1z6d: Difference between revisions

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[[Image:1z6d.gif|left|200px]]
[[Image:1z6d.gif|left|200px]]


{{Structure
<!--
|PDB= 1z6d |SIZE=350|CAPTION= <scene name='initialview01'>1z6d</scene>, resolution 1.54&Aring;
The line below this paragraph, containing "STRUCTURE_1z6d", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=IMP:INOSINIC+ACID'>IMP</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Pancreatic_ribonuclease Pancreatic ribonuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.27.5 3.1.27.5] </span>
or leave the SCENE parameter empty for the default display.
|GENE=  
-->
|DOMAIN=
{{STRUCTURE_1z6d| PDB=1z6d  | SCENE= }}  
|RELATEDENTRY=[[1o0f|1O0F]], [[1o0o|1O0O]], [[1o0h|1O0H]], [[1o0m|1O0M]], [[1o0n|1O0N]], [[1z6s|1Z6S]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1z6d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1z6d OCA], [http://www.ebi.ac.uk/pdbsum/1z6d PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1z6d RCSB]</span>
}}


'''Ribonuclease A- IMP complex'''
'''Ribonuclease A- IMP complex'''
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[[Category: Leonidas, D D.]]
[[Category: Leonidas, D D.]]
[[Category: Oikonomakos, N G.]]
[[Category: Oikonomakos, N G.]]
[[Category: hydrolase]]
[[Category: Hydrolase]]
[[Category: ribonuclease]]
[[Category: Ribonuclease]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 17:13:38 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 01:29:44 2008''

Revision as of 17:13, 3 May 2008

File:1z6d.gif

Template:STRUCTURE 1z6d

Ribonuclease A- IMP complex


OverviewOverview

The binding of inosine 5' phosphate (IMP) to ribonuclease A has been studied by kinetic and X-ray crystallographic experiments at high (1.5 A) resolution. IMP is a competitive inhibitor of the enzyme with respect to C>p and binds to the catalytic cleft by anchoring three IMP molecules in a novel binding mode. The three IMP molecules are connected to each other by hydrogen bond and van der Waals interactions and collectively occupy the B1R1P1B2P0P(-1) region of the ribonucleolytic active site. One of the IMP molecules binds with its nucleobase in the outskirts of the B2 subsite and interacts with Glu111 while its phosphoryl group binds in P1. Another IMP molecule binds by following the retro-binding mode previously observed only for guanosines with its nucleobase at B1 and the phosphoryl group in P(-1). The third IMP molecule binds in a novel mode towards the C-terminus. The RNase A-IMP complex provides structural evidence for the functional components of subsite P(-1) while it further supports the role inferred by other studies to Asn71 as the primary structural determinant for the adenine specificity of the B2 subsite. Comparative structural analysis of the IMP and AMP complexes highlights key aspects of the specificity of the base binding subsites of RNase A and provides a structural explanation for their potencies. The binding of IMP suggests ways to develop more potent inhibitors of the pancreatic RNase superfamily using this nucleotide as the starting point.

About this StructureAbout this Structure

1Z6D is a Single protein structure of sequence from Bos taurus. Full crystallographic information is available from OCA.

ReferenceReference

The binding of IMP to ribonuclease A., Hatzopoulos GN, Leonidas DD, Kardakaris R, Kobe J, Oikonomakos NG, FEBS J. 2005 Aug;272(15):3988-4001. PMID:16045769 Page seeded by OCA on Sat May 3 17:13:38 2008

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