1d7h
From Proteopedia
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|PDB= 1d7h |SIZE=350|CAPTION= <scene name='initialview01'>1d7h</scene>, resolution 1.90Å | |PDB= 1d7h |SIZE=350|CAPTION= <scene name='initialview01'>1d7h</scene>, resolution 1.90Å | ||
|SITE= | |SITE= | ||
- | |LIGAND= <scene name='pdbligand= | + | |LIGAND= <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=NH4:AMMONIUM+ION'>NH4</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene> |
- | |ACTIVITY= [http://en.wikipedia.org/wiki/Peptidylprolyl_isomerase Peptidylprolyl isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.2.1.8 5.2.1.8] | + | |ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Peptidylprolyl_isomerase Peptidylprolyl isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.2.1.8 5.2.1.8] </span> |
|GENE= | |GENE= | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY=[[1d6o|1D6O]], [[1d7h|1D7H]], [[1d7i|1D7I]], [[1d7j|1D7J]] | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1d7h FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1d7h OCA], [http://www.ebi.ac.uk/pdbsum/1d7h PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1d7h RCSB]</span> | ||
}} | }} | ||
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[[Category: Taylor, P.]] | [[Category: Taylor, P.]] | ||
[[Category: Walkinshaw, M D.]] | [[Category: Walkinshaw, M D.]] | ||
- | [[Category: DMS]] | ||
- | [[Category: NH4]] | ||
- | [[Category: SO4]] | ||
[[Category: dmso]] | [[Category: dmso]] | ||
[[Category: fkbp]] | [[Category: fkbp]] | ||
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[[Category: isomerase]] | [[Category: isomerase]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:36:08 2008'' |
Revision as of 16:36, 30 March 2008
| |||||||
, resolution 1.90Å | |||||||
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Ligands: | , , | ||||||
Activity: | Peptidylprolyl isomerase, with EC number 5.2.1.8 | ||||||
Related: | 1D6O, 1D7H, 1D7I, 1D7J
| ||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
FKBP COMPLEXED WITH DMSO
Overview
A new crystal form of native FK506 binding protein (FKBP) has been obtained which has proved useful in ligand binding studies. Three different small molecule ligand complexes and the native enzyme have been determined at higher resolution than 2.0 A. Dissociation constants of the related small molecule ligands vary from 20 mM for dimethylsulphoxide to 200 microM for tetrahydrothiophene 1-oxide. Comparison of the four available crystal structures shows that the protein structures are identical to within experimental error, but there are differences in the water structure in the active site. Analysis of the calculated buried surface areas of these related ligands provides an estimated van der Waals contribution to the binding energy of -0.5 kJ/A(2) for non-polar interactions between ligand and protein.
About this Structure
1D7H is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
X-ray structures of small ligand-FKBP complexes provide an estimate for hydrophobic interaction energies., Burkhard P, Taylor P, Walkinshaw MD, J Mol Biol. 2000 Jan 28;295(4):953-62. PMID:10656803
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