Skip to main content Skip to navigation Skip to search
Open toolbar

Accessibility

Disclaimer
Home

Main menu

  • Home
  • Download
  • Information
  • Contact

Mobile Main Menu

  • Home
  • Download
  • Information
  • Contact
AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

Breadcrumb

  1. Home
YPL273W SAM4 / SGDID:S000006194
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
Yeast Systematic Name Yeast Symbol SGDID Analog Name Analog Description EC Organism Disease Structure Uniprot Human ID Human Symbol HHsearch Probability HHsearch E_value HHsearch P_value HHsearch Score Flag Disease related Flag Homo sapiens Flag Mus musculus Flag Danio rerio Flag Drosophila melanogaster Flag Caenorhabditis elegans Flag Arabidopsis thaliana Flag Escherichia coli
YPL273W SAM4 SGDID:S000006194
BHMT
Betaine--homocysteine S-methyltransferase 1 (EC 2.1.1.5)
2.1.1.5 Homo sapiens
Vascular Disease,Amino Acid Metabolic Disorder,Homocystinuria,Bardet-Biedl Syndrome,Placental Abruption,Liver Cirrhosis,Choline Deficiency Disease,Homocysteinemia,Neural Tube Defects,Hypermethioninemia,Orofacial Cleft,Glycine N-Methyltransferase Deficiency,Methylmalonic Acidemia And Homocysteinemia, Cblx Type
4m3p_c Q93088 ENSG00000145692 BHMT 100.00 5.00E-62 3.50E-66 448.40 1 1 0 0 0 0 0 0
YPL273W SAM4 SGDID:S000006194
Bhmt
Betaine--homocysteine S-methyltransferase 1 (EC 2.1.1.5)
2.1.1.5 Rattus norvegicus
1umy_d O09171 100.00 6.40E-62 4.50E-66 447.40 0 0 0 0 0 0 0 0
YPL273W SAM4 SGDID:S000006194
TM_0268
TM_0268
2.1.1.13 Thermotoga maritima
1q7q_a Q9WYA5 100.00 7.90E-61 5.60E-65 461.10 0 0 0 0 0 0 0 0
YPL273W SAM4 SGDID:S000006194
mmuM yagD b0261 JW0253
Homocysteine S-methyltransferase (EC 2.1.1.10) (S-methylmethionine:homocysteine methyltransferase)
2.1.1.10 Escherichia coli
5dml_a Q47690 100.00 1.90E-64 1.30E-68 452.10 0 0 0 0 0 0 0 1
YPL273W SAM4 SGDID:S000006194
BHMT
Betaine--homocysteine S-methyltransferase 1 (EC 2.1.1.5)
2.1.1.5 Homo sapiens
Vascular Disease,Amino Acid Metabolic Disorder,Homocystinuria,Bardet-Biedl Syndrome,Placental Abruption,Liver Cirrhosis,Choline Deficiency Disease,Homocysteinemia,Neural Tube Defects,Hypermethioninemia,Orofacial Cleft,Glycine N-Methyltransferase Deficiency,Methylmalonic Acidemia And Homocysteinemia, Cblx Type
1lt7_a Q93088 100.00 5.30E-65 3.70E-69 464.40 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab