Detail Information of Protein

Basic Information:

Symbol MOSPD2
Protein Name Motile sperm domain-containing protein 2
Species Human
Entrez ID 158747
Uniprot ID Q8NHP6
Membrane Contact Site ER-Endosome; Endosome-ER
Location (from literature) ER
Cell line/Tissue HeLa cells; HEK293T cells
Experimental Method Low throughput experimental methods
Protein Sequence
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Complex Information:

Complex ID Subunit of complex Subcellular location Species More
CMCS00013 MOSPD2; STARD3NL ER-Endosome; Endosome-ER Human more
CMCS00014 MOSPD2; STARD3 ER-Endosome; Endosome-ER Human more
CMCS00015 MOSPD2; OSBPL1A ER-Endosome; Endosome-ER Human more
CMCS00072 MOSPD2; CERT1 ER-Endosome; Endosome-ER Human more

Expression Overview of MOSPD2:

Homology Information of MOSPD2:

Uniprot ID Q8NHP6
EggNOG KOG1470
HOGENOM CLU_028924_1_0_1
OrthoDB 2168468at2759
TreeFam TF351054
GeneTree ENSGT00390000016713

References:

Pubmed ID 29858488
DOI 10.15252/embr.201745453
Description Consequently, MOSPD2 and these organelle‐bound proteins mediate the formation of contact sites between the ER and endosomes, mitochondria, or Golgi.; ll these proteins, by binding VAP proteins, are known to build contact sites between the ER and endosomes (STARD3, STARD3NL, ORP1L), mitochondria (PTPIP51), and Golgi (STARD11).
Description of experimental evidence The protein was validated by immunofluorescence, colocalization analysis, SDS–PAGE, western blot, coomassie blue staining, pull‐down assays, GFP‐Trap, mass spectrometry analysis, electron microscopy and immunoprecipitation in HeLa cells and HEK293T cells.
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Pubmed ID 33124732
DOI 10.15252/embj.2019104369
Description The endoplasmic reticulum possesses three major receptors, VAP‐A, VAP‐B, and MOSPD2, which interact with proteins at the surface of other organelles to build contacts; onventional FFATs (illustrated here with STARD11/CERT) which allow the formation of a stable complex between VAPs/MOSPD2 and thus the formation of MCSs.
Description of experimental evidence The protein was validated by pull‐down assays, immunoprecipitation,SDS–PAGE, western blot, CIP treatment, coomassie blue staining, mass spectrometry analysis, immunofluorescence and colocalization analysis in HeLa cells.
More related results

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