Heat shock protein 47 and 65-kDa FK506-binding protein weakly but synergistically interact during collagen folding in the endoplasmic reticulum

Ziploc-ing the structure 2.0: Endoplasmic reticulum-resident peptidyl prolyl isomerases show different activities toward hydroxyproline

(2017) Yoshihiro Ishikawa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen

(2017) Ivan Duran et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Regulation of Calcium Homeostasis by ER Redox: A Close-Up of the ER/Mitochondria Connection

(2017) Alexander L. Chernorudskiy et al.   JOURNAL OF MOLECULAR BIOLOGY

Biology of Hsp47 (Serpin H1), a collagen-specific molecular chaperone

(2017) Shinya Ito et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Mapping the Interactome of a Major Mammalian Endoplasmic Reticulum Heat Shock Protein 90

(2017) Feng Hong et al.   PLoS One

FKBP65-dependent peptidyl-prolyl isomerase activity potentiates the lysyl hydroxylase 2-driven collagen cross-link switch

(2017) Yulong Chen et al.   Scientific Reports

Molecular insights into prolyl and lysyl hydroxylation of fibrillar collagens in health and disease

(2016) Rutger A. F. Gjaltema et al.   CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY

Cyclophilin-B Modulates Collagen Cross-linking by Differentially Affecting Lysine Hydroxylation in the Helical and Telopeptidyl Domains of Tendon Type I Collagen

(2016) Masahiko Terajima et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2

(2016) Rutger A. F. Gjaltema et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Intracellular mechanisms of molecular recognition and sorting for transport of large extracellular matrix molecules

(2016) Yoshihiro Ishikawa et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Co- and Post-Translational Protein Folding in the ER

(2016) Lars Ellgaard et al.   TRAFFIC

Ziploc-ing the structure: Triple helix formation is coordinated by rough endoplasmic reticulum resident PPIases

(2015) Yoshihiro Ishikawa et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Osteogenesis imperfecta due to mutations in non-collagenous genes

(2014) Joan C. Marini et al.   CURRENT OPINION IN PEDIATRICS

Connective tissue alterations in Fkbp10−/− mice

(2014) Caressa D. Lietman et al.   HUMAN MOLECULAR GENETICS

HSP47 and FKBP65 cooperate in the synthesis of type I procollagen

(2014) Ivan Duran et al.   HUMAN MOLECULAR GENETICS

A Substrate Preference for the Rough Endoplasmic Reticulum Resident Protein FKBP22 during Collagen Biosynthesis

(2014) Yoshihiro Ishikawa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Elastin Binding Protein and FKBP65 Modulate in Vitro Self-Assembly of Human Tropoelastin

(2013) Ming Miao et al.   BIOCHEMISTRY

Orchestration of secretory protein folding by ER chaperones

(2013) Tali Gidalevitz et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

A molecular ensemble in the rER for procollagen maturation

(2013) Yoshihiro Ishikawa et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype ofFKBP10  Mutations

(2013) Aileen M. Barnes et al.   HUMAN MUTATION

Posttranslational Modifications in Type I Collagen from Different Tissues Extracted from Wild Type and Prolyl 3-Hydroxylase 1 Null Mice

(2013) Elena Pokidysheva et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Concave Face of Decorin Mediates Reversible Dimerization and Collagen Binding

(2013) Mehwaesh Islam et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

(2012) U. Schwarze et al.   HUMAN MOLECULAR GENETICS

An Interaction Map of Endoplasmic Reticulum Chaperones and Foldases

(2012) Gregor Jansen et al.   MOLECULAR & CELLULAR PROTEOMICS

A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta

(2012) Masaki Takagi et al.   PLoS One

Molecular basis for the action of the collagen-specific chaperone Hsp47/SERPINH1 and its structure-specific client recognition

(2012) C. Widmer et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Endoplasmic reticulum stress or mutation of an EF-hand Ca2+-binding domain directs the FKBP65 rotamase to an ERAD-based proteolysis

(2011) Lindsey A. Murphy et al.   CELL STRESS & CHAPERONES

Serpin structure, function and dysfunction

(2011) J. A. HUNTINGTON   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Protein Folding and Quality Control in the ER

(2011) K. Araki et al.   Cold Spring Harbor Perspectives in Biology

Endoplasmic-Reticulum Calcium Depletion and Disease

(2011) D. Mekahli et al.   Cold Spring Harbor Perspectives in Biology

Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta

(2010) Yasemin Alanay et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta

(2010) Helena E. Christiansen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Effect of FKBP65, a putative elastin chaperone, on the coacervation of tropoelastin in vitro

(2010) Kevin L.Y. Cheung et al.   Biochemistry and Cell Biology

Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome

(2010) Brian P Kelley et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Characterisation of serpin polymers in vitro and in vivo

(2010) Didier Belorgey et al.   METHODS

Chaperoning osteogenesis: new protein-folding disease paradigms

(2010) Elena Makareeva et al.   TRENDS IN CELL BIOLOGY

Revisiting absorbance at 230nm as a protein unfolding probe

(2009) Pei-Fen Liu et al.   ANALYTICAL BIOCHEMISTRY

Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex

(2009) Weizhong Chang et al.   HUMAN MOLECULAR GENETICS

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations

(2009) John F. Bateman et al.   NATURE REVIEWS GENETICS

The Rough Endoplasmic Reticulum-resident FK506-binding Protein FKBP65 Is a Molecular Chaperone That Interacts with Collagens

(2008) Yoshihiro Ishikawa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Crystal structure of a stable dimer reveals the molecular basis of serpin polymerization

(2008) Masayuki Yamasaki et al.   NATURE