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 | COG1850 | ribulose-bisphosphate carboxylase activity | 0.030230 |
2 | COG1969 | Ni Fe-hydrogenase, b-type cytochrome subunit | 0.026399 |
3 | COG2723 | 6-phospho-beta-galactosidase activity | -0.026337 |
4 | COG0375 | protein maturation | 0.024789 |
5 | COG0378 | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | 0.023158 |
6 | COG0374 | Belongs to the NiFe NiFeSe hydrogenase large subunit family | 0.023050 |
7 | COG0349 | Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides | -0.022868 |
8 | COG1435 | thymidine kinase activity | -0.022743 |
9 | COG1740 | oxidoreductase activity, acting on hydrogen as donor, iron-sulfur protein as acceptor | 0.022635 |
10 | COG0298 | carbon dioxide binding | 0.021989 |
11 | COG0409 | Hydrogenase expression formation protein | 0.021989 |
12 | COG0068 | Along with HypE, it catalyzes the synthesis of the CN ligands of the active site iron of NiFe -hydrogenases using carbamoylphosphate as a substrate. It functions as a carbamoyl transferase using carbamoylphosphate as a substrate and transferring the carboxamido moiety in an ATP-dependent reaction to the thiolate of the C-terminal cysteine of HypE yielding a protein-S-carboxamide | 0.021682 |
13 | COG4451 | ribulose bisphosphate carboxylase, small | 0.021403 |
14 | COG2962 | Rard protein | -0.021290 |
15 | COG0295 | cytidine deaminase activity | -0.020900 |
16 | COG2008 | Catalyzes the cleavage of L-allo-threonine and L- threonine to glycine and acetaldehyde | -0.020720 |
17 | COG1533 | DNA photolyase activity | 0.020715 |
18 | COG1773 | rubredoxin | 0.020559 |
19 | COG2862 | Uncharacterized protein family, UPF0114 | 0.019902 |
20 | COG1633 | Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) | 0.019681 |
21 | COG3666 | COG3666 Transposase and inactivated derivatives | 0.019050 |
22 | COG0644 | oxidoreductase | 0.018668 |
23 | 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 | -0.018619 |
24 | COG0680 | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | 0.018566 |
25 | COG0602 | queuosine metabolic process | 0.018553 |
26 | COG0017 | Asparaginyl-tRNA synthetase | -0.018505 |
27 | COG2020 | methyltransferase activity | 0.018480 |
28 | COG0584 | glycerophosphoryl diester phosphodiesterase | -0.018479 |
29 | COG0247 | lactate metabolic process | 0.018438 |
30 | COG2818 | Glycosylase | -0.018428 |
31 | COG3743 | rRNA binding | -0.018345 |
32 | COG2195 | Cleaves the N-terminal amino acid of tripeptides | -0.018325 |
33 | COG0309 | Hydrogenase expression formation protein (HypE) | 0.018158 |
34 | COG0421 | Catalyzes the irreversible transfer of a propylamine group from the amino donor S-adenosylmethioninamine (decarboxy- AdoMet) to putrescine (1,4-diaminobutane) to yield spermidine | 0.017942 |
35 | 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 | 0.017895 |
36 | COG3883 | PFAM NLP P60 protein | -0.017739 |
37 | COG0011 | TIGRFAM Protein of | 0.017500 |
38 | COG3005 | denitrification pathway | 0.017450 |
39 | COG3344 | reverse transcriptase | -0.017349 |
40 | COG0561 | phosphatase activity | -0.017267 |
41 | COG2348 | transferase activity, transferring amino-acyl groups | -0.017131 |
42 | 339P0 | KaiB | 0.016885 |
43 | COG2986 | histidine ammonia-lyase | -0.016623 |
44 | COG1145 | 4fe-4S ferredoxin, iron-sulfur binding domain protein | 0.016620 |
45 | COG1566 | PFAM secretion protein HlyD family protein | 0.016582 |
46 | COG0058 | SHG alpha-glucan phosphorylase activity | 0.016441 |
47 | COG0580 | Belongs to the MIP aquaporin (TC 1.A.8) family | -0.016212 |
48 | COG3533 | Beta-L-arabinofuranosidase, GH127 | -0.016167 |
49 | COG4907 | membrane protein (DUF2207) | -0.016139 |
50 | COG0371 | Dehydrogenase | 0.016127 |
51 | COG4785 | May be involved in cell division | -0.016126 |
52 | COG2076 | Multidrug Resistance protein | 0.016076 |
53 | COG3865 | 3-Demethylubiquinone-9 3-methyltransferase | 0.016069 |
54 | COG5424 | Ring cyclization and eight-electron oxidation of 3a-(2- amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline- 7,9-dicarboxylic-acid to PQQ | 0.016047 |
55 | COG2187 | AAA domain | 0.015974 |
56 | COG1438 | arginine binding | -0.015894 |
57 | COG1979 | alcohol dehydrogenase | -0.015881 |
58 | COG1738 | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | -0.015826 |
59 | COG1926 | phosphoribosyltransferase | 0.015824 |
60 | COG1289 | transmembrane transporter activity | 0.015785 |
61 | COG4091 | Methyl-accepting Chemotaxis protein | 0.015754 |
62 | COG2115 | Belongs to the xylose isomerase family | -0.015727 |
63 | COG3940 | Belongs to the glycosyl hydrolase 43 family | -0.015713 |
64 | COG1652 | LysM domain | -0.015623 |
65 | COG1950 | PFAM Membrane protein of | 0.015595 |
66 | COG0384 | phenazine biosynthesis protein PhzF | -0.015576 |
67 | COG4695 | Portal protein | -0.015555 |
68 | COG0620 | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | 0.015541 |
69 | COG0075 | 2-aminoethylphosphonate-pyruvate transaminase activity | 0.015520 |
70 | COG1054 | Belongs to the UPF0176 family | -0.015519 |
71 | COG1820 | Belongs to the metallo-dependent hydrolases superfamily. NagA family | -0.015468 |
72 | COG1236 | Exonuclease of the beta-lactamase fold involved in RNA processing | 0.015448 |
73 | 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 | 0.015434 |
74 | COG0738 | Major facilitator superfamily | -0.015413 |
75 | COG4916 | TIR domain | 0.015382 |
76 | COG1011 | Hydrolase | -0.015324 |
77 | COG1429 | ligase activity, forming nitrogen-metal bonds | 0.015260 |
78 | COG4260 | virion core protein, lumpy skin disease virus | -0.015196 |
79 | COG2379 | hydroxypyruvate reductase | 0.015152 |
80 | COG2049 | 5-oxoprolinase (ATP-hydrolyzing) activity | 0.015099 |
81 | COG0850 | regulation of cytokinetic process | 0.015076 |
82 | COG0589 | response to stress | 0.015047 |
83 | COG1434 | Gram-negative-bacterium-type cell wall biogenesis | 0.014960 |
84 | COG2055 | Belongs to the LDH2 MDH2 oxidoreductase family | -0.014928 |
85 | COG4325 | translation initiation factor activity | -0.014928 |
86 | COG3395 | kinase activity | 0.014761 |
87 | COG4309 | conserved protein (DUF2249) | -0.014580 |
88 | COG5405 | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | 0.014566 |
89 | COG0287 | Prephenate dehydrogenase | 0.014503 |
90 | COG0657 | acetylesterase activity | -0.014492 |
91 | COG4301 | Catalyzes the SAM-dependent triple methylation of the alpha-amino group of histidine to form hercynine, a step in the biosynthesis pathway of ergothioneine | 0.014441 |
92 | COG1981 | membrane | 0.014437 |
93 | COG1416 | DNA-binding transcription factor activity | 0.014424 |
94 | COG1144 | Oxidoreductase | 0.014367 |
95 | COG3507 | Belongs to the glycosyl hydrolase 43 family | -0.014355 |
96 | COG2191 | Formylmethanofuran dehydrogenase, subunit e | 0.014352 |
97 | COG1501 | Belongs to the glycosyl hydrolase 31 family | -0.014287 |
98 | COG1487 | ribonuclease activity | 0.014266 |
99 | COG4989 | oxidoreductase activity | -0.014227 |
100 | COG3712 | iron ion homeostasis | 0.014224 |
101 | COG1733 | regulation of RNA biosynthetic process | -0.014115 |
102 | COG1151 | hydroxylamine reductase activity | 0.014105 |
103 | COG4181 | ATPase activity | -0.014088 |
104 | COG1898 | dTDP-4-dehydrorhamnose 3,5-epimerase activity | 0.014049 |
105 | COG1366 | Belongs to the anti-sigma-factor antagonist family | -0.014046 |
106 | 2ZCCT | Glyoxalase-like domain | -0.013990 |
107 | COG0189 | ligase activity | 0.013978 |
108 | COG4185 | zeta toxin | -0.013953 |
109 | COG0860 | N-Acetylmuramoyl-L-alanine amidase | 0.013883 |
110 | 2ZMC1 | -0.013867 | |
111 | COG3358 | COGs COG3358 conserved | -0.013858 |
112 | COG1594 | Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and or for immediate growth after restoration of oxygen | -0.013852 |
113 | COG3521 | Type VI secretion | 0.013791 |
114 | COG0814 | amino acid | -0.013783 |
115 | COG5283 | actin binding | -0.013779 |
116 | COG3705 | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | 0.013766 |
117 | COG4912 | Dna alkylation repair | -0.013742 |
118 | COG3185 | 4-Hydroxyphenylpyruvate dioxygenase | -0.013710 |
119 | COG0535 | radical SAM domain protein | 0.013702 |
120 | COG2932 | Transcriptional regulator | 0.013698 |
121 | COG2257 | FlhB HrpN YscU SpaS Family | 0.013669 |
122 | 33D9H | Peptidase propeptide and YPEB domain | 0.013650 |
123 | COG5330 | Evidence 4 Homologs of previously reported genes of | 0.013611 |
124 | COG2069 | CO dehydrogenase acetyl-CoA synthase delta subunit | 0.013521 |
125 | COG2391 | methyltransferase activity | 0.013494 |
126 | 32YPT | -0.013448 | |
127 | COG0338 | D12 class N6 adenine-specific DNA methyltransferase | -0.013443 |
128 | 2Z9II | PEGA domain | -0.013439 |
129 | 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 | -0.013429 |
130 | COG1393 | Belongs to the ArsC family | 0.013425 |
131 | COG0134 | indole-3-glycerol-phosphate synthase activity | 0.013417 |
132 | COG4972 | Pilus assembly protein | -0.013358 |
133 | COG1058 | Belongs to the CinA family | 0.013352 |
134 | 32STP | 0.013335 | |
135 | COG3954 | Phosphoribulokinase | 0.013326 |
136 | COG2025 | fatty acid beta-oxidation using acyl-CoA dehydrogenase | -0.013312 |
137 | COG2086 | electron transfer activity | -0.013312 |
138 | COG2166 | iron-sulfur cluster assembly | -0.013268 |
139 | COG2936 | dipeptidyl-peptidase activity | -0.013253 |
140 | COG3642 | lipopolysaccharide core region biosynthetic process | 0.013248 |
141 | COG1443 | Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) | -0.013241 |
142 | COG0035 | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | -0.013216 |
143 | COG1609 | Transcriptional regulator | -0.013210 |
144 | COG0396 | ATPase activity | -0.013190 |
145 | COG0719 | Fe-S assembly protein | -0.013190 |
146 | COG4774 | siderophore transport | 0.013164 |
147 | COG1433 | Dinitrogenase iron-molybdenum cofactor | 0.013141 |
148 | COG3345 | alpha-galactosidase | -0.013140 |
149 | COG1474 | Belongs to the peptidase S16 family | -0.013107 |
150 | COG0474 | ATPase, P-type transporting, HAD superfamily, subfamily IC | 0.013067 |
151 | COG2222 | sugar isomerase | -0.013060 |
152 | COG3381 | protein complex oligomerization | 0.013002 |
153 | COG3342 | major pilin protein fima | -0.012986 |
154 | COG2220 | Zn-dependent hydrolases of the beta-lactamase fold | -0.012979 |
155 | COG5501 | 0.012954 | |
156 | COG1972 | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | -0.012950 |
157 | COG2356 | endonuclease I | -0.012890 |
158 | COG2893 | phosphoenolpyruvate-dependent sugar phosphotransferase system | 0.012866 |
159 | COG1956 | GAF domain-containing protein | -0.012816 |
160 | COG5403 | PFAM Bacterial protein of | -0.012814 |
161 | COG0311 | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | -0.012792 |
162 | COG0146 | N-methylhydantoinase B acetone carboxylase alpha subunit | 0.012785 |
163 | COG2603 | Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA | 0.012770 |
164 | COG4653 | Phage capsid family | -0.012768 |
165 | COG3886 | PLD-like domain | -0.012756 |
166 | COG1514 | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | 0.012721 |
167 | COG0423 | glycine-tRNA ligase activity | -0.012718 |
168 | COG1092 | Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA | -0.012700 |
169 | COG3349 | Catalyzes the conversion of zeta-carotene to lycopene via the intermediary of neurosporene. It carries out two consecutive desaturations (introduction of double bonds) at positions C-7 and C-7' | 0.012690 |
170 | COG1538 | Outer membrane efflux protein | 0.012679 |
171 | COG5271 | translation initiation factor activity | 0.012650 |
172 | COG5646 | InterPro IPR014922 | -0.012646 |
173 | COG2048 | Heterodisulfide reductase, subunit B | 0.012645 |
174 | COG3104 | oligopeptide transport | -0.012643 |
175 | COG1739 | Uncharacterized protein family UPF0029 | -0.012571 |
176 | COG1723 | PFAM Uncharacterised ACR, YagE family COG1723 | 0.012567 |
177 | COG2138 | Cobalamin (vitamin B12) biosynthesis CbiX protein | 0.012550 |
178 | COG1209 | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | 0.012537 |
179 | COG4799 | Acetyl-CoA carboxylase, carboxyltransferase component subunits alpha and beta | -0.012519 |
180 | COG1018 | Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress | -0.012486 |
181 | COG5625 | HemY protein N-terminus | 0.012462 |
182 | COG0627 | Serine hydrolase involved in the detoxification of formaldehyde | -0.012450 |
183 | COG2313 | pseudouridylate synthase activity | -0.012449 |
184 | COG1764 | response to oxidative stress | -0.012442 |
185 | COG0400 | carboxylic ester hydrolase activity | -0.012433 |
186 | COG3921 | Protein conserved in bacteria | 0.012425 |
187 | COG2866 | Carboxypeptidase | -0.012411 |
188 | COG2937 | Belongs to the GPAT DAPAT family | -0.012409 |
189 | COG3246 | L-lysine catabolic process to acetate | 0.012371 |
190 | COG2353 | YceI-like domain | -0.012367 |
191 | COG4067 | protein conserved in archaea | -0.012343 |
192 | COG1492 | cobalamin metabolic process | 0.012340 |
193 | COG0001 | glutamate-1-semialdehyde 2,1-aminomutase activity | 0.012323 |
194 | 32SEB | 0.012298 | |
195 | 2ZITU | Cupin domain | 0.012266 |
196 | COG1618 | nucleotide phosphatase activity, acting on free nucleotides | 0.012254 |
197 | COG5107 | Psort location Cytoplasmic, score 8.96 | -0.012254 |
198 | COG3809 | Transcription factor zinc-finger | -0.012252 |
199 | 33N16 | -0.012241 | |
200 | COG3093 | addiction module antidote protein HigA | 0.012238 |
201 | COG1273 | With LigD forms a non-homologous end joining (NHEJ) DNA repair enzyme, which repairs dsDNA breaks with reduced fidelity. Binds linear dsDNA with 5'- and 3'- overhangs but not closed circular dsDNA nor ssDNA. Recruits and stimulates the ligase activity of LigD | 0.012236 |
202 | COG5153 | cell wall organization | 0.012234 |
203 | COG2963 | transposase activity | -0.012231 |
204 | COG5470 | NIPSNAP family containing protein | 0.012180 |
205 | 2ZBES | 0.012174 | |
206 | 30ICB | -0.012172 | |
207 | COG1760 | l-serine dehydratase | -0.012172 |
208 | COG2221 | Nitrite and sulphite reductase 4Fe-4S | 0.012162 |
209 | COG4764 | Protein conserved in bacteria | -0.012161 |
210 | COG1560 | Kdo2-lipid A biosynthetic process | -0.012135 |
211 | COG1742 | UPF0060 membrane protein | 0.012111 |
212 | 32YVX | Protein of unknown function (DUF2905) | 0.012103 |
213 | COG3000 | fatty acid hydroxylase | -0.012102 |
214 | COG4174 | ABC transporter (Permease) | -0.012081 |
215 | COG1641 | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | 0.012060 |
216 | COG0550 | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | -0.012048 |
217 | COG0158 | D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1 | 0.012021 |
218 | COG3402 | PFAM membrane-flanked domain | -0.011949 |
219 | COG5483 | Protein of unknown function, DUF488 | 0.011943 |
220 | COG0705 | Rhomboid family | 0.011942 |
221 | COG3914 | O-linked N-acetylglucosamine transferase SPINDLY family | 0.011911 |
222 | COG4630 | Xanthine dehydrogenase iron-sulfur cluster and FAD-binding subunit A | 0.011904 |
223 | COG1270 | Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group | 0.011888 |
224 | COG2175 | clavaminate synthase activity | -0.011885 |
225 | COG0852 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | 0.011857 |
226 | COG1476 | TRANSCRIPTIONal | -0.011841 |
227 | COG4196 | transglutaminase domain protein | 0.011832 |
228 | COG0780 | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | 0.011813 |
229 | COG1239 | Involved in chlorophyll biosynthesis. Catalyzes the insertion of magnesium ion into protoporphyrin IX to yield Mg- protoporphyrin IX | 0.011797 |
230 | COG0661 | Is probably a protein kinase regulator of UbiI activity which is involved in aerobic coenzyme Q (ubiquinone) biosynthesis | 0.011790 |
231 | COG3975 | serine-type endopeptidase activity | 0.011740 |
232 | COG2185 | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | -0.011726 |
233 | COG2233 | PERMEase | -0.011708 |
234 | 2ZC4V | -0.011705 | |
235 | COG3222 | Protein conserved in bacteria | -0.011695 |
236 | COG2894 | cell division | 0.011685 |
237 | COG3913 | Uncharacterized protein conserved in bacteria (DUF2094) | 0.011673 |
238 | COG1320 | monovalent cation:proton antiporter activity | 0.011621 |
239 | COG1863 | multisubunit Na H antiporter MnhE subunit | 0.011621 |
240 | COG2089 | acid synthase | 0.011535 |
241 | 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 | 0.011527 |
242 | COG0759 | Could be involved in insertion of integral membrane proteins into the membrane | 0.011524 |
243 | COG3646 | Phage regulatory protein | -0.011517 |
244 | COG0176 | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | 0.011514 |
245 | 30BPJ | -0.011474 | |
246 | COG1032 | radical SAM domain protein | 0.011474 |
247 | COG1865 | Adenosylcobinamide amidohydrolase | 0.011470 |
248 | 344FT | Cupin domain | 0.011453 |
249 | COG1284 | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | -0.011439 |
250 | COG1622 | oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor | -0.011421 |