1ha3: Difference between revisions
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|PDB= 1ha3 |SIZE=350|CAPTION= <scene name='initialview01'>1ha3</scene>, resolution 2.00Å | |PDB= 1ha3 |SIZE=350|CAPTION= <scene name='initialview01'>1ha3</scene>, resolution 2.00Å | ||
|SITE= <scene name='pdbsite=GDA:Gdp+Binding+Site+For+Chain+A'>GDA</scene>, <scene name='pdbsite=GDB:Gdp+Binding+Site+For+Chain+B'>GDB</scene>, <scene name='pdbsite=MAA:Mau+Binding+Site+For+Chain+A+Symmetry+Related+Subunits+C+...'>MAA</scene>, <scene name='pdbsite=MAB:Mau+Binding+Site+For+Chain+B+Symmetry+Related+Subunits+C+...'>MAB</scene>, <scene name='pdbsite=MGA:Mg+Binding+Site+For+Chain+A'>MGA</scene> and <scene name='pdbsite=MGB:Mg+Binding+Site+For+Chain+B'>MGB</scene> | |SITE= <scene name='pdbsite=GDA:Gdp+Binding+Site+For+Chain+A'>GDA</scene>, <scene name='pdbsite=GDB:Gdp+Binding+Site+For+Chain+B'>GDB</scene>, <scene name='pdbsite=MAA:Mau+Binding+Site+For+Chain+A+Symmetry+Related+Subunits+C+...'>MAA</scene>, <scene name='pdbsite=MAB:Mau+Binding+Site+For+Chain+B+Symmetry+Related+Subunits+C+...'>MAB</scene>, <scene name='pdbsite=MGA:Mg+Binding+Site+For+Chain+A'>MGA</scene> and <scene name='pdbsite=MGB:Mg+Binding+Site+For+Chain+B'>MGB</scene> | ||
|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=GDP:GUANOSINE-5 | |LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=GDP:GUANOSINE-5'-DIPHOSPHATE'>GDP</scene>, <scene name='pdbligand=MAU:N-METHYL+KIRROMYCIN'>MAU</scene> and <scene name='pdbligand=BME:BETA-MERCAPTOETHANOL'>BME</scene> | ||
|ACTIVITY= [http://en.wikipedia.org/wiki/dGTPase dGTPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.5.1 3.1.5.1] | |ACTIVITY= [http://en.wikipedia.org/wiki/dGTPase dGTPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.5.1 3.1.5.1] | ||
|GENE= TUFB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=271 Thermus aquaticus]) | |GENE= TUFB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=271 Thermus aquaticus]) | ||
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[[Category: ribosome]] | [[Category: ribosome]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 23 12:03:48 2008'' | ||
Revision as of 13:03, 23 March 2008
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| , resolution 2.00Å | |||||||
|---|---|---|---|---|---|---|---|
| Sites: | , , , , and | ||||||
| Ligands: | , , and | ||||||
| Gene: | TUFB (Thermus aquaticus) | ||||||
| Activity: | dGTPase, with EC number 3.1.5.1 | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
ELONGATION FACTOR TU IN COMPLEX WITH AURODOX
OverviewOverview
Aurodox is a member of the family of kirromycin antibiotics, which inhibit protein biosynthesis by binding to elongation factor Tu (EF-Tu). We have determined the crystal structure of the 1:1:1 complex of Thermus thermophilus EF-Tu with GDP and aurodox to 2.0-A resolution. During its catalytic cycle, EF-Tu adopts two strikingly different conformations depending on the nucleotide bound: the GDP form and the GTP form. In the present structure, a GTP complex-like conformation of EF-Tu is observed, although GDP is bound to the nucleotide-binding site. This is consistent with previous proposals that aurodox fixes EF-Tu on the ribosome by locking it in its GTP form. Binding of EF-Tu.GDP to aminoacyl-tRNA and mutually exclusive binding of kirromycin and elongation factor Ts to EF-Tu can be explained on the basis of the structure. For many previously observed mutations that provide resistance to kirromycin, it can now be understood how they prevent interaction with the antibiotic. An unexpected feature of the structure is the reorientation of the His-85 side chain toward the nucleotide-binding site. We propose that this residue stabilizes the transition state of GTP hydrolysis, explaining the acceleration of the reaction by kirromycin-type antibiotics.
About this StructureAbout this Structure
1HA3 is a Single protein structure of sequence from Thermus aquaticus. Full crystallographic information is available from OCA.
ReferenceReference
Conformational change of elongation factor Tu (EF-Tu) induced by antibiotic binding. Crystal structure of the complex between EF-Tu.GDP and aurodox., Vogeley L, Palm GJ, Mesters JR, Hilgenfeld R, J Biol Chem. 2001 May 18;276(20):17149-55. Epub 2001 Jan 30. PMID:11278992
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