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Literature summary for 4.1.2.55 extracted from

  • Theodossis, A.; Walden, H.; Westwick, E.J.; Connaris, H.; Lamble, H.J.; Hough, D.W.; Danson, M.J.; Taylor, G.L.
    The structural basis for substrate promiscuity in 2-keto-3-deoxygluconate aldolase from the Entner-Doudoroff pathway in Sulfolobus solfataricus (2004), J. Biol. Chem., 279, 43886-43892.
    View publication on PubMed

Crystallization (Commentary)

Crystallization (Comment) Organism
trapping of Schiff base complexes with natural substrates pyruvate, 2-dehydro-3-deoxy-D-gluconate, 2-dehydro-3-deoxy-D-galactonate and pyruvate plus D-glyceraldehyde at physiological pH by rapid soaking at low temperature followed by flash freezing prior to X-ray data collection. The complexes explain the substrate promiscuity of the enzyme with a rigid ligand-binding site able to accommodate both 2-dehydro-3-deoxy-D-gluconate and 2-dehydro-3-deoxy-D-galactonate Saccharolobus solfataricus

Organism

Organism UniProt Comment Textmining
Saccharolobus solfataricus O54288
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-dehydro-3-deoxy-D-galactonate lack of stereoselectivity in the condensation reaction of pyruvate and D-glyceraldehyde, forming a mixture of 2-dehydro-3-deoxy-D-gluconate and 2-dehydro-3-deoxy-D-galactonate Saccharolobus solfataricus pyruvate + D-glyceraldehyde
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r
2-dehydro-3-deoxy-D-gluconate lack of stereoselectivity in the condensation reaction of pyruvate and D-glyceraldehyde, forming a mixture of 2-dehydro-3-deoxy-D-gluconate and 2-dehydro-3-deoxy-D-galactonate Saccharolobus solfataricus pyruvate + D-glyceraldehyde
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r

Synonyms

Synonyms Comment Organism
KDGA
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Saccharolobus solfataricus