(Q24535911)

6 July 2017

title

A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme (English)

1 reference

6 July 2017

7

Kurt von Figura

0 references

Andrea Preusser-Kunze

2

object named as

Andrea Preusser-Kunze

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author name string

Dirk Roeser

1

1 reference

6 July 2017

Andrea Preusser-Kunze

2

1 reference

6 July 2017

Bernhard Schmidt

3

1 reference

6 July 2017

Kathrin Gasow

4

1 reference

6 July 2017

Julia G Wittmann

5

1 reference

6 July 2017

Thomas Dierks

6

1 reference

6 July 2017

Markus Georg Rudolph

8

1 reference

6 July 2017

language of work or name

English

0 references

publication date

20 December 2005

1 reference

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

6 July 2017

published in

1 reference

6 July 2017

volume

103

1 reference

6 July 2017

issue

1

1 reference

6 July 2017

page(s)

81-86

1 reference

Sulphatase activities are regulated by the interaction of sulphatase-modifying factor 1 with SUMF2

6 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

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24 March 2017

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Structure of Rab escort protein-1 in complex with Rab geranylgeranyltransferase

24 March 2017

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Crystal structures of two rat MHC class Ia (RT1-A) molecules that are associated differentially with peptide transporter alleles TAP-A and TAP-B

24 March 2017

1 reference

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Structure of myohemerythrin in the azidomet state at 1.7/1.3 A resolution

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Free R value: a novel statistical quantity for assessing the accuracy of crystal structures

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

The CCP4 suite: programs for protein crystallography

24 March 2017

1 reference

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Raster3D Version 2.0. A program for photorealistic molecular graphics

24 March 2017

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The atomic structure of protein-protein recognition sites

24 March 2017

1 reference

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An extensively modified version of MolScript that includes greatly enhanced coloring capabilities

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Shape complementarity at protein/protein interfaces

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Satisfying hydrogen bonding potential in proteins

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Oxygenases without requirement for cofactors or metal ions

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Identification of 16 sulfamidase gene mutations including the common R74C in patients with mucopolysaccharidosis type IIIA (Sanfilippo A)

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

The molecular surface package

24 March 2017

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.0507592102

De novo calcium/sulfur SAD phasing of the human formylglycine-generating enzyme using in-house data

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Expression, localization, structural, and functional characterization of pFGE, the paralog of the Calpha-formylglycine-generating enzyme

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Crystal structure of human pFGE, the paralog of the Calpha-formylglycine-generating enzyme

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Molecular characterization of the human Calpha-formylglycine-generating enzyme

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Structural and thermodynamic correlates of T cell signaling

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Molecular basis of iduronate-2-sulphatase gene mutations in patients with mucopolysaccharidosis type II (Hunter syndrome).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Conversion of cysteine to formylglycine: a protein modification in the endoplasmic reticulum

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Characterization of posttranslational formylglycine formation by luminal components of the endoplasmic reticulum

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0507592102

Antibody catalysis of the oxidation of water

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0507592102

A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1324989

Detection of four novel mutations in the iduronate-2-sulfatase gene. Mutations in brief no. 123. Online

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16368756

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16368756

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0507592102

1 reference

OpenCitations bibliographic resource ID

6 July 2017

0 references

2310853

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

6 July 2017

1 reference