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Items: 1 to 20 of 104

1.

Multidomain Carbohydrate-binding Proteins Involved in Bacteroides thetaiotaomicron Starch Metabolism.

Cameron EA, Maynard MA, Smith CJ, Smith TJ, Koropatkin NM, Martens EC.

J Biol Chem. 2012 Oct 5;287(41):34614-25. doi: 10.1074/jbc.M112.397380. Epub 2012 Aug 21.

2.

Multifunctional nutrient-binding proteins adapt human symbiotic bacteria for glycan competition in the gut by separately promoting enhanced sensing and catalysis.

Cameron EA, Kwiatkowski KJ, Lee BH, Hamaker BR, Koropatkin NM, Martens EC.

MBio. 2014 Sep 9;5(5):e01441-14. doi: 10.1128/mBio.01441-14.

5.
6.

Superresolution imaging captures carbohydrate utilization dynamics in human gut symbionts.

Karunatilaka KS, Cameron EA, Martens EC, Koropatkin NM, Biteen JS.

MBio. 2014 Nov 11;5(6):e02172. doi: 10.1128/mBio.02172-14.

7.

Structure of Bacteroides thetaiotaomicron BT2081 at 2.05 Å resolution: the first structural representative of a new protein family that may play a role in carbohydrate metabolism.

Yeh AP, Abdubek P, Astakhova T, Axelrod HL, Bakolitsa C, Cai X, Carlton D, Chen C, Chiu HJ, Chiu M, Clayton T, Das D, Deller MC, Duan L, Ellrott K, Farr CL, Feuerhelm J, Grant JC, Grzechnik A, Han GW, Jaroszewski L, Jin KK, Klock HE, Knuth MW, Kozbial P, Krishna SS, Kumar A, Lam WW, Marciano D, McMullan D, Miller MD, Morse AT, Nigoghossian E, Nopakun A, Okach L, Puckett C, Reyes R, Tien HJ, Trame CB, van den Bedem H, Weekes D, Wooten T, Xu Q, Hodgson KO, Wooley J, Elsliger MA, Deacon AM, Godzik A, Lesley SA, Wilson IA.

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Oct 1;66(Pt 10):1287-96. doi: 10.1107/S1744309110028228. Epub 2010 Aug 4.

8.

A structural and functional analysis of alpha-glucan recognition by family 25 and 26 carbohydrate-binding modules reveals a conserved mode of starch recognition.

Boraston AB, Healey M, Klassen J, Ficko-Blean E, Lammerts van Bueren A, Law V.

J Biol Chem. 2006 Jan 6;281(1):587-98. Epub 2005 Oct 17.

10.

Starch catabolism by a prominent human gut symbiont is directed by the recognition of amylose helices.

Koropatkin NM, Martens EC, Gordon JI, Smith TJ.

Structure. 2008 Jul;16(7):1105-15. doi: 10.1016/j.str.2008.03.017.

11.
12.

Structure of the GH76 α-mannanase homolog, BT2949, from the gut symbiont Bacteroides thetaiotaomicron.

Thompson AJ, Cuskin F, Spears RJ, Dabin J, Turkenburg JP, Gilbert HJ, Davies GJ.

Acta Crystallogr D Biol Crystallogr. 2015 Feb;71(Pt 2):408-15. doi: 10.1107/S1399004714026443. Epub 2015 Jan 23.

13.
14.

Location and characterization of genes involved in binding of starch to the surface of Bacteroides thetaiotaomicron.

Tancula E, Feldhaus MJ, Bedzyk LA, Salyers AA.

J Bacteriol. 1992 Sep;174(17):5609-16.

15.

A discrete genetic locus confers xyloglucan metabolism in select human gut Bacteroidetes.

Larsbrink J, Rogers TE, Hemsworth GR, McKee LS, Tauzin AS, Spadiut O, Klinter S, Pudlo NA, Urs K, Koropatkin NM, Creagh AL, Haynes CA, Kelly AG, Cederholm SN, Davies GJ, Martens EC, Brumer H.

Nature. 2014 Feb 27;506(7489):498-502. doi: 10.1038/nature12907. Epub 2014 Jan 19.

16.

SusG: a unique cell-membrane-associated alpha-amylase from a prominent human gut symbiont targets complex starch molecules.

Koropatkin NM, Smith TJ.

Structure. 2010 Feb 10;18(2):200-15. doi: 10.1016/j.str.2009.12.010.

17.

Suggested alternative starch utilization system from the human gut bacterium Bacteroides thetaiotaomicron.

Chaudet MM, Rose DR.

Biochem Cell Biol. 2016 Jun;94(3):241-6. doi: 10.1139/bcb-2016-0002. Epub 2016 Feb 10.

PMID:
27093479
18.

Molecular Dissection of Xyloglucan Recognition in a Prominent Human Gut Symbiont.

Tauzin AS, Kwiatkowski KJ, Orlovsky NI, Smith CJ, Creagh AL, Haynes CA, Wawrzak Z, Brumer H, Koropatkin NM.

MBio. 2016 Apr 26;7(2):e02134-15. doi: 10.1128/mBio.02134-15.

20.

Structure of a SusD homologue, BT1043, involved in mucin O-glycan utilization in a prominent human gut symbiont.

Koropatkin N, Martens EC, Gordon JI, Smith TJ.

Biochemistry. 2009 Feb 24;48(7):1532-42. doi: 10.1021/bi801942a.

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