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1rzy

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(New page: 200px<br /><applet load="1rzy" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rzy, resolution 1.80&Aring;" /> '''Crystal structure of...)
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[[Image:1rzy.jpg|left|200px]]<br /><applet load="1rzy" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1rzy, resolution 1.80&Aring;" />
caption="1rzy, resolution 1.80&Aring;" />
'''Crystal structure of rabbit Hint complexed with N-ethylsulfamoyladenosine'''<br />
'''Crystal structure of rabbit Hint complexed with N-ethylsulfamoyladenosine'''<br />
==Overview==
==Overview==
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Hint, histidine triad nucleotide-binding protein, is a universally, conserved enzyme that hydrolyzes AMP linked to lysine and, in yeast, functions as a positive regulator of the RNA polymerase II C-terminal, domain kinase, Kin28. To explore the biochemical and structural bases for, the adenosine phosphoramidate hydrolase activity of rabbit Hint, we, synthesized novel substrates linking a p-nitroaniline group to adenylate, (AMP-pNA) and inhibitors that consist of an adenosine group and, 5'-sulfamoyl (AdoOSO(2)NH(2)) or N-ethylsulfamoyl (AdoOSO(2)NHCH(2)CH(3)), group. AMP-pNA is a suitable substrate for Hint that allowed, characterization of the inhibitors; titration of each inhibitor into, AMP-pNA assays revealed their K(i) values. The N-ethylsulfamoyl derivative, has a 13-fold binding advantage over the sulfamoyl adenosine. The 1.8-A, cocrystal structure of rabbit Hint with N-ethylsulfamoyl adenosine, revealed a binding site for the ethyl group against Trp-123, a residue, that reaches across the Hint dimer interface to interact with the alkyl, portion of the inhibitor and, presumably, the alkyl portion of a lysyl, substrate. Ser-107 is positioned to donate a hydrogen bond to the leaving, group nitrogen. Consistent with a role in acid-base catalysis, the Hint, S107A mutant protein displayed depressed catalytic activity.
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Hint, histidine triad nucleotide-binding protein, is a universally conserved enzyme that hydrolyzes AMP linked to lysine and, in yeast, functions as a positive regulator of the RNA polymerase II C-terminal domain kinase, Kin28. To explore the biochemical and structural bases for the adenosine phosphoramidate hydrolase activity of rabbit Hint, we synthesized novel substrates linking a p-nitroaniline group to adenylate (AMP-pNA) and inhibitors that consist of an adenosine group and 5'-sulfamoyl (AdoOSO(2)NH(2)) or N-ethylsulfamoyl (AdoOSO(2)NHCH(2)CH(3)) group. AMP-pNA is a suitable substrate for Hint that allowed characterization of the inhibitors; titration of each inhibitor into AMP-pNA assays revealed their K(i) values. The N-ethylsulfamoyl derivative has a 13-fold binding advantage over the sulfamoyl adenosine. The 1.8-A cocrystal structure of rabbit Hint with N-ethylsulfamoyl adenosine revealed a binding site for the ethyl group against Trp-123, a residue that reaches across the Hint dimer interface to interact with the alkyl portion of the inhibitor and, presumably, the alkyl portion of a lysyl substrate. Ser-107 is positioned to donate a hydrogen bond to the leaving group nitrogen. Consistent with a role in acid-base catalysis, the Hint S107A mutant protein displayed depressed catalytic activity.
==About this Structure==
==About this Structure==
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1RZY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with 5AS as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1RZY OCA].
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1RZY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with <scene name='pdbligand=5AS:'>5AS</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RZY OCA].
==Reference==
==Reference==
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[[Category: Adams, M.]]
[[Category: Adams, M.]]
[[Category: Baraniak, J.]]
[[Category: Baraniak, J.]]
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[[Category: Blackburn, G.M.]]
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[[Category: Blackburn, G M.]]
[[Category: Brenner, C.]]
[[Category: Brenner, C.]]
[[Category: Kaczmarek, R.]]
[[Category: Kaczmarek, R.]]
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[[Category: Krakowiak, A.K.]]
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[[Category: Krakowiak, A K.]]
[[Category: Mekhalfia, A.]]
[[Category: Mekhalfia, A.]]
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[[Category: Pace, H.C.]]
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[[Category: Pace, H C.]]
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[[Category: Stec, W.J.]]
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[[Category: Stec, W J.]]
[[Category: 5AS]]
[[Category: 5AS]]
[[Category: hit protein; protein-inhibitor complex]]
[[Category: hit protein; protein-inhibitor complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 01:59:40 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:56:26 2008''

Revision as of 12:56, 21 February 2008


1rzy, resolution 1.80Å

Drag the structure with the mouse to rotate

Crystal structure of rabbit Hint complexed with N-ethylsulfamoyladenosine

Overview

Hint, histidine triad nucleotide-binding protein, is a universally conserved enzyme that hydrolyzes AMP linked to lysine and, in yeast, functions as a positive regulator of the RNA polymerase II C-terminal domain kinase, Kin28. To explore the biochemical and structural bases for the adenosine phosphoramidate hydrolase activity of rabbit Hint, we synthesized novel substrates linking a p-nitroaniline group to adenylate (AMP-pNA) and inhibitors that consist of an adenosine group and 5'-sulfamoyl (AdoOSO(2)NH(2)) or N-ethylsulfamoyl (AdoOSO(2)NHCH(2)CH(3)) group. AMP-pNA is a suitable substrate for Hint that allowed characterization of the inhibitors; titration of each inhibitor into AMP-pNA assays revealed their K(i) values. The N-ethylsulfamoyl derivative has a 13-fold binding advantage over the sulfamoyl adenosine. The 1.8-A cocrystal structure of rabbit Hint with N-ethylsulfamoyl adenosine revealed a binding site for the ethyl group against Trp-123, a residue that reaches across the Hint dimer interface to interact with the alkyl portion of the inhibitor and, presumably, the alkyl portion of a lysyl substrate. Ser-107 is positioned to donate a hydrogen bond to the leaving group nitrogen. Consistent with a role in acid-base catalysis, the Hint S107A mutant protein displayed depressed catalytic activity.

About this Structure

1RZY is a Single protein structure of sequence from Oryctolagus cuniculus with as ligand. Full crystallographic information is available from OCA.

Reference

Biochemical, crystallographic, and mutagenic characterization of hint, the AMP-lysine hydrolase, with novel substrates and inhibitors., Krakowiak A, Pace HC, Blackburn GM, Adams M, Mekhalfia A, Kaczmarek R, Baraniak J, Stec WJ, Brenner C, J Biol Chem. 2004 Apr 30;279(18):18711-6. Epub 2004 Feb 24. PMID:14982931

Page seeded by OCA on Thu Feb 21 14:56:26 2008

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