1wva

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[[Image:1wva.gif|left|200px]]
[[Image:1wva.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1wva |SIZE=350|CAPTION= <scene name='initialview01'>1wva</scene>, resolution 1.94&Aring;
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The line below this paragraph, containing "STRUCTURE_1wva", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</scene>, <scene name='pdbligand=S2C:S-2-(BORONOETHYL)-L-CYSTEINE'>S2C</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Arginase Arginase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.3.1 3.5.3.1] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1wva| PDB=1wva | SCENE= }}
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|RELATEDENTRY=[[1wvb|1WVB]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1wva FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wva OCA], [http://www.ebi.ac.uk/pdbsum/1wva PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1wva RCSB]</span>
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}}
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'''Crystal structure of human arginase I from twinned crystal'''
'''Crystal structure of human arginase I from twinned crystal'''
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[[Category: Rodriguez, P C.]]
[[Category: Rodriguez, P C.]]
[[Category: Sabio, G.]]
[[Category: Sabio, G.]]
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[[Category: bec inhibitor]]
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[[Category: Bec inhibitor]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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[[Category: twinned crystal]]
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[[Category: Twinned crystal]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 14:11:05 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:41:28 2008''
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Revision as of 11:11, 3 May 2008

Template:STRUCTURE 1wva

Crystal structure of human arginase I from twinned crystal


Overview

Human arginase I is a potential target for therapeutic intervention in diseases linked to compromised l-arginine homeostasis. Here, we report high-affinity binding of the reaction coordinate analogue inhibitors 2(S)-amino-6-boronohexanoic acid (ABH, Kd = 5 nM) and S-(2-boronoethyl)-l-cysteine (BEC, Kd = 270 nM) to human arginase I, and we report x-ray crystal structures of the respective enzyme-inhibitor complexes at 1.29- and 1.94-A resolution determined from crystals twinned by hemihedry. The ultrahigh-resolution structure of the human arginase I-ABH complex yields an unprecedented view of the binuclear manganese cluster and illuminates the structural basis for nanomolar affinity: bidentate inner-sphere boronate-manganese coordination interactions and fully saturated hydrogen bond networks with inhibitor alpha-amino and alpha-carboxylate groups. These interactions are therefore implicated in the stabilization of the transition state for l-arginine hydrolysis. Electron density maps also reveal that active-site residue H141 is protonated as the imidazolium cation. The location of H141 is such that it could function as a general acid to protonate the leaving amino group of l-ornithine during catalysis, and this is a revised mechanistic proposal for arginase. This work serves as a foundation for studying the structural and chemical biology of arginase I in the immune response, and we demonstrate the inhibition of arginase activity by ABH in human and murine myeloid cells.

About this Structure

1WVA is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystal structure of human arginase I at 1.29-A resolution and exploration of inhibition in the immune response., Di Costanzo L, Sabio G, Mora A, Rodriguez PC, Ochoa AC, Centeno F, Christianson DW, Proc Natl Acad Sci U S A. 2005 Sep 13;102(37):13058-63. Epub 2005 Sep 2. PMID:16141327 Page seeded by OCA on Sat May 3 14:11:05 2008

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