NC_007109.1|WP_011270680.1|356451_357303_+|glycosyltransferase-family-2-protein |
gnl|CDD|133005 |
cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.
|
1.27295e-73 |
NC_007109.1|WP_187145859.1|373808_373967_+|nucleotidyltransferase-domain-containing-protein |
gnl|CDD|143393 |
cd05403, NT_KNTase_like, Nucleotidyltransferase (NT) domain of Staphylococcus aureus kanamycin nucleotidyltransferase, and similar proteins. S. aureus KNTase is a plasmid encoded enzyme which confers resistance to a wide range of aminoglycoside antibiotics which have a 4'- or 4''-hydroxyl group in the equatorial position, such as kanamycin A. This enzyme transfers a nucleoside monophosphate group from a nucleotide (ATP,GTP, or UTP) to the 4'-hydroxyl group of kanamycin A. This enzyme is a homodimer, having two NT active sites. The nucleotide and antibiotic binding sites of each active site include residues from each monomer. Included in this subgroup is Escherichia coli AadA5 which confers resistance to the antibiotic spectinomycin and is a putative aminoglycoside-3'-adenylyltransferase. It is part of the aadA5 cassette of a class 1 integron. This subgroup also includes Haemophilus influenzae HI0073 which forms a 2:2 heterotetramer with an unrelated protein HI0074. Structurally HI0074 is related to the substrate-binding domain of S. aureus KNTase. The genes encoding HI0073 and HI0074 form an operon. Little is known about the substrate specificity or function of two-component NTs. The characterized members of this subgroup may not be representive of the function of this subgroup. This subgroup belongs to the Pol beta-like NT superfamily. In the majority of enzymes in this superfamily, two carboxylates, Dx[D/E], together with a third more distal carboxylate, co-ordinate two divalent metal cations involved in a two-metal ion mechanism of nucleotide addition. These carboxylate residues are conserved in this subgroup.
|
0.000197009 |
NC_007109.1|WP_011270690.1|369343_370021_+|7-carboxy-7-deazaguanine-synthase-QueE |
gnl|CDD|223675 |
COG0602, NrdG, Organic radical activating enzymes [Posttranslational modification, protein turnover, chaperones].
|
6.29164e-57 |
NC_007109.1|WP_011270694.1|372443_373541_+|redox-regulated-ATPase-YchF |
gnl|CDD|236583 |
PRK09601, PRK09601, redox-regulated ATPase YchF.
|
0 |
NC_007109.1|WP_011270691.1|370433_371045_+|50S-ribosomal-protein-L25/general-stress-protein-Ctc |
gnl|CDD|235534 |
PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.
|
9.21479e-76 |
NC_007109.1|WP_041405310.1|361730_362030_-|tyrosine-type-recombinase/integrase |
gnl|CDD|334163 |
pfam00589, Phage_integrase, Phage integrase family. Members of this family cleave DNA substrates by a series of staggered cuts, during which the protein becomes covalently linked to the DNA through a catalytic tyrosine residue at the carboxy end of the alignment. The catalytic site residues in CRE recombinase are Arg-173, His-289, Arg-292 and Tyr-324.
|
6.20777e-08 |
NC_007109.1|WP_081427805.1|372132_372447_+|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.
|
8.33772e-12 |
NC_007109.1|WP_011270688.1|368274_368409_-|50S-ribosomal-protein-L34 |
gnl|CDD|179004 |
PRK00399, rpmH, 50S ribosomal protein L34; Reviewed.
|
1.24213e-10 |
NC_007109.1|WP_011270678.1|354667_354928_-|type-II-toxin-antitoxin-system-RelB/DinJ-family-antitoxin |
gnl|CDD|274102 |
TIGR02384, Putative_antitoxin_RelB, addiction module antitoxin, RelB/DinJ family. Plasmids may be maintained stably in bacterial populations through the action of addiction modules, in which a toxin and antidote are encoded in a cassette on the plasmid. In any daughter cell that lacks the plasmid, the toxin persists and is lethal after the antidote protein is depleted. Toxin/antitoxin pairs are also found on main chromosomes, and likely represent selfish DNA. Sequences in the seed for this alignment all were found adjacent to toxin genes. The resulting model appears to describe a narrower set of proteins than pfam04221, although many in the scope of this model are not obviously paired with toxin proteins. Several toxin/antitoxin pairs may occur in a single species. [Cellular processes, Toxin production and resistance, Mobile and extrachromosomal element functions, Other].
|
5.61456e-15 |
NC_007109.1|WP_011270677.1|354394_354664_-|type-II-toxin-antitoxin-system-YafQ-family-toxin |
gnl|CDD|379750 |
pfam15738, YafQ_toxin, Bacterial toxin of type II toxin-antitoxin system, YafQ. YafQ is a family of bacterial toxin ribonucleases of type II toxin-antitoxin systems. The E.coli gene is expressed from the dinB operon. The cognate antitoxin for the E. coli protein is DinJ, in family RelB_antitoxin, pfam02604.
|
6.31139e-42 |
NC_007109.1|WP_011270682.1|358800_359511_+|phosphoribosylaminoimidazolesuccinocarboxamide-synthase |
gnl|CDD|181800 |
PRK09362, PRK09362, phosphoribosylaminoimidazole-succinocarboxamide synthase; Reviewed.
|
5.21691e-119 |
NC_007109.1|WP_004997924.1|368935_369142_-|50S-ribosomal-protein-L35 |
gnl|CDD|234676 |
PRK00172, rpmI, 50S ribosomal protein L35; Reviewed.
|
1.43258e-19 |
NC_007109.1|WP_011270692.1|371328_371886_+|aminoacyl-tRNA-hydrolase |
gnl|CDD|223271 |
COG0193, Pth, Peptidyl-tRNA hydrolase [Translation, ribosomal structure and biogenesis].
|
4.09043e-92 |
NC_007109.1|WP_011270406.1|363778_364579_+|AAA-family-ATPase |
gnl|CDD|181681 |
PRK09183, PRK09183, transposase/IS protein; Provisional.
|
1.91848e-162 |
NC_007109.1|WP_156110739.1|362398_362557_+|hypothetical-protein |
gnl|CDD|293786 |
sd00045, ANK, ankyrin repeats. Ankyrin repeats are one of the most abundant repeat motifs, and generally function as scaffolds for protein-protein interactions in processes including cell cycle, transcriptional regulation, signal transduction, vesicular trafficking, and inflammatory response. Although predominantly found in eukaryotic proteins, they are also found in some bacterial and viral proteins. Less is known of their physiological roles in prokaryotes. Some bacterial ANK proteins play key roles in microbial pathogenesis by mimicking or manipulating host function(s). The pathogen Providencia alcalifaciens N-formyltransferase ankyrin repeats function in small molecule binding and allosteric control. Ankyrin-repeat proteins have been associated with a number of human diseases.
|
0.00515489 |
NC_007109.1|WP_011270687.1|367898_368255_-|ribonuclease-P-protein-component |
gnl|CDD|100883 |
PRK01492, rnpA, ribonuclease P protein component.
|
8.58617e-58 |
NC_007109.1|WP_011270681.1|357381_358620_+|insulinase-family-protein |
gnl|CDD|223685 |
COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].
|
1.12344e-120 |
NC_007109.1|WP_011270689.1|368561_368915_-|50S-ribosomal-protein-L20 |
gnl|CDD|179959 |
PRK05185, rplT, 50S ribosomal protein L20; Provisional.
|
4.461e-61 |
NC_007109.1|WP_011270679.1|355087_356107_+|cytochrome-d-ubiquinol-oxidase-subunit-II |
gnl|CDD|224213 |
COG1294, AppB, Cytochrome bd-type quinol oxidase, subunit 2 [Energy production and conversion].
|
1.96871e-117 |