylation, protein-import, regulation-of-protein-phosphorylation, secretion, secretory-pathway, snare-complex-assembly, t-cell-activation, transport, vesicle-docking, vesicle-fusion

Quite a number of genes have been found to play important roles in Membrane Docking, such as C2, EEA1, HNRNPC, KAT5, PEX14, PLA2G4A, PLEK, RAB5A, RABEP1, SLC2A4, SNAP23, SNAP25, STXBP3, SYT1, VAMP2, VTI1B. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this pathway. Plesae stay updated.