Prolyl 3-hydroxylase 1, enzyme characterization and identification of a novel family of enzymes
about
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaProlyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaLack of cyclophilin B in osteogenesis imperfecta with normal collagen foldingProlyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bonesProlyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complexThe prolyl 3-hydroxylases P3H2 and P3H3 are novel targets for epigenetic silencing in breast cancerCharacterization of recombinant human prolyl 3-hydroxylase isoenzyme 2, an enzyme modifying the basement membrane collagen IVIdentification of a human trans-3-hydroxy-L-proline dehydratase, the first characterized member of a novel family of proline racemase-like enzymesA novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfectaNull mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfectaProlyl 4-hydroxylaseCRTAP and LEPRE1 mutations in recessive osteogenesis imperfectaBone collagen: new clues to its mineralization mechanism from recessive osteogenesis imperfectaPost-translational hydroxylation by 2OG/Fe(II)-dependent oxygenases as a novel regulatory mechanism in bacteriaDifferential effects of collagen prolyl 3-hydroxylation on skeletal tissuesTranscriptome meta-analysis reveals a dysregulation in extra cellular matrix and cell junction associated gene signatures during Dengue virus infectionCrystal structures of wild-type and mutated cyclophilin B that causes hyperelastosis cutis in the American quarter horseCore glycosylation of collagen is initiated by two beta(1-O)galactosyltransferases.Inhibition of 2-oxoglutarate dependent oxygenasesPrediction and analysis of protein hydroxyproline and hydroxylysineA role for prolyl 3-hydroxylase 2 in post-translational modification of fibril-forming collagensSevere osteogenesis imperfecta in cyclophilin B-deficient miceDistribution and prediction of catalytic domains in 2-oxoglutarate dependent dioxygenases.Generalized connective tissue disease in Crtap-/- mouse.Procollagen triple helix assembly: an unconventional chaperone-assisted folding paradigm.Location of 3-hydroxyproline residues in collagen types I, II, III, and V/XI implies a role in fibril supramolecular assembly.CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VIIMutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.Insights on the evolution of prolyl 3-hydroxylation sites from comparative analysis of chicken and Xenopus fibrillar collagens.Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasisThe aberrance of the 4S diastereomer of 4-hydroxyproline.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.Structure of the ribosomal oxygenase OGFOD1 provides insights into the regio- and stereoselectivity of prolyl hydroxylases2-Oxoglutarate-dependent dioxygenases are sensors of energy metabolism, oxygen availability, and iron homeostasis: potential role in the regulation of aging process.A novel 3-hydroxyproline (3Hyp)-rich motif marks the triple-helical C terminus of tendon type I collagen.Chaperoning osteogenesis: new protein-folding disease paradigms.Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes.The rough endoplasmic reticulum-resident FK506-binding protein FKBP65 is a molecular chaperone that interacts with collagens.Evolutionary origins of C-terminal (GPP)n 3-hydroxyproline formation in vertebrate tendon collagen.COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke.
P2860
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P2860
Prolyl 3-hydroxylase 1, enzyme characterization and identification of a novel family of enzymes
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
name
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@ast
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en-gb
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@nl
type
label
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@ast
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en-gb
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@nl
prefLabel
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@ast
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en-gb
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@nl
P2860
P921
P3181
P356
P1476
Prolyl 3-hydroxylase 1, enzyme ...... n of a novel family of enzymes
@en
P2093
Janice A Vranka
Lynn Y Sakai
P2860
P304
P3181
P356
10.1074/JBC.M312807200
P407
P577
2004-05-28T00:00:00Z