Literature DB >> 1375171

Solution structure of FK506 bound to FKBP-12.

C A Lepre1, J A Thomson, J M Moore.   

Abstract

The complex of the immunosuppressant FK506 bound to FKBP-12 has been studied in solution using 1H and inverse-detected 13C NMR methods. The resonances of bound, 13C-labelled FK506 were assigned and a set of 66 intraligand NOE distance restraints were used to calculate the structure of the bound ligand by distance geometry and restrained molecular dynamics methods. The structure of bound FK506 in solution closely resembles that seen in the X-ray structure [17], except for the allyl region. The differences reflect the influence of intermolecular crystal contacts and have implications for interpretation of the interaction of the FK506/FKBP complex with its putative biological receptor.

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Year:  1992        PMID: 1375171     DOI: 10.1016/0014-5793(92)80292-o

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


  8 in total

1.  Automated detection of problem restraints in NMR data sets using the FINGAR genetic algorithm method.

Authors:  D A Pearlman
Journal:  J Biomol NMR       Date:  1999-04       Impact factor: 2.835

2.  FINGAR: A new genetic algorithm-based method for fitting NMR data.

Authors:  D A Pearlman
Journal:  J Biomol NMR       Date:  1996-07       Impact factor: 2.835

3.  Practical applications of time-averaged restrained molecular dynamics to ligand-receptor systems: FK506 bound to the Q50R,A95H,K98I triple mutant of FKBP-13.

Authors:  C A Lepre; D A Pearlman; O Futer; D J Livingston; J M Moore
Journal:  J Biomol NMR       Date:  1996-07       Impact factor: 2.835

4.  Dynamic NMR studies of ligand-receptor interactions: design and analysis of a rapidly exchanging complex of FKBP-12/FK506 with a 24 kDa calcineurin fragment.

Authors:  J Fejzo; C A Lepre; J W Peng; M S Su; J A Thomson; J M Moore
Journal:  Protein Sci       Date:  1996-09       Impact factor: 6.725

5.  How is an NMR structure best defined? An analysis of molecular dynamics distance-based approaches.

Authors:  D A Pearlman
Journal:  J Biomol NMR       Date:  1994-01       Impact factor: 2.835

Review 6.  Role of calcineurin in neurodegeneration produced by misfolded proteins and endoplasmic reticulum stress.

Authors:  Abhisek Mukherjee; Claudio Soto
Journal:  Curr Opin Cell Biol       Date:  2011-02-02       Impact factor: 8.382

7.  Mapping the ligand binding site at protein side-chains in protein-ligand complexes through NOE difference spectroscopy.

Authors:  C Eichmüller; M Tollinger; B Kräutler; R Konrat
Journal:  J Biomol NMR       Date:  2001-07       Impact factor: 2.835

Review 8.  The chemistry of signal transduction.

Authors:  J Clardy
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-03       Impact factor: 11.205

  8 in total

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