Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 6

1.

BAR scaffolds drive membrane fission by crowding disordered domains.

Snead WT, Zeno WF, Kago G, Perkins RW, Richter JB, Zhao C, Lafer EM, Stachowiak JC.

J Cell Biol. 2018 Nov 30. pii: jcb.201807119. doi: 10.1083/jcb.201807119. [Epub ahead of print]

PMID:
30504247
2.

Ubiquitin-like domains can target to the proteasome but proteolysis requires a disordered region.

Yu H, Kago G, Yellman CM, Matouschek A.

EMBO J. 2016 Jul 15;35(14):1522-36. doi: 10.15252/embj.201593147. Epub 2016 May 27.

3.

Conserved Sequence Preferences Contribute to Substrate Recognition by the Proteasome.

Yu H, Singh Gautam AK, Wilmington SR, Wylie D, Martinez-Fonts K, Kago G, Warburton M, Chavali S, Inobe T, Finkelstein IJ, Babu MM, Matouschek A.

J Biol Chem. 2016 Jul 8;291(28):14526-39. doi: 10.1074/jbc.M116.727578. Epub 2016 May 17.

4.

Sequence composition of disordered regions fine-tunes protein half-life.

Fishbain S, Inobe T, Israeli E, Chavali S, Yu H, Kago G, Babu MM, Matouschek A.

Nat Struct Mol Biol. 2015 Mar;22(3):214-21. doi: 10.1038/nsmb.2958. Epub 2015 Feb 2.

5.

Structural analysis of a fungal methionine synthase with substrates and inhibitors.

Ubhi D, Kago G, Monzingo AF, Robertus JD.

J Mol Biol. 2014 Apr 17;426(8):1839-47. doi: 10.1016/j.jmb.2014.02.006. Epub 2014 Feb 11.

PMID:
24524835
6.

Exploring naphthyl-carbohydrazides as inhibitors of influenza A viruses.

Barman S, You L, Chen R, Codrea V, Kago G, Edupuganti R, Robertus J, Krug RM, Anslyn EV.

Eur J Med Chem. 2014 Jan;71:81-90. doi: 10.1016/j.ejmech.2013.10.063. Epub 2013 Nov 7.

Supplemental Content

Support Center