1l9o: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px<br /><applet load="1l9o" size="450" color="white" frame="true" align="right" spinBox="true" caption="1l9o, resolution 1.70Å" /> '''CRYSTAL STRUCTURE OF...
 
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:1l9o.jpg|left|200px]]<br /><applet load="1l9o" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1l9o.jpg|left|200px]]<br /><applet load="1l9o" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1l9o, resolution 1.70&Aring;" />
caption="1l9o, resolution 1.70&Aring;" />
'''CRYSTAL STRUCTURE OF NITRITE SOAKED I257A VARIANT OF THE COPPER-CONTAINING NITRITE REDUCTASE FROM ALCALIGENES FAECALIS'''<br />
'''CRYSTAL STRUCTURE OF NITRITE SOAKED I257A VARIANT OF THE COPPER-CONTAINING NITRITE REDUCTASE FROM ALCALIGENES FAECALIS'''<br />


==Overview==
==Overview==
Unlike the heme cd(1)-based nitrite reductase enzymes, the molecular, mechanism of copper-containing nitrite reductases remains controversial. A, key source of controversy is the productive binding mode of nitrite in the, active site. To identify and characterize the molecular determinants, associated with nitrite binding, we applied a combinatorial mutagenesis, approach to generate a small library of six variants at position 257 in, nitrite reductase from Alcaligenes faecalis S-6. The activities of these, six variants span nearly two orders of magnitude with one variant, I257V, the only observed natural substitution for Ile257, showing greater, activity than the native enzyme. High-resolution (&gt; 1.8 A) nitrite-soaked, crystal structures of these variants display different modes of nitrite, binding that correlate well with the altered activities. These studies, identify for the first time that the highly conserved Ile257 in the native, enzyme is a key molecular determinant in directing a catalytically, competent mode of nitrite binding in the active site. The O-coordinate, bidentate binding mode of nitrite observed in native and mutant forms with, high activity supports a catalytic model distinct from the heme cd(1), NiRs. (The atomic coordinates for I257V[NO(2)(-)], I257L[NO(2)(-)], I257A[NO(2)(-)], I257T[NO(2)(-)], I257M[NO(2)(-)] and I257G[NO(2)(-)], AfNiR have been deposited in the Protein Data Bank [PDB identification, codes are listed in Table 2].)
Unlike the heme cd(1)-based nitrite reductase enzymes, the molecular mechanism of copper-containing nitrite reductases remains controversial. A key source of controversy is the productive binding mode of nitrite in the active site. To identify and characterize the molecular determinants associated with nitrite binding, we applied a combinatorial mutagenesis approach to generate a small library of six variants at position 257 in nitrite reductase from Alcaligenes faecalis S-6. The activities of these six variants span nearly two orders of magnitude with one variant, I257V, the only observed natural substitution for Ile257, showing greater activity than the native enzyme. High-resolution (&gt; 1.8 A) nitrite-soaked crystal structures of these variants display different modes of nitrite binding that correlate well with the altered activities. These studies identify for the first time that the highly conserved Ile257 in the native enzyme is a key molecular determinant in directing a catalytically competent mode of nitrite binding in the active site. The O-coordinate bidentate binding mode of nitrite observed in native and mutant forms with high activity supports a catalytic model distinct from the heme cd(1) NiRs. (The atomic coordinates for I257V[NO(2)(-)], I257L[NO(2)(-)], I257A[NO(2)(-)], I257T[NO(2)(-)], I257M[NO(2)(-)] and I257G[NO(2)(-)] AfNiR have been deposited in the Protein Data Bank [PDB identification codes are listed in Table 2].)


==About this Structure==
==About this Structure==
1L9O is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Alcaligenes_faecalis Alcaligenes faecalis] with CU and NO2 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Nitrite_reductase_(NO-forming) Nitrite reductase (NO-forming)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.7.2.1 1.7.2.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1L9O OCA].  
1L9O is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Alcaligenes_faecalis Alcaligenes faecalis] with <scene name='pdbligand=CU:'>CU</scene> and <scene name='pdbligand=NO2:'>NO2</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Nitrite_reductase_(NO-forming) Nitrite reductase (NO-forming)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.7.2.1 1.7.2.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1L9O OCA].  


==Reference==
==Reference==
Line 14: Line 14:
[[Category: Nitrite reductase (NO-forming)]]
[[Category: Nitrite reductase (NO-forming)]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Boulanger, M.J.]]
[[Category: Boulanger, M J.]]
[[Category: Murphy, M.E.P.]]
[[Category: Murphy, M E.P.]]
[[Category: CU]]
[[Category: CU]]
[[Category: NO2]]
[[Category: NO2]]
[[Category: greek key motif]]
[[Category: greek key motif]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 20:24:18 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:42:52 2008''