| NZ_CP020478.1|WP_082199636.1|769990_770314_+|ribonuclease-P-protein-component |
gnl|CDD|223667 |
COG0594, RnpA, RNase P protein component [Translation, ribosomal structure and biogenesis].
|
1.77536e-20 |
| NZ_CP020478.1|WP_082199623.1|757329_757995_+|response-regulator-transcription-factor |
gnl|CDD|223816 |
COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].
|
5.8132e-61 |
| NZ_CP020478.1|WP_082199632.1|767080_767455_+|YbgC/FadM-family-acyl-CoA-thioesterase |
gnl|CDD|274304 |
TIGR02799, Acyl-CoA_thioesterase_YbgC, tol-pal system-associated acyl-CoA thioesterase. The tol-pal system consists of five critical genes. Inner membrane proteins TolQ and TolR convert protomotive force to energy that is transduced through TolA to an outer membrane complex of TolB and Pal. The system is known to be required to maintain outer membrane integrity. In a system with several homologous parts, ExbB and ExbD transduces energy through TonB to a variety of outer membrane proteins, many of which are siderophore receptors. The tol-pal system therefore may also be involved in transport. This family consists of a protein nearly always found in operons with the genes of the tol-pal system. The significance of this thioesterase to the tol-pal system is unclear, but either of two observations may be relevant. First, Pal, or peptidoglycan-associated lipoprotein, has a conserved N-terminal cleavage and acylation that makes it a lipoprotein. Second, the tol-pal system is implicated not only in the import of certain organics but also in the maintenance of outer membrane integrity (by an unknown mechanism).
|
7.75115e-41 |
| NZ_CP020478.1|WP_082199624.1|757987_759190_+|HAMP-domain-containing-histidine-kinase |
gnl|CDD|223715 |
COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].
|
6.8638e-37 |
| NZ_CP020478.1|WP_082199622.1|756630_757227_-|bacteriohemerythrin |
gnl|CDD|225331 |
COG2703, COG2703, Hemerythrin [Inorganic ion transport and metabolism].
|
2.02396e-43 |
| NZ_CP020478.1|WP_082199637.1|770646_772260_+|membrane-protein-insertase-YidC |
gnl|CDD|234942 |
PRK01318, PRK01318, membrane protein insertase; Provisional.
|
2.18107e-180 |
| NZ_CP020478.1|WP_082199627.1|760649_763181_-|hypothetical-protein |
gnl|CDD|225463 |
COG2911, COG2911, Uncharacterized protein conserved in bacteria [Function unknown].
|
4.79281e-06 |
| NZ_CP020478.1|WP_082199631.1|766478_767084_+|thiamine-phosphate-synthase |
gnl|CDD|223429 |
COG0352, ThiE, Thiamine monophosphate synthase [Coenzyme metabolism].
|
1.51493e-55 |
| NZ_CP020478.1|WP_082199626.1|759374_760067_-|laccase |
gnl|CDD|224413 |
COG1496, yfiH, Multicopper polyphenol oxidase (laccase) [Secondary metabolites biosynthesis, transport and catabolism].
|
2.73304e-50 |
| NZ_CP020478.1|WP_082200745.1|760030_760639_-|riboflavin-synthase |
gnl|CDD|236455 |
PRK09289, PRK09289, riboflavin synthase.
|
3.4364e-79 |
| NZ_CP020478.1|WP_004277342.1|769859_769994_+|50S-ribosomal-protein-L34 |
gnl|CDD|179004 |
PRK00399, rpmH, 50S ribosomal protein L34; Reviewed.
|
3.75934e-11 |
| NZ_CP020478.1|WP_082200746.1|770301_770646_+|membrane-protein-insertion-efficiency-factor-YidD |
gnl|CDD|223830 |
COG0759, COG0759, Uncharacterized conserved protein [Function unknown].
|
3.56783e-29 |
| NZ_CP020478.1|WP_082199635.1|769244_769724_-|GNAT-family-N-acetyltransferase |
gnl|CDD|366181 |
pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.
|
2.90407e-12 |
| NZ_CP020478.1|WP_082199628.1|763341_763602_+|co-chaperone-GroES |
gnl|CDD|178988 |
PRK00364, groES, co-chaperonin GroES; Reviewed.
|
4.02798e-37 |
| NZ_CP020478.1|WP_082199630.1|765355_766489_+|2-iminoacetate-synthase-ThiH |
gnl|CDD|236425 |
PRK09240, thiH, 2-iminoacetate synthase ThiH.
|
0 |
| NZ_CP020478.1|WP_082199634.1|768639_769248_-|hypothetical-protein |
gnl|CDD|381680 |
cd10030, UDG-F4_TTUDGA_SPO1dp_like, Uracil DNA glycosylase family 4, includes Thermotoga maritima TTUDGA, Bacillus phage SPO1 DNA polymerase, and similar proteins. Uracil DNA glycosylase family 4 includes Thermotoga maritima TTUDGA, a robust uracil DNA glycosylase that shares narrow substrate specificity and high catalytic efficiency with family 1, acting on double-stranded and single-stranded uracil-containing DNA. Members of this family possess four conserved cysteine residues required to coordinate the [4Fe-4S] iron-sulfur cluster. This family also includes the N-terminal domain of Bacillus phage SPO1 DNA polymerase. Bacteriophage SPO1 is one of a group of large, lytic, tailed bacteriophages of Bacillus subtilis, and contains hydroxymethyluracil (hmUra) in place of thymine in their DNA. It has been speculated that this UDG domain may help discriminate between hmUra containing SPO1 DNA and thymine-containing host DNA. Uracil-DNA glycosylases (UDGs) initiate repair of uracils in DNA. Uracil in DNA can arise as a result of mis-incorporation of dUMP residues by DNA polymerase or via deamination of cytosine. Uracil in DNA mispaired with guanine is one of the major pro-mutagenic events, causing G:C->A:T mutations. Thus, UDG is an essential enzyme for maintaining the integrity of genetic information. UDGs have been classified into various families on the basis of their substrate specificity, conserved motifs, and structural similarities. Although these families demonstrate different substrate specificities, often the function of one enzyme can be complemented by the other.
|
4.93787e-30 |
| NZ_CP020478.1|WP_082199621.1|756235_756616_-|ribbon-helix-helix-protein,-CopG-family |
gnl|CDD|227054 |
COG4710, COG4710, Predicted DNA-binding protein with an HTH domain [General function prediction only].
|
4.02289e-21 |
