sulfotransferase 1A1 isoform X1 [Homo sapiens]

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Insights into the substrate binding mechanism of SULT1A1 through molecular dynamics with excited normal modes simulations. [Sci Rep. 2021]
Insights into the substrate binding mechanism of SULT1A1 through molecular dynamics with excited normal modes simulations.
Dudas B, Toth D, Perahia D, Nicot AB, Balog E, Miteva MA. Sci Rep. 2021 Jun 23; 11(1):13129. Epub 2021 Jun 23.
Investigating the molecular mechanism of hydroxylated bromdiphenyl ethers to inhibit the thyroid hormone sulfotransferase SULT1A1. [Chemosphere. 2021]
Investigating the molecular mechanism of hydroxylated bromdiphenyl ethers to inhibit the thyroid hormone sulfotransferase SULT1A1.
Ma G, Geng L, Lu Y, Wei X, Yu H. Chemosphere. 2021 Jan; 263:128353. Epub 2020 Sep 16.
Evaluation of a conserved tryptophanyl residue in donor substrate binding and catalysis by a phenol sulfotransferase (SULT1A1). [Arch Biochem Biophys. 2020]
Evaluation of a conserved tryptophanyl residue in donor substrate binding and catalysis by a phenol sulfotransferase (SULT1A1).
Beckmann JD, Chodavarapu S, Doyle B. Arch Biochem Biophys. 2020 Nov 30; 695:108621. Epub 2020 Oct 10.

RefSeq genomic sequence
See the genomic reference sequence for the SULT1A1 gene (NG_028128.1).
RefSeq mRNA
See reference mRNA sequence for the SULT1A1 gene (XM_017023604.2).
RefSeq protein isoforms
See 34 reference sequence protein isoforms for the SULT1A1 gene.

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SNP
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txid1279[Organism] (44076043)
Protein
Homo sapiens calcium voltage-gated channel subunit alpha1 D (CACNA1D), transcrip...
Homo sapiens calcium voltage-gated channel subunit alpha1 D (CACNA1D), transcript variant 2, mRNA
gi|1519245652|ref|NM_001128840.3|

Nucleotide
Hepatic methionine adenosyltransferase deficiency
Hepatic methionine adenosyltransferase deficiency

MedGen
C0268621[conceptid] (1)
MedGen
PROTEIN S HEERLEN
PROTEIN S HEERLEN

MedGen

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