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1ZTU
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STRUCTURE OF THE CHROMOPHORE BINDING DOMAIN OF BACTERIAL PHYTOCHROME
Descriptor:Bacteriophytochrome, BILIVERDINE IX ALPHA
Authors:Wagner, J.R., Brunzelle, J.S., Forest, K.T., Vierstra, R.D.
Deposit date:2005-05-27
Release date:2005-11-15
Last modified:2017-10-11
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:A light-sensing knot revealed by the structure of the chromophore-binding domain of phytochrome.
Nature, 438, 2005
2O9B
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CRYSTAL STRUCTURE OF BACTERIOPHYTOCHROME CHROMOPHORE BINDING DOMAIN
Descriptor:Bacteriophytochrome, 3-[2-[(Z)-[3-(2-carboxyethyl)-5-[(Z)-(4-ethenyl-3-methyl-5-oxidanylidene-pyrrol-2-ylidene)methyl]-4-methyl-pyrrol-1-ium-2-ylidene]methyl]-5-[(Z)-[(3E)-3-ethylidene-4-methyl-5-oxidanylidene-pyrrolidin-2-ylidene]methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid
Authors:Wagner, J.R., Brunzelle, J.S., Vierstra, R.D., Forest, K.T.
Deposit date:2006-12-13
Release date:2007-03-06
Last modified:2017-10-18
Method:X-RAY DIFFRACTION (2.15 Å)
Cite:High resolution structure of deinococcus bacteriophytochrome yields new insights into phytochrome architecture and evolution.
J.Biol.Chem., 282, 2007
2O9C
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CRYSTAL STRUCTURE OF BACTERIOPHYTOCHROME CHROMOPHORE BINDING DOMAIN AT 1.45 ANGSTROM RESOLUTION
Descriptor:Bacteriophytochrome, 3-[2-[(Z)-[3-(2-carboxyethyl)-5-[(Z)-(4-ethenyl-3-methyl-5-oxidanylidene-pyrrol-2-ylidene)methyl]-4-methyl-pyrrol-1-ium-2-ylidene]methyl]-5-[(Z)-[(3E)-3-ethylidene-4-methyl-5-oxidanylidene-pyrrolidin-2-ylidene]methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid
Authors:Wagner, J.R., Brunzelle, J.S., Vierstra, R.D., Forest, K.T.
Deposit date:2006-12-13
Release date:2007-03-06
Last modified:2018-01-24
Method:X-RAY DIFFRACTION (1.45 Å)
Cite:High resolution structure of deinococcus bacteriophytochrome yields new insights into phytochrome architecture and evolution.
J.Biol.Chem., 282, 2007
1PY5
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CRYSTAL STRUCTURE OF TGF-BETA RECEPTOR I KINASE WITH INHIBITOR
Descriptor:TGF-beta receptor type I, SULFATE ION, 4-(3-PYRIDIN-2-YL-1H-PYRAZOL-4-YL)QUINOLINE
Authors:Zhang, F., Sawyer, J.S.
Deposit date:2003-07-08
Release date:2004-07-13
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole inhibitors of the transforming growth factor-beta type I receptor kinase domain.
Bioorg.Med.Chem.Lett., 14, 2004
1RW8
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CRYSTAL STRUCTURE OF TGF-BETA RECEPTOR I KINASE WITH ATP SITE INHIBITOR
Descriptor:TGF-beta receptor type I, 3-(4-FLUOROPHENYL)-2-(6-METHYLPYRIDIN-2-YL)-5,6-DIHYDRO-4H-PYRROLO[1,2-B]PYRAZOLE
Authors:Zhang, F., Sawyer, J.S.
Deposit date:2003-12-16
Release date:2005-02-01
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole inhibitors of the transforming growth factor-beta type I receptor kinase domain.
Bioorg.Med.Chem.Lett., 14, 2004