1eep: Difference between revisions

New page: left|200px<br /><applet load="1eep" size="450" color="white" frame="true" align="right" spinBox="true" caption="1eep, resolution 2.40Å" /> '''2.4 A RESOLUTION CRY...
 
No edit summary
Line 1: Line 1:
[[Image:1eep.jpg|left|200px]]<br /><applet load="1eep" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1eep.jpg|left|200px]]<br /><applet load="1eep" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1eep, resolution 2.40&Aring;" />
caption="1eep, resolution 2.40&Aring;" />
'''2.4 A RESOLUTION CRYSTAL STRUCTURE OF BORRELIA BURGDORFERI INOSINE 5'-MONPHOSPHATE DEHYDROGENASE IN COMPLEX WITH A SULFATE ION'''<br />
'''2.4 A RESOLUTION CRYSTAL STRUCTURE OF BORRELIA BURGDORFERI INOSINE 5'-MONPHOSPHATE DEHYDROGENASE IN COMPLEX WITH A SULFATE ION'''<br />


==Overview==
==Overview==
The conversion of inosine 5'-monophosphate (IMP) to xanthosine, 5'-monophosphate (XMP) is the committed and rate-limiting reaction in de, novo guanine nucleotide biosynthesis. Inosine 5'- monophosphate, dehydrogenase (IMPDH) is the enzyme that catalyzes the oxidation of IMP to, XMP with the concomitant reduction of nicotinamide adenine dinucleotide, (from NAD(+) to NADH). Because of its critical role in purine, biosynthesis, IMPDH is a drug design target for anticancer, antiinfective, and immunosuppressive chemotherapy. We have determined the crystal, structure of IMPDH from Borrelia burgdorferi, the bacterial spirochete, that causes Lyme disease, with a sulfate ion bound in the IMP phosphate, binding site. This is the first structure of IMPDH in the absence of, substrate or cofactor where the active-site loop (loop 6), which contains, the essential catalytic residue Cys 229, is clearly defined in the, electron density. We report that a seven residue region of loop 6, including Cys229, is tilted more than 6 A away from its position in, substrate- or substrate analogue-bound structures of IMPDH, suggestive of, a conformational change. The location of this loop between beta6 and, alpha6 links IMPDH to a family of beta/alpha barrel enzymes known to, utilize this loop as a functional lid during catalysis. Least-squares, minimization, root-mean-square deviation analysis, and inspection of the, molecular surface of the loop 6 region in the substrate-free B., burgdorferi IMPDH and XMP-bound Chinese hamster IMPDH show that loop 6, follows a similar pattern of hinged rigid-body motion and indicates that, IMPDH may be using loop 6 to bind and sequester substrate and to recruit, an essential catalytic residue.
The conversion of inosine 5'-monophosphate (IMP) to xanthosine 5'-monophosphate (XMP) is the committed and rate-limiting reaction in de novo guanine nucleotide biosynthesis. Inosine 5'- monophosphate dehydrogenase (IMPDH) is the enzyme that catalyzes the oxidation of IMP to XMP with the concomitant reduction of nicotinamide adenine dinucleotide (from NAD(+) to NADH). Because of its critical role in purine biosynthesis, IMPDH is a drug design target for anticancer, antiinfective, and immunosuppressive chemotherapy. We have determined the crystal structure of IMPDH from Borrelia burgdorferi, the bacterial spirochete that causes Lyme disease, with a sulfate ion bound in the IMP phosphate binding site. This is the first structure of IMPDH in the absence of substrate or cofactor where the active-site loop (loop 6), which contains the essential catalytic residue Cys 229, is clearly defined in the electron density. We report that a seven residue region of loop 6, including Cys229, is tilted more than 6 A away from its position in substrate- or substrate analogue-bound structures of IMPDH, suggestive of a conformational change. The location of this loop between beta6 and alpha6 links IMPDH to a family of beta/alpha barrel enzymes known to utilize this loop as a functional lid during catalysis. Least-squares minimization, root-mean-square deviation analysis, and inspection of the molecular surface of the loop 6 region in the substrate-free B. burgdorferi IMPDH and XMP-bound Chinese hamster IMPDH show that loop 6 follows a similar pattern of hinged rigid-body motion and indicates that IMPDH may be using loop 6 to bind and sequester substrate and to recruit an essential catalytic residue.


==About this Structure==
==About this Structure==
1EEP is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Borrelia_burgdorferi Borrelia burgdorferi] with SO4 as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/IMP_dehydrogenase IMP dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.205 1.1.1.205] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1EEP OCA].  
1EEP is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Borrelia_burgdorferi Borrelia burgdorferi] with <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/IMP_dehydrogenase IMP dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.205 1.1.1.205] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EEP OCA].  


==Reference==
==Reference==
Line 16: Line 16:
[[Category: Cahoon, M.]]
[[Category: Cahoon, M.]]
[[Category: Hedstrom, L.]]
[[Category: Hedstrom, L.]]
[[Category: McMillan, F.M.]]
[[Category: McMillan, F M.]]
[[Category: Petsko, G.A.]]
[[Category: Petsko, G A.]]
[[Category: Ringe, D.]]
[[Category: Ringe, D.]]
[[Category: White, A.]]
[[Category: White, A.]]
Line 28: Line 28:
[[Category: tim barrel]]
[[Category: tim barrel]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 13:56:49 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:26:56 2008''

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA