1d9s

<StructureSection load='1d9s' size='340' side='right'caption='[[1d9s]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>

<table><tr><td colspan='2'>[[1d9s]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1D9S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1D9S FirstGlance]. <br>

</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1d9s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1d9s OCA], [https://pdbe.org/1d9s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1d9s RCSB], [https://www.ebi.ac.uk/pdbsum/1d9s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1d9s ProSAT]</span></td></tr>

[[https://www.uniprot.org/uniprot/CDN2B_MOUSE CDN2B_MOUSE]] Interacts strongly with CDK4 and CDK6. Potent inhibitor. Potential effector of TGF-beta induced cell cycle arrest (By similarity).

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== Publication Abstract from PubMed ==

The INK4 (inhibitor of cyclin-dependent kinase 4) family consists of four tumor-suppressor proteins: p15(INK4B), p16(INK4A), p18(INK4C), and p19(INK4D). While their sequences and structures are highly homologous, they show appreciable differences in conformational flexibility, stability, and aggregation tendency. Here, p16 and p18 were first compared directly by NMR for line broadening and disappearance, then investigated by three different approaches in search of the causes of these differences. From denaturation experiments it was found that both proteins are marginally stable with low denaturation stability (1.94 and 2.98 kcal/mol, respectively). Heteronuclear (1)H-(15)N nuclear Overhauser enhancement measurements revealed very limited conformational flexibility on the pico- to nanosecond time-scale for both p16 and p18. H/(2)H exchange of amide protons monitored by NMR on three proteins (p16, p18 as well as p15), however, revealed markedly different rates in the order p18&lt;p16&lt;/=p15. A subset of very slowly exchanging residues (about 19 in total) was identified in p18, including 16 residues in the region of the fourth ankyrin repeat, probably as a result of a stabilizing effect by the extra ankyrin repeat. Thus, while INK4 proteins may have similar low thermodynamic stability as well as limited flexibility on the pico- to nanosecond time-scale, they display pronounced differences in the conformational flexibility on the time-scale of minutes to hours. Further analyses suggested that differences in H/(2)H exchange rates reflect differences in the kinetic stability of the INK4 proteins, which in turn is related to differences in the aggregation tendency.

Tumor suppressor INK4: comparisons of conformational properties between p16(INK4A) and p18(INK4C).,Yuan C, Li J, Selby TL, Byeon IJ, Tsai MD J Mol Biol. 1999 Nov 19;294(1):201-11. PMID:10556039<ref>PMID:10556039</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>

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<div class="pdbe-citations 1d9s" style="background-color:#fffaf0;"></div>

== References ==

<references/>

[[Category: Lk3 transgenic mice]]

[[Category: Byeon, I J.L]]

[[Category: Ji, L]]

[[Category: Selby, T L]]

[[Category: Tsai, M D]]

[[Category: Yuan, C]]

[[Category: Signaling protein]]