1meo

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1meo.jpg|left|200px]]<br /><applet load="1meo" size="350" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1meo.jpg|left|200px]]
-
caption="1meo, resolution 1.72&Aring;" />
+
 
-
'''human glycinamide ribonucleotide Transformylase at pH 4.2'''<br />
+
{{Structure
 +
|PDB= 1meo |SIZE=350|CAPTION= <scene name='initialview01'>1meo</scene>, resolution 1.72&Aring;
 +
|SITE=
 +
|LIGAND= <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene> and <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene>
 +
|ACTIVITY= [http://en.wikipedia.org/wiki/Phosphoribosylglycinamide_formyltransferase Phosphoribosylglycinamide formyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.1.2.2 2.1.2.2]
 +
|GENE= GART ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
 +
}}
 +
 
 +
'''human glycinamide ribonucleotide Transformylase at pH 4.2'''
 +
 
==Overview==
==Overview==
Line 7: Line 16:
==About this Structure==
==About this Structure==
-
1MEO 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=PO4:'>PO4</scene> and <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Phosphoribosylglycinamide_formyltransferase Phosphoribosylglycinamide formyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.1.2.2 2.1.2.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MEO OCA].
+
1MEO is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MEO OCA].
==Reference==
==Reference==
-
Crystal structures of human GAR Tfase at low and high pH and with substrate beta-GAR., Zhang Y, Desharnais J, Greasley SE, Beardsley GP, Boger DL, Wilson IA, Biochemistry. 2002 Dec 3;41(48):14206-15. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12450384 12450384]
+
Crystal structures of human GAR Tfase at low and high pH and with substrate beta-GAR., Zhang Y, Desharnais J, Greasley SE, Beardsley GP, Boger DL, Wilson IA, Biochemistry. 2002 Dec 3;41(48):14206-15. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/12450384 12450384]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Phosphoribosylglycinamide formyltransferase]]
[[Category: Phosphoribosylglycinamide formyltransferase]]
Line 24: Line 33:
[[Category: purine biosynthesis]]
[[Category: purine biosynthesis]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:54:29 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 12:42:33 2008''

Revision as of 10:42, 20 March 2008


PDB ID 1meo

Drag the structure with the mouse to rotate
, resolution 1.72Å
Ligands: and
Gene: GART (Homo sapiens)
Activity: Phosphoribosylglycinamide formyltransferase, with EC number 2.1.2.2
Coordinates: save as pdb, mmCIF, xml



human glycinamide ribonucleotide Transformylase at pH 4.2


Overview

Glycinamide ribonucleotide transformylase (GAR Tfase) is a key folate-dependent enzyme in the de novo purine biosynthesis pathway and, as such, has been the target for antitumor drug design. Here, we describe the crystal structures of the human GAR Tfase (purN) component of the human trifunctional protein (purD-purM-purN) at various pH values and in complex with its substrate. Human GAR Tfase exhibits pH-dependent enzyme activity with its maximum around pH 7.5-8. Comparison of unliganded human GAR Tfase structures at pH 4.2 and pH 8.5 reveals conformational differences in the substrate binding loop, which at pH 4.2 occupies the binding cleft and prohibits substrate binding, while at pH 8.5 is permissive for substrate binding. The crystal structure of GAR Tfase with its natural substrate, beta-glycinamide ribonucleotide (beta-GAR), at pH 8.5 confirms this conformational isomerism. Surprisingly, several important structural differences are found between human GAR Tfase and previously reported E. coli GAR Tfase structures, which have been used as the primary template for drug design studies. While the E. coli structure gave valuable insights into the active site and formyl transfer mechanism, differences in structure and inhibition between the bacterial and mammalian enzymes suggest that the human GAR Tfase structure is now the appropriate template for the design of anti-cancer agents.

About this Structure

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

Reference

Crystal structures of human GAR Tfase at low and high pH and with substrate beta-GAR., Zhang Y, Desharnais J, Greasley SE, Beardsley GP, Boger DL, Wilson IA, Biochemistry. 2002 Dec 3;41(48):14206-15. PMID:12450384

Page seeded by OCA on Thu Mar 20 12:42:33 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools