236 related articles for article (PubMed ID: 11248037)
1. Reverse engineering the (beta/alpha )8 barrel fold.
Silverman JA; Balakrishnan R; Harbury PB
Proc Natl Acad Sci U S A; 2001 Mar; 98(6):3092-7. PubMed ID: 11248037
[TBL] [Abstract][Full Text] [Related]
2. Folding of beta/alpha-unit scrambled forms of S. cerevisiae triosephosphate isomerase: Evidence for autonomy of substructure formation and plasticity of hydrophobic and hydrogen bonding interactions in core of (beta/alpha)8-barrel.
Shukla A; Guptasarma P
Proteins; 2004 May; 55(3):548-57. PubMed ID: 15103619
[TBL] [Abstract][Full Text] [Related]
3. Recurrent alpha beta loop structures in TIM barrel motifs show a distinct pattern of conserved structural features.
Scheerlinck JP; Lasters I; Claessens M; De Maeyer M; Pio F; Delhaise P; Wodak SJ
Proteins; 1992 Apr; 12(4):299-313. PubMed ID: 1374562
[TBL] [Abstract][Full Text] [Related]
4. Stabilization of human triosephosphate isomerase by improvement of the stability of individual alpha-helices in dimeric as well as monomeric forms of the protein.
Mainfroid V; Mande SC; Hol WG; Martial JA; Goraj K
Biochemistry; 1996 Apr; 35(13):4110-7. PubMed ID: 8672446
[TBL] [Abstract][Full Text] [Related]
5. In vivo fragment complementation of a (beta/alpha)(8) barrel protein: generation of variability by recombination.
Soberón X; Fuentes-Gallego P; Saab-Rincón G
FEBS Lett; 2004 Feb; 560(1-3):167-72. PubMed ID: 14988017
[TBL] [Abstract][Full Text] [Related]
6. Kinetic and structural properties of triosephosphate isomerase from Helicobacter pylori.
Chu CH; Lai YJ; Huang H; Sun YJ
Proteins; 2008 Apr; 71(1):396-406. PubMed ID: 17957775
[TBL] [Abstract][Full Text] [Related]
7. Structural effects of a dimer interface mutation on catalytic activity of triosephosphate isomerase. The role of conserved residues and complementary mutations.
Banerjee M; Balaram H; Balaram P
FEBS J; 2009 Aug; 276(15):4169-83. PubMed ID: 19583769
[TBL] [Abstract][Full Text] [Related]
8. The importance of hinge sequence for loop function and catalytic activity in the reaction catalyzed by triosephosphate isomerase.
Xiang J; Sun J; Sampson NS
J Mol Biol; 2001 Apr; 307(4):1103-12. PubMed ID: 11286559
[TBL] [Abstract][Full Text] [Related]
9. The importance of surface loops for stabilizing an eightfold beta alpha barrel protein.
Urfer R; Kirschner K
Protein Sci; 1992 Jan; 1(1):31-45. PubMed ID: 1304881
[TBL] [Abstract][Full Text] [Related]
10. Mechanism of activation of human heparanase investigated by protein engineering.
Nardella C; Lahm A; Pallaoro M; Brunetti M; Vannini A; Steinkühler C
Biochemistry; 2004 Feb; 43(7):1862-73. PubMed ID: 14967027
[TBL] [Abstract][Full Text] [Related]
11. Protein design through systematic catalytic loop exchange in the (beta/alpha)8 fold.
Ochoa-Leyva A; Soberón X; Sánchez F; Argüello M; Montero-Morán G; Saab-Rincón G
J Mol Biol; 2009 Apr; 387(4):949-64. PubMed ID: 19233201
[TBL] [Abstract][Full Text] [Related]
12. Evolutionary potential of (beta/alpha)8-barrels: functional promiscuity produced by single substitutions in the enolase superfamily.
Schmidt DM; Mundorff EC; Dojka M; Bermudez E; Ness JE; Govindarajan S; Babbitt PC; Minshull J; Gerlt JA
Biochemistry; 2003 Jul; 42(28):8387-93. PubMed ID: 12859183
[TBL] [Abstract][Full Text] [Related]
13. Directed evolution of new catalytic activity using the alpha/beta-barrel scaffold.
Altamirano MM; Blackburn JM; Aguayo C; Fersht AR
Nature; 2000 Feb; 403(6770):617-22. PubMed ID: 10688189
[TBL] [Abstract][Full Text] [Related]
14. Exhaustive mutagenesis of six secondary active-site residues in Escherichia coli chorismate mutase shows the importance of hydrophobic side chains and a helix N-capping position for stability and catalysis.
Lassila JK; Keeffe JR; Kast P; Mayo SL
Biochemistry; 2007 Jun; 46(23):6883-91. PubMed ID: 17506527
[TBL] [Abstract][Full Text] [Related]
15. Evolutionary walk between (β/α)(8) barrels: catalytic migration from triosephosphate isomerase to thiamin phosphate synthase.
Saab-Rincón G; Olvera L; Olvera M; Rudiño-Piñera E; Benites E; Soberón X; Morett E
J Mol Biol; 2012 Feb; 416(2):255-70. PubMed ID: 22226942
[TBL] [Abstract][Full Text] [Related]
16. Structural insights into N-terminal to C-terminal interactions and implications for thermostability of a (β/α)8-triosephosphate isomerase barrel enzyme.
Mahanta P; Bhardwaj A; Kumar K; Reddy VS; Ramakumar S
FEBS J; 2015 Sep; 282(18):3543-55. PubMed ID: 26102498
[TBL] [Abstract][Full Text] [Related]
17. The central cavity from the (alpha/alpha)6 barrel structure of Anabaena sp. CH1 N-acetyl-D-glucosamine 2-epimerase contains two key histidine residues for reversible conversion.
Lee YC; Wu HM; Chang YN; Wang WC; Hsu WH
J Mol Biol; 2007 Mar; 367(3):895-908. PubMed ID: 17292397
[TBL] [Abstract][Full Text] [Related]
18. 3(10)-Helix adjoining alpha-helix and beta-strand: sequence and structural features and their conservation.
Pal L; Dasgupta B; Chakrabarti P
Biopolymers; 2005 Jun; 78(3):147-62. PubMed ID: 15759287
[TBL] [Abstract][Full Text] [Related]
19. Prediction of secondary structure by evolutionary comparison: application to the alpha subunit of tryptophan synthase.
Crawford IP; Niermann T; Kirschner K
Proteins; 1987; 2(2):118-29. PubMed ID: 3328860
[TBL] [Abstract][Full Text] [Related]
20. Structural elements to convert Escherichia coli alpha-xylosidase (YicI) into alpha-glucosidase.
Okuyama M; Kaneko A; Mori H; Chiba S; Kimura A
FEBS Lett; 2006 May; 580(11):2707-11. PubMed ID: 16631751
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
