1n4s: Difference between revisions

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New page: left|200px<br /><applet load="1n4s" size="450" color="white" frame="true" align="right" spinBox="true" caption="1n4s, resolution 2.60Å" /> '''Protein Geranylgeran...
 
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[[Image:1n4s.gif|left|200px]]<br /><applet load="1n4s" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1n4s.gif|left|200px]]<br /><applet load="1n4s" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1n4s, resolution 2.60&Aring;" />
caption="1n4s, resolution 2.60&Aring;" />
'''Protein Geranylgeranyltransferase type-I Complexed with GGPP and a Geranylgeranylated KKKSKTKCVIL Peptide Product'''<br />
'''Protein Geranylgeranyltransferase type-I Complexed with GGPP and a Geranylgeranylated KKKSKTKCVIL Peptide Product'''<br />


==Overview==
==Overview==
Protein geranylgeranyltransferase type-I (GGTase-I), one of two CaaX, prenyltransferases, is an essential enzyme in eukaryotes. GGTase-I, catalyzes C-terminal lipidation of &gt;100 proteins, including many GTP-, binding regulatory proteins. We present the first structural information, for mammalian GGTase-I, including a series of substrate and product, complexes that delineate the path of the chemical reaction. These, structures reveal that all protein prenyltransferases share a common, reaction mechanism and identify specific residues that play a dominant, role in determining prenyl group specificity. This hypothesis was, confirmed by converting farnesyltransferase (15-C prenyl substrate) into, GGTase-I (20-C prenyl substrate) with a single point mutation. GGTase-I, discriminates against farnesyl diphosphate (FPP) at the product turnover, step through the inability of a 15-C FPP to displace the 20-C, prenyl-peptide product. Understanding these key features of specificity is, expected to contribute to optimization of anti-cancer and anti-parasite, drugs.
Protein geranylgeranyltransferase type-I (GGTase-I), one of two CaaX prenyltransferases, is an essential enzyme in eukaryotes. GGTase-I catalyzes C-terminal lipidation of &gt;100 proteins, including many GTP- binding regulatory proteins. We present the first structural information for mammalian GGTase-I, including a series of substrate and product complexes that delineate the path of the chemical reaction. These structures reveal that all protein prenyltransferases share a common reaction mechanism and identify specific residues that play a dominant role in determining prenyl group specificity. This hypothesis was confirmed by converting farnesyltransferase (15-C prenyl substrate) into GGTase-I (20-C prenyl substrate) with a single point mutation. GGTase-I discriminates against farnesyl diphosphate (FPP) at the product turnover step through the inability of a 15-C FPP to displace the 20-C prenyl-peptide product. Understanding these key features of specificity is expected to contribute to optimization of anti-cancer and anti-parasite drugs.


==About this Structure==
==About this Structure==
1N4S is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with ZN, CL, TTH and GRG as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1N4S OCA].  
1N4S is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=CL:'>CL</scene>, <scene name='pdbligand=TTH:'>TTH</scene> and <scene name='pdbligand=GRG:'>GRG</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1N4S OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
[[Category: Beese, L.S.]]
[[Category: Beese, L S.]]
[[Category: Casey, P.J.]]
[[Category: Casey, P J.]]
[[Category: Reid, T.S.]]
[[Category: Reid, T S.]]
[[Category: Taylor, J.S.]]
[[Category: Taylor, J S.]]
[[Category: CL]]
[[Category: CL]]
[[Category: GRG]]
[[Category: GRG]]
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[[Category: rap2b]]
[[Category: rap2b]]


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