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Journal Abstract Search

903 related items for PubMed ID: 18400533

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  • 2. Solution structure of the N-terminal domain of a potential copper-translocating P-type ATPase from Bacillus subtilis in the apo and Cu(I) loaded states.
    Banci L, Bertini I, Ciofi-Baffoni S, D'Onofrio M, Gonnelli L, Marhuenda-Egea FC, Ruiz-Dueñas FJ.
    J Mol Biol; 2002 Mar 29; 317(3):415-29. PubMed ID: 11922674
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  • 5. The ATP-dependent CodWX (HslVU) protease in Bacillus subtilis is an N-terminal serine protease.
    Kang MS, Lim BK, Seong IS, Seol JH, Tanahashi N, Tanaka K, Chung CH.
    EMBO J; 2001 Feb 15; 20(4):734-42. PubMed ID: 11179218
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  • 7. The X-ray structure of the type II secretion system complex formed by the N-terminal domain of EpsE and the cytoplasmic domain of EpsL of Vibrio cholerae.
    Abendroth J, Murphy P, Sandkvist M, Bagdasarian M, Hol WG.
    J Mol Biol; 2005 May 13; 348(4):845-55. PubMed ID: 15843017
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  • 8. The N-terminal region of the bacterial DNA polymerase PolC features a pair of domains, both distantly related to domain V of the DNA polymerase III τ subunit.
    Timinskas K, Venclovas Č.
    FEBS J; 2011 Sep 13; 278(17):3109-18. PubMed ID: 21740522
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  • 10. Negative regulation of AAA + ATPase assembly by two component receiver domains: a transcription activation mechanism that is conserved in mesophilic and extremely hyperthermophilic bacteria.
    Doucleff M, Chen B, Maris AE, Wemmer DE, Kondrashkina E, Nixon BT.
    J Mol Biol; 2005 Oct 21; 353(2):242-55. PubMed ID: 16169010
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  • 12. Structure and function of the arginine repressor-operator complex from Bacillus subtilis.
    Garnett JA, Marincs F, Baumberg S, Stockley PG, Phillips SE.
    J Mol Biol; 2008 May 30; 379(2):284-98. PubMed ID: 18455186
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  • 13. Interplay between an AAA module and an integrin I domain may regulate the function of magnesium chelatase.
    Fodje MN, Hansson A, Hansson M, Olsen JG, Gough S, Willows RD, Al-Karadaghi S.
    J Mol Biol; 2001 Aug 03; 311(1):111-22. PubMed ID: 11469861
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  • 14. Structural basis for transcription-coupled repair: the N terminus of Mfd resembles UvrB with degenerate ATPase motifs.
    Assenmacher N, Wenig K, Lammens A, Hopfner KP.
    J Mol Biol; 2006 Jan 27; 355(4):675-83. PubMed ID: 16309703
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  • 15. Dimer stabilization upon activation of the transcriptional antiterminator LicT.
    Declerck N, Dutartre H, Receveur V, Dubois V, Royer C, Aymerich S, van Tilbeurgh H.
    J Mol Biol; 2001 Dec 07; 314(4):671-81. PubMed ID: 11733988
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  • 17. RNA recognition by transcriptional antiterminators of the BglG/SacY family: mapping of SacY RNA binding site.
    Declerck N, Minh NL, Yang Y, Bloch V, Kochoyan M, Aymerich S.
    J Mol Biol; 2002 Jun 21; 319(5):1035-48. PubMed ID: 12079345
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  • 20. Structure of the alkalohyperthermophilic Archaeoglobus fulgidus lipase contains a unique C-terminal domain essential for long-chain substrate binding.
    Chen CK, Lee GC, Ko TP, Guo RT, Huang LM, Liu HJ, Ho YF, Shaw JF, Wang AH.
    J Mol Biol; 2009 Jul 24; 390(4):672-85. PubMed ID: 19447113
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