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Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function

Biochimica et biophysica acta, 2014-04, Vol.1841 (4), p.574-580

2014

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Large scale production of the active human ASCT2 (SLC1A5) transporter in Pichia pastoris — functional and kinetic asymmetry revealed in proteoliposomes

Biochimica et biophysica acta, 2013-09, Vol.1828 (9), p.2238-2246

2013

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Substrate-bound outward-open structure of a Na + -coupled sialic acid symporter reveals a new Na + site

Nature communications, 2018-05, Vol.9 (1), p.1753-14, Article 1753

2018

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The human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease

Biochimica et biophysica acta, 2012-03, Vol.1818 (3), p.559-565

2012

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Over-expression in Escherichia coli, purification and reconstitution in liposomes of the third member of the OCTN sub-family: The mouse carnitine transporter OCTN3

Biochemical and biophysical research communications, 2012-05, Vol.422 (1), p.59-63

2012

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Acetylcholine and acetylcarnitine transport in peritoneum: Role of the SLC22A4 (OCTN1) transporter

Biochimica et biophysica acta, 2016-04, Vol.1858 (4), p.653-660

2016

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Over-expression in Escherichia coli and characterization of two recombinant isoforms of human FAD synthetase

Biochemical and biophysical research communications, 2006-06, Vol.344 (3), p.1008-1016

2006

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Conformation-dependent accessibility of Cys-136 and Cys-155 of the mitochondrial rat carnitine/acylcarnitine carrier to membrane-impermeable SH reagents

Biochimica et biophysica acta, 2007-11, Vol.1767 (11), p.1331-1339

2007

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The involvement of sodium in the function of the human amino acid transporter ASCT2

FEBS letters, 2021-12, Vol.595 (24), p.3030-3041

2021

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The Sodium Sialic Acid Symporter From Staphylococcus aureus Has Altered Substrate Specificity

Frontiers in chemistry, 2018, Vol.6, p.233-233

2018

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Glutamine transport. From energy supply to sensing and beyond

Biochimica et biophysica acta, 2016-08, Vol.1857 (8), p.1147-1157

2016

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Cysteine is not a substrate but a specific modulator of human ASCT2 (SLC1A5) transporter

FEBS letters, 2015-11, Vol.589 (23), p.3617-3623

2015

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OCTN1 (SLC22A4) displays two different transport pathways for organic cations or zwitterions

Biochimica et biophysica acta. Biomembranes, 2024-02, Vol.1866 (2), p.184263-184263, Article 184263

2024

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Glutathione controls the redox state of the mitochondrial carnitine/acylcarnitine carrier Cys residues by glutathionylation

Biochimica et biophysica acta, 2013-11, Vol.1830 (11), p.5299-5304

2013

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Novel insights into the transport mechanism of the human amino acid transporter LAT1 (SLC7A5). Probing critical residues for substrate translocation

Biochimica et biophysica acta. General subjects, 2017-04, Vol.1861 (4), p.727-736

2017

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Structural insights into the bifunctional enzyme human FAD synthase

Structure (London), 2024-07, Vol.32 (7), p.953-965.e5

2024

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Insights into the transport side of the human SLC38A9 transceptor

Biochimica et biophysica acta. Biomembranes, 2019-09, Vol.1861 (9), p.1558-1567

2019

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Nitric oxide inhibits the mitochondrial carnitine/acylcarnitine carrier through reversible S-nitrosylation of cysteine 136

Biochimica et biophysica acta. Bioenergetics, 2017-07, Vol.1858 (7), p.475-482

2017

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In silico investigation on structure–function relationship of members belonging to the human SLC52 transporter family

Proteins, structure, function, and bioinformatics, 2023-05, Vol.91 (5), p.619-633

2023

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Tryptophan 224 of the rat mitochondrial carnitine/acylcarnitine carrier is crucial for the antiport mechanism

Biochimica et biophysica acta. Bioenergetics, 2019-09, Vol.1860 (9), p.708-716

2019

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The mitochondrial carnitine/acylcarnitine carrier is regulated by hydrogen sulfide via interaction with C136 and C155

Biochimica et biophysica acta, 2016-01, Vol.1860 (1), p.20-27

2016

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Reconstitution into liposomes of the B degrees -like glutamine-neutral amino acid transporter from renal cell plasma membrane

Biochimica et biophysica acta, 2008-10, Vol.1778 (10), p.2258

2008

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Human FAD synthase is a bi-functional enzyme with a FAD hydrolase activity in the molybdopterin binding domain

Biochemical and biophysical research communications, 2015-09, Vol.465 (3), p.443-449

2015

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Identification by site-directed mutagenesis of a hydrophobic binding site of the mitochondrial carnitine/acylcarnitine carrier involved in the interaction with acyl groups

Biochimica et biophysica acta, 2012-05, Vol.1817 (5), p.697-704

2012

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Site-directed mutagenesis of charged amino acids of the human mitochondrial carnitine/acylcarnitine carrier: Insight into the molecular mechanism of transport

Biochimica et biophysica acta, 2010-06, Vol.1797 (6-7), p.839-845

2010

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Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function

Large scale production of the active human ASCT2 (SLC1A5) transporter in Pichia pastoris — functional and kinetic asymmetry revealed in proteoliposomes

Substrate-bound outward-open structure of a Na + -coupled sialic acid symporter reveals a new Na + site

The human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease

Over-expression in Escherichia coli, purification and reconstitution in liposomes of the third member of the OCTN sub-family: The mouse carnitine transporter OCTN3

Acetylcholine and acetylcarnitine transport in peritoneum: Role of the SLC22A4 (OCTN1) transporter

Over-expression in Escherichia coli and characterization of two recombinant isoforms of human FAD synthetase

Conformation-dependent accessibility of Cys-136 and Cys-155 of the mitochondrial rat carnitine/acylcarnitine carrier to membrane-impermeable SH reagents

The involvement of sodium in the function of the human amino acid transporter ASCT2

The Sodium Sialic Acid Symporter From Staphylococcus aureus Has Altered Substrate Specificity

Glutamine transport. From energy supply to sensing and beyond

Cysteine is not a substrate but a specific modulator of human ASCT2 (SLC1A5) transporter

OCTN1 (SLC22A4) displays two different transport pathways for organic cations or zwitterions

Glutathione controls the redox state of the mitochondrial carnitine/acylcarnitine carrier Cys residues by glutathionylation

Novel insights into the transport mechanism of the human amino acid transporter LAT1 (SLC7A5). Probing critical residues for substrate translocation

Structural insights into the bifunctional enzyme human FAD synthase

Insights into the transport side of the human SLC38A9 transceptor

Nitric oxide inhibits the mitochondrial carnitine/acylcarnitine carrier through reversible S-nitrosylation of cysteine 136

In silico investigation on structure–function relationship of members belonging to the human SLC52 transporter family

Tryptophan 224 of the rat mitochondrial carnitine/acylcarnitine carrier is crucial for the antiport mechanism

The mitochondrial carnitine/acylcarnitine carrier is regulated by hydrogen sulfide via interaction with C136 and C155

Reconstitution into liposomes of the B degrees -like glutamine-neutral amino acid transporter from renal cell plasma membrane

Human FAD synthase is a bi-functional enzyme with a FAD hydrolase activity in the molybdopterin binding domain

Identification by site-directed mutagenesis of a hydrophobic binding site of the mitochondrial carnitine/acylcarnitine carrier involved in the interaction with acyl groups

Site-directed mutagenesis of charged amino acids of the human mitochondrial carnitine/acylcarnitine carrier: Insight into the molecular mechanism of transport

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