ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HNFLJBMO_00001 | 4e-279 | 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 | ||
HNFLJBMO_00002 | 1.8e-108 | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | ||
HNFLJBMO_00003 | 4.3e-113 | xerD | D | recombinase XerD | ||
HNFLJBMO_00004 | 1.1e-124 | cvfB | S | S1 domain | ||
HNFLJBMO_00005 | 2.4e-51 | yeaL | S | Protein of unknown function (DUF441) | ||
HNFLJBMO_00006 | 4.5e-58 | 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 | |||
HNFLJBMO_00007 | 5.8e-100 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HNFLJBMO_00008 | 3.2e-56 | 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 | ||
HNFLJBMO_00009 | 1.2e-58 | 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 | ||
HNFLJBMO_00010 | 4.6e-37 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
HNFLJBMO_00011 | 1.9e-216 | 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 | ||
HNFLJBMO_00012 | 7e-79 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
HNFLJBMO_00013 | 6e-123 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
HNFLJBMO_00014 | 4.5e-179 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
HNFLJBMO_00015 | 5.9e-100 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
HNFLJBMO_00016 | 4.8e-72 | |||||
HNFLJBMO_00018 | 3.7e-12 | |||||
HNFLJBMO_00019 | 1.6e-42 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HNFLJBMO_00020 | 1e-27 | ysxB | J | Cysteine protease Prp | ||
HNFLJBMO_00021 | 8.3e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HNFLJBMO_00022 | 3.4e-107 | 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 | |
HNFLJBMO_00023 | 4.4e-207 | 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 | ||
HNFLJBMO_00024 | 1e-67 | rplO | J | Binds to the 23S rRNA | ||
HNFLJBMO_00025 | 2.1e-22 | rpmD | J | Ribosomal protein L30 | ||
HNFLJBMO_00026 | 1.3e-82 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HNFLJBMO_00027 | 9.6e-56 | 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 | ||
HNFLJBMO_00028 | 3.2e-87 | 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 | ||
HNFLJBMO_00029 | 2.5e-65 | 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 | ||
HNFLJBMO_00030 | 4.4e-28 | 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 | ||
HNFLJBMO_00031 | 1.3e-91 | 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 | ||
HNFLJBMO_00032 | 7e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HNFLJBMO_00033 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HNFLJBMO_00034 | 8e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HNFLJBMO_00035 | 9e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HNFLJBMO_00036 | 3.1e-72 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HNFLJBMO_00037 | 5.2e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HNFLJBMO_00038 | 1.5e-53 | 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 | ||
HNFLJBMO_00039 | 1e-44 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HNFLJBMO_00040 | 1.4e-142 | 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 | ||
HNFLJBMO_00041 | 2.9e-39 | 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 | ||
HNFLJBMO_00042 | 1e-100 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HNFLJBMO_00043 | 4.5e-109 | 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 | ||
HNFLJBMO_00044 | 3.7e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HNFLJBMO_00045 | 6.2e-166 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HNFLJBMO_00046 | 6.5e-79 | K | rpiR family | |||
HNFLJBMO_00047 | 2.2e-53 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
HNFLJBMO_00048 | 8.5e-147 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
HNFLJBMO_00049 | 4.9e-21 | K | Acetyltransferase (GNAT) domain | |||
HNFLJBMO_00050 | 8.3e-119 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HNFLJBMO_00051 | 2e-17 | |||||
HNFLJBMO_00052 | 1.9e-104 | azlC | E | AzlC protein | ||
HNFLJBMO_00053 | 1.3e-38 | azlD | S | branched-chain amino acid | ||
HNFLJBMO_00054 | 3.6e-66 | I | alpha/beta hydrolase fold | |||
HNFLJBMO_00055 | 2.8e-26 | |||||
HNFLJBMO_00056 | 1.2e-58 | 3.6.1.27 | I | phosphatase | ||
HNFLJBMO_00057 | 1.6e-22 | |||||
HNFLJBMO_00058 | 4.5e-94 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HNFLJBMO_00059 | 6.3e-90 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
HNFLJBMO_00060 | 1.1e-76 | E | GDSL-like Lipase/Acylhydrolase family | |||
HNFLJBMO_00061 | 9.2e-56 | S | Protein of unknown function (DUF975) | |||
HNFLJBMO_00062 | 7.3e-149 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
HNFLJBMO_00063 | 4e-230 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
HNFLJBMO_00064 | 2.9e-179 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
HNFLJBMO_00065 | 2.8e-166 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
HNFLJBMO_00066 | 4.7e-178 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
HNFLJBMO_00069 | 2.3e-34 | S | Protein of unknown function (DUF4256) | |||
HNFLJBMO_00070 | 2.5e-128 | metQ | M | Belongs to the nlpA lipoprotein family | ||
HNFLJBMO_00071 | 2.4e-31 | metI | U | ABC transporter permease | ||
HNFLJBMO_00072 | 6.2e-151 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HNFLJBMO_00074 | 3.3e-265 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
HNFLJBMO_00075 | 1.3e-172 | npr | 1.11.1.1 | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
HNFLJBMO_00076 | 2.3e-106 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
HNFLJBMO_00077 | 3.9e-84 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
HNFLJBMO_00078 | 3e-84 | drgA | C | nitroreductase | ||
HNFLJBMO_00079 | 8.8e-135 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
HNFLJBMO_00080 | 9.6e-68 | metI | P | ABC transporter permease | ||
HNFLJBMO_00081 | 1.5e-149 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HNFLJBMO_00082 | 7.4e-107 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
HNFLJBMO_00083 | 1e-143 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
HNFLJBMO_00084 | 1.4e-45 | yphJ | 4.1.1.44 | S | decarboxylase | |
HNFLJBMO_00085 | 1.1e-55 | yphH | S | Cupin domain | ||
HNFLJBMO_00086 | 2.4e-46 | C | Flavodoxin | |||
HNFLJBMO_00087 | 3.6e-56 | S | CAAX protease self-immunity | |||
HNFLJBMO_00088 | 1.6e-55 | jag | S | R3H domain protein | ||
HNFLJBMO_00089 | 9.1e-54 | K | Transcriptional regulator C-terminal region | |||
HNFLJBMO_00090 | 2.7e-44 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
HNFLJBMO_00091 | 1.1e-286 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HNFLJBMO_00092 | 2.2e-111 | dat | 2.6.1.21 | EH | PFAM aminotransferase, class IV | |
HNFLJBMO_00093 | 9.5e-08 | S | SdpI/YhfL protein family | |||
HNFLJBMO_00094 | 6.6e-71 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
HNFLJBMO_00095 | 6.7e-47 | hmpT | S | ECF-type riboflavin transporter, S component | ||
HNFLJBMO_00096 | 1.1e-300 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
HNFLJBMO_00097 | 3e-210 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
HNFLJBMO_00098 | 1.7e-76 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
HNFLJBMO_00099 | 1.4e-131 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HNFLJBMO_00100 | 4.2e-56 | 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 | ||
HNFLJBMO_00101 | 1.5e-274 | dnaK | O | Heat shock 70 kDa protein | ||
HNFLJBMO_00102 | 1.2e-160 | 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 | ||
HNFLJBMO_00103 | 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 | ||
HNFLJBMO_00104 | 2.3e-68 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
HNFLJBMO_00105 | 8.4e-119 | ytbE | S | reductase | ||
HNFLJBMO_00106 | 3e-41 | ytcD | K | HxlR-like helix-turn-helix | ||
HNFLJBMO_00107 | 1.9e-101 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
HNFLJBMO_00108 | 4.5e-67 | ybbL | S | ABC transporter | ||
HNFLJBMO_00109 | 6.2e-163 | oxlT | P | Major Facilitator Superfamily | ||
HNFLJBMO_00110 | 4.7e-53 | 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 | |
HNFLJBMO_00111 | 2.9e-24 | S | Short repeat of unknown function (DUF308) | |||
HNFLJBMO_00112 | 5e-116 | KT | Putative sugar diacid recognition | |||
HNFLJBMO_00113 | 1.8e-181 | EG | GntP family permease | |||
HNFLJBMO_00114 | 6.7e-151 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HNFLJBMO_00115 | 1.5e-43 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HNFLJBMO_00116 | 1.3e-20 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HNFLJBMO_00117 | 6.5e-59 | ctpA | 3.6.3.54 | P | P-type ATPase | |
HNFLJBMO_00118 | 2e-47 | pts33BCA | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Pts system | |
HNFLJBMO_00119 | 6.8e-169 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HNFLJBMO_00120 | 7.5e-101 | 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 | ||
HNFLJBMO_00121 | 4.2e-56 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
HNFLJBMO_00122 | 1.8e-126 | minD | D | Belongs to the ParA family | ||
HNFLJBMO_00123 | 8.3e-77 | 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 | ||
HNFLJBMO_00124 | 1.5e-54 | mreD | M | rod shape-determining protein MreD | ||
HNFLJBMO_00125 | 2.1e-88 | mreC | M | Involved in formation and maintenance of cell shape | ||
HNFLJBMO_00126 | 3.6e-156 | mreB | D | cell shape determining protein MreB | ||
HNFLJBMO_00127 | 4.5e-21 | K | Cold shock | |||
HNFLJBMO_00128 | 5.3e-79 | radC | L | DNA repair protein | ||
HNFLJBMO_00129 | 3.7e-137 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HNFLJBMO_00130 | 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 | |
HNFLJBMO_00131 | 3.2e-196 | 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 | |
HNFLJBMO_00132 | 2.5e-161 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
HNFLJBMO_00133 | 1.7e-152 | mdtG | EGP | Major facilitator Superfamily | ||
HNFLJBMO_00134 | 9.1e-106 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
HNFLJBMO_00135 | 5.5e-223 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
HNFLJBMO_00136 | 8.7e-231 | 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 | |
HNFLJBMO_00137 | 3.6e-17 | yneR | ||||
HNFLJBMO_00138 | 4.3e-248 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
HNFLJBMO_00139 | 1.6e-40 | 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 | ||
HNFLJBMO_00140 | 1.6e-60 | yiiE | S | Protein of unknown function (DUF1211) | ||
HNFLJBMO_00141 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
HNFLJBMO_00142 | 1.8e-151 | gtf1 | 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 |
HNFLJBMO_00143 | 2.5e-08 | L | Helix-turn-helix domain | |||
HNFLJBMO_00145 | 1.4e-10 | L | Helix-turn-helix domain | |||
HNFLJBMO_00146 | 4e-16 | L | hmm pf00665 | |||
HNFLJBMO_00147 | 1.9e-48 | L | hmm pf00665 | |||
HNFLJBMO_00148 | 3.9e-157 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HNFLJBMO_00150 | 2.8e-230 | 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 | |
HNFLJBMO_00151 | 1.2e-63 | C | FMN binding | |||
HNFLJBMO_00152 | 6.7e-206 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HNFLJBMO_00153 | 1.7e-54 | rplI | J | Binds to the 23S rRNA | ||
HNFLJBMO_00154 | 6.7e-263 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HNFLJBMO_00155 | 1.4e-06 | |||||
HNFLJBMO_00161 | 5.1e-08 | |||||
HNFLJBMO_00168 | 3.5e-179 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
HNFLJBMO_00169 | 1.4e-40 | rpmE2 | J | Ribosomal protein L31 | ||
HNFLJBMO_00170 | 8e-61 | |||||
HNFLJBMO_00172 | 3.2e-114 | secA2 | 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 | ||
HNFLJBMO_00173 | 1.2e-70 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
HNFLJBMO_00174 | 1.7e-87 | S | hydrolase | |||
HNFLJBMO_00175 | 2.5e-205 | ywfO | S | HD domain protein | ||
HNFLJBMO_00176 | 9.8e-86 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HNFLJBMO_00177 | 1.8e-32 | ywiB | S | Domain of unknown function (DUF1934) | ||
HNFLJBMO_00178 | 9.9e-42 | 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 | ||
HNFLJBMO_00179 | 3.3e-289 | 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 | |
HNFLJBMO_00182 | 1.6e-201 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HNFLJBMO_00183 | 9.5e-235 | prdA | 1.21.4.1 | EJ | Glycine/sarcosine/betaine reductase component B subunits | |
HNFLJBMO_00184 | 3.2e-26 | S | Psort location Cytoplasmic, score | |||
HNFLJBMO_00185 | 5.8e-66 | prdB | 1.21.4.1, 1.21.4.2 | S | the current gene model (or a revised gene model) may contain a premature stop | |
HNFLJBMO_00186 | 4.3e-31 | S | the current gene model (or a revised gene model) may contain a premature stop | |||
HNFLJBMO_00187 | 4.7e-73 | prdD | S | An automated process has identified a potential problem with this gene model | ||
HNFLJBMO_00188 | 2.7e-66 | 3.5.1.1 | EJ | Glycine/sarcosine/betaine reductase component B subunits | ||
HNFLJBMO_00189 | 7e-144 | 5.1.1.4 | E | Proline racemase | ||
HNFLJBMO_00190 | 3e-69 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HNFLJBMO_00191 | 2.5e-56 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
HNFLJBMO_00192 | 1.3e-142 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HNFLJBMO_00193 | 6.8e-106 | 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 | |
HNFLJBMO_00194 | 1.8e-116 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
HNFLJBMO_00195 | 3.1e-42 | yxjI | ||||
HNFLJBMO_00196 | 6.9e-70 | 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 | ||
HNFLJBMO_00197 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HNFLJBMO_00198 | 2.5e-61 | phaJ | I | N-terminal half of MaoC dehydratase | ||
HNFLJBMO_00199 | 3.8e-222 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HNFLJBMO_00200 | 2.7e-233 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
HNFLJBMO_00201 | 1.2e-245 | yjbQ | P | TrkA C-terminal domain protein | ||
HNFLJBMO_00202 | 1.8e-30 | |||||
HNFLJBMO_00203 | 1.1e-60 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HNFLJBMO_00204 | 5.5e-77 | 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 | ||
HNFLJBMO_00205 | 6.5e-126 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HNFLJBMO_00206 | 2.2e-108 | 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 | ||
HNFLJBMO_00207 | 1.5e-110 | 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 | |
HNFLJBMO_00208 | 6.1e-101 | 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 | ||
HNFLJBMO_00209 | 1.4e-52 | rplQ | J | Ribosomal protein L17 | ||
HNFLJBMO_00210 | 1.3e-155 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNFLJBMO_00211 | 2.3e-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 | ||
HNFLJBMO_00212 | 4.4e-56 | 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 | ||
HNFLJBMO_00213 | 2.5e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HNFLJBMO_00214 | 4.8e-34 | 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 | ||
HNFLJBMO_00215 | 4.3e-15 | S | Protein of unknown function (DUF2929) | |||
HNFLJBMO_00216 | 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 | ||
HNFLJBMO_00217 | 4.3e-203 | 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 | |
HNFLJBMO_00218 | 3.7e-41 | XK27_04120 | S | Putative amino acid metabolism | ||
HNFLJBMO_00219 | 1.3e-159 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
HNFLJBMO_00220 | 2.5e-92 | 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 | |
HNFLJBMO_00222 | 5.8e-81 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
HNFLJBMO_00223 | 1.5e-130 | 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 | |
HNFLJBMO_00224 | 1.7e-152 | nhaC | C | Na H antiporter NhaC | ||
HNFLJBMO_00225 | 8.5e-94 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
HNFLJBMO_00226 | 1.5e-27 | yazA | L | GIY-YIG catalytic domain protein | ||
HNFLJBMO_00227 | 7.2e-128 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HNFLJBMO_00228 | 3.6e-128 | 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 | ||
HNFLJBMO_00229 | 6.2e-103 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
HNFLJBMO_00230 | 1.9e-75 | K | Helix-turn-helix domain, rpiR family | |||
HNFLJBMO_00231 | 3.3e-92 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
HNFLJBMO_00232 | 1.3e-127 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
HNFLJBMO_00233 | 6.5e-90 | nanK | GK | ROK family | ||
HNFLJBMO_00234 | 1.1e-53 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
HNFLJBMO_00235 | 4.7e-65 | G | Xylose isomerase domain protein TIM barrel | |||
HNFLJBMO_00236 | 7.9e-155 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
HNFLJBMO_00237 | 3.9e-207 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
HNFLJBMO_00238 | 1.3e-74 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
HNFLJBMO_00239 | 4.7e-112 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
HNFLJBMO_00240 | 7.7e-41 | S | Iron-sulfur cluster assembly protein | |||
HNFLJBMO_00241 | 1.6e-121 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
HNFLJBMO_00242 | 3.9e-187 | 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 | |
HNFLJBMO_00243 | 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 | |
HNFLJBMO_00244 | 2.1e-36 | yrzL | S | Belongs to the UPF0297 family | ||
HNFLJBMO_00245 | 2.3e-59 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HNFLJBMO_00246 | 1.9e-33 | yrzB | S | Belongs to the UPF0473 family | ||
HNFLJBMO_00247 | 1.4e-15 | 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 | ||
HNFLJBMO_00248 | 2.3e-16 | cvpA | S | Colicin V production protein | ||
HNFLJBMO_00249 | 6.5e-311 | 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 | ||
HNFLJBMO_00250 | 9.9e-41 | trxA | O | Belongs to the thioredoxin family | ||
HNFLJBMO_00251 | 1.1e-60 | yslB | S | Protein of unknown function (DUF2507) | ||
HNFLJBMO_00252 | 1.5e-72 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
HNFLJBMO_00253 | 1.5e-41 | S | Phosphoesterase | |||
HNFLJBMO_00255 | 5.1e-102 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
HNFLJBMO_00256 | 7.1e-109 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
HNFLJBMO_00257 | 5.1e-231 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HNFLJBMO_00258 | 2.2e-27 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HNFLJBMO_00259 | 4.9e-102 | 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 | |
HNFLJBMO_00260 | 4.2e-61 | marR | K | Transcriptional regulator, MarR family | ||
HNFLJBMO_00261 | 9.8e-66 | 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 | |
HNFLJBMO_00262 | 7.5e-225 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HNFLJBMO_00263 | 7e-152 | V | Pfam:Methyltransf_26 | |||
HNFLJBMO_00266 | 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 | |
HNFLJBMO_00267 | 1.8e-208 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
HNFLJBMO_00268 | 1.9e-67 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
HNFLJBMO_00269 | 5.4e-157 | XK27_09615 | S | reductase | ||
HNFLJBMO_00270 | 1.2e-39 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
HNFLJBMO_00271 | 1.2e-148 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HNFLJBMO_00272 | 1.2e-53 | cps3I | G | Acyltransferase family | ||
HNFLJBMO_00273 | 3.6e-14 | |||||
HNFLJBMO_00274 | 4.1e-57 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HNFLJBMO_00275 | 3.8e-159 | 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) | |
HNFLJBMO_00276 | 1.2e-225 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
HNFLJBMO_00277 | 7.5e-39 | 2.7.1.191 | G | PTS system fructose IIA component | ||
HNFLJBMO_00278 | 3.2e-123 | G | PTS system mannose/fructose/sorbose family IID component | |||
HNFLJBMO_00279 | 4.4e-101 | G | PTS system sorbose-specific iic component | |||
HNFLJBMO_00280 | 4.5e-64 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
HNFLJBMO_00281 | 8.7e-81 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
HNFLJBMO_00282 | 8.6e-141 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HNFLJBMO_00283 | 4.3e-184 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
HNFLJBMO_00285 | 2.9e-117 | pepL | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
HNFLJBMO_00286 | 2.2e-196 | 1.3.5.4 | C | FMN_bind | ||
HNFLJBMO_00287 | 2.2e-56 | 3.1.3.48 | K | Transcriptional regulator | ||
HNFLJBMO_00288 | 1.4e-160 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
HNFLJBMO_00289 | 7e-197 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
HNFLJBMO_00290 | 4.4e-75 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
HNFLJBMO_00291 | 2.4e-129 | yxjG | 2.1.1.14 | E | Cobalamin-independent synthase, Catalytic domain | |
HNFLJBMO_00292 | 1e-99 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HNFLJBMO_00293 | 9.5e-82 | S | Belongs to the UPF0246 family | |||
HNFLJBMO_00294 | 7.9e-12 | S | CAAX protease self-immunity | |||
HNFLJBMO_00295 | 1.2e-59 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
HNFLJBMO_00296 | 1.5e-15 | |||||
HNFLJBMO_00297 | 9.7e-37 | ptsH | G | phosphocarrier protein HPR | ||
HNFLJBMO_00298 | 6.9e-285 | 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) | |
HNFLJBMO_00299 | 6.3e-54 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HNFLJBMO_00300 | 1.6e-191 | 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 | ||
HNFLJBMO_00301 | 3.4e-180 | 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 | ||
HNFLJBMO_00302 | 5e-33 | 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 | ||
HNFLJBMO_00303 | 3e-19 | yggT | S | YGGT family | ||
HNFLJBMO_00304 | 1.2e-82 | ylmH | S | S4 domain protein | ||
HNFLJBMO_00305 | 3.9e-62 | divIVA | D | DivIVA domain protein | ||
HNFLJBMO_00306 | 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) | |
HNFLJBMO_00307 | 4.8e-115 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
HNFLJBMO_00308 | 2.7e-21 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
HNFLJBMO_00310 | 2.1e-15 | S | by MetaGeneAnnotator | |||
HNFLJBMO_00315 | 7.1e-12 | N | Bacterial Ig-like domain 2 | |||
HNFLJBMO_00316 | 2.4e-27 | S | Calcineurin-like phosphoesterase | |||
HNFLJBMO_00318 | 3.5e-100 | M | Prophage endopeptidase tail | |||
HNFLJBMO_00319 | 7.7e-274 | rny | D | peptidase | ||
HNFLJBMO_00320 | 2e-141 | S | Phage tail protein | |||
HNFLJBMO_00321 | 4e-283 | M | Phage tail tape measure protein TP901 | |||
HNFLJBMO_00322 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HNFLJBMO_00323 | 1e-160 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HNFLJBMO_00324 | 2.1e-301 | 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 | |
HNFLJBMO_00325 | 1.4e-54 | |||||
HNFLJBMO_00326 | 4.8e-158 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HNFLJBMO_00327 | 1.5e-63 | ymfM | S | Helix-turn-helix domain | ||
HNFLJBMO_00328 | 2.4e-90 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HNFLJBMO_00329 | 2.4e-149 | ymfH | S | Peptidase M16 | ||
HNFLJBMO_00330 | 5.3e-109 | ymfF | S | Peptidase M16 inactive domain protein | ||
HNFLJBMO_00336 | 5.8e-79 | copY | K | Penicillinase repressor | ||
HNFLJBMO_00337 | 0.0 | 3.6.3.4 | P | haloacid dehalogenase-like hydrolase | ||
HNFLJBMO_00338 | 2.4e-40 | S | membrane protein (DUF2078) | |||
HNFLJBMO_00339 | 4.8e-16 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
HNFLJBMO_00340 | 1.5e-33 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
HNFLJBMO_00341 | 5e-117 | K | response regulator | |||
HNFLJBMO_00342 | 6.2e-164 | baeS | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_00343 | 2.4e-47 | baeS | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_00344 | 5.9e-146 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HNFLJBMO_00345 | 1.4e-67 | spx4 | 1.20.4.1 | P | ArsC family | |
HNFLJBMO_00346 | 6e-34 | L | Helix-turn-helix domain | |||
HNFLJBMO_00349 | 3.5e-98 | cadD | P | Cadmium resistance transporter | ||
HNFLJBMO_00350 | 1.1e-14 | tnp | L | Transposase IS66 family | ||
HNFLJBMO_00351 | 5.4e-85 | dps | P | Ferritin-like domain | ||
HNFLJBMO_00352 | 3e-125 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | ||
HNFLJBMO_00353 | 4.3e-58 | tlpA2 | L | Transposase IS200 like | ||
HNFLJBMO_00354 | 1.8e-160 | L | transposase, IS605 OrfB family | |||
HNFLJBMO_00355 | 9.2e-29 | yaaL | S | Protein of unknown function (DUF2508) | ||
HNFLJBMO_00356 | 2.2e-97 | 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 | ||
HNFLJBMO_00357 | 7e-34 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
HNFLJBMO_00358 | 5.1e-211 | 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 | |
HNFLJBMO_00359 | 3.3e-62 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HNFLJBMO_00360 | 3.2e-75 | rsmC | 2.1.1.172 | J | Methyltransferase | |
HNFLJBMO_00361 | 2.7e-27 | nrdH | O | Glutaredoxin | ||
HNFLJBMO_00362 | 6.3e-45 | nrdI | F | NrdI Flavodoxin like | ||
HNFLJBMO_00363 | 1e-157 | 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 | |
HNFLJBMO_00364 | 6.6e-97 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HNFLJBMO_00365 | 3.6e-158 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HNFLJBMO_00366 | 1.1e-39 | ybjQ | S | Belongs to the UPF0145 family | ||
HNFLJBMO_00367 | 9.7e-08 | |||||
HNFLJBMO_00368 | 3e-95 | V | ABC transporter, ATP-binding protein | |||
HNFLJBMO_00369 | 1.1e-41 | gntR1 | K | Transcriptional regulator, GntR family | ||
HNFLJBMO_00370 | 2.4e-185 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
HNFLJBMO_00371 | 2.8e-65 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
HNFLJBMO_00372 | 3.8e-262 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
HNFLJBMO_00373 | 2.2e-107 | terC | P | Integral membrane protein TerC family | ||
HNFLJBMO_00374 | 1.6e-38 | K | Transcriptional regulator | |||
HNFLJBMO_00375 | 9.8e-96 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HNFLJBMO_00376 | 1.6e-100 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HNFLJBMO_00377 | 4.5e-102 | tcyB | E | ABC transporter | ||
HNFLJBMO_00379 | 3.7e-13 | ponA | V | the current gene model (or a revised gene model) may contain a frame shift | ||
HNFLJBMO_00380 | 2.3e-187 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
HNFLJBMO_00381 | 7.8e-303 | 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 | |
HNFLJBMO_00382 | 2e-209 | mtlR | K | Mga helix-turn-helix domain | ||
HNFLJBMO_00383 | 4.9e-176 | yjcE | P | Sodium proton antiporter | ||
HNFLJBMO_00384 | 8.4e-104 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HNFLJBMO_00385 | 1.4e-49 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
HNFLJBMO_00386 | 5.6e-69 | dhaL | 2.7.1.121 | S | Dak2 | |
HNFLJBMO_00387 | 2e-151 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
HNFLJBMO_00388 | 1.9e-114 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
HNFLJBMO_00389 | 1.7e-61 | K | Bacterial regulatory proteins, tetR family | |||
HNFLJBMO_00390 | 1.9e-208 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HNFLJBMO_00392 | 1.7e-111 | endA | F | DNA RNA non-specific endonuclease | ||
HNFLJBMO_00393 | 4.1e-75 | XK27_02070 | S | Nitroreductase family | ||
HNFLJBMO_00394 | 1.1e-193 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
HNFLJBMO_00395 | 3.5e-33 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
HNFLJBMO_00396 | 4.7e-294 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
HNFLJBMO_00397 | 1.2e-221 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HNFLJBMO_00398 | 6.9e-214 | G | phosphotransferase system | |||
HNFLJBMO_00399 | 9.7e-91 | licT | K | CAT RNA binding domain | ||
HNFLJBMO_00400 | 7.2e-114 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HNFLJBMO_00401 | 2.7e-58 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
HNFLJBMO_00402 | 5.1e-77 | azlC | E | branched-chain amino acid | ||
HNFLJBMO_00403 | 2.6e-31 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
HNFLJBMO_00404 | 1.5e-56 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
HNFLJBMO_00405 | 2.6e-13 | |||||
HNFLJBMO_00407 | 3.2e-135 | S | D5 N terminal like | |||
HNFLJBMO_00408 | 3.3e-45 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
HNFLJBMO_00415 | 1e-07 | K | Helix-turn-helix XRE-family like proteins | |||
HNFLJBMO_00416 | 1.1e-82 | S | overlaps another CDS with the same product name | |||
HNFLJBMO_00418 | 6e-57 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
HNFLJBMO_00419 | 3.6e-24 | L | Eco57I restriction-modification methylase | |||
HNFLJBMO_00420 | 3.2e-47 | L | COG1961 Site-specific recombinases, DNA invertase Pin homologs | |||
HNFLJBMO_00421 | 4.1e-73 | |||||
HNFLJBMO_00422 | 2.8e-22 | |||||
HNFLJBMO_00423 | 5.4e-44 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
HNFLJBMO_00424 | 1.6e-92 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HNFLJBMO_00425 | 2.9e-26 | yneF | S | UPF0154 protein | ||
HNFLJBMO_00426 | 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 | |
HNFLJBMO_00427 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HNFLJBMO_00428 | 6.2e-64 | srtA | 3.4.22.70 | M | sortase family | |
HNFLJBMO_00430 | 5.2e-72 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
HNFLJBMO_00431 | 2.5e-21 | 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 | |
HNFLJBMO_00432 | 1.1e-102 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
HNFLJBMO_00433 | 8.1e-93 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
HNFLJBMO_00434 | 3.5e-26 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
HNFLJBMO_00435 | 6.1e-187 | rodA | D | Belongs to the SEDS family | ||
HNFLJBMO_00436 | 1.3e-13 | S | Protein of unknown function (DUF2969) | |||
HNFLJBMO_00437 | 9e-27 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
HNFLJBMO_00438 | 3.4e-167 | mbl | D | Cell shape determining protein MreB Mrl | ||
HNFLJBMO_00440 | 1.6e-38 | M | Glycosyl transferase family 8 | |||
HNFLJBMO_00441 | 1.2e-55 | nss | M | transferase activity, transferring glycosyl groups | ||
HNFLJBMO_00443 | 7.6e-15 | arbx | M | family 8 | ||
HNFLJBMO_00444 | 1.4e-07 | M | Glycosyltransferase like family 2 | |||
HNFLJBMO_00445 | 2e-66 | nss | M | transferase activity, transferring glycosyl groups | ||
HNFLJBMO_00446 | 9.6e-109 | gtf2 | M | A stabilizing protein 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. Stabilizes the glycosylation activity of Gtf1 | ||
HNFLJBMO_00447 | 9e-34 | yxaB | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 |
HNFLJBMO_00448 | 2.1e-36 | M | LysM domain protein | |||
HNFLJBMO_00449 | 9.5e-277 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
HNFLJBMO_00450 | 1.4e-85 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
HNFLJBMO_00451 | 1e-34 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
HNFLJBMO_00452 | 7.7e-101 | hrtB | V | ABC transporter permease | ||
HNFLJBMO_00453 | 7.5e-195 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HNFLJBMO_00454 | 3e-14 | S | Acyltransferase family | |||
HNFLJBMO_00455 | 2.2e-66 | sip | L | Belongs to the 'phage' integrase family | ||
HNFLJBMO_00457 | 1.9e-59 | 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 | |
HNFLJBMO_00458 | 5e-87 | S | Alpha beta hydrolase | |||
HNFLJBMO_00459 | 1.2e-43 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
HNFLJBMO_00460 | 3.6e-140 | V | MatE | |||
HNFLJBMO_00461 | 1.4e-156 | gmuE | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
HNFLJBMO_00462 | 2e-64 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
HNFLJBMO_00463 | 4.3e-97 | V | ABC transporter | |||
HNFLJBMO_00464 | 9.6e-132 | bacI | V | MacB-like periplasmic core domain | ||
HNFLJBMO_00465 | 9e-74 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HNFLJBMO_00466 | 1.7e-26 | |||||
HNFLJBMO_00467 | 2.1e-180 | yhdP | S | Transporter associated domain | ||
HNFLJBMO_00468 | 6e-79 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
HNFLJBMO_00469 | 0.0 | L | Helicase C-terminal domain protein | |||
HNFLJBMO_00470 | 9.6e-251 | 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 | |
HNFLJBMO_00471 | 6.9e-62 | yeeE | S | Sulphur transport | ||
HNFLJBMO_00472 | 9.7e-15 | yraQ | S | Predicted permease | ||
HNFLJBMO_00473 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
HNFLJBMO_00475 | 2.4e-50 | L | PFAM Integrase catalytic | |||
HNFLJBMO_00476 | 4.8e-82 | yitS | S | EDD domain protein, DegV family | ||
HNFLJBMO_00477 | 5.6e-57 | racA | K | Domain of unknown function (DUF1836) | ||
HNFLJBMO_00478 | 3e-115 | queH | 1.17.99.6, 3.1.26.4 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
HNFLJBMO_00479 | 1.3e-15 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
HNFLJBMO_00480 | 1.1e-166 | potE2 | E | amino acid | ||
HNFLJBMO_00483 | 1.2e-213 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HNFLJBMO_00484 | 2.8e-186 | 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 | ||
HNFLJBMO_00485 | 1e-154 | 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 | ||
HNFLJBMO_00486 | 1.1e-29 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
HNFLJBMO_00487 | 3e-60 | 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 | |
HNFLJBMO_00488 | 3.5e-153 | phoH | T | phosphate starvation-inducible protein PhoH | ||
HNFLJBMO_00489 | 1.7e-94 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HNFLJBMO_00490 | 7.6e-74 | glcR | K | DeoR C terminal sensor domain | ||
HNFLJBMO_00491 | 1.3e-60 | yceE | S | haloacid dehalogenase-like hydrolase | ||
HNFLJBMO_00492 | 4.3e-41 | S | CAAX protease self-immunity | |||
HNFLJBMO_00493 | 7e-34 | S | Domain of unknown function (DUF4811) | |||
HNFLJBMO_00494 | 2.7e-197 | lmrB | EGP | Major facilitator Superfamily | ||
HNFLJBMO_00495 | 1.9e-32 | merR | K | MerR HTH family regulatory protein | ||
HNFLJBMO_00496 | 1e-39 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
HNFLJBMO_00497 | 9.1e-71 | S | Protein of unknown function (DUF554) | |||
HNFLJBMO_00498 | 9.4e-101 | malR | K | Transcriptional regulator, LacI family | ||
HNFLJBMO_00499 | 4.3e-213 | malT | G | Transporter, major facilitator family protein | ||
HNFLJBMO_00500 | 5.9e-79 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
HNFLJBMO_00501 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
HNFLJBMO_00502 | 2.4e-84 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
HNFLJBMO_00503 | 2.2e-27 | M | family 8 | |||
HNFLJBMO_00505 | 3.9e-30 | S | Enterocin A Immunity | |||
HNFLJBMO_00506 | 5.8e-223 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HNFLJBMO_00507 | 4.3e-19 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
HNFLJBMO_00508 | 1e-90 | rfbP | M | Bacterial sugar transferase | ||
HNFLJBMO_00509 | 2.4e-125 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HNFLJBMO_00510 | 2.1e-111 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
HNFLJBMO_00511 | 6.5e-81 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
HNFLJBMO_00512 | 1.7e-73 | epsB | M | biosynthesis protein | ||
HNFLJBMO_00514 | 5.5e-115 | cps2J | S | Polysaccharide biosynthesis protein | ||
HNFLJBMO_00517 | 1.2e-155 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
HNFLJBMO_00518 | 1.5e-188 | iolF | EGP | Major facilitator Superfamily | ||
HNFLJBMO_00519 | 5.8e-216 | rhaB | 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 | |
HNFLJBMO_00520 | 4e-40 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
HNFLJBMO_00521 | 4.8e-219 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
HNFLJBMO_00522 | 6.9e-110 | 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 | |
HNFLJBMO_00524 | 7.1e-187 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
HNFLJBMO_00529 | 2.2e-131 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HNFLJBMO_00530 | 1.4e-186 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HNFLJBMO_00531 | 6.3e-159 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HNFLJBMO_00532 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HNFLJBMO_00533 | 7.3e-119 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HNFLJBMO_00535 | 1.6e-55 | ctsR | K | Belongs to the CtsR family | ||
HNFLJBMO_00536 | 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 | ||
HNFLJBMO_00537 | 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 | |
HNFLJBMO_00538 | 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 | |
HNFLJBMO_00539 | 4.7e-148 | mepA | V | MATE efflux family protein | ||
HNFLJBMO_00540 | 1.6e-152 | lsa | S | ABC transporter | ||
HNFLJBMO_00541 | 1.8e-80 | 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 | |
HNFLJBMO_00542 | 5.7e-108 | puuD | S | peptidase C26 | ||
HNFLJBMO_00543 | 2.2e-201 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HNFLJBMO_00544 | 1.1e-25 | |||||
HNFLJBMO_00545 | 6.6e-49 | argR | K | Regulates arginine biosynthesis genes | ||
HNFLJBMO_00546 | 4.4e-120 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HNFLJBMO_00547 | 7.5e-80 | 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 | |
HNFLJBMO_00548 | 1.7e-105 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
HNFLJBMO_00549 | 3e-311 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
HNFLJBMO_00550 | 2.2e-276 | yfmR | S | ABC transporter, ATP-binding protein | ||
HNFLJBMO_00551 | 7.5e-156 | 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 | |
HNFLJBMO_00552 | 4.7e-56 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
HNFLJBMO_00553 | 2.6e-129 | EGP | Major Facilitator Superfamily | |||
HNFLJBMO_00554 | 6.3e-99 | EGP | Major Facilitator Superfamily | |||
HNFLJBMO_00555 | 1.7e-72 | K | Transcriptional regulator, LysR family | |||
HNFLJBMO_00556 | 0.0 | O | Belongs to the peptidase S8 family | |||
HNFLJBMO_00557 | 2.1e-26 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
HNFLJBMO_00559 | 4.5e-252 | L | Transposase DDE domain group 1 | |||
HNFLJBMO_00560 | 8.5e-93 | apt | 2.4.2.7 | F | purine ribonucleoside salvage | |
HNFLJBMO_00561 | 3.8e-167 | aadK | G | adenylyltransferase | ||
HNFLJBMO_00562 | 6.8e-141 | Q | Protein of unknown function (DUF1698) | |||
HNFLJBMO_00563 | 3.1e-164 | L | Nucleotidyltransferase domain | |||
HNFLJBMO_00564 | 1.6e-32 | K | Cro/C1-type HTH DNA-binding domain | |||
HNFLJBMO_00565 | 2.3e-295 | L | Recombinase | |||
HNFLJBMO_00566 | 1.1e-71 | S | Recombinase | |||
HNFLJBMO_00567 | 7.5e-83 | L | COG1961 Site-specific recombinases, DNA invertase Pin homologs | |||
HNFLJBMO_00568 | 8.7e-144 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
HNFLJBMO_00569 | 6.4e-12 | |||||
HNFLJBMO_00570 | 1.7e-68 | 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 | ||
HNFLJBMO_00571 | 1.8e-97 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
HNFLJBMO_00572 | 3.9e-127 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
HNFLJBMO_00573 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HNFLJBMO_00574 | 7.4e-173 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HNFLJBMO_00575 | 6.9e-43 | yodB | K | Transcriptional regulator, HxlR family | ||
HNFLJBMO_00576 | 2.1e-67 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
HNFLJBMO_00577 | 3.2e-73 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HNFLJBMO_00578 | 1e-32 | asp3 | S | Accessory Sec system protein Asp3 | ||
HNFLJBMO_00579 | 7.5e-105 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
HNFLJBMO_00580 | 8.5e-52 | asp1 | S | Accessory Sec system protein Asp1 | ||
HNFLJBMO_00581 | 1.5e-199 | L | Transposase DDE domain group 1 | |||
HNFLJBMO_00582 | 2.7e-66 | |||||
HNFLJBMO_00583 | 1.9e-181 | L | Transposase DDE domain group 1 | |||
HNFLJBMO_00584 | 5e-132 | 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 | |
HNFLJBMO_00585 | 5e-104 | K | response regulator | |||
HNFLJBMO_00586 | 1.6e-168 | T | PhoQ Sensor | |||
HNFLJBMO_00587 | 6.7e-146 | lmrP | E | Major Facilitator Superfamily | ||
HNFLJBMO_00588 | 3.3e-85 | 1.1.1.1 | C | Zinc-binding dehydrogenase | ||
HNFLJBMO_00590 | 3.4e-41 | S | Protein of unknown function (DUF1211) | |||
HNFLJBMO_00591 | 1.1e-166 | helD | 3.6.4.12 | L | DNA helicase | |
HNFLJBMO_00592 | 5.2e-67 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HNFLJBMO_00593 | 6.2e-58 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
HNFLJBMO_00594 | 3.9e-163 | XK27_08315 | M | Sulfatase | ||
HNFLJBMO_00595 | 5.3e-80 | S | Bacterial membrane protein YfhO | |||
HNFLJBMO_00596 | 1.4e-120 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
HNFLJBMO_00597 | 1.7e-44 | |||||
HNFLJBMO_00598 | 7e-86 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HNFLJBMO_00599 | 1.8e-95 | EG | EamA-like transporter family | |||
HNFLJBMO_00600 | 8.9e-73 | yjjH | S | Calcineurin-like phosphoesterase | ||
HNFLJBMO_00601 | 2.2e-85 | sip | L | Belongs to the 'phage' integrase family | ||
HNFLJBMO_00602 | 9.2e-16 | psiE | S | Phosphate-starvation-inducible E | ||
HNFLJBMO_00603 | 5.4e-208 | mmuP | E | amino acid | ||
HNFLJBMO_00604 | 6.9e-114 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
HNFLJBMO_00605 | 5.3e-40 | K | LytTr DNA-binding domain | |||
HNFLJBMO_00606 | 7.8e-18 | S | Protein of unknown function (DUF3021) | |||
HNFLJBMO_00607 | 4.5e-151 | yfeX | P | Peroxidase | ||
HNFLJBMO_00608 | 2.2e-12 | tetR | K | Transcriptional regulator C-terminal region | ||
HNFLJBMO_00609 | 3.4e-208 | 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 | |
HNFLJBMO_00610 | 9e-179 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HNFLJBMO_00611 | 1.2e-49 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
HNFLJBMO_00612 | 3e-162 | ytbD | EGP | Major facilitator Superfamily | ||
HNFLJBMO_00613 | 6.1e-99 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
HNFLJBMO_00614 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HNFLJBMO_00615 | 3.5e-197 | fbp | 3.1.3.11 | G | phosphatase activity | |
HNFLJBMO_00616 | 3.4e-268 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
HNFLJBMO_00617 | 3.1e-50 | comEA | L | Competence protein ComEA | ||
HNFLJBMO_00618 | 2e-69 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HNFLJBMO_00619 | 1.3e-79 | 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 | ||
HNFLJBMO_00620 | 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) | |
HNFLJBMO_00621 | 9.7e-108 | dnaI | L | Primosomal protein DnaI | ||
HNFLJBMO_00622 | 2.8e-79 | dnaB | L | replication initiation and membrane attachment | ||
HNFLJBMO_00623 | 6.1e-66 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HNFLJBMO_00624 | 7.8e-50 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HNFLJBMO_00625 | 1.5e-107 | 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 | |
HNFLJBMO_00626 | 8.5e-237 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HNFLJBMO_00627 | 3.3e-192 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
HNFLJBMO_00629 | 1.2e-192 | clpB | O | Belongs to the ClpA ClpB family | ||
HNFLJBMO_00631 | 8.1e-12 | 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 | ||
HNFLJBMO_00632 | 9.7e-118 | sip | L | Belongs to the 'phage' integrase family | ||
HNFLJBMO_00635 | 4.6e-45 | L | Primase C terminal 1 (PriCT-1) | |||
HNFLJBMO_00636 | 1.4e-78 | S | DNA primase | |||
HNFLJBMO_00637 | 5.9e-10 | |||||
HNFLJBMO_00638 | 5.1e-260 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HNFLJBMO_00639 | 3.6e-169 | 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 | ||
HNFLJBMO_00640 | 2e-131 | 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 | ||
HNFLJBMO_00641 | 7.2e-259 | 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 | ||
HNFLJBMO_00642 | 6.1e-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 | ||
HNFLJBMO_00643 | 1.3e-81 | 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 | ||
HNFLJBMO_00644 | 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 | ||
HNFLJBMO_00645 | 5.1e-92 | dedA | S | SNARE associated Golgi protein | ||
HNFLJBMO_00646 | 7.8e-32 | S | Protein of unknown function (DUF1461) | |||
HNFLJBMO_00647 | 2.9e-113 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HNFLJBMO_00648 | 2.8e-52 | yutD | S | Protein of unknown function (DUF1027) | ||
HNFLJBMO_00649 | 3e-57 | S | Calcineurin-like phosphoesterase | |||
HNFLJBMO_00650 | 2.7e-183 | cycA | E | Amino acid permease | ||
HNFLJBMO_00651 | 2e-69 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HNFLJBMO_00652 | 3e-14 | |||||
HNFLJBMO_00655 | 1.7e-74 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HNFLJBMO_00656 | 7.1e-35 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
HNFLJBMO_00657 | 5.2e-65 | hly | S | protein, hemolysin III | ||
HNFLJBMO_00658 | 2.5e-176 | XK27_08315 | M | Sulfatase | ||
HNFLJBMO_00661 | 1.9e-167 | mdtG | EGP | Major facilitator Superfamily | ||
HNFLJBMO_00662 | 8.3e-251 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
HNFLJBMO_00663 | 5.7e-84 | treR | K | UTRA | ||
HNFLJBMO_00664 | 9.5e-259 | treB | G | phosphotransferase system | ||
HNFLJBMO_00665 | 4.6e-63 | 3.1.3.73 | G | phosphoglycerate mutase | ||
HNFLJBMO_00666 | 2.4e-82 | pncA | Q | isochorismatase | ||
HNFLJBMO_00667 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
HNFLJBMO_00668 | 2.9e-102 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
HNFLJBMO_00669 | 8.6e-171 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HNFLJBMO_00670 | 1.1e-25 | K | Transcriptional regulator, HxlR family | |||
HNFLJBMO_00671 | 8.8e-53 | L | Protein involved in initiation of plasmid replication | |||
HNFLJBMO_00672 | 5.3e-18 | |||||
HNFLJBMO_00675 | 4e-48 | L | Resolvase, N terminal domain | |||
HNFLJBMO_00676 | 5.9e-50 | S | Filamentation induced by cAMP protein fic | |||
HNFLJBMO_00677 | 2.3e-105 | K | Psort location CytoplasmicMembrane, score | |||
HNFLJBMO_00678 | 2.6e-169 | bcrA | V | ABC transporter | ||
HNFLJBMO_00679 | 1.7e-126 | S | ABC-2 family transporter protein | |||
HNFLJBMO_00681 | 8.3e-25 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
HNFLJBMO_00682 | 6.2e-87 | L | Replication initiation factor | |||
HNFLJBMO_00683 | 3.1e-29 | L | Single-strand binding protein family | |||
HNFLJBMO_00684 | 2.3e-55 | L | Phage integrase, N-terminal SAM-like domain | |||
HNFLJBMO_00688 | 9e-76 | L | Lactococcus lactis RepB C-terminus | |||
HNFLJBMO_00689 | 1.7e-142 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
HNFLJBMO_00690 | 2.2e-190 | yddH | M | NlpC p60 family protein | ||
HNFLJBMO_00691 | 1.2e-59 | S | Conjugative transposon protein TcpC | |||
HNFLJBMO_00692 | 9.8e-39 | S | Conjugative transposon protein TcpC | |||
HNFLJBMO_00693 | 4.4e-86 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HNFLJBMO_00694 | 4.5e-284 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HNFLJBMO_00695 | 3.3e-103 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HNFLJBMO_00696 | 1.1e-99 | glnH | ET | ABC transporter | ||
HNFLJBMO_00697 | 1.2e-85 | gluC | P | ABC transporter permease | ||
HNFLJBMO_00698 | 9.6e-78 | glnP | P | ABC transporter permease | ||
HNFLJBMO_00699 | 2.1e-160 | steT | E | amino acid | ||
HNFLJBMO_00700 | 7.7e-12 | M | Lysin motif | |||
HNFLJBMO_00701 | 2e-86 | 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 | |
HNFLJBMO_00702 | 9.4e-81 | lytH | 3.5.1.28 | M | Ami_3 | |
HNFLJBMO_00706 | 2.8e-279 | 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 | |
HNFLJBMO_00707 | 2.4e-44 | S | Repeat protein | |||
HNFLJBMO_00708 | 4.7e-56 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
HNFLJBMO_00709 | 1.3e-80 | 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 | |
HNFLJBMO_00710 | 4.2e-297 | S | membrane | |||
HNFLJBMO_00711 | 2.3e-279 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
HNFLJBMO_00712 | 1.8e-27 | S | Protein of unknown function (DUF3290) | |||
HNFLJBMO_00713 | 8.7e-299 | 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) | |
HNFLJBMO_00714 | 3.4e-204 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
HNFLJBMO_00716 | 7.6e-55 | clpP | 3.4.21.92 | OU | Clp protease | |
HNFLJBMO_00717 | 8.5e-82 | S | Phage portal protein | |||
HNFLJBMO_00718 | 6.2e-182 | S | Terminase | |||
HNFLJBMO_00719 | 3.8e-14 | |||||
HNFLJBMO_00720 | 8.7e-26 | V | HNH nucleases | |||
HNFLJBMO_00721 | 5.4e-22 | |||||
HNFLJBMO_00723 | 2.3e-25 | arpU | S | Phage transcriptional regulator, ArpU family | ||
HNFLJBMO_00736 | 9.7e-71 | |||||
HNFLJBMO_00737 | 1.6e-25 | |||||
HNFLJBMO_00740 | 3.2e-83 | 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 | |
HNFLJBMO_00741 | 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 | |
HNFLJBMO_00742 | 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 | |
HNFLJBMO_00743 | 3.5e-35 | FbpA | K | Fibronectin-binding protein | ||
HNFLJBMO_00744 | 2.7e-204 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
HNFLJBMO_00745 | 2.5e-141 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
HNFLJBMO_00746 | 1e-193 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
HNFLJBMO_00747 | 6.9e-160 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
HNFLJBMO_00748 | 6.5e-158 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HNFLJBMO_00749 | 2.4e-92 | yueF | S | AI-2E family transporter | ||
HNFLJBMO_00750 | 2.6e-97 | ygaC | J | Belongs to the UPF0374 family | ||
HNFLJBMO_00751 | 6.5e-193 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HNFLJBMO_00752 | 4.6e-16 | 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 | |
HNFLJBMO_00753 | 3.7e-153 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HNFLJBMO_00754 | 3.3e-90 | stp | 3.1.3.16 | T | phosphatase | |
HNFLJBMO_00755 | 7.5e-191 | KLT | serine threonine protein kinase | |||
HNFLJBMO_00756 | 1.8e-111 | 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 | |
HNFLJBMO_00757 | 3.8e-58 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HNFLJBMO_00758 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
HNFLJBMO_00759 | 1.5e-122 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
HNFLJBMO_00760 | 1.1e-199 | nupG | F | Nucleoside | ||
HNFLJBMO_00761 | 4.1e-105 | 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 | ||
HNFLJBMO_00762 | 2.2e-49 | 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 | |
HNFLJBMO_00763 | 3.4e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HNFLJBMO_00764 | 2.1e-204 | 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 | ||
HNFLJBMO_00765 | 2.4e-221 | gdhA | 1.4.1.4 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
HNFLJBMO_00766 | 2.1e-243 | E | Amino acid permease | |||
HNFLJBMO_00767 | 3.8e-08 | E | Amino acid permease | |||
HNFLJBMO_00768 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
HNFLJBMO_00769 | 2.5e-136 | pfoS | S | Phosphotransferase system, EIIC | ||
HNFLJBMO_00770 | 1.9e-117 | ldhA | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
HNFLJBMO_00771 | 2.5e-101 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
HNFLJBMO_00772 | 1.5e-07 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
HNFLJBMO_00773 | 6.7e-17 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
HNFLJBMO_00774 | 9.9e-58 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
HNFLJBMO_00775 | 7.2e-53 | perR | P | Belongs to the Fur family | ||
HNFLJBMO_00776 | 1.1e-207 | 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) | |
HNFLJBMO_00781 | 1.5e-69 | S | RRXRR protein | |||
HNFLJBMO_00783 | 9.5e-246 | yhcA | V | ABC transporter, ATP-binding protein | ||
HNFLJBMO_00784 | 2.6e-223 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
HNFLJBMO_00785 | 6.4e-69 | G | Transporter, major facilitator family protein | |||
HNFLJBMO_00786 | 3.3e-311 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
HNFLJBMO_00787 | 1.5e-43 | S | zinc-ribbon domain | |||
HNFLJBMO_00788 | 2.7e-114 | 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 | |
HNFLJBMO_00789 | 3e-122 | pstA | P | Phosphate transport system permease protein PstA | ||
HNFLJBMO_00790 | 5.4e-119 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HNFLJBMO_00791 | 2.7e-96 | pstS | P | Phosphate | ||
HNFLJBMO_00792 | 3.9e-41 | yjbH | Q | Thioredoxin | ||
HNFLJBMO_00793 | 1.5e-38 | |||||
HNFLJBMO_00794 | 7.3e-14 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
HNFLJBMO_00795 | 1.4e-49 | I | Alpha/beta hydrolase family | |||
HNFLJBMO_00796 | 1.4e-94 | S | Bacterial membrane protein, YfhO | |||
HNFLJBMO_00797 | 1.9e-53 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HNFLJBMO_00798 | 2.4e-190 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HNFLJBMO_00799 | 9e-24 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
HNFLJBMO_00800 | 4.1e-108 | spo0J | K | Belongs to the ParB family | ||
HNFLJBMO_00801 | 6.5e-118 | soj | D | Sporulation initiation inhibitor | ||
HNFLJBMO_00802 | 2.8e-82 | noc | K | Belongs to the ParB family | ||
HNFLJBMO_00803 | 4.7e-102 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HNFLJBMO_00804 | 4.5e-126 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HNFLJBMO_00805 | 8.4e-110 | 3.1.4.46 | C | phosphodiesterase | ||
HNFLJBMO_00806 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
HNFLJBMO_00807 | 1.7e-184 | L | Probable transposase | |||
HNFLJBMO_00808 | 7.9e-62 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
HNFLJBMO_00810 | 4.3e-54 | queT | S | QueT transporter | ||
HNFLJBMO_00811 | 3.9e-34 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
HNFLJBMO_00812 | 1.2e-100 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HNFLJBMO_00813 | 2.1e-153 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HNFLJBMO_00814 | 4.3e-61 | uspA | T | universal stress protein | ||
HNFLJBMO_00816 | 1.4e-12 | yajC | U | Preprotein translocase | ||
HNFLJBMO_00817 | 2.3e-207 | 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) | |
HNFLJBMO_00818 | 1e-182 | 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) | |
HNFLJBMO_00819 | 1.2e-93 | 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 | |
HNFLJBMO_00820 | 2.4e-192 | cycA | E | Amino acid permease | ||
HNFLJBMO_00821 | 1.8e-186 | ytgP | S | Polysaccharide biosynthesis protein | ||
HNFLJBMO_00822 | 9.2e-104 | tatD | L | hydrolase, TatD family | ||
HNFLJBMO_00823 | 3.4e-87 | 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 | |
HNFLJBMO_00824 | 7e-132 | 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 | |
HNFLJBMO_00825 | 2.2e-64 | tal | 2.2.1.2 | G | Transaldolase/Fructose-6-phosphate aldolase | |
HNFLJBMO_00826 | 3.1e-36 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
HNFLJBMO_00827 | 2.7e-135 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
HNFLJBMO_00828 | 4.8e-83 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
HNFLJBMO_00829 | 4.5e-43 | gutM | K | Glucitol operon activator protein (GutM) | ||
HNFLJBMO_00830 | 1.5e-104 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
HNFLJBMO_00831 | 1.4e-61 | IQ | NAD dependent epimerase/dehydratase family | |||
HNFLJBMO_00832 | 3e-26 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
HNFLJBMO_00833 | 1.2e-24 | yktA | S | Belongs to the UPF0223 family | ||
HNFLJBMO_00834 | 6.3e-76 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
HNFLJBMO_00835 | 4.6e-77 | typA | T | GTP-binding protein TypA | ||
HNFLJBMO_00836 | 4e-211 | yhgF | K | Tex-like protein N-terminal domain protein | ||
HNFLJBMO_00837 | 3.6e-44 | ydcK | S | Belongs to the SprT family | ||
HNFLJBMO_00839 | 4.6e-116 | 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 | |
HNFLJBMO_00840 | 4.5e-129 | mleP2 | S | Sodium Bile acid symporter family | ||
HNFLJBMO_00841 | 8e-25 | arbx | M | family 8 | ||
HNFLJBMO_00842 | 8.8e-168 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HNFLJBMO_00843 | 4.3e-89 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HNFLJBMO_00844 | 6e-58 | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
HNFLJBMO_00845 | 3.7e-96 | yicL | EG | EamA-like transporter family | ||
HNFLJBMO_00846 | 6e-223 | pepF | E | Oligopeptidase F | ||
HNFLJBMO_00847 | 8.6e-109 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HNFLJBMO_00848 | 1.7e-178 | metC | 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
HNFLJBMO_00849 | 2.3e-140 | gldA | 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
HNFLJBMO_00850 | 1.4e-61 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
HNFLJBMO_00851 | 2.1e-24 | relB | L | RelB antitoxin | ||
HNFLJBMO_00852 | 4.9e-172 | S | Putative peptidoglycan binding domain | |||
HNFLJBMO_00853 | 6.8e-69 | rny | D | Peptidase family M23 | ||
HNFLJBMO_00855 | 2.3e-138 | tetA | EGP | Major facilitator Superfamily | ||
HNFLJBMO_00856 | 1.8e-32 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
HNFLJBMO_00857 | 4.8e-233 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
HNFLJBMO_00858 | 7.6e-136 | 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 | |
HNFLJBMO_00860 | 4.5e-09 | D | Antitoxin Phd_YefM, type II toxin-antitoxin system | |||
HNFLJBMO_00861 | 3e-08 | XK27_10540 | S | ParE toxin of type II toxin-antitoxin system, parDE | ||
HNFLJBMO_00862 | 1.6e-147 | dtpT | U | amino acid peptide transporter | ||
HNFLJBMO_00863 | 5.1e-54 | fld | C | Flavodoxin | ||
HNFLJBMO_00864 | 1.2e-143 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
HNFLJBMO_00865 | 1.2e-152 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HNFLJBMO_00866 | 4.7e-12 | mltD | CBM50 | M | Lysin motif | |
HNFLJBMO_00867 | 3.8e-93 | yihY | S | Belongs to the UPF0761 family | ||
HNFLJBMO_00868 | 2.4e-78 | repE | K | Primase C terminal 1 (PriCT-1) | ||
HNFLJBMO_00871 | 6.8e-104 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
HNFLJBMO_00872 | 1.6e-71 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
HNFLJBMO_00873 | 4.4e-77 | desR | K | helix_turn_helix, Lux Regulon | ||
HNFLJBMO_00874 | 3.2e-57 | salK | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_00875 | 4.2e-53 | yvfS | V | ABC-2 type transporter | ||
HNFLJBMO_00876 | 1e-79 | yvfR | V | ABC transporter | ||
HNFLJBMO_00877 | 3.5e-99 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HNFLJBMO_00878 | 2.5e-78 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
HNFLJBMO_00879 | 5.5e-29 | |||||
HNFLJBMO_00880 | 1.1e-41 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
HNFLJBMO_00881 | 1.8e-179 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
HNFLJBMO_00882 | 6.9e-80 | |||||
HNFLJBMO_00883 | 1.2e-45 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
HNFLJBMO_00884 | 7.3e-94 | C | Luciferase-like monooxygenase | |||
HNFLJBMO_00885 | 1.3e-24 | 1.5.1.38 | S | FMN reductase | ||
HNFLJBMO_00886 | 4.3e-26 | 1.5.1.38 | S | NADPH-dependent FMN reductase | ||
HNFLJBMO_00887 | 1.5e-117 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
HNFLJBMO_00888 | 3.9e-76 | L | haloacid dehalogenase-like hydrolase | |||
HNFLJBMO_00889 | 3.1e-61 | EG | EamA-like transporter family | |||
HNFLJBMO_00890 | 1.2e-117 | K | AI-2E family transporter | |||
HNFLJBMO_00891 | 2.4e-172 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
HNFLJBMO_00892 | 2.1e-123 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HNFLJBMO_00894 | 4e-16 | |||||
HNFLJBMO_00895 | 6.1e-103 | V | domain protein | |||
HNFLJBMO_00896 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
HNFLJBMO_00897 | 1.3e-68 | pts13C | 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 | ||
HNFLJBMO_00898 | 3.2e-108 | pepE | 3.4.13.21 | E | Alpha/beta hydrolase of unknown function (DUF915) | |
HNFLJBMO_00899 | 4.2e-298 | S | Bacterial membrane protein YfhO | |||
HNFLJBMO_00900 | 7e-169 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HNFLJBMO_00901 | 9e-30 | yqkB | S | Belongs to the HesB IscA family | ||
HNFLJBMO_00902 | 1.8e-65 | yxkH | G | Polysaccharide deacetylase | ||
HNFLJBMO_00903 | 1.8e-07 | |||||
HNFLJBMO_00904 | 7e-33 | K | LysR substrate binding domain | |||
HNFLJBMO_00905 | 4.7e-220 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HNFLJBMO_00906 | 7.9e-30 | O | ADP-ribosylglycohydrolase | |||
HNFLJBMO_00907 | 3.7e-168 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HNFLJBMO_00908 | 1.4e-108 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HNFLJBMO_00909 | 2.6e-07 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
HNFLJBMO_00910 | 2e-219 | 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 | |
HNFLJBMO_00911 | 1.4e-17 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
HNFLJBMO_00912 | 6e-81 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HNFLJBMO_00913 | 9.1e-95 | yeaN | P | Major Facilitator Superfamily | ||
HNFLJBMO_00914 | 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 | ||
HNFLJBMO_00915 | 1.1e-163 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HNFLJBMO_00916 | 1.7e-30 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
HNFLJBMO_00917 | 1.9e-08 | 2.3.1.19 | K | Cro/C1-type HTH DNA-binding domain | ||
HNFLJBMO_00920 | 4.3e-82 | thrE | S | Putative threonine/serine exporter | ||
HNFLJBMO_00921 | 6.3e-49 | S | Threonine/Serine exporter, ThrE | |||
HNFLJBMO_00922 | 1.2e-120 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HNFLJBMO_00923 | 4.2e-86 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HNFLJBMO_00924 | 1.9e-34 | trxA | O | Belongs to the thioredoxin family | ||
HNFLJBMO_00925 | 9.4e-22 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HNFLJBMO_00926 | 1.3e-20 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HNFLJBMO_00927 | 3.3e-65 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
HNFLJBMO_00928 | 3e-70 | lepB | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
HNFLJBMO_00929 | 1.1e-244 | lutB | C | 4Fe-4S dicluster domain | ||
HNFLJBMO_00930 | 6.9e-117 | lutA | C | Cysteine-rich domain | ||
HNFLJBMO_00931 | 2e-208 | yfnA | E | Amino Acid | ||
HNFLJBMO_00932 | 6.2e-61 | casE | S | CRISPR_assoc | ||
HNFLJBMO_00933 | 3.6e-54 | S | Putative HNHc nuclease | |||
HNFLJBMO_00937 | 1.2e-09 | selB | J | Elongation factor SelB, winged helix | ||
HNFLJBMO_00938 | 8.8e-111 | sufS | 2.8.1.7, 4.4.1.16 | E | Serine hydroxymethyltransferase | |
HNFLJBMO_00939 | 7e-110 | selA | 2.9.1.1 | H | Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis | |
HNFLJBMO_00940 | 9e-29 | yitW | S | Iron-sulfur cluster assembly protein | ||
HNFLJBMO_00941 | 2.4e-176 | rnfC | C | RnfC Barrel sandwich hybrid domain | ||
HNFLJBMO_00942 | 2.7e-100 | selD | 2.7.9.3 | E | Synthesizes selenophosphate from selenide and ATP | |
HNFLJBMO_00943 | 3.6e-152 | comEC | S | Competence protein ComEC | ||
HNFLJBMO_00944 | 2.3e-47 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
HNFLJBMO_00945 | 1.6e-223 | 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 | ||
HNFLJBMO_00946 | 8.2e-154 | yacL | S | domain protein | ||
HNFLJBMO_00947 | 2.4e-31 | M | Glycosyltransferase like family 2 | |||
HNFLJBMO_00949 | 2.8e-09 | S | Protein of unknown function (DUF805) | |||
HNFLJBMO_00951 | 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 | |
HNFLJBMO_00952 | 3e-101 | ftsW | D | Belongs to the SEDS family | ||
HNFLJBMO_00953 | 3.3e-148 | manN | G | system, mannose fructose sorbose family IID component | ||
HNFLJBMO_00954 | 7e-115 | manY | G | PTS system | ||
HNFLJBMO_00955 | 3.5e-148 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
HNFLJBMO_00956 | 6.8e-26 | ykuJ | S | Protein of unknown function (DUF1797) | ||
HNFLJBMO_00957 | 1.7e-129 | 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 | ||
HNFLJBMO_00958 | 1e-126 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
HNFLJBMO_00959 | 2e-161 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
HNFLJBMO_00960 | 7.5e-56 | P | Plays a role in the regulation of phosphate uptake | |||
HNFLJBMO_00961 | 1.8e-148 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
HNFLJBMO_00962 | 1.1e-79 | S | VIT family | |||
HNFLJBMO_00963 | 9.4e-84 | S | membrane | |||
HNFLJBMO_00964 | 2.7e-171 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
HNFLJBMO_00965 | 4.5e-228 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HNFLJBMO_00966 | 8.5e-36 | 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 | ||
HNFLJBMO_00968 | 3.7e-23 | K | Acetyltransferase (GNAT) domain | |||
HNFLJBMO_00969 | 8.1e-112 | natA | S | Domain of unknown function (DUF4162) | ||
HNFLJBMO_00970 | 1.5e-63 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
HNFLJBMO_00971 | 3.3e-134 | S | interspecies interaction between organisms | |||
HNFLJBMO_00972 | 6.7e-206 | G | glycerol-3-phosphate transporter | |||
HNFLJBMO_00973 | 5e-98 | |||||
HNFLJBMO_00974 | 3.1e-09 | 3.2.1.14 | GH18 | |||
HNFLJBMO_00975 | 2.4e-53 | zur | P | Belongs to the Fur family | ||
HNFLJBMO_00976 | 5.2e-103 | dam2 | 2.1.1.72 | L | DNA methyltransferase | |
HNFLJBMO_00977 | 3.1e-79 | sip | L | Belongs to the 'phage' integrase family | ||
HNFLJBMO_00978 | 7.1e-172 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
HNFLJBMO_00980 | 4.7e-106 | yxeH | S | hydrolase | ||
HNFLJBMO_00982 | 2.8e-95 | S | Domain of unknown function DUF87 | |||
HNFLJBMO_00984 | 4.1e-229 | V | ABC transporter transmembrane region | |||
HNFLJBMO_00985 | 4e-216 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
HNFLJBMO_00986 | 1e-09 | K | LytTr DNA-binding domain | |||
HNFLJBMO_00987 | 3.7e-19 | M | domain protein | |||
HNFLJBMO_00989 | 1.2e-16 | 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 | |
HNFLJBMO_00990 | 8.9e-147 | 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 | |
HNFLJBMO_00991 | 1e-103 | 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 | |
HNFLJBMO_00992 | 9.7e-75 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
HNFLJBMO_00993 | 8.3e-178 | thrC | 4.2.3.1 | E | Threonine synthase | |
HNFLJBMO_00994 | 3.4e-127 | 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 | |
HNFLJBMO_00995 | 1.1e-261 | U | COG3505 Type IV secretory pathway, VirD4 components | |||
HNFLJBMO_00996 | 7.7e-80 | |||||
HNFLJBMO_01000 | 5.3e-12 | D | Antitoxin component of a toxin-antitoxin (TA) module | |||
HNFLJBMO_01002 | 2.1e-65 | H | Methyltransferase domain | |||
HNFLJBMO_01003 | 5.9e-76 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
HNFLJBMO_01004 | 9.6e-41 | wecD | M | Acetyltransferase (GNAT) family | ||
HNFLJBMO_01007 | 3.1e-40 | K | Transcriptional regulator | |||
HNFLJBMO_01009 | 6.2e-210 | glnP | P | ABC transporter | ||
HNFLJBMO_01010 | 9.3e-168 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
HNFLJBMO_01011 | 6.3e-103 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
HNFLJBMO_01012 | 7.8e-78 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
HNFLJBMO_01013 | 4.3e-149 | EGP | Sugar (and other) transporter | |||
HNFLJBMO_01015 | 2.4e-13 | |||||
HNFLJBMO_01024 | 2.6e-16 | S | RelB antitoxin | |||
HNFLJBMO_01025 | 4.6e-37 | |||||
HNFLJBMO_01027 | 3.7e-26 | radC | L | DNA repair protein | ||
HNFLJBMO_01028 | 2.4e-59 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HNFLJBMO_01030 | 3.1e-111 | K | response regulator | |||
HNFLJBMO_01031 | 1.2e-82 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
HNFLJBMO_01032 | 9.7e-43 | M | transferase activity, transferring glycosyl groups | |||
HNFLJBMO_01033 | 4.5e-53 | asp | S | Asp23 family, cell envelope-related function | ||
HNFLJBMO_01034 | 1.3e-238 | yloV | S | DAK2 domain fusion protein YloV | ||
HNFLJBMO_01035 | 4e-247 | 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) | |
HNFLJBMO_01036 | 6.5e-204 | pipD | E | Dipeptidase | ||
HNFLJBMO_01037 | 3.6e-43 | |||||
HNFLJBMO_01038 | 2.6e-64 | K | helix_turn_helix, arabinose operon control protein | |||
HNFLJBMO_01039 | 5.2e-54 | S | Membrane | |||
HNFLJBMO_01040 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
HNFLJBMO_01041 | 1e-58 | L | Helicase C-terminal domain protein | |||
HNFLJBMO_01042 | 9.5e-161 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
HNFLJBMO_01043 | 7.6e-236 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
HNFLJBMO_01044 | 3.1e-143 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
HNFLJBMO_01045 | 3.1e-36 | ypmB | S | Protein conserved in bacteria | ||
HNFLJBMO_01046 | 3.6e-24 | yozE | S | Belongs to the UPF0346 family | ||
HNFLJBMO_01047 | 4.7e-133 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
HNFLJBMO_01048 | 4.9e-97 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HNFLJBMO_01049 | 2e-32 | dprA | LU | DNA protecting protein DprA | ||
HNFLJBMO_01050 | 1.8e-82 | L | Transposase, IS116 IS110 IS902 family | |||
HNFLJBMO_01051 | 1.4e-51 | |||||
HNFLJBMO_01052 | 7.2e-77 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
HNFLJBMO_01053 | 1.5e-144 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HNFLJBMO_01054 | 5.4e-13 | |||||
HNFLJBMO_01055 | 3.4e-48 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
HNFLJBMO_01056 | 3.7e-212 | yfnA | E | Amino Acid | ||
HNFLJBMO_01057 | 7.7e-135 | 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 | |
HNFLJBMO_01058 | 4.1e-89 | 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 | |
HNFLJBMO_01059 | 1e-177 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HNFLJBMO_01060 | 6.8e-86 | tdk | 2.7.1.21 | F | thymidine kinase | |
HNFLJBMO_01061 | 3.1e-240 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HNFLJBMO_01062 | 7.1e-295 | 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 | ||
HNFLJBMO_01063 | 1.3e-55 | 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 | ||
HNFLJBMO_01064 | 6.2e-42 | L | Helicase C-terminal domain protein | |||
HNFLJBMO_01066 | 3.4e-39 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HNFLJBMO_01067 | 1.7e-109 | aatB | ET | ABC transporter substrate-binding protein | ||
HNFLJBMO_01068 | 1.6e-118 | 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 | ||
HNFLJBMO_01069 | 9.7e-24 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HNFLJBMO_01070 | 5.6e-137 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
HNFLJBMO_01071 | 7.3e-105 | |||||
HNFLJBMO_01072 | 3.2e-117 | |||||
HNFLJBMO_01073 | 1.3e-41 | dut | S | dUTPase | ||
HNFLJBMO_01074 | 2.1e-94 | 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 | ||
HNFLJBMO_01075 | 3.7e-46 | yqhY | S | Asp23 family, cell envelope-related function | ||
HNFLJBMO_01078 | 3.3e-29 | M | Glycosyl transferases group 1 | |||
HNFLJBMO_01079 | 3.4e-83 | qorB | 1.6.5.2 | GM | NmrA-like family | |
HNFLJBMO_01080 | 8e-40 | K | Transcriptional regulator | |||
HNFLJBMO_01081 | 1.4e-31 | S | CHY zinc finger | |||
HNFLJBMO_01083 | 9.2e-16 | |||||
HNFLJBMO_01087 | 1.2e-210 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
HNFLJBMO_01088 | 1.9e-174 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
HNFLJBMO_01089 | 5.3e-223 | ybeC | E | amino acid | ||
HNFLJBMO_01090 | 6e-84 | XK27_00825 | S | Sulfite exporter TauE/SafE | ||
HNFLJBMO_01091 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
HNFLJBMO_01092 | 1.7e-60 | K | DeoR C terminal sensor domain | |||
HNFLJBMO_01093 | 1e-38 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
HNFLJBMO_01094 | 9.2e-36 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
HNFLJBMO_01095 | 1.4e-181 | gatC | G | PTS system sugar-specific permease component | ||
HNFLJBMO_01096 | 5.6e-120 | gatD | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
HNFLJBMO_01097 | 2.8e-167 | gutB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
HNFLJBMO_01098 | 6.6e-87 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
HNFLJBMO_01099 | 3e-44 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
HNFLJBMO_01100 | 2.3e-213 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
HNFLJBMO_01103 | 8.8e-24 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
HNFLJBMO_01105 | 1.5e-68 | 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
HNFLJBMO_01106 | 1.6e-167 | yjjP | S | Putative threonine/serine exporter | ||
HNFLJBMO_01107 | 4.8e-109 | glcU | U | sugar transport | ||
HNFLJBMO_01108 | 5.9e-15 | K | regulatory protein TetR | |||
HNFLJBMO_01109 | 6.9e-37 | |||||
HNFLJBMO_01110 | 3.4e-92 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HNFLJBMO_01111 | 1e-64 | 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 | |
HNFLJBMO_01112 | 1.7e-46 | 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 | |
HNFLJBMO_01113 | 3.2e-160 | 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 | |
HNFLJBMO_01114 | 7.5e-63 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HNFLJBMO_01115 | 1.7e-09 | S | Helix-turn-helix domain | |||
HNFLJBMO_01116 | 7.5e-43 | S | Phage regulatory protein Rha (Phage_pRha) | |||
HNFLJBMO_01119 | 1e-106 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
HNFLJBMO_01120 | 5.1e-16 | |||||
HNFLJBMO_01122 | 3.8e-267 | 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 | ||
HNFLJBMO_01123 | 1.8e-116 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HNFLJBMO_01124 | 5.6e-40 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HNFLJBMO_01125 | 1.8e-32 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HNFLJBMO_01126 | 3e-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 | ||
HNFLJBMO_01127 | 6e-93 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HNFLJBMO_01128 | 1.5e-186 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HNFLJBMO_01129 | 1.4e-153 | 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) |
HNFLJBMO_01131 | 2.3e-38 | |||||
HNFLJBMO_01132 | 4.1e-27 | gcvR | T | Belongs to the UPF0237 family | ||
HNFLJBMO_01133 | 6.7e-219 | XK27_08635 | S | UPF0210 protein | ||
HNFLJBMO_01134 | 9e-88 | fruR | K | DeoR C terminal sensor domain | ||
HNFLJBMO_01135 | 4.1e-151 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
HNFLJBMO_01136 | 3.3e-283 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
HNFLJBMO_01137 | 2e-49 | cps3F | ||||
HNFLJBMO_01138 | 2.1e-83 | S | Membrane | |||
HNFLJBMO_01139 | 1.8e-254 | E | Amino acid permease | |||
HNFLJBMO_01140 | 3.4e-226 | cadA | P | P-type ATPase | ||
HNFLJBMO_01141 | 6.4e-114 | degV | S | EDD domain protein, DegV family | ||
HNFLJBMO_01142 | 1.1e-148 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
HNFLJBMO_01143 | 5.6e-57 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HNFLJBMO_01144 | 7.2e-27 | ydiI | Q | Thioesterase superfamily | ||
HNFLJBMO_01145 | 4.3e-144 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
HNFLJBMO_01146 | 1.9e-139 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
HNFLJBMO_01147 | 4.7e-81 | S | L,D-transpeptidase catalytic domain | |||
HNFLJBMO_01148 | 1.5e-165 | EGP | Major facilitator Superfamily | |||
HNFLJBMO_01149 | 1.4e-21 | K | helix_turn_helix multiple antibiotic resistance protein | |||
HNFLJBMO_01150 | 5.1e-225 | pipD | E | Dipeptidase | ||
HNFLJBMO_01151 | 7e-126 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HNFLJBMO_01152 | 2.6e-32 | ywjH | S | Protein of unknown function (DUF1634) | ||
HNFLJBMO_01153 | 1.7e-119 | yxaA | S | membrane transporter protein | ||
HNFLJBMO_01154 | 5.7e-47 | S | Plasmid replication protein | |||
HNFLJBMO_01157 | 8.4e-38 | XK27_10050 | K | Peptidase S24-like | ||
HNFLJBMO_01158 | 4.1e-14 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
HNFLJBMO_01159 | 6.5e-80 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
HNFLJBMO_01160 | 1e-83 | holB | 2.7.7.7 | L | DNA polymerase III | |
HNFLJBMO_01161 | 1.4e-40 | yabA | L | Involved in initiation control of chromosome replication | ||
HNFLJBMO_01162 | 3.2e-92 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HNFLJBMO_01163 | 5.5e-82 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
HNFLJBMO_01164 | 2.3e-139 | ansA | 3.5.1.1 | EJ | Asparaginase | |
HNFLJBMO_01165 | 4.1e-69 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
HNFLJBMO_01166 | 3.4e-60 | hchA | S | intracellular protease amidase | ||
HNFLJBMO_01167 | 3.1e-134 | glpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
HNFLJBMO_01168 | 3.7e-113 | lacI3 | K | helix_turn _helix lactose operon repressor | ||
HNFLJBMO_01169 | 1.3e-14 | malL | 3.2.1.10 | GH13 | G | Psort location Cytoplasmic, score |
HNFLJBMO_01170 | 7.6e-125 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
HNFLJBMO_01172 | 1.5e-112 | casC | L | CT1975-like protein | ||
HNFLJBMO_01173 | 8.1e-22 | casB | S | CRISPR-associated protein Cse2 (CRISPR_cse2) | ||
HNFLJBMO_01174 | 1.2e-151 | casA | L | the current gene model (or a revised gene model) may contain a frame shift | ||
HNFLJBMO_01175 | 1.5e-74 | cas3 | L | CRISPR-associated helicase cas3 | ||
HNFLJBMO_01176 | 2.2e-204 | G | PTS system Galactitol-specific IIC component | |||
HNFLJBMO_01177 | 2e-93 | M | Exporter of polyketide antibiotics | |||
HNFLJBMO_01178 | 9.5e-48 | M | Exporter of polyketide antibiotics | |||
HNFLJBMO_01179 | 1.5e-83 | 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 | |
HNFLJBMO_01180 | 2.6e-78 | 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 | |
HNFLJBMO_01181 | 9.6e-126 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
HNFLJBMO_01182 | 5.3e-70 | M | Domain of unknown function (DUF4422) | |||
HNFLJBMO_01183 | 4.7e-59 | cps3F | ||||
HNFLJBMO_01184 | 1.4e-209 | yjeM | E | Amino Acid | ||
HNFLJBMO_01186 | 1.2e-31 | 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 | ||
HNFLJBMO_01187 | 9.2e-88 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HNFLJBMO_01188 | 1.2e-171 | patA | 2.6.1.1 | E | Aminotransferase | |
HNFLJBMO_01189 | 3e-17 | L | hmm pf00665 | |||
HNFLJBMO_01190 | 3e-38 | S | Sulfite exporter TauE/SafE | |||
HNFLJBMO_01191 | 1.8e-70 | K | Sugar-specific transcriptional regulator TrmB | |||
HNFLJBMO_01192 | 4.6e-168 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
HNFLJBMO_01193 | 1.7e-150 | 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 | ||
HNFLJBMO_01194 | 7.8e-198 | 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 | ||
HNFLJBMO_01195 | 3.9e-249 | 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 | |
HNFLJBMO_01196 | 9.7e-300 | 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 | ||
HNFLJBMO_01197 | 5e-23 | ykzG | S | Belongs to the UPF0356 family | ||
HNFLJBMO_01199 | 4.7e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HNFLJBMO_01200 | 2.5e-71 | yqeG | S | HAD phosphatase, family IIIA | ||
HNFLJBMO_01201 | 3e-180 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
HNFLJBMO_01202 | 1e-29 | yhbY | J | RNA-binding protein | ||
HNFLJBMO_01203 | 3.5e-77 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HNFLJBMO_01204 | 4e-282 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
HNFLJBMO_01205 | 2.5e-11 | ftsL | D | cell division protein FtsL | ||
HNFLJBMO_01206 | 4.5e-99 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HNFLJBMO_01207 | 2.3e-109 | 2.1.1.72, 3.1.21.3 | V | N-6 DNA Methylase | ||
HNFLJBMO_01209 | 5.7e-07 | L | Integrase core domain | |||
HNFLJBMO_01210 | 1.7e-42 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
HNFLJBMO_01211 | 2.2e-117 | prmA | J | Ribosomal protein L11 methyltransferase | ||
HNFLJBMO_01212 | 9.7e-74 | draG | O | ADP-ribosylglycohydrolase | ||
HNFLJBMO_01213 | 2.3e-181 | pepS | E | Thermophilic metalloprotease (M29) | ||
HNFLJBMO_01214 | 3.4e-78 | rapL | 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | |
HNFLJBMO_01215 | 1.2e-21 | rapL | 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | |
HNFLJBMO_01216 | 3.5e-117 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HNFLJBMO_01217 | 4.1e-102 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
HNFLJBMO_01218 | 6.8e-144 | pbuO_1 | S | Permease family | ||
HNFLJBMO_01219 | 6.6e-157 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
HNFLJBMO_01220 | 3.3e-105 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
HNFLJBMO_01221 | 1.3e-183 | lmrB | EGP | Major facilitator Superfamily | ||
HNFLJBMO_01222 | 2.1e-54 | bioY | S | BioY family | ||
HNFLJBMO_01223 | 1.4e-94 | S | Predicted membrane protein (DUF2207) | |||
HNFLJBMO_01224 | 1.4e-19 | |||||
HNFLJBMO_01225 | 4.4e-37 | M | Glycosyltransferase group 2 family protein | |||
HNFLJBMO_01226 | 7.4e-54 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
HNFLJBMO_01227 | 2.8e-58 | ktrA | P | TrkA-N domain | ||
HNFLJBMO_01228 | 1.2e-114 | ntpJ | P | Potassium uptake protein | ||
HNFLJBMO_01229 | 1.6e-183 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HNFLJBMO_01230 | 1e-281 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
HNFLJBMO_01231 | 3.5e-216 | scrB | 3.2.1.26 | GH32 | G | invertase |
HNFLJBMO_01232 | 1.7e-147 | scrR | K | helix_turn _helix lactose operon repressor | ||
HNFLJBMO_01233 | 8.3e-187 | 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 | |
HNFLJBMO_01234 | 9.1e-83 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
HNFLJBMO_01235 | 4.5e-187 | mtnE | 2.6.1.83 | E | Aminotransferase | |
HNFLJBMO_01237 | 2.7e-15 | |||||
HNFLJBMO_01238 | 1.6e-112 | rssA | S | Phospholipase, patatin family | ||
HNFLJBMO_01239 | 4.1e-15 | ywzB | S | Protein of unknown function (DUF1146) | ||
HNFLJBMO_01240 | 4.1e-38 | M | group 2 family protein | |||
HNFLJBMO_01241 | 6.6e-63 | licT | K | transcriptional antiterminator | ||
HNFLJBMO_01242 | 1.1e-100 | 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 | |
HNFLJBMO_01243 | 8.5e-37 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HNFLJBMO_01244 | 3.6e-220 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
HNFLJBMO_01245 | 4e-65 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
HNFLJBMO_01246 | 3.2e-57 | lssY | 3.6.1.27 | I | phosphatidate phosphatase activity | |
HNFLJBMO_01247 | 5.4e-128 | comFA | L | Helicase C-terminal domain protein | ||
HNFLJBMO_01248 | 2.5e-23 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
HNFLJBMO_01249 | 1.7e-118 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
HNFLJBMO_01250 | 9.5e-95 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
HNFLJBMO_01251 | 1.1e-98 | IQ | reductase | |||
HNFLJBMO_01252 | 4.2e-35 | K | helix_turn_helix, mercury resistance | |||
HNFLJBMO_01253 | 3.5e-113 | S | Aldo keto reductase | |||
HNFLJBMO_01254 | 1.8e-106 | L | Belongs to the 'phage' integrase family | |||
HNFLJBMO_01255 | 2.9e-22 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
HNFLJBMO_01256 | 1e-43 | 2.7.13.3 | T | protein histidine kinase activity | ||
HNFLJBMO_01257 | 1.4e-215 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HNFLJBMO_01258 | 3.5e-22 | S | Cytochrome B5 | |||
HNFLJBMO_01259 | 7.8e-49 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain (presumed) | |
HNFLJBMO_01260 | 1.9e-08 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
HNFLJBMO_01261 | 8.1e-37 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
HNFLJBMO_01262 | 2.2e-20 | |||||
HNFLJBMO_01263 | 4.5e-08 | S | Protein of unknown function (DUF3343) | |||
HNFLJBMO_01265 | 1.7e-40 | |||||
HNFLJBMO_01266 | 2.8e-34 | K | GNAT family | |||
HNFLJBMO_01267 | 7.6e-210 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
HNFLJBMO_01268 | 1.2e-167 | clcA | P | chloride | ||
HNFLJBMO_01269 | 2.8e-19 | secG | U | Preprotein translocase | ||
HNFLJBMO_01271 | 6.4e-45 | S | Haloacid dehalogenase-like hydrolase | |||
HNFLJBMO_01272 | 1.7e-07 | comGB | NU | type II secretion system | ||
HNFLJBMO_01273 | 3.1e-120 | comGA | NU | Type II IV secretion system protein | ||
HNFLJBMO_01274 | 2.3e-85 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
HNFLJBMO_01275 | 6.5e-34 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HNFLJBMO_01276 | 2e-129 | L | Belongs to the 'phage' integrase family | |||
HNFLJBMO_01277 | 1.4e-51 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
HNFLJBMO_01278 | 2.4e-164 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HNFLJBMO_01279 | 4.1e-75 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
HNFLJBMO_01280 | 1e-47 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
HNFLJBMO_01281 | 8.1e-38 | K | transcriptional regulator PadR family | |||
HNFLJBMO_01282 | 3.2e-19 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
HNFLJBMO_01283 | 2.4e-16 | S | Putative adhesin | |||
HNFLJBMO_01284 | 9.4e-94 | cca | 2.7.7.19, 2.7.7.72 | J | Aminoglycoside-2''-adenylyltransferase | |
HNFLJBMO_01285 | 7e-200 | L | transposition, DNA-mediated | |||
HNFLJBMO_01286 | 2.2e-16 | pspC | KT | PspC domain | ||
HNFLJBMO_01287 | 3.9e-13 | S | Enterocin A Immunity | |||
HNFLJBMO_01288 | 1.5e-235 | 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 | |
HNFLJBMO_01289 | 1.6e-260 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
HNFLJBMO_01290 | 7.4e-100 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HNFLJBMO_01291 | 8.2e-167 | 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 | |
HNFLJBMO_01292 | 9.5e-120 | potB | P | ABC transporter permease | ||
HNFLJBMO_01293 | 1.3e-103 | potC | U | Binding-protein-dependent transport system inner membrane component | ||
HNFLJBMO_01294 | 1.1e-158 | potD | P | ABC transporter | ||
HNFLJBMO_01295 | 7.8e-132 | ABC-SBP | S | ABC transporter | ||
HNFLJBMO_01296 | 4.3e-113 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
HNFLJBMO_01297 | 1e-107 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
HNFLJBMO_01298 | 7.4e-67 | M | ErfK YbiS YcfS YnhG | |||
HNFLJBMO_01299 | 4.1e-54 | 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 | ||
HNFLJBMO_01300 | 1.4e-224 | 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 | ||
HNFLJBMO_01301 | 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 | ||
HNFLJBMO_01303 | 2.2e-116 | ynjE | 2.8.1.11 | P | Rhodanese Homology Domain | |
HNFLJBMO_01304 | 4.2e-96 | trxB2 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
HNFLJBMO_01310 | 7.7e-39 | |||||
HNFLJBMO_01311 | 1.3e-172 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HNFLJBMO_01316 | 4.3e-56 | K | LytTr DNA-binding domain | |||
HNFLJBMO_01317 | 1.8e-22 | 2.7.13.3 | T | GHKL domain | ||
HNFLJBMO_01318 | 2.2e-128 | arlS | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_01320 | 2.5e-08 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
HNFLJBMO_01321 | 4e-07 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HNFLJBMO_01322 | 1.8e-131 | ylbL | T | Belongs to the peptidase S16 family | ||
HNFLJBMO_01323 | 5e-60 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HNFLJBMO_01324 | 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 | ||
HNFLJBMO_01325 | 4.7e-139 | yabM | S | Polysaccharide biosynthesis protein | ||
HNFLJBMO_01326 | 3.6e-31 | yabO | J | S4 domain protein | ||
HNFLJBMO_01327 | 2.3e-18 | divIC | D | Septum formation initiator | ||
HNFLJBMO_01328 | 1.1e-40 | yabR | J | RNA binding | ||
HNFLJBMO_01329 | 4.8e-91 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HNFLJBMO_01330 | 1.3e-158 | ccpA | K | catabolite control protein A | ||
HNFLJBMO_01331 | 3e-48 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HNFLJBMO_01332 | 1.7e-236 | 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 | |
HNFLJBMO_01333 | 5.1e-141 | 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 | ||
HNFLJBMO_01334 | 6.3e-266 | 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 | |
HNFLJBMO_01335 | 4.1e-58 | 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 | ||
HNFLJBMO_01336 | 2.4e-39 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HNFLJBMO_01337 | 1.8e-15 | 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 | ||
HNFLJBMO_01338 | 4.5e-97 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HNFLJBMO_01339 | 5e-100 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HNFLJBMO_01340 | 3.9e-43 | L | HTH-like domain | |||
HNFLJBMO_01341 | 1.6e-27 | L | Helix-turn-helix domain | |||
HNFLJBMO_01342 | 1.1e-293 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
HNFLJBMO_01343 | 1.8e-76 | 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 | ||
HNFLJBMO_01344 | 6.3e-188 | nhaC | C | Na H antiporter NhaC | ||
HNFLJBMO_01345 | 1e-64 | ypsA | S | Belongs to the UPF0398 family | ||
HNFLJBMO_01346 | 2.1e-196 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
HNFLJBMO_01348 | 2.4e-34 | 2.3.1.178 | M | GNAT acetyltransferase | ||
HNFLJBMO_01349 | 1.2e-16 | J | GNAT acetyltransferase | |||
HNFLJBMO_01350 | 1.3e-68 | maa | 2.3.1.79 | S | Maltose acetyltransferase | |
HNFLJBMO_01351 | 3.7e-56 | 3.6.1.27 | I | Acid phosphatase homologues | ||
HNFLJBMO_01352 | 5.1e-81 | XK27_07525 | 3.6.1.55 | F | Hydrolase, nudix family | |
HNFLJBMO_01354 | 1.3e-99 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HNFLJBMO_01355 | 1.5e-62 | bCE_4747 | S | Beta-lactamase superfamily domain | ||
HNFLJBMO_01356 | 1.4e-290 | ybiT | S | ABC transporter, ATP-binding protein | ||
HNFLJBMO_01357 | 1e-78 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HNFLJBMO_01358 | 1.3e-24 | |||||
HNFLJBMO_01359 | 5.8e-112 | dkg | S | reductase | ||
HNFLJBMO_01361 | 1.5e-20 | rimL | 1.1.1.25 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
HNFLJBMO_01362 | 2.3e-168 | 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) | |
HNFLJBMO_01363 | 2.5e-192 | 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 | |
HNFLJBMO_01364 | 5.6e-47 | EGP | Transmembrane secretion effector | |||
HNFLJBMO_01365 | 5.2e-137 | purR | 2.4.2.7 | F | pur operon repressor | |
HNFLJBMO_01366 | 2.5e-44 | adhR | K | helix_turn_helix, mercury resistance | ||
HNFLJBMO_01367 | 9.7e-184 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
HNFLJBMO_01369 | 1.2e-103 | pfoS | S | Phosphotransferase system, EIIC | ||
HNFLJBMO_01370 | 2.9e-126 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HNFLJBMO_01371 | 2.9e-149 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
HNFLJBMO_01372 | 2.1e-194 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
HNFLJBMO_01373 | 3.8e-188 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
HNFLJBMO_01374 | 2.3e-159 | 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 | ||
HNFLJBMO_01375 | 2.6e-182 | rny | S | Endoribonuclease that initiates mRNA decay | ||
HNFLJBMO_01376 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HNFLJBMO_01377 | 2.2e-226 | 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 | ||
HNFLJBMO_01378 | 5.5e-89 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
HNFLJBMO_01379 | 3.7e-141 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_01380 | 2.5e-113 | K | response regulator | |||
HNFLJBMO_01381 | 3.4e-89 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
HNFLJBMO_01382 | 3.4e-92 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
HNFLJBMO_01383 | 8.6e-272 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
HNFLJBMO_01384 | 3.1e-69 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
HNFLJBMO_01385 | 5.5e-243 | lysP | E | amino acid | ||
HNFLJBMO_01386 | 3.6e-190 | 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) | |
HNFLJBMO_01387 | 7.9e-08 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
HNFLJBMO_01388 | 4.8e-78 | 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 | |
HNFLJBMO_01389 | 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 | |
HNFLJBMO_01390 | 2.3e-54 | 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 | ||
HNFLJBMO_01391 | 5.1e-57 | 3.1.3.18 | J | HAD-hyrolase-like | ||
HNFLJBMO_01392 | 3.4e-42 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HNFLJBMO_01393 | 1.4e-127 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HNFLJBMO_01394 | 1.3e-75 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HNFLJBMO_01395 | 3.5e-204 | pyrP | F | Permease | ||
HNFLJBMO_01396 | 7.4e-115 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HNFLJBMO_01397 | 1.1e-154 | S | peptidoglycan catabolic process | |||
HNFLJBMO_01398 | 8.7e-32 | S | phage tail | |||
HNFLJBMO_01399 | 2e-60 | S | Prophage endopeptidase tail | |||
HNFLJBMO_01401 | 1.2e-67 | S | Domain of unknown function (DUF2479) | |||
HNFLJBMO_01407 | 7e-22 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
HNFLJBMO_01408 | 3e-117 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
HNFLJBMO_01409 | 2.9e-160 | Z012_01130 | S | Fic/DOC family | ||
HNFLJBMO_01410 | 2.3e-163 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HNFLJBMO_01411 | 4.5e-179 | 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) | |
HNFLJBMO_01412 | 5.9e-111 | galR | K | Transcriptional regulator | ||
HNFLJBMO_01413 | 8.9e-289 | lacS | G | Transporter | ||
HNFLJBMO_01414 | 1.1e-55 | repB | L | Initiator Replication protein | ||
HNFLJBMO_01415 | 2.6e-17 | pre | D | Plasmid recombination enzyme | ||
HNFLJBMO_01416 | 4.6e-72 | catB | 2.3.1.28 | V | This enzyme is an effector of chloramphenicol resistance in bacteria | |
HNFLJBMO_01417 | 4.1e-41 | L | Replication initiation factor | |||
HNFLJBMO_01418 | 4.1e-240 | tetL | EGP | Major Facilitator Superfamily | ||
HNFLJBMO_01419 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
HNFLJBMO_01420 | 4.9e-247 | 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) | |
HNFLJBMO_01421 | 3.6e-207 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNFLJBMO_01422 | 6.4e-56 | 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) | ||
HNFLJBMO_01423 | 1.6e-108 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HNFLJBMO_01424 | 7e-71 | yacP | S | YacP-like NYN domain | ||
HNFLJBMO_01425 | 2.1e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HNFLJBMO_01426 | 2.6e-11 | 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 | ||
HNFLJBMO_01427 | 7.7e-84 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HNFLJBMO_01428 | 5e-67 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HNFLJBMO_01429 | 1.6e-115 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HNFLJBMO_01430 | 7.6e-75 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HNFLJBMO_01431 | 9.7e-15 | K | Cro/C1-type HTH DNA-binding domain | |||
HNFLJBMO_01434 | 2e-77 | S | Siphovirus Gp157 | |||
HNFLJBMO_01435 | 5.4e-240 | res | L | Helicase C-terminal domain protein | ||
HNFLJBMO_01436 | 5.6e-117 | L | AAA domain | |||
HNFLJBMO_01437 | 8.1e-85 | |||||
HNFLJBMO_01438 | 2.8e-140 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
HNFLJBMO_01439 | 3e-229 | S | Virulence-associated protein E | |||
HNFLJBMO_01440 | 1.2e-49 | S | VRR_NUC | |||
HNFLJBMO_01444 | 1.4e-32 | arpU | S | Phage transcriptional regulator, ArpU family | ||
HNFLJBMO_01445 | 1.4e-08 | T | SpoVT / AbrB like domain | |||
HNFLJBMO_01446 | 6.3e-17 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
HNFLJBMO_01449 | 8.9e-90 | L | HNH nucleases | |||
HNFLJBMO_01450 | 4.3e-83 | L | Phage terminase, small subunit | |||
HNFLJBMO_01451 | 0.0 | S | Phage Terminase | |||
HNFLJBMO_01453 | 6.7e-207 | S | Phage portal protein | |||
HNFLJBMO_01454 | 4.2e-119 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
HNFLJBMO_01455 | 4.4e-222 | S | Phage capsid family | |||
HNFLJBMO_01456 | 4.8e-22 | S | Phage gp6-like head-tail connector protein | |||
HNFLJBMO_01457 | 4.2e-59 | S | Phage head-tail joining protein | |||
HNFLJBMO_01458 | 1.9e-65 | S | Bacteriophage HK97-gp10, putative tail-component | |||
HNFLJBMO_01459 | 5.4e-65 | S | Protein of unknown function (DUF806) | |||
HNFLJBMO_01460 | 6.1e-123 | S | Phage tail tube protein | |||
HNFLJBMO_01461 | 8.2e-54 | S | Phage tail assembly chaperone proteins, TAC | |||
HNFLJBMO_01463 | 1.3e-35 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
HNFLJBMO_01464 | 3.5e-86 | K | response regulator | |||
HNFLJBMO_01465 | 1e-84 | phoR | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_01466 | 4.1e-08 | KT | PspC domain protein | |||
HNFLJBMO_01467 | 1.6e-26 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
HNFLJBMO_01468 | 7.4e-132 | 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 | ||
HNFLJBMO_01469 | 1.1e-112 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HNFLJBMO_01470 | 6.1e-273 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
HNFLJBMO_01471 | 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 | ||
HNFLJBMO_01472 | 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 | ||
HNFLJBMO_01473 | 1.1e-83 | 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) | |
HNFLJBMO_01474 | 5.9e-80 | ylbE | GM | NAD dependent epimerase dehydratase family protein | ||
HNFLJBMO_01475 | 5.1e-113 | yitU | 3.1.3.104 | S | hydrolase | |
HNFLJBMO_01476 | 1.5e-60 | speG | J | Acetyltransferase (GNAT) domain | ||
HNFLJBMO_01477 | 1.8e-189 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HNFLJBMO_01478 | 1.1e-23 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
HNFLJBMO_01479 | 1.7e-231 | tetP | J | elongation factor G | ||
HNFLJBMO_01481 | 2.7e-94 | pstS | P | T5orf172 | ||
HNFLJBMO_01482 | 4.8e-258 | yeeB | L | DEAD-like helicases superfamily | ||
HNFLJBMO_01483 | 1.2e-248 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
HNFLJBMO_01484 | 1.5e-59 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
HNFLJBMO_01485 | 3.6e-213 | yjeM | E | Amino Acid | ||
HNFLJBMO_01486 | 5.6e-190 | glnPH2 | P | ABC transporter permease | ||
HNFLJBMO_01487 | 2.3e-112 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HNFLJBMO_01488 | 2.2e-44 | E | GDSL-like Lipase/Acylhydrolase | |||
HNFLJBMO_01489 | 5e-133 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
HNFLJBMO_01490 | 7.6e-275 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HNFLJBMO_01491 | 6.4e-48 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HNFLJBMO_01492 | 9e-20 | yaaA | S | S4 domain protein YaaA | ||
HNFLJBMO_01493 | 8.4e-154 | 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 | ||
HNFLJBMO_01494 | 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 | |
HNFLJBMO_01495 | 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 | |
HNFLJBMO_01496 | 4.8e-45 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HNFLJBMO_01497 | 3.3e-63 | 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 | ||
HNFLJBMO_01498 | 6.2e-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 | ||
HNFLJBMO_01499 | 5.6e-110 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
HNFLJBMO_01500 | 5.6e-117 | S | Glycosyl transferase family 2 | |||
HNFLJBMO_01501 | 5.7e-64 | D | peptidase | |||
HNFLJBMO_01502 | 1.9e-167 | 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 | |
HNFLJBMO_01503 | 3.7e-310 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HNFLJBMO_01504 | 4.1e-71 | S | Protein of unknown function (DUF1361) | |||
HNFLJBMO_01505 | 8.5e-127 | 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 | |
HNFLJBMO_01506 | 5.3e-68 | ybbR | S | YbbR-like protein | ||
HNFLJBMO_01507 | 2.6e-226 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HNFLJBMO_01508 | 8.3e-28 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
HNFLJBMO_01509 | 5.3e-131 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
HNFLJBMO_01510 | 4.2e-21 | cutC | P | Participates in the control of copper homeostasis | ||
HNFLJBMO_01511 | 8.1e-198 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
HNFLJBMO_01512 | 2.7e-127 | 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 | |
HNFLJBMO_01513 | 5e-91 | smc | D | Required for chromosome condensation and partitioning | ||
HNFLJBMO_01514 | 7.2e-146 | 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) | ||
HNFLJBMO_01515 | 1.2e-39 | 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 | ||
HNFLJBMO_01516 | 5e-204 | 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 | |
HNFLJBMO_01517 | 3.6e-42 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HNFLJBMO_01518 | 3.8e-27 | ylqC | S | Belongs to the UPF0109 family | ||
HNFLJBMO_01519 | 1.5e-57 | 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 | ||
HNFLJBMO_01520 | 1.9e-114 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HNFLJBMO_01521 | 3.3e-61 | pat | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
HNFLJBMO_01522 | 3.7e-134 | K | Transcriptional regulator | |||
HNFLJBMO_01523 | 8.3e-144 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
HNFLJBMO_01524 | 1.1e-114 | glcR | K | DeoR C terminal sensor domain | ||
HNFLJBMO_01526 | 4.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HNFLJBMO_01527 | 1.6e-38 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HNFLJBMO_01528 | 2.8e-69 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
HNFLJBMO_01529 | 1.5e-25 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
HNFLJBMO_01530 | 4.7e-158 | glk | 2.7.1.2 | G | Glucokinase | |
HNFLJBMO_01531 | 1.4e-45 | yqhL | P | Rhodanese-like protein | ||
HNFLJBMO_01532 | 2.8e-16 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
HNFLJBMO_01533 | 5.4e-111 | 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) | |
HNFLJBMO_01534 | 1.8e-205 | ynbB | 4.4.1.1 | P | aluminum resistance | |
HNFLJBMO_01535 | 1.3e-45 | glnR | K | Transcriptional regulator | ||
HNFLJBMO_01536 | 2e-247 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HNFLJBMO_01537 | 5.9e-35 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HNFLJBMO_01538 | 1e-98 | fhuC | P | ABC transporter | ||
HNFLJBMO_01539 | 2.1e-103 | znuB | U | ABC 3 transport family | ||
HNFLJBMO_01540 | 1.5e-55 | S | ECF transporter, substrate-specific component | |||
HNFLJBMO_01541 | 4.7e-103 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HNFLJBMO_01542 | 1.9e-88 | S | NADPH-dependent FMN reductase | |||
HNFLJBMO_01543 | 1.2e-27 | K | helix_turn_helix, mercury resistance | |||
HNFLJBMO_01544 | 1.2e-67 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HNFLJBMO_01546 | 2.6e-154 | EGP | Major facilitator Superfamily | |||
HNFLJBMO_01547 | 3.9e-58 | S | Haloacid dehalogenase-like hydrolase | |||
HNFLJBMO_01548 | 1.6e-88 | yvyE | 3.4.13.9 | S | YigZ family | |
HNFLJBMO_01549 | 9.5e-38 | S | CAAX protease self-immunity | |||
HNFLJBMO_01550 | 5.8e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
HNFLJBMO_01551 | 8.6e-62 | S | Glycosyltransferase like family 2 | |||
HNFLJBMO_01552 | 3.6e-141 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HNFLJBMO_01553 | 9.4e-101 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
HNFLJBMO_01554 | 1.8e-179 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HNFLJBMO_01555 | 2.1e-130 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
HNFLJBMO_01556 | 4.6e-117 | nagZ | 3.2.1.52 | G | Glycosyl hydrolase family 3 N terminal domain | |
HNFLJBMO_01557 | 4.4e-27 | S | zinc-ribbon domain | |||
HNFLJBMO_01558 | 2.5e-83 | S | response to antibiotic | |||
HNFLJBMO_01559 | 1.6e-159 | mgtE | P | Acts as a magnesium transporter | ||
HNFLJBMO_01560 | 5.4e-92 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
HNFLJBMO_01561 | 7.6e-117 | 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 | |
HNFLJBMO_01562 | 2.5e-94 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
HNFLJBMO_01563 | 8.1e-256 | topB | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
HNFLJBMO_01564 | 3.1e-34 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HNFLJBMO_01565 | 1.7e-193 | pbuX | F | xanthine permease | ||
HNFLJBMO_01566 | 3.3e-74 | 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 | |
HNFLJBMO_01567 | 6.3e-61 | acmC | 3.2.1.96 | NU | mannosyl-glycoprotein | |
HNFLJBMO_01568 | 3.2e-64 | S | ECF transporter, substrate-specific component | |||
HNFLJBMO_01569 | 9.6e-127 | mleP | S | Sodium Bile acid symporter family | ||
HNFLJBMO_01570 | 7e-247 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
HNFLJBMO_01571 | 6.2e-72 | mleR | K | LysR family | ||
HNFLJBMO_01572 | 3.1e-56 | K | transcriptional | |||
HNFLJBMO_01573 | 2.6e-41 | K | Bacterial regulatory proteins, tetR family | |||
HNFLJBMO_01574 | 6.1e-60 | T | Belongs to the universal stress protein A family | |||
HNFLJBMO_01575 | 1.2e-44 | K | Copper transport repressor CopY TcrY | |||
HNFLJBMO_01576 | 7e-50 | fhaB | M | Rib/alpha-like repeat | ||
HNFLJBMO_01577 | 1e-148 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
HNFLJBMO_01578 | 1.9e-95 | ypuA | S | Protein of unknown function (DUF1002) | ||
HNFLJBMO_01579 | 1.1e-07 | |||||
HNFLJBMO_01581 | 4.6e-90 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HNFLJBMO_01582 | 4.9e-96 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
HNFLJBMO_01583 | 2.1e-89 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
HNFLJBMO_01584 | 3.3e-243 | 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 | |
HNFLJBMO_01585 | 1.4e-129 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
HNFLJBMO_01586 | 3.6e-150 | S | Tetratricopeptide repeat protein | |||
HNFLJBMO_01587 | 1.1e-100 | EG | EamA-like transporter family | |||
HNFLJBMO_01588 | 6.2e-168 | rarA | L | recombination factor protein RarA | ||
HNFLJBMO_01590 | 3.4e-73 | usp6 | T | universal stress protein | ||
HNFLJBMO_01591 | 3.8e-54 | tag | 3.2.2.20 | L | glycosylase | |
HNFLJBMO_01592 | 2.2e-199 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HNFLJBMO_01593 | 3.5e-125 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HNFLJBMO_01595 | 3.5e-115 | sip | L | Belongs to the 'phage' integrase family | ||
HNFLJBMO_01596 | 5.7e-17 | K | Transcriptional regulator | |||
HNFLJBMO_01604 | 1.9e-42 | ybl78 | L | DnaD domain protein | ||
HNFLJBMO_01605 | 4.8e-09 | |||||
HNFLJBMO_01608 | 1.7e-93 | sip | L | Belongs to the 'phage' integrase family | ||
HNFLJBMO_01609 | 5.8e-37 | ogt | 2.1.1.63 | H | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
HNFLJBMO_01610 | 2.7e-48 | S | Domain of unknown function (DUF956) | |||
HNFLJBMO_01611 | 6.3e-115 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HNFLJBMO_01612 | 7.2e-82 | 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 | ||
HNFLJBMO_01613 | 4.9e-105 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HNFLJBMO_01614 | 5.1e-102 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
HNFLJBMO_01615 | 4.1e-157 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HNFLJBMO_01616 | 1.7e-259 | 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 | |
HNFLJBMO_01617 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HNFLJBMO_01618 | 2.7e-66 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
HNFLJBMO_01619 | 4.8e-170 | nusA | K | Participates in both transcription termination and antitermination | ||
HNFLJBMO_01620 | 1.4e-39 | ylxR | K | Protein of unknown function (DUF448) | ||
HNFLJBMO_01621 | 6.9e-26 | ylxQ | J | ribosomal protein | ||
HNFLJBMO_01622 | 1.6e-127 | mocA | S | Oxidoreductase | ||
HNFLJBMO_01623 | 2e-159 | yfmL | L | DEAD DEAH box helicase | ||
HNFLJBMO_01624 | 2e-20 | S | Domain of unknown function (DUF3284) | |||
HNFLJBMO_01626 | 1e-279 | kup | P | Transport of potassium into the cell | ||
HNFLJBMO_01628 | 6.8e-73 | gshR | 1.8.1.7 | C | Glutathione reductase | |
HNFLJBMO_01629 | 4.9e-179 | proV | E | ABC transporter, ATP-binding protein | ||
HNFLJBMO_01630 | 5.3e-263 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
HNFLJBMO_01631 | 2.6e-119 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HNFLJBMO_01632 | 1.5e-31 | |||||
HNFLJBMO_01633 | 2e-111 | ampC | V | Beta-lactamase | ||
HNFLJBMO_01634 | 3.5e-110 | cobQ | S | glutamine amidotransferase | ||
HNFLJBMO_01635 | 1e-219 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
HNFLJBMO_01636 | 1.1e-34 | tetR | K | transcriptional regulator | ||
HNFLJBMO_01639 | 1e-09 | 3.1.3.48 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
HNFLJBMO_01641 | 7.3e-18 | |||||
HNFLJBMO_01642 | 2e-120 | L | Mrr N-terminal domain | |||
HNFLJBMO_01644 | 6.4e-36 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
HNFLJBMO_01645 | 7.6e-210 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HNFLJBMO_01646 | 9.8e-146 | yegS | 2.7.1.107 | G | Lipid kinase | |
HNFLJBMO_01647 | 5.6e-256 | 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) | |
HNFLJBMO_01648 | 1.6e-234 | 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) | |
HNFLJBMO_01649 | 1.7e-37 | 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) | |
HNFLJBMO_01650 | 7.1e-161 | camS | S | sex pheromone | ||
HNFLJBMO_01651 | 2.3e-279 | 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 | |
HNFLJBMO_01652 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HNFLJBMO_01653 | 3.5e-144 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
HNFLJBMO_01655 | 1.2e-140 | hprA | 1.1.1.29 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HNFLJBMO_01656 | 1.4e-304 | 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 | ||
HNFLJBMO_01657 | 2.2e-214 | 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 | ||
HNFLJBMO_01658 | 6.9e-198 | oatA | I | Acyltransferase | ||
HNFLJBMO_01659 | 2.4e-144 | C | Aldo/keto reductase family | |||
HNFLJBMO_01660 | 5e-66 | pgm3 | G | phosphoglycerate mutase family | ||
HNFLJBMO_01661 | 5.1e-57 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | |
HNFLJBMO_01662 | 1.1e-85 | 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 | ||
HNFLJBMO_01663 | 1.2e-218 | yifK | E | Amino acid permease | ||
HNFLJBMO_01665 | 2.4e-28 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
HNFLJBMO_01668 | 3.3e-79 | L | Replication protein | |||
HNFLJBMO_01671 | 5.8e-59 | L | Psort location Cytoplasmic, score | |||
HNFLJBMO_01672 | 8.1e-266 | 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 |
HNFLJBMO_01673 | 2.6e-163 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
HNFLJBMO_01674 | 4e-119 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
HNFLJBMO_01675 | 9.4e-195 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
HNFLJBMO_01676 | 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 |
HNFLJBMO_01677 | 1.2e-175 | 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 |
HNFLJBMO_01678 | 3.4e-24 | S | Domain of unknown function (DUF4828) | |||
HNFLJBMO_01679 | 4.9e-29 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
HNFLJBMO_01680 | 1.4e-160 | 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 | |
HNFLJBMO_01681 | 3.6e-44 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
HNFLJBMO_01682 | 5.1e-49 | 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 | ||
HNFLJBMO_01683 | 5.5e-82 | H | Nodulation protein S (NodS) | |||
HNFLJBMO_01684 | 1.3e-122 | ylbM | S | Belongs to the UPF0348 family | ||
HNFLJBMO_01685 | 3.5e-57 | yceD | S | Uncharacterized ACR, COG1399 | ||
HNFLJBMO_01686 | 1.9e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HNFLJBMO_01687 | 2.8e-11 | K | DeoR C terminal sensor domain | |||
HNFLJBMO_01688 | 6.6e-30 | fcsR | K | DeoR C terminal sensor domain | ||
HNFLJBMO_01689 | 2.6e-295 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
HNFLJBMO_01690 | 8.9e-132 | rhaB | 2.7.1.5, 2.7.1.51 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
HNFLJBMO_01691 | 3.5e-180 | xylB | 2.7.1.17 | GH19 | EGP | Major facilitator Superfamily |
HNFLJBMO_01692 | 3.9e-48 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
HNFLJBMO_01693 | 2.2e-178 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
HNFLJBMO_01694 | 3.8e-50 | S | Membrane | |||
HNFLJBMO_01695 | 1.4e-75 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
HNFLJBMO_01696 | 4.2e-240 | sufB | O | assembly protein SufB | ||
HNFLJBMO_01697 | 4.9e-41 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HNFLJBMO_01698 | 1.1e-146 | sufS | 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 | |
HNFLJBMO_01699 | 2.1e-145 | sufD | O | FeS assembly protein SufD | ||
HNFLJBMO_01700 | 8.1e-116 | sufC | O | FeS assembly ATPase SufC | ||
HNFLJBMO_01701 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HNFLJBMO_01702 | 2.8e-96 | 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 | |
HNFLJBMO_01703 | 8.8e-58 | 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 | |
HNFLJBMO_01704 | 7.5e-178 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
HNFLJBMO_01705 | 4.1e-11 | |||||
HNFLJBMO_01707 | 9.9e-223 | lmrA | V | ABC transporter, ATP-binding protein | ||
HNFLJBMO_01708 | 3.9e-254 | yfiC | V | ABC transporter | ||
HNFLJBMO_01710 | 3.2e-45 | yjcF | K | protein acetylation | ||
HNFLJBMO_01711 | 1.1e-54 | L | phosphatase homologous to the C-terminal domain of histone macroH2A1 | |||
HNFLJBMO_01712 | 8.7e-72 | lemA | S | LemA family | ||
HNFLJBMO_01713 | 1.3e-114 | htpX | O | Belongs to the peptidase M48B family | ||
HNFLJBMO_01715 | 2.2e-270 | helD | 3.6.4.12 | L | DNA helicase | |
HNFLJBMO_01716 | 1.4e-141 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HNFLJBMO_01717 | 1.1e-30 | S | (CBS) domain | |||
HNFLJBMO_01718 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HNFLJBMO_01719 | 5.6e-127 | |||||
HNFLJBMO_01720 | 5.1e-152 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HNFLJBMO_01721 | 1.6e-42 | VPA1512 | ET | Bacterial extracellular solute-binding proteins, family 3 | ||
HNFLJBMO_01722 | 4.2e-26 | K | Bacterial regulatory proteins, tetR family | |||
HNFLJBMO_01723 | 2.9e-96 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HNFLJBMO_01724 | 4.8e-30 | 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 | |
HNFLJBMO_01725 | 1.2e-102 | 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 | |
HNFLJBMO_01726 | 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 | |
HNFLJBMO_01727 | 5.5e-227 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HNFLJBMO_01728 | 2.4e-139 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HNFLJBMO_01729 | 1.2e-74 | 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 | |
HNFLJBMO_01730 | 8.5e-234 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HNFLJBMO_01731 | 6e-161 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HNFLJBMO_01732 | 1.4e-16 | |||||
HNFLJBMO_01734 | 8.9e-141 | 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 | |
HNFLJBMO_01735 | 5.8e-101 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
HNFLJBMO_01736 | 7.6e-218 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
HNFLJBMO_01737 | 1.6e-138 | G | Xylose isomerase-like TIM barrel | |||
HNFLJBMO_01738 | 4.6e-117 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HNFLJBMO_01739 | 3e-216 | 1.3.5.4 | C | FAD binding domain | ||
HNFLJBMO_01740 | 8.4e-138 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
HNFLJBMO_01741 | 4.5e-71 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
HNFLJBMO_01742 | 2.4e-142 | xerS | L | Phage integrase family | ||
HNFLJBMO_01743 | 9.3e-128 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
HNFLJBMO_01744 | 8.8e-171 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNFLJBMO_01745 | 2.1e-102 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HNFLJBMO_01746 | 3.2e-82 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
HNFLJBMO_01747 | 6.3e-90 | ybhR | V | ABC transporter | ||
HNFLJBMO_01748 | 3.9e-100 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HNFLJBMO_01749 | 5.9e-98 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
HNFLJBMO_01750 | 2.9e-72 | ecsB | U | ABC transporter | ||
HNFLJBMO_01751 | 9.8e-95 | ecsA | V | ABC transporter, ATP-binding protein | ||
HNFLJBMO_01752 | 7e-53 | hit | FG | histidine triad | ||
HNFLJBMO_01754 | 1.5e-113 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HNFLJBMO_01755 | 2.1e-126 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HNFLJBMO_01756 | 2e-21 | yheA | S | Belongs to the UPF0342 family | ||
HNFLJBMO_01757 | 1.5e-284 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNFLJBMO_01760 | 2.6e-86 | ykuT | M | mechanosensitive ion channel | ||
HNFLJBMO_01761 | 2.4e-177 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HNFLJBMO_01762 | 3e-61 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HNFLJBMO_01763 | 1.5e-45 | ykuL | S | CBS domain | ||
HNFLJBMO_01764 | 1.3e-118 | gla | U | Major intrinsic protein | ||
HNFLJBMO_01765 | 5.8e-30 | S | Uncharacterized protein conserved in bacteria (DUF2188) | |||
HNFLJBMO_01766 | 2.3e-18 | |||||
HNFLJBMO_01769 | 1.6e-140 | K | Phage regulatory protein | |||
HNFLJBMO_01770 | 1.7e-10 | K | Helix-turn-helix XRE-family like proteins | |||
HNFLJBMO_01771 | 2.9e-23 | 3.4.21.88 | K | Helix-turn-helix domain | ||
HNFLJBMO_01772 | 1.1e-15 | S | Pfam:DUF955 | |||
HNFLJBMO_01774 | 9.6e-28 | S | Short C-terminal domain | |||
HNFLJBMO_01775 | 8.9e-19 | L | nuclease | |||
HNFLJBMO_01776 | 7.3e-13 | |||||
HNFLJBMO_01779 | 5.7e-85 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
HNFLJBMO_01780 | 6.9e-92 | T | Calcineurin-like phosphoesterase superfamily domain | |||
HNFLJBMO_01781 | 4.2e-49 | lytE | M | LysM domain protein | ||
HNFLJBMO_01782 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNFLJBMO_01783 | 7.4e-177 | 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 | |
HNFLJBMO_01793 | 2.1e-07 | |||||
HNFLJBMO_01799 | 3.7e-114 | 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 | ||
HNFLJBMO_01800 | 6.7e-149 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
HNFLJBMO_01801 | 1.4e-198 | frdC | 1.3.5.4 | C | FAD binding domain | |
HNFLJBMO_01802 | 3.4e-205 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
HNFLJBMO_01803 | 9.3e-37 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
HNFLJBMO_01804 | 6.7e-72 | ywlG | S | Belongs to the UPF0340 family | ||
HNFLJBMO_01805 | 1.7e-128 | C | Oxidoreductase | |||
HNFLJBMO_01806 | 2.4e-178 | L | transposase, IS605 OrfB family | |||
HNFLJBMO_01807 | 1.5e-69 | tlpA2 | L | Transposase IS200 like | ||
HNFLJBMO_01808 | 1.6e-174 | spoVK | O | PFAM ATPase family associated with various cellular activities (AAA) | ||
HNFLJBMO_01809 | 8.9e-44 | S | Domain of unknown function (DUF3841) | |||
HNFLJBMO_01810 | 4.9e-56 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
HNFLJBMO_01811 | 1.5e-103 | S | Domain of unknown function (DUF4343) | |||
HNFLJBMO_01812 | 0.0 | L | helicase activity | |||
HNFLJBMO_01813 | 1.1e-210 | K | DNA binding | |||
HNFLJBMO_01814 | 0.0 | res | 2.1.1.72, 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
HNFLJBMO_01815 | 3.3e-222 | mod | 2.1.1.72, 3.1.21.5 | L | DNA methylase | |
HNFLJBMO_01816 | 2.8e-98 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HNFLJBMO_01817 | 2.4e-33 | S | CAAX protease self-immunity | |||
HNFLJBMO_01818 | 2.4e-33 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HNFLJBMO_01819 | 1.8e-271 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HNFLJBMO_01820 | 2.5e-269 | aha1 | P | COG COG0474 Cation transport ATPase | ||
HNFLJBMO_01821 | 4.1e-296 | ydaO | E | amino acid | ||
HNFLJBMO_01822 | 5.2e-36 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
HNFLJBMO_01823 | 4.8e-43 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HNFLJBMO_01824 | 6.4e-59 | |||||
HNFLJBMO_01825 | 5.3e-27 | xlyB | 3.5.1.28 | CBM50 | M | LysM domain |
HNFLJBMO_01826 | 6.6e-19 | glpE | P | Rhodanese Homology Domain | ||
HNFLJBMO_01827 | 6.5e-197 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HNFLJBMO_01828 | 2.2e-201 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
HNFLJBMO_01829 | 3e-155 | amtB | P | ammonium transporter | ||
HNFLJBMO_01830 | 9e-116 | 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 | |
HNFLJBMO_01831 | 6.6e-46 | argR | K | Regulates arginine biosynthesis genes | ||
HNFLJBMO_01832 | 1.7e-138 | arcT | 2.6.1.1 | E | Cys/Met metabolism PLP-dependent enzyme | |
HNFLJBMO_01833 | 2e-87 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HNFLJBMO_01834 | 9e-114 | K | response regulator | |||
HNFLJBMO_01835 | 1.5e-272 | vicK | 2.7.13.3 | T | Histidine kinase | |
HNFLJBMO_01836 | 1.3e-102 | yycH | S | YycH protein | ||
HNFLJBMO_01837 | 2.1e-79 | yycI | S | YycH protein | ||
HNFLJBMO_01838 | 6.8e-30 | yyaQ | S | YjbR | ||
HNFLJBMO_01839 | 1.7e-116 | vicX | 3.1.26.11 | S | domain protein | |
HNFLJBMO_01840 | 9.6e-146 | htrA | 3.4.21.107 | O | serine protease | |
HNFLJBMO_01842 | 1.1e-35 | 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 | ||
HNFLJBMO_01843 | 1.8e-172 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HNFLJBMO_01844 | 3.1e-36 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
HNFLJBMO_01845 | 1.5e-22 | S | Family of unknown function (DUF5322) | |||
HNFLJBMO_01846 | 3.8e-256 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HNFLJBMO_01847 | 1.8e-38 | |||||
HNFLJBMO_01848 | 2.8e-125 | rapZ | S | Displays ATPase and GTPase activities | ||
HNFLJBMO_01849 | 8.2e-153 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HNFLJBMO_01850 | 1.8e-149 | whiA | K | May be required for sporulation | ||
HNFLJBMO_01851 | 1.1e-99 | 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 | |
HNFLJBMO_01853 | 2.9e-137 | cggR | K | Putative sugar-binding domain | ||
HNFLJBMO_01854 | 6.1e-180 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HNFLJBMO_01855 | 1.3e-208 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HNFLJBMO_01856 | 2.3e-128 | 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) | |
HNFLJBMO_01857 | 9.5e-234 | 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 | |
HNFLJBMO_01858 | 3.5e-70 | mltD | CBM50 | M | NlpC P60 family protein | |
HNFLJBMO_01859 | 1.8e-52 | manO | S | Domain of unknown function (DUF956) | ||
HNFLJBMO_01860 | 2.1e-147 | manN | G | system, mannose fructose sorbose family IID component | ||
HNFLJBMO_01861 | 8e-119 | manY | G | PTS system sorbose-specific iic component | ||
HNFLJBMO_01862 | 9e-152 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
HNFLJBMO_01863 | 4.1e-80 | rbsB | G | sugar-binding domain protein | ||
HNFLJBMO_01864 | 5.1e-99 | baeS | T | Histidine kinase | ||
HNFLJBMO_01865 | 3.9e-79 | baeR | K | Bacterial regulatory proteins, luxR family | ||
HNFLJBMO_01866 | 1.8e-120 | G | Bacterial extracellular solute-binding protein | |||
HNFLJBMO_01867 | 3.2e-181 | pbuG | S | permease | ||
HNFLJBMO_01868 | 3.1e-202 | oppA | E | ABC transporter, substratebinding protein | ||
HNFLJBMO_01869 | 7.9e-142 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HNFLJBMO_01870 | 3.7e-169 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HNFLJBMO_01871 | 1.3e-180 | oppD | P | Belongs to the ABC transporter superfamily | ||
HNFLJBMO_01872 | 1.4e-154 | oppF | P | Belongs to the ABC transporter superfamily |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)