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4TQX
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MOLECULAR BASIS OF STREPTOCOCCUS MUTANS SORTASE A INHIBITION BY CHALCONE.
Descriptor:Sortase, TETRAETHYLENE GLYCOL, ACETIC ACID, ...
Authors:Wallock-Richards, D.J., Marles-Wright, J., Clarke, D.J., Maitra, A., Dodds, M., Hanley, B., Campopiano, D.J.
Deposit date:2014-06-12
Release date:2015-05-20
Last modified:2017-08-30
Method:X-RAY DIFFRACTION (1.37 Å)
Cite:Molecular basis of Streptococcus mutans sortase A inhibition by the flavonoid natural product trans-chalcone.
Chem.Commun.(Camb.), 51, 2015
1OB8
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HOLLIDAY JUNCTION RESOLVING ENZYME
Descriptor:HOLLIDAY-JUNCTION RESOLVASE, SULFATE ION, 1,2-ETHANEDIOL
Authors:Middleton, C.L., Parker, J.L., Richard, D.J., White, M.F., Bond, C.S.
Deposit date:2003-01-28
Release date:2004-10-15
Last modified:2019-03-06
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Substrate Recognition and Catalysis by the Holliday Junction Resolving Enzyme Hje.
Nucleic Acids Res., 32, 2004
1OB9
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HOLLIDAY JUNCTION RESOLVING ENZYME
Descriptor:HOLLIDAY JUNCTION RESOLVASE, 1,2-ETHANEDIOL, FORMIC ACID
Authors:Middleton, C.L., Parker, J.L., Richard, D.J., White, M.F., Bond, C.S.
Deposit date:2003-01-28
Release date:2004-10-15
Last modified:2019-03-06
Method:X-RAY DIFFRACTION (2 Å)
Cite:Substrate Recognition and Catalysis by the Holliday Junction Resolving Enzyme Hje.
Nucleic Acids Res., 32, 2004
2MNA
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THE STRUCTURAL BASIS OF DNA BINDING BY THE SINGLE-STRANDED DNA-BINDING PROTEIN FROM SULFOLOBUS SOLFATARICUS
Descriptor:ssDNA, Single-stranded DNA binding protein (SSB)
Authors:Gamsjaeger, R., Kariawasam, R., Gimenez, A.X., Touma, C.F., McIlwain, E., Bernardo, R.E., Shepherd, N.E., Ataide, S.F., Dong, A.Q., Richard, D.J., White, M.F., Cubeddu, L.
Deposit date:2014-04-02
Release date:2014-12-17
Method:SOLUTION NMR
Cite:The structural basis of DNA binding by the single-stranded DNA-binding protein from Sulfolobus solfataricus
Biochem.J., 465, 2015
3IBE
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CRYSTAL STRUCTURE OF A PYRAZOLOPYRIMIDINE INHIBITOR BOUND TO PI3 KINASE GAMMA
Descriptor:Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, SULFATE ION, 1-(4-{4-morpholin-4-yl-1-[1-(pyridin-3-ylcarbonyl)piperidin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-yl}phenyl)-3-pyridin-4-ylurea
Authors:Bard, J., Svenson, K.
Deposit date:2009-07-15
Release date:2009-09-01
Last modified:2017-11-01
Method:X-RAY DIFFRACTION (2.798 Å)
Cite:ATP-Competitive Inhibitors of the Mammalian Target of Rapamycin: Design and Synthesis of Highly Potent and Selective Pyrazolopyrimidines.
J.Med.Chem., 52, 2009