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 | COG1702 | phosphate starvation-inducible protein PhoH | -0.014517 |
2 | COG0799 | negative regulation of ribosome biogenesis | -0.013804 |
3 | COG1932 | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | -0.013356 |
4 | 2ZAUC | 0.011399 | |
5 | COG0705 | Rhomboid family | -0.011075 |
6 | COG3247 | response to pH | -0.010622 |
7 | COG1775 | 2-hydroxyglutaryl-CoA dehydratase, D-component | 0.010513 |
8 | COG0782 | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus | -0.010426 |
9 | COG4152 | abc transporter atp-binding protein | -0.010426 |
10 | COG1983 | PspC domain protein | -0.010365 |
11 | COG3270 | Specifically methylates the cytosine at position 1407 (m5C1407) of 16S rRNA | -0.010264 |
12 | COG0342 | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | 0.010090 |
13 | COG5426 | von Willebrand factor, type A | -0.009953 |
14 | COG4108 | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | -0.009923 |
15 | COG0396 | ATPase activity | -0.009914 |
16 | COG0719 | Fe-S assembly protein | -0.009914 |
17 | COG1399 | metal-binding, possibly nucleic acid-binding protein | -0.009904 |
18 | COG0546 | phosphoglycolate phosphatase activity | -0.009809 |
19 | COG1825 | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | -0.009715 |
20 | COG4566 | intracellular signal transduction | -0.009694 |
21 | COG1475 | DNA binding | -0.009607 |
22 | COG1539 | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | -0.009572 |
23 | COG4485 | Bacterial membrane protein, YfhO | -0.009492 |
24 | COG0593 | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | -0.009433 |
25 | COG4992 | N2-acetyl-L-ornithine:2-oxoglutarate 5-aminotransferase activity | -0.009326 |
26 | COG1243 | radical SAM domain protein | 0.009261 |
27 | COG1623 | Has also diadenylate cyclase activity, catalyzing the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP). c- di-AMP acts as a signaling molecule that couples DNA integrity with progression of sporulation. The rise in c-di-AMP level generated by DisA while scanning the chromosome, operates as a positive signal that advances sporulation | 0.009261 |
28 | COG5438 | YibE/F-like protein | 0.009148 |
29 | 3204A | 0.009096 | |
30 | COG0590 | tRNA wobble adenosine to inosine editing | -0.009038 |
31 | COG0174 | glutamine synthetase | -0.009002 |
32 | COG2084 | Dehydrogenase | -0.008880 |
33 | COG0428 | transporter | -0.008867 |
34 | COG1494 | fructose-1,6-bisphosphatase | 0.008830 |
35 | COG1785 | Belongs to the alkaline phosphatase family | -0.008809 |
36 | COG0828 | Belongs to the bacterial ribosomal protein bS21 family | -0.008802 |
37 | COG2843 | Capsule synthesis protein | -0.008772 |
38 | COG1748 | Saccharopine dehydrogenase | -0.008752 |
39 | COG0372 | Belongs to the citrate synthase family | -0.008705 |
40 | COG0385 | Bile acid | -0.008538 |
41 | COG3201 | nicotinamide mononucleotide transporter | -0.008487 |
42 | COG0620 | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | -0.008469 |
43 | COG2151 | metal-sulfur cluster biosynthetic enzyme | -0.008440 |
44 | COG1297 | OPT oligopeptide transporter protein | -0.008367 |
45 | COG0819 | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | -0.008328 |
46 | COG1583 | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA) | 0.008306 |
47 | COG3250 | beta-galactosidase activity | -0.008290 |
48 | COG2261 | transglycosylase associated protein | -0.008289 |
49 | COG0205 | 6-phosphofructokinase activity | -0.008262 |
50 | COG1954 | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | 0.008202 |
51 | COG0483 | inositol monophosphate 1-phosphatase activity | -0.008196 |
52 | 33J3F | the current gene model (or a revised gene model) may contain a frame shift | 0.008127 |
53 | COG0021 | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | -0.008087 |
54 | COG0607 | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | -0.008045 |
55 | COG2214 | Heat shock protein DnaJ domain protein | 0.008016 |
56 | 33QJ0 | 0.007977 | |
57 | COG1329 | Transcriptional regulator | -0.007936 |
58 | COG0369 | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component | -0.007905 |
59 | COG0530 | calcium, potassium:sodium antiporter activity | -0.007889 |
60 | COG4555 | ABC transporter | -0.007876 |
61 | COG1296 | Branched-chain amino acid permease (Azaleucine resistance) | -0.007874 |
62 | COG1522 | sequence-specific DNA binding | -0.007858 |
63 | COG0731 | radical SAM domain protein | 0.007856 |
64 | COG2081 | HI0933 family | -0.007830 |
65 | COG4399 | Belongs to the UPF0754 family | 0.007828 |
66 | COG2246 | polysaccharide biosynthetic process | -0.007792 |
67 | COG1587 | Uroporphyrinogen-III synthase | -0.007780 |
68 | COG2050 | protein possibly involved in aromatic compounds catabolism | -0.007743 |
69 | COG2169 | Transcriptional regulator | -0.007737 |
70 | COG5340 | Psort location Cytoplasmic, score | -0.007638 |
71 | COG3395 | kinase activity | 0.007564 |
72 | COG2088 | sporulation resulting in formation of a cellular spore | 0.007560 |
73 | COG4748 | type I restriction enzyme | -0.007556 |
74 | COG0026 | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | -0.007504 |
75 | 32YHG | Putative adhesin | -0.007478 |
76 | COG0623 | enoyl-[acyl-carrier-protein] reductase (NADH) activity | -0.007476 |
77 | COG1680 | COG1680 Beta-lactamase class C and other penicillin binding | -0.007439 |
78 | COG1433 | Dinitrogenase iron-molybdenum cofactor | 0.007436 |
79 | COG0586 | Pfam SNARE associated Golgi protein | -0.007391 |
80 | COG3493 | citrate carrier protein | 0.007367 |
81 | COG1004 | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | -0.007362 |
82 | COG3976 | FMN-binding domain protein | 0.007346 |
83 | COG0394 | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | -0.007342 |
84 | COG0276 | Catalyzes the ferrous insertion into protoporphyrin IX | -0.007338 |
85 | COG3980 | spore coat polysaccharide biosynthesis protein | 0.007333 |
86 | COG3883 | PFAM NLP P60 protein | -0.007318 |
87 | COG0232 | Belongs to the dGTPase family. Type 2 subfamily | -0.007305 |
88 | COG2884 | Cell division ATP-binding protein ftsE | -0.007302 |
89 | COG0214 | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | 0.007295 |
90 | 33YTS | 0.007286 | |
91 | 30FW8 | 0.007255 | |
92 | 32SQE | Psort location CytoplasmicMembrane, score | 0.007255 |
93 | 32YCW | Domain of unknown function (DUF4363) | 0.007255 |
94 | 32ZH6 | Small, acid-soluble spore protein Tlp | 0.007255 |
95 | 33BU4 | 0.007255 | |
96 | 33HSY | 0.007255 | |
97 | 33NPR | 4Fe-4S single cluster domain of Ferredoxin I | 0.007255 |
98 | COG2604 | Protein of unknown function DUF115 | 0.007255 |
99 | COG2836 | Biogenesis protein | 0.007255 |
100 | COG2179 | HAD superfamily (subfamily IIIA) phosphatase, TIGR01668 | -0.007254 |
101 | COG3027 | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | -0.007241 |
102 | COG0538 | isocitrate dehydrogenase activity | -0.007228 |
103 | COG3576 | pyridoxamine 5-phosphate | 0.007226 |
104 | COG0737 | Belongs to the 5'-nucleotidase family | -0.007211 |
105 | COG2807 | transmembrane transport | -0.007204 |
106 | COG2089 | acid synthase | 0.007193 |
107 | COG1861 | Spore coat polysaccharide biosynthesis protein F CMP-KDO synthetase | 0.007184 |
108 | COG4734 | Psort location Cytoplasmic, score | -0.007150 |
109 | COG0176 | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | -0.007142 |
110 | COG0266 | class I DNA-(apurinic or apyrimidinic site) endonuclease activity | -0.007134 |
111 | COG2951 | lytic endotransglycosylase activity | -0.007132 |
112 | COG0610 | Subunit R is required for both nuclease and ATPase activities, but not for modification | -0.007121 |
113 | COG0710 | 3-dehydroquinate dehydratase activity | -0.007111 |
114 | COG5305 | Membrane | 0.007065 |
115 | COG3581 | 4 iron, 4 sulfur cluster binding | 0.007054 |
116 | COG2992 | FlgJ-related protein | 0.007037 |
117 | 2Z7IF | 0.007037 | |
118 | 2Z81M | 0.007037 | |
119 | 2Z8JZ | 0.007037 | |
120 | 2ZANH | 0.007037 | |
121 | 2ZB1T | 0.007037 | |
122 | 2ZB2U | 0.007037 | |
123 | 2ZB4K | 0.007037 | |
124 | 2ZBE8 | SIR2-like domain | 0.007037 |
125 | 2ZCBC | 0.007037 | |
126 | 2ZI92 | 0.007037 | |
127 | 2ZN7A | 0.007037 | |
128 | 2ZNS3 | 0.007037 | |
129 | 3059E | 0.007037 | |
130 | 30I98 | 0.007037 | |
131 | 311NS | 0.007037 | |
132 | 31WHG | 0.007037 | |
133 | 32R07 | 0.007037 | |
134 | 32TDI | 0.007037 | |
135 | 32TJ3 | Domain of unknown function (DUF4911) | 0.007037 |
136 | 32WIG | 0.007037 | |
137 | 32XIJ | L,D-transpeptidase catalytic domain | 0.007037 |
138 | 32Y2K | Hydrid cluster protein-associated redox disulfide domain protein | 0.007037 |
139 | 32YZT | 0.007037 | |
140 | 331VG | 0.007037 | |
141 | 33KNY | Type IV leader peptidase family | 0.007037 |
142 | COG4752 | Belongs to the RNA methyltransferase TrmD family | 0.007037 |
143 | COG3451 | type IV secretory pathway VirB4 | -0.007029 |
144 | 33MNE | Domain of unknown function (DUF1904) | 0.007021 |
145 | COG4185 | zeta toxin | 0.007015 |
146 | COG4492 | Belongs to the UPF0735 family | 0.007011 |
147 | COG2860 | membrane | -0.007006 |
148 | COG4533 | DNA binding | 0.006998 |
149 | COG4604 | ABC transporter, ATP-binding protein | 0.006988 |
150 | 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) | 0.006977 |
151 | COG0850 | regulation of cytokinetic process | 0.006956 |
152 | 2Z7V1 | 0.006946 | |
153 | COG0378 | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | 0.006940 |
154 | COG3878 | Protein conserved in bacteria | 0.006929 |
155 | COG3872 | metal-dependent enzyme | 0.006927 |
156 | COG0504 | CTP synthase activity | -0.006926 |
157 | COG2129 | metallophosphoesterase | -0.006907 |
158 | COG4892 | Cytochrome b5 | 0.006869 |
159 | COG3682 | Transcriptional regulator | -0.006856 |
160 | COG3274 | enterobacterial common antigen metabolic process | -0.006804 |
161 | COG0794 | Belongs to the SIS family. GutQ KpsF subfamily | 0.006802 |
162 | 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 | -0.006795 |
163 | COG0524 | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | -0.006790 |
164 | COG3478 | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | 0.006764 |
165 | 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 | -0.006742 |
166 | COG0135 | phosphoribosylanthranilate isomerase activity | -0.006741 |
167 | 32TBR | Protein of unknown function (DUF2974) | -0.006724 |
168 | COG4990 | cell redox homeostasis | -0.006720 |
169 | COG1322 | Protein conserved in bacteria | -0.006696 |
170 | 32ZT4 | 0.006690 | |
171 | 2Z8TW | 0.006690 | |
172 | 30H27 | 0.006690 | |
173 | 30U2T | Psort location Cytoplasmic, score | 0.006690 |
174 | 32ZVE | 0.006690 | |
175 | COG0667 | Aldo Keto reductase | -0.006672 |
176 | COG0611 | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 | -0.006662 |
177 | COG4211 | Belongs to the binding-protein-dependent transport system permease family | 0.006649 |
178 | COG0320 | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | -0.006647 |
179 | COG0509 | glycine decarboxylation via glycine cleavage system | -0.006629 |
180 | COG1244 | Elongator protein 3, MiaB family, Radical SAM | 0.006619 |
181 | 2ZCKR | 0.006618 | |
182 | COG0741 | lytic transglycosylase activity | -0.006607 |
183 | COG1668 | transmembrane transport | -0.006603 |
184 | COG0738 | Major facilitator superfamily | -0.006595 |
185 | COG3331 | DNA recombination | -0.006579 |
186 | 3471B | Helix-turn-helix XRE-family like proteins | 0.006574 |
187 | 2Z9AH | 0.006564 | |
188 | COG3807 | Bacterial SH3 domain | 0.006563 |
189 | COG1194 | a g-specific adenine glycosylase | -0.006557 |
190 | COG2771 | luxR family | -0.006534 |
191 | COG3276 | selenocysteine insertion sequence binding | 0.006532 |
192 | 32RV1 | Domain of Unknown Function with PDB structure (DUF3862) | 0.006523 |
193 | COG2915 | High frequency lysogenization protein hflD homolog | -0.006523 |
194 | COG2365 | Tyrosine phosphatase family | -0.006520 |
195 | COG3326 | Membrane | -0.006510 |
196 | 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 | 0.006477 |
197 | COG2870 | Catalyzes the ADP transfer from ATP to D-glycero-beta-D- manno-heptose 1-phosphate, yielding ADP-D-glycero-beta-D-manno- heptose | 0.006474 |
198 | COG2926 | Belongs to the UPF0265 family | 0.006474 |
199 | COG4807 | Protein conserved in bacteria | 0.006474 |
200 | COG0374 | Belongs to the NiFe NiFeSe hydrogenase large subunit family | 0.006468 |
201 | COG1740 | oxidoreductase activity, acting on hydrogen as donor, iron-sulfur protein as acceptor | 0.006468 |
202 | COG5337 | Spore coat protein CotH | -0.006444 |
203 | COG0112 | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | -0.006438 |
204 | COG4545 | Glutaredoxin-related protein | 0.006430 |
205 | COG2166 | iron-sulfur cluster assembly | -0.006427 |
206 | COG1001 | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | 0.006426 |
207 | COG3246 | L-lysine catabolic process to acetate | 0.006425 |
208 | 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 | -0.006425 |
209 | COG4980 | gas vesicle protein | -0.006421 |
210 | COG4392 | branched-chain amino acid | -0.006383 |
211 | COG1342 | Belongs to the UPF0251 family | 0.006379 |
212 | COG1808 | Membrane | -0.006359 |
213 | COG0328 | RNA-DNA hybrid ribonuclease activity | -0.006347 |
214 | COG1516 | flagellar protein fliS | 0.006338 |
215 | COG0599 | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | -0.006331 |
216 | COG1893 | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | -0.006327 |
217 | COG0134 | indole-3-glycerol-phosphate synthase activity | -0.006324 |
218 | COG1362 | aminopeptidase activity | 0.006322 |
219 | COG1712 | Catalyzes the reversible NADPH-dependent reductive amination of L-2-amino-6-oxopimelate, the acyclic form of L- tetrahydrodipicolinate, to generate the meso compound, D,L-2,6- diaminopimelate | -0.006320 |
220 | COG3525 | Glycosyl hydrolase, family 20, catalytic domain | -0.006318 |
221 | COG2259 | Doxx family | -0.006291 |
222 | 2Z7T7 | Psort location CytoplasmicMembrane, score | -0.006287 |
223 | COG0002 | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | -0.006277 |
224 | COG0548 | Belongs to the acetylglutamate kinase family. ArgB subfamily | -0.006277 |
225 | COG0159 | tryptophan synthase activity | -0.006277 |
226 | COG0547 | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | -0.006277 |
227 | COG3862 | protein with conserved CXXC pairs | 0.006274 |
228 | COG3152 | Membrane | -0.006272 |
229 | COG2073 | Cobalamin biosynthesis protein cbiG | 0.006267 |
230 | COG2082 | Precorrin-8x methylmutase | 0.006267 |
231 | COG2099 | Precorrin-6x reductase | 0.006267 |
232 | COG0392 | lysyltransferase activity | -0.006258 |
233 | COG1574 | metal-dependent hydrolase with the TIM-barrel fold | -0.006234 |
234 | 2Z974 | Psort location Cytoplasmic, score | 0.006224 |
235 | COG1754 | DNA topoisomerase type I activity | -0.006216 |
236 | COG5002 | protein histidine kinase activity | -0.006211 |
237 | COG3935 | DnaD domain protein | -0.006206 |
238 | COG3620 | sequence-specific DNA binding | -0.006191 |
239 | COG2813 | Specifically methylates the guanine in position | -0.006187 |
240 | COG1197 | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | -0.006166 |
241 | COG4915 | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | -0.006164 |
242 | COG2221 | Nitrite and sulphite reductase 4Fe-4S | 0.006157 |
243 | COG3086 | response to oxidative stress | 0.006142 |
244 | COG1961 | COG1961 Site-specific recombinases, DNA invertase Pin homologs | -0.006125 |
245 | 33E6K | 0.006116 | |
246 | COG4936 | Histidine kinase | 0.006103 |
247 | COG3710 | Transcriptional regulator | -0.006088 |
248 | COG1253 | flavin adenine dinucleotide binding | -0.006080 |
249 | 32UC7 | Glycosyltransferase family 52 | 0.006074 |
250 | COG1266 | CAAX protease self-immunity | -0.006064 |