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 | COG0130 | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | 0.228171 |
2 | COG1187 | pseudouridine synthase activity | 0.224135 |
3 | COG0101 | tRNA pseudouridine synthase activity | 0.223922 |
4 | COG0564 | pseudouridine synthase activity | 0.220204 |
5 | COG0729 | surface antigen | -0.096443 |
6 | 32UTB | -0.094707 | |
7 | 33AGD | -0.094707 | |
8 | 33Z2K | -0.094224 | |
9 | 30YFD | -0.094177 | |
10 | 34AYS | -0.091903 | |
11 | COG3590 | peptidase | -0.089289 |
12 | COG3226 | Transcriptional regulator | -0.087331 |
13 | COG1266 | CAAX protease self-immunity | -0.086023 |
14 | COG1376 | ErfK ybiS ycfS ynhG family protein | -0.082616 |
15 | COG4977 | sequence-specific DNA binding | -0.080644 |
16 | COG3604 | Transcriptional regulator | -0.070647 |
17 | COG4774 | siderophore transport | -0.067795 |
18 | COG0580 | Belongs to the MIP aquaporin (TC 1.A.8) family | -0.066730 |
19 | 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) | -0.056154 |
20 | COG0329 | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | -0.052014 |
21 | COG0625 | glutathione transferase activity | -0.051192 |
22 | COG0543 | 2 iron, 2 sulfur cluster binding | -0.050868 |
23 | 32TDU | -0.049390 | |
24 | COG1062 | S-(hydroxymethyl)glutathione dehydrogenase activity | -0.048172 |
25 | COG3347 | Dehydrogenase | -0.045532 |
26 | COG4638 | Rieske (2fe-2S) | -0.044809 |
27 | COG3620 | sequence-specific DNA binding | 0.044798 |
28 | 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 | -0.044449 |
29 | COG5517 | Aromatic-ring-hydroxylating dioxygenase beta subunit | -0.042988 |
30 | COG2514 | catechol 2,3-dioxygenase activity | -0.042212 |
31 | COG2146 | nitrite reductase [NAD(P)H] activity | -0.041851 |
32 | COG3917 | 2-hydroxychromene-2-carboxylate isomerase | -0.041686 |
33 | 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) | -0.041485 |
34 | COG3239 | Fatty acid desaturase | -0.041377 |
35 | 2Z9D2 | Psort location CytoplasmicMembrane, score | -0.041062 |
36 | COG5639 | conserved small protein | -0.040571 |
37 | COG2055 | Belongs to the LDH2 MDH2 oxidoreductase family | -0.040401 |
38 | COG0135 | phosphoribosylanthranilate isomerase activity | -0.039511 |
39 | COG0841 | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | -0.039345 |
40 | COG3883 | PFAM NLP P60 protein | 0.039342 |
41 | COG3324 | translation initiation factor activity | 0.038945 |
42 | COG4581 | dead DEAH box helicase | 0.038363 |
43 | COG1605 | Chorismate mutase | 0.038137 |
44 | COG0692 | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | 0.037801 |
45 | COG3934 | Belongs to the glycosyl hydrolase 5 (cellulase A) family | 0.037141 |
46 | COG1664 | Polymer-forming cytoskeletal | -0.036148 |
47 | COG0596 | Alpha beta hydrolase | -0.035764 |
48 | COG2337 | Toxic component of a toxin-antitoxin (TA) module | 0.035546 |
49 | COG4105 | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | -0.035527 |
50 | COG3835 | regulator | 0.035509 |
51 | COG3442 | glutamine amidotransferase | 0.034340 |
52 | COG4775 | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | -0.033922 |
53 | COG4795 | General secretion pathway protein | -0.033620 |
54 | COG2877 | 3-deoxy-8-phosphooctulonate synthase activity | -0.033200 |
55 | COG3546 | catalase activity | 0.033056 |
56 | COG1004 | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | -0.032789 |
57 | COG3246 | L-lysine catabolic process to acetate | 0.032553 |
58 | COG3634 | alkyl hydroperoxide reductase activity | -0.032481 |
59 | COG1113 | amino acid transport | 0.032435 |
60 | COG4585 | Histidine kinase | 0.032265 |
61 | COG1324 | tolerance protein | -0.032121 |
62 | COG1172 | Belongs to the binding-protein-dependent transport system permease family | -0.031963 |
63 | COG1022 | Amp-dependent synthetase and ligase | -0.031870 |
64 | COG1481 | regulation of sporulation | 0.031807 |
65 | COG4913 | Putative exonuclease SbcCD, C subunit | 0.031752 |
66 | COG3264 | Mechanosensitive ion channel | -0.031687 |
67 | COG3608 | succinylglutamate desuccinylase aspartoacylase | -0.031673 |
68 | COG4559 | Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system | -0.031393 |
69 | 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 | -0.031363 |
70 | COG1969 | Ni Fe-hydrogenase, b-type cytochrome subunit | -0.031205 |
71 | COG0234 | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | -0.031159 |
72 | 32Y4N | CotJB protein | 0.031105 |
73 | COG2199 | diguanylate cyclase activity | -0.030959 |
74 | COG0632 | four-way junction helicase activity | -0.030889 |
75 | COG1702 | phosphate starvation-inducible protein PhoH | 0.030752 |
76 | COG1584 | GPR1 FUN34 yaaH family protein | -0.030534 |
77 | COG2005 | Transcriptional regulator | 0.030526 |
78 | 345K5 | -0.030422 | |
79 | 2ZQPU | Outer membrane efflux protein | -0.030353 |
80 | COG3610 | response to peptide | 0.030244 |
81 | COG1983 | PspC domain protein | 0.029950 |
82 | COG3688 | RNA-binding protein containing a PIN domain | 0.029878 |
83 | COG1211 | 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase activity | 0.029750 |
84 | COG1597 | lipid kinase activity | 0.029744 |
85 | COG1251 | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | -0.029556 |
86 | COG0811 | peptide transport | -0.029548 |
87 | 30URY | An automated process has identified a potential problem with this gene model | -0.029517 |
88 | COG1649 | PFAM Uncharacterised BCR, COG1649 | -0.029494 |
89 | COG1011 | Hydrolase | 0.029455 |
90 | COG1178 | ABC-type Fe3 transport system permease component | -0.029285 |
91 | COG5435 | protein kinase activity | 0.029217 |
92 | COG4752 | Belongs to the RNA methyltransferase TrmD family | -0.029203 |
93 | COG5621 | secreted hydrolase | -0.029115 |
94 | COG1082 | Xylose isomerase domain protein TIM barrel | 0.029061 |
95 | COG3214 | Protein conserved in bacteria | 0.028992 |
96 | COG2826 | transposase and inactivated derivatives, IS30 family | -0.028952 |
97 | COG2313 | pseudouridylate synthase activity | -0.028883 |
98 | COG1942 | 4-Oxalocrotonate Tautomerase | -0.028858 |
99 | COG0688 | phosphatidylethanolamine metabolic process | -0.028857 |
100 | COG4232 | protein-disulfide reductase activity | -0.028770 |
101 | 31H4F | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | -0.028711 |
102 | COG2358 | TRAP transporter, solute receptor (TAXI family | -0.028602 |
103 | COG1234 | tRNA 3'-trailer cleavage | 0.028511 |
104 | COG1971 | Probably functions as a manganese efflux pump | 0.028418 |
105 | COG3653 | N-Acyl-D-aspartate D-glutamate deacylase | -0.028385 |
106 | COG5577 | PFAM Coat F domain | 0.028347 |
107 | COG2339 | peptidase activity | 0.028308 |
108 | COG0531 | amino acid | 0.028177 |
109 | COG1280 | lysine exporter protein (LysE YggA) | -0.028144 |
110 | 31XUS | sporulation protein | 0.028116 |
111 | COG1077 | Cell shape determining protein MreB Mrl | -0.028104 |
112 | COG0616 | signal peptide processing | -0.028060 |
113 | 33Y7F | -0.028016 | |
114 | COG3412 | dihydroxyacetone kinase, phosphotransfer subunit | -0.027965 |
115 | COG1600 | 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) | -0.027949 |
116 | COG5506 | Protein of unknown function (DUF1694) | -0.027864 |
117 | COG3851 | Histidine kinase | 0.027840 |
118 | COG1017 | nitric oxide dioxygenase activity | 0.027803 |
119 | COG3764 | Sortase (surface protein transpeptidase) | 0.027791 |
120 | COG4941 | Belongs to the sigma-70 factor family | 0.027772 |
121 | COG4667 | esterase of the alpha-beta hydrolase superfamily | 0.027759 |
122 | COG5569 | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | -0.027742 |
123 | COG1299 | protein-N(PI)-phosphohistidine-fructose phosphotransferase system transporter activity | 0.027732 |
124 | COG3402 | PFAM membrane-flanked domain | 0.027618 |
125 | COG4970 | Tfp pilus assembly protein FimT | -0.027446 |
126 | COG4569 | acetaldehyde dehydrogenase (acetylating) activity | -0.027443 |
127 | COG0330 | HflC and HflK could | -0.027433 |
128 | COG2501 | S4 domain | 0.027290 |
129 | 32Z9Y | DNA-templated transcription, termination | 0.026901 |
130 | COG3386 | PFAM SMP-30 Gluconolaconase | 0.026852 |
131 | COG2986 | histidine ammonia-lyase | -0.026796 |
132 | COG0795 | lipopolysaccharide-transporting ATPase activity | -0.026727 |
133 | COG1799 | cell septum assembly | 0.026716 |
134 | COG3504 | Conjugal transfer protein | -0.026714 |
135 | COG1620 | l-lactate permease | 0.026692 |
136 | COG4200 | ABC-2 family transporter protein | 0.026658 |
137 | 31RN5 | Bacterial regulatory proteins, tetR family | 0.026557 |
138 | COG4841 | protein insertion into membrane | 0.026554 |
139 | COG2948 | multi-organism process | -0.026457 |
140 | COG1316 | TRANSCRIPTIONal | 0.026376 |
141 | COG3021 | interspecies interaction between organisms | 0.026373 |
142 | COG0741 | lytic transglycosylase activity | -0.026213 |
143 | COG2303 | Involved in the biosynthesis of the osmoprotectant glycine betaine. Catalyzes the oxidation of choline to betaine aldehyde and betaine aldehyde to glycine betaine at the same rate | 0.026167 |
144 | COG2379 | hydroxypyruvate reductase | -0.026164 |
145 | 338TK | 0.026144 | |
146 | COG2353 | YceI-like domain | -0.026138 |
147 | 3172B | Bacterial PH domain | 0.026131 |
148 | COG0437 | 4 iron, 4 sulfur cluster binding | -0.026087 |
149 | COG2606 | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | 0.026053 |
150 | COG1637 | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | 0.026004 |
151 | 324HC | Sigma-70 region 2 | -0.025965 |
152 | COG1350 | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | -0.025963 |
153 | COG2267 | carboxylic ester hydrolase activity | 0.025871 |
154 | COG3540 | Alkaline phosphatase | 0.025806 |
155 | COG2376 | Dihydroxyacetone kinase | -0.025770 |
156 | COG4666 | Tripartite ATP-independent periplasmic transporter, DctM component | -0.025709 |
157 | COG1450 | Type ii and iii secretion system protein | -0.025697 |
158 | COG2966 | Psort location CytoplasmicMembrane, score | 0.025688 |
159 | COG3702 | type iv secretory pathway | -0.025673 |
160 | COG1076 | Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA | -0.025626 |
161 | COG1452 | involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane | -0.025614 |
162 | COG0459 | protein refolding | -0.025379 |
163 | COG0817 | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | -0.025289 |
164 | COG0721 | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | -0.025191 |
165 | COG2346 | COG2346, Truncated hemoglobins | 0.025157 |
166 | COG3600 | Phage-associated protein | -0.025125 |
167 | COG2061 | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | 0.025106 |
168 | COG0859 | PFAM glycosyl transferase family 9 | -0.025093 |
169 | COG0851 | Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell | -0.025093 |
170 | 339JQ | Spore cortex biosynthesis protein YabQ | 0.025036 |
171 | COG3736 | Type IV secretory pathway, component VirB8 | -0.024945 |
172 | 2ZU9X | Mut7-C ubiquitin | 0.024941 |
173 | COG3937 | granule-associated protein | 0.024935 |
174 | 33HRU | -0.024904 | |
175 | COG0037 | tRNA processing | -0.024904 |
176 | COG3475 | LICD family | 0.024831 |
177 | COG3601 | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | 0.024808 |
178 | COG2312 | Erythromycin esterase | 0.024808 |
179 | COG2169 | Transcriptional regulator | 0.024756 |
180 | COG1032 | radical SAM domain protein | -0.024754 |
181 | COG3643 | Formiminotransferase domain | -0.024713 |
182 | COG0144 | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | -0.024651 |
183 | COG4388 | Caudovirus prohead serine protease | 0.024601 |
184 | 2Z7YI | Psort location Cytoplasmic, score | -0.024593 |
185 | 32SBU | Tryptophan transporter | 0.024577 |
186 | COG5504 | Zn-dependent protease | 0.024576 |
187 | COG1804 | L-carnitine dehydratase bile acid-inducible protein F | 0.024540 |
188 | 349CY | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | -0.024493 |
189 | COG2364 | Membrane | 0.024470 |
190 | 330YS | 0.024460 | |
191 | COG1523 | belongs to the glycosyl hydrolase 13 family | -0.024352 |
192 | COG1560 | Kdo2-lipid A biosynthetic process | -0.024338 |
193 | COG2825 | PFAM Outer membrane chaperone Skp (OmpH) | -0.024296 |
194 | COG3311 | Transcriptional regulator | -0.024289 |
195 | COG3002 | Belongs to the UPF0753 family | -0.024255 |
196 | COG1363 | Peptidase, m42 | 0.024250 |
197 | COG0388 | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | -0.024228 |
198 | COG0486 | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | -0.024222 |
199 | COG2268 | Band 7 protein | 0.024125 |
200 | COG4572 | Cation transport regulator | 0.024117 |
201 | COG0389 | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | 0.024051 |
202 | COG0848 | biopolymer transport protein | -0.024024 |
203 | COG4670 | ketone body catabolic process | -0.024016 |
204 | COG2020 | methyltransferase activity | -0.023950 |
205 | 333DA | 0.023917 | |
206 | 334N1 | 0.023853 | |
207 | COG4651 | solute:proton antiporter activity | -0.023773 |
208 | COG1735 | metal-dependent hydrolase with the TIM-barrel fold | 0.023715 |
209 | 32RKH | 0.023582 | |
210 | COG3164 | Protein of unknown function | -0.023559 |
211 | 33BU4 | 0.023527 | |
212 | COG0523 | cobalamin synthesis protein | 0.023484 |
213 | COG1212 | Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria | -0.023481 |
214 | COG1115 | amino acid carrier protein | 0.023466 |
215 | COG0849 | cell division | -0.023460 |
216 | 32YI8 | 0.023439 | |
217 | COG1691 | (AIR) carboxylase | 0.023431 |
218 | COG3119 | arylsulfatase activity | 0.023429 |
219 | 33160 | -0.023408 | |
220 | COG4688 | A helicase nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme degrades any linearized DNA that is unable to undergo homologous recombination. In the holoenzyme this subunit has ssDNA-dependent ATPase and 5'-3' helicase activity. When added to pre-assembled RecBC greatly stimulates nuclease activity and augments holoenzyme processivity. Negatively regulates the RecA-loading ability of RecBCD | 0.023379 |
221 | COG0496 | Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates | -0.023365 |
222 | COG2949 | membrane | -0.023353 |
223 | COG3328 | transposase activity | 0.023332 |
224 | COG4924 | 0.023278 | |
225 | COG4668 | phosphoenolpyruvate-dependent sugar phosphotransferase system | 0.023272 |
226 | COG0573 | inorganic phosphate transmembrane transporter activity | 0.023196 |
227 | 2ZQ9P | 0.023144 | |
228 | 33IIW | 0.023131 | |
229 | COG3577 | Aspartyl protease | -0.023127 |
230 | COG0702 | epimerase | 0.023114 |
231 | COG2367 | Beta-lactamase | 0.023102 |
232 | 30A7P | 0.023078 | |
233 | COG1242 | 4 iron, 4 sulfur cluster binding | 0.023065 |
234 | COG5266 | PFAM Nickel transport complex, NikM subunit, transmembrane | -0.023055 |
235 | 337A1 | -0.023001 | |
236 | COG2094 | Belongs to the DNA glycosylase MPG family | 0.022936 |
237 | 32YQ0 | -0.022908 | |
238 | COG1754 | DNA topoisomerase type I activity | -0.022872 |
239 | COG0672 | )-iron permease | 0.022866 |
240 | 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 | -0.022853 |
241 | 2ZITU | Cupin domain | -0.022852 |
242 | 31S9P | sporulation protein YtxC | 0.022847 |
243 | 335XQ | sh3 domain protein | 0.022839 |
244 | 33EHP | 0.022807 | |
245 | 3454B | Mannose-6-phosphate isomerase | -0.022790 |
246 | COG0154 | amidase activity | -0.022788 |
247 | COG1904 | glucuronate isomerase | -0.022757 |
248 | COG2964 | Protein conserved in bacteria | -0.022692 |
249 | COG1366 | Belongs to the anti-sigma-factor antagonist family | 0.022677 |
250 | COG1099 | with the TIM-barrel fold | 0.022659 |