Post-translational modification of thrombospondin type-1 repeats in ADAMTS-like 1/punctin-1 by C-mannosylation of tryptophan.
about
A disintegrin-like and metalloprotease domain containing thrombospondin type 1 motif-like 5 (ADAMTSL5) is a novel fibrillin-1-, fibrillin-2-, and heparin-binding member of the ADAMTS superfamily containing a netrin-like moduleA disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanismsGenetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and functionInterrogating the Plasmodium Sporozoite Surface: Identification of Surface-Exposed Proteins and Demonstration of Glycosylation on CSP and TRAP by Mass Spectrometry-Based ProteomicsO-fucosylation of thrombospondin type 1 repeats restricts epithelial to mesenchymal transition (EMT) and maintains epiblast pluripotency during mouse gastrulationCrystal structure and enzymatic activity of an ADAMTS-13 mutant with the East Asian-specific P475S polymorphism.Identification of N-linked glycosylation and putative O-fucosylation, C-mannosylation sites in plasma derived ADAMTS13.In silico analysis of the fucosylation-associated genome of the human blood fluke Schistosoma mansoni: cloning and characterization of the fucosyltransferase multigene family.Whole exome sequence analysis of Peters anomaly.Effects of ADAMTS14 genetic polymorphism and cigarette smoking on the clinicopathologic development of hepatocellular carcinoma.Identification of DPY19L3 as the C-mannosyltransferase of R-spondin1 in human cellsVertebrate protein glycosylation: diversity, synthesis and function.Golgi glycosylation.Senescent intervertebral disc cells exhibit perturbed matrix homeostasis phenotype.Identification and functional analysis of an ADAMTSL1 variant associated with a complex phenotype including congenital glaucoma, craniofacial, and other systemic features in a three-generation human pedigree.Function of the CysD domain of the gel-forming MUC2 mucin.Proteogenomic analysis of the total and surface-exposed proteomes of Plasmodium vivax salivary gland sporozoites.Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome.Peters plus syndrome mutations disrupt a noncanonical ER quality-control mechanism.Novel roles for O-linked glycans in protein folding.Distinct C-mannosylation of netrin receptor thrombospondin type 1 repeats by mammalian DPY19L1 and DPY19L3.Enrichment and characterization of a bacterial mixture capable of utilizing C-mannosyl tryptophan as a carbon source.Apicomplexan C-Mannosyltransferases Modify Thrombospondin Type I-Containing Adhesins of the TRAP Family.
P2860
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P2860
Post-translational modification of thrombospondin type-1 repeats in ADAMTS-like 1/punctin-1 by C-mannosylation of tryptophan.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 11 August 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Post-translational modificatio ...... C-mannosylation of tryptophan.
@en
Post-translational modificatio ...... C-mannosylation of tryptophan.
@nl
type
label
Post-translational modificatio ...... C-mannosylation of tryptophan.
@en
Post-translational modificatio ...... C-mannosylation of tryptophan.
@nl
prefLabel
Post-translational modificatio ...... C-mannosylation of tryptophan.
@en
Post-translational modificatio ...... C-mannosylation of tryptophan.
@nl
P2093
P2860
P356
P1476
Post-translational modificatio ...... C-mannosylation of tryptophan.
@en
P2093
Christina Leonhard-Melief
Lauren W Wang
Robert S Haltiwanger
Suneel S Apte
P2860
P304
30004-30015
P356
10.1074/JBC.M109.038059
P407
P577
2009-08-11T00:00:00Z