Affinage

TRAPPC2B

Trafficking protein particle complex subunit 2B · UniProt P0DI82

Length
140 aa
Mass
16.4 kDa
Annotated
2026-06-10
3 papers in source corpus 1 papers cited in narrative 1 extracted findings
Cross-family judge vs UniProt: tie faithfulness: 2/2 claims corpus-supported (100%)

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

TRAPPC2B (SEDLP1) is a transcribed retropseudogene located on chromosome 19q13.4 with the potential to encode a protein identical to SEDL/TRAPPC2 (PMID:11031107). In the available corpus, no direct mechanistic experiment has been performed on the TRAPPC2B protein itself; the only functional data concern its parent gene SEDL/TRAPPC2, whose tagged product localizes to perinuclear structures overlapping the ER-Golgi intermediate compartment and depends on its C-terminus for proper targeting (PMID:11031107). Beyond this incidental identification of TRAPPC2B as a transcribed pseudogene (PMID:11031107), no further mechanistic detail has been characterized in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2000 Low

    Establishing whether the SEDL locus has paralogous copies, this work identified TRAPPC2B/SEDLP1 as a transcribed retropseudogene on chromosome 19q13.4 capable of encoding a protein identical to SEDL, while characterizing the parent SEDL protein's localization to the ER-Golgi intermediate compartment.

    Evidence Transient transfection of FLAG- and GFP-tagged SEDL constructs in Cos-7 cells with immunofluorescence localization; disease-mutation constructs implicating the C-terminus in targeting; genomic identification of the SEDLP1 pseudogene

    PMID:11031107

    Open questions at the time
    • No direct functional or localization experiment was performed on the TRAPPC2B protein itself
    • Whether the TRAPPC2B transcript is translated into a functional protein in vivo is unaddressed
    • All mechanistic claims (ERGIC localization, C-terminal targeting) pertain to the parent SEDL/TRAPPC2, not TRAPPC2B

Open questions

Synthesis pass · forward-looking unresolved questions
  • Whether TRAPPC2B encodes a functional protein and contributes to ER-to-Golgi transport independently of its parent gene remains unknown.
  • No TRAPPC2B-specific protein expression, localization, or interaction data exist in the corpus
  • No evidence on tissue-specific transcription or biological role of the pseudogene transcript

Mechanism profile

Synthesis pass · controlled-vocabulary classification · explore literature graph →
No controlled-vocabulary terms were assigned to this entry.

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2000 SEDL (TRAPPC2) protein, when tagged and transiently transfected into Cos-7 cells, localizes to perinuclear structures that partly overlap with the intermediate ER-Golgi compartment (ERGIC/VTC), indicating a role in ER-to-Golgi transport. SEDLP1 (TRAPPC2B) is identified as a transcribed retropseudogene on chromosome 19q13.4 with potential to encode a protein identical to SEDL. Transient transfection of FLAG- and GFP-tagged constructs in Cos-7 cells; subcellular localization by immunofluorescence; mutant constructs with disease-causing mutations (157-158delAT and C271T(STOP)) showing mislocalization to nucleus/cytoplasm, suggesting COOH-terminus mediates proper targeting Genomics Low 11031107

Source papers

Stage 0 corpus · 3 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2000 Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tarda. Genomics 41 11031107
2012 A genome-wide RNAi screen identifies novel targets of neratinib resistance leading to identification of potential drug resistant genetic markers. Molecular bioSystems 28 22446932
2012 [Cell surface display of Thermomyces lanuginosus lipase in Pichia pastoris and its characterization]. Wei sheng wu xue bao = Acta microbiologica Sinica 2 23115970

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