Literature DB >> 10981718

Three-dimensional NMR structure of the sixth ligand-binding module of the human LDL receptor: comparison of two adjacent modules with different ligand binding specificities.

D Clayton1, I M Brereton, P A Kroon, R Smith.   

Abstract

The sixth ligand-binding module of the low-density lipoprotein receptor contributes to the binding of apolipoprotein B100-containing lipoproteins. 1H NMR spectroscopy, DYANA and X-PLOR structure calculations were used to determine that this module has a well defined structure with a backbone conformation similar to other modules. Structures from calculations that simulated the presence of a calcium ion showed increased resolution without large increases in energy, increased deviations from idealised geometry or violations of experimental constraints. Investigation of the surface properties of this module indicates there are significant differences from the fifth module, which binds apolipoprotein E-containing lipoproteins in addition to apolipoprotein B100-containing lipoproteins.

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Year:  2000        PMID: 10981718     DOI: 10.1016/s0014-5793(00)01842-1

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  2 in total

1.  The crystal structure of a multidomain protease inhibitor (HAI-1) reveals the mechanism of its auto-inhibition.

Authors:  Min Liu; Cai Yuan; Jan K Jensen; Baoyu Zhao; Yunbin Jiang; Longguang Jiang; Mingdong Huang
Journal:  J Biol Chem       Date:  2017-03-27       Impact factor: 5.157

2.  Structural basis for ligand capture and release by the endocytic receptor ApoER2.

Authors:  Hidenori Hirai; Norihisa Yasui; Keitaro Yamashita; Sanae Tabata; Masaki Yamamoto; Junichi Takagi; Terukazu Nogi
Journal:  EMBO Rep       Date:  2017-04-26       Impact factor: 8.807

  2 in total

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