(Q53628160)

16 May 2018

title

Ca2+-dependent interface formation in fibrillin-1. (English)

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16 May 2018

author

Sacha Jensen

1

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16 May 2018

Christina Redfield

4

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16 May 2018

author name string

Adam R Corbett

2

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16 May 2018

Vroni Knott

3

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16 May 2018

Penny A Handford

5

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16 May 2018

language of work or name

English

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publication date

13 January 2005

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16 May 2018

Journal of Biological Chemistry

published in

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16 May 2018

volume

280

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16 May 2018

issue

14

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16 May 2018

page(s)

14076-14084

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16 May 2018

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

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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

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

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Extraction of extendable beaded structures and their identification as fibrillin-containing extracellular matrix microfibrils

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Solution structure and dynamics of a calcium binding epidermal growth factor-like domain pair from the neonatal region of human fibrillin-1

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Calcium stabilizes fibrillin-1 against proteolytic degradation.

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EGF-like domain calcium affinity modulated by N-terminal domain linkage in human fibrillin-1.

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Fibrillin-1: organization in microfibrils and structural properties

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A Gly --> Ser change causes defective folding in vitro of calcium-binding epidermal growth factor-like domains from factor IX and fibrillin-1.

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21 January 2018

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Structural consequences of cysteine substitutions C1977Y and C1977R in calcium-binding epidermal growth factor-like domain 30 of human fibrillin-1.

21 January 2018

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Structure of the integrin binding fragment from fibrillin-1 gives new insights into microfibril organization

21 January 2018

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Effects of the N2144S mutation on backbone dynamics of a TB-cbEGF domain pair from human fibrillin-1.

21 January 2018

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The high affinity calcium-binding sites in the epidermal growth factor module region of vitamin K-dependent protein S.

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Metal ion dependency of microfibrils supports a rod-like conformation for fibrillin-1 calcium-binding epidermal growth factor-like domains

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Mutations in calcium-binding epidermal growth factor modules render fibrillin-1 susceptible to proteolysis. A potential disease-causing mechanism in Marfan syndrome

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Solution structure of the transforming growth factor beta-binding protein-like module, a domain associated with matrix fibrils

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Fibrillin-1, a calcium binding protein of extracellular matrix

21 January 2018

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

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RASMOL: biomolecular graphics for all

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M412832200

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16 May 2018

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16 May 2018