Model Internals
Each PhenDB model is trained on sets of bacterial ENOGs (orthologous groups from EggNOG 4.5), which have or have not been identified in the training genomes. Each ENOG is given a weight, with the magnitude of the weight being the importance of that ENOG for the final prediction. The sign of the weight indicates whether the presence (positive weight) or absence (negative weight) of this ENOG is indicative of the trait.
This table lists the 250 highest-ranking ENOGs of this model.
rank in model | enog name | enog description | weight in model |
---|---|---|---|
1 | COG0287 | Prephenate dehydrogenase | -0.020239 |
2 | COG2150 | ACT domain | -0.017302 |
3 | COG0133 | tryptophan synthase activity | -0.016293 |
4 | COG0726 | polysaccharide deacetylase | -0.015847 |
5 | COG2927 | DNA polymerase III (CHI subunit) | 0.015256 |
6 | COG0440 | acetolactate synthase activity | -0.015113 |
7 | COG0031 | Belongs to the cysteine synthase cystathionine beta- synthase family | -0.014968 |
8 | COG0134 | indole-3-glycerol-phosphate synthase activity | -0.014333 |
9 | COG3127 | ABC-type transport system involved in lysophospholipase L1, biosynthesis, permease component | -0.013916 |
10 | COG1636 | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | -0.013727 |
11 | COG0169 | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | -0.013526 |
12 | COG0826 | peptidase U32 | -0.013332 |
13 | COG0843 | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | 0.013319 |
14 | COG1622 | oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor | 0.013319 |
15 | COG1845 | cytochrome c oxidase, subunit III | 0.013319 |
16 | COG0853 | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | -0.013255 |
17 | COG3226 | Transcriptional regulator | -0.013148 |
18 | COG2252 | PERMEase | -0.013100 |
19 | COG0652 | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | -0.013074 |
20 | COG0052 | Belongs to the universal ribosomal protein uS2 family | 0.013053 |
21 | COG0159 | tryptophan synthase activity | -0.013021 |
22 | COG0325 | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | -0.012913 |
23 | COG0345 | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | -0.012865 |
24 | COG0091 | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | 0.012821 |
25 | COG0333 | Belongs to the bacterial ribosomal protein bL32 family | 0.012648 |
26 | COG0251 | oxidation-reduction process | -0.012616 |
27 | COG0379 | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | -0.012500 |
28 | COG0275 | rRNA processing | 0.012490 |
29 | COG0547 | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | -0.012444 |
30 | COG0048 | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | 0.012435 |
31 | COG0051 | transcription antitermination factor activity, RNA binding | 0.012435 |
32 | COG0080 | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | 0.012435 |
33 | COG0085 | RNA polymerase activity | 0.012435 |
34 | COG0087 | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | 0.012435 |
35 | COG0090 | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | 0.012435 |
36 | COG0092 | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | 0.012435 |
37 | COG0093 | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | 0.012435 |
38 | COG0094 | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | 0.012435 |
39 | COG0097 | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | 0.012435 |
40 | COG0099 | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | 0.012435 |
41 | COG0100 | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | 0.012435 |
42 | COG0185 | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | 0.012435 |
43 | COG0186 | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | 0.012435 |
44 | COG0197 | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | 0.012435 |
45 | COG0199 | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | 0.012435 |
46 | COG0202 | RNA polymerase activity | 0.012435 |
47 | COG0211 | Belongs to the bacterial ribosomal protein bL27 family | 0.012435 |
48 | COG0227 | Belongs to the bacterial ribosomal protein bL28 family | 0.012435 |
49 | COG0228 | four-way junction DNA binding | 0.012435 |
50 | COG0261 | This protein binds to 23S rRNA in the presence of protein L20 | 0.012435 |
51 | COG0292 | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | 0.012435 |
52 | COG0305 | Participates in initiation and elongation during chromosome replication | 0.012435 |
53 | COG0361 | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | 0.012435 |
54 | COG0443 | Heat shock 70 kDa protein | 0.012435 |
55 | COG0480 | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | 0.012435 |
56 | COG0522 | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | 0.012435 |
57 | COG0587 | DNA-directed DNA polymerase activity | 0.012435 |
58 | COG0691 | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | 0.012435 |
59 | COG0673 | inositol 2-dehydrogenase activity | -0.012411 |
60 | COG0365 | Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA | -0.012403 |
61 | COG0014 | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | -0.012402 |
62 | COG0414 | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | -0.012394 |
63 | COG1052 | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | -0.012369 |
64 | COG0096 | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | 0.012344 |
65 | COG0098 | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | 0.012344 |
66 | COG0102 | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | 0.012344 |
67 | COG3125 | oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor | 0.012321 |
68 | COG0174 | glutamine synthetase | -0.012185 |
69 | COG0088 | Forms part of the polypeptide exit tunnel | 0.012056 |
70 | COG0290 | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | 0.012056 |
71 | COG0576 | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | 0.012056 |
72 | COG0347 | Belongs to the P(II) protein family | -0.011991 |
73 | COG0482 | sulfurtransferase activity | 0.011888 |
74 | COG0200 | Binds to the 23S rRNA | 0.011865 |
75 | COG1702 | phosphate starvation-inducible protein PhoH | -0.011817 |
76 | COG0532 | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | 0.011812 |
77 | COG0508 | dehydrogenase complex catalyzes the overall conversion of | 0.011751 |
78 | COG0316 | Belongs to the HesB IscA family | 0.011737 |
79 | COG0413 | 3-methyl-2-oxobutanoate hydroxymethyltransferase activity | -0.011722 |
80 | COG0239 | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | -0.011695 |
81 | COG2084 | Dehydrogenase | -0.011683 |
82 | COG0254 | rRNA binding | 0.011672 |
83 | COG0824 | Thioesterase | -0.011606 |
84 | COG1454 | alcohol dehydrogenase | -0.011530 |
85 | COG0067 | glutamate synthase | -0.011459 |
86 | COG1089 | Catalyzes the conversion of GDP-D-mannose to GDP-4- dehydro-6-deoxy-D-mannose | -0.011455 |
87 | COG0184 | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | 0.011437 |
88 | COG0257 | Belongs to the bacterial ribosomal protein bL36 family | 0.011421 |
89 | COG0789 | Transcriptional regulator | -0.011413 |
90 | COG0034 | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | -0.011323 |
91 | COG0041 | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | -0.011323 |
92 | COG0047 | phosphoribosylformylglycinamidine synthase activity | -0.011323 |
93 | COG0263 | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | -0.011278 |
94 | COG0050 | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | 0.011272 |
95 | COG0062 | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | -0.011213 |
96 | COG0135 | phosphoribosylanthranilate isomerase activity | -0.011204 |
97 | COG0267 | Belongs to the bacterial ribosomal protein bL33 family | 0.011190 |
98 | COG1191 | sigma factor activity | -0.011125 |
99 | COG0785 | Cytochrome C biogenesis protein | -0.011112 |
100 | COG1995 | Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) | -0.011083 |
101 | COG0049 | tRNA binding | 0.011069 |
102 | COG3830 | Belongs to the UPF0237 family | -0.010980 |
103 | COG1918 | ferrous iron import across plasma membrane | -0.010974 |
104 | COG0445 | tRNA wobble uridine modification | 0.010947 |
105 | COG1045 | serine acetyltransferase | -0.010919 |
106 | COG2022 | thiamine diphosphate biosynthetic process | -0.010896 |
107 | COG2021 | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | -0.010873 |
108 | COG1605 | Chorismate mutase | -0.010854 |
109 | COG0402 | S-adenosylhomocysteine deaminase activity | -0.010819 |
110 | COG2913 | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | 0.010795 |
111 | COG0568 | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | 0.010789 |
112 | COG0538 | isocitrate dehydrogenase activity | -0.010757 |
113 | COG0179 | Fumarylacetoacetate (FAA) hydrolase | -0.010722 |
114 | COG0129 | dihydroxy-acid dehydratase activity | -0.010663 |
115 | COG0640 | Transcriptional regulator | -0.010599 |
116 | COG0151 | Belongs to the GarS family | -0.010580 |
117 | COG4172 | Belongs to the ABC transporter superfamily | -0.010531 |
118 | COG1193 | negative regulation of DNA recombination | -0.010517 |
119 | COG0077 | Prephenate dehydratase | -0.010514 |
120 | COG0299 | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | -0.010487 |
121 | COG1301 | dicarboxylic acid transport | 0.010472 |
122 | COG0004 | ammonium transporteR | -0.010422 |
123 | COG1666 | GTP binding | -0.010399 |
124 | COG0836 | Belongs to the mannose-6-phosphate isomerase type 2 family | -0.010353 |
125 | COG1521 | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | -0.010255 |
126 | COG0847 | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. The epsilon subunit contain the editing function and is a proofreading 3'-5' exonuclease | 0.010250 |
127 | COG0648 | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | 0.010232 |
128 | COG0432 | Pfam Uncharacterised protein family UPF0047 | -0.010208 |
129 | COG0601 | transmembrane transport | -0.010194 |
130 | COG0138 | bifunctional purine biosynthesis protein purh | -0.010181 |
131 | COG0634 | Belongs to the purine pyrimidine phosphoribosyltransferase family | -0.010149 |
132 | COG2133 | pyrroloquinoline quinone binding | -0.010147 |
133 | COG0086 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | 0.010122 |
134 | COG0800 | Aldolase | -0.010120 |
135 | COG0335 | large ribosomal subunit rRNA binding | 0.010090 |
136 | COG0546 | phosphoglycolate phosphatase activity | -0.010089 |
137 | COG1080 | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | -0.010079 |
138 | COG2608 | mercury ion transmembrane transporter activity | -0.010069 |
139 | COG1912 | Pfam S-adenosyl-l-methionine hydroxide adenosyltransferase | -0.010062 |
140 | COG1959 | 2 iron, 2 sulfur cluster binding | -0.010018 |
141 | COG0234 | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | 0.010013 |
142 | COG0633 | Ferredoxin | 0.009991 |
143 | COG2249 | NAD(P)H dehydrogenase (quinone) activity | -0.009958 |
144 | COG0459 | protein refolding | 0.009939 |
145 | COG0157 | Belongs to the NadC ModD family | -0.009920 |
146 | COG0173 | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | 0.009905 |
147 | COG0746 | molybdenum cofactor guanylyltransferase activity | -0.009888 |
148 | COG1610 | YqeY-like protein | -0.009844 |
149 | COG2770 | Histidine kinase | -0.009782 |
150 | COG1778 | Involved in the biosynthesis of lipopolysaccharides (LPSs). Catalyzes the hydrolysis of 3-deoxy-D-manno-octulosonate 8-phosphate (KDO 8-P) to 3-deoxy-D-manno-octulosonate (KDO) and inorganic phosphate | -0.009777 |
151 | COG1296 | Branched-chain amino acid permease (Azaleucine resistance) | -0.009776 |
152 | COG4839 | cell division protein FtsL | -0.009768 |
153 | COG0428 | transporter | -0.009742 |
154 | COG0566 | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | 0.009697 |
155 | COG0386 | Belongs to the glutathione peroxidase family | -0.009681 |
156 | COG0038 | chloride channel | -0.009664 |
157 | COG0535 | radical SAM domain protein | -0.009654 |
158 | COG0230 | Belongs to the bacterial ribosomal protein bL34 family | 0.009630 |
159 | COG0284 | orotidine-5'-phosphate decarboxylase activity | -0.009630 |
160 | COG1160 | GTP binding | 0.009624 |
161 | COG0002 | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | -0.009598 |
162 | COG0466 | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner | 0.009590 |
163 | COG1723 | PFAM Uncharacterised ACR, YagE family COG1723 | 0.009585 |
164 | COG1368 | sulfuric ester hydrolase activity | -0.009548 |
165 | COG0667 | Aldo Keto reductase | -0.009545 |
166 | COG0005 | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | -0.009539 |
167 | COG1989 | Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue | -0.009526 |
168 | COG0351 | phosphomethylpyrimidine kinase | -0.009520 |
169 | COG0123 | including yeast histone deacetylase and acetoin utilization protein | -0.009510 |
170 | COG0540 | Belongs to the ATCase OTCase family | -0.009504 |
171 | COG2189 | Belongs to the N(4) N(6)-methyltransferase family | -0.009483 |
172 | COG1208 | COG1208 Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis translation initiation factor 2B, gamma epsilon subunits eIF-2Bgamma eIF-2Bepsilon | -0.009477 |
173 | COG0119 | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | -0.009447 |
174 | COG1249 | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | 0.009402 |
175 | COG0370 | Transporter of a GTP-driven Fe(2 ) uptake system | -0.009380 |
176 | COG0293 | Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit | 0.009370 |
177 | COG3448 | diguanylate cyclase activity | -0.009364 |
178 | COG1847 | R3H domain protein | -0.009347 |
179 | COG1364 | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | -0.009328 |
180 | COG2127 | Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation | -0.009311 |
181 | COG0362 | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | 0.009306 |
182 | COG2873 | o-acetylhomoserine | -0.009294 |
183 | COG0019 | diaminopimelate decarboxylase activity | -0.009275 |
184 | COG3202 | ADP transmembrane transporter activity | 0.009267 |
185 | COG1011 | Hydrolase | -0.009266 |
186 | COG0735 | belongs to the Fur family | -0.009265 |
187 | COG3837 | Cupin domain | -0.009259 |
188 | COG2104 | thiamine diphosphate biosynthetic process | -0.009259 |
189 | COG5002 | protein histidine kinase activity | -0.009248 |
190 | COG1473 | amidohydrolase | -0.009218 |
191 | COG2957 | Belongs to the agmatine deiminase family | -0.009194 |
192 | COG0165 | Argininosuccinate lyase | -0.009168 |
193 | COG2510 | membrane | -0.009161 |
194 | COG0564 | pseudouridine synthase activity | 0.009143 |
195 | COG2827 | Endonuclease containing a URI domain | -0.009135 |
196 | COG0791 | NLP P60 protein | -0.009122 |
197 | COG2151 | metal-sulfur cluster biosynthetic enzyme | -0.008995 |
198 | COG0605 | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | 0.008961 |
199 | COG0533 | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | 0.008955 |
200 | COG3967 | Belongs to the short-chain dehydrogenases reductases (SDR) family | -0.008954 |
201 | COG3167 | carbon utilization | -0.008903 |
202 | COG1216 | Glycosyl transferase, family 2 | -0.008844 |
203 | COG0066 | 3-isopropylmalate dehydratase activity | -0.008836 |
204 | COG3960 | tartronate-semialdehyde synthase activity | -0.008811 |
205 | COG2951 | lytic endotransglycosylase activity | -0.008802 |
206 | COG0109 | protoheme IX farnesyltransferase activity | 0.008755 |
207 | COG0730 | response to heat | -0.008748 |
208 | COG1125 | glycine betaine transport | -0.008737 |
209 | COG1174 | glycine betaine transport | -0.008737 |
210 | COG4221 | oxidoreductase activity | -0.008734 |
211 | COG0683 | leucine binding | -0.008715 |
212 | COG2759 | Belongs to the formate--tetrahydrofolate ligase family | -0.008683 |
213 | COG4966 | pilus assembly protein PilW | -0.008665 |
214 | COG0539 | negative regulation of cytoplasmic translation | 0.008664 |
215 | COG2921 | Belongs to the UPF0250 family | -0.008657 |
216 | COG0659 | secondary active sulfate transmembrane transporter activity | -0.008655 |
217 | COG0476 | Involved in molybdopterin and thiamine biosynthesis, family 2 | -0.008634 |
218 | COG4166 | transmembrane transport | -0.008630 |
219 | COG0291 | Belongs to the bacterial ribosomal protein bL35 family | 0.008619 |
220 | COG0510 | thiamine kinase activity | 0.008616 |
221 | COG4968 | Prepilin-type N-terminal cleavage methylation domain | -0.008605 |
222 | COG0315 | cyclic pyranopterin monophosphate synthase activity | -0.008584 |
223 | COG2896 | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | -0.008584 |
224 | COG0008 | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | 0.008552 |
225 | COG0060 | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | 0.008552 |
226 | COG0172 | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | 0.008552 |
227 | COG0233 | cytoplasmic translational termination | 0.008552 |
228 | COG0358 | DNA primase activity | 0.008552 |
229 | COG0013 | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | 0.008552 |
230 | COG0105 | UTP biosynthetic process | 0.008525 |
231 | COG0410 | ABC transporter | -0.008501 |
232 | COG0411 | ABC transporter | -0.008483 |
233 | COG0059 | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | -0.008482 |
234 | COG0525 | valine-tRNA ligase activity | 0.008477 |
235 | COG3133 | Outer membrane lipoprotein | 0.008469 |
236 | COG1254 | Belongs to the acylphosphatase family | -0.008447 |
237 | COG0344 | acyl-phosphate glycerol-3-phosphate acyltransferase activity | -0.008428 |
238 | COG2905 | signal-transduction protein containing cAMP-binding and CBS domains | -0.008425 |
239 | COG0150 | phosphoribosylformylglycinamidine cyclo-ligase activity | -0.008413 |
240 | COG1219 | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | 0.008408 |
241 | COG0069 | glutamate synthase activity | -0.008391 |
242 | COG0124 | histidyl-tRNA synthetase | 0.008373 |
243 | COG0143 | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | 0.008373 |
244 | COG0162 | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | 0.008373 |
245 | COG0180 | Tryptophanyl-tRNA synthetase | 0.008373 |
246 | COG0015 | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | -0.008370 |
247 | COG1765 | OsmC-like protein | -0.008358 |
248 | 34CD0 | Thioredoxin | 0.008345 |
249 | COG0203 | ribosomal protein L17 | 0.008342 |
250 | COG0238 | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | 0.008342 |