The X-ray crystal structures of human alpha-phosphomannomutase 1 reveal the structural basis of congenital disorder of glycosylation type 1a
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Analysis of the Structural Determinants Underlying Discrimination between Substrate and Solvent in β-Phosphoglucomutase Catalysis † ‡Bacillus cereus Phosphopentomutase Is an Alkaline Phosphatase Family Member That Exhibits an Altered Entry Point into the Catalytic CycleThe X-ray crystallographic structure and specificity profile of HAD superfamily phosphohydrolase BT1666: Comparison of paralogous functions inB. thetaiotaomicronEvolutionary and Structural Analyses of Mammalian Haloacid Dehalogenase-type Phosphatases AUM and Chronophin Provide Insight into the Basis of Their Different Substrate SpecificitiesHigh-resolution structure of an atypical α-phosphoglucomutase related to eukaryotic phosphomannomutasesConformational response to ligand binding in phosphomannomutase2: insights into inborn glycosylation disorder.Molecular analysis of phosphomannomutase (PMM) genes reveals a unique PMM duplication event in diverse Triticeae species and the main PMM isozymes in bread wheat tissues.Panoramic view of a superfamily of phosphatases through substrate profilingPhosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblasts.Effect of Temperature Downshift on the Transcriptomic Responses of Chinese Hamster Ovary Cells Using Recombinant Human Tissue Plasminogen Activator Production Culture.Synaptic roles for phosphomannomutase type 2 in a new Drosophila congenital disorder of glycosylation disease modelConsequences of domain insertion on sequence-structure divergence in a superfold.Molecular dynamics simulations reveal that Tyr-317 phosphorylation reduces Shc binding affinity for phosphotyrosyl residues of epidermal growth factor receptorTowards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.Beyond structural genomics: computational approaches for the identification of ligand binding sites in protein structures.Expression analysis revealing destabilizing mutations in phosphomannomutase 2 deficiency (PMM2-CDG): expression analysis of PMM2-CDG mutations.Mammalian phosphomannomutase PMM1 is the brain IMP-sensitive glucose-1,6-bisphosphataseBiochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylationPhosphoglucomutase is absent in Trypanosoma brucei and redundantly substituted by phosphomannomutase and phospho-N-acetylglucosamine mutase.Production and crystallization of α-phosphoglucomutase from Lactococcus lactis.The molecular landscape of phosphomannose mutase deficiency in iberian peninsula: identification of 15 population-specific mutationsStructure-guided approach for detecting large domain inserts in protein sequences as illustrated using the haloacid dehalogenase superfamily.A qualitative description of the peptide sharing between poliovirus and Homo sapiens.A Temperature-sensitive mutation in the Arabidopsis thaliana phosphomannomutase gene disrupts protein glycosylation and triggers cell death.A mutant of phosphomannomutase1 retains full enzymatic activity, but is not activated by IMP: Possible implications for the disease PMM2-CDG.The Effects of PMM2-CDG-Causing Mutations on the Folding, Activity, and Stability of the PMM2 Protein.Molecular cloning and functional analysis of the phosphomannomutase (PMM) gene from Dendrobium officinale and evidence for the involvement of an abiotic stress response during germination.DFT investigation on the reaction mechanism catalyzed by α-phosphomannomutase1 in protonated/deprotonated states.The α-Phosphoglucomutase ofLactococcus lactisIs Unrelated to the α-d-Phosphohexomutase Superfamily and Is Encoded by the Essential GenepgmHCongenital Disorder of Glycosylation Type Ia: Searching for the Origin of Common Mutations inPMM2
P2860
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P2860
The X-ray crystal structures of human alpha-phosphomannomutase 1 reveal the structural basis of congenital disorder of glycosylation type 1a
description
2006 nî lūn-bûn
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2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
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
name
The X-ray crystal structures o ...... order of glycosylation type 1a
@ast
The X-ray crystal structures o ...... order of glycosylation type 1a
@en
The X-ray crystal structures o ...... order of glycosylation type 1a
@en-gb
The X-ray crystal structures o ...... order of glycosylation type 1a
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type
label
The X-ray crystal structures o ...... order of glycosylation type 1a
@ast
The X-ray crystal structures o ...... order of glycosylation type 1a
@en
The X-ray crystal structures o ...... order of glycosylation type 1a
@en-gb
The X-ray crystal structures o ...... order of glycosylation type 1a
@nl
prefLabel
The X-ray crystal structures o ...... order of glycosylation type 1a
@ast
The X-ray crystal structures o ...... order of glycosylation type 1a
@en
The X-ray crystal structures o ...... order of glycosylation type 1a
@en-gb
The X-ray crystal structures o ...... order of glycosylation type 1a
@nl
P2093
P2860
P921
P356
P1476
The X-ray crystal structures o ...... order of glycosylation type 1a
@en
P2093
Chunchun Zhang
Jianying Dai
Nicholas R Silvaggi
Zhibing Lu
P2860
P304
P356
10.1074/JBC.M601505200
P407
P577
2006-05-26T00:00:00Z