1jii

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|PDB= 1jii |SIZE=350|CAPTION= <scene name='initialview01'>1jii</scene>, resolution 3.2&Aring;
|PDB= 1jii |SIZE=350|CAPTION= <scene name='initialview01'>1jii</scene>, resolution 3.2&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=383:[2-AMINO-3-(4-HYDROXY-PHENYL)-PROPIONYLAMINO]- (2,4,5,8-TETRAHYDROXY-7-OXA-2-AZA-BICYCLO[3.2.1]OCT-3-YL)- ACETIC ACID'>383</scene>
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|LIGAND= <scene name='pdbligand=383:[2-AMINO-3-(4-HYDROXY-PHENYL)-PROPIONYLAMINO]-+(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZA-BICYCLO[3.2.1]OCT-3-YL)-+ACETIC+ACID'>383</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Tyrosine--tRNA_ligase Tyrosine--tRNA ligase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.1.1.1 6.1.1.1]
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Tyrosine--tRNA_ligase Tyrosine--tRNA ligase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.1.1.1 6.1.1.1] </span>
|GENE=
|GENE=
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|DOMAIN=
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|RELATEDENTRY=[[1jij|1JIJ]], [[1jik|1JIK]], [[1jil|1JIL]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1jii FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1jii OCA], [http://www.ebi.ac.uk/pdbsum/1jii PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1jii RCSB]</span>
}}
}}
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[[Category: Qiu, X.]]
[[Category: Qiu, X.]]
[[Category: Smith, W W.]]
[[Category: Smith, W W.]]
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[[Category: 383]]
 
[[Category: staphylococcus aureus]]
[[Category: staphylococcus aureus]]
[[Category: structure based inhibitor design]]
[[Category: structure based inhibitor design]]
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[[Category: tyrosyl-trna synthetase]]
[[Category: tyrosyl-trna synthetase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 12:03:55 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:34:11 2008''

Revision as of 18:34, 30 March 2008


PDB ID 1jii

Drag the structure with the mouse to rotate
, resolution 3.2Å
Ligands:
Activity: Tyrosine--tRNA ligase, with EC number 6.1.1.1
Related: 1JIJ, 1JIK, 1JIL


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Crystal structure of S. aureus TyrRS in complex with SB-219383


Overview

SB-219383 and its analogues are a class of potent and specific inhibitors of bacterial tyrosyl-tRNA synthetases. Crystal structures of these inhibitors have been solved in complex with the tyrosyl-tRNA synthetase from Staphylococcus aureus, the bacterium that is largely responsible for hospital-acquired infections. The full-length enzyme yielded crystals that diffracted to 2.8 A resolution, but a truncated version of the enzyme allowed the resolution to be extended to 2.2 A. These inhibitors not only occupy the known substrate binding sites in unique ways, but also reveal a butyl binding pocket. It was reported that the Bacillus stearothermophilus TyrRS T51P mutant has much increased catalytic activity. The S. aureus enzyme happens to have a proline at position 51. Therefore, our structures may contribute to the understanding of the catalytic mechanism and provide the structural basis for designing novel antimicrobial agents.

About this Structure

1JII is a Single protein structure of sequence from Staphylococcus aureus. Full crystallographic information is available from OCA.

Reference

Crystal structure of Staphylococcus aureus tyrosyl-tRNA synthetase in complex with a class of potent and specific inhibitors., Qiu X, Janson CA, Smith WW, Green SM, McDevitt P, Johanson K, Carter P, Hibbs M, Lewis C, Chalker A, Fosberry A, Lalonde J, Berge J, Brown P, Houge-Frydrych CS, Jarvest RL, Protein Sci. 2001 Oct;10(10):2008-16. PMID:11567092

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