| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| KKLOAAPI_00001 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
| KKLOAAPI_00002 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
| KKLOAAPI_00003 | 2.7e-154 | ymdB | S | YmdB-like protein | ||
| KKLOAAPI_00004 | 2.1e-216 | rny | S | Endoribonuclease that initiates mRNA decay | ||
| KKLOAAPI_00005 | 5e-191 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
| KKLOAAPI_00006 | 9.4e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
| KKLOAAPI_00007 | 3.7e-97 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
| KKLOAAPI_00008 | 5.7e-110 | ymfM | S | Helix-turn-helix domain | ||
| KKLOAAPI_00009 | 2.9e-251 | ymfH | S | Peptidase M16 | ||
| KKLOAAPI_00010 | 9.4e-231 | ymfF | S | Peptidase M16 inactive domain protein | ||
| KKLOAAPI_00011 | 3.8e-254 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
| KKLOAAPI_00012 | 1.5e-155 | aatB | ET | ABC transporter substrate-binding protein | ||
| KKLOAAPI_00013 | 2.5e-115 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
| KKLOAAPI_00014 | 4.6e-109 | glnP | P | ABC transporter permease | ||
| KKLOAAPI_00015 | 1.7e-145 | minD | D | Belongs to the ParA family | ||
| KKLOAAPI_00016 | 1.1e-116 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
| KKLOAAPI_00017 | 1.6e-88 | mreD | M | rod shape-determining protein MreD | ||
| KKLOAAPI_00018 | 2.6e-144 | mreC | M | Involved in formation and maintenance of cell shape | ||
| KKLOAAPI_00019 | 2.8e-161 | mreB | D | cell shape determining protein MreB | ||
| KKLOAAPI_00020 | 6.6e-116 | radC | L | DNA repair protein | ||
| KKLOAAPI_00021 | 1.4e-248 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
| KKLOAAPI_00022 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
| KKLOAAPI_00023 | 3e-89 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
| KKLOAAPI_00024 | 4e-234 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
| KKLOAAPI_00025 | 1.8e-226 | thiI | 2.8.1.4 | H | 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 | |
| KKLOAAPI_00026 | 2.9e-218 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
| KKLOAAPI_00028 | 0.0 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
| KKLOAAPI_00029 | 5e-81 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
| KKLOAAPI_00030 | 3.1e-107 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
| KKLOAAPI_00031 | 5.2e-113 | yktB | S | Belongs to the UPF0637 family | ||
| KKLOAAPI_00032 | 2.3e-81 | yueI | S | Protein of unknown function (DUF1694) | ||
| KKLOAAPI_00033 | 3.1e-110 | S | Protein of unknown function (DUF1648) | |||
| KKLOAAPI_00034 | 3.3e-43 | czrA | K | Helix-turn-helix domain | ||
| KKLOAAPI_00035 | 3.3e-231 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
| KKLOAAPI_00036 | 9.2e-42 | 2.7.1.191 | G | PTS system fructose IIA component | ||
| KKLOAAPI_00037 | 2.7e-104 | G | PTS system mannose fructose sorbose family IID component | |||
| KKLOAAPI_00038 | 3.6e-103 | G | PTS system sorbose-specific iic component | |||
| KKLOAAPI_00039 | 6e-66 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
| KKLOAAPI_00040 | 5.9e-95 | cytR | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | |
| KKLOAAPI_00041 | 0.0 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
| KKLOAAPI_00042 | 8e-238 | rarA | L | recombination factor protein RarA | ||
| KKLOAAPI_00043 | 1.5e-38 | |||||
| KKLOAAPI_00044 | 6.2e-82 | usp6 | T | universal stress protein | ||
| KKLOAAPI_00045 | 4.1e-201 | bla2 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
| KKLOAAPI_00046 | 3.3e-161 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
| KKLOAAPI_00047 | 1.5e-294 | glpQ3 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
| KKLOAAPI_00048 | 5.4e-214 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
| KKLOAAPI_00049 | 3.6e-188 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
| KKLOAAPI_00050 | 6e-177 | S | Protein of unknown function (DUF2785) | |||
| KKLOAAPI_00051 | 1.4e-167 | hicD1 | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
| KKLOAAPI_00052 | 2.2e-148 | metQ | M | Belongs to the nlpA lipoprotein family | ||
| KKLOAAPI_00053 | 1.4e-111 | metI | U | ABC transporter permease | ||
| KKLOAAPI_00054 | 4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
| KKLOAAPI_00055 | 3.6e-48 | gcsH2 | E | glycine cleavage | ||
| KKLOAAPI_00056 | 9.3e-220 | rodA | D | Belongs to the SEDS family | ||
| KKLOAAPI_00057 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
| KKLOAAPI_00058 | 2.3e-43 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
| KKLOAAPI_00059 | 3.5e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
| KKLOAAPI_00060 | 2.1e-102 | J | Acetyltransferase (GNAT) domain | |||
| KKLOAAPI_00061 | 4.4e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
| KKLOAAPI_00062 | 1.1e-50 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
| KKLOAAPI_00063 | 2.1e-263 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
| KKLOAAPI_00064 | 2.3e-165 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
| KKLOAAPI_00065 | 2.7e-280 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
| KKLOAAPI_00066 | 1.8e-90 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
| KKLOAAPI_00067 | 6e-51 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
| KKLOAAPI_00068 | 2.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
| KKLOAAPI_00069 | 6.5e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
| KKLOAAPI_00070 | 1e-232 | pyrP | F | Permease | ||
| KKLOAAPI_00071 | 4.7e-114 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
| KKLOAAPI_00072 | 2.9e-232 | glyA | 2.1.2.1 | E | 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 | |
| KKLOAAPI_00073 | 7.7e-191 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
| KKLOAAPI_00074 | 8.6e-159 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
| KKLOAAPI_00075 | 1.2e-197 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
| KKLOAAPI_00076 | 9.3e-109 | tdk | 2.7.1.21 | F | thymidine kinase | |
| KKLOAAPI_00077 | 1.5e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
| KKLOAAPI_00078 | 5.9e-137 | cobQ | S | glutamine amidotransferase | ||
| KKLOAAPI_00079 | 9.8e-196 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
| KKLOAAPI_00080 | 4.1e-192 | ampC | V | Beta-lactamase | ||
| KKLOAAPI_00081 | 1.4e-29 | |||||
| KKLOAAPI_00082 | 1e-203 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
| KKLOAAPI_00083 | 1.9e-58 | |||||
| KKLOAAPI_00084 | 2.4e-125 | |||||
| KKLOAAPI_00085 | 0.0 | yfiC | V | ABC transporter | ||
| KKLOAAPI_00086 | 0.0 | ycfI | V | ABC transporter, ATP-binding protein | ||
| KKLOAAPI_00087 | 3.3e-65 | S | Protein of unknown function (DUF1093) | |||
| KKLOAAPI_00088 | 3.8e-135 | yxkH | G | Polysaccharide deacetylase | ||
| KKLOAAPI_00089 | 6.3e-48 | K | IrrE N-terminal-like domain | |||
| KKLOAAPI_00091 | 1.3e-29 | hol | S | Bacteriophage holin | ||
| KKLOAAPI_00092 | 5.2e-47 | |||||
| KKLOAAPI_00093 | 8.2e-189 | lys | M | Glycosyl hydrolases family 25 | ||
| KKLOAAPI_00095 | 4.2e-19 | |||||
| KKLOAAPI_00096 | 4.6e-61 | |||||
| KKLOAAPI_00099 | 0.0 | S | Calcineurin-like phosphoesterase | |||
| KKLOAAPI_00100 | 2.9e-10 | |||||
| KKLOAAPI_00102 | 2.6e-67 | S | Prophage endopeptidase tail | |||
| KKLOAAPI_00103 | 3.7e-63 | S | Phage tail protein | |||
| KKLOAAPI_00104 | 0.0 | S | peptidoglycan catabolic process | |||
| KKLOAAPI_00105 | 3.2e-99 | S | Bacteriophage Gp15 protein | |||
| KKLOAAPI_00107 | 8.4e-77 |
Showing 1 to 100 of 2,935 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)