Hsp47 and cyclophilin B traverse the endoplasmic reticulum with procollagen into pre-Golgi intermediate vesicles. A role for Hsp47 and cyclophilin B in the export of procollagen from the endoplasmic reticulum.
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Lack of cyclophilin B in osteogenesis imperfecta with normal collagen foldingProteomics of endoplasmic reticulum-Golgi intermediate compartment (ERGIC) membranes from brefeldin A-treated HepG2 cells identifies ERGIC-32, a new cycling protein that interacts with human Erv46Developmental regulation of FKBP65. An ER-localized extracellular matrix binding-proteinHaploinsufficiency of RanBP2 is neuroprotective against light-elicited and age-dependent degeneration of photoreceptor neuronsFrom Drosophila to humans: reflections on the roles of the prolyl isomerases and chaperones, cyclophilins, in cell function and diseaseIdentification of two CyP-40-like cyclophilins in Saccharomyces cerevisiae, one of which is required for normal growth.The molecular interactions of heat shock protein 47 (Hsp47) and their implications for collagen biosynthesisNascent lipidated apolipoprotein B is transported to the Golgi as an incompletely folded intermediate as probed by its association with network of endoplasmic reticulum molecular chaperones, GRP94, ERp72, BiP, calreticulin, and cyclophilin BSevere osteogenesis imperfecta in cyclophilin B-deficient miceActivation of CD147 with cyclophilin a induces the expression of IFITM1 through ERK and PI3K in THP-1 cells.Developmental regulation and coordinate reexpression of FKBP65 with extracellular matrix proteins after lung injury suggest a specialized function for this endoplasmic reticulum immunophilin.An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1·cartilage-associated protein·cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.Chaperoning osteogenesis: new protein-folding disease paradigms.Redistribution of cyclophilin A to viral factories during vaccinia virus infection and its incorporation into mature particlesMolecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta.Identification of tropoelastin as a ligand for the 65-kD FK506-binding protein, FKBP65, in the secretory pathway.Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix.Cyclophilin B enhances HIV-1 infectionPPIB mutations cause severe osteogenesis imperfecta.New perspectives on osteogenesis imperfectaThe ubiquitin-proteasome system in retinal health and disease.Exposure to tetrabromobisphenol A induces cellular dysfunction in osteoblastic MC3T3-E1 cells.Mechanism of resistance of hepatitis C virus replicons to structurally distinct cyclophilin inhibitors.Change in cellular localization of a rheumatoid arthritis-related antigen (RA-A47) with downregulation upon stimulation by inflammatory cytokines in chondrocytes.Hsp47 binds to the KDEL receptor and cell surface expression is modulated by cytoplasmic and endosomal pH.Deletion of the collagen-specific molecular chaperone Hsp47 causes endoplasmic reticulum stress-mediated apoptosis of hepatic stellate cells.Mapping Hsp47 binding site(s) using CNBr peptides derived from type I and type II collagen.Cloning and biochemical characterization of the cyclophilin homologues from the free-living nematode Caenorhabditis elegans.A substrate preference for the rough endoplasmic reticulum resident protein FKBP22 during collagen biosynthesis.Cyclophilin B mediates cyclosporin A incorporation in human blood T-lymphocytes through the specific binding of complexed drug to the cell surface.Mutation in cyclophilin B that causes hyperelastosis cutis in American Quarter Horse does not affect peptidylprolyl cis-trans isomerase activity but shows altered cyclophilin B-protein interactions and affects collagen foldingStructure-function studies on hsp47: pH-dependent inhibition of collagen fibril formation in vitro.The pH sensitivity of murine heat shock protein 47 (HSP47) binding to collagen is affected by mutations in the breach histidine cluster.Bergenin increases osteogenic differentiation and prevents methylglyoxal-induced cytotoxicity in MC3T3-E1 osteoblasts.
P2860
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P2860
Hsp47 and cyclophilin B traverse the endoplasmic reticulum with procollagen into pre-Golgi intermediate vesicles. A role for Hsp47 and cyclophilin B in the export of procollagen from the endoplasmic reticulum.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Hsp47 and cyclophilin B traver ...... rom the endoplasmic reticulum.
@en
type
label
Hsp47 and cyclophilin B traver ...... rom the endoplasmic reticulum.
@en
prefLabel
Hsp47 and cyclophilin B traver ...... rom the endoplasmic reticulum.
@en
P2093
P2860
P356
P1476
Hsp47 and cyclophilin B traver ...... rom the endoplasmic reticulum.
@en
P2093
P2860
P304
18323-18328
P356
10.1074/JBC.270.31.18323
P407
P577
1995-08-01T00:00:00Z