Reaction Details |
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Target | N-acetyllactosaminide alpha-1,3-galactosyltransferase |
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Ligand | BDBM50118213 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_219109 |
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Ki | 128000±n/a nM |
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Citation | Vaghefi, MM; Bernacki, RJ; Dalley, NK; Wilson, BE; Robins, RK Synthesis of glycopyranosylphosphonate analogues of certain natural nucleoside diphosphate sugars as potential inhibitors of glycosyltransferases. J Med Chem30:1383-91 (1987) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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N-acetyllactosaminide alpha-1,3-galactosyltransferase |
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Name: | N-acetyllactosaminide alpha-1,3-galactosyltransferase |
Synonyms: | GGTA1_MOUSE | Galactosyltransferase | Ggta-1 | Ggta1 | UDP-galactose:beta-D-galactosyl-1,4-N-acetyl-D-glucosaminide alpha-1,3-galactosyltransferase |
Type: | PROTEIN |
Mol. Mass.: | 46474.57 |
Organism: | Mus musculus |
Description: | ChEMBL_219109 |
Residue: | 394 |
Sequence: | MITMLQDLHVNKISMSRSKSETSLPSSRSGSQEKIMNVKGKVILLMLIVSTVVVVFWEYV
NRIPEVGENRWQKDWWFPSWFKNGTHSYQEDNVEGRREKGRNGDRIEEPQLWDWFNPKNR
PDVLTVTPWKAPIVWEGTYDTALLEKYYATQKLTVGLTVFAVGKYIEHYLEDFLESADMY
FMVGHRVIFYVMIDDTSRMPVVHLNPLHSLQVFEIRSEKRWQDISMMRMKTIGEHILAHI
QHEVDFLFCMDVDQVFQDNFGVETLGQLVAQLQAWWYKASPEKFTYERRELSAAYIPFGE
GDFYYHAAIFGGTPTHILNLTRECFKGILQDKKHDIEAQWHDESHLNKYFLFNKPTKILS
PEYCWDYQIGLPSDIKSVKVAWQTKEYNLVRNNV
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BDBM50118213 |
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n/a |
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Name | BDBM50118213 |
Synonyms: | 5'-UTP | CHEMBL336296 | H4utp | UTP | uridine 5'-(tetrahydrogen triphosphate) | uridine 5'-triphosphoric acid |
Type | Small organic molecule |
Emp. Form. | C9H15N2O15P3 |
Mol. Mass. | 484.1411 |
SMILES | O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r| |
Structure |
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