2aeb: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px<br /> <applet load="2aeb" size="450" color="white" frame="true" align="right" spinBox="true" caption="2aeb, resolution 1.29Å" /> '''Crystal structure o...
 
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:2aeb.gif|left|200px]]<br />
[[Image:2aeb.gif|left|200px]]<br /><applet load="2aeb" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2aeb" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2aeb, resolution 1.29&Aring;" />
caption="2aeb, resolution 1.29&Aring;" />
'''Crystal structure of human arginase I at 1.29 A resolution and exploration of inhibition in immune response.'''<br />
'''Crystal structure of human arginase I at 1.29 A resolution and exploration of inhibition in immune response.'''<br />


==Overview==
==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.
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==
==About this Structure==
2AEB 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 MN and AB5 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2AEB OCA].  
2AEB 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=MN:'>MN</scene> and <scene name='pdbligand=AB5:'>AB5</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2AEB OCA].  


==Reference==
==Reference==
Line 16: Line 15:
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Centeno, F.]]
[[Category: Centeno, F.]]
[[Category: Christianson, D.W.]]
[[Category: Christianson, D W.]]
[[Category: Costanzo, L.Di.]]
[[Category: Costanzo, L Di.]]
[[Category: Mora, A.]]
[[Category: Mora, A.]]
[[Category: Ochoa, A.C.]]
[[Category: Ochoa, A C.]]
[[Category: Rodriguez, P.C.]]
[[Category: Rodriguez, P C.]]
[[Category: Sabio, G.]]
[[Category: Sabio, G.]]
[[Category: AB5]]
[[Category: AB5]]
Line 29: Line 28:
[[Category: perfectly twinned crystal]]
[[Category: perfectly twinned crystal]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:49:44 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:26:29 2008''