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Literature summary extracted from

  • Ganu, R.; Garrow, T.; Koutmos, M.; Rund, L.; Schook, L.B.
    Splicing variants of the porcine betaine-homocysteine S-methyltransferase gene: implications for mammalian metabolism (2013), Gene, 529, 228-237.
    View publication on PubMedView publication on EuropePMC

Crystallization (Commentary)

EC Number Crystallization (Comment) Organism
2.1.1.5 dominant structural feature of wild type BHMT is an (betaalpha)8 barrel. A modeled structure of truncated BHMT suggests that this protein would assume a horseshoe fold and lack methyltransferase activity Sus scrofa

Organism

EC Number Organism UniProt Comment Textmining
2.1.1.5 Sus scrofa
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Source Tissue

EC Number Source Tissue Comment Organism Textmining
2.1.1.5 fetus low BHMT activity is detected in the G30 fetus, and slightly increased levels of activity are observed in the liver from G45 and G90 fetuses Sus scrofa
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2.1.1.5 kidney transcripts are expressed at significant levels in the liver and kidney from day 45 of gestation onward Sus scrofa
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2.1.1.5 liver transcripts are expressed at significant levels in the liver and kidney from day 45 of gestation onward Sus scrofa
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Expression

EC Number Organism Comment Expression
2.1.1.5 Sus scrofa during fetal development, a total of ten splice variants of BHMT are expressed at varying levels across a wide range of porcine tissues. Two variants contain an identical ORF that encodes a C-terminal truncated form of BHMT additional information