Molecular recognition in the assembly of collagens: terminal noncollagenous domains are key recognition modules in the formation of triple helical protomers.
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Aegyptin displays high-affinity for the von Willebrand factor binding site (RGQOGVMGF) in collagen and inhibits carotid thrombus formation in vivoThree novel collagen VI chains, alpha4(VI), alpha5(VI), and alpha6(VI)Collagen structure and stabilityThe molecular structure of human tissue type XV presents a unique conformation among the collagensRNA protein interactions governing expression of the most abundant protein in human body, type I collagenRole of the podocyte (and glomerular endothelium) in building the GBMUbiquitous amyloidsCol4a1 mutations cause progressive retinal neovascular defects and retinopathySolution Structure of an ABC Collagen Heterotrimer Reveals a Single-register Helix Stabilized by Electrostatic InteractionsCrystal Structure of Human Collagen XVIII Trimerization Domain: A Novel Collagen Trimerization FoldCrystal structure of the human collagen XV trimerization domain: A potent trimerizing unit common to multiplexin collagensStructural Insights into Charge Pair Interactions in Triple Helical Collagen-like ProteinsDiversity, Structures, and Collagen-Degrading Mechanisms of Bacterial Collagenolytic ProteasesMammalian collagen IVBacterial collagen-like proteins that form triple-helical structuresMutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patients.Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta.The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature.Expanding the family of collagen proteins: recombinant bacterial collagens of varying composition form triple-helices of similar stability.Identification of the NC1 domain of {alpha}3 chain as critical for {alpha}3{alpha}4{alpha}5 type IV collagen network assembly.Vitamin a deficiency and alterations in the extracellular matrix.Spatio-temporal modification of collagen scaffolds mediated by triple helical propensity.Dissecting a bacterial collagen domain from Streptococcus pyogenes: sequence and length-dependent variations in triple helix stability and folding.COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta.A novel functional role of collagen glycosylation: interaction with the endocytic collagen receptor uparap/ENDO180Hypohalous acids contribute to renal extracellular matrix damage in experimental diabetesCOL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke.COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.Glomerular basement membrane and related glomerular diseaseAkt mediated phosphorylation of LARP6; critical step in biosynthesis of type I collagen.Mapping structural landmarks, ligand binding sites, and missense mutations to the collagen IV heterotrimers predicts major functional domains, novel interactions, and variation in phenotypes in inherited diseases affecting basement membranes.Thrombogenic collagen-mimetic peptides: Self-assembly of triple helix-based fibrils driven by hydrophobic interactions.A role for collagen IV cross-links in conferring immune privilege to the Goodpasture autoantigen: structural basis for the crypticity of B cell epitopes.Type IV collagen-derived angiogenesis inhibitorsNonmuscle myosin-dependent synthesis of type I collagen.Extracellular chloride signals collagen IV network assembly during basement membrane formationIdentification and characterization of CTRP9, a novel secreted glycoprotein, from adipose tissue that reduces serum glucose in mice and forms heterotrimers with adiponectinNanoscale protein architecture of the kidney glomerular basement membrane.Trimeric reassembly of the globular domain of human C1qCOL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome.
P2860
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P2860
Molecular recognition in the assembly of collagens: terminal noncollagenous domains are key recognition modules in the formation of triple helical protomers.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Molecular recognition in the a ...... n of triple helical protomers.
@ast
Molecular recognition in the a ...... n of triple helical protomers.
@en
type
label
Molecular recognition in the a ...... n of triple helical protomers.
@ast
Molecular recognition in the a ...... n of triple helical protomers.
@en
prefLabel
Molecular recognition in the a ...... n of triple helical protomers.
@ast
Molecular recognition in the a ...... n of triple helical protomers.
@en
P2093
P2860
P356
P1476
Molecular recognition in the a ...... on of triple helical protomers
@en
P2093
Arthur Veis
Jamshid Khoshnoodi
Jean-Philippe Cartailler
P2860
P304
38117-38121
P356
10.1074/JBC.R600025200
P407
P577
2006-11-02T00:00:00Z