2q7o: Difference between revisions

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==Overview==
==Overview==
Human purine nucleoside phosphorylase (PNP) was crystallized with, transition-state analogue inhibitors Immucillin-H and DADMe-Immucillin-H, synthesized with ribosyl mimics of l-stereochemistry. The inhibitors, demonstrate that major driving forces for tight binding of these analogues, are the leaving group interaction and the cationic mimicry of the, transition state, even though large geometric changes occur with, d-Immucillins and l-Immucillins bound to human PNP.
Human purine nucleoside phosphorylase (PNP) was crystallized with transition-state analogue inhibitors Immucillin-H and DADMe-Immucillin-H synthesized with ribosyl mimics of l-stereochemistry. The inhibitors demonstrate that major driving forces for tight binding of these analogues are the leaving group interaction and the cationic mimicry of the transition state, even though large geometric changes occur with d-Immucillins and l-Immucillins bound to human PNP.


==About this Structure==
==About this Structure==
2Q7O is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=PO4:'>PO4</scene> and <scene name='pdbligand=IMH:'>IMH</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Purine-nucleoside_phosphorylase Purine-nucleoside phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.1 2.4.2.1] Known structural/functional Sites: <scene name='pdbsite=AC1:Po4 Binding Site For Residue E 290'>AC1</scene> and <scene name='pdbsite=AC2:Imh Binding Site For Residue E 291'>AC2</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q7O OCA].  
2Q7O is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=PO4:'>PO4</scene> and <scene name='pdbligand=IMH:'>IMH</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Purine-nucleoside_phosphorylase Purine-nucleoside phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.1 2.4.2.1] Known structural/functional Sites: <scene name='pdbsite=AC1:Po4+Binding+Site+For+Residue+E+290'>AC1</scene> and <scene name='pdbsite=AC2:Imh+Binding+Site+For+Residue+E+291'>AC2</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q7O OCA].  


==Reference==
==Reference==
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[[Category: Purine-nucleoside phosphorylase]]
[[Category: Purine-nucleoside phosphorylase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Almo, S.C.]]
[[Category: Almo, S C.]]
[[Category: Rinaldo-Matthis, A.]]
[[Category: Rinaldo-Matthis, A.]]
[[Category: Schramm, V.L.]]
[[Category: Schramm, V L.]]
[[Category: IMH]]
[[Category: IMH]]
[[Category: PO4]]
[[Category: PO4]]
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[[Category: transferase]]
[[Category: transferase]]


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Revision as of 19:36, 21 February 2008

File:2q7o.jpg


2q7o, resolution 2.900Å

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Structure of human purine nucleoside phosphorylase in complex with L-Immucillin-H

OverviewOverview

Human purine nucleoside phosphorylase (PNP) was crystallized with transition-state analogue inhibitors Immucillin-H and DADMe-Immucillin-H synthesized with ribosyl mimics of l-stereochemistry. The inhibitors demonstrate that major driving forces for tight binding of these analogues are the leaving group interaction and the cationic mimicry of the transition state, even though large geometric changes occur with d-Immucillins and l-Immucillins bound to human PNP.

About this StructureAbout this Structure

2Q7O is a Single protein structure of sequence from Homo sapiens with and as ligands. Active as Purine-nucleoside phosphorylase, with EC number 2.4.2.1 Known structural/functional Sites: and . Full crystallographic information is available from OCA.

ReferenceReference

L-Enantiomers of transition state analogue inhibitors bound to human purine nucleoside phosphorylase., Rinaldo-Matthis A, Murkin AS, Ramagopal UA, Clinch K, Mee SP, Evans GB, Tyler PC, Furneaux RH, Almo SC, Schramm VL, J Am Chem Soc. 2008 Jan 23;130(3):842-4. Epub 2007 Dec 23. PMID:18154341

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