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1A18
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PHENANTHROLINE MODIFIED MURINE ADIPOCYTE LIPID BINDING PROTEIN
分子名称:ADIPOCYTE LIPID BINDING PROTEIN
著者Ory, J., Mazhary, A., Kuang, H., Davies, R., Distefano, M., Banaszak, L.
登録日1997-12-23
公開日1998-07-01
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structural characterization of two synthetic catalysts based on adipocyte lipid-binding protein.
Protein Eng., 11, 1998
1A2D
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PYRIDOXAMINE MODIFIED MURINE ADIPOCYTE LIPID BINDING PROTEIN
分子名称:ADIPOCYTE LIPID BINDING PROTEIN, CHLORIDE ION
著者Ory, J., Mazhary, A., Kuang, H., Davies, R., Distefano, M., Banaszak, L.
登録日1997-12-29
公開日1998-07-01
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structural characterization of two synthetic catalysts based on adipocyte lipid-binding protein.
Protein Eng., 11, 1998
4RM8
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CRYSTAL STRUCTURE OF HUMAN EZRIN IN SPACE GROUP P21
分子名称:Ezrin
著者Phang, J.M., Harrop, S.J., Davies, R., Duff, A.P., Wilk, K.E., Curmi, P.M.G.
登録日2014-10-20
公開日2015-12-09
最終更新日2017-09-27
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Structural characterization suggests models for monomeric and dimeric forms of full-length ezrin.
Biochem. J., 473, 2016
4RM9
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CRYSTAL STRUCTURE OF HUMAN EZRIN IN SPACE GROUP C2221
分子名称:Ezrin
著者Phang, J.M., Harrop, S.J., Davies, R., Duff, A.P., Wilk, K.E., Curmi, P.M.G.
登録日2014-10-21
公開日2015-12-09
最終更新日2017-09-27
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structural characterization suggests models for monomeric and dimeric forms of full-length ezrin.
Biochem. J., 473, 2016
4UU9
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CRYSTAL STRUCTURE OF THE HUMAN C5A IN COMPLEX WITH MEDI7814 A NEUTRALISING ANTIBODY
分子名称:MEDI7814, COMPLEMENT C5, SULFATE ION
著者Colley, C., Sridharan, S., Dobson, C., Popovic, B., Debreczeni, J.E., Hargreaves, D., Edwards, B., Brennan, J., England, L., Fung, S., An Eghobamien, L., Sivars, U., Woods, R., Flavell, L., Renshaw, G.J., Wickson, K., Wilkinson, T., Davies, R., Bonnell, J., Warrener, P., Howes, R., Vaughan, T.
登録日2014-07-25
公開日2015-08-12
最終更新日2019-02-27
実験手法X-RAY DIFFRACTION (2.12 Å)
主引用文献Structure and characterization of a high affinity C5a monoclonal antibody that blocks binding to C5aR1 and C5aR2 receptors.
MAbs, 10, 2018