This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.

Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1mx4

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1mx4.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1mx4.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1mx4| PDB=1mx4 | SCENE= }}
{{STRUCTURE_1mx4| PDB=1mx4 | SCENE= }}
-
'''Structure of p18INK4c (F82Q)'''
+
===Structure of p18INK4c (F82Q)===
-
==Overview==
+
<!--
-
p18(INK4c) is a member of the INK4 family of proteins that regulate the G(1) to S cell cycle transition by binding to and inhibiting the pRb kinase activity of cyclin-dependent kinases 4 and 6. The p16(INK4a) member of the INK4 protein family is altered in a variety of cancers and structure-function studies of the INK4 proteins reveal that the vast majority of missense tumor-derived p16(INK4a) mutations reduce protein thermodynamic stability. Based on this observation, we used p18(INK4c) as a model to test the proposal that INK4 proteins with increased stability might have enhanced cell cycle inhibitory activity. Structure-based mutagenesis was used to prepare p18(INK4c) mutant proteins with a predicted increase in stability. Using this approach, we report the generation of three mutant p18(INK4C) proteins, F71N, F82Q, and F92N, with increased stability toward thermal denaturation of which the F71N mutant also showed an increased stability to chemical denaturation. The x-ray crystal structures of the F71N, F82Q, and F92N p18INK4C mutant proteins were determined to reveal the structural basis for their increased stability properties. Significantly, the F71N mutant also showed enhanced CDK6 interaction and cell cycle inhibitory activity in vivo, as measured using co-immunoprecipitation and transient transfection assays, respectively. These studies show that a structure-based approach to increase the thermodynamic stability of INK4 proteins can be exploited to prepare more biologically active molecules with potential applications for the development of molecules to treat p16(INK4a)-mediated cancers.
+
The line below this paragraph, {{ABSTRACT_PUBMED_12370184}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 12370184 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_12370184}}
==About this Structure==
==About this Structure==
Line 28: Line 32:
[[Category: Venkataramani, R N.]]
[[Category: Venkataramani, R N.]]
[[Category: Ankyrin repeat]]
[[Category: Ankyrin repeat]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 01:49:34 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 05:14:59 2008''

Revision as of 02:15, 28 July 2008

Image:1mx4.png

Template:STRUCTURE 1mx4

Structure of p18INK4c (F82Q)

Template:ABSTRACT PUBMED 12370184

About this Structure

1MX4 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structure-based design of p18INK4c proteins with increased thermodynamic stability and cell cycle inhibitory activity., Venkataramani RN, MacLachlan TK, Chai X, El-Deiry WS, Marmorstein R, J Biol Chem. 2002 Dec 13;277(50):48827-33. Epub 2002 Oct 4. PMID:12370184

Page seeded by OCA on Mon Jul 28 05:14:59 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1mx4"
Personal tools