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ProteinQ21114011· pop 5· linked from 359 articles

CD1e molecule

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Also known as hCD1e, differentiation antigen CD1-alpha-3, T-cell surface glycoprotein CD1e, membrane-associated, CD1E, leukocyte differentiation antigen, CD1E antigen, e polypeptide, R2G1, thymocyte antigen CD1E

T-cell surface glycoprotein CD1e, membrane-associated is a protein that in humans is encoded by the CD1E gene.

Protein · UniProt

T-cell surface glycoprotein CD1e, membrane-associated

Gene
CD1E
Organism
Homo sapiens (Human)
Length
388 aa
Molecular mass
43,626 Da
Evidence
1: Evidence at protein level

T-cell surface glycoprotein CD1e, soluble binds diacetylated lipids, including phosphatidyl inositides and diacylated sulfoglycolipids, and is required for the presentation of glycolipid antigens on the cell surface. The membrane-associated form is not active

3D-structureAdaptive immunityAlternative splicingDisulfide bondEndosomeGlycoproteinGolgi apparatusImmunity
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Swiss-Prot (reviewed) · via UniProt

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T-cell surface glycoprotein CD1e, membrane-associated is a protein that in humans is encoded by the CD1E gene.

This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes within Golgi compartments, endosomes, and lysosomes, and is cleaved into a stable soluble form. The soluble form is required for the intracellular processing of some glycolipids into a form that can be presented by other CD1 family members. Several alternatively spliced transcript variants encoding different isoforms have been described. Additional transcript variants have been found; however, their biological validity has not been determined.

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