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Molecular cloning and primary structure of Kell blood group protein

Molecular cloning and primary structure of Kell blood group protein

http://www.wikidata.org/entity/Q33264546

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The Kell protein of the common K2 phenotype is a catalytically active metalloprotease, whereas the rare Kell K1 antigen is inactive. Identification of novel substrates for the Kell protein Organization and chromosomal localization of the human ECEL1 (XCE) gene encoding a zinc metallopeptidase involved in the nervous control of respiration Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens Crystal Structure of Mycobacterium tuberculosis Zinc-dependent Metalloprotease-1 (Zmp1), a Metalloprotease Involved in Pathogenicity Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens A fourth isoform of endothelin-converting enzyme (ECE-1) is generated from an additional promoter molecular cloning and characterization FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization Constitutive phosphorylation of human endothelin-converting enzyme-1 isoforms Transcriptional regulation of the KEL gene and Kell protein expression in erythroid and non-erythroid cells Biochemical and physical characterisation of urinary nanovesicles following CHAPS treatment Molecular identification and characterization of novel membrane-bound metalloprotease, the soluble secreted form of which hydrolyzes a variety of vasoactive peptides Neprilysin degrades both amyloid beta peptides 1-40 and 1-42 most rapidly and efficiently among thiorphan- and phosphoramidon-sensitive endopeptidases Neonatal lethality in mice deficient in XCE, a novel member of the endothelin-converting enzyme and neutral endopeptidase family A three-dimensional model of the neprilysin 2 active site based on the X-ray structure of neprilysin. Identification of residues involved in substrate hydrolysis and inhibitor binding of neprilysin 2 Cell-specific activity of neprilysin 2 isoforms and enzymic specificity compared with neprilysin Association of XK and Kell blood group proteins Structural and functional impacts of amino acid substitutions that create blood group antigens: implications for immunogenicity.Dynamic changes in the secondary structure of ECE-1 and XCE account for their different substrate specificities.The neprilysin (NEP) family of zinc metalloendopeptidases: genomics and function.Kell expression on myeloid progenitor cells.Transient loss of proteins carrying Kell and Lutheran red cell antigens during consecutive relapses of autoimmune thrombocytopenia.Identification of an endothelin-converting enzyme-2-specific fluorigenic substrate and development of an in vitro and ex vivo enzymatic assay Insights into the Holley- and Joseph- phenotypes.Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.Families of zinc metalloproteases.Resolution of translation start site for the human Kell glycoprotein.Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic rickets.Molecular Basis of KELnull Phenotype in Brazilians.Characterization of human blood group scFv antibodies derived from a V gene phage-display library.The value of DNA analysis for antigens of the Kell and Kx blood group systems.Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETI Another example of a KEL1 variant red cell phenotype due to a threonine to serine change at position 193 of Kell glycoprotein.Xkr8 phospholipid scrambling complex in apoptotic phosphatidylserine exposure.Advances In Mycobacterium Tuberculosis Therapeutics Discovery Utlizing Structural Biology.Endothelin-3-converting enzyme activity of the KEL1 and KEL6 phenotypes of the Kell blood group system.Targeting SOX17 in human embryonic stem cells creates unique strategies for isolating and analyzing developing endoderm Expression profiles of mouse Kell, XK, and XPLAC mRNA.Blood group antigens defined by the amino acid sequences of red cell surface proteins.Overexpression of Phex in osteoblasts fails to rescue the Hyp mouse phenotype.Molecular defects underlying the Kell null phenotype.

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P2860

Molecular cloning and primary structure of Kell blood group protein

http://www.wikidata.org/entity/Q33264546

description

1991 nî lūn-bûn

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1991 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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1991 թվականի հուլիսին հրատարակված գիտական հոդված

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1991年の論文

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1991年論文

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1991年論文

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1991年論文

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1991年論文

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1991年論文

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1991年论文

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name

Molecular cloning and primary structure of Kell blood group protein

@ast

Molecular cloning and primary structure of Kell blood group protein

@en

Molecular cloning and primary structure of Kell blood group protein.

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type

label

Molecular cloning and primary structure of Kell blood group protein

@ast

Molecular cloning and primary structure of Kell blood group protein

@en

Molecular cloning and primary structure of Kell blood group protein.

@nl

prefLabel

Molecular cloning and primary structure of Kell blood group protein

@ast

Molecular cloning and primary structure of Kell blood group protein

@en

Molecular cloning and primary structure of Kell blood group protein.

@nl

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PNAS.88.14.6353

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Molecular cloning and primary structure of Kell blood group protein

@en

P2093

C M Redman

http://www.w3.org/2001/XMLSchema#string

E D Zambas

http://www.w3.org/2001/XMLSchema#string

S Lee

http://www.w3.org/2001/XMLSchema#string

W L Marsh

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P2860

DNA sequencing with chain-terminating inhibitors

Common acute lymphoblastic leukemia antigen (CALLA) is active neutral endopeptidase 24.11 ("enkephalinase"): direct evidence by cDNA transfection analysis

Organization of the gene encoding common acute lymphoblastic leukemia antigen (neutral endopeptidase 24.11): multiple miniexons and separate 5' untranslated regions

Improved tools for biological sequence comparison.

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

A simple method for displaying the hydropathic character of a protein

Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing

Molecular cloning and amino acid sequence of rat enkephalinase

Eukaryotic transcriptional regulatory proteins

Predicting the orientation of eukaryotic membrane-spanning proteins.

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6353-6357

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14

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1712490

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protein structure

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52081

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