Insights into molecular properties of the human monocarboxylate transporter 8 by combining functional with structural information (Q35161452)

6 August 2017

title

Insights into molecular properties of the human monocarboxylate transporter 8 by combining functional with structural information (English)

1 reference

6 August 2017

Ulrich Schweizer

2

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Josef Köhrle

object named as

Josef Köhrle

4

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author name string

Gunnar Kleinau

1

1 reference

6 August 2017

Anita Kinne

3

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6 August 2017

Annette Grüters

5

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6 August 2017

Heiko Krude

6

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6 August 2017

Heike Biebermann

7

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6 August 2017

publication date

3 August 2011

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6 August 2017

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6 August 2017

volume

4 Suppl 1

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6 August 2017

page(s)

S4

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Evidence of Evolutionary Conservation of Function between the Thyroxine Transporter Oatp1c1 and Major Facilitator Superfamily Members

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Essential molecular determinants for thyroid hormone transport and first structural implications for monocarboxylate transporter 8.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Genetics and phenomics of thyroid hormone transport by MCT8.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Evidence for a homodimeric structure of human monocarboxylate transporter 8.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Surface translocation and tri-iodothyronine uptake of mutant MCT8 proteins are cell type-dependent

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Studies on the DIDS-binding site of monocarboxylate transporter 1 suggest a homology model of the open conformation and a plausible translocation cycle

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

The role of charged residues in the transmembrane helices of monocarboxylate transporter 1 and its ancillary protein basigin in determining plasma membrane expression and catalytic activity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Structure of the multidrug transporter EmrD from Escherichia coli

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Thyroid hormone transporters

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Predicting the three-dimensional structure of the human facilitative glucose transporter glut1 by a novel evolutionary homology strategy: insights on the molecular mechanism of substrate migration, and binding sites for glucose and inhibitory molecu

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

The evolution of transmembrane helix kinks and the structural diversity of G protein-coupled receptors

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Structure and mechanism of the glycerol-3-phosphate transporter from Escherichia coli

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Structure and mechanism of the lactose permease of Escherichia coli

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3155110

Proline substitutions are not easily accommodated in a membrane protein

13 July 2018

1 reference

https://api.crossref.org/works/10.1186/1756-6614-4-S1-S4

Structural mimicry of proline kinks: tertiary packing interactions support local structural distortions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186/1756-6614-4-S1-S4

A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1186/1756-6614-4-S1-S4

Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186/1756-6614-4-S1-S4

Structural rearrangements in the thyroid hormone receptor hinge domain and their putative role in the receptor function

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21835051

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1756-6614-4-S1-S4

1 reference

Dimensions Publication ID

6 August 2017

0 references

1 reference

6 August 2017

1 reference