1E1Y
Flavopiridol inhibits glycogen phosphorylase by binding at the inhibitor site
Summary for 1E1Y
Entry DOI | 10.2210/pdb1e1y/pdb |
Related | 1A8I 1ABB 1AXR 1B4D 1BX3 1GPA 1GPB 1GPY 1NOI 1NOJ 1NOK 1PYG 2AMV 2GPA 2GPB 2GPN 2PRI 2PRJ 2SKC 2SKD 2SKE 3AMV 3GPB 4GPB 5GPB 6GPB 7GPB 8GPB 9GPB |
Descriptor | GLYCOGEN PHOSPHORYLASE, MUSCLE FORM, 2-(2-CHLORO-PHENYL)-5,7-DIHYDROXY-8-(3-HYDROXY-1-METHYL-PIPERIDIN-4-YL)-4H-BENZOPYRAN-4-ONE, PHOSPHITE ION, ... (6 entities in total) |
Functional Keywords | allosteric inhibition, transferase |
Biological source | ORYCTOLAGUS CUNICULUS (RABBIT) |
Total number of polymer chains | 1 |
Total formula weight | 98199.31 |
Authors | Oikonomakos, N.G.,Zographos, S.E.,Skamnaki, V.T.,Tsitsanou, K.E.,Johnson, L.N. (deposition date: 2000-05-11, release date: 2000-05-17, Last modification date: 2023-12-06) |
Primary citation | Oikonomakos, N.G.,Schnier, J.B.,Zographos, S.E.,Skamnaki, V.T.,Tsitsanou, K.E.,Johnson, L.N. Flavopiridol Inhibits Glycogen Phosphorylase by Binding at the Inhibitor Site J.Biol.Chem., 275:34566-, 2000 Cited by PubMed: 10924512DOI: 10.1074/JBC.M004485200 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.23 Å) |
Structure validation
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