| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| KCMLOAMG_00001 | 6e-74 | yxeA | V | FtsX-like permease family | ||
| KCMLOAMG_00002 | 1.4e-127 | devA | 3.6.3.25 | V | ATPases associated with a variety of cellular activities | |
| KCMLOAMG_00003 | 6.4e-34 | |||||
| KCMLOAMG_00004 | 4.8e-137 | tipA | K | TipAS antibiotic-recognition domain | ||
| KCMLOAMG_00006 | 1.4e-138 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
| KCMLOAMG_00007 | 3.6e-143 | ecfT | U | Transmembrane (T) component of an 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 | ||
| KCMLOAMG_00008 | 3.2e-158 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common 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 | |
| KCMLOAMG_00009 | 1.8e-153 | ecfA1 | P | ATP-binding (A) component of a common 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 | ||
| KCMLOAMG_00010 | 2.1e-120 | |||||
| KCMLOAMG_00011 | 3.1e-60 | rplQ | J | Ribosomal protein L17 | ||
| KCMLOAMG_00012 | 3.6e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
| KCMLOAMG_00013 | 4e-63 | rpsK | J | 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 | ||
| KCMLOAMG_00014 | 2.1e-58 | rpsM | J | 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 | ||
| KCMLOAMG_00015 | 6.6e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
| KCMLOAMG_00016 | 1.4e-33 | infA | J | 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 | ||
| KCMLOAMG_00017 | 1.4e-121 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
| KCMLOAMG_00018 | 9.8e-231 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
| KCMLOAMG_00019 | 2.2e-62 | rplO | J | Binds to the 23S rRNA | ||
| KCMLOAMG_00020 | 1.7e-24 | rpmD | J | Ribosomal protein L30 | ||
| KCMLOAMG_00021 | 1.2e-83 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
| KCMLOAMG_00022 | 4.6e-58 | rplR | J | This is one 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 | ||
| KCMLOAMG_00023 | 2.3e-93 | rplF | J | 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 | ||
| KCMLOAMG_00024 | 1e-66 | rpsH | J | 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 | ||
| KCMLOAMG_00025 | 1.1e-95 | rplE | J | 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 | ||
| KCMLOAMG_00026 | 2.4e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
| KCMLOAMG_00027 | 2.1e-58 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
| KCMLOAMG_00028 | 1.4e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
| KCMLOAMG_00029 | 1.1e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
| KCMLOAMG_00030 | 2.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
| KCMLOAMG_00031 | 3.7e-109 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
| KCMLOAMG_00032 | 1.1e-54 | rplV | J | 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 | ||
| KCMLOAMG_00033 | 2.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
| KCMLOAMG_00034 | 3.9e-156 | rplB | J | 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 | ||
| KCMLOAMG_00035 | 2e-46 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
| KCMLOAMG_00036 | 5.9e-109 | rplD | J | Forms part of the polypeptide exit tunnel | ||
| KCMLOAMG_00037 | 3e-113 | rplC | J | 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 | ||
| KCMLOAMG_00038 | 1.2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
| KCMLOAMG_00039 | 1.2e-68 | psiE | S | Phosphate-starvation-inducible E | ||
| KCMLOAMG_00040 | 3.8e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
| KCMLOAMG_00041 | 2.5e-197 | yfjR | K | WYL domain | ||
| KCMLOAMG_00042 | 0.0 | fusA | J | 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 | ||
| KCMLOAMG_00043 | 8.4e-84 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
| KCMLOAMG_00044 | 3.6e-70 | rpsL | J | 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 | ||
| KCMLOAMG_00045 | 0.0 | M | domain protein | |||
| KCMLOAMG_00046 | 3.1e-38 | 3.4.23.43 | ||||
| KCMLOAMG_00047 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_00048 | 3.2e-30 | 3.4.23.43 | ||||
| KCMLOAMG_00049 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
| KCMLOAMG_00050 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
| KCMLOAMG_00051 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
| KCMLOAMG_00052 | 1.8e-78 | ctsR | K | Belongs to the CtsR family | ||
| KCMLOAMG_00061 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
| KCMLOAMG_00062 | 2.4e-71 | S | COG NOG38524 non supervised orthologous group | |||
| KCMLOAMG_00065 | 6.1e-35 | |||||
| KCMLOAMG_00066 | 3e-292 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
| KCMLOAMG_00067 | 2.9e-190 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
| KCMLOAMG_00068 | 8.5e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
| KCMLOAMG_00069 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
| KCMLOAMG_00070 | 5.9e-97 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
| KCMLOAMG_00071 | 9.1e-245 | tilS | 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
| KCMLOAMG_00072 | 6.1e-82 | yabR | J | RNA binding | ||
| KCMLOAMG_00073 | 4.4e-65 | divIC | D | cell cycle | ||
| KCMLOAMG_00074 | 1.8e-38 | yabO | J | S4 domain protein | ||
| KCMLOAMG_00075 | 4.2e-281 | yabM | S | Polysaccharide biosynthesis protein | ||
| KCMLOAMG_00076 | 0.0 | mfd | L | 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 | ||
| KCMLOAMG_00077 | 2.4e-101 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
| KCMLOAMG_00078 | 4.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
| KCMLOAMG_00079 | 5.9e-263 | S | Putative peptidoglycan binding domain | |||
| KCMLOAMG_00080 | 1.3e-96 | padR | K | Transcriptional regulator PadR-like family | ||
| KCMLOAMG_00081 | 2.4e-246 | XK27_06930 | S | ABC-2 family transporter protein | ||
| KCMLOAMG_00082 | 9.9e-114 | 1.6.5.2 | S | Flavodoxin-like fold | ||
| KCMLOAMG_00083 | 5.1e-119 | S | (CBS) domain | |||
| KCMLOAMG_00084 | 6.8e-130 | yciB | M | ErfK YbiS YcfS YnhG | ||
| KCMLOAMG_00085 | 1.2e-279 | gltD | 1.4.1.13, 1.4.1.14 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
| KCMLOAMG_00086 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
| KCMLOAMG_00087 | 1.7e-85 | S | QueT transporter | |||
| KCMLOAMG_00088 | 5.6e-62 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
| KCMLOAMG_00089 | 2.4e-37 | |||||
| KCMLOAMG_00090 | 3.5e-216 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
| KCMLOAMG_00091 | 1.7e-63 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
| KCMLOAMG_00092 | 4.5e-264 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
| KCMLOAMG_00093 | 1.3e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
| KCMLOAMG_00094 | 2.3e-147 | |||||
| KCMLOAMG_00095 | 1.5e-123 | S | Tetratricopeptide repeat | |||
| KCMLOAMG_00096 | 1.7e-122 | |||||
| KCMLOAMG_00097 | 3e-72 | |||||
| KCMLOAMG_00098 | 3.3e-42 | rpmE2 | J | Ribosomal protein L31 | ||
| KCMLOAMG_00099 | 7.4e-236 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
| KCMLOAMG_00100 | 6.4e-08 | |||||
| KCMLOAMG_00102 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
| KCMLOAMG_00103 | 7e-220 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
| KCMLOAMG_00106 | 3e-151 | S | Protein of unknown function (DUF1211) | |||
| KCMLOAMG_00107 | 5.9e-62 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
| KCMLOAMG_00108 | 3.5e-79 | ywiB | S | Domain of unknown function (DUF1934) | ||
| KCMLOAMG_00109 | 8.7e-156 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
| KCMLOAMG_00110 | 9.6e-266 | ywfO | S | HD domain protein | ||
| KCMLOAMG_00111 | 2.4e-83 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
| KCMLOAMG_00112 | 4.2e-176 | S | DUF218 domain | |||
| KCMLOAMG_00113 | 1.8e-60 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
| KCMLOAMG_00114 | 4.3e-74 | |||||
| KCMLOAMG_00115 | 1e-51 | nudA | S | ASCH | ||
| KCMLOAMG_00116 | 1e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
| KCMLOAMG_00117 | 1.5e-213 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
| KCMLOAMG_00118 | 3.5e-219 | ysaA | V | RDD family | ||
| KCMLOAMG_00119 | 1.3e-151 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
| KCMLOAMG_00120 | 6.5e-119 | ybbL | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_00121 | 1.8e-123 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
| KCMLOAMG_00122 | 6.7e-159 | czcD | P | cation diffusion facilitator family transporter | ||
| KCMLOAMG_00123 | 9e-164 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
| KCMLOAMG_00124 | 1.1e-37 | veg | S | Biofilm formation stimulator VEG | ||
| KCMLOAMG_00125 | 5.5e-153 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
| KCMLOAMG_00126 | 5e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
| KCMLOAMG_00127 | 1.3e-145 | tatD | L | hydrolase, TatD family | ||
| KCMLOAMG_00128 | 5e-79 | manR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |
| KCMLOAMG_00129 | 9.5e-186 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
| KCMLOAMG_00130 | 4.5e-171 | yqhA | G | Aldose 1-epimerase | ||
| KCMLOAMG_00131 | 1.3e-125 | T | LytTr DNA-binding domain | |||
| KCMLOAMG_00132 | 1.1e-167 | 2.7.13.3 | T | GHKL domain | ||
| KCMLOAMG_00133 | 9.2e-304 | V | ABC transporter | |||
| KCMLOAMG_00134 | 0.0 | V | ABC transporter | |||
| KCMLOAMG_00135 | 1.3e-28 | K | Transcriptional | |||
| KCMLOAMG_00136 | 5.7e-66 | |||||
| KCMLOAMG_00137 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
| KCMLOAMG_00138 | 4.1e-173 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
| KCMLOAMG_00139 | 4.8e-11 | gluP | 3.4.21.105 | S | proteolysis | |
| KCMLOAMG_00140 | 8.6e-153 | yunF | F | Protein of unknown function DUF72 | ||
| KCMLOAMG_00141 | 3.8e-92 | 3.6.1.55 | F | NUDIX domain | ||
| KCMLOAMG_00142 | 1.5e-169 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
| KCMLOAMG_00143 | 5.3e-107 | yiiE | S | Protein of unknown function (DUF1211) | ||
| KCMLOAMG_00144 | 5.7e-129 | cobB | K | Sir2 family | ||
| KCMLOAMG_00145 | 2.8e-17 | |||||
| KCMLOAMG_00146 | 2.8e-168 | |||||
| KCMLOAMG_00147 | 2.5e-97 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
| KCMLOAMG_00149 | 1.6e-161 | ypuA | S | Protein of unknown function (DUF1002) | ||
| KCMLOAMG_00150 | 2.5e-172 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
| KCMLOAMG_00151 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
| KCMLOAMG_00152 | 9.5e-286 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
| KCMLOAMG_00153 | 1e-173 | S | Aldo keto reductase | |||
| KCMLOAMG_00154 | 9.3e-155 | bioC | 2.1.1.187, 2.1.1.197 | Q | Protein-L-isoaspartate(D-aspartate) O-methyltransferase (PCMT) | |
| KCMLOAMG_00155 | 1.7e-90 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
| KCMLOAMG_00156 | 1e-238 | dinF | V | MatE | ||
| KCMLOAMG_00158 | 3.3e-110 | S | TPM domain | |||
| KCMLOAMG_00159 | 3.1e-102 | lemA | S | LemA family | ||
| KCMLOAMG_00160 | 6.3e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
| KCMLOAMG_00161 | 5.4e-74 | EGP | Major Facilitator Superfamily | |||
| KCMLOAMG_00162 | 2e-252 | gshR | 1.8.1.7 | C | Glutathione reductase | |
| KCMLOAMG_00163 | 6.6e-176 | proV | E | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_00164 | 4.9e-274 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
| KCMLOAMG_00166 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
| KCMLOAMG_00167 | 2.7e-146 | rlrG | K | Transcriptional regulator | ||
| KCMLOAMG_00168 | 4.8e-174 | shetA | P | Voltage-dependent anion channel | ||
| KCMLOAMG_00169 | 2.5e-133 | nodJ | V | ABC-2 type transporter | ||
| KCMLOAMG_00170 | 4.9e-134 | nodI | V | ABC transporter | ||
| KCMLOAMG_00171 | 1.4e-130 | ydfF | K | Transcriptional | ||
| KCMLOAMG_00172 | 3.6e-109 | S | CAAX protease self-immunity | |||
| KCMLOAMG_00174 | 1.5e-276 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_00175 | 3.6e-109 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
| KCMLOAMG_00176 | 7.2e-71 | K | MarR family | |||
| KCMLOAMG_00177 | 0.0 | uvrA3 | L | excinuclease ABC | ||
| KCMLOAMG_00178 | 1.9e-189 | yghZ | C | Aldo keto reductase family protein | ||
| KCMLOAMG_00179 | 1.8e-142 | S | hydrolase | |||
| KCMLOAMG_00180 | 1.2e-58 | |||||
| KCMLOAMG_00181 | 4.8e-12 | |||||
| KCMLOAMG_00182 | 1.3e-42 | |||||
| KCMLOAMG_00183 | 5.1e-28 | |||||
| KCMLOAMG_00185 | 3e-62 | V | ABC transporter | |||
| KCMLOAMG_00187 | 2.6e-118 | yoaK | S | Protein of unknown function (DUF1275) | ||
| KCMLOAMG_00188 | 3.1e-127 | yjhF | G | Phosphoglycerate mutase family | ||
| KCMLOAMG_00189 | 5.8e-149 | yitU | 3.1.3.104 | S | hydrolase | |
| KCMLOAMG_00190 | 3.6e-90 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
| KCMLOAMG_00191 | 1.7e-165 | K | LysR substrate binding domain | |||
| KCMLOAMG_00192 | 3.9e-226 | EK | Aminotransferase, class I | |||
| KCMLOAMG_00194 | 2.9e-45 | |||||
| KCMLOAMG_00195 | 9.4e-58 | |||||
| KCMLOAMG_00196 | 5.6e-193 | 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 | ||
| KCMLOAMG_00197 | 7.3e-116 | ydfK | S | Protein of unknown function (DUF554) | ||
| KCMLOAMG_00198 | 5.1e-89 | |||||
| KCMLOAMG_00200 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
| KCMLOAMG_00201 | 3.7e-168 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
| KCMLOAMG_00202 | 1.1e-130 | rpl | K | Helix-turn-helix domain, rpiR family | ||
| KCMLOAMG_00203 | 1.8e-297 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
| KCMLOAMG_00204 | 2.3e-136 | K | UTRA domain | |||
| KCMLOAMG_00205 | 1.4e-253 | fucA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
| KCMLOAMG_00206 | 3.3e-161 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
| KCMLOAMG_00207 | 8.6e-129 | G | PTS system sorbose-specific iic component | |||
| KCMLOAMG_00208 | 5.9e-149 | G | PTS system mannose/fructose/sorbose family IID component | |||
| KCMLOAMG_00209 | 3.4e-63 | K | Transcriptional regulator | |||
| KCMLOAMG_00210 | 6e-247 | ypiB | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00211 | 6.1e-87 | |||||
| KCMLOAMG_00212 | 5e-223 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
| KCMLOAMG_00213 | 5.1e-246 | G | PTS system sugar-specific permease component | |||
| KCMLOAMG_00214 | 3.6e-45 | sgcB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
| KCMLOAMG_00215 | 5.2e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
| KCMLOAMG_00216 | 1.2e-109 | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | ||
| KCMLOAMG_00217 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
| KCMLOAMG_00218 | 2.3e-48 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
| KCMLOAMG_00219 | 2.3e-48 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00220 | 5.3e-294 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
| KCMLOAMG_00221 | 6.1e-160 | ypbG | 2.7.1.2 | GK | ROK family | |
| KCMLOAMG_00222 | 1.2e-249 | S | Metal-independent alpha-mannosidase (GH125) | |||
| KCMLOAMG_00223 | 0.0 | mngB | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
| KCMLOAMG_00224 | 1.4e-232 | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
| KCMLOAMG_00225 | 5e-136 | K | UbiC transcription regulator-associated domain protein | |||
| KCMLOAMG_00226 | 1.1e-133 | fcsR | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_00227 | 1.7e-145 | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | ||
| KCMLOAMG_00228 | 1.6e-76 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
| KCMLOAMG_00229 | 1.5e-231 | ywtG | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00230 | 1.9e-294 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 2.7.1.51 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
| KCMLOAMG_00231 | 0.0 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
| KCMLOAMG_00232 | 2e-166 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
| KCMLOAMG_00233 | 7e-258 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
| KCMLOAMG_00234 | 3.8e-56 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
| KCMLOAMG_00235 | 4.5e-285 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
| KCMLOAMG_00236 | 5.7e-88 | iolF | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00237 | 1.4e-122 | iolF | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00238 | 1.4e-192 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
| KCMLOAMG_00239 | 6.4e-215 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
| KCMLOAMG_00240 | 4.6e-64 | S | Protein of unknown function (DUF1093) | |||
| KCMLOAMG_00241 | 9.5e-95 | |||||
| KCMLOAMG_00242 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
| KCMLOAMG_00243 | 1.9e-306 | plyA3 | M | Right handed beta helix region | ||
| KCMLOAMG_00244 | 5e-81 | |||||
| KCMLOAMG_00245 | 1.6e-269 | M | Heparinase II/III N-terminus | |||
| KCMLOAMG_00247 | 6e-66 | G | PTS system fructose IIA component | |||
| KCMLOAMG_00248 | 3.6e-143 | agaD | G | PTS system mannose/fructose/sorbose family IID component | ||
| KCMLOAMG_00249 | 6.4e-132 | G | PTS system sorbose-specific iic component | |||
| KCMLOAMG_00250 | 5.4e-81 | agaV | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
| KCMLOAMG_00251 | 7e-204 | ugl | 3.2.1.180 | GH88 | S | Glycosyl Hydrolase Family 88 |
| KCMLOAMG_00252 | 5.4e-102 | Z012_03480 | S | Psort location Cytoplasmic, score | ||
| KCMLOAMG_00253 | 1.6e-108 | K | Bacterial transcriptional regulator | |||
| KCMLOAMG_00254 | 4.5e-144 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
| KCMLOAMG_00255 | 1e-137 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
| KCMLOAMG_00256 | 3e-87 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
| KCMLOAMG_00257 | 3.5e-151 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
| KCMLOAMG_00258 | 5.1e-122 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
| KCMLOAMG_00259 | 0.0 | CP_0954 | 4.2.2.1 | PL8 | N | Polysaccharide lyase family 8, N terminal alpha-helical domain |
| KCMLOAMG_00260 | 2.1e-206 | rafA | 3.2.1.22 | G | Melibiase | |
| KCMLOAMG_00261 | 7.8e-40 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
| KCMLOAMG_00262 | 3.1e-65 | G | PTS system mannose/fructose/sorbose family IID component | |||
| KCMLOAMG_00263 | 4.4e-64 | G | PTS system sorbose-specific iic component | |||
| KCMLOAMG_00264 | 2.1e-22 | 2.7.1.191 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
| KCMLOAMG_00266 | 4.6e-53 | araR | K | Transcriptional regulator | ||
| KCMLOAMG_00267 | 1.6e-271 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain | |
| KCMLOAMG_00268 | 6.9e-295 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
| KCMLOAMG_00269 | 1.5e-209 | V | ABC-type multidrug transport system, ATPase and permease components | |||
| KCMLOAMG_00270 | 1.1e-108 | K | Transcriptional activator, Rgg GadR MutR family | |||
| KCMLOAMG_00271 | 3.3e-86 | K | Helix-turn-helix domain, rpiR family | |||
| KCMLOAMG_00272 | 1.5e-10 | K | Helix-turn-helix domain, rpiR family | |||
| KCMLOAMG_00273 | 2.1e-82 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
| KCMLOAMG_00275 | 1.7e-133 | L | Transposase, IS116 IS110 IS902 family | |||
| KCMLOAMG_00276 | 1.8e-136 | 4.1.2.14 | S | KDGP aldolase | ||
| KCMLOAMG_00277 | 4.2e-203 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
| KCMLOAMG_00278 | 4.4e-216 | dho | 3.5.2.3 | S | Amidohydrolase family | |
| KCMLOAMG_00279 | 1e-106 | S | Domain of unknown function (DUF4310) | |||
| KCMLOAMG_00280 | 8.3e-137 | S | Domain of unknown function (DUF4311) | |||
| KCMLOAMG_00281 | 6e-53 | S | Domain of unknown function (DUF4312) | |||
| KCMLOAMG_00282 | 3.4e-61 | S | Glycine-rich SFCGS | |||
| KCMLOAMG_00283 | 2.4e-54 | S | PRD domain | |||
| KCMLOAMG_00284 | 0.0 | K | Mga helix-turn-helix domain | |||
| KCMLOAMG_00285 | 1.3e-122 | tal | 2.2.1.2 | H | Pfam:Transaldolase | |
| KCMLOAMG_00286 | 6.7e-63 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
| KCMLOAMG_00287 | 3.6e-194 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
| KCMLOAMG_00288 | 2.2e-102 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
| KCMLOAMG_00289 | 1.8e-87 | gutM | K | Glucitol operon activator protein (GutM) | ||
| KCMLOAMG_00290 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
| KCMLOAMG_00291 | 2.2e-145 | IQ | NAD dependent epimerase/dehydratase family | |||
| KCMLOAMG_00292 | 1.6e-137 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
| KCMLOAMG_00293 | 4.1e-150 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
| KCMLOAMG_00294 | 3.6e-168 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
| KCMLOAMG_00295 | 2.2e-137 | repA | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_00296 | 7.4e-115 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
| KCMLOAMG_00297 | 3.7e-45 | sgaB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
| KCMLOAMG_00298 | 5.3e-281 | ulaA | S | PTS system sugar-specific permease component | ||
| KCMLOAMG_00299 | 1.1e-80 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
| KCMLOAMG_00300 | 3.4e-213 | ulaG | S | Beta-lactamase superfamily domain | ||
| KCMLOAMG_00301 | 0.0 | O | Belongs to the peptidase S8 family | |||
| KCMLOAMG_00302 | 2.2e-41 | |||||
| KCMLOAMG_00303 | 6.6e-154 | bglK_1 | GK | ROK family | ||
| KCMLOAMG_00304 | 1.7e-179 | aspG | 3.4.19.5, 3.5.1.1, 3.5.1.26 | E | Asparaginase | |
| KCMLOAMG_00305 | 9.1e-253 | 3.5.1.18 | E | Peptidase family M20/M25/M40 | ||
| KCMLOAMG_00306 | 3.5e-129 | ymfC | K | UTRA | ||
| KCMLOAMG_00307 | 5.3e-215 | uhpT | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00308 | 1.7e-206 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
| KCMLOAMG_00309 | 1.9e-95 | S | Domain of unknown function (DUF4428) | |||
| KCMLOAMG_00310 | 4e-278 | xylB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
| KCMLOAMG_00311 | 1.2e-204 | C | Zinc-binding dehydrogenase | |||
| KCMLOAMG_00312 | 1.3e-151 | manZ | G | PTS system mannose/fructose/sorbose family IID component | ||
| KCMLOAMG_00313 | 3.7e-137 | G | PTS system sorbose-specific iic component | |||
| KCMLOAMG_00314 | 8.5e-84 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
| KCMLOAMG_00315 | 2.3e-69 | ahaA | 2.7.1.191 | G | PTS system fructose IIA component | |
| KCMLOAMG_00316 | 2.6e-245 | licR | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | K | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
| KCMLOAMG_00317 | 3.7e-162 | G | Fructose-bisphosphate aldolase class-II | |||
| KCMLOAMG_00318 | 5.7e-280 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
| KCMLOAMG_00319 | 4.7e-252 | gatC | G | PTS system sugar-specific permease component | ||
| KCMLOAMG_00320 | 1.6e-48 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00321 | 4.2e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
| KCMLOAMG_00322 | 6.9e-161 | gatY | G | Fructose-bisphosphate aldolase class-II | ||
| KCMLOAMG_00323 | 2.4e-133 | farR | K | Helix-turn-helix domain | ||
| KCMLOAMG_00324 | 2e-91 | yjgM | K | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_00325 | 3.4e-112 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
| KCMLOAMG_00327 | 5.2e-96 | K | Helix-turn-helix domain | |||
| KCMLOAMG_00328 | 0.0 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
| KCMLOAMG_00329 | 9.6e-132 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
| KCMLOAMG_00330 | 4.5e-108 | pncA | Q | Isochorismatase family | ||
| KCMLOAMG_00331 | 9.5e-264 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
| KCMLOAMG_00332 | 3.6e-131 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
| KCMLOAMG_00333 | 3.3e-68 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
| KCMLOAMG_00334 | 3.2e-240 | ugpB | G | Bacterial extracellular solute-binding protein | ||
| KCMLOAMG_00335 | 6.4e-148 | ugpE | G | ABC transporter permease | ||
| KCMLOAMG_00336 | 2.8e-163 | ugpA | P | ABC-type sugar transport systems, permease components | ||
| KCMLOAMG_00337 | 2.8e-210 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
| KCMLOAMG_00338 | 5.4e-226 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_00339 | 1.4e-147 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
| KCMLOAMG_00340 | 1.7e-190 | blaA6 | V | Beta-lactamase | ||
| KCMLOAMG_00341 | 1.7e-146 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
| KCMLOAMG_00342 | 3.4e-161 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
| KCMLOAMG_00343 | 5.8e-80 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
| KCMLOAMG_00344 | 1.6e-149 | G | PTS system mannose/fructose/sorbose family IID component | |||
| KCMLOAMG_00345 | 1.8e-129 | G | PTS system sorbose-specific iic component | |||
| KCMLOAMG_00347 | 2.8e-199 | S | endonuclease exonuclease phosphatase family protein | |||
| KCMLOAMG_00348 | 2.1e-171 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
| KCMLOAMG_00349 | 4.2e-158 | 1.1.1.346 | S | reductase | ||
| KCMLOAMG_00350 | 4.2e-74 | adhR | K | helix_turn_helix, mercury resistance | ||
| KCMLOAMG_00351 | 9.7e-143 | Q | Methyltransferase | |||
| KCMLOAMG_00352 | 1.7e-51 | sugE | U | Multidrug resistance protein | ||
| KCMLOAMG_00354 | 8.6e-59 | |||||
| KCMLOAMG_00355 | 3.5e-36 | |||||
| KCMLOAMG_00356 | 4.2e-107 | S | alpha beta | |||
| KCMLOAMG_00357 | 2.7e-80 | MA20_25245 | K | FR47-like protein | ||
| KCMLOAMG_00358 | 1.5e-57 | hisB | 2.7.7.71, 3.1.3.15, 3.1.3.82, 3.1.3.83, 4.2.1.19, 5.3.1.28, 6.3.2.10 | GT9 | E | HAD-hyrolase-like |
| KCMLOAMG_00359 | 6.3e-134 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
| KCMLOAMG_00360 | 5.4e-86 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_00361 | 3.5e-123 | |||||
| KCMLOAMG_00362 | 3.6e-68 | 6.3.3.2 | S | ASCH | ||
| KCMLOAMG_00363 | 6.1e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
| KCMLOAMG_00364 | 4.1e-198 | ybiR | P | Citrate transporter | ||
| KCMLOAMG_00365 | 2.1e-101 | |||||
| KCMLOAMG_00366 | 1.9e-250 | E | Peptidase dimerisation domain | |||
| KCMLOAMG_00367 | 2.1e-296 | E | ABC transporter, substratebinding protein | |||
| KCMLOAMG_00369 | 3.1e-135 | |||||
| KCMLOAMG_00370 | 0.0 | cadA | P | P-type ATPase | ||
| KCMLOAMG_00371 | 1e-75 | hsp3 | O | Hsp20/alpha crystallin family | ||
| KCMLOAMG_00372 | 5.9e-70 | S | Iron-sulphur cluster biosynthesis | |||
| KCMLOAMG_00373 | 3.8e-206 | htrA | 3.4.21.107 | O | serine protease | |
| KCMLOAMG_00374 | 1e-14 | |||||
| KCMLOAMG_00375 | 2.7e-154 | vicX | 3.1.26.11 | S | domain protein | |
| KCMLOAMG_00376 | 1.1e-141 | yycI | S | YycH protein | ||
| KCMLOAMG_00377 | 5.3e-259 | yycH | S | YycH protein | ||
| KCMLOAMG_00378 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_00379 | 8.1e-131 | K | response regulator | |||
| KCMLOAMG_00380 | 1.1e-121 | S | Alpha/beta hydrolase family | |||
| KCMLOAMG_00381 | 9.3e-259 | arpJ | P | ABC transporter permease | ||
| KCMLOAMG_00382 | 5.1e-234 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
| KCMLOAMG_00383 | 1.4e-267 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
| KCMLOAMG_00384 | 2.6e-213 | S | Bacterial protein of unknown function (DUF871) | |||
| KCMLOAMG_00385 | 3.5e-73 | S | Domain of unknown function (DUF3284) | |||
| KCMLOAMG_00386 | 1.7e-238 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
| KCMLOAMG_00387 | 6.9e-130 | K | UbiC transcription regulator-associated domain protein | |||
| KCMLOAMG_00388 | 3e-51 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00389 | 4.9e-54 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
| KCMLOAMG_00390 | 1.7e-107 | speG | J | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_00391 | 1.9e-81 | F | NUDIX domain | |||
| KCMLOAMG_00392 | 2.3e-90 | S | AAA domain | |||
| KCMLOAMG_00393 | 2.5e-112 | ycaC | Q | Isochorismatase family | ||
| KCMLOAMG_00394 | 1.5e-253 | ydiC1 | EGP | Major Facilitator Superfamily | ||
| KCMLOAMG_00395 | 3.5e-211 | yeaN | P | Transporter, major facilitator family protein | ||
| KCMLOAMG_00396 | 4.3e-172 | iolS | C | Aldo keto reductase | ||
| KCMLOAMG_00397 | 4.4e-64 | manO | S | Domain of unknown function (DUF956) | ||
| KCMLOAMG_00398 | 8.7e-170 | manN | G | system, mannose fructose sorbose family IID component | ||
| KCMLOAMG_00399 | 1.6e-122 | manY | G | PTS system | ||
| KCMLOAMG_00400 | 3.7e-182 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
| KCMLOAMG_00401 | 9.8e-220 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_00402 | 2.3e-187 | K | Helix-turn-helix XRE-family like proteins | |||
| KCMLOAMG_00403 | 4.2e-150 | K | Helix-turn-helix XRE-family like proteins | |||
| KCMLOAMG_00404 | 1.3e-157 | K | sequence-specific DNA binding | |||
| KCMLOAMG_00408 | 1.6e-304 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
| KCMLOAMG_00409 | 4e-287 | glnP | P | ABC transporter permease | ||
| KCMLOAMG_00410 | 4.1e-133 | glnQ | E | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_00411 | 2e-40 | |||||
| KCMLOAMG_00412 | 1.5e-236 | malE | G | Bacterial extracellular solute-binding protein | ||
| KCMLOAMG_00413 | 1e-09 | |||||
| KCMLOAMG_00414 | 6.3e-123 | S | Protein of unknown function (DUF975) | |||
| KCMLOAMG_00415 | 1.5e-58 | yqkB | S | Iron-sulphur cluster biosynthesis | ||
| KCMLOAMG_00416 | 1.2e-52 | |||||
| KCMLOAMG_00417 | 1.9e-80 | S | Bacterial PH domain | |||
| KCMLOAMG_00418 | 9.4e-286 | ydbT | S | Bacterial PH domain | ||
| KCMLOAMG_00419 | 1.3e-142 | S | AAA ATPase domain | |||
| KCMLOAMG_00420 | 1e-164 | yniA | G | Phosphotransferase enzyme family | ||
| KCMLOAMG_00421 | 2.6e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
| KCMLOAMG_00422 | 2.7e-255 | glnP | P | ABC transporter | ||
| KCMLOAMG_00423 | 1.1e-264 | glnP | P | ABC transporter | ||
| KCMLOAMG_00424 | 3.4e-100 | ydaF | J | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_00425 | 6.3e-103 | S | Stage II sporulation protein M | |||
| KCMLOAMG_00426 | 3.2e-167 | yeaC | S | ATPase family associated with various cellular activities (AAA) | ||
| KCMLOAMG_00427 | 1e-131 | yeaD | S | Protein of unknown function DUF58 | ||
| KCMLOAMG_00428 | 0.0 | yebA | E | Transglutaminase/protease-like homologues | ||
| KCMLOAMG_00429 | 2.8e-12 | |||||
| KCMLOAMG_00430 | 7e-214 | lsgC | M | Glycosyl transferases group 1 | ||
| KCMLOAMG_00431 | 1.3e-254 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
| KCMLOAMG_00432 | 2.2e-110 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
| KCMLOAMG_00433 | 5.1e-56 | yjdF | S | Protein of unknown function (DUF2992) | ||
| KCMLOAMG_00436 | 1.3e-96 | |||||
| KCMLOAMG_00438 | 2.7e-149 | 1.1.1.31 | I | NAD binding domain of 6-phosphogluconate dehydrogenase | ||
| KCMLOAMG_00439 | 7.2e-68 | |||||
| KCMLOAMG_00440 | 1.6e-131 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
| KCMLOAMG_00441 | 2e-169 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
| KCMLOAMG_00442 | 1.6e-226 | ptsG | G | phosphotransferase system | ||
| KCMLOAMG_00443 | 4e-100 | K | CAT RNA binding domain | |||
| KCMLOAMG_00445 | 8.8e-170 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
| KCMLOAMG_00446 | 5.5e-180 | D | Alpha beta | |||
| KCMLOAMG_00447 | 5.9e-185 | lipA | I | Carboxylesterase family | ||
| KCMLOAMG_00448 | 1e-215 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
| KCMLOAMG_00449 | 1e-78 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
| KCMLOAMG_00450 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
| KCMLOAMG_00451 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
| KCMLOAMG_00452 | 9.6e-132 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
| KCMLOAMG_00453 | 8.6e-150 | S | haloacid dehalogenase-like hydrolase | |||
| KCMLOAMG_00454 | 2.8e-44 | |||||
| KCMLOAMG_00455 | 2e-14 | |||||
| KCMLOAMG_00456 | 1.3e-137 | |||||
| KCMLOAMG_00457 | 8.2e-221 | spiA | K | IrrE N-terminal-like domain | ||
| KCMLOAMG_00458 | 8.1e-151 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
| KCMLOAMG_00459 | 1e-125 | V | ABC transporter | |||
| KCMLOAMG_00460 | 8.1e-208 | bacI | V | MacB-like periplasmic core domain | ||
| KCMLOAMG_00461 | 2.8e-179 | |||||
| KCMLOAMG_00462 | 0.0 | M | Leucine rich repeats (6 copies) | |||
| KCMLOAMG_00463 | 3e-223 | mtnE | 2.6.1.83 | E | Aminotransferase | |
| KCMLOAMG_00464 | 1.1e-141 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
| KCMLOAMG_00465 | 1.1e-149 | M | NLPA lipoprotein | |||
| KCMLOAMG_00468 | 8.1e-199 | gldA | 1.1.1.1, 1.1.1.6 | C | dehydrogenase | |
| KCMLOAMG_00469 | 3.3e-225 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
| KCMLOAMG_00470 | 2.6e-80 | S | Threonine/Serine exporter, ThrE | |||
| KCMLOAMG_00471 | 3.2e-133 | thrE | S | Putative threonine/serine exporter | ||
| KCMLOAMG_00473 | 3.8e-31 | |||||
| KCMLOAMG_00474 | 1.4e-271 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_00476 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
| KCMLOAMG_00477 | 6.9e-251 | mnmE | S | 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 | ||
| KCMLOAMG_00478 | 1.9e-138 | jag | S | R3H domain protein | ||
| KCMLOAMG_00479 | 6.4e-138 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
| KCMLOAMG_00480 | 1.9e-59 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
| KCMLOAMG_00481 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
| KCMLOAMG_00482 | 3.5e-252 | dnaA | L | 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 | ||
| KCMLOAMG_00483 | 5.2e-204 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
| KCMLOAMG_00484 | 2.9e-31 | yaaA | S | S4 domain protein YaaA | ||
| KCMLOAMG_00485 | 1.6e-202 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
| KCMLOAMG_00486 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
| KCMLOAMG_00487 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
| KCMLOAMG_00488 | 6.4e-112 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
| KCMLOAMG_00489 | 1.6e-73 | ssb_2 | L | Single-strand binding protein family | ||
| KCMLOAMG_00490 | 2.7e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
| KCMLOAMG_00491 | 1.1e-69 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
| KCMLOAMG_00492 | 1.2e-35 | rpsR | J | 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 | ||
| KCMLOAMG_00494 | 1.5e-91 | yhbO | 3.5.1.124 | S | DJ-1/PfpI family | |
| KCMLOAMG_00495 | 4e-281 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
| KCMLOAMG_00496 | 3.8e-182 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
| KCMLOAMG_00497 | 2.1e-28 | |||||
| KCMLOAMG_00498 | 1.5e-82 | V | Best Blastp hit gi 7514214 pir G75157 'abc transporter, ATP-binding protein, puta tive PAB2069 - Pyrococcus abyssi (strain Orsay)' gi 5457852 emb CAB49342.1 '(AJ248284) ABC transporter, ATP-binding protein, puta tive Pyrococcus abyssi ', score 77, E-value 3.00E-13 | |||
| KCMLOAMG_00499 | 6.7e-162 | V | ABC transporter | |||
| KCMLOAMG_00500 | 1.1e-187 | amtB | P | Ammonium Transporter Family | ||
| KCMLOAMG_00501 | 7.8e-213 | P | Pyridine nucleotide-disulphide oxidoreductase | |||
| KCMLOAMG_00502 | 6.9e-125 | usp | 3.5.1.28 | CBM50 | D | CHAP domain |
| KCMLOAMG_00503 | 0.0 | ylbB | V | ABC transporter permease | ||
| KCMLOAMG_00504 | 8.3e-128 | macB | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_00505 | 2.5e-95 | K | transcriptional regulator | |||
| KCMLOAMG_00506 | 2.9e-153 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
| KCMLOAMG_00507 | 1.4e-45 | |||||
| KCMLOAMG_00508 | 4.1e-128 | S | membrane transporter protein | |||
| KCMLOAMG_00509 | 2.1e-103 | S | Protein of unknown function (DUF1211) | |||
| KCMLOAMG_00510 | 1.7e-113 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
| KCMLOAMG_00511 | 1.3e-54 | |||||
| KCMLOAMG_00512 | 8.1e-287 | pipD | E | Dipeptidase | ||
| KCMLOAMG_00513 | 2.3e-105 | S | Membrane | |||
| KCMLOAMG_00514 | 1.9e-84 | |||||
| KCMLOAMG_00515 | 2.2e-52 | |||||
| KCMLOAMG_00516 | 4.9e-52 | |||||
| KCMLOAMG_00517 | 1.1e-179 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
| KCMLOAMG_00518 | 2.4e-122 | azlC | E | branched-chain amino acid | ||
| KCMLOAMG_00519 | 1.5e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
| KCMLOAMG_00520 | 0.0 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
| KCMLOAMG_00521 | 0.0 | M | Glycosyl hydrolase family 59 | |||
| KCMLOAMG_00522 | 1.4e-116 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
| KCMLOAMG_00523 | 4.6e-177 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
| KCMLOAMG_00524 | 1.2e-279 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
| KCMLOAMG_00525 | 1.7e-217 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
| KCMLOAMG_00526 | 0.0 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
| KCMLOAMG_00527 | 3.9e-266 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
| KCMLOAMG_00528 | 5.6e-245 | G | Major Facilitator | |||
| KCMLOAMG_00529 | 1.2e-126 | kdgR | K | FCD domain | ||
| KCMLOAMG_00530 | 1.5e-190 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
| KCMLOAMG_00531 | 0.0 | M | Glycosyl hydrolase family 59 | |||
| KCMLOAMG_00532 | 5.6e-58 | |||||
| KCMLOAMG_00533 | 1e-64 | S | pyridoxamine 5-phosphate | |||
| KCMLOAMG_00534 | 2.6e-242 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_00536 | 0.0 | ydgH | S | MMPL family | ||
| KCMLOAMG_00537 | 5.9e-106 | K | Tetracycline repressor, C-terminal all-alpha domain | |||
| KCMLOAMG_00538 | 9.7e-122 | S | Sulfite exporter TauE/SafE | |||
| KCMLOAMG_00539 | 1.3e-246 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
| KCMLOAMG_00540 | 3.3e-69 | S | An automated process has identified a potential problem with this gene model | |||
| KCMLOAMG_00541 | 1e-148 | S | Protein of unknown function (DUF3100) | |||
| KCMLOAMG_00543 | 1.9e-110 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
| KCMLOAMG_00544 | 7.8e-174 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
| KCMLOAMG_00545 | 4.7e-106 | opuCB | E | ABC transporter permease | ||
| KCMLOAMG_00546 | 1.6e-214 | opuCA | E | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_00547 | 0.0 | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | ||
| KCMLOAMG_00548 | 6.2e-32 | copZ | P | Heavy-metal-associated domain | ||
| KCMLOAMG_00549 | 1.2e-100 | dps | P | Belongs to the Dps family | ||
| KCMLOAMG_00550 | 6.8e-116 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
| KCMLOAMG_00551 | 1.3e-96 | K | Bacterial regulatory proteins, tetR family | |||
| KCMLOAMG_00552 | 1.6e-83 | S | Protein of unknown function with HXXEE motif | |||
| KCMLOAMG_00554 | 1e-159 | S | CAAX protease self-immunity | |||
| KCMLOAMG_00556 | 2.5e-136 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
| KCMLOAMG_00557 | 1.4e-228 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
| KCMLOAMG_00558 | 1.1e-104 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
| KCMLOAMG_00559 | 7.3e-133 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
| KCMLOAMG_00560 | 1.5e-181 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
| KCMLOAMG_00561 | 2.4e-304 | norB | EGP | Major Facilitator | ||
| KCMLOAMG_00562 | 5.2e-110 | K | Bacterial regulatory proteins, tetR family | |||
| KCMLOAMG_00563 | 3.8e-41 | |||||
| KCMLOAMG_00564 | 5.1e-64 | |||||
| KCMLOAMG_00566 | 6.8e-107 | 1.1.1.133, 5.1.3.13 | M | dTDP-4-dehydrorhamnose 3,5-epimerase | ||
| KCMLOAMG_00567 | 2.8e-137 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
| KCMLOAMG_00568 | 3.5e-163 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
| KCMLOAMG_00569 | 1.9e-217 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
| KCMLOAMG_00570 | 1.1e-71 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
| KCMLOAMG_00571 | 6.2e-257 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
| KCMLOAMG_00572 | 6.4e-257 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
| KCMLOAMG_00573 | 9e-184 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
| KCMLOAMG_00574 | 5.7e-197 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
| KCMLOAMG_00575 | 6.6e-63 | |||||
| KCMLOAMG_00576 | 8.6e-38 | K | sequence-specific DNA binding | |||
| KCMLOAMG_00577 | 2.5e-71 | 3.6.1.55 | L | NUDIX domain | ||
| KCMLOAMG_00578 | 1.5e-150 | EG | EamA-like transporter family | |||
| KCMLOAMG_00579 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_00581 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
| KCMLOAMG_00582 | 5.1e-70 | rplI | J | Binds to the 23S rRNA | ||
| KCMLOAMG_00583 | 1.7e-246 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
| KCMLOAMG_00584 | 4e-220 | |||||
| KCMLOAMG_00585 | 0.0 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
| KCMLOAMG_00586 | 2.2e-160 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
| KCMLOAMG_00587 | 2.3e-198 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
| KCMLOAMG_00588 | 1.8e-156 | K | Helix-turn-helix domain, rpiR family | |||
| KCMLOAMG_00589 | 9.1e-107 | K | Transcriptional regulator C-terminal region | |||
| KCMLOAMG_00590 | 5.4e-127 | V | ABC transporter, ATP-binding protein | |||
| KCMLOAMG_00591 | 0.0 | ylbB | V | ABC transporter permease | ||
| KCMLOAMG_00592 | 2.5e-205 | 4.1.1.52 | S | Amidohydrolase | ||
| KCMLOAMG_00593 | 4.9e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
| KCMLOAMG_00594 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
| KCMLOAMG_00595 | 6e-55 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
| KCMLOAMG_00596 | 5.9e-152 | K | Helix-turn-helix XRE-family like proteins | |||
| KCMLOAMG_00597 | 9.7e-27 | S | Phospholipase_D-nuclease N-terminal | |||
| KCMLOAMG_00598 | 3.4e-121 | yxlF | V | ABC transporter | ||
| KCMLOAMG_00599 | 2e-103 | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | |||
| KCMLOAMG_00600 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
| KCMLOAMG_00601 | 2.1e-120 | |||||
| KCMLOAMG_00602 | 1.4e-181 | yveB | 2.7.4.29 | I | PAP2 superfamily | |
| KCMLOAMG_00603 | 1.8e-206 | mccF | V | LD-carboxypeptidase | ||
| KCMLOAMG_00605 | 2.5e-42 | |||||
| KCMLOAMG_00606 | 1.1e-206 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
| KCMLOAMG_00607 | 1.1e-40 | |||||
| KCMLOAMG_00608 | 8.5e-111 | |||||
| KCMLOAMG_00609 | 1.5e-224 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_00610 | 5.7e-86 | |||||
| KCMLOAMG_00611 | 2.9e-201 | T | PhoQ Sensor | |||
| KCMLOAMG_00612 | 1.6e-120 | K | Transcriptional regulatory protein, C terminal | |||
| KCMLOAMG_00613 | 8.2e-90 | ogt | 2.1.1.63 | L | Methyltransferase | |
| KCMLOAMG_00614 | 1.2e-191 | ldhD3 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
| KCMLOAMG_00615 | 4.5e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00616 | 1.3e-51 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
| KCMLOAMG_00617 | 8e-85 | |||||
| KCMLOAMG_00618 | 7.2e-253 | celD | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
| KCMLOAMG_00619 | 3.5e-290 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
| KCMLOAMG_00620 | 5.8e-132 | K | UTRA | |||
| KCMLOAMG_00621 | 6.1e-40 | |||||
| KCMLOAMG_00622 | 4e-57 | ypaA | S | Protein of unknown function (DUF1304) | ||
| KCMLOAMG_00623 | 1.2e-53 | S | Protein of unknown function (DUF1516) | |||
| KCMLOAMG_00624 | 1.4e-254 | pbuO | S | permease | ||
| KCMLOAMG_00625 | 3.4e-52 | S | DsrE/DsrF-like family | |||
| KCMLOAMG_00626 | 4.9e-187 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
| KCMLOAMG_00627 | 4.5e-43 | |||||
| KCMLOAMG_00628 | 5.6e-106 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
| KCMLOAMG_00629 | 0.0 | |||||
| KCMLOAMG_00631 | 4.1e-123 | yqcC | S | WxL domain surface cell wall-binding | ||
| KCMLOAMG_00632 | 6.2e-183 | ynjC | S | Cell surface protein | ||
| KCMLOAMG_00633 | 9.2e-270 | L | Mga helix-turn-helix domain | |||
| KCMLOAMG_00634 | 7e-149 | yhaI | S | Protein of unknown function (DUF805) | ||
| KCMLOAMG_00635 | 2.7e-57 | |||||
| KCMLOAMG_00636 | 1.6e-252 | rarA | L | recombination factor protein RarA | ||
| KCMLOAMG_00637 | 6.4e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
| KCMLOAMG_00638 | 3.2e-133 | K | DeoR C terminal sensor domain | |||
| KCMLOAMG_00639 | 5.1e-284 | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
| KCMLOAMG_00640 | 6.4e-162 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
| KCMLOAMG_00641 | 7.3e-242 | sgaT | 2.7.1.194 | S | PTS system sugar-specific permease component | |
| KCMLOAMG_00642 | 2.2e-159 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase superfamily domain | |
| KCMLOAMG_00643 | 7.7e-137 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
| KCMLOAMG_00644 | 5.7e-248 | bmr3 | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00647 | 1.7e-89 | |||||
| KCMLOAMG_00649 | 8.6e-47 | V | ATPase activity | |||
| KCMLOAMG_00650 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_00651 | 6.3e-15 | |||||
| KCMLOAMG_00653 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
| KCMLOAMG_00654 | 1.8e-303 | oppA | E | ABC transporter, substratebinding protein | ||
| KCMLOAMG_00655 | 2.2e-76 | |||||
| KCMLOAMG_00656 | 8.6e-117 | |||||
| KCMLOAMG_00657 | 9.3e-122 | |||||
| KCMLOAMG_00658 | 2.5e-118 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_00659 | 1.6e-74 | |||||
| KCMLOAMG_00660 | 3e-81 | S | NUDIX domain | |||
| KCMLOAMG_00661 | 2.3e-212 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
| KCMLOAMG_00662 | 0.0 | fnq20 | 1.13.12.16 | S | FAD-NAD(P)-binding | |
| KCMLOAMG_00663 | 4.7e-260 | nox | 1.6.3.4 | C | NADH oxidase | |
| KCMLOAMG_00664 | 1.7e-116 | |||||
| KCMLOAMG_00665 | 1.6e-233 | S | TPM domain | |||
| KCMLOAMG_00666 | 4e-129 | yxaA | S | Sulfite exporter TauE/SafE | ||
| KCMLOAMG_00667 | 1e-55 | ywjH | S | Protein of unknown function (DUF1634) | ||
| KCMLOAMG_00669 | 6.5e-65 | |||||
| KCMLOAMG_00670 | 1.6e-51 | |||||
| KCMLOAMG_00671 | 1.9e-83 | fld | C | Flavodoxin | ||
| KCMLOAMG_00672 | 3.4e-36 | |||||
| KCMLOAMG_00673 | 6.7e-27 | |||||
| KCMLOAMG_00674 | 4.4e-172 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
| KCMLOAMG_00675 | 9.1e-71 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
| KCMLOAMG_00676 | 6.4e-38 | S | Transglycosylase associated protein | |||
| KCMLOAMG_00677 | 1.5e-89 | S | Protein conserved in bacteria | |||
| KCMLOAMG_00678 | 2.5e-29 | |||||
| KCMLOAMG_00679 | 5.1e-61 | asp23 | S | Asp23 family, cell envelope-related function | ||
| KCMLOAMG_00680 | 7.9e-65 | asp2 | S | Asp23 family, cell envelope-related function | ||
| KCMLOAMG_00681 | 1.8e-129 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
| KCMLOAMG_00682 | 1.7e-114 | S | Protein of unknown function (DUF969) | |||
| KCMLOAMG_00683 | 6.7e-146 | S | Protein of unknown function (DUF979) | |||
| KCMLOAMG_00684 | 6.5e-119 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
| KCMLOAMG_00685 | 2.3e-105 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
| KCMLOAMG_00687 | 1e-127 | cobQ | S | glutamine amidotransferase | ||
| KCMLOAMG_00688 | 2.2e-66 | |||||
| KCMLOAMG_00689 | 2.3e-133 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
| KCMLOAMG_00690 | 2.4e-142 | noc | K | Belongs to the ParB family | ||
| KCMLOAMG_00691 | 2.5e-138 | soj | D | Sporulation initiation inhibitor | ||
| KCMLOAMG_00692 | 2e-155 | spo0J | K | Belongs to the ParB family | ||
| KCMLOAMG_00693 | 1.3e-30 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
| KCMLOAMG_00694 | 2.8e-185 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
| KCMLOAMG_00695 | 1.6e-140 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
| KCMLOAMG_00696 | 5.1e-268 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
| KCMLOAMG_00697 | 1.5e-118 | |||||
| KCMLOAMG_00698 | 2.5e-121 | K | response regulator | |||
| KCMLOAMG_00699 | 1.2e-219 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_00700 | 1.4e-237 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
| KCMLOAMG_00702 | 3.6e-85 | greA | K | 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. GreA releases sequences of 2 to 3 nucleotides | ||
| KCMLOAMG_00703 | 2.7e-296 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
| KCMLOAMG_00704 | 5.4e-141 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
| KCMLOAMG_00705 | 4.4e-163 | yvgN | C | Aldo keto reductase | ||
| KCMLOAMG_00706 | 1.6e-140 | iolR | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_00707 | 1.5e-267 | iolT | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00708 | 6.1e-274 | iolA | 1.2.1.18, 1.2.1.27 | C | Belongs to the aldehyde dehydrogenase family | |
| KCMLOAMG_00709 | 8.4e-156 | iolB | 5.3.1.30 | G | Involved in the isomerization of 5-deoxy-glucuronate (5DG) to 5-dehydro-2-deoxy-D-gluconate (DKG or 2-deoxy-5-keto-D- gluconate) | |
| KCMLOAMG_00710 | 1.4e-178 | iolC | 2.7.1.92 | H | Catalyzes the phosphorylation of 5-dehydro-2-deoxy-D- gluconate (2-deoxy-5-keto-D-gluconate or DKG) to 6-phospho-5- dehydro-2-deoxy-D-gluconate (DKGP) | |
| KCMLOAMG_00711 | 0.0 | iolD | 3.7.1.22 | E | Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) | |
| KCMLOAMG_00712 | 3.2e-192 | iolG | 1.1.1.18, 1.1.1.369 | C | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
| KCMLOAMG_00713 | 1.8e-195 | iolG2 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
| KCMLOAMG_00714 | 1.8e-175 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
| KCMLOAMG_00715 | 9.6e-158 | iolJ | 4.1.2.13, 4.1.2.29 | G | Fructose-bisphosphate aldolase class-II | |
| KCMLOAMG_00716 | 1.1e-65 | iolK | S | Tautomerase enzyme | ||
| KCMLOAMG_00717 | 3.9e-131 | iolI | 5.3.99.11 | G | Xylose isomerase-like TIM barrel | |
| KCMLOAMG_00718 | 1.3e-170 | iolH | G | Xylose isomerase-like TIM barrel | ||
| KCMLOAMG_00719 | 2.1e-146 | gntR | K | rpiR family | ||
| KCMLOAMG_00720 | 4.4e-167 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
| KCMLOAMG_00721 | 3.9e-303 | gntK | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
| KCMLOAMG_00722 | 2.8e-204 | gntP | EG | Gluconate | ||
| KCMLOAMG_00723 | 7.6e-58 | |||||
| KCMLOAMG_00724 | 4.1e-130 | fhuC | 3.6.3.35 | P | ABC transporter | |
| KCMLOAMG_00725 | 3e-134 | znuB | U | ABC 3 transport family | ||
| KCMLOAMG_00726 | 3.2e-166 | T | Calcineurin-like phosphoesterase superfamily domain | |||
| KCMLOAMG_00727 | 1.9e-161 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
| KCMLOAMG_00728 | 0.0 | pepF | E | oligoendopeptidase F | ||
| KCMLOAMG_00729 | 5.7e-200 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
| KCMLOAMG_00730 | 2.3e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
| KCMLOAMG_00731 | 1.1e-71 | T | Sh3 type 3 domain protein | |||
| KCMLOAMG_00732 | 2.2e-134 | glcR | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_00733 | 2.6e-146 | M | Glycosyltransferase like family 2 | |||
| KCMLOAMG_00734 | 4.8e-134 | XK27_06755 | S | Protein of unknown function (DUF975) | ||
| KCMLOAMG_00735 | 2.2e-52 | |||||
| KCMLOAMG_00736 | 1.8e-107 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
| KCMLOAMG_00737 | 2.1e-174 | draG | O | ADP-ribosylglycohydrolase | ||
| KCMLOAMG_00738 | 8.9e-292 | S | ABC transporter | |||
| KCMLOAMG_00739 | 2e-135 | ksgA | 2.1.1.182, 2.1.1.197, 2.5.1.134 | J | rRNA (adenine-N6,N6-)-dimethyltransferase activity | |
| KCMLOAMG_00740 | 6.1e-35 | |||||
| KCMLOAMG_00743 | 2.4e-71 | S | COG NOG38524 non supervised orthologous group | |||
| KCMLOAMG_00744 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
| KCMLOAMG_00745 | 1.7e-43 | trxC | O | Belongs to the thioredoxin family | ||
| KCMLOAMG_00746 | 5.6e-133 | thrE | S | Putative threonine/serine exporter | ||
| KCMLOAMG_00747 | 3.5e-74 | S | Threonine/Serine exporter, ThrE | |||
| KCMLOAMG_00748 | 1.4e-212 | livJ | E | Receptor family ligand binding region | ||
| KCMLOAMG_00749 | 1.5e-150 | livH | U | Branched-chain amino acid transport system / permease component | ||
| KCMLOAMG_00750 | 1.7e-120 | livM | E | Branched-chain amino acid transport system / permease component | ||
| KCMLOAMG_00751 | 3.6e-140 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
| KCMLOAMG_00752 | 1.8e-122 | livF | E | ABC transporter | ||
| KCMLOAMG_00753 | 1.2e-52 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
| KCMLOAMG_00754 | 1.4e-167 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
| KCMLOAMG_00755 | 5.2e-232 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
| KCMLOAMG_00756 | 1.1e-115 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
| KCMLOAMG_00757 | 2.3e-231 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
| KCMLOAMG_00758 | 1.1e-127 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
| KCMLOAMG_00759 | 1.7e-143 | p75 | M | NlpC P60 family protein | ||
| KCMLOAMG_00760 | 4.7e-260 | nox | 1.6.3.4 | C | NADH oxidase | |
| KCMLOAMG_00761 | 5.5e-261 | lacE-1 | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
| KCMLOAMG_00762 | 2.1e-144 | K | CAT RNA binding domain | |||
| KCMLOAMG_00763 | 5.2e-57 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
| KCMLOAMG_00764 | 2.4e-235 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
| KCMLOAMG_00765 | 1.2e-157 | sepS16B | ||||
| KCMLOAMG_00766 | 1.8e-119 | |||||
| KCMLOAMG_00767 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
| KCMLOAMG_00768 | 1.6e-238 | malE | G | Bacterial extracellular solute-binding protein | ||
| KCMLOAMG_00769 | 1.7e-82 | |||||
| KCMLOAMG_00770 | 3.7e-195 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
| KCMLOAMG_00771 | 9e-130 | XK27_08435 | K | UTRA | ||
| KCMLOAMG_00772 | 1.3e-218 | agaS | G | SIS domain | ||
| KCMLOAMG_00773 | 2.1e-224 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
| KCMLOAMG_00774 | 0.0 | bgaC | 3.2.1.23 | G | Glycosyl hydrolases family 35 | |
| KCMLOAMG_00775 | 8.1e-82 | manX_1 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
| KCMLOAMG_00776 | 1.5e-140 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
| KCMLOAMG_00777 | 3e-145 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
| KCMLOAMG_00778 | 7.8e-64 | XK27_08465 | 2.7.1.191 | G | PTS system fructose IIA component | |
| KCMLOAMG_00779 | 2.9e-295 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
| KCMLOAMG_00780 | 0.0 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
| KCMLOAMG_00781 | 6.8e-205 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
| KCMLOAMG_00782 | 2.3e-226 | 4.4.1.8 | E | Aminotransferase, class I | ||
| KCMLOAMG_00783 | 2.6e-181 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
| KCMLOAMG_00784 | 2.7e-252 | 2.7.1.207 | U | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
| KCMLOAMG_00785 | 6.7e-59 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00786 | 4.2e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
| KCMLOAMG_00787 | 3.8e-193 | ypdE | E | M42 glutamyl aminopeptidase | ||
| KCMLOAMG_00788 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
| KCMLOAMG_00789 | 3.6e-235 | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | ||
| KCMLOAMG_00790 | 3.2e-292 | E | ABC transporter, substratebinding protein | |||
| KCMLOAMG_00791 | 2.3e-116 | S | Acetyltransferase (GNAT) family | |||
| KCMLOAMG_00793 | 2.2e-274 | nisT | V | ABC transporter | ||
| KCMLOAMG_00794 | 9.1e-267 | L | Transposase DDE domain | |||
| KCMLOAMG_00795 | 1.8e-34 | |||||
| KCMLOAMG_00796 | 2.8e-27 | |||||
| KCMLOAMG_00797 | 5.7e-95 | S | ABC-type cobalt transport system, permease component | |||
| KCMLOAMG_00798 | 8.7e-243 | P | ABC transporter | |||
| KCMLOAMG_00799 | 1.2e-109 | P | cobalt transport | |||
| KCMLOAMG_00800 | 1e-125 | tenA | 3.5.99.2 | K | 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 | |
| KCMLOAMG_00801 | 1.1e-81 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
| KCMLOAMG_00802 | 5.4e-150 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
| KCMLOAMG_00803 | 3.7e-103 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
| KCMLOAMG_00804 | 3.6e-149 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
| KCMLOAMG_00805 | 1.9e-272 | E | Amino acid permease | |||
| KCMLOAMG_00806 | 2.8e-185 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
| KCMLOAMG_00807 | 8.3e-61 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
| KCMLOAMG_00808 | 1.3e-269 | rbsA | 3.6.3.17 | G | ABC transporter | |
| KCMLOAMG_00809 | 1e-152 | rbsC | U | Belongs to the binding-protein-dependent transport system permease family | ||
| KCMLOAMG_00810 | 1.1e-157 | rbsB | G | Periplasmic binding protein domain | ||
| KCMLOAMG_00811 | 1.4e-162 | rbsK | 2.7.1.15 | H | 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 | |
| KCMLOAMG_00812 | 9.3e-44 | K | DNA-binding helix-turn-helix protein | |||
| KCMLOAMG_00813 | 2.5e-36 | |||||
| KCMLOAMG_00818 | 3.2e-155 | S | Protein of unknown function (DUF2785) | |||
| KCMLOAMG_00819 | 0.0 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
| KCMLOAMG_00820 | 5e-53 | |||||
| KCMLOAMG_00821 | 4.9e-87 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
| KCMLOAMG_00822 | 1.7e-80 | |||||
| KCMLOAMG_00823 | 4.5e-62 | |||||
| KCMLOAMG_00824 | 6.7e-94 | |||||
| KCMLOAMG_00825 | 2.3e-238 | ydiC1 | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00826 | 2.1e-68 | K | helix_turn_helix multiple antibiotic resistance protein | |||
| KCMLOAMG_00827 | 1.6e-102 | |||||
| KCMLOAMG_00828 | 1e-28 | |||||
| KCMLOAMG_00829 | 1e-165 | GKT | transcriptional antiterminator | |||
| KCMLOAMG_00830 | 2.1e-46 | ptxB | 2.7.1.194, 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
| KCMLOAMG_00831 | 2.6e-204 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
| KCMLOAMG_00832 | 5.1e-48 | |||||
| KCMLOAMG_00833 | 1.2e-149 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
| KCMLOAMG_00834 | 4.2e-86 | 6.3.4.4 | S | Zeta toxin | ||
| KCMLOAMG_00835 | 6.2e-155 | rihB | 3.2.2.1 | F | Nucleoside | |
| KCMLOAMG_00836 | 9.8e-213 | dcuD | C | Tripartite ATP-independent periplasmic transporter, DctM component | ||
| KCMLOAMG_00837 | 7.6e-43 | K | Acetyltransferase (GNAT) family | |||
| KCMLOAMG_00838 | 3.7e-118 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
| KCMLOAMG_00839 | 1.5e-88 | 4.1.2.13 | G | DeoC/LacD family aldolase | ||
| KCMLOAMG_00840 | 9.9e-39 | glpP | K | 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 | ||
| KCMLOAMG_00841 | 1.1e-180 | 2.7.1.53 | G | Belongs to the FGGY kinase family | ||
| KCMLOAMG_00842 | 1.8e-91 | IQ | KR domain | |||
| KCMLOAMG_00843 | 3.2e-125 | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | ||
| KCMLOAMG_00844 | 2e-156 | gatC | G | COG3775 Phosphotransferase system, galactitol-specific IIC component | ||
| KCMLOAMG_00845 | 3e-286 | K | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
| KCMLOAMG_00846 | 6.4e-154 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
| KCMLOAMG_00847 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | phosphotransferase system | |
| KCMLOAMG_00848 | 5.4e-239 | sorE | E | Alcohol dehydrogenase GroES-like domain | ||
| KCMLOAMG_00849 | 2.2e-163 | sorC | K | sugar-binding domain protein | ||
| KCMLOAMG_00850 | 4.1e-131 | IQ | NAD dependent epimerase/dehydratase family | |||
| KCMLOAMG_00851 | 3.6e-62 | sorF | 2.7.1.191, 2.7.1.206 | G | PTS system fructose IIA component | |
| KCMLOAMG_00852 | 1.9e-78 | sorB | 2.7.1.191, 2.7.1.206 | G | PTS system sorbose subfamily IIB component | |
| KCMLOAMG_00853 | 3.6e-130 | sorA | U | PTS system sorbose-specific iic component | ||
| KCMLOAMG_00854 | 1.2e-149 | sorM | G | system, mannose fructose sorbose family IID component | ||
| KCMLOAMG_00855 | 4.9e-149 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
| KCMLOAMG_00856 | 1.4e-238 | P | transporter | |||
| KCMLOAMG_00857 | 1.2e-172 | C | FAD dependent oxidoreductase | |||
| KCMLOAMG_00858 | 4.9e-109 | K | Transcriptional regulator, LysR family | |||
| KCMLOAMG_00859 | 1.1e-158 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
| KCMLOAMG_00860 | 2.7e-97 | S | UPF0397 protein | |||
| KCMLOAMG_00861 | 0.0 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
| KCMLOAMG_00862 | 7.2e-147 | cbiQ | P | cobalt transport | ||
| KCMLOAMG_00863 | 3.4e-25 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00864 | 5.7e-21 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
| KCMLOAMG_00865 | 1.1e-162 | U | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
| KCMLOAMG_00866 | 9.7e-20 | 2.7.1.200, 2.7.1.202 | GKT | to transcription antiterminator BglG family | ||
| KCMLOAMG_00867 | 2.6e-266 | L | Transposase DDE domain | |||
| KCMLOAMG_00868 | 2.4e-39 | 2.7.1.194, 2.7.1.202 | GKT | antiterminator | ||
| KCMLOAMG_00869 | 5.7e-200 | 3.2.1.86 | GT1 | G | Glycosyl hydrolase family 1 | |
| KCMLOAMG_00870 | 3.5e-82 | S | Putative transposase | |||
| KCMLOAMG_00871 | 7.8e-60 | S | Putative transposase | |||
| KCMLOAMG_00872 | 1.8e-147 | L | PFAM Integrase catalytic region | |||
| KCMLOAMG_00873 | 6.9e-90 | L | Helix-turn-helix domain | |||
| KCMLOAMG_00874 | 2.8e-143 | K | helix_turn_helix, arabinose operon control protein | |||
| KCMLOAMG_00875 | 0.0 | K | Sigma-54 interaction domain | |||
| KCMLOAMG_00876 | 8.1e-57 | levA | G | PTS system fructose IIA component | ||
| KCMLOAMG_00877 | 1.1e-86 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
| KCMLOAMG_00878 | 4.1e-137 | M | PTS system sorbose-specific iic component | |||
| KCMLOAMG_00879 | 1.8e-145 | levD | G | PTS system mannose/fructose/sorbose family IID component | ||
| KCMLOAMG_00880 | 3.5e-49 | |||||
| KCMLOAMG_00882 | 9e-108 | S | Haloacid dehalogenase-like hydrolase | |||
| KCMLOAMG_00883 | 6.2e-129 | fruR | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_00884 | 3.9e-108 | 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | ||
| KCMLOAMG_00885 | 5.3e-93 | hxlB | 4.1.2.43, 5.3.1.27 | M | SIS domain | |
| KCMLOAMG_00886 | 0.0 | mtlF | 2.7.1.197 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
| KCMLOAMG_00887 | 2.9e-173 | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | ||
| KCMLOAMG_00888 | 8.2e-210 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
| KCMLOAMG_00889 | 7.1e-223 | G | Major Facilitator Superfamily | |||
| KCMLOAMG_00890 | 3.9e-227 | E | Peptidase family M20/M25/M40 | |||
| KCMLOAMG_00891 | 1.9e-97 | K | Transcriptional regulator, LysR family | |||
| KCMLOAMG_00893 | 0.0 | ebgA | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
| KCMLOAMG_00894 | 2e-277 | ygjI | E | Amino Acid | ||
| KCMLOAMG_00895 | 6.3e-263 | lysP | E | amino acid | ||
| KCMLOAMG_00896 | 2.5e-163 | K | helix_turn_helix, arabinose operon control protein | |||
| KCMLOAMG_00897 | 0.0 | GK | helix_turn_helix, arabinose operon control protein | |||
| KCMLOAMG_00898 | 4.3e-209 | G | Major Facilitator Superfamily | |||
| KCMLOAMG_00899 | 1.5e-272 | abgB | 3.5.1.47 | S | Peptidase dimerisation domain | |
| KCMLOAMG_00900 | 1.9e-18 | hxlR | K | Transcriptional regulator, HxlR family | ||
| KCMLOAMG_00901 | 4.4e-57 | pnb | C | nitroreductase | ||
| KCMLOAMG_00902 | 5.7e-119 | |||||
| KCMLOAMG_00903 | 6.7e-08 | K | DNA-templated transcription, initiation | |||
| KCMLOAMG_00904 | 1.3e-17 | S | YvrJ protein family | |||
| KCMLOAMG_00905 | 1.8e-144 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
| KCMLOAMG_00906 | 1.5e-86 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
| KCMLOAMG_00907 | 1.9e-184 | hrtB | V | ABC transporter permease | ||
| KCMLOAMG_00908 | 1.3e-120 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
| KCMLOAMG_00909 | 5.5e-261 | npr | 1.11.1.1 | C | NADH oxidase | |
| KCMLOAMG_00910 | 3.7e-151 | S | hydrolase | |||
| KCMLOAMG_00911 | 7.6e-45 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
| KCMLOAMG_00912 | 5.6e-138 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
| KCMLOAMG_00914 | 4.7e-10 | |||||
| KCMLOAMG_00917 | 8.5e-151 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
| KCMLOAMG_00918 | 3.2e-189 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
| KCMLOAMG_00919 | 2.5e-175 | |||||
| KCMLOAMG_00920 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
| KCMLOAMG_00921 | 9.4e-17 | |||||
| KCMLOAMG_00922 | 4e-104 | K | Bacterial regulatory proteins, tetR family | |||
| KCMLOAMG_00923 | 9.6e-59 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
| KCMLOAMG_00924 | 2.5e-101 | dhaL | 2.7.1.121 | S | Dak2 | |
| KCMLOAMG_00925 | 1.6e-188 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
| KCMLOAMG_00926 | 2.6e-76 | ohr | O | OsmC-like protein | ||
| KCMLOAMG_00927 | 1.9e-20 | |||||
| KCMLOAMG_00928 | 2.9e-12 | |||||
| KCMLOAMG_00930 | 5.2e-55 | |||||
| KCMLOAMG_00931 | 2.2e-252 | L | Exonuclease | |||
| KCMLOAMG_00932 | 6.5e-28 | relB | L | RelB antitoxin | ||
| KCMLOAMG_00933 | 7e-29 | |||||
| KCMLOAMG_00934 | 1.2e-48 | K | Helix-turn-helix domain | |||
| KCMLOAMG_00935 | 4.8e-205 | yceJ | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_00936 | 1.2e-103 | tag | 3.2.2.20 | L | glycosylase | |
| KCMLOAMG_00937 | 2e-32 | |||||
| KCMLOAMG_00938 | 1e-167 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
| KCMLOAMG_00939 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
| KCMLOAMG_00940 | 3.4e-43 | |||||
| KCMLOAMG_00941 | 7e-152 | V | Beta-lactamase | |||
| KCMLOAMG_00942 | 1.6e-191 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
| KCMLOAMG_00943 | 8.7e-136 | H | Protein of unknown function (DUF1698) | |||
| KCMLOAMG_00944 | 1.1e-139 | puuD | S | peptidase C26 | ||
| KCMLOAMG_00945 | 1.3e-106 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
| KCMLOAMG_00946 | 1.3e-78 | K | Psort location Cytoplasmic, score | |||
| KCMLOAMG_00947 | 4.8e-257 | 6.3.1.2 | E | Glutamine synthetase N-terminal domain | ||
| KCMLOAMG_00948 | 3.8e-223 | S | Amidohydrolase | |||
| KCMLOAMG_00949 | 2.4e-248 | E | Amino acid permease | |||
| KCMLOAMG_00950 | 2.5e-74 | K | helix_turn_helix, mercury resistance | |||
| KCMLOAMG_00951 | 3.2e-161 | morA2 | S | reductase | ||
| KCMLOAMG_00952 | 2.6e-194 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
| KCMLOAMG_00953 | 4e-59 | hxlR | K | Transcriptional regulator, HxlR family | ||
| KCMLOAMG_00954 | 2e-127 | S | membrane transporter protein | |||
| KCMLOAMG_00955 | 7.5e-61 | |||||
| KCMLOAMG_00956 | 1.5e-248 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
| KCMLOAMG_00957 | 1.6e-29 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
| KCMLOAMG_00958 | 5.6e-188 | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
| KCMLOAMG_00959 | 4.6e-38 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_00960 | 1.8e-212 | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | GKT | Mga helix-turn-helix domain | ||
| KCMLOAMG_00961 | 1.1e-196 | |||||
| KCMLOAMG_00962 | 5.4e-130 | XK27_12140 | V | ATPases associated with a variety of cellular activities | ||
| KCMLOAMG_00963 | 6e-299 | S | Psort location CytoplasmicMembrane, score | |||
| KCMLOAMG_00964 | 2.2e-125 | K | Transcriptional regulatory protein, C terminal | |||
| KCMLOAMG_00965 | 3.3e-195 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
| KCMLOAMG_00966 | 3.6e-160 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_00967 | 1.6e-197 | |||||
| KCMLOAMG_00968 | 2.3e-105 | |||||
| KCMLOAMG_00969 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
| KCMLOAMG_00970 | 8.4e-276 | ycaM | E | amino acid | ||
| KCMLOAMG_00971 | 2.2e-238 | G | MFS/sugar transport protein | |||
| KCMLOAMG_00972 | 7.6e-91 | S | Protein of unknown function (DUF1440) | |||
| KCMLOAMG_00973 | 5.1e-161 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
| KCMLOAMG_00974 | 2.7e-174 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
| KCMLOAMG_00976 | 1.5e-138 | |||||
| KCMLOAMG_00978 | 1e-212 | metC | 4.4.1.8 | E | cystathionine | |
| KCMLOAMG_00979 | 8.6e-145 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
| KCMLOAMG_00980 | 2.2e-120 | tcyB | E | ABC transporter | ||
| KCMLOAMG_00981 | 2.2e-117 | |||||
| KCMLOAMG_00982 | 2.5e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
| KCMLOAMG_00983 | 3.5e-75 | S | WxL domain surface cell wall-binding | |||
| KCMLOAMG_00984 | 1.2e-172 | S | Cell surface protein | |||
| KCMLOAMG_00985 | 5.5e-43 | |||||
| KCMLOAMG_00986 | 2.2e-245 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
| KCMLOAMG_00988 | 1.7e-133 | L | Transposase, IS116 IS110 IS902 family | |||
| KCMLOAMG_00989 | 5e-120 | S | WxL domain surface cell wall-binding | |||
| KCMLOAMG_00990 | 4.7e-61 | |||||
| KCMLOAMG_00991 | 7.4e-113 | N | WxL domain surface cell wall-binding | |||
| KCMLOAMG_00992 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
| KCMLOAMG_00993 | 1.1e-167 | yicL | EG | EamA-like transporter family | ||
| KCMLOAMG_00994 | 2e-300 | |||||
| KCMLOAMG_00995 | 1.1e-144 | CcmA5 | V | ABC transporter | ||
| KCMLOAMG_00996 | 6.2e-78 | S | ECF-type riboflavin transporter, S component | |||
| KCMLOAMG_00997 | 6.1e-146 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
| KCMLOAMG_00998 | 1.5e-163 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
| KCMLOAMG_00999 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
| KCMLOAMG_01000 | 0.0 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01001 | 0.0 | V | ABC transporter | |||
| KCMLOAMG_01002 | 7.2e-220 | oxlT | P | Major Facilitator Superfamily | ||
| KCMLOAMG_01003 | 8.5e-128 | treR | K | UTRA | ||
| KCMLOAMG_01004 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
| KCMLOAMG_01005 | 0.0 | treB | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
| KCMLOAMG_01006 | 2e-212 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
| KCMLOAMG_01007 | 2.5e-267 | yfnA | E | Amino Acid | ||
| KCMLOAMG_01008 | 2.5e-172 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
| KCMLOAMG_01009 | 1.9e-250 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
| KCMLOAMG_01010 | 4.6e-31 | K | 'Cold-shock' DNA-binding domain | |||
| KCMLOAMG_01011 | 4.1e-69 | |||||
| KCMLOAMG_01012 | 3.5e-76 | O | OsmC-like protein | |||
| KCMLOAMG_01013 | 2.3e-281 | lsa | S | ABC transporter | ||
| KCMLOAMG_01014 | 1e-113 | ylbE | GM | NAD(P)H-binding | ||
| KCMLOAMG_01015 | 2.9e-159 | yeaE | S | Aldo/keto reductase family | ||
| KCMLOAMG_01016 | 1.9e-256 | yifK | E | Amino acid permease | ||
| KCMLOAMG_01017 | 1.4e-282 | S | Protein of unknown function (DUF3800) | |||
| KCMLOAMG_01018 | 0.0 | yjcE | P | Sodium proton antiporter | ||
| KCMLOAMG_01019 | 2.2e-56 | S | Protein of unknown function (DUF3021) | |||
| KCMLOAMG_01020 | 4.8e-68 | K | LytTr DNA-binding domain | |||
| KCMLOAMG_01021 | 3.1e-148 | cylB | V | ABC-2 type transporter | ||
| KCMLOAMG_01022 | 1.4e-156 | cylA | V | ABC transporter | ||
| KCMLOAMG_01023 | 8.3e-145 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
| KCMLOAMG_01024 | 8.7e-116 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
| KCMLOAMG_01025 | 2.6e-52 | ybjQ | S | Belongs to the UPF0145 family | ||
| KCMLOAMG_01026 | 5.1e-95 | nudC | 1.3.7.1, 3.6.1.22 | L | NUDIX domain | |
| KCMLOAMG_01027 | 2e-158 | 3.5.1.10 | C | nadph quinone reductase | ||
| KCMLOAMG_01028 | 1.3e-243 | amt | P | ammonium transporter | ||
| KCMLOAMG_01029 | 1.4e-178 | yfeX | P | Peroxidase | ||
| KCMLOAMG_01030 | 1.1e-118 | yhiD | S | MgtC family | ||
| KCMLOAMG_01031 | 2.7e-146 | F | DNA RNA non-specific endonuclease | |||
| KCMLOAMG_01033 | 1.2e-10 | |||||
| KCMLOAMG_01034 | 2.3e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01035 | 3.3e-276 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
| KCMLOAMG_01036 | 2e-111 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
| KCMLOAMG_01037 | 1.9e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
| KCMLOAMG_01038 | 0.0 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
| KCMLOAMG_01039 | 5.9e-296 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
| KCMLOAMG_01040 | 1.8e-133 | epsG | 2.4.1.293 | GT2 | M | Glycosyltransferase like family 2 |
| KCMLOAMG_01041 | 6.5e-138 | lacT | K | PRD domain | ||
| KCMLOAMG_01042 | 0.0 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
| KCMLOAMG_01043 | 4.7e-247 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
| KCMLOAMG_01044 | 1.9e-50 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
| KCMLOAMG_01045 | 6.2e-221 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
| KCMLOAMG_01046 | 5.5e-194 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
| KCMLOAMG_01047 | 1.1e-283 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
| KCMLOAMG_01048 | 4.3e-162 | K | Transcriptional regulator | |||
| KCMLOAMG_01049 | 6.9e-192 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
| KCMLOAMG_01051 | 4.3e-70 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
| KCMLOAMG_01052 | 1.7e-48 | 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_01053 | 2.3e-249 | gatC | G | PTS system sugar-specific permease component | ||
| KCMLOAMG_01055 | 1.5e-29 | |||||
| KCMLOAMG_01056 | 4.7e-188 | V | Beta-lactamase | |||
| KCMLOAMG_01057 | 1.4e-124 | S | Domain of unknown function (DUF4867) | |||
| KCMLOAMG_01058 | 9.3e-175 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
| KCMLOAMG_01059 | 1.6e-185 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
| KCMLOAMG_01060 | 9.9e-94 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
| KCMLOAMG_01061 | 6.1e-73 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
| KCMLOAMG_01062 | 1.9e-141 | lacR | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_01063 | 5e-116 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
| KCMLOAMG_01064 | 2.4e-209 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
| KCMLOAMG_01065 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
| KCMLOAMG_01066 | 1.3e-14 | |||||
| KCMLOAMG_01067 | 5.3e-86 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
| KCMLOAMG_01068 | 1.6e-211 | mutY | L | A G-specific adenine glycosylase | ||
| KCMLOAMG_01069 | 1.9e-149 | cytC6 | I | alpha/beta hydrolase fold | ||
| KCMLOAMG_01070 | 2.9e-120 | yrkL | S | Flavodoxin-like fold | ||
| KCMLOAMG_01072 | 6.9e-87 | S | Short repeat of unknown function (DUF308) | |||
| KCMLOAMG_01073 | 3e-153 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
| KCMLOAMG_01074 | 2.7e-199 | |||||
| KCMLOAMG_01075 | 3.9e-07 | |||||
| KCMLOAMG_01076 | 4e-116 | ywnB | S | NmrA-like family | ||
| KCMLOAMG_01077 | 0.0 | bglB | 3.2.1.21 | GH3 | G | hydrolase, family 3 |
| KCMLOAMG_01078 | 6.1e-166 | XK27_00670 | S | ABC transporter substrate binding protein | ||
| KCMLOAMG_01079 | 2.6e-164 | XK27_00670 | S | ABC transporter | ||
| KCMLOAMG_01080 | 7.6e-156 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
| KCMLOAMG_01081 | 9.8e-141 | cmpC | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01082 | 1.1e-170 | yhfP | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
| KCMLOAMG_01083 | 0.0 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
| KCMLOAMG_01084 | 5.8e-180 | ykcC | GT2 | M | Glycosyl transferase family 2 | |
| KCMLOAMG_01085 | 0.0 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
| KCMLOAMG_01086 | 6.4e-72 | S | GtrA-like protein | |||
| KCMLOAMG_01087 | 1.3e-128 | K | cheY-homologous receiver domain | |||
| KCMLOAMG_01088 | 7.3e-239 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
| KCMLOAMG_01089 | 1.7e-66 | yqkB | S | Belongs to the HesB IscA family | ||
| KCMLOAMG_01090 | 1.7e-122 | drgA | C | Nitroreductase family | ||
| KCMLOAMG_01091 | 9.2e-206 | lctO | C | IMP dehydrogenase / GMP reductase domain | ||
| KCMLOAMG_01094 | 2.3e-07 | Z012_04635 | K | Helix-turn-helix domain | ||
| KCMLOAMG_01096 | 4.2e-06 | mutR | K | Helix-turn-helix | ||
| KCMLOAMG_01098 | 5.4e-181 | K | sequence-specific DNA binding | |||
| KCMLOAMG_01099 | 3.1e-56 | K | Transcriptional regulator PadR-like family | |||
| KCMLOAMG_01100 | 4e-42 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
| KCMLOAMG_01101 | 6.6e-50 | |||||
| KCMLOAMG_01102 | 1.1e-184 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
| KCMLOAMG_01103 | 9.8e-56 | |||||
| KCMLOAMG_01104 | 3.4e-80 | |||||
| KCMLOAMG_01105 | 2.3e-207 | yubA | S | AI-2E family transporter | ||
| KCMLOAMG_01106 | 7.4e-26 | |||||
| KCMLOAMG_01107 | 1e-97 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
| KCMLOAMG_01108 | 3.2e-75 | |||||
| KCMLOAMG_01109 | 1.1e-167 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
| KCMLOAMG_01110 | 2.7e-106 | ywrF | S | Flavin reductase like domain | ||
| KCMLOAMG_01111 | 8.8e-96 | |||||
| KCMLOAMG_01112 | 1.4e-104 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
| KCMLOAMG_01113 | 8.8e-62 | yeaO | S | Protein of unknown function, DUF488 | ||
| KCMLOAMG_01114 | 8.6e-173 | corA | P | CorA-like Mg2+ transporter protein | ||
| KCMLOAMG_01115 | 2.4e-161 | mleR | K | LysR family | ||
| KCMLOAMG_01116 | 0.0 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
| KCMLOAMG_01117 | 1.1e-170 | mleP | S | Sodium Bile acid symporter family | ||
| KCMLOAMG_01118 | 1e-87 | 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 | |
| KCMLOAMG_01119 | 3.4e-94 | |||||
| KCMLOAMG_01120 | 9.9e-172 | K | sequence-specific DNA binding | |||
| KCMLOAMG_01121 | 1.1e-284 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_01122 | 0.0 | pepF | E | Oligopeptidase F | ||
| KCMLOAMG_01123 | 2.5e-77 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
| KCMLOAMG_01124 | 1.8e-59 | |||||
| KCMLOAMG_01125 | 0.0 | yfgQ | P | E1-E2 ATPase | ||
| KCMLOAMG_01126 | 1.8e-178 | 3.4.11.5 | I | Releases the N-terminal proline from various substrates | ||
| KCMLOAMG_01127 | 1.8e-59 | |||||
| KCMLOAMG_01128 | 1.1e-93 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
| KCMLOAMG_01129 | 2.9e-194 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
| KCMLOAMG_01130 | 1.6e-120 | gph | 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
| KCMLOAMG_01131 | 1.5e-77 | K | Transcriptional regulator | |||
| KCMLOAMG_01132 | 8e-179 | D | Alpha beta | |||
| KCMLOAMG_01133 | 3.8e-84 | nrdI | F | Belongs to the NrdI family | ||
| KCMLOAMG_01134 | 4.1e-158 | dkgB | S | reductase | ||
| KCMLOAMG_01135 | 1.8e-120 | |||||
| KCMLOAMG_01136 | 2.8e-162 | S | Alpha beta hydrolase | |||
| KCMLOAMG_01137 | 1e-116 | yviA | S | Protein of unknown function (DUF421) | ||
| KCMLOAMG_01138 | 3.5e-74 | S | Protein of unknown function (DUF3290) | |||
| KCMLOAMG_01139 | 2.7e-221 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
| KCMLOAMG_01140 | 1.6e-87 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
| KCMLOAMG_01141 | 6e-103 | yjbF | S | SNARE associated Golgi protein | ||
| KCMLOAMG_01142 | 3.9e-102 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
| KCMLOAMG_01143 | 9e-195 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
| KCMLOAMG_01144 | 3.6e-207 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
| KCMLOAMG_01145 | 5.2e-228 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
| KCMLOAMG_01146 | 1.4e-45 | yajC | U | Preprotein translocase | ||
| KCMLOAMG_01147 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
| KCMLOAMG_01148 | 3.9e-116 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
| KCMLOAMG_01149 | 1.1e-289 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
| KCMLOAMG_01150 | 3.1e-206 | dinB | 2.7.7.7 | L | 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 | |
| KCMLOAMG_01151 | 5.2e-240 | ytoI | K | DRTGG domain | ||
| KCMLOAMG_01152 | 1.8e-178 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
| KCMLOAMG_01153 | 5.6e-250 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
| KCMLOAMG_01154 | 4.3e-172 | |||||
| KCMLOAMG_01155 | 0.0 | alaS | 6.1.1.7 | J | 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 | |
| KCMLOAMG_01156 | 3.9e-209 | |||||
| KCMLOAMG_01157 | 4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
| KCMLOAMG_01158 | 2.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
| KCMLOAMG_01159 | 2.3e-53 | yrzB | S | Belongs to the UPF0473 family | ||
| KCMLOAMG_01160 | 2e-36 | zapA | D | 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 | ||
| KCMLOAMG_01161 | 8.6e-93 | cvpA | S | Colicin V production protein | ||
| KCMLOAMG_01162 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
| KCMLOAMG_01163 | 6.6e-53 | trxA | O | Belongs to the thioredoxin family | ||
| KCMLOAMG_01164 | 1.2e-293 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
| KCMLOAMG_01165 | 4.5e-238 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
| KCMLOAMG_01166 | 1.2e-36 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
| KCMLOAMG_01167 | 2.1e-246 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
| KCMLOAMG_01168 | 1.2e-82 | yslB | S | Protein of unknown function (DUF2507) | ||
| KCMLOAMG_01169 | 5.3e-278 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
| KCMLOAMG_01170 | 4.1e-95 | S | Phosphoesterase | |||
| KCMLOAMG_01171 | 5.2e-133 | gla | U | Major intrinsic protein | ||
| KCMLOAMG_01172 | 8.7e-84 | ykuL | S | CBS domain | ||
| KCMLOAMG_01173 | 2.7e-155 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
| KCMLOAMG_01174 | 1.8e-156 | ykuT | M | mechanosensitive ion channel | ||
| KCMLOAMG_01176 | 1.9e-78 | ytxH | S | YtxH-like protein | ||
| KCMLOAMG_01177 | 2.5e-92 | niaR | S | 3H domain | ||
| KCMLOAMG_01178 | 2.8e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
| KCMLOAMG_01179 | 2.3e-179 | ccpA | K | catabolite control protein A | ||
| KCMLOAMG_01180 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
| KCMLOAMG_01181 | 4e-127 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
| KCMLOAMG_01182 | 6.3e-134 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
| KCMLOAMG_01183 | 1.9e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
| KCMLOAMG_01184 | 2.8e-257 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
| KCMLOAMG_01185 | 6.1e-54 | |||||
| KCMLOAMG_01186 | 1.9e-187 | yibE | S | overlaps another CDS with the same product name | ||
| KCMLOAMG_01187 | 5.9e-116 | yibF | S | overlaps another CDS with the same product name | ||
| KCMLOAMG_01188 | 5.3e-115 | S | Calcineurin-like phosphoesterase | |||
| KCMLOAMG_01189 | 1.3e-265 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
| KCMLOAMG_01190 | 2.6e-109 | yutD | S | Protein of unknown function (DUF1027) | ||
| KCMLOAMG_01191 | 1.7e-145 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
| KCMLOAMG_01192 | 7.3e-115 | S | Protein of unknown function (DUF1461) | |||
| KCMLOAMG_01193 | 8.9e-116 | dedA | S | SNARE-like domain protein | ||
| KCMLOAMG_01194 | 1.5e-86 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
| KCMLOAMG_01195 | 4.7e-185 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
| KCMLOAMG_01196 | 1.7e-110 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
| KCMLOAMG_01197 | 4.3e-64 | yugI | 5.3.1.9 | J | general stress protein | |
| KCMLOAMG_01198 | 6.1e-35 | |||||
| KCMLOAMG_01199 | 2.4e-71 | S | COG NOG38524 non supervised orthologous group | |||
| KCMLOAMG_01200 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
| KCMLOAMG_01226 | 1.3e-93 | sigH | K | Sigma-70 region 2 | ||
| KCMLOAMG_01227 | 1.9e-297 | ybeC | E | amino acid | ||
| KCMLOAMG_01228 | 1.5e-230 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
| KCMLOAMG_01229 | 1e-195 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
| KCMLOAMG_01230 | 4.5e-167 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
| KCMLOAMG_01231 | 2.6e-219 | patA | 2.6.1.1 | E | Aminotransferase | |
| KCMLOAMG_01232 | 5.1e-44 | ykuJ | S | Protein of unknown function (DUF1797) | ||
| KCMLOAMG_01233 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
| KCMLOAMG_01234 | 5.3e-80 | perR | P | Belongs to the Fur family | ||
| KCMLOAMG_01235 | 6.1e-35 | |||||
| KCMLOAMG_01236 | 2.4e-71 | S | COG NOG38524 non supervised orthologous group | |||
| KCMLOAMG_01237 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
| KCMLOAMG_01238 | 9.3e-13 | |||||
| KCMLOAMG_01242 | 1.5e-99 | |||||
| KCMLOAMG_01243 | 1.7e-210 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
| KCMLOAMG_01244 | 7.3e-275 | emrY | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_01245 | 1.1e-80 | merR | K | MerR HTH family regulatory protein | ||
| KCMLOAMG_01246 | 8.1e-266 | lmrB | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_01247 | 1e-112 | S | Domain of unknown function (DUF4811) | |||
| KCMLOAMG_01248 | 9.7e-118 | 3.6.1.27 | I | Acid phosphatase homologues | ||
| KCMLOAMG_01249 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
| KCMLOAMG_01250 | 2.4e-279 | ytgP | S | Polysaccharide biosynthesis protein | ||
| KCMLOAMG_01251 | 1.7e-128 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
| KCMLOAMG_01252 | 3.3e-35 | yhcC | S | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | ||
| KCMLOAMG_01253 | 1.5e-139 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
| KCMLOAMG_01254 | 5.1e-95 | FNV0100 | F | NUDIX domain | ||
| KCMLOAMG_01256 | 4.8e-87 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
| KCMLOAMG_01257 | 7.4e-225 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
| KCMLOAMG_01258 | 3.8e-222 | cpdA | S | Calcineurin-like phosphoesterase | ||
| KCMLOAMG_01259 | 1.5e-37 | gcvR | T | Belongs to the UPF0237 family | ||
| KCMLOAMG_01260 | 1.3e-243 | XK27_08635 | S | UPF0210 protein | ||
| KCMLOAMG_01261 | 3.1e-211 | coiA | 3.6.4.12 | S | Competence protein | |
| KCMLOAMG_01262 | 1.5e-115 | yjbH | Q | Thioredoxin | ||
| KCMLOAMG_01263 | 1.2e-103 | yjbK | S | CYTH | ||
| KCMLOAMG_01264 | 2.7e-123 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
| KCMLOAMG_01265 | 1.4e-150 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
| KCMLOAMG_01266 | 2.1e-171 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
| KCMLOAMG_01267 | 3.1e-203 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
| KCMLOAMG_01268 | 4.4e-112 | cutC | P | Participates in the control of copper homeostasis | ||
| KCMLOAMG_01269 | 3.5e-146 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
| KCMLOAMG_01270 | 3.9e-198 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
| KCMLOAMG_01271 | 1.2e-61 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
| KCMLOAMG_01272 | 3.5e-42 | rpsN | J | 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 | ||
| KCMLOAMG_01273 | 2e-191 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
| KCMLOAMG_01274 | 5.7e-172 | corA | P | CorA-like Mg2+ transporter protein | ||
| KCMLOAMG_01275 | 6.2e-154 | rrmA | 2.1.1.187 | H | Methyltransferase | |
| KCMLOAMG_01276 | 2.1e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
| KCMLOAMG_01277 | 5.4e-71 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
| KCMLOAMG_01278 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
| KCMLOAMG_01279 | 6.1e-230 | ymfF | S | Peptidase M16 inactive domain protein | ||
| KCMLOAMG_01280 | 2.2e-243 | ymfH | S | Peptidase M16 | ||
| KCMLOAMG_01281 | 1.3e-128 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
| KCMLOAMG_01282 | 2e-116 | ymfM | S | Helix-turn-helix domain | ||
| KCMLOAMG_01283 | 1.6e-103 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
| KCMLOAMG_01284 | 4e-226 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
| KCMLOAMG_01285 | 3.3e-189 | 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 | ||
| KCMLOAMG_01286 | 1.3e-12 | |||||
| KCMLOAMG_01287 | 1.7e-242 | rny | S | Endoribonuclease that initiates mRNA decay | ||
| KCMLOAMG_01288 | 6.8e-116 | yvyE | 3.4.13.9 | S | YigZ family | |
| KCMLOAMG_01289 | 1.3e-235 | comFA | L | Helicase C-terminal domain protein | ||
| KCMLOAMG_01290 | 5.3e-89 | comFC | S | Competence protein | ||
| KCMLOAMG_01291 | 5.4e-98 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
| KCMLOAMG_01292 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
| KCMLOAMG_01293 | 8.9e-176 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
| KCMLOAMG_01294 | 1.9e-124 | ftsE | D | ABC transporter | ||
| KCMLOAMG_01295 | 1.8e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
| KCMLOAMG_01296 | 6.5e-196 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
| KCMLOAMG_01297 | 5.2e-130 | K | response regulator | |||
| KCMLOAMG_01298 | 6.4e-304 | phoR | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_01299 | 1.2e-155 | pstS | P | Phosphate | ||
| KCMLOAMG_01300 | 3.4e-161 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
| KCMLOAMG_01301 | 1.1e-156 | pstA | P | Phosphate transport system permease protein PstA | ||
| KCMLOAMG_01302 | 6.9e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
| KCMLOAMG_01303 | 7.1e-141 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
| KCMLOAMG_01304 | 1e-119 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
| KCMLOAMG_01305 | 5.5e-214 | yvlB | S | Putative adhesin | ||
| KCMLOAMG_01306 | 2.1e-31 | |||||
| KCMLOAMG_01307 | 1.3e-46 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
| KCMLOAMG_01308 | 2.8e-174 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
| KCMLOAMG_01309 | 1.1e-155 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
| KCMLOAMG_01310 | 2e-194 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
| KCMLOAMG_01311 | 1.5e-180 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
| KCMLOAMG_01312 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
| KCMLOAMG_01313 | 7.9e-117 | yfbR | S | HD containing hydrolase-like enzyme | ||
| KCMLOAMG_01314 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
| KCMLOAMG_01315 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
| KCMLOAMG_01316 | 6.7e-85 | S | Short repeat of unknown function (DUF308) | |||
| KCMLOAMG_01317 | 1.3e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
| KCMLOAMG_01318 | 1.7e-190 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
| KCMLOAMG_01319 | 1.6e-171 | whiA | K | May be required for sporulation | ||
| KCMLOAMG_01320 | 5.5e-80 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
| KCMLOAMG_01321 | 2.5e-101 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
| KCMLOAMG_01323 | 3.6e-188 | cggR | K | Putative sugar-binding domain | ||
| KCMLOAMG_01324 | 2.2e-193 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
| KCMLOAMG_01325 | 1.5e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
| KCMLOAMG_01326 | 1.7e-139 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
| KCMLOAMG_01327 | 3.7e-246 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
| KCMLOAMG_01328 | 5.9e-64 | |||||
| KCMLOAMG_01329 | 7e-292 | clcA | P | chloride | ||
| KCMLOAMG_01330 | 1.7e-60 | |||||
| KCMLOAMG_01331 | 9.3e-31 | secG | U | Preprotein translocase | ||
| KCMLOAMG_01332 | 5.4e-138 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
| KCMLOAMG_01333 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
| KCMLOAMG_01334 | 3.2e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
| KCMLOAMG_01335 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
| KCMLOAMG_01336 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
| KCMLOAMG_01337 | 4.2e-113 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
| KCMLOAMG_01338 | 8.7e-50 | |||||
| KCMLOAMG_01339 | 1.2e-235 | YSH1 | S | Metallo-beta-lactamase superfamily | ||
| KCMLOAMG_01340 | 4.4e-239 | malE | G | Bacterial extracellular solute-binding protein | ||
| KCMLOAMG_01341 | 4.2e-147 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
| KCMLOAMG_01342 | 2.6e-166 | malG | P | ABC-type sugar transport systems, permease components | ||
| KCMLOAMG_01343 | 1e-193 | malK | P | ATPases associated with a variety of cellular activities | ||
| KCMLOAMG_01344 | 4.4e-103 | 3.2.2.20 | K | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_01345 | 9e-92 | yxjI | ||||
| KCMLOAMG_01346 | 2e-158 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
| KCMLOAMG_01347 | 4.6e-131 | ung | 3.2.2.27 | L | 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 | |
| KCMLOAMG_01348 | 4.2e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
| KCMLOAMG_01349 | 1.2e-82 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
| KCMLOAMG_01350 | 1.5e-166 | natA | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01351 | 5.3e-218 | ysdA | CP | ABC-2 family transporter protein | ||
| KCMLOAMG_01352 | 3.1e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
| KCMLOAMG_01353 | 1.6e-148 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
| KCMLOAMG_01354 | 9.5e-158 | murB | 1.3.1.98 | M | Cell wall formation | |
| KCMLOAMG_01355 | 0.0 | yjcE | P | Sodium proton antiporter | ||
| KCMLOAMG_01356 | 2.9e-96 | puuR | K | Cupin domain | ||
| KCMLOAMG_01357 | 4.5e-205 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
| KCMLOAMG_01358 | 1.7e-148 | potB | P | ABC transporter permease | ||
| KCMLOAMG_01359 | 8.9e-145 | potC | P | ABC transporter permease | ||
| KCMLOAMG_01360 | 3.6e-207 | potD | P | ABC transporter | ||
| KCMLOAMG_01361 | 5.2e-14 | T | SpoVT / AbrB like domain | |||
| KCMLOAMG_01363 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
| KCMLOAMG_01364 | 5.8e-118 | K | Transcriptional regulator | |||
| KCMLOAMG_01365 | 2.7e-184 | V | ABC transporter | |||
| KCMLOAMG_01366 | 2.1e-126 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
| KCMLOAMG_01367 | 1e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
| KCMLOAMG_01368 | 7e-166 | ybbR | S | YbbR-like protein | ||
| KCMLOAMG_01369 | 9.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
| KCMLOAMG_01370 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
| KCMLOAMG_01371 | 0.0 | pepF2 | E | Oligopeptidase F | ||
| KCMLOAMG_01372 | 9.7e-91 | S | VanZ like family | |||
| KCMLOAMG_01373 | 3.4e-132 | yebC | K | Transcriptional regulatory protein | ||
| KCMLOAMG_01374 | 1.5e-131 | comGA | NU | Type II IV secretion system protein | ||
| KCMLOAMG_01375 | 1.2e-164 | comGB | NU | type II secretion system | ||
| KCMLOAMG_01376 | 5.1e-48 | |||||
| KCMLOAMG_01378 | 1.1e-47 | |||||
| KCMLOAMG_01379 | 1.1e-80 | |||||
| KCMLOAMG_01380 | 4.6e-49 | |||||
| KCMLOAMG_01381 | 4.5e-183 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
| KCMLOAMG_01382 | 3.3e-72 | |||||
| KCMLOAMG_01383 | 1.2e-247 | cycA | E | Amino acid permease | ||
| KCMLOAMG_01384 | 3.8e-142 | arbV | 2.3.1.51 | I | Phosphate acyltransferases | |
| KCMLOAMG_01385 | 9.5e-163 | arbx | M | Glycosyl transferase family 8 | ||
| KCMLOAMG_01386 | 1.5e-180 | arbY | M | family 8 | ||
| KCMLOAMG_01387 | 9.1e-164 | arbZ | I | Phosphate acyltransferases | ||
| KCMLOAMG_01388 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
| KCMLOAMG_01389 | 1.9e-175 | sip | L | Belongs to the 'phage' integrase family | ||
| KCMLOAMG_01390 | 6e-22 | sip | L | Belongs to the 'phage' integrase family | ||
| KCMLOAMG_01393 | 2.1e-29 | |||||
| KCMLOAMG_01394 | 4.4e-17 | |||||
| KCMLOAMG_01395 | 1.1e-21 | |||||
| KCMLOAMG_01397 | 1.9e-23 | |||||
| KCMLOAMG_01398 | 2.9e-148 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
| KCMLOAMG_01399 | 1.9e-300 | S | Phage plasmid primase, P4 | |||
| KCMLOAMG_01400 | 3.9e-51 | S | Phage head-tail joining protein | |||
| KCMLOAMG_01402 | 5.1e-24 | L | Phage-associated protein | |||
| KCMLOAMG_01403 | 5.3e-78 | terS | L | Phage terminase, small subunit | ||
| KCMLOAMG_01404 | 0.0 | terL | S | overlaps another CDS with the same product name | ||
| KCMLOAMG_01405 | 2.5e-20 | |||||
| KCMLOAMG_01406 | 1e-218 | S | Phage portal protein | |||
| KCMLOAMG_01407 | 1.9e-273 | S | Phage capsid family | |||
| KCMLOAMG_01408 | 7.4e-46 | S | Phage gp6-like head-tail connector protein | |||
| KCMLOAMG_01410 | 2.9e-16 | |||||
| KCMLOAMG_01411 | 2.2e-14 | ytgB | S | Transglycosylase associated protein | ||
| KCMLOAMG_01413 | 3.8e-69 | S | SdpI/YhfL protein family | |||
| KCMLOAMG_01414 | 3.1e-133 | K | response regulator | |||
| KCMLOAMG_01415 | 4.6e-272 | yclK | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_01416 | 1.3e-93 | yhbS | S | acetyltransferase | ||
| KCMLOAMG_01417 | 7.6e-31 | |||||
| KCMLOAMG_01418 | 5.2e-72 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
| KCMLOAMG_01419 | 3.8e-82 | |||||
| KCMLOAMG_01420 | 5.3e-59 | |||||
| KCMLOAMG_01421 | 5.5e-250 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
| KCMLOAMG_01423 | 8.1e-176 | S | response to antibiotic | |||
| KCMLOAMG_01425 | 1.3e-213 | tnpB | L | Putative transposase DNA-binding domain | ||
| KCMLOAMG_01426 | 8.3e-108 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
| KCMLOAMG_01427 | 4.5e-28 | yjgN | S | Bacterial protein of unknown function (DUF898) | ||
| KCMLOAMG_01428 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
| KCMLOAMG_01429 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
| KCMLOAMG_01430 | 1.2e-203 | camS | S | sex pheromone | ||
| KCMLOAMG_01431 | 4.9e-45 | gatC | 6.3.5.6, 6.3.5.7 | J | 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) | |
| KCMLOAMG_01432 | 3.3e-264 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
| KCMLOAMG_01433 | 6.1e-279 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | 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) | |
| KCMLOAMG_01434 | 2.9e-193 | yegS | 2.7.1.107 | G | Lipid kinase | |
| KCMLOAMG_01435 | 2.4e-248 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
| KCMLOAMG_01436 | 1.2e-216 | yttB | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_01437 | 3.9e-145 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
| KCMLOAMG_01438 | 2e-163 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
| KCMLOAMG_01439 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
| KCMLOAMG_01440 | 3.7e-76 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_01441 | 6.8e-164 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
| KCMLOAMG_01442 | 5e-120 | qmcA | O | prohibitin homologues | ||
| KCMLOAMG_01443 | 3.2e-29 | |||||
| KCMLOAMG_01444 | 7.5e-132 | lys | M | Glycosyl hydrolases family 25 | ||
| KCMLOAMG_01445 | 1.1e-59 | S | Protein of unknown function (DUF1093) | |||
| KCMLOAMG_01447 | 2e-61 | S | Domain of unknown function (DUF4828) | |||
| KCMLOAMG_01448 | 1.7e-177 | mocA | S | Oxidoreductase | ||
| KCMLOAMG_01449 | 4.5e-236 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
| KCMLOAMG_01450 | 6.8e-48 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
| KCMLOAMG_01451 | 1.9e-71 | S | Domain of unknown function (DUF3284) | |||
| KCMLOAMG_01453 | 5.7e-07 | |||||
| KCMLOAMG_01454 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
| KCMLOAMG_01456 | 2.4e-239 | pepS | E | Thermophilic metalloprotease (M29) | ||
| KCMLOAMG_01457 | 2.7e-111 | K | Bacterial regulatory proteins, tetR family | |||
| KCMLOAMG_01458 | 1.4e-259 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
| KCMLOAMG_01459 | 7.3e-178 | yihY | S | Belongs to the UPF0761 family | ||
| KCMLOAMG_01460 | 1.9e-80 | fld | C | Flavodoxin | ||
| KCMLOAMG_01461 | 2.2e-159 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
| KCMLOAMG_01462 | 5.8e-194 | M | Glycosyltransferase like family 2 | |||
| KCMLOAMG_01464 | 4.5e-29 | |||||
| KCMLOAMG_01465 | 4.9e-125 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
| KCMLOAMG_01466 | 6.8e-198 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
| KCMLOAMG_01467 | 8.8e-170 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
| KCMLOAMG_01469 | 6.8e-307 | bglH | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
| KCMLOAMG_01470 | 0.0 | S | Bacterial membrane protein YfhO | |||
| KCMLOAMG_01471 | 2.6e-308 | S | Psort location CytoplasmicMembrane, score | |||
| KCMLOAMG_01472 | 1.6e-83 | S | Fic/DOC family | |||
| KCMLOAMG_01473 | 2.1e-171 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
| KCMLOAMG_01474 | 2.3e-108 | |||||
| KCMLOAMG_01475 | 8.6e-168 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
| KCMLOAMG_01476 | 2.1e-31 | cspC | K | Cold shock protein | ||
| KCMLOAMG_01477 | 2.5e-13 | chpR | T | PFAM SpoVT AbrB | ||
| KCMLOAMG_01478 | 8.1e-82 | yvbK | 3.1.3.25 | K | GNAT family | |
| KCMLOAMG_01479 | 2.3e-108 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
| KCMLOAMG_01480 | 1.2e-100 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
| KCMLOAMG_01481 | 9.5e-242 | pbuX | F | xanthine permease | ||
| KCMLOAMG_01482 | 1.9e-203 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
| KCMLOAMG_01483 | 1.8e-245 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
| KCMLOAMG_01484 | 1.2e-103 | |||||
| KCMLOAMG_01485 | 8e-129 | |||||
| KCMLOAMG_01486 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
| KCMLOAMG_01487 | 3.7e-108 | vanZ | V | VanZ like family | ||
| KCMLOAMG_01488 | 2.9e-151 | glcU | U | sugar transport | ||
| KCMLOAMG_01489 | 7.3e-258 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
| KCMLOAMG_01490 | 4.2e-225 | L | Pfam:Integrase_AP2 | |||
| KCMLOAMG_01491 | 8.8e-30 | |||||
| KCMLOAMG_01492 | 1.4e-61 | S | Pyridoxamine 5'-phosphate oxidase | |||
| KCMLOAMG_01495 | 7.8e-50 | S | Domain of unknown function (DUF4352) | |||
| KCMLOAMG_01496 | 1.6e-56 | |||||
| KCMLOAMG_01497 | 1.1e-15 | |||||
| KCMLOAMG_01498 | 2.3e-14 | E | IrrE N-terminal-like domain | |||
| KCMLOAMG_01499 | 1.7e-38 | K | Helix-turn-helix XRE-family like proteins | |||
| KCMLOAMG_01504 | 1.2e-97 | |||||
| KCMLOAMG_01506 | 2.1e-13 | |||||
| KCMLOAMG_01509 | 1e-151 | recT | L | RecT family | ||
| KCMLOAMG_01510 | 5.5e-132 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
| KCMLOAMG_01511 | 7.4e-135 | L | Replication initiation and membrane attachment | |||
| KCMLOAMG_01513 | 6.6e-63 | S | Hypothetical protein (DUF2513) | |||
| KCMLOAMG_01514 | 2e-08 | K | Cro/C1-type HTH DNA-binding domain | |||
| KCMLOAMG_01515 | 2.9e-49 | |||||
| KCMLOAMG_01516 | 7.6e-39 | |||||
| KCMLOAMG_01517 | 3e-65 | S | magnesium ion binding | |||
| KCMLOAMG_01518 | 8.5e-20 | |||||
| KCMLOAMG_01519 | 1.7e-27 | |||||
| KCMLOAMG_01520 | 1.3e-35 | S | Protein of unknown function (DUF1642) | |||
| KCMLOAMG_01523 | 9.1e-77 | |||||
| KCMLOAMG_01524 | 2.3e-156 | |||||
| KCMLOAMG_01525 | 2.2e-218 | S | GcrA cell cycle regulator | |||
| KCMLOAMG_01526 | 8.1e-54 | |||||
| KCMLOAMG_01527 | 8.9e-28 | S | Helix-turn-helix of insertion element transposase | |||
| KCMLOAMG_01528 | 1.3e-248 | S | Terminase-like family | |||
| KCMLOAMG_01529 | 2.7e-253 | S | Phage portal protein | |||
| KCMLOAMG_01530 | 1.2e-180 | S | head morphogenesis protein, SPP1 gp7 family | |||
| KCMLOAMG_01531 | 2.7e-96 | S | Domain of unknown function (DUF4355) | |||
| KCMLOAMG_01532 | 9e-184 | gpG | ||||
| KCMLOAMG_01533 | 6.7e-60 | S | Phage gp6-like head-tail connector protein | |||
| KCMLOAMG_01534 | 8.7e-50 | |||||
| KCMLOAMG_01535 | 1.4e-57 | S | Bacteriophage HK97-gp10, putative tail-component | |||
| KCMLOAMG_01536 | 8e-67 | S | Protein of unknown function (DUF3168) | |||
| KCMLOAMG_01537 | 1e-102 | S | Phage tail tube protein | |||
| KCMLOAMG_01538 | 1.3e-49 | S | Phage tail assembly chaperone protein, TAC | |||
| KCMLOAMG_01539 | 2.3e-54 | |||||
| KCMLOAMG_01540 | 7.2e-293 | S | phage tail tape measure protein | |||
| KCMLOAMG_01541 | 1.7e-266 | S | Phage tail protein | |||
| KCMLOAMG_01542 | 0.0 | S | cellulase activity | |||
| KCMLOAMG_01543 | 8.7e-15 | |||||
| KCMLOAMG_01544 | 3.4e-53 | |||||
| KCMLOAMG_01545 | 2.2e-43 | hol | S | Bacteriophage holin | ||
| KCMLOAMG_01546 | 1e-207 | M | Glycosyl hydrolases family 25 | |||
| KCMLOAMG_01548 | 3.3e-46 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
| KCMLOAMG_01549 | 1.4e-113 | F | DNA/RNA non-specific endonuclease | |||
| KCMLOAMG_01550 | 4.1e-77 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
| KCMLOAMG_01551 | 3.5e-79 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
| KCMLOAMG_01552 | 1.8e-138 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
| KCMLOAMG_01553 | 1.7e-173 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
| KCMLOAMG_01554 | 5.8e-85 | guaD | 3.5.4.12, 3.5.4.3, 3.5.4.33 | FJ | MafB19-like deaminase | |
| KCMLOAMG_01560 | 1.1e-210 | L | PFAM transposase, IS4 family protein | |||
| KCMLOAMG_01563 | 1.2e-17 | |||||
| KCMLOAMG_01564 | 3.3e-193 | yttB | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_01565 | 6.3e-284 | pipD | E | Dipeptidase | ||
| KCMLOAMG_01567 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_01570 | 8.7e-09 | |||||
| KCMLOAMG_01571 | 1.5e-132 | G | Phosphoglycerate mutase family | |||
| KCMLOAMG_01572 | 1.1e-121 | K | Bacterial regulatory proteins, tetR family | |||
| KCMLOAMG_01573 | 0.0 | ycfI | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01574 | 0.0 | yfiC | V | ABC transporter | ||
| KCMLOAMG_01575 | 2.5e-138 | S | NADPH-dependent FMN reductase | |||
| KCMLOAMG_01576 | 2.3e-164 | 1.13.11.2 | S | glyoxalase | ||
| KCMLOAMG_01577 | 8.9e-192 | ampC | V | Beta-lactamase | ||
| KCMLOAMG_01578 | 1e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
| KCMLOAMG_01579 | 6e-111 | tdk | 2.7.1.21 | F | thymidine kinase | |
| KCMLOAMG_01580 | 4.8e-191 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
| KCMLOAMG_01581 | 3.6e-154 | 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 | |
| KCMLOAMG_01582 | 1.2e-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 | |
| KCMLOAMG_01583 | 2e-233 | 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 | |
| KCMLOAMG_01584 | 4.4e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
| KCMLOAMG_01585 | 3.3e-124 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
| KCMLOAMG_01586 | 1.6e-26 | 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 | ||
| KCMLOAMG_01587 | 2.6e-51 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
| KCMLOAMG_01588 | 2.9e-88 | 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 | ||
| KCMLOAMG_01589 | 2.8e-285 | 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 | |
| KCMLOAMG_01590 | 1.2e-163 | 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 | ||
| KCMLOAMG_01591 | 1.8e-08 | |||||
| KCMLOAMG_01592 | 1.2e-248 | 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 | |
| KCMLOAMG_01593 | 1.6e-52 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
| KCMLOAMG_01594 | 6.4e-32 | ywzB | S | Protein of unknown function (DUF1146) | ||
| KCMLOAMG_01595 | 4.5e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
| KCMLOAMG_01596 | 1.4e-25 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
| KCMLOAMG_01597 | 1.6e-54 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
| KCMLOAMG_01598 | 1.3e-31 | S | Protein of unknown function (DUF2969) | |||
| KCMLOAMG_01599 | 7.6e-222 | rodA | D | Belongs to the SEDS family | ||
| KCMLOAMG_01600 | 1.2e-46 | gcvH | E | glycine cleavage | ||
| KCMLOAMG_01601 | 4.2e-214 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
| KCMLOAMG_01602 | 1.9e-147 | P | Belongs to the nlpA lipoprotein family | |||
| KCMLOAMG_01603 | 5e-148 | P | Belongs to the nlpA lipoprotein family | |||
| KCMLOAMG_01604 | 9.1e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
| KCMLOAMG_01605 | 1.1e-105 | metI | P | ABC transporter permease | ||
| KCMLOAMG_01606 | 1.9e-141 | sufC | O | FeS assembly ATPase SufC | ||
| KCMLOAMG_01607 | 1.3e-190 | sufD | O | FeS assembly protein SufD | ||
| KCMLOAMG_01608 | 2.1e-224 | csdA | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
| KCMLOAMG_01609 | 7.2e-77 | nifU | C | SUF system FeS assembly protein, NifU family | ||
| KCMLOAMG_01610 | 1.2e-279 | sufB | O | assembly protein SufB | ||
| KCMLOAMG_01611 | 1.8e-26 | |||||
| KCMLOAMG_01612 | 8.4e-66 | yueI | S | Protein of unknown function (DUF1694) | ||
| KCMLOAMG_01613 | 1.2e-180 | S | Protein of unknown function (DUF2785) | |||
| KCMLOAMG_01614 | 4.4e-158 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
| KCMLOAMG_01615 | 1.5e-83 | usp6 | T | universal stress protein | ||
| KCMLOAMG_01616 | 1.7e-39 | |||||
| KCMLOAMG_01617 | 6e-239 | rarA | L | recombination factor protein RarA | ||
| KCMLOAMG_01618 | 0.0 | 6.3.2.2, 6.3.2.4 | M | Mur ligase middle domain protein | ||
| KCMLOAMG_01619 | 1.7e-72 | yueI | S | Protein of unknown function (DUF1694) | ||
| KCMLOAMG_01620 | 1.6e-106 | yktB | S | Belongs to the UPF0637 family | ||
| KCMLOAMG_01621 | 8.4e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
| KCMLOAMG_01622 | 1.6e-149 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
| KCMLOAMG_01623 | 4.8e-120 | G | Phosphoglycerate mutase family | |||
| KCMLOAMG_01624 | 1.2e-154 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
| KCMLOAMG_01625 | 3.9e-165 | IQ | NAD dependent epimerase/dehydratase family | |||
| KCMLOAMG_01626 | 2.7e-137 | pnuC | H | nicotinamide mononucleotide transporter | ||
| KCMLOAMG_01627 | 8.9e-133 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
| KCMLOAMG_01628 | 5.8e-157 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
| KCMLOAMG_01629 | 3.6e-307 | oppA | E | ABC transporter, substratebinding protein | ||
| KCMLOAMG_01630 | 3.7e-152 | T | GHKL domain | |||
| KCMLOAMG_01631 | 4.7e-120 | T | Transcriptional regulatory protein, C terminal | |||
| KCMLOAMG_01632 | 2.7e-166 | bcrA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
| KCMLOAMG_01633 | 4.1e-128 | S | ABC-2 family transporter protein | |||
| KCMLOAMG_01634 | 9.7e-158 | K | Transcriptional regulator | |||
| KCMLOAMG_01635 | 3.6e-78 | yphH | S | Cupin domain | ||
| KCMLOAMG_01636 | 2.7e-54 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
| KCMLOAMG_01637 | 3e-105 | K | Psort location Cytoplasmic, score | |||
| KCMLOAMG_01638 | 1.7e-162 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_01639 | 6.5e-84 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_01640 | 9.7e-155 | S | Uncharacterised protein, DegV family COG1307 | |||
| KCMLOAMG_01641 | 3.1e-102 | desR | K | helix_turn_helix, Lux Regulon | ||
| KCMLOAMG_01642 | 7.5e-200 | desK | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_01643 | 1.5e-127 | yvfS | V | ABC-2 type transporter | ||
| KCMLOAMG_01644 | 5.7e-158 | yvfR | V | ABC transporter | ||
| KCMLOAMG_01645 | 2.5e-275 | |||||
| KCMLOAMG_01646 | 2.5e-181 | |||||
| KCMLOAMG_01647 | 0.0 | D | Putative exonuclease SbcCD, C subunit | |||
| KCMLOAMG_01648 | 2.2e-132 | S | Protein of unknown function C-terminus (DUF2399) | |||
| KCMLOAMG_01649 | 2.2e-82 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_01650 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
| KCMLOAMG_01651 | 7.4e-82 | |||||
| KCMLOAMG_01652 | 1.1e-138 | puuD | S | peptidase C26 | ||
| KCMLOAMG_01653 | 1e-227 | steT | E | Amino acid permease | ||
| KCMLOAMG_01656 | 2.1e-135 | L | Transposase DDE domain | |||
| KCMLOAMG_01657 | 9.7e-60 | S | SIR2-like domain | |||
| KCMLOAMG_01658 | 2.9e-74 | S | Domain of unknown function DUF87 | |||
| KCMLOAMG_01659 | 9.1e-267 | L | Transposase DDE domain | |||
| KCMLOAMG_01660 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_01661 | 1.2e-78 | S | cog cog0433 | |||
| KCMLOAMG_01662 | 2.2e-16 | S | Domain of unknown function (DUF4263) | |||
| KCMLOAMG_01663 | 2.1e-111 | 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 | ||
| KCMLOAMG_01664 | 1.7e-84 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
| KCMLOAMG_01665 | 1.2e-273 | 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 | ||
| KCMLOAMG_01666 | 3.9e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
| KCMLOAMG_01667 | 1.5e-225 | 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 | |
| KCMLOAMG_01668 | 1.3e-114 | rex | K | CoA binding domain | ||
| KCMLOAMG_01669 | 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 | |
| KCMLOAMG_01670 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
| KCMLOAMG_01671 | 8.7e-116 | S | Haloacid dehalogenase-like hydrolase | |||
| KCMLOAMG_01672 | 2e-118 | radC | L | DNA repair protein | ||
| KCMLOAMG_01673 | 1e-179 | mreB | D | cell shape determining protein MreB | ||
| KCMLOAMG_01674 | 8.5e-151 | mreC | M | Involved in formation and maintenance of cell shape | ||
| KCMLOAMG_01675 | 4.7e-83 | mreD | M | rod shape-determining protein MreD | ||
| KCMLOAMG_01676 | 1.4e-113 | 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 | ||
| KCMLOAMG_01677 | 1.3e-140 | minD | D | Belongs to the ParA family | ||
| KCMLOAMG_01678 | 4.7e-109 | artQ | P | ABC transporter permease | ||
| KCMLOAMG_01679 | 3.8e-111 | glnQ | 3.6.3.21 | E | ABC transporter | |
| KCMLOAMG_01680 | 2.1e-151 | aatB | ET | ABC transporter substrate-binding protein | ||
| KCMLOAMG_01682 | 3.1e-270 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
| KCMLOAMG_01683 | 4.2e-53 | |||||
| KCMLOAMG_01684 | 4.8e-78 | mraZ | K | Belongs to the MraZ family | ||
| KCMLOAMG_01685 | 1.8e-170 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
| KCMLOAMG_01686 | 6.2e-58 | ftsL | D | cell division protein FtsL | ||
| KCMLOAMG_01687 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
| KCMLOAMG_01688 | 9.2e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
| KCMLOAMG_01689 | 5e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
| KCMLOAMG_01690 | 1.4e-198 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
| KCMLOAMG_01691 | 1.3e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
| KCMLOAMG_01692 | 6.9e-224 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
| KCMLOAMG_01693 | 3.1e-218 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
| KCMLOAMG_01694 | 6.7e-78 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
| KCMLOAMG_01695 | 3.4e-43 | yggT | D | integral membrane protein | ||
| KCMLOAMG_01696 | 6.4e-145 | ylmH | S | S4 domain protein | ||
| KCMLOAMG_01697 | 1.9e-80 | divIVA | D | DivIVA protein | ||
| KCMLOAMG_01698 | 0.0 | ileS | 6.1.1.5 | J | 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) | |
| KCMLOAMG_01699 | 8.2e-37 | cspA | K | Cold shock protein | ||
| KCMLOAMG_01700 | 1.5e-145 | pstS | P | Phosphate | ||
| KCMLOAMG_01701 | 3.6e-263 | ydiC1 | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_01702 | 6.2e-208 | yaaN | P | Toxic anion resistance protein (TelA) | ||
| KCMLOAMG_01703 | 6.9e-116 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
| KCMLOAMG_01704 | 3.1e-98 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
| KCMLOAMG_01705 | 5.8e-34 | |||||
| KCMLOAMG_01706 | 2.4e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
| KCMLOAMG_01707 | 9.9e-219 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
| KCMLOAMG_01708 | 2.6e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
| KCMLOAMG_01709 | 0.0 | uvrA2 | L | ABC transporter | ||
| KCMLOAMG_01710 | 2.8e-218 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
| KCMLOAMG_01712 | 1.3e-122 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
| KCMLOAMG_01713 | 1.4e-116 | S | Repeat protein | |||
| KCMLOAMG_01714 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
| KCMLOAMG_01715 | 4.6e-243 | els | S | Sterol carrier protein domain | ||
| KCMLOAMG_01716 | 8.5e-184 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| KCMLOAMG_01717 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
| KCMLOAMG_01718 | 4.9e-31 | ykzG | S | Belongs to the UPF0356 family | ||
| KCMLOAMG_01720 | 2.4e-72 | |||||
| KCMLOAMG_01721 | 2.5e-25 | |||||
| KCMLOAMG_01722 | 1.2e-100 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
| KCMLOAMG_01723 | 2.1e-135 | S | E1-E2 ATPase | |||
| KCMLOAMG_01724 | 1.1e-209 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
| KCMLOAMG_01725 | 1.8e-181 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
| KCMLOAMG_01726 | 3.1e-242 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
| KCMLOAMG_01727 | 2.4e-259 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
| KCMLOAMG_01728 | 8.3e-157 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
| KCMLOAMG_01729 | 3.2e-46 | yktA | S | Belongs to the UPF0223 family | ||
| KCMLOAMG_01730 | 5e-145 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
| KCMLOAMG_01731 | 0.0 | typA | T | GTP-binding protein TypA | ||
| KCMLOAMG_01732 | 6.5e-210 | ftsW | D | Belongs to the SEDS family | ||
| KCMLOAMG_01733 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
| KCMLOAMG_01734 | 2.5e-56 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
| KCMLOAMG_01735 | 1.7e-99 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
| KCMLOAMG_01736 | 4e-84 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
| KCMLOAMG_01737 | 7.9e-194 | ylbL | T | Belongs to the peptidase S16 family | ||
| KCMLOAMG_01738 | 4.2e-105 | comEA | L | Competence protein ComEA | ||
| KCMLOAMG_01739 | 0.0 | comEC | S | Competence protein ComEC | ||
| KCMLOAMG_01740 | 2.2e-193 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
| KCMLOAMG_01741 | 2.3e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
| KCMLOAMG_01742 | 5.4e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
| KCMLOAMG_01743 | 1.5e-126 | |||||
| KCMLOAMG_01744 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
| KCMLOAMG_01745 | 1.6e-160 | S | Tetratricopeptide repeat | |||
| KCMLOAMG_01746 | 1.2e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
| KCMLOAMG_01747 | 1.7e-82 | M | Protein of unknown function (DUF3737) | |||
| KCMLOAMG_01748 | 4.8e-134 | cobB | K | Sir2 family | ||
| KCMLOAMG_01749 | 1.7e-63 | pcaC | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
| KCMLOAMG_01750 | 9.3e-65 | rmeD | K | helix_turn_helix, mercury resistance | ||
| KCMLOAMG_01751 | 0.0 | yknV | V | ABC transporter | ||
| KCMLOAMG_01752 | 2.1e-196 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
| KCMLOAMG_01753 | 2.9e-232 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
| KCMLOAMG_01754 | 3.1e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
| KCMLOAMG_01755 | 2.3e-47 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
| KCMLOAMG_01756 | 2.3e-20 | |||||
| KCMLOAMG_01757 | 6.1e-258 | glnPH2 | P | ABC transporter permease | ||
| KCMLOAMG_01758 | 2.4e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
| KCMLOAMG_01759 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
| KCMLOAMG_01760 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
| KCMLOAMG_01761 | 9.4e-156 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
| KCMLOAMG_01762 | 7.7e-132 | fruR | K | DeoR C terminal sensor domain | ||
| KCMLOAMG_01763 | 1.6e-233 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
| KCMLOAMG_01764 | 0.0 | oatA | I | Acyltransferase | ||
| KCMLOAMG_01765 | 1.5e-183 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
| KCMLOAMG_01766 | 9.6e-141 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
| KCMLOAMG_01767 | 1.3e-46 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
| KCMLOAMG_01768 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
| KCMLOAMG_01769 | 3.5e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
| KCMLOAMG_01770 | 9.6e-95 | M1-874 | K | Domain of unknown function (DUF1836) | ||
| KCMLOAMG_01771 | 4.7e-301 | cpdB | 3.1.3.6, 3.1.4.16 | F | 5'-nucleotidase, C-terminal domain | |
| KCMLOAMG_01772 | 9.2e-145 | |||||
| KCMLOAMG_01773 | 1.3e-19 | S | Protein of unknown function (DUF2929) | |||
| KCMLOAMG_01774 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
| KCMLOAMG_01775 | 3.5e-177 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
| KCMLOAMG_01776 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
| KCMLOAMG_01777 | 7.2e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
| KCMLOAMG_01778 | 3.4e-163 | cvfB | S | S1 domain | ||
| KCMLOAMG_01779 | 3.3e-166 | xerD | D | recombinase XerD | ||
| KCMLOAMG_01780 | 3.4e-67 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
| KCMLOAMG_01781 | 7.3e-127 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
| KCMLOAMG_01782 | 3.3e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
| KCMLOAMG_01783 | 9.4e-138 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
| KCMLOAMG_01784 | 2.4e-96 | U | 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 | |||
| KCMLOAMG_01785 | 1.4e-45 | fer | C | 4Fe-4S single cluster domain of Ferredoxin I | ||
| KCMLOAMG_01786 | 1e-179 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
| KCMLOAMG_01787 | 1.3e-265 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
| KCMLOAMG_01788 | 3.8e-55 | M | Lysin motif | |||
| KCMLOAMG_01789 | 2.6e-115 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
| KCMLOAMG_01790 | 1.1e-218 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
| KCMLOAMG_01791 | 5.3e-245 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
| KCMLOAMG_01792 | 2e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
| KCMLOAMG_01793 | 2.6e-236 | S | Tetratricopeptide repeat protein | |||
| KCMLOAMG_01794 | 4.8e-149 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
| KCMLOAMG_01795 | 9.5e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
| KCMLOAMG_01796 | 9.6e-85 | |||||
| KCMLOAMG_01797 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01798 | 4.2e-191 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
| KCMLOAMG_01799 | 8.8e-92 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
| KCMLOAMG_01800 | 8.1e-114 | hly | S | protein, hemolysin III | ||
| KCMLOAMG_01801 | 6.6e-148 | DegV | S | EDD domain protein, DegV family | ||
| KCMLOAMG_01802 | 7.8e-157 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
| KCMLOAMG_01803 | 2.4e-113 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
| KCMLOAMG_01804 | 1.8e-95 | msrA | 1.8.4.11, 1.8.4.12 | C | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
| KCMLOAMG_01805 | 2.3e-40 | yozE | S | Belongs to the UPF0346 family | ||
| KCMLOAMG_01806 | 8e-258 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
| KCMLOAMG_01807 | 6.8e-56 | |||||
| KCMLOAMG_01809 | 1.6e-126 | S | Domain of unknown function (DUF4918) | |||
| KCMLOAMG_01810 | 8.8e-156 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
| KCMLOAMG_01811 | 9.6e-138 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
| KCMLOAMG_01812 | 1.5e-144 | dprA | LU | DNA protecting protein DprA | ||
| KCMLOAMG_01813 | 0.0 | topA | 5.99.1.2 | L | 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 | |
| KCMLOAMG_01814 | 6.1e-249 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
| KCMLOAMG_01815 | 4.7e-168 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
| KCMLOAMG_01816 | 5.5e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
| KCMLOAMG_01817 | 2.5e-256 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
| KCMLOAMG_01818 | 6.2e-173 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
| KCMLOAMG_01819 | 6.9e-110 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
| KCMLOAMG_01820 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
| KCMLOAMG_01821 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
| KCMLOAMG_01822 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
| KCMLOAMG_01823 | 2.1e-170 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
| KCMLOAMG_01824 | 5.2e-181 | K | LysR substrate binding domain | |||
| KCMLOAMG_01825 | 9.5e-172 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
| KCMLOAMG_01826 | 5.8e-208 | xerS | L | Belongs to the 'phage' integrase family | ||
| KCMLOAMG_01827 | 0.0 | ysaB | V | FtsX-like permease family | ||
| KCMLOAMG_01828 | 2.2e-134 | XK27_05695 | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_01829 | 1e-173 | T | Histidine kinase-like ATPases | |||
| KCMLOAMG_01830 | 1.7e-128 | T | Transcriptional regulatory protein, C terminal | |||
| KCMLOAMG_01831 | 3e-218 | EGP | Transmembrane secretion effector | |||
| KCMLOAMG_01832 | 7.1e-68 | msi198 | K | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_01833 | 5.9e-70 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_01834 | 7.5e-112 | nfnB | 1.5.1.34 | C | Nitroreductase family | |
| KCMLOAMG_01835 | 3.2e-147 | Q | Fumarylacetoacetate (FAA) hydrolase family | |||
| KCMLOAMG_01836 | 8.3e-207 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
| KCMLOAMG_01837 | 2.3e-51 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
| KCMLOAMG_01838 | 1.4e-56 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
| KCMLOAMG_01839 | 1e-131 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
| KCMLOAMG_01840 | 3.1e-133 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
| KCMLOAMG_01841 | 3e-113 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
| KCMLOAMG_01842 | 2.4e-104 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
| KCMLOAMG_01843 | 1.7e-09 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
| KCMLOAMG_01844 | 3.2e-226 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
| KCMLOAMG_01845 | 3.5e-109 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
| KCMLOAMG_01846 | 9.2e-217 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
| KCMLOAMG_01847 | 1.3e-207 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
| KCMLOAMG_01848 | 1.5e-100 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
| KCMLOAMG_01849 | 3.2e-161 | degV | S | EDD domain protein, DegV family | ||
| KCMLOAMG_01850 | 1.3e-06 | |||||
| KCMLOAMG_01851 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
| KCMLOAMG_01852 | 6.2e-51 | S | MazG-like family | |||
| KCMLOAMG_01853 | 3.2e-193 | pfoS | S | Phosphotransferase system, EIIC | ||
| KCMLOAMG_01854 | 5.3e-113 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
| KCMLOAMG_01855 | 4.7e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
| KCMLOAMG_01856 | 4.2e-153 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
| KCMLOAMG_01857 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
| KCMLOAMG_01858 | 1e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
| KCMLOAMG_01859 | 2.1e-238 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
| KCMLOAMG_01860 | 7.3e-180 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
| KCMLOAMG_01861 | 2.6e-236 | pyrP | F | Permease | ||
| KCMLOAMG_01862 | 1.7e-96 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
| KCMLOAMG_01863 | 1.4e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
| KCMLOAMG_01864 | 1.2e-81 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
| KCMLOAMG_01865 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
| KCMLOAMG_01866 | 1.4e-63 | S | Family of unknown function (DUF5322) | |||
| KCMLOAMG_01867 | 2.7e-67 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
| KCMLOAMG_01868 | 5.7e-109 | XK27_02070 | S | Nitroreductase family | ||
| KCMLOAMG_01869 | 2.8e-279 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
| KCMLOAMG_01870 | 3.3e-55 | |||||
| KCMLOAMG_01871 | 3.1e-270 | K | Mga helix-turn-helix domain | |||
| KCMLOAMG_01872 | 4.5e-38 | nrdH | O | Glutaredoxin | ||
| KCMLOAMG_01873 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
| KCMLOAMG_01874 | 4e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
| KCMLOAMG_01875 | 4.5e-163 | K | Transcriptional regulator | |||
| KCMLOAMG_01876 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
| KCMLOAMG_01877 | 4.8e-193 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
| KCMLOAMG_01878 | 1.5e-33 | |||||
| KCMLOAMG_01879 | 1e-173 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
| KCMLOAMG_01880 | 1.6e-216 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
| KCMLOAMG_01882 | 1.8e-66 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
| KCMLOAMG_01883 | 1.2e-105 | ypsA | S | Belongs to the UPF0398 family | ||
| KCMLOAMG_01884 | 3.3e-120 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
| KCMLOAMG_01885 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
| KCMLOAMG_01886 | 1.2e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
| KCMLOAMG_01887 | 2.8e-114 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
| KCMLOAMG_01888 | 4e-110 | dnaD | L | DnaD domain protein | ||
| KCMLOAMG_01889 | 2.3e-256 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
| KCMLOAMG_01890 | 6.9e-220 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
| KCMLOAMG_01891 | 6.1e-85 | ypmB | S | Protein conserved in bacteria | ||
| KCMLOAMG_01892 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
| KCMLOAMG_01893 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
| KCMLOAMG_01894 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
| KCMLOAMG_01895 | 4.6e-166 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
| KCMLOAMG_01896 | 9.6e-178 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
| KCMLOAMG_01897 | 3.4e-194 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
| KCMLOAMG_01898 | 3.5e-260 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
| KCMLOAMG_01899 | 7.2e-175 | |||||
| KCMLOAMG_01900 | 5.9e-140 | |||||
| KCMLOAMG_01901 | 9.7e-61 | yitW | S | Iron-sulfur cluster assembly protein | ||
| KCMLOAMG_01902 | 1.9e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
| KCMLOAMG_01903 | 7.2e-270 | V | (ABC) transporter | |||
| KCMLOAMG_01904 | 1.3e-307 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_01905 | 6.3e-148 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
| KCMLOAMG_01906 | 7.1e-127 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
| KCMLOAMG_01907 | 4.4e-196 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
| KCMLOAMG_01908 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
| KCMLOAMG_01909 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
| KCMLOAMG_01910 | 8.8e-175 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
| KCMLOAMG_01911 | 6.5e-93 | 2.3.1.128, 5.2.1.8 | J | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_01912 | 1.1e-06 | S | ABC-2 family transporter protein | |||
| KCMLOAMG_01913 | 3.7e-123 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_01914 | 3.5e-54 | |||||
| KCMLOAMG_01915 | 1.4e-147 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
| KCMLOAMG_01916 | 1.2e-168 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
| KCMLOAMG_01917 | 1.8e-63 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
| KCMLOAMG_01918 | 1.5e-65 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
| KCMLOAMG_01919 | 1.4e-83 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
| KCMLOAMG_01920 | 7.7e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
| KCMLOAMG_01921 | 1.6e-68 | yqeY | S | YqeY-like protein | ||
| KCMLOAMG_01922 | 2.9e-21 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
| KCMLOAMG_01923 | 7.2e-155 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
| KCMLOAMG_01924 | 7.9e-168 | nfo | 3.1.21.2 | L | 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 | |
| KCMLOAMG_01925 | 4.4e-169 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
| KCMLOAMG_01926 | 1.1e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
| KCMLOAMG_01927 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
| KCMLOAMG_01928 | 1.4e-242 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
| KCMLOAMG_01929 | 1e-268 | |||||
| KCMLOAMG_01930 | 1.5e-158 | V | ABC transporter | |||
| KCMLOAMG_01931 | 7.7e-79 | FG | adenosine 5'-monophosphoramidase activity | |||
| KCMLOAMG_01932 | 5.2e-248 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
| KCMLOAMG_01933 | 7.9e-114 | 3.1.3.18 | J | HAD-hyrolase-like | ||
| KCMLOAMG_01934 | 1e-75 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
| KCMLOAMG_01935 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
| KCMLOAMG_01936 | 4e-53 | |||||
| KCMLOAMG_01937 | 5.8e-124 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
| KCMLOAMG_01938 | 3e-173 | prmA | J | Ribosomal protein L11 methyltransferase | ||
| KCMLOAMG_01939 | 3.6e-85 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
| KCMLOAMG_01940 | 9.4e-112 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
| KCMLOAMG_01941 | 3.1e-37 | |||||
| KCMLOAMG_01942 | 9.7e-62 | S | Protein of unknown function (DUF1093) | |||
| KCMLOAMG_01943 | 8.9e-26 | |||||
| KCMLOAMG_01944 | 3.2e-61 | |||||
| KCMLOAMG_01946 | 6.9e-18 | M | Host cell surface-exposed lipoprotein | |||
| KCMLOAMG_01947 | 2.2e-145 | hutG | 3.5.3.8 | E | N-formylglutamate amidohydrolase | |
| KCMLOAMG_01948 | 1.2e-54 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
| KCMLOAMG_01949 | 3.7e-90 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
| KCMLOAMG_01950 | 1.7e-93 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
| KCMLOAMG_01951 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
| KCMLOAMG_01952 | 7.1e-62 | |||||
| KCMLOAMG_01953 | 1.4e-81 | 6.3.3.2 | S | ASCH | ||
| KCMLOAMG_01954 | 5.9e-32 | |||||
| KCMLOAMG_01955 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
| KCMLOAMG_01956 | 4.1e-188 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
| KCMLOAMG_01957 | 1e-286 | dnaK | O | Heat shock 70 kDa protein | ||
| KCMLOAMG_01958 | 1.4e-99 | grpE | O | 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 | ||
| KCMLOAMG_01959 | 8.4e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
| KCMLOAMG_01960 | 1.7e-223 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
| KCMLOAMG_01961 | 2.5e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
| KCMLOAMG_01962 | 8.1e-160 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
| KCMLOAMG_01963 | 1.5e-118 | terC | P | membrane | ||
| KCMLOAMG_01964 | 7.8e-58 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
| KCMLOAMG_01965 | 0.0 | infB | J | 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 | ||
| KCMLOAMG_01966 | 5.4e-44 | ylxQ | J | ribosomal protein | ||
| KCMLOAMG_01967 | 1.5e-46 | ylxR | K | Protein of unknown function (DUF448) | ||
| KCMLOAMG_01968 | 2.5e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
| KCMLOAMG_01969 | 1e-84 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
| KCMLOAMG_01970 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
| KCMLOAMG_01971 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
| KCMLOAMG_01972 | 1e-229 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
| KCMLOAMG_01973 | 4.3e-141 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
| KCMLOAMG_01974 | 9.5e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
| KCMLOAMG_01975 | 4e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
| KCMLOAMG_01976 | 2.2e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
| KCMLOAMG_01977 | 2e-155 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
| KCMLOAMG_01978 | 1.8e-131 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
| KCMLOAMG_01979 | 4.9e-47 | yazA | L | GIY-YIG catalytic domain protein | ||
| KCMLOAMG_01980 | 4.8e-134 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
| KCMLOAMG_01981 | 2.2e-122 | plsC | 2.3.1.51 | I | Acyltransferase | |
| KCMLOAMG_01982 | 6.6e-201 | bcaP | E | Amino Acid | ||
| KCMLOAMG_01983 | 2.9e-137 | yejC | S | Protein of unknown function (DUF1003) | ||
| KCMLOAMG_01984 | 0.0 | mdlB | V | ABC transporter | ||
| KCMLOAMG_01985 | 0.0 | mdlA | V | ABC transporter | ||
| KCMLOAMG_01986 | 4.8e-29 | yneF | S | UPF0154 protein | ||
| KCMLOAMG_01987 | 1.1e-37 | ynzC | S | UPF0291 protein | ||
| KCMLOAMG_01988 | 1.1e-25 | |||||
| KCMLOAMG_01989 | 6.5e-57 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
| KCMLOAMG_01990 | 3.1e-147 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
| KCMLOAMG_01991 | 7.6e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
| KCMLOAMG_01992 | 8.4e-38 | ylqC | S | Belongs to the UPF0109 family | ||
| KCMLOAMG_01993 | 1e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
| KCMLOAMG_01994 | 1.2e-229 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
| KCMLOAMG_01995 | 1.3e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
| KCMLOAMG_01996 | 1.8e-24 | |||||
| KCMLOAMG_01997 | 8.8e-53 | |||||
| KCMLOAMG_01998 | 9.8e-183 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
| KCMLOAMG_01999 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
| KCMLOAMG_02000 | 1.9e-124 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
| KCMLOAMG_02001 | 0.0 | oppA1 | E | ABC transporter substrate-binding protein | ||
| KCMLOAMG_02002 | 8.2e-136 | oppC | EP | Binding-protein-dependent transport system inner membrane component | ||
| KCMLOAMG_02003 | 2.8e-174 | oppB | P | ABC transporter permease | ||
| KCMLOAMG_02004 | 1.4e-178 | oppF | P | Belongs to the ABC transporter superfamily | ||
| KCMLOAMG_02005 | 4.4e-194 | oppD | P | Belongs to the ABC transporter superfamily | ||
| KCMLOAMG_02006 | 8.9e-37 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
| KCMLOAMG_02007 | 4e-187 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
| KCMLOAMG_02008 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
| KCMLOAMG_02009 | 4.7e-286 | yloV | S | DAK2 domain fusion protein YloV | ||
| KCMLOAMG_02010 | 2.3e-57 | asp | S | Asp23 family, cell envelope-related function | ||
| KCMLOAMG_02011 | 2.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
| KCMLOAMG_02012 | 3.1e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
| KCMLOAMG_02013 | 1.5e-115 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
| KCMLOAMG_02014 | 4.3e-169 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
| KCMLOAMG_02015 | 0.0 | KLT | serine threonine protein kinase | |||
| KCMLOAMG_02016 | 2e-135 | stp | 3.1.3.16 | T | phosphatase | |
| KCMLOAMG_02017 | 8.7e-251 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
| KCMLOAMG_02018 | 6.5e-176 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
| KCMLOAMG_02019 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
| KCMLOAMG_02020 | 1.4e-215 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
| KCMLOAMG_02021 | 2.9e-35 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
| KCMLOAMG_02022 | 3.2e-115 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
| KCMLOAMG_02023 | 1.6e-120 | rssA | S | Patatin-like phospholipase | ||
| KCMLOAMG_02024 | 3e-50 | |||||
| KCMLOAMG_02025 | 1.7e-307 | recN | L | May be involved in recombinational repair of damaged DNA | ||
| KCMLOAMG_02026 | 2e-74 | argR | K | Regulates arginine biosynthesis genes | ||
| KCMLOAMG_02027 | 3e-153 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
| KCMLOAMG_02028 | 9.7e-147 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
| KCMLOAMG_02029 | 1.6e-32 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
| KCMLOAMG_02030 | 1.1e-245 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
| KCMLOAMG_02031 | 5e-151 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
| KCMLOAMG_02032 | 2e-66 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
| KCMLOAMG_02033 | 1.5e-72 | yqhY | S | Asp23 family, cell envelope-related function | ||
| KCMLOAMG_02034 | 6.3e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
| KCMLOAMG_02035 | 7e-203 | ypdF | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
| KCMLOAMG_02036 | 1.7e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
| KCMLOAMG_02037 | 1e-54 | ysxB | J | Cysteine protease Prp | ||
| KCMLOAMG_02038 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
| KCMLOAMG_02039 | 1.3e-32 | |||||
| KCMLOAMG_02040 | 4.1e-14 | |||||
| KCMLOAMG_02041 | 7.4e-233 | ywhK | S | Membrane | ||
| KCMLOAMG_02043 | 5.4e-263 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_02044 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
| KCMLOAMG_02045 | 5.8e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
| KCMLOAMG_02046 | 1e-60 | glnR | K | Transcriptional regulator | ||
| KCMLOAMG_02047 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
| KCMLOAMG_02048 | 5.9e-241 | ynbB | 4.4.1.1 | P | aluminum resistance | |
| KCMLOAMG_02049 | 5.7e-180 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
| KCMLOAMG_02050 | 9.8e-25 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
| KCMLOAMG_02051 | 3.7e-72 | yqhL | P | Rhodanese-like protein | ||
| KCMLOAMG_02052 | 2e-177 | glk | 2.7.1.2 | G | Glucokinase | |
| KCMLOAMG_02053 | 1.1e-40 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
| KCMLOAMG_02054 | 9.6e-121 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
| KCMLOAMG_02055 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
| KCMLOAMG_02056 | 0.0 | S | Bacterial membrane protein YfhO | |||
| KCMLOAMG_02057 | 2.9e-53 | yneR | S | Belongs to the HesB IscA family | ||
| KCMLOAMG_02058 | 5.8e-115 | vraR | K | helix_turn_helix, Lux Regulon | ||
| KCMLOAMG_02059 | 2.3e-182 | vraS | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_02060 | 2.3e-122 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
| KCMLOAMG_02061 | 9e-78 | greA | K | 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. GreA releases sequences of 2 to 3 nucleotides | ||
| KCMLOAMG_02062 | 4.7e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
| KCMLOAMG_02063 | 1.1e-206 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
| KCMLOAMG_02064 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
| KCMLOAMG_02065 | 6.4e-201 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
| KCMLOAMG_02066 | 6.9e-68 | yodB | K | Transcriptional regulator, HxlR family | ||
| KCMLOAMG_02067 | 5.6e-94 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
| KCMLOAMG_02068 | 2.1e-137 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
| KCMLOAMG_02069 | 6e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
| KCMLOAMG_02070 | 3.8e-179 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
| KCMLOAMG_02071 | 3.6e-288 | arlS | 2.7.13.3 | T | Histidine kinase | |
| KCMLOAMG_02072 | 7.9e-123 | K | response regulator | |||
| KCMLOAMG_02073 | 1.6e-271 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
| KCMLOAMG_02074 | 5.6e-140 | M | Peptidase family M23 | |||
| KCMLOAMG_02075 | 1.6e-165 | L | Probable transposase | |||
| KCMLOAMG_02076 | 2.2e-58 | L | Probable transposase | |||
| KCMLOAMG_02077 | 7.1e-18 | yhcX | S | Psort location Cytoplasmic, score | ||
| KCMLOAMG_02079 | 7.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
| KCMLOAMG_02080 | 1.1e-206 | ylbM | S | Belongs to the UPF0348 family | ||
| KCMLOAMG_02081 | 1.9e-138 | yqeM | Q | Methyltransferase | ||
| KCMLOAMG_02082 | 1.9e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
| KCMLOAMG_02083 | 2.5e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
| KCMLOAMG_02084 | 9.4e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
| KCMLOAMG_02085 | 1.1e-47 | yhbY | J | RNA-binding protein | ||
| KCMLOAMG_02086 | 4e-217 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
| KCMLOAMG_02087 | 2.4e-95 | yqeG | S | HAD phosphatase, family IIIA | ||
| KCMLOAMG_02088 | 8.9e-167 | ykcA | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
| KCMLOAMG_02089 | 7.3e-191 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
| KCMLOAMG_02090 | 1.8e-121 | mhqD | S | Dienelactone hydrolase family | ||
| KCMLOAMG_02091 | 4.4e-180 | 3.5.1.10 | C | Alcohol dehydrogenase GroES-like domain | ||
| KCMLOAMG_02092 | 1.5e-100 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
| KCMLOAMG_02093 | 1.1e-56 | rplT | J | 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 | ||
| KCMLOAMG_02094 | 9e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
| KCMLOAMG_02095 | 8.9e-78 | infC | J | 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 | ||
| KCMLOAMG_02096 | 9e-72 | K | Transcriptional regulator | |||
| KCMLOAMG_02097 | 3.1e-232 | EGP | Major Facilitator Superfamily | |||
| KCMLOAMG_02098 | 1.7e-136 | cobB | K | Sir2 family | ||
| KCMLOAMG_02099 | 2.4e-127 | S | SseB protein N-terminal domain | |||
| KCMLOAMG_02100 | 3.6e-64 | |||||
| KCMLOAMG_02101 | 7.2e-61 | yrgI | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
| KCMLOAMG_02102 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
| KCMLOAMG_02103 | 1.2e-169 | dnaI | L | Primosomal protein DnaI | ||
| KCMLOAMG_02104 | 5.1e-251 | dnaB | L | replication initiation and membrane attachment | ||
| KCMLOAMG_02105 | 3.3e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
| KCMLOAMG_02106 | 1e-102 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
| KCMLOAMG_02107 | 5.5e-158 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
| KCMLOAMG_02108 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
| KCMLOAMG_02109 | 2.3e-117 | ybhL | S | Inhibitor of apoptosis-promoting Bax1 | ||
| KCMLOAMG_02111 | 6.7e-190 | S | Cell surface protein | |||
| KCMLOAMG_02113 | 8.4e-137 | S | WxL domain surface cell wall-binding | |||
| KCMLOAMG_02114 | 0.0 | N | domain, Protein | |||
| KCMLOAMG_02115 | 5.9e-264 | K | Mga helix-turn-helix domain | |||
| KCMLOAMG_02116 | 1.2e-252 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
| KCMLOAMG_02117 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
| KCMLOAMG_02119 | 9.9e-112 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
| KCMLOAMG_02120 | 7.2e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
| KCMLOAMG_02122 | 2.9e-119 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
| KCMLOAMG_02123 | 1.2e-148 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
| KCMLOAMG_02124 | 2.8e-224 | ecsB | U | ABC transporter | ||
| KCMLOAMG_02125 | 2.2e-131 | ecsA | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_02126 | 1.1e-74 | hit | FG | histidine triad | ||
| KCMLOAMG_02127 | 4.8e-47 | yhaH | S | YtxH-like protein | ||
| KCMLOAMG_02128 | 1.3e-157 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
| KCMLOAMG_02129 | 9.6e-183 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
| KCMLOAMG_02130 | 4.6e-55 | yheA | S | Control of competence regulator ComK, YlbF/YmcA | ||
| KCMLOAMG_02131 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
| KCMLOAMG_02132 | 9.4e-68 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
| KCMLOAMG_02133 | 1.1e-65 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
| KCMLOAMG_02134 | 5.3e-75 | argR | K | Regulates arginine biosynthesis genes | ||
| KCMLOAMG_02135 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
| KCMLOAMG_02137 | 1.2e-67 | |||||
| KCMLOAMG_02138 | 1.5e-20 | |||||
| KCMLOAMG_02139 | 1.2e-177 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
| KCMLOAMG_02140 | 1.2e-303 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
| KCMLOAMG_02141 | 5.1e-122 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
| KCMLOAMG_02142 | 1.5e-65 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
| KCMLOAMG_02143 | 1.2e-137 | yhfI | S | Metallo-beta-lactamase superfamily | ||
| KCMLOAMG_02144 | 2.9e-90 | traP | 1.14.99.57, 6.2.1.3 | S | Antibiotic biosynthesis monooxygenase | |
| KCMLOAMG_02145 | 0.0 | V | ABC transporter (permease) | |||
| KCMLOAMG_02146 | 1.3e-137 | bceA | V | ABC transporter | ||
| KCMLOAMG_02147 | 1e-122 | K | response regulator | |||
| KCMLOAMG_02148 | 1.3e-207 | T | PhoQ Sensor | |||
| KCMLOAMG_02149 | 3.2e-109 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
| KCMLOAMG_02150 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
| KCMLOAMG_02151 | 1.6e-76 | copR | K | Copper transport repressor CopY TcrY | ||
| KCMLOAMG_02152 | 2e-217 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
| KCMLOAMG_02153 | 3.5e-288 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
| KCMLOAMG_02154 | 7.8e-100 | purN | 2.1.2.2 | F | 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 | |
| KCMLOAMG_02155 | 1.6e-185 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
| KCMLOAMG_02156 | 2e-277 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
| KCMLOAMG_02157 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| KCMLOAMG_02158 | 3.3e-129 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| KCMLOAMG_02159 | 6.4e-41 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| KCMLOAMG_02160 | 2.3e-133 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
| KCMLOAMG_02161 | 5.1e-212 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
| KCMLOAMG_02162 | 2.2e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
| KCMLOAMG_02163 | 1.6e-103 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
| KCMLOAMG_02165 | 1.8e-254 | iolT | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_02166 | 7.4e-12 | |||||
| KCMLOAMG_02167 | 0.0 | ptsI | 2.7.3.9 | G | 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) | |
| KCMLOAMG_02168 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
| KCMLOAMG_02169 | 2e-28 | |||||
| KCMLOAMG_02170 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
| KCMLOAMG_02171 | 4.3e-46 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
| KCMLOAMG_02172 | 2.3e-303 | prfC | J | 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 | ||
| KCMLOAMG_02173 | 8.7e-243 | hlyX | S | Transporter associated domain | ||
| KCMLOAMG_02174 | 6.8e-207 | yueF | S | AI-2E family transporter | ||
| KCMLOAMG_02175 | 2.1e-73 | S | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_02176 | 2.8e-96 | |||||
| KCMLOAMG_02177 | 1.4e-104 | ygaC | J | Belongs to the UPF0374 family | ||
| KCMLOAMG_02178 | 4.1e-139 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
| KCMLOAMG_02179 | 6.7e-292 | frvR | K | Mga helix-turn-helix domain | ||
| KCMLOAMG_02180 | 9.9e-58 | |||||
| KCMLOAMG_02181 | 9.4e-253 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
| KCMLOAMG_02182 | 1.3e-79 | F | Nucleoside 2-deoxyribosyltransferase | |||
| KCMLOAMG_02183 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
| KCMLOAMG_02184 | 2.5e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
| KCMLOAMG_02185 | 1.4e-210 | mvaA | 1.1.1.34, 1.1.1.88 | C | Belongs to the HMG-CoA reductase family | |
| KCMLOAMG_02186 | 5e-210 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
| KCMLOAMG_02187 | 2.4e-47 | |||||
| KCMLOAMG_02188 | 8.8e-161 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
| KCMLOAMG_02189 | 1.8e-101 | V | Restriction endonuclease | |||
| KCMLOAMG_02190 | 4.1e-158 | 5.1.3.3 | G | Aldose 1-epimerase | ||
| KCMLOAMG_02191 | 1.4e-209 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
| KCMLOAMG_02192 | 4.4e-101 | S | ECF transporter, substrate-specific component | |||
| KCMLOAMG_02194 | 6.6e-81 | yodP | 2.3.1.264 | K | FR47-like protein | |
| KCMLOAMG_02195 | 5.8e-82 | ydcK | S | Belongs to the SprT family | ||
| KCMLOAMG_02196 | 7.3e-130 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_02197 | 1.3e-128 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
| KCMLOAMG_02198 | 8.9e-176 | XK27_08835 | S | ABC transporter | ||
| KCMLOAMG_02199 | 3.1e-72 | |||||
| KCMLOAMG_02200 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
| KCMLOAMG_02202 | 2.7e-216 | V | Beta-lactamase | |||
| KCMLOAMG_02203 | 1.7e-151 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
| KCMLOAMG_02204 | 1.1e-220 | V | Beta-lactamase | |||
| KCMLOAMG_02205 | 6.1e-274 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
| KCMLOAMG_02206 | 6.6e-125 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
| KCMLOAMG_02207 | 1.7e-218 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
| KCMLOAMG_02208 | 4.5e-138 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
| KCMLOAMG_02209 | 0.0 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
| KCMLOAMG_02210 | 6.5e-284 | sprD | D | Domain of Unknown Function (DUF1542) | ||
| KCMLOAMG_02211 | 2.1e-261 | mga | K | Mga helix-turn-helix domain | ||
| KCMLOAMG_02213 | 1.7e-156 | yjjH | S | Calcineurin-like phosphoesterase | ||
| KCMLOAMG_02214 | 3e-257 | dtpT | U | amino acid peptide transporter | ||
| KCMLOAMG_02215 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_02216 | 1.4e-65 | |||||
| KCMLOAMG_02217 | 2.1e-73 | S | function, without similarity to other proteins | |||
| KCMLOAMG_02218 | 2.2e-260 | G | MFS/sugar transport protein | |||
| KCMLOAMG_02219 | 1.3e-231 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
| KCMLOAMG_02220 | 1e-56 | |||||
| KCMLOAMG_02221 | 0.0 | pckG | 4.1.1.32, 4.1.1.49 | C | Phosphoenolpyruvate carboxykinase | |
| KCMLOAMG_02222 | 2.7e-24 | S | Virus attachment protein p12 family | |||
| KCMLOAMG_02223 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
| KCMLOAMG_02224 | 1.7e-82 | feoA | P | FeoA | ||
| KCMLOAMG_02225 | 1.9e-117 | E | lipolytic protein G-D-S-L family | |||
| KCMLOAMG_02229 | 1.2e-117 | ywnB | S | NAD(P)H-binding | ||
| KCMLOAMG_02230 | 1.9e-91 | S | MucBP domain | |||
| KCMLOAMG_02231 | 1.3e-85 | |||||
| KCMLOAMG_02233 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
| KCMLOAMG_02234 | 2.4e-71 | S | COG NOG38524 non supervised orthologous group | |||
| KCMLOAMG_02237 | 6.1e-35 | |||||
| KCMLOAMG_02238 | 7.6e-212 | serS | 6.1.1.11 | J | 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) | |
| KCMLOAMG_02239 | 1.4e-300 | frvR | K | Mga helix-turn-helix domain | ||
| KCMLOAMG_02240 | 2e-296 | frvR | K | Mga helix-turn-helix domain | ||
| KCMLOAMG_02241 | 9.4e-267 | lysP | E | amino acid | ||
| KCMLOAMG_02243 | 5.3e-130 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
| KCMLOAMG_02244 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
| KCMLOAMG_02245 | 1.6e-97 | |||||
| KCMLOAMG_02246 | 8.8e-98 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_02247 | 3.6e-188 | S | Bacterial protein of unknown function (DUF916) | |||
| KCMLOAMG_02248 | 9.9e-103 | |||||
| KCMLOAMG_02249 | 2e-18 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
| KCMLOAMG_02250 | 1.4e-156 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
| KCMLOAMG_02251 | 1.7e-156 | I | alpha/beta hydrolase fold | |||
| KCMLOAMG_02252 | 9.7e-48 | |||||
| KCMLOAMG_02253 | 2.5e-68 | |||||
| KCMLOAMG_02254 | 7.9e-46 | |||||
| KCMLOAMG_02255 | 2.6e-155 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
| KCMLOAMG_02256 | 7.2e-124 | citR | K | FCD | ||
| KCMLOAMG_02257 | 4.5e-266 | oadA | 2.1.3.1, 4.1.1.3, 6.4.1.1, 6.4.1.7 | C | Conserved carboxylase domain | |
| KCMLOAMG_02258 | 5.2e-101 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
| KCMLOAMG_02259 | 4.7e-285 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
| KCMLOAMG_02260 | 1.7e-154 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
| KCMLOAMG_02261 | 2.2e-48 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
| KCMLOAMG_02262 | 9.3e-181 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
| KCMLOAMG_02264 | 1.3e-196 | oadB | 4.1.1.3 | C | Na+-transporting oxaloacetate decarboxylase beta subunit | |
| KCMLOAMG_02265 | 6.7e-37 | gcdC | 2.3.1.12 | I | Biotin-requiring enzyme | |
| KCMLOAMG_02266 | 1.8e-48 | |||||
| KCMLOAMG_02267 | 2.2e-241 | citM | C | Citrate transporter | ||
| KCMLOAMG_02268 | 1.3e-41 | |||||
| KCMLOAMG_02269 | 2.5e-98 | kptA | J | Removes the 2'-phosphate from RNA via an intermediate in which the phosphate is ADP-ribosylated by NAD followed by a presumed transesterification to release the RNA and generate ADP- ribose 1''-2''-cyclic phosphate (APPR P). May function as an ADP- ribosylase | ||
| KCMLOAMG_02270 | 7.9e-88 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_02271 | 2.4e-107 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
| KCMLOAMG_02272 | 3.7e-57 | K | Transcriptional regulator PadR-like family | |||
| KCMLOAMG_02273 | 4.6e-64 | ORF00048 | ||||
| KCMLOAMG_02274 | 1.6e-137 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
| KCMLOAMG_02275 | 6.1e-163 | yjjC | V | ABC transporter | ||
| KCMLOAMG_02276 | 1.1e-284 | M | Exporter of polyketide antibiotics | |||
| KCMLOAMG_02277 | 1.8e-113 | K | Transcriptional regulator | |||
| KCMLOAMG_02278 | 2.2e-257 | ypiB | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_02279 | 6.7e-128 | S | membrane transporter protein | |||
| KCMLOAMG_02280 | 1.9e-184 | K | Helix-turn-helix domain | |||
| KCMLOAMG_02281 | 1.8e-147 | L | PFAM Integrase catalytic region | |||
| KCMLOAMG_02282 | 2e-89 | L | Helix-turn-helix domain | |||
| KCMLOAMG_02283 | 3.8e-159 | S | Alpha beta hydrolase | |||
| KCMLOAMG_02284 | 3.6e-61 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
| KCMLOAMG_02285 | 1.6e-126 | skfE | V | ATPases associated with a variety of cellular activities | ||
| KCMLOAMG_02286 | 1e-16 | |||||
| KCMLOAMG_02287 | 2.6e-266 | L | Transposase DDE domain | |||
| KCMLOAMG_02288 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_02289 | 3.8e-67 | |||||
| KCMLOAMG_02290 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_02291 | 9.3e-72 | |||||
| KCMLOAMG_02292 | 1.1e-87 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_02293 | 5.7e-158 | oppF | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
| KCMLOAMG_02294 | 6.8e-198 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
| KCMLOAMG_02295 | 1.7e-48 | |||||
| KCMLOAMG_02296 | 8.8e-173 | amiD | P | N-terminal TM domain of oligopeptide transport permease C | ||
| KCMLOAMG_02297 | 5e-168 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
| KCMLOAMG_02298 | 2.3e-311 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
| KCMLOAMG_02299 | 6.7e-38 | |||||
| KCMLOAMG_02300 | 1.3e-285 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_02301 | 2.3e-282 | V | ABC transporter transmembrane region | |||
| KCMLOAMG_02302 | 9.3e-68 | S | Iron-sulphur cluster biosynthesis | |||
| KCMLOAMG_02303 | 4.2e-134 | 2.7.1.39 | S | Phosphotransferase enzyme family | ||
| KCMLOAMG_02304 | 1.9e-114 | zmp3 | O | Zinc-dependent metalloprotease | ||
| KCMLOAMG_02305 | 2.7e-23 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
| KCMLOAMG_02307 | 0.0 | lytN | 3.5.1.104 | M | LysM domain | |
| KCMLOAMG_02308 | 2.6e-47 | lciIC | K | Helix-turn-helix XRE-family like proteins | ||
| KCMLOAMG_02309 | 1.5e-37 | L | Plasmid pRiA4b ORF-3-like protein | |||
| KCMLOAMG_02311 | 1.3e-24 | K | Cro/C1-type HTH DNA-binding domain | |||
| KCMLOAMG_02313 | 2.5e-15 | M | LysM domain | |||
| KCMLOAMG_02314 | 4.1e-66 | L | Transposase DDE domain | |||
| KCMLOAMG_02315 | 2.6e-266 | L | Transposase DDE domain | |||
| KCMLOAMG_02316 | 2.7e-176 | S | cog cog0433 | |||
| KCMLOAMG_02317 | 1.5e-92 | S | SIR2-like domain | |||
| KCMLOAMG_02318 | 2.5e-302 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
| KCMLOAMG_02320 | 2e-177 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
| KCMLOAMG_02321 | 3.7e-52 | |||||
| KCMLOAMG_02322 | 1.2e-40 | |||||
| KCMLOAMG_02323 | 1.8e-275 | pipD | E | Dipeptidase | ||
| KCMLOAMG_02324 | 3.6e-82 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
| KCMLOAMG_02325 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
| KCMLOAMG_02326 | 1e-27 | |||||
| KCMLOAMG_02327 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
| KCMLOAMG_02328 | 1.2e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
| KCMLOAMG_02329 | 2.9e-81 | yjhE | S | Phage tail protein | ||
| KCMLOAMG_02330 | 1.4e-216 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
| KCMLOAMG_02331 | 4e-181 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
| KCMLOAMG_02332 | 1.2e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
| KCMLOAMG_02333 | 1.1e-169 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
| KCMLOAMG_02334 | 0.0 | V | FtsX-like permease family | |||
| KCMLOAMG_02335 | 1.4e-136 | cysA | V | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_02336 | 0.0 | E | amino acid | |||
| KCMLOAMG_02337 | 4.1e-164 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
| KCMLOAMG_02338 | 4.5e-236 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
| KCMLOAMG_02339 | 5.7e-111 | nodB3 | G | Polysaccharide deacetylase | ||
| KCMLOAMG_02340 | 0.0 | M | Sulfatase | |||
| KCMLOAMG_02341 | 3e-174 | S | EpsG family | |||
| KCMLOAMG_02342 | 7.4e-83 | epsG | 2.7.10.1 | D | Capsular exopolysaccharide family | |
| KCMLOAMG_02343 | 3.6e-99 | ywqC | M | capsule polysaccharide biosynthetic process | ||
| KCMLOAMG_02344 | 1.6e-247 | S | polysaccharide biosynthetic process | |||
| KCMLOAMG_02345 | 2.2e-199 | M | Glycosyl transferases group 1 | |||
| KCMLOAMG_02346 | 1.6e-121 | tagF | 2.7.8.12 | M | Glycosyltransferase like family 2 | |
| KCMLOAMG_02347 | 2.6e-212 | S | Bacterial membrane protein, YfhO | |||
| KCMLOAMG_02348 | 1.2e-266 | L | Transposase DDE domain | |||
| KCMLOAMG_02349 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_02350 | 1.1e-300 | M | Glycosyl hydrolases family 25 | |||
| KCMLOAMG_02351 | 5.8e-179 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
| KCMLOAMG_02352 | 7.2e-112 | icaC | M | Acyltransferase family | ||
| KCMLOAMG_02353 | 1.3e-158 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
| KCMLOAMG_02354 | 7.8e-200 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
| KCMLOAMG_02355 | 6.2e-85 | |||||
| KCMLOAMG_02356 | 1.5e-253 | wcaJ | M | Bacterial sugar transferase | ||
| KCMLOAMG_02357 | 1.1e-133 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
| KCMLOAMG_02358 | 1.6e-113 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
| KCMLOAMG_02359 | 6e-174 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
| KCMLOAMG_02360 | 1.1e-110 | glnP | P | ABC transporter permease | ||
| KCMLOAMG_02361 | 7.9e-109 | gluC | P | ABC transporter permease | ||
| KCMLOAMG_02362 | 1e-148 | glnH | ET | ABC transporter substrate-binding protein | ||
| KCMLOAMG_02364 | 1.8e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
| KCMLOAMG_02365 | 2.8e-171 | |||||
| KCMLOAMG_02367 | 1.2e-84 | zur | P | Belongs to the Fur family | ||
| KCMLOAMG_02368 | 1.8e-08 | |||||
| KCMLOAMG_02369 | 9.3e-112 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
| KCMLOAMG_02370 | 1.1e-66 | K | Acetyltransferase (GNAT) domain | |||
| KCMLOAMG_02371 | 2.3e-117 | spl | M | NlpC/P60 family | ||
| KCMLOAMG_02372 | 1e-240 | tyrS | 6.1.1.1 | J | 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) | |
| KCMLOAMG_02373 | 2.6e-161 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
| KCMLOAMG_02374 | 1.4e-53 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
| KCMLOAMG_02375 | 1.1e-172 | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | ||
| KCMLOAMG_02376 | 0.0 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
| KCMLOAMG_02377 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
| KCMLOAMG_02378 | 2e-285 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
| KCMLOAMG_02379 | 7.9e-200 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
| KCMLOAMG_02380 | 6.3e-197 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
| KCMLOAMG_02381 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
| KCMLOAMG_02382 | 8.8e-203 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
| KCMLOAMG_02383 | 2.1e-115 | ylcC | 3.4.22.70 | M | Sortase family | |
| KCMLOAMG_02384 | 9.8e-144 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
| KCMLOAMG_02385 | 0.0 | fbp | 3.1.3.11 | G | phosphatase activity | |
| KCMLOAMG_02386 | 1.8e-63 | nrp | 1.20.4.1 | P | ArsC family | |
| KCMLOAMG_02387 | 0.0 | clpL | O | associated with various cellular activities | ||
| KCMLOAMG_02388 | 7.6e-143 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
| KCMLOAMG_02389 | 1.2e-158 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
| KCMLOAMG_02390 | 4.4e-202 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
| KCMLOAMG_02391 | 1.1e-80 | L | Transposase DDE domain | |||
| KCMLOAMG_02392 | 2.5e-180 | L | Integrase core domain | |||
| KCMLOAMG_02393 | 9.7e-103 | L | Bacterial dnaA protein | |||
| KCMLOAMG_02394 | 4.9e-77 | cpsE | M | Bacterial sugar transferase | ||
| KCMLOAMG_02395 | 7.9e-84 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
| KCMLOAMG_02396 | 1.2e-74 | sacB | GT2,GT4 | H | Stealth protein CR1, conserved region 1 | |
| KCMLOAMG_02397 | 9.3e-28 | L | Transposase IS66 family | |||
| KCMLOAMG_02398 | 2.1e-86 | L | Transposase IS66 family | |||
| KCMLOAMG_02399 | 1.2e-266 | L | Transposase DDE domain | |||
| KCMLOAMG_02400 | 5.8e-65 | glfT1 | 1.1.1.133 | S | Glycosyltransferase like family 2 | |
| KCMLOAMG_02401 | 4e-25 | |||||
| KCMLOAMG_02402 | 2.5e-64 | cps1D | M | Domain of unknown function (DUF4422) | ||
| KCMLOAMG_02403 | 2.8e-62 | GT2,GT4 | M | Glycosyltransferase GT-D fold | ||
| KCMLOAMG_02404 | 9.3e-71 | 1.1.1.133 | S | Glycosyltransferase like family 2 | ||
| KCMLOAMG_02405 | 6.8e-79 | M | Core-2/I-Branching enzyme | |||
| KCMLOAMG_02406 | 2.7e-210 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
| KCMLOAMG_02407 | 1.4e-198 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
| KCMLOAMG_02408 | 3.5e-108 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
| KCMLOAMG_02409 | 3.7e-128 | epsB | M | biosynthesis protein | ||
| KCMLOAMG_02410 | 1.6e-129 | E | lipolytic protein G-D-S-L family | |||
| KCMLOAMG_02411 | 4.9e-82 | ccl | S | QueT transporter | ||
| KCMLOAMG_02412 | 4.6e-126 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
| KCMLOAMG_02413 | 1.4e-36 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
| KCMLOAMG_02414 | 6.4e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
| KCMLOAMG_02415 | 5.6e-115 | gpm5 | 3.1.3.3, 5.4.2.11 | G | Phosphoglycerate mutase family | |
| KCMLOAMG_02416 | 3.4e-180 | oppF | P | Belongs to the ABC transporter superfamily | ||
| KCMLOAMG_02417 | 1.9e-197 | oppD | P | Belongs to the ABC transporter superfamily | ||
| KCMLOAMG_02418 | 3.1e-176 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
| KCMLOAMG_02419 | 3e-162 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
| KCMLOAMG_02420 | 3.7e-304 | oppA | E | ABC transporter, substratebinding protein | ||
| KCMLOAMG_02421 | 4.3e-256 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_02422 | 2.2e-99 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
| KCMLOAMG_02423 | 3.1e-130 | yrjD | S | LUD domain | ||
| KCMLOAMG_02424 | 8e-290 | lutB | C | 4Fe-4S dicluster domain | ||
| KCMLOAMG_02425 | 3.1e-147 | lutA | C | Cysteine-rich domain | ||
| KCMLOAMG_02426 | 9.1e-101 | |||||
| KCMLOAMG_02427 | 9.5e-53 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
| KCMLOAMG_02428 | 6.5e-212 | S | Bacterial protein of unknown function (DUF871) | |||
| KCMLOAMG_02429 | 4.6e-70 | S | Domain of unknown function (DUF3284) | |||
| KCMLOAMG_02430 | 4e-270 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
| KCMLOAMG_02431 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
| KCMLOAMG_02432 | 1.9e-138 | S | Belongs to the UPF0246 family | |||
| KCMLOAMG_02433 | 1.4e-136 | XK27_05520 | S | Uncharacterized protein conserved in bacteria (DUF2087) | ||
| KCMLOAMG_02434 | 0.0 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
| KCMLOAMG_02435 | 3.9e-110 | |||||
| KCMLOAMG_02436 | 9e-102 | S | WxL domain surface cell wall-binding | |||
| KCMLOAMG_02437 | 1.3e-145 | frlD | 2.7.1.218 | G | pfkB family carbohydrate kinase | |
| KCMLOAMG_02438 | 0.0 | G | Phosphodiester glycosidase | |||
| KCMLOAMG_02439 | 9.1e-267 | L | Transposase DDE domain | |||
| KCMLOAMG_02440 | 3.2e-289 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase N-terminal region | |
| KCMLOAMG_02441 | 1.2e-205 | S | Protein of unknown function (DUF917) | |||
| KCMLOAMG_02442 | 2.1e-222 | F | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
| KCMLOAMG_02443 | 4e-118 | |||||
| KCMLOAMG_02444 | 0.0 | S | Protein of unknown function (DUF1524) | |||
| KCMLOAMG_02445 | 0.0 | 3.4.21.53 | O | Putative ATP-dependent Lon protease | ||
| KCMLOAMG_02446 | 0.0 | S | PglZ domain | |||
| KCMLOAMG_02447 | 0.0 | 2.1.1.72 | V | Eco57I restriction-modification methylase | ||
| KCMLOAMG_02448 | 2.8e-191 | L | Belongs to the 'phage' integrase family | |||
| KCMLOAMG_02449 | 0.0 | 2.1.1.72 | V | Eco57I restriction-modification methylase | ||
| KCMLOAMG_02450 | 0.0 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
| KCMLOAMG_02451 | 2.5e-93 | S | Domain of unknown function (DUF1788) | |||
| KCMLOAMG_02452 | 1.3e-100 | S | Putative inner membrane protein (DUF1819) | |||
| KCMLOAMG_02453 | 1.8e-212 | ykiI | ||||
| KCMLOAMG_02454 | 0.0 | pip | V | domain protein | ||
| KCMLOAMG_02455 | 0.0 | scrA | 2.7.1.211 | G | phosphotransferase system | |
| KCMLOAMG_02456 | 0.0 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
| KCMLOAMG_02457 | 2.8e-177 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
| KCMLOAMG_02458 | 1.1e-299 | scrB | 3.2.1.26 | GH32 | G | invertase |
| KCMLOAMG_02460 | 1.5e-158 | azoB | GM | NmrA-like family | ||
| KCMLOAMG_02461 | 6.5e-234 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
| KCMLOAMG_02462 | 2e-143 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
| KCMLOAMG_02463 | 5.4e-147 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
| KCMLOAMG_02464 | 6.2e-260 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
| KCMLOAMG_02465 | 1.2e-76 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
| KCMLOAMG_02466 | 2.3e-51 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
| KCMLOAMG_02467 | 3.1e-223 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
| KCMLOAMG_02468 | 7.3e-127 | IQ | reductase | |||
| KCMLOAMG_02469 | 2.5e-164 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
| KCMLOAMG_02470 | 5.3e-173 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
| KCMLOAMG_02471 | 4.5e-33 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
| KCMLOAMG_02472 | 3e-173 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
| KCMLOAMG_02473 | 2.1e-76 | marR | K | Winged helix DNA-binding domain | ||
| KCMLOAMG_02474 | 9e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
| KCMLOAMG_02475 | 7.4e-191 | I | carboxylic ester hydrolase activity | |||
| KCMLOAMG_02476 | 3.5e-227 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
| KCMLOAMG_02477 | 7.1e-62 | P | Rhodanese-like domain | |||
| KCMLOAMG_02478 | 6.8e-84 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
| KCMLOAMG_02479 | 4.3e-26 | |||||
| KCMLOAMG_02480 | 3.7e-67 | K | MarR family | |||
| KCMLOAMG_02481 | 1.2e-10 | S | response to antibiotic | |||
| KCMLOAMG_02482 | 1.5e-151 | S | Putative esterase | |||
| KCMLOAMG_02483 | 2.5e-176 | |||||
| KCMLOAMG_02484 | 3.5e-103 | rmaB | K | Transcriptional regulator, MarR family | ||
| KCMLOAMG_02485 | 5.4e-83 | F | NUDIX domain | |||
| KCMLOAMG_02486 | 3.5e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
| KCMLOAMG_02487 | 4.4e-29 | |||||
| KCMLOAMG_02488 | 1.7e-124 | S | zinc-ribbon domain | |||
| KCMLOAMG_02489 | 2.7e-202 | pbpX1 | V | Beta-lactamase | ||
| KCMLOAMG_02490 | 1.5e-181 | K | AI-2E family transporter | |||
| KCMLOAMG_02491 | 1.1e-127 | srtA | 3.4.22.70 | M | Sortase family | |
| KCMLOAMG_02492 | 1.5e-65 | gtcA | S | Teichoic acid glycosylation protein | ||
| KCMLOAMG_02493 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
| KCMLOAMG_02494 | 1.5e-169 | gbuC | E | glycine betaine | ||
| KCMLOAMG_02495 | 9.4e-126 | proW | E | glycine betaine | ||
| KCMLOAMG_02496 | 1e-221 | gbuA | 3.6.3.32 | E | glycine betaine | |
| KCMLOAMG_02497 | 6.2e-134 | sfsA | S | Belongs to the SfsA family | ||
| KCMLOAMG_02498 | 2e-66 | usp1 | T | Universal stress protein family | ||
| KCMLOAMG_02499 | 3.1e-250 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
| KCMLOAMG_02500 | 7.1e-153 | thrB | 2.7.1.39, 4.2.3.1 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
| KCMLOAMG_02501 | 8.8e-284 | thrC | 4.2.3.1 | E | Threonine synthase | |
| KCMLOAMG_02502 | 1.8e-231 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
| KCMLOAMG_02503 | 1.8e-251 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
| KCMLOAMG_02504 | 6.2e-168 | yqiK | S | SPFH domain / Band 7 family | ||
| KCMLOAMG_02505 | 1.5e-68 | |||||
| KCMLOAMG_02506 | 1.7e-153 | pfoS | S | Phosphotransferase system, EIIC | ||
| KCMLOAMG_02507 | 1.6e-180 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
| KCMLOAMG_02508 | 5.4e-217 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
| KCMLOAMG_02509 | 1e-37 | E | lactoylglutathione lyase activity | |||
| KCMLOAMG_02510 | 2.2e-120 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
| KCMLOAMG_02511 | 1.5e-146 | S | Alpha/beta hydrolase family | |||
| KCMLOAMG_02512 | 9.5e-101 | K | Bacterial regulatory proteins, tetR family | |||
| KCMLOAMG_02513 | 4.7e-173 | XK27_06930 | V | domain protein | ||
| KCMLOAMG_02514 | 2.4e-170 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
| KCMLOAMG_02515 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
| KCMLOAMG_02516 | 8.5e-08 | |||||
| KCMLOAMG_02517 | 8.8e-206 | S | Calcineurin-like phosphoesterase | |||
| KCMLOAMG_02518 | 8.8e-162 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
| KCMLOAMG_02519 | 9.6e-175 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
| KCMLOAMG_02520 | 7.6e-222 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
| KCMLOAMG_02521 | 4.4e-166 | natA | S | ABC transporter | ||
| KCMLOAMG_02522 | 1e-208 | ysdA | CP | ABC-2 family transporter protein | ||
| KCMLOAMG_02523 | 3.6e-64 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
| KCMLOAMG_02524 | 2.6e-163 | CcmA | V | ABC transporter | ||
| KCMLOAMG_02525 | 4.8e-114 | VPA0052 | I | ABC-2 family transporter protein | ||
| KCMLOAMG_02526 | 9.9e-146 | IQ | reductase | |||
| KCMLOAMG_02527 | 3.5e-258 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
| KCMLOAMG_02528 | 0.0 | bglP | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
| KCMLOAMG_02529 | 1.7e-159 | licT | K | CAT RNA binding domain | ||
| KCMLOAMG_02530 | 3.6e-291 | cydC | V | ABC transporter transmembrane region | ||
| KCMLOAMG_02531 | 3.5e-310 | cydD | CO | ABC transporter transmembrane region | ||
| KCMLOAMG_02532 | 1.7e-75 | ynhH | S | NusG domain II | ||
| KCMLOAMG_02533 | 1.2e-173 | M | Peptidoglycan-binding domain 1 protein | |||
| KCMLOAMG_02534 | 1.4e-36 | XK27_02675 | K | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_02535 | 4.6e-115 | S | CRISPR-associated protein (Cas_Csn2) | |||
| KCMLOAMG_02536 | 1.1e-47 | cas2 | L | 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). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
| KCMLOAMG_02537 | 6.6e-170 | cas1 | L | 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 spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
| KCMLOAMG_02538 | 0.0 | cas9 | L | 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 spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
| KCMLOAMG_02539 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
| KCMLOAMG_02540 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
| KCMLOAMG_02541 | 5e-182 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
| KCMLOAMG_02542 | 6.8e-278 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
| KCMLOAMG_02543 | 2.4e-237 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
| KCMLOAMG_02544 | 1.5e-173 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
| KCMLOAMG_02545 | 1.7e-37 | |||||
| KCMLOAMG_02546 | 4.9e-87 | |||||
| KCMLOAMG_02547 | 2.7e-24 | |||||
| KCMLOAMG_02548 | 5.2e-162 | yicL | EG | EamA-like transporter family | ||
| KCMLOAMG_02549 | 2.8e-111 | tag | 3.2.2.20 | L | glycosylase | |
| KCMLOAMG_02551 | 4.2e-77 | usp5 | T | universal stress protein | ||
| KCMLOAMG_02552 | 4.7e-64 | K | Helix-turn-helix XRE-family like proteins | |||
| KCMLOAMG_02553 | 1e-144 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
| KCMLOAMG_02554 | 3.8e-223 | queG | 1.17.99.6 | C | Domain of unknown function (DUF1730) | |
| KCMLOAMG_02555 | 1.4e-62 | |||||
| KCMLOAMG_02556 | 1.4e-87 | bioY | S | BioY family | ||
| KCMLOAMG_02558 | 4.2e-102 | Q | methyltransferase | |||
| KCMLOAMG_02559 | 1.6e-100 | T | Sh3 type 3 domain protein | |||
| KCMLOAMG_02560 | 7.1e-115 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
| KCMLOAMG_02561 | 1.8e-136 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
| KCMLOAMG_02562 | 4.9e-257 | yhdP | S | Transporter associated domain | ||
| KCMLOAMG_02563 | 1.9e-144 | S | Alpha beta hydrolase | |||
| KCMLOAMG_02564 | 7.8e-196 | I | Acyltransferase | |||
| KCMLOAMG_02565 | 3.1e-262 | lmrB | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_02566 | 8.8e-84 | S | Domain of unknown function (DUF4811) | |||
| KCMLOAMG_02567 | 1.1e-95 | maf | D | nucleoside-triphosphate diphosphatase activity | ||
| KCMLOAMG_02568 | 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 | ||
| KCMLOAMG_02569 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
| KCMLOAMG_02570 | 2.2e-67 | L | hmm pf00665 | |||
| KCMLOAMG_02571 | 4e-34 | L | Helix-turn-helix domain | |||
| KCMLOAMG_02572 | 0.0 | ydaO | E | amino acid | ||
| KCMLOAMG_02573 | 1.1e-56 | S | Domain of unknown function (DUF1827) | |||
| KCMLOAMG_02574 | 4.5e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
| KCMLOAMG_02575 | 6.7e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
| KCMLOAMG_02576 | 4.2e-110 | ydiL | S | CAAX protease self-immunity | ||
| KCMLOAMG_02577 | 1.1e-195 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
| KCMLOAMG_02578 | 3.2e-187 | |||||
| KCMLOAMG_02579 | 3e-159 | ytrB | V | ABC transporter | ||
| KCMLOAMG_02580 | 1e-60 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
| KCMLOAMG_02581 | 4.2e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
| KCMLOAMG_02582 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
| KCMLOAMG_02583 | 3.6e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| KCMLOAMG_02584 | 1.8e-187 | tsaD | 2.3.1.234 | 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. 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 | |
| KCMLOAMG_02585 | 2.3e-98 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
| KCMLOAMG_02586 | 2.7e-129 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
| KCMLOAMG_02587 | 1.7e-117 | |||||
| KCMLOAMG_02588 | 5.6e-08 | |||||
| KCMLOAMG_02589 | 7.3e-89 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
| KCMLOAMG_02590 | 1.5e-180 | ansA | 3.5.1.1 | EJ | Asparaginase | |
| KCMLOAMG_02591 | 1.1e-143 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
| KCMLOAMG_02592 | 1.7e-151 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
| KCMLOAMG_02593 | 1.7e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
| KCMLOAMG_02594 | 4.3e-175 | holB | 2.7.7.7 | L | DNA polymerase III | |
| KCMLOAMG_02595 | 7.8e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
| KCMLOAMG_02596 | 7.4e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
| KCMLOAMG_02597 | 8.7e-38 | S | Protein of unknown function (DUF2508) | |||
| KCMLOAMG_02598 | 1.3e-108 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
| KCMLOAMG_02599 | 1.5e-33 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
| KCMLOAMG_02600 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
| KCMLOAMG_02601 | 1.2e-86 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
| KCMLOAMG_02602 | 1.2e-49 | |||||
| KCMLOAMG_02603 | 3.4e-106 | rsmC | 2.1.1.172 | J | Methyltransferase | |
| KCMLOAMG_02604 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
| KCMLOAMG_02605 | 1.6e-224 | tnpB | L | Putative transposase DNA-binding domain | ||
| KCMLOAMG_02607 | 1.7e-67 | |||||
| KCMLOAMG_02608 | 7.3e-172 | ccpB | 5.1.1.1 | K | lacI family | |
| KCMLOAMG_02609 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
| KCMLOAMG_02610 | 6e-155 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
| KCMLOAMG_02611 | 3.8e-55 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
| KCMLOAMG_02612 | 7.7e-83 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
| KCMLOAMG_02613 | 9.8e-225 | mdtG | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_02614 | 2.9e-156 | K | acetyltransferase | |||
| KCMLOAMG_02615 | 3.1e-90 | |||||
| KCMLOAMG_02616 | 7.7e-222 | yceI | G | Sugar (and other) transporter | ||
| KCMLOAMG_02617 | 4.5e-226 | |||||
| KCMLOAMG_02618 | 8.6e-292 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
| KCMLOAMG_02619 | 3.3e-302 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
| KCMLOAMG_02620 | 2.1e-260 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
| KCMLOAMG_02621 | 3.2e-95 | yqaB | S | Acetyltransferase (GNAT) domain | ||
| KCMLOAMG_02622 | 3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
| KCMLOAMG_02623 | 4.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
| KCMLOAMG_02624 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
| KCMLOAMG_02625 | 3.4e-261 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
| KCMLOAMG_02626 | 3.6e-91 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Cobalamin adenosyltransferase | |
| KCMLOAMG_02627 | 3.8e-88 | S | ECF transporter, substrate-specific component | |||
| KCMLOAMG_02628 | 5.2e-63 | S | Domain of unknown function (DUF4430) | |||
| KCMLOAMG_02629 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
| KCMLOAMG_02630 | 5e-78 | F | nucleoside 2-deoxyribosyltransferase | |||
| KCMLOAMG_02631 | 3.2e-158 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
| KCMLOAMG_02632 | 1.5e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
| KCMLOAMG_02633 | 1.5e-22 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
| KCMLOAMG_02634 | 8.5e-22 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
| KCMLOAMG_02635 | 2e-172 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
| KCMLOAMG_02636 | 2.5e-164 | menA | 2.5.1.74 | M | UbiA prenyltransferase family | |
| KCMLOAMG_02637 | 4.8e-196 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
| KCMLOAMG_02638 | 8e-224 | tnpB | L | Putative transposase DNA-binding domain | ||
| KCMLOAMG_02639 | 4.6e-139 | cad | S | FMN_bind | ||
| KCMLOAMG_02640 | 0.0 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
| KCMLOAMG_02641 | 1.7e-81 | ynhH | S | NusG domain II | ||
| KCMLOAMG_02642 | 5.2e-99 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
| KCMLOAMG_02643 | 1.1e-178 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
| KCMLOAMG_02644 | 4.6e-80 | |||||
| KCMLOAMG_02645 | 1.4e-147 | T | Calcineurin-like phosphoesterase superfamily domain | |||
| KCMLOAMG_02646 | 1.1e-49 | |||||
| KCMLOAMG_02647 | 1.9e-95 | |||||
| KCMLOAMG_02648 | 1.1e-156 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_02649 | 1.6e-219 | |||||
| KCMLOAMG_02650 | 1.4e-193 | |||||
| KCMLOAMG_02651 | 1.3e-122 | 1.5.1.40 | S | Rossmann-like domain | ||
| KCMLOAMG_02652 | 4.2e-192 | XK27_00915 | C | Luciferase-like monooxygenase | ||
| KCMLOAMG_02653 | 1.2e-97 | yacP | S | YacP-like NYN domain | ||
| KCMLOAMG_02654 | 7e-144 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
| KCMLOAMG_02655 | 5.5e-74 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
| KCMLOAMG_02656 | 9.3e-272 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
| KCMLOAMG_02657 | 7.9e-144 | K | sequence-specific DNA binding | |||
| KCMLOAMG_02658 | 1.8e-246 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
| KCMLOAMG_02659 | 2.8e-105 | |||||
| KCMLOAMG_02661 | 1.8e-147 | L | PFAM Integrase catalytic region | |||
| KCMLOAMG_02662 | 2e-89 | L | Helix-turn-helix domain | |||
| KCMLOAMG_02663 | 2.8e-258 | gltX | 6.1.1.17, 6.1.1.24 | J | 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) | |
| KCMLOAMG_02664 | 1.9e-139 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
| KCMLOAMG_02665 | 1.6e-156 | S | Membrane | |||
| KCMLOAMG_02666 | 1.8e-60 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
| KCMLOAMG_02667 | 3.3e-226 | inlJ | M | MucBP domain | ||
| KCMLOAMG_02668 | 4e-113 | K | sequence-specific DNA binding | |||
| KCMLOAMG_02669 | 1.8e-201 | yacL | S | domain protein | ||
| KCMLOAMG_02670 | 8.5e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
| KCMLOAMG_02671 | 7.3e-100 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
| KCMLOAMG_02672 | 4.2e-49 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
| KCMLOAMG_02673 | 8.8e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
| KCMLOAMG_02674 | 1.4e-261 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
| KCMLOAMG_02675 | 7.7e-197 | |||||
| KCMLOAMG_02676 | 7.3e-209 | S | ABC-2 family transporter protein | |||
| KCMLOAMG_02677 | 7.3e-166 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_02678 | 0.0 | kup | P | Transport of potassium into the cell | ||
| KCMLOAMG_02679 | 0.0 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
| KCMLOAMG_02680 | 1.5e-92 | ccpN | K | Domain in cystathionine beta-synthase and other proteins. | ||
| KCMLOAMG_02681 | 2.9e-122 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
| KCMLOAMG_02682 | 1.5e-200 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
| KCMLOAMG_02683 | 7.2e-46 | |||||
| KCMLOAMG_02684 | 9.6e-195 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
| KCMLOAMG_02685 | 1.2e-08 | yhjA | S | CsbD-like | ||
| KCMLOAMG_02686 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_02687 | 1.8e-151 | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | ||
| KCMLOAMG_02688 | 1.9e-191 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_02689 | 7.7e-116 | udp | 2.4.2.3, 3.2.2.4 | F | Phosphorylase superfamily | |
| KCMLOAMG_02690 | 1.1e-170 | EGP | Major facilitator Superfamily | |||
| KCMLOAMG_02691 | 4.1e-95 | KT | Purine catabolism regulatory protein-like family | |||
| KCMLOAMG_02692 | 9.4e-171 | L | Transposase DDE domain | |||
| KCMLOAMG_02693 | 5.4e-08 | |||||
| KCMLOAMG_02694 | 2.5e-32 | |||||
| KCMLOAMG_02695 | 7.4e-34 | |||||
| KCMLOAMG_02696 | 4.9e-224 | pimH | EGP | Major facilitator Superfamily | ||
| KCMLOAMG_02697 | 2e-225 | proA | 1.2.1.41 | E | 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 | |
| KCMLOAMG_02698 | 8.6e-148 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
| KCMLOAMG_02700 | 3.8e-96 | |||||
| KCMLOAMG_02701 | 1.8e-134 | 3.4.22.70 | M | Sortase family | ||
| KCMLOAMG_02702 | 4.6e-296 | M | Cna protein B-type domain | |||
| KCMLOAMG_02703 | 1.4e-264 | M | domain protein | |||
| KCMLOAMG_02704 | 0.0 | M | domain protein | |||
| KCMLOAMG_02705 | 3.3e-103 | |||||
| KCMLOAMG_02706 | 3.5e-227 | N | Uncharacterized conserved protein (DUF2075) | |||
| KCMLOAMG_02707 | 2.7e-207 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
| KCMLOAMG_02708 | 6.5e-111 | K | Helix-turn-helix XRE-family like proteins | |||
| KCMLOAMG_02709 | 5.2e-56 | K | Transcriptional regulator PadR-like family | |||
| KCMLOAMG_02710 | 4.2e-136 | |||||
| KCMLOAMG_02711 | 2.7e-135 | |||||
| KCMLOAMG_02712 | 1.5e-43 | S | Enterocin A Immunity | |||
| KCMLOAMG_02713 | 1.6e-186 | tas | C | Aldo/keto reductase family | ||
| KCMLOAMG_02714 | 2.5e-253 | yjjP | S | Putative threonine/serine exporter | ||
| KCMLOAMG_02715 | 7.8e-58 | |||||
| KCMLOAMG_02716 | 4.8e-228 | mesE | M | Transport protein ComB | ||
| KCMLOAMG_02717 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
| KCMLOAMG_02719 | 1.4e-78 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
| KCMLOAMG_02720 | 9e-78 | greA | K | 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. GreA releases sequences of 2 to 3 nucleotides | ||
| KCMLOAMG_02721 | 5.4e-50 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
| KCMLOAMG_02722 | 1.6e-49 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
| KCMLOAMG_02723 | 1.1e-206 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
| KCMLOAMG_02724 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
| KCMLOAMG_02725 | 2.2e-104 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
| KCMLOAMG_02726 | 2.4e-84 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
| KCMLOAMG_02727 | 6.9e-68 | yodB | K | Transcriptional regulator, HxlR family | ||
| KCMLOAMG_02728 | 9.3e-31 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
| KCMLOAMG_02729 | 1.4e-40 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
| KCMLOAMG_02730 | 1.7e-37 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
| KCMLOAMG_02731 | 2.2e-78 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
| KCMLOAMG_02732 | 3.8e-137 | plnD | K | LytTr DNA-binding domain | ||
| KCMLOAMG_02735 | 1.4e-44 | spiA | S | Enterocin A Immunity | ||
| KCMLOAMG_02736 | 2.9e-20 | |||||
| KCMLOAMG_02740 | 5.8e-133 | S | CAAX protease self-immunity | |||
| KCMLOAMG_02741 | 2.5e-69 | K | Transcriptional regulator | |||
| KCMLOAMG_02742 | 1.4e-251 | EGP | Major Facilitator Superfamily | |||
| KCMLOAMG_02743 | 2.4e-53 | |||||
| KCMLOAMG_02744 | 2.3e-54 | S | Enterocin A Immunity | |||
| KCMLOAMG_02745 | 2.6e-180 | S | Aldo keto reductase | |||
| KCMLOAMG_02746 | 1.2e-129 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
| KCMLOAMG_02747 | 1.5e-214 | yqiG | C | Oxidoreductase | ||
| KCMLOAMG_02748 | 1.3e-16 | S | Short C-terminal domain | |||
| KCMLOAMG_02749 | 3.3e-253 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
| KCMLOAMG_02750 | 2.2e-135 | |||||
| KCMLOAMG_02751 | 2e-17 | |||||
| KCMLOAMG_02752 | 5.3e-279 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
| KCMLOAMG_02753 | 0.0 | pacL | P | P-type ATPase | ||
| KCMLOAMG_02754 | 9.8e-64 | |||||
| KCMLOAMG_02755 | 1.2e-225 | EGP | Major Facilitator Superfamily | |||
| KCMLOAMG_02756 | 4.2e-311 | mco | Q | Multicopper oxidase | ||
| KCMLOAMG_02757 | 1e-24 | |||||
| KCMLOAMG_02758 | 3.2e-110 | 2.5.1.105 | P | Cation efflux family | ||
| KCMLOAMG_02759 | 8.7e-51 | czrA | K | Transcriptional regulator, ArsR family | ||
| KCMLOAMG_02760 | 1.2e-174 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
| KCMLOAMG_02761 | 9.5e-145 | mtsB | U | ABC 3 transport family | ||
| KCMLOAMG_02762 | 1.9e-130 | mntB | 3.6.3.35 | P | ABC transporter | |
| KCMLOAMG_02763 | 2.7e-42 | rpsN | J | 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 | ||
| KCMLOAMG_02764 | 2e-166 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
| KCMLOAMG_02765 | 1.4e-118 | GM | NmrA-like family | |||
| KCMLOAMG_02766 | 1.8e-84 | |||||
| KCMLOAMG_02767 | 3.9e-162 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
| KCMLOAMG_02768 | 4.7e-20 | |||||
| KCMLOAMG_02770 | 5.9e-53 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
| KCMLOAMG_02771 | 8.2e-67 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
| KCMLOAMG_02772 | 1.2e-285 | G | MFS/sugar transport protein | |||
| KCMLOAMG_02773 | 0.0 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase concanavalin-like domain | ||
| KCMLOAMG_02774 | 4.6e-169 | ssuA | P | NMT1-like family | ||
| KCMLOAMG_02775 | 1.9e-294 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
| KCMLOAMG_02776 | 5.6e-236 | yfiQ | I | Acyltransferase family | ||
| KCMLOAMG_02777 | 1.7e-120 | ssuB | P | ATPases associated with a variety of cellular activities | ||
| KCMLOAMG_02778 | 1.6e-146 | ssuC | U | Binding-protein-dependent transport system inner membrane component | ||
| KCMLOAMG_02779 | 1.4e-121 | S | B3/4 domain | |||
| KCMLOAMG_02780 | 2.3e-09 | |||||
| KCMLOAMG_02781 | 3.5e-13 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
| KCMLOAMG_02782 | 7.3e-14 | |||||
| KCMLOAMG_02783 | 0.0 | V | ABC transporter | |||
| KCMLOAMG_02784 | 0.0 | V | ATPases associated with a variety of cellular activities | |||
| KCMLOAMG_02785 | 2.5e-209 | EGP | Transmembrane secretion effector | |||
| KCMLOAMG_02786 | 1.1e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
| KCMLOAMG_02787 | 7e-80 | rplM | J | 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 | ||
| KCMLOAMG_02788 | 1.1e-102 | K | Bacterial regulatory proteins, tetR family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)