Search Results

Overview

Uniprot IDP49755
Protein NameTransmembrane emp24 domain-containing protein 10
Gene NameTMED10
OrganismHomo sapiens

Kla Sites from experimental identification

Position Flanking peptide
127 QLVILDMKHGVEAKN
133 MKHGVEAKNYEEIAK
143 EEIAKVEKLKPLEVE
50 CLREEIHKDLLVTGA
75 GGLRSHLKITDSAGH
87 AGHILYSKEDATKGK

Function

Cargo receptor involved in protein vesicular trafficking and quality control in the endoplasmic reticulum (ER) and Golgi (PubMed:10052452, PubMed:11726511, PubMed:16641999, PubMed:17288597, PubMed:19296914, PubMed:20427317, PubMed:21219331, PubMed:27569046). The p24 protein family is a group of transmembrane proteins that bind coat protein complex I/COPI and coat protein complex II/COPII involved in vesicular trafficking between the membranes (PubMed:10052452). Acts at the lumenal side for incorporation of secretory cargo molecules into transport vesicles and involved in vesicle coat formation at the cytoplasmic side (PubMed:20427317, PubMed:27569046). Mainly functions in the early secretory pathway and cycles between the ER, ER-Golgi intermediate compartment (ERGIC) and Golgi, mediating cargo transport through COPI and COPII-coated vesicles (PubMed:10052452, PubMed:10852829, PubMed:12237308). In COPII vesicle-mediated anterograde transport, involved in the transport of GPI-anchored proteins by acting together with TMED2 as their cargo receptor; the function specifically implies SEC24C and SEC24D of the COPII vesicle coat and lipid raft-like microdomains of the ER (PubMed:20427317, PubMed:27569046). Recognizes GPI anchors structural remodeled in the ER by the GPI inositol-deacylase/PGAP1 and the metallophosphoesterase MPPE1/PGAP5 (By similarity). In COPI vesicle-mediated retrograde transport, involved in the biogenesis of COPI vesicles and vesicle coat recruitment (PubMed:11726511). Involved in trafficking of amyloid beta A4 protein and soluble APP-beta release (independent from the modulation of gamma-secretase activity) (PubMed:17288597). Involved in the KDELR2-mediated retrograde transport of the toxin A subunit (CTX-A-K63)together with COPI and the COOH terminus of KDELR2 (By similarity). On Golgi membranes, acts as a primary receptor for ARF1-GDP, a GTP-binding protein involved in COPI-vesicle formation (PubMed:11726511). Increases coatomer-dependent GTPase-activating activity of ARFGAP2 which mediates the hydrolysis of ARF1-bound GTP and therefore modulates protein trafficking from the Golgi apparatus (PubMed:19296914). Involved in the exocytic trafficking of G protein-coupled receptors F2LR1/PAR2 (trypsin and tryspin-like enzyme receptor), OPRM1 (opioid receptor) and P2RY4 (UTD and UDP receptor) from the Golgi to the plasma membrane, thus contributing to receptor resensitization (PubMed:21219331). In addition to its cargo receptor activity, may also act as a protein channel after oligomerization, facilitating the post-translational entry of leaderless cytoplasmic cargo into the ERGIC (PubMed:32272059). Involved in the translocation into ERGIC, the vesicle entry and the secretion of leaderless cargos (lacking the secretion signal sequence), including the mature form of interleukin 1/IL-1 family members, the alpha-crystallin B chain HSPB5, the carbohydrate-binding proteins galectin-1/LGALS1 and galectin-3/LGALS3, the microtubule-associated protein Tau/MAPT, and the annexin A1/ANXA1; the translocation process is dependent on cargo protein unfolding and enhanced by chaperones HSP90AB1 and HSP90B1/GRP9 (PubMed:32272059). Could also associates with the presenilin-dependent gamma-secretase complex in order to regulate gamma-cleavages of the amyloid beta A4 protein to yield amyloid-beta 40/Abeta40 (PubMed:16641999)

Protein Sequence

10 MSGLSGPPAR 20 RGPFPLALLL 30 LFLLGPRLVL 40 AISFHLPINS 50 RKCLREEIHK 60 DLLVTGAYEI 70 SDQSGGAGGL 80 RSHLKITDSA 90 GHILYSKEDA 100 TKGKFAFTTE 110 DYDMFEVCFE 120 SKGTGRIPDQ 130 LVILDMKHGV 140 EAKNYEEIAK 150 VEKLKPLEVE 160 LRRLEDLSES 170 IVNDFAYMKK 180 REEEMRDTNE 190 STNTRVLYFS 200 IFSMFCLIGL 210 ATWQVFYLRR FFKAKKLIE

Gene Ontology

Classification GO ID Description
Cellular Component GO:0005801 cis-Golgi network
Cellular Component GO:0030137 COPI-coated vesicle
Cellular Component GO:0030134 COPII-coated ER to Golgi transport vesicle
Cellular Component GO:0005783 endoplasmic reticulum
Cellular Component GO:0005789 endoplasmic reticulum membrane
Cellular Component GO:0005793 endoplasmic reticulum-Golgi intermediate compartment
Cellular Component GO:0033116 endoplasmic reticulum-Golgi intermediate compartment membrane
Cellular Component GO:0012507 ER to Golgi transport vesicle membrane
Cellular Component GO:0070765 gamma-secretase complex
Cellular Component GO:0005794 Golgi apparatus
Cellular Component GO:0000139 Golgi membrane
Cellular Component GO:0042470 melanosome
Cellular Component GO:0016020 membrane
Cellular Component GO:0005886 plasma membrane
Cellular Component GO:0030667 secretory granule membrane
Cellular Component GO:0030140 trans-Golgi network transport vesicle
Cellular Component GO:0030133 transport vesicle
Cellular Component GO:0042589 zymogen granule membrane
Molecular Function GO:0008320 protein transmembrane transporter activity
Molecular Function GO:0019905 syntaxin binding
Biological Process GO:0048205 COPI coating of Golgi vesicle
Biological Process GO:0035964 COPI-coated vesicle budding
Biological Process GO:0048208 COPII vesicle coating
Biological Process GO:0106273 cytosol to ERGIC protein transport
Biological Process GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport
Biological Process GO:0007030 Golgi organization
Biological Process GO:0006886 intracellular protein transport
Biological Process GO:0032732 positive regulation of interleukin-1 production
Biological Process GO:0050714 positive regulation of protein secretion
Biological Process GO:0106272 protein localization to ERGIC
Biological Process GO:0045055 regulated exocytosis
Biological Process GO:1902003 regulation of amyloid-beta formation
Biological Process GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
Biological Process GO:0035459 vesicle cargo loading
Biological Process GO:0048199 vesicle targeting, to, from or within Golgi

Reference

[1] Yang Z, Yan C, Ma J, Peng P, Ren X et al.. Lactylome analysis suggests lactylation-dependent mechanisms of metabolic adaptation in hepatocellular carcinoma.. Nat Metab 5(1):61-79. 2023 Jan. PMID: 36593272.