1qsl: Difference between revisions

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New page: left|200px<br /><applet load="1qsl" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qsl, resolution 2.20Å" /> '''KLENOW FRAGMENT COMP...
 
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[[Image:1qsl.gif|left|200px]]<br /><applet load="1qsl" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1qsl.gif|left|200px]]<br /><applet load="1qsl" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1qsl, resolution 2.20&Aring;" />
caption="1qsl, resolution 2.20&Aring;" />
'''KLENOW FRAGMENT COMPLEXED WITH SINGLE-STRANDED SUBSTRATE AND EUROPIUM (III) ION'''<br />
'''KLENOW FRAGMENT COMPLEXED WITH SINGLE-STRANDED SUBSTRATE AND EUROPIUM (III) ION'''<br />


==Overview==
==Overview==
BACKGROUND: Biochemical and biophysical experiments have shown that two, catalytically essential divalent metal ions (termed 'A' and 'B') bind to, the 3'-5' exonuclease active site of the Klenow fragment (KF) of, Escherichia coli DNA polymerase I. X-ray crystallographic studies have, established the normal positions in the KF 3'-5' exonuclease (KF exo), active site of the two cations and the single-stranded DNA substrate., Lanthanide (III) luminescence studies have demonstrated, however, that, only a single europium (III) ion (Eu3+) binds to the KF exo active site., Furthermore, Eu3+ does not support catalysis by KF exo or several other, two-metal-ion phosphoryl-transfer enzymes. RESULTS: A crystal structure of, KF complexed with both Eu3+ and substrate single-stranded, oligodeoxynucleotide shows that a lone Eu3+ is bound near to metal-ion, site A. Comparison of this structure to a relevant native structure, reveals that the bound Eu3+ causes a number of changes to the KF exo, active site. The scissile phosphate of the substrate is displaced from its, normal position by about 1 A when Eu3+ is bound and the presence of Eu3+, in the active site precludes the binding of the essential metal ion B., CONCLUSIONS: The substantial, lanthanide-induced differences in metal-ion, and substrate binding to KF exo account for the inhibition of this enzyme, by Eu3+. These changes also explain the inability of KF exo to bind more, than one cation in the presence of lanthanides. The mechanistic similarity, between KF exo and other two-metal-ion phosphoryl-transfer enzymes, suggests that the principles of lanthanide (III) ion binding and, inhibition ascertained from this study will probably apply to most members, of this class of enzymes.
BACKGROUND: Biochemical and biophysical experiments have shown that two catalytically essential divalent metal ions (termed 'A' and 'B') bind to the 3'-5' exonuclease active site of the Klenow fragment (KF) of Escherichia coli DNA polymerase I. X-ray crystallographic studies have established the normal positions in the KF 3'-5' exonuclease (KF exo) active site of the two cations and the single-stranded DNA substrate. Lanthanide (III) luminescence studies have demonstrated, however, that only a single europium (III) ion (Eu3+) binds to the KF exo active site. Furthermore, Eu3+ does not support catalysis by KF exo or several other two-metal-ion phosphoryl-transfer enzymes. RESULTS: A crystal structure of KF complexed with both Eu3+ and substrate single-stranded oligodeoxynucleotide shows that a lone Eu3+ is bound near to metal-ion site A. Comparison of this structure to a relevant native structure reveals that the bound Eu3+ causes a number of changes to the KF exo active site. The scissile phosphate of the substrate is displaced from its normal position by about 1 A when Eu3+ is bound and the presence of Eu3+ in the active site precludes the binding of the essential metal ion B. CONCLUSIONS: The substantial, lanthanide-induced differences in metal-ion and substrate binding to KF exo account for the inhibition of this enzyme by Eu3+. These changes also explain the inability of KF exo to bind more than one cation in the presence of lanthanides. The mechanistic similarity between KF exo and other two-metal-ion phosphoryl-transfer enzymes suggests that the principles of lanthanide (III) ion binding and inhibition ascertained from this study will probably apply to most members of this class of enzymes.


==About this Structure==
==About this Structure==
1QSL is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with EU as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/DNA-directed_DNA_polymerase DNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.7 2.7.7.7] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1QSL OCA].  
1QSL is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=EU:'>EU</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/DNA-directed_DNA_polymerase DNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.7 2.7.7.7] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QSL OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Aschheim, K.]]
[[Category: Aschheim, K.]]
[[Category: Brautigam, C.A.]]
[[Category: Brautigam, C A.]]
[[Category: Steitz, T.A.]]
[[Category: Steitz, T A.]]
[[Category: EU]]
[[Category: EU]]
[[Category: exonuclease]]
[[Category: exonuclease]]
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[[Category: two metal ions]]
[[Category: two metal ions]]


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