Related ArticlesNMR solution structure of Thermotoga maritima protein TM1509 reveals a Zn-metalloprotease-like tertiary structure.
J Struct Funct Genomics. 2005;6(1):51-62
Authors: Penhoat CH, Li Z, Atreya HS, Kim S, Yee A, Xiao R, Murray D, Arrowsmith CH, Szyperski T
The 150-residue protein TM1509 is encoded in gene YF09_THEMA of Thermotoga maritima. TM1509 has so far no functional annotation and belongs to protein family UPF0054 (PFAM accession number: PF02130) which contains at least 146 members. The NMR structure of TM1509 reveals an alpha+beta fold comprising a four stranded beta-sheet with topology A( upward arrow), B( upward arrow), D( upward arrow), C( downward arrow) as well as five alpha-helices I-V. The structures of most members of family PF02130 can be reliably constructed using the TM1509 NMR structure, demonstrating high leverage for exploration of fold space. A multiple sequence alignment of TM1509 with homologues of family UPF0054 shows that three polypeptide segments, as well as a putative zinc-binding consensus motif HGXLHLXGYDH located at the C-terminal end of alpha-helix IV, are highly conserved. The spatial arrangement of the three His residues of this UPF0054 consensus motif is similar to the arrangement found for the His residues in the HEXXHXXGXXH zinc-binding consensus motif of matrix metallo-proteases (MMPs). Moreover, the other conserved polypeptide segments form a large cavity which encloses the putative Zn-binding pocket and might confer specificity during catalysis. However, TM1509 and the other members of the UPF0054 family do not have the crucial Glu residue in position 2 of the MMP consensus motif. Intriguingly, the TM1509 structure indicates that the Asp in the UPF0054 consensus motif (Asp 111 in TM1509) may overtake the catalytic role of the Glu. This suggests that protein family UPF0054 might contain members of a hitherto uncharacterized class of metalloproteases.
The structure and dynamic properties of the complete histidine phosphotransfer domain of the chemotaxis specific histidine autokinase CheA from Thermotoga maritima
The structure and dynamic properties of the complete histidine phosphotransfer domain of the chemotaxis specific histidine autokinase CheA from Thermotoga maritima
Abstract The bacterial histidine autokinase CheA contains a histidine phosphotransfer (Hpt) domain that accepts a phosphate from the catalytic domain and donates the phosphate to either target response regulator protein, CheY or CheB. The Hpt domain forms a helix-bundle structure with a conserved four-helix bundle motif and a variable fifth helix. Observation of two nearly equally populated conformations in the crystal...
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[NMR paper] NMR structure of the conserved hypothetical protein TM0487 from Thermotoga maritima: implications for 216 homologous DUF59 proteins.
NMR structure of the conserved hypothetical protein TM0487 from Thermotoga maritima: implications for 216 homologous DUF59 proteins.
Related Articles NMR structure of the conserved hypothetical protein TM0487 from Thermotoga maritima: implications for 216 homologous DUF59 proteins.
Protein Sci. 2005 Nov;14(11):2880-6
Authors: Almeida MS, Herrmann T, Peti W, Wilson IA, Wüthrich K
The NMR structure of the conserved hypothetical protein TM0487 from Thermotoga maritima represents an alpha/beta-topology formed by the regular secondary structures...
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[NMR paper] NMR structure determination of the conserved hypothetical protein TM1816 from Thermotoga maritima.
NMR structure determination of the conserved hypothetical protein TM1816 from Thermotoga maritima.
Related Articles NMR structure determination of the conserved hypothetical protein TM1816 from Thermotoga maritima.
Proteins. 2005 Aug 15;60(3):552-7
Authors: Columbus L, Peti W, Etezady-Esfarjani T, Herrmann T, Wüthrich K
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[NMR paper] NMR structure of the conserved hypothetical protein TM0979 from Thermotoga maritima.
NMR structure of the conserved hypothetical protein TM0979 from Thermotoga maritima.
Related Articles NMR structure of the conserved hypothetical protein TM0979 from Thermotoga maritima.
Proteins. 2005 May 1;59(2):387-90
Authors: Peti W, Herrmann T, Zagnitko O, Grzechnik SK, Wüthrich K
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[NMR paper] NMR for structural proteomics of Thermotoga maritima: screening and structure determi
NMR for structural proteomics of Thermotoga maritima: screening and structure determination.
Related Articles NMR for structural proteomics of Thermotoga maritima: screening and structure determination.
J Struct Funct Genomics. 2004;5(3):205-15
Authors: Peti W, Etezady-Esfarjani T, Herrmann T, Klock HE, Lesley SA, Wüthrich K
This paper describes the NMR screening of 141 small (
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[NMR paper] NMR assignment of the conserved hypothetical protein TM1290 of Thermotoga maritima.
NMR assignment of the conserved hypothetical protein TM1290 of Thermotoga maritima.
Related Articles NMR assignment of the conserved hypothetical protein TM1290 of Thermotoga maritima.
J Biomol NMR. 2003 Feb;25(2):167-8
Authors: Etezady-Esfarjani T, Peti W, Wüthrich K
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[NMR paper] NMR assignment of the full-length ribosomal protein L11 from Thermotoga maritima.
NMR assignment of the full-length ribosomal protein L11 from Thermotoga maritima.
Related Articles NMR assignment of the full-length ribosomal protein L11 from Thermotoga maritima.
J Biomol NMR. 2003 Feb;25(2):163-4
Authors: Ilin S, Hoskins A, Schwalbe H, Wöhnert J
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[NMR paper] An NMR-derived model for the solution structure of oxidized Thermotoga maritima 1[Fe4
An NMR-derived model for the solution structure of oxidized Thermotoga maritima 1 ferredoxin.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www3.interscience.wiley.com-aboutus-images-wiley_interscience_pubmed_logo_FREE_120x27.gif Related Articles An NMR-derived model for the solution structure of oxidized Thermotoga maritima 1 ferredoxin.
Eur J Biochem. 1996 May 1;237(3):726-35
Authors: Sticht H, Wildegger G, Bentrop D, Darimont B, Sterner R, Rösch P
The solution structure of the 60-residue 1 ferredoxin from the hyperthermophilic...