1mly: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px<br /><applet load="1mly" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mly, resolution 1.81Å" /> '''Crystal Structure of...
 
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:1mly.gif|left|200px]]<br /><applet load="1mly" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1mly.gif|left|200px]]<br /><applet load="1mly" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1mly, resolution 1.81&Aring;" />
caption="1mly, resolution 1.81&Aring;" />
'''Crystal Structure of 7,8-Diaminopelargonic Acid Synthase in complex with the cis isomer of amiclenomycin'''<br />
'''Crystal Structure of 7,8-Diaminopelargonic Acid Synthase in complex with the cis isomer of amiclenomycin'''<br />


==Overview==
==Overview==
The antibiotic amiclenomycin blocks the biosynthesis of biotin by, inhibiting the pyridoxal-phosphate-dependent enzyme diaminopelargonic acid, synthase. Inactivation of the enzyme is stereoselective, i.e. the cis, isomer of amiclenomycin is a potent inhibitor, whereas the trans isomer is, much less reactive. The crystal structure of the complex of the holoenzyme, and amiclenomycin at 1.8 A resolution reveals that the internal aldimine, linkage between the cofactor and the side chain of the catalytic residue, Lys-274 is broken. Instead, a covalent bond is formed between the 4-amino, nitrogen of amiclenomycin and the C4' carbon atom of pyridoxal-phosphate., The electron density for the bound inhibitor suggests that aromatization, of the cyclohexadiene ring has occurred upon formation of the covalent, adduct. This process could be initiated by proton abstraction at the C4, carbon atom of the cyclohexadiene ring, possibly by the proximal side, chain of Lys-274, leading to the tautomer Schiff base followed by the, removal of the second allylic hydrogen. The carboxyl tail of the, amiclenomycin moiety forms a salt link to the conserved residue Arg-391 in, the substrate-binding site. Modeling suggests steric hindrance at the, active site as the determinant of the weak inhibiting potency of the trans, isomer.
The antibiotic amiclenomycin blocks the biosynthesis of biotin by inhibiting the pyridoxal-phosphate-dependent enzyme diaminopelargonic acid synthase. Inactivation of the enzyme is stereoselective, i.e. the cis isomer of amiclenomycin is a potent inhibitor, whereas the trans isomer is much less reactive. The crystal structure of the complex of the holoenzyme and amiclenomycin at 1.8 A resolution reveals that the internal aldimine linkage between the cofactor and the side chain of the catalytic residue Lys-274 is broken. Instead, a covalent bond is formed between the 4-amino nitrogen of amiclenomycin and the C4' carbon atom of pyridoxal-phosphate. The electron density for the bound inhibitor suggests that aromatization of the cyclohexadiene ring has occurred upon formation of the covalent adduct. This process could be initiated by proton abstraction at the C4 carbon atom of the cyclohexadiene ring, possibly by the proximal side chain of Lys-274, leading to the tautomer Schiff base followed by the removal of the second allylic hydrogen. The carboxyl tail of the amiclenomycin moiety forms a salt link to the conserved residue Arg-391 in the substrate-binding site. Modeling suggests steric hindrance at the active site as the determinant of the weak inhibiting potency of the trans isomer.


==About this Structure==
==About this Structure==
1MLY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with ACZ, NA and PLP as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Adenosylmethionine--8-amino-7-oxononanoate_transaminase Adenosylmethionine--8-amino-7-oxononanoate transaminase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.6.1.62 2.6.1.62] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1MLY OCA].  
1MLY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=ACZ:'>ACZ</scene>, <scene name='pdbligand=NA:'>NA</scene> and <scene name='pdbligand=PLP:'>PLP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Adenosylmethionine--8-amino-7-oxononanoate_transaminase Adenosylmethionine--8-amino-7-oxononanoate transaminase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.6.1.62 2.6.1.62] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MLY OCA].  


==Reference==
==Reference==
Line 26: Line 26:
[[Category: subclass ii]]
[[Category: subclass ii]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 21:31:04 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:56:32 2008''