Ontology highlight
ABSTRACT:
SUBMITTER: Granero-Molto F
PROVIDER: S-EPMC2459293 | biostudies-literature | 2008 Jul
REPOSITORIES: biostudies-literature
Granero-Moltó Froilán F Sarmah Swapnalee S O'Rear Lynda L Spagnoli Anna A Abrahamson Dale D Saus Juan J Hudson Billy G BG Knapik Ela W EW
The Journal of biological chemistry 20080418 29
Human Goodpasture antigen-binding protein (GPBP) is an atypical protein kinase that phosphorylates the Goodpasture auto-antigen, the alpha3 chain of collagen IV. The COL4A3BP gene is alternatively spliced producing two protein isoforms: GPBP and GPBPDelta26. The latter lacks a serine-rich domain composed of 26 amino acid residues. Both isoforms also function as ceramide transfer proteins (CERT). Here, we explored the function of Gpbp and GpbpDelta26/CERT during embryogenesis in zebrafish. We clo ...[more]