(Q52552045)

3 May 2018

title

Calcium stabilizes fibrillin-1 against proteolytic degradation. (English)

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3 May 2018

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D P Reinhardt

1

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3 May 2018

R N Ono

series ordinal

2

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3 May 2018

L Y Sakai

series ordinal

3

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3 May 2018

language of work or name

English

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publication date

1 January 1997

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3 May 2018

Journal of Biological Chemistry

number of pages

6

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based on heuristic

inferred from page(s)

published in

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3 May 2018

volume

272

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3 May 2018

issue

2

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3 May 2018

page(s)

1231-1236

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3 May 2018

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

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Fibrillin Binds Calcium and Is Coded by cDNAs That Reveal a Multidomain Structure and Alternatively Spliced Exons at the 5′ End

21 January 2018

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Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

21 January 2018

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Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices

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Fibulin is an extracellular matrix and plasma glycoprotein with repeated domain structure

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Sequence of extracellular mouse protein BM-90/fibulin and its calcium-dependent binding to other basement-membrane ligands

21 January 2018

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Structure and expression of fibulin-2, a novel extracellular matrix protein with multiple EGF-like repeats and consensus motifs for calcium binding

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Fibulin-2 (FBLN2): human cDNA sequence, mRNA expression, and mapping of the gene on human and mouse chromosomes

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Amino acid sequence and domain structure of entactin. Homology with epidermal growth factor precursor and low density lipoprotein receptor

21 January 2018

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Isolation and sequence of the cDNA for human protein S, a regulator of blood coagulation

21 January 2018

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Nucleotide sequence from the neurogenic locus notch implies a gene product that shares homology with proteins containing EGF-like repeats

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The Caenorhabditis elegans lin-12 gene encodes a transmembrane protein with overall similarity to Drosophila Notch

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Xotch, the Xenopus homolog of Drosophila notch

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TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms

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The calcium binding properties and molecular organization of epidermal growth factor-like domains in human fibrillin-1.

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Fibrillin-1: organization in microfibrils and structural properties

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Specific EGF repeats of Notch mediate interactions with Delta and serrate: Implications for notch as a multifunctional receptor

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Fibrillin-1 and fibulin-2 interact and are colocalized in some tissues

21 January 2018

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Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils

21 January 2018

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Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders

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Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly

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Low nidogen affinity of laminin-5 can be attributed to two serine residues in EGF-like motif gamma 2III4.

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High-efficiency transformation of mammalian cells by plasmid DNA

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

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The structure of a Ca2+-binding epidermal growth factor-like domain: Its role in protein-protein interactions

21 January 2018

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Calcium binding properties of an epidermal growth factor-like domain pair from human fibrillin-1.

21 January 2018

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Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndrome

21 January 2018

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Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders

21 January 2018

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Catabolism of intact fibrillin microfibrils by neutrophil elastase, chymotrypsin and trypsin.

21 January 2018

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Haemophilia B (sixth edition): a database of point mutations and short additions and deletions

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Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome

21 January 2018

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Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome

21 January 2018

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Recurrent mis-splicing of fibrillin exon 32 in two patients with neonatal Marfan syndrome

21 January 2018

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Fibrillin domain folding and calcium binding: significance to Marfan syndrome

21 January 2018

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Partial sequence of a candidate gene for the Marfan syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.272.2.1231

1 reference

3 May 2018

1 reference

3 May 2018