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1 T. maritima (Tm) RNase III catalytic activity exhibits a
2 T. maritima cellobiose-binding protein binds a variety o
3 T. maritima CheC, as well as CheX, dephosphorylate CheY,
4 T. maritima CheW and CheY were both soluble and were eas
5 T. maritima FliN is primarily a dimer in solution, and T
6 T. maritima is unable to grow on myo-inositol as a singl
7 T. maritima RRF also inhibited the E. coli RRF reaction
8 T. maritima TrmE was overexpressed in Escherichia coli a
10 Here, we present the crystal structure of a T. maritima cellobiose-binding protein (tm0031) that is
11 yeast, B. stearothermophilus, T. brucei and T. maritima PGK, and may therefore have a role in the in
14 to published data for DHFR from E. coli and T. maritima shows a decreasing trend in efficiency of hy
15 a FliN is primarily a dimer in solution, and T. maritima FliN and FliM together form a stable FliM(1)
17 ficient methylation, the interaction between T. maritima CheR and T. maritima MCPs is of relatively l
20 nated products can be further metabolized by T. maritima in a previously uncharacterized SAH degradat
22 formational differences between the E. coli, T. maritima, and yeast synthetases suggest the possibili
24 ction for IscU-type proteins, we demonstrate T. maritima IscU-mediated reconstitution of human apofer
28 r RRF activity and therefore responsible for T. maritima RRF inhibition of the E. coli RRF reaction.
29 nine and L-allo-threonine are substrates for T. maritima TA, enzymatic assays revealed a strong prefe
32 fied recombinant tagaturonate epimerase from T. maritima was directly confirmed and kinetically chara
33 es from P. furiosus and of the POR gene from T. maritima, all of which comprise four different subuni
35 s of the putative laminarinase, Lam16A, from T. maritima comprise a highly thermostable family 4 CBM
36 osphate transport system regulator PhoU from T. maritima (a 235-residue mainly alpha-helical protein)
37 ydrogenase that was previously purified from T. maritima does not use either reduced ferredoxin or NA
38 occus jannaschii resulted in fivefold higher T. maritima cell densities when compared with monocultur
39 troglodytes, 9-12 in T. caudata and 10-14 in T. maritima, with some colonies having individuals of mo
40 8, 118 to 122, 154 to 160, and 172 to 176 in T. maritima RRF differed totally from that of E. coli RR
41 CheA binds CheY with identical affinity in T. maritima and E. coli at the vastly different temperat
42 ated during chloramphenicol challenge and in T. maritima bound in exopolysaccharide aggregates during
43 ng a pathway for polysaccharide formation in T. maritima, these results point to the existence of pep
44 at Lys81 (equivalent to Lys150 and Lys82 in T. maritima) for the Bacillus subtilis enzyme suggesting
45 ns and MCPs indicate that MCP methylation in T. maritima occurs independently of a pentapeptide-bindi
46 wide ranging collection of such networks in T. maritima suggests that this organism is capable of ad
49 acturonate to mannonate catabolic pathway in T. maritima was reconstituted in vitro using a mixture o
50 uence for chemoreceptor methylation sites in T. maritima that is distinct from the previously identif
51 ng a putative signaling peptide and tmRNA in T. maritima is intriguing, since this overlapping arrang
53 high structural homology of their monomers, T. maritima MreB and actin filaments display different a
55 f WT and mutated (NMBD deletion or mutation) T. maritima CopA, comparing it with Archaeoglobus fulgid
59 occludes approximately 35 bp, association of T. maritima HU with DNA of sufficient length to accommod
61 terize the molten globule characteristics of T. maritima IscU by near-ultraviolet circular dichroism,
66 rectly confirmed for the purified product of T. maritima gene dipA cloned and expressed in Escherichi
67 Furthermore, the biophysical properties of T. maritima MreB filaments, including high rigidity and
69 d to infer the phylogenetic relationships of T. maritima, one of the deepest-branching eubacteria kno
71 pporting the reticulate origin of samples of T. maritima in southwestern France and T. sinuatocollis/
72 Here, we present the crystal structure of T. maritima SecA in isolation, determined in its ADP-bou
77 The results indicate that the recombinant T. maritima two-component proteins overexpressed in E. c
79 b-families based on EDTA resistance and that T. maritima ExoVII is the first member of the branch tha
80 al denaturation experiments demonstrate that T. maritima IscU is a thermally stable protein with a th
84 rcular dichroism spectroscopy indicates that T. maritima endonuclease IV has secondary structure simi
85 rophoretic mobility shift analyses show that T. maritima HU (TmHU) binds double-stranded DNA with hig
92 sed on cumulative GC skew analysis, both the T. maritima and T. neapolitana lineages contain one or t
93 AdoMet-DCs are structurally conserved in the T. maritima AdoMetDC despite very limited primary sequen
94 carbohydrate-active proteins encoded in the T. maritima genome was followed using a targeted cDNA mi
96 reduces the subunit dissociation rate of the T. maritima CheA dimer by interacting with the regulator
97 ike genes are clustered in 15 regions of the T. maritima genome that range in size from 4 to 20 kilob
101 Sequence comparisons establish that the T. maritima and Slr0387 proteins have loops of similar l
102 that of E. coli endonuclease IV and that the T. maritima endonuclease IV structure is more stable tha
106 commodating RNAP in the DNA channel, whereas T. maritima sigma1.1 must be rearranged to fit therein.
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