Magnesium transporter subtype 1 (MAGT1) is a newly evolved and conserved magnesium membrane transporter with channel-like properties present in human epithelial cells. It has been documented that the predominant form of MAGT1 in vivo is oxidized, which is consistent with the transient formation of mixed disulfides between MAGT1 and a glycoprotein substrate. In this process, the lumenally oriented active site CVVC motif in MAGT1 is required for glycosylation of STT3B-dependent acceptor sites, which is an important mechanism to achieve N-glycosylation of cysteine proximal acceptor sites.
Basic Information of MAGT1 | |
Protein Name | Magnesium transporter protein 1 |
Gene Name | MAGT1 |
Aliases | Implantation-associated protein |
Organism | Homo sapiens (Human) |
UniProt ID | Q9H0U3 |
TransmMAGT1rane Times | 4 |
Length (aa) | 335 |
Sequence | MAARWRFWCVSVTMVVALLIVCDVPSASAQRKKEMVLSEKVSQLMEWTNKRPVIRMNGDKFRRLVKAPPRNYSVIVMFTALQLHRQCVVCKQADEEFQILANSWRYSSAFTNRIFFAMVDFDEGSDVFQMLNMNSAPTFINFPAKGKPKRGDTYELQVRGFSAEQIARWIADRTDVNIRVIRPPNYAGPLMLGLLLAVIGGLVYLRRSNMEFLFNKTGWAFAALCFVLAMTSGQMWNHIRGPPYAHKNPHTGHVNYIHGSSQAQFVAETHIVLLFNGGVTLGMVLLCEAATSDMDIGKRKIMCVAGIGLVVLFFSWMLSIFRSKYHGYPYSFLMS |
The basic function of MAGT1 is believed to import Mg2+ into the cytoplasm. Magnesium (Mg2+) has been reported to exert regulatory functions in immune cells, thereby affecting proliferation, cell cycle, and differentiation. Recently, Mg2+ transporters and channels have been identified to regulate Mg2+ homeostasis in T lymphocytes. Among them, MAGT1 has been proposed to play a key role in the regulation of free cytoplasmic magnesium concentration and is associated with X-linked immunodeficiency and Mg2+ deficiency, EBV infection and neoplasia syndrome. Patients who are deficient in MAGT1 often exhibit chronic EBV infection, which may induce EBV-associated lymphoproliferative disorders, such as Hodgkin, Burkitt or non-Hodgkin B-cell lymphoma. In addition, MAGT1 can catalyze the cotranslational transfer of high-mannose sugars to nascent polypeptides during N-linked glycosylation in the rough endoplasmic reticulum lumen.
Fig.1 The top panel shows the MAGTs transmembrane domain (TM), the actuator domain (A), the phosphorylation domain (P) and the nucleotide-binding domain (N). MAGT transports Mg2+ ions to the cytoplasm as a function of ATP hydrolysis, and (m) represents an unknown stoichiometry. (Subramani, 2016)
This article finds that proteins involved in the transcellular Ca2+ and Mg2+ transport pathways increase, while the expression of paracellular transporters remains unchanged during lactation.
This article suggests that MagT1 is a major magnesium transporter/channel that is deeply involved in the development of flies by affecting developmental signaling pathways.
This study demonstrates for the first time that abolishing MAGT1 function leads to imbalances in cation homeostasis and developmental responses in B cells.
This article shows that the mgtE protein provides the primary pathway for magnesium import in Bacillus subtilis and that other putative transporters may be used for more specialized growth conditions.
This article suggests that Mg2+ transported by OsMGT1 in the root mature region enhances the activity of OsHKT1; 5 and restricts the accumulation of Na on the shoots.
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