ORF_ID e_value Gene_name EC_number CAZy COGs Description
NJMBNHFK_00001 1.3e-257 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
NJMBNHFK_00002 6.3e-202 dnaN 2.7.7.7 L Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria
NJMBNHFK_00003 1.1e-29 yyzM S Protein conserved in bacteria
NJMBNHFK_00004 1.1e-203 ychF J ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner
NJMBNHFK_00005 1.4e-104 pth 3.1.1.29 J The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis
NJMBNHFK_00006 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
NJMBNHFK_00007 1.7e-39 yabO J Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog)
NJMBNHFK_00008 2.7e-61 divIC D Septum formation initiator
NJMBNHFK_00010 8.7e-240 XK27_09285 3.5.2.6 V Beta-lactamase enzyme family
NJMBNHFK_00011 5e-240 tilS 2.4.2.8, 6.3.4.19 D Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine
NJMBNHFK_00012 3.4e-97 hpt 2.4.2.8, 6.3.4.19 F Belongs to the purine pyrimidine phosphoribosyltransferase family
NJMBNHFK_00013 0.0 ftsH O Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins
NJMBNHFK_00014 1.3e-137 L Transposase
NJMBNHFK_00015 1.1e-92 L Transposase
NJMBNHFK_00016 1.6e-55 L transposition
NJMBNHFK_00017 1.9e-86 L Integrase core domain protein
NJMBNHFK_00030 5.3e-11
NJMBNHFK_00036 5.5e-139 mreC M Involved in formation and maintenance of cell shape
NJMBNHFK_00037 6.3e-88 mreD M Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins
NJMBNHFK_00038 1.7e-90 usp 3.5.1.28 CBM50 S CHAP domain
NJMBNHFK_00039 1.2e-174 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)
NJMBNHFK_00040 2.9e-218 araT 2.6.1.1 E Aminotransferase
NJMBNHFK_00041 2.6e-143 recO L Involved in DNA repair and RecF pathway recombination
NJMBNHFK_00042 1.3e-179 plsX 2.3.1.15 I Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA
NJMBNHFK_00043 4.2e-34 acpP1 IQ Carrier of the growing fatty acid chain in fatty acid biosynthesis
NJMBNHFK_00044 2e-129 purC 4.1.1.21, 4.3.2.2, 6.3.2.6 F Belongs to the SAICAR synthetase family
NJMBNHFK_00045 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
NJMBNHFK_00046 1.3e-276 purF 2.4.2.14 F Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine
NJMBNHFK_00047 1.8e-184 purM 6.3.3.1, 6.3.4.13 F Phosphoribosylformylglycinamidine cyclo-ligase
NJMBNHFK_00048 1.4e-101 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
NJMBNHFK_00049 2.3e-295 purH 2.1.2.3, 3.5.4.10 F Bifunctional purine biosynthesis protein PurH
NJMBNHFK_00050 6.1e-79 L transposase activity
NJMBNHFK_00051 1.3e-49 L transposition
NJMBNHFK_00052 6.3e-34 L Integrase core domain protein
NJMBNHFK_00053 2.3e-161 S CHAP domain
NJMBNHFK_00054 3.4e-241 purD 6.3.4.13 F Belongs to the GARS family
NJMBNHFK_00055 4.9e-76 purE 5.4.99.18 F Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR)
NJMBNHFK_00056 2.2e-204 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)
NJMBNHFK_00057 9.2e-141 1.1.1.169 H Ketopantoate reductase
NJMBNHFK_00058 8.7e-248 purB 4.3.2.2 F Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily
NJMBNHFK_00059 0.0 argS 6.1.1.19 J Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA
NJMBNHFK_00060 1.2e-09 L Transposase
NJMBNHFK_00061 7.8e-211 ugd 1.1.1.22 M Belongs to the UDP-glucose GDP-mannose dehydrogenase family
NJMBNHFK_00062 8.3e-221 nodC 2.4.1.212 GT2 M Chitin synthase
NJMBNHFK_00063 3.1e-89 FNV0100 F Belongs to the Nudix hydrolase family
NJMBNHFK_00064 3.5e-28 3.4.13.21 I Protein conserved in bacteria
NJMBNHFK_00067 1.3e-57 T Toxic component of a toxin-antitoxin (TA) module
NJMBNHFK_00069 8.2e-70 argR K Regulates arginine biosynthesis genes
NJMBNHFK_00070 1e-57 ymcA 3.6.3.21 S Belongs to the UPF0342 family
NJMBNHFK_00071 0.0 mutS L that it carries out the mismatch recognition step. This protein has a weak ATPase activity
NJMBNHFK_00072 7e-34 S Protein of unknown function (DUF3021)
NJMBNHFK_00073 1.2e-61 KT phosphorelay signal transduction system
NJMBNHFK_00075 0.0 mutL L This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex
NJMBNHFK_00077 7.8e-103 ruvA 3.6.4.12 L The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB
NJMBNHFK_00078 6.4e-107 tag 3.2.2.20 L 3-methyladenine DNA glycosylase
NJMBNHFK_00079 1e-232 cinA 3.5.1.42 S Belongs to the CinA family
NJMBNHFK_00080 2.8e-197 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
NJMBNHFK_00081 2.3e-66 spxA_2 1.20.4.1 P Belongs to the ArsC family
NJMBNHFK_00087 2.6e-10
NJMBNHFK_00090 1.9e-07
NJMBNHFK_00095 0.0 polC 2.7.7.7 L Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity
NJMBNHFK_00096 8.6e-237 pepS E COG2309 Leucyl aminopeptidase (aminopeptidase T)
NJMBNHFK_00097 5.5e-36 XK27_02060 S Transglycosylase associated protein
NJMBNHFK_00098 1.7e-54 badR K DNA-binding transcription factor activity
NJMBNHFK_00099 1e-96 S reductase
NJMBNHFK_00100 2.3e-31 L Integrase core domain protein
NJMBNHFK_00101 6.2e-36 L transposition
NJMBNHFK_00102 1.9e-22 yocD 3.4.17.13 V carboxypeptidase activity
NJMBNHFK_00103 3.8e-87 yocD 3.4.17.13 V proteins, homologs of microcin C7 resistance protein MccF
NJMBNHFK_00106 1.3e-137 rpsB J Belongs to the universal ribosomal protein uS2 family
NJMBNHFK_00107 1.7e-182 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
NJMBNHFK_00108 1.1e-83 S Putative small multi-drug export protein
NJMBNHFK_00109 6.2e-76 ctsR K Belongs to the CtsR family
NJMBNHFK_00110 0.0 clpC O Belongs to the ClpA ClpB family
NJMBNHFK_00111 3.2e-151 dacA 3.4.16.4 M Belongs to the peptidase S11 family
NJMBNHFK_00112 1.8e-32 dacA 3.4.16.4 M Belongs to the peptidase S11 family
NJMBNHFK_00113 1.4e-231 dacA 3.4.16.4 M Belongs to the peptidase S11 family
NJMBNHFK_00114 0.0 pnp 2.7.7.8 J Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction
NJMBNHFK_00115 6.9e-144 S SseB protein N-terminal domain
NJMBNHFK_00116 1.1e-112 cysE 2.3.1.30 E serine acetyltransferase
NJMBNHFK_00117 1.7e-259 cysS 6.1.1.16, 6.3.1.13 J Belongs to the class-I aminoacyl-tRNA synthetase family
NJMBNHFK_00118 4.2e-68 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)
NJMBNHFK_00121 5.7e-135 trmH 2.1.1.185 J Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
NJMBNHFK_00122 1e-84 yacP S RNA-binding protein containing a PIN domain
NJMBNHFK_00123 3.4e-155 degV S DegV family
NJMBNHFK_00125 1.8e-31 K helix-turn-helix
NJMBNHFK_00126 6.1e-182 panE 1.1.1.169 H Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid
NJMBNHFK_00127 2e-79 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
NJMBNHFK_00128 9.5e-65 rpsI J Belongs to the universal ribosomal protein uS9 family
NJMBNHFK_00129 1.5e-35 K sequence-specific DNA binding
NJMBNHFK_00131 0.0 S Lantibiotic dehydratase, C terminus
NJMBNHFK_00132 2.4e-231 spaC2 V Lanthionine synthetase C family protein
NJMBNHFK_00133 4.3e-183 EGP Major facilitator Superfamily
NJMBNHFK_00134 5.9e-24 3.6.4.12
NJMBNHFK_00135 5.9e-91 3.6.4.12 K Divergent AAA domain protein
NJMBNHFK_00136 7.4e-225 int L Belongs to the 'phage' integrase family
NJMBNHFK_00137 1.8e-38 S Helix-turn-helix domain
NJMBNHFK_00138 4.9e-173
NJMBNHFK_00140 3.4e-75 isp2 S pathogenesis
NJMBNHFK_00141 5.7e-91 tnp L Transposase
NJMBNHFK_00142 3.3e-225 capA M Bacterial capsule synthesis protein
NJMBNHFK_00143 3.6e-39 gcvR T UPF0237 protein
NJMBNHFK_00144 1.9e-242 XK27_08635 S UPF0210 protein
NJMBNHFK_00145 2.2e-38 ais G alpha-ribazole phosphatase activity
NJMBNHFK_00146 1.6e-143 vanY 3.4.17.14 M D-alanyl-D-alanine carboxypeptidase
NJMBNHFK_00147 1.3e-102 acmA 3.2.1.17 NU amidase activity
NJMBNHFK_00148 5.3e-198 hrcA K Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons
NJMBNHFK_00149 1.3e-71 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
NJMBNHFK_00150 9.8e-298 dnaK O Heat shock 70 kDa protein
NJMBNHFK_00151 4.2e-190 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
NJMBNHFK_00152 2.5e-138 truA 5.4.99.12 J Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs
NJMBNHFK_00153 6.2e-137 thiD 2.7.1.35, 2.7.1.49, 2.7.4.7 H phosphomethylpyrimidine kinase
NJMBNHFK_00154 1.7e-60 hmpT S membrane
NJMBNHFK_00167 0.0 amiA E ABC transporter, substrate-binding protein, family 5
NJMBNHFK_00168 1.3e-168 L Transposase
NJMBNHFK_00169 9.9e-19 S Domain of unknown function (DUF4649)
NJMBNHFK_00170 1.8e-56 amd 3.5.1.47 E COG1473 Metal-dependent amidase aminoacylase carboxypeptidase
NJMBNHFK_00171 1.5e-233 cfa 2.1.1.317, 2.1.1.79 M cyclopropane-fatty-acyl-phospholipid synthase
NJMBNHFK_00172 6.5e-87
NJMBNHFK_00173 1.6e-77 sigH K DNA-templated transcription, initiation
NJMBNHFK_00174 3.5e-149 ykuT M mechanosensitive ion channel
NJMBNHFK_00175 7.1e-218 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
NJMBNHFK_00176 4.8e-73 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
NJMBNHFK_00177 7.6e-310 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
NJMBNHFK_00178 1.1e-83 XK27_03960 S Protein of unknown function (DUF3013)
NJMBNHFK_00179 3.7e-81 mutT3 3.6.1.13, 3.6.1.55 L NUDIX domain
NJMBNHFK_00180 2e-177 prmA J Ribosomal protein L11 methyltransferase
NJMBNHFK_00181 4.4e-135 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
NJMBNHFK_00182 1.4e-42 F nucleotide catabolic process
NJMBNHFK_00183 5.4e-139 cpdB 3.1.3.6, 3.1.4.16 F Belongs to the 5'-nucleotidase family
NJMBNHFK_00184 7.7e-140 cpdB 3.1.3.6, 3.1.4.16 F Belongs to the 5'-nucleotidase family
NJMBNHFK_00185 2.3e-51 cpdB 3.1.3.6, 3.1.4.16 F Belongs to the 5'-nucleotidase family
NJMBNHFK_00186 1.8e-83 nrdI F Belongs to the NrdI family
NJMBNHFK_00187 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
NJMBNHFK_00188 2.3e-75 dtd J rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality
NJMBNHFK_00189 1.4e-09 dex 3.2.1.11 GH66 G Glycosyl hydrolase family 66
NJMBNHFK_00190 2e-27 dex 3.2.1.11 GH66 G Glycosyl hydrolase family 66
NJMBNHFK_00191 2.1e-58 dex 3.2.1.11 GH66 G Glycosyl hydrolase family 66
NJMBNHFK_00192 3.9e-46 dex 3.2.1.11 GH66 G Glycosyl hydrolase family 66
NJMBNHFK_00193 1.7e-237 ilvA 4.3.1.19 E Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA
NJMBNHFK_00194 3.3e-112 def 3.5.1.31, 3.5.1.88 J Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions
NJMBNHFK_00195 5.3e-113 fnr5 K Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases
NJMBNHFK_00196 6.5e-202 yhjX P Major Facilitator
NJMBNHFK_00197 9.2e-43 rpsO J Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome
NJMBNHFK_00198 5e-94 V VanZ like family
NJMBNHFK_00199 1e-123 glnQ E abc transporter atp-binding protein
NJMBNHFK_00200 5.8e-275 glnP P ABC transporter
NJMBNHFK_00201 9.1e-153 uppP 3.6.1.27 V Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin
NJMBNHFK_00202 1.3e-134 mecA NOT Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis
NJMBNHFK_00203 1.9e-185 tagO 2.7.8.33, 2.7.8.35 M transferase
NJMBNHFK_00204 9.5e-144 sufC O ABC-type transport system involved in Fe-S cluster assembly, ATPase component
NJMBNHFK_00205 1.4e-234 sufD O assembly protein SufD
NJMBNHFK_00206 7.7e-238 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
NJMBNHFK_00207 2.5e-74 nifU C SUF system FeS assembly protein, NifU family
NJMBNHFK_00208 2.2e-273 sufB O assembly protein SufB
NJMBNHFK_00209 7e-10 oppA E ABC transporter substrate-binding protein
NJMBNHFK_00210 2e-138 oppA E ABC transporter substrate-binding protein
NJMBNHFK_00211 4.2e-27 oppB P ABC-type dipeptide oligopeptide nickel transport systems, permease components
NJMBNHFK_00212 6.6e-11 oppC EP ABC-type dipeptide oligopeptide nickel transport systems, permease components
NJMBNHFK_00213 1.7e-33 oppC EP ABC-type dipeptide oligopeptide nickel transport systems, permease components
NJMBNHFK_00214 2.5e-09 oppC EP ABC-type dipeptide oligopeptide nickel transport systems, permease components
NJMBNHFK_00215 1.4e-38 oppC EP ABC-type dipeptide oligopeptide nickel transport systems, permease components
NJMBNHFK_00216 3e-27 oppD P Belongs to the ABC transporter superfamily
NJMBNHFK_00217 2.5e-32 oppD P Belongs to the ABC transporter superfamily
NJMBNHFK_00218 1.2e-62 oppD P Belongs to the ABC transporter superfamily
NJMBNHFK_00219 3.1e-43 oppD P Belongs to the ABC transporter superfamily
NJMBNHFK_00220 7.5e-62 oppF P Belongs to the ABC transporter superfamily
NJMBNHFK_00221 4.4e-62 oppF P Belongs to the ABC transporter superfamily
NJMBNHFK_00222 6.4e-23
NJMBNHFK_00223 2.1e-157 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
NJMBNHFK_00224 7.4e-183 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
NJMBNHFK_00225 1.9e-223 EGP Major facilitator Superfamily
NJMBNHFK_00226 3.1e-72 adcR K transcriptional
NJMBNHFK_00227 2.2e-136 adcC P ABC transporter, ATP-binding protein
NJMBNHFK_00228 1.6e-127 adcB P ABC transporter (Permease
NJMBNHFK_00229 1.4e-162 mleP2 S Transporter, auxin efflux carrier (AEC) family protein
NJMBNHFK_00230 5.6e-65 ptsG 2.7.1.199, 2.7.1.208 G pts system
NJMBNHFK_00231 2.1e-150 ptsG 2.7.1.199, 2.7.1.208, 2.7.1.211 G pts system
NJMBNHFK_00232 1.4e-105 ptsG 2.7.1.199, 2.7.1.208, 2.7.1.211 G phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1
NJMBNHFK_00233 6.8e-158 rgfB 3.1.3.90 L Endonuclease/Exonuclease/phosphatase family
NJMBNHFK_00234 2.8e-257 pgi 5.3.1.9 G Belongs to the GPI family
NJMBNHFK_00235 1.9e-127 yeeN K transcriptional regulatory protein
NJMBNHFK_00236 9.8e-50 yajC U protein transport
NJMBNHFK_00237 1.1e-141 uppS 2.5.1.31 H Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids
NJMBNHFK_00238 2.2e-145 cdsA 2.7.7.41 S Belongs to the CDS family
NJMBNHFK_00239 1.4e-231 rseP 3.4.21.107, 3.4.21.116 M zinc metalloprotease
NJMBNHFK_00240 0.0 proS 6.1.1.15 J Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS
NJMBNHFK_00241 0.0 WQ51_06230 S ABC transporter substrate binding protein
NJMBNHFK_00242 5.2e-142 cmpC S abc transporter atp-binding protein
NJMBNHFK_00243 1.3e-42 groS O Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter
NJMBNHFK_00244 4.1e-287 groL O Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions
NJMBNHFK_00245 4.4e-37 L Transposase
NJMBNHFK_00246 6.4e-18 L transposase activity
NJMBNHFK_00247 1.5e-30 L transposition
NJMBNHFK_00250 4.7e-43
NJMBNHFK_00251 6.8e-56 S TM2 domain
NJMBNHFK_00252 1.2e-165 rluA 5.4.99.23 J Responsible for synthesis of pseudouridine from uracil
NJMBNHFK_00253 0.0 pbp2A 2.4.1.129, 3.4.16.4 GT51 M penicillin-binding protein
NJMBNHFK_00254 3.3e-21 rpmG J Belongs to the bacterial ribosomal protein bL33 family
NJMBNHFK_00255 5.7e-25 secE U Belongs to the SecE SEC61-gamma family
NJMBNHFK_00256 8.4e-96 nusG K Participates in transcription elongation, termination and antitermination
NJMBNHFK_00257 4.6e-85 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 I phosphatidate phosphatase activity
NJMBNHFK_00258 6e-55 cof Q phosphatase activity
NJMBNHFK_00259 6.2e-35 cof Q phosphatase activity
NJMBNHFK_00260 1.6e-137 glcR K transcriptional regulator (DeoR family)
NJMBNHFK_00261 0.0 leuS 6.1.1.4 J Belongs to the class-I aminoacyl-tRNA synthetase family
NJMBNHFK_00263 3.8e-40 K transcriptional
NJMBNHFK_00265 2.6e-76 S thiolester hydrolase activity
NJMBNHFK_00266 1e-139 S COG1073 Hydrolases of the alpha beta superfamily
NJMBNHFK_00267 5.7e-280 pncB 6.3.4.21 H Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP
NJMBNHFK_00268 2.1e-151 nadE 6.3.1.5 H Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source
NJMBNHFK_00269 1.9e-77 yhaI L Membrane
NJMBNHFK_00270 5.1e-259 pepC 3.4.22.40 E aminopeptidase
NJMBNHFK_00271 1.6e-249 L Transposase
NJMBNHFK_00272 0.0 ponA 2.4.1.129, 3.4.16.4 GT51 M penicillin-binding protein
NJMBNHFK_00273 2.5e-109 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
NJMBNHFK_00274 3.1e-95 ypsA S Belongs to the UPF0398 family
NJMBNHFK_00275 2.5e-50 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
NJMBNHFK_00276 1.5e-222 rlmL 2.1.1.173, 2.1.1.264 L Belongs to the methyltransferase superfamily
NJMBNHFK_00277 2.5e-296 mapZ D Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning
NJMBNHFK_00278 0.0 snf 2.7.11.1 L Superfamily II DNA RNA helicases, SNF2 family'
NJMBNHFK_00279 2.5e-23
NJMBNHFK_00280 2.6e-255 mpl 6.3.2.4, 6.3.2.45, 6.3.2.8 M Belongs to the MurCDEF family
NJMBNHFK_00281 7.3e-80 XK27_09675 K -acetyltransferase
NJMBNHFK_00282 0.0 mltG ADL Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation
NJMBNHFK_00283 1.6e-77 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
NJMBNHFK_00284 5.2e-59 L Integrase core domain protein
NJMBNHFK_00285 2.9e-165 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
NJMBNHFK_00286 7e-46 acyP 3.6.1.7 C Belongs to the acylphosphatase family
NJMBNHFK_00287 6.4e-131 spoU 2.1.1.185 J Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
NJMBNHFK_00288 6.1e-93 XK27_09705 6.1.1.14 S HD superfamily hydrolase
NJMBNHFK_00289 8.8e-98 ybhL S Belongs to the BI1 family
NJMBNHFK_00292 9.6e-244 lysA 4.1.1.20 E Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine
NJMBNHFK_00293 3.7e-91 K transcriptional regulator
NJMBNHFK_00294 7.6e-36 yneF S UPF0154 protein
NJMBNHFK_00295 3.8e-148 murI 5.1.1.3 M Provides the (R)-glutamate required for cell wall biosynthesis
NJMBNHFK_00296 7.1e-186 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
NJMBNHFK_00297 3.5e-99 XK27_09740 S Phosphoesterase
NJMBNHFK_00298 7.8e-85 ykuL S CBS domain
NJMBNHFK_00299 4.5e-135 xerD L tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site
NJMBNHFK_00300 3.8e-120 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
NJMBNHFK_00301 3e-99 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
NJMBNHFK_00302 6.1e-140 rluB 5.4.99.19, 5.4.99.21, 5.4.99.22 J Belongs to the pseudouridine synthase RsuA family
NJMBNHFK_00303 1.2e-39 yidD S Could be involved in insertion of integral membrane proteins into the membrane
NJMBNHFK_00304 1.2e-258 trkH P Cation transport protein
NJMBNHFK_00305 1.5e-247 trkA P Potassium transporter peripheral membrane component
NJMBNHFK_00306 7.9e-96 trmL 2.1.1.207 J Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily
NJMBNHFK_00307 3.2e-90 ribU 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
NJMBNHFK_00308 4.8e-114 bcrC 3.6.1.27 I Membrane-associated phospholipid phosphatase
NJMBNHFK_00309 5.6e-161 K sequence-specific DNA binding
NJMBNHFK_00310 1.2e-32 V protein secretion by the type I secretion system
NJMBNHFK_00311 7.4e-36 V ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain
NJMBNHFK_00312 4.3e-57 V ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain
NJMBNHFK_00313 1.6e-25 V protein secretion by the type I secretion system
NJMBNHFK_00314 1.8e-27 comA V protein secretion by the type I secretion system
NJMBNHFK_00315 3.4e-68 comA V ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain
NJMBNHFK_00316 3.7e-51 yhaI L Membrane
NJMBNHFK_00317 6.7e-36 S Domain of unknown function (DUF4173)
NJMBNHFK_00318 9.2e-132 S Domain of unknown function (DUF4173)
NJMBNHFK_00319 6.8e-95 ureI S AmiS/UreI family transporter
NJMBNHFK_00320 7.6e-46 ureA 3.5.1.5 E Belongs to the urease gamma subunit family
NJMBNHFK_00321 7.8e-54 ureB 3.5.1.5 E Belongs to the urease beta subunit family
NJMBNHFK_00322 0.0 ureC 3.5.1.5 E Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family
NJMBNHFK_00323 6.6e-78 ureE O enzyme active site formation
NJMBNHFK_00324 5.3e-130 ureF O Required for maturation of urease via the functional incorporation of the urease nickel metallocenter
NJMBNHFK_00325 9.5e-112 ureG KO Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG
NJMBNHFK_00326 1.3e-159 ureD O Required for maturation of urease via the functional incorporation of the urease nickel metallocenter
NJMBNHFK_00327 2.7e-177 cbiM P PDGLE domain
NJMBNHFK_00328 1.1e-136 P cobalt transport protein
NJMBNHFK_00329 1.6e-131 cbiO P ABC transporter
NJMBNHFK_00330 5.3e-153 ET amino acid transport
NJMBNHFK_00331 0.0 Q 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
NJMBNHFK_00332 0.0 3.3.1.1, 3.6.1.55, 3.6.1.67 F NUDIX domain
NJMBNHFK_00333 3.8e-205 EGP Transmembrane secretion effector
NJMBNHFK_00334 1.8e-153 ET amino acid transport
NJMBNHFK_00335 7.1e-164 metQ M Belongs to the NlpA lipoprotein family
NJMBNHFK_00336 4.9e-87 dapE 3.5.1.18 E COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases
NJMBNHFK_00337 1.2e-61 dapE 3.5.1.18 E succinyl-diaminopimelate desuccinylase activity
NJMBNHFK_00338 1.4e-62 dapE 3.5.1.18 E succinyl-diaminopimelate desuccinylase activity
NJMBNHFK_00339 1.2e-189 metN P Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system
NJMBNHFK_00340 5.2e-98 metI P ABC transporter (Permease
NJMBNHFK_00341 3.9e-210 sstT E Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system)
NJMBNHFK_00342 5.5e-158 salL 2.5.1.63, 2.5.1.94 S S-adenosyl-l-methionine hydroxide adenosyltransferase
NJMBNHFK_00343 8e-94 S UPF0397 protein
NJMBNHFK_00344 0.0 ykoD P abc transporter atp-binding protein
NJMBNHFK_00345 1.2e-146 cbiQ P cobalt transport
NJMBNHFK_00346 0.0 tkt 2.2.1.1 G 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
NJMBNHFK_00347 1.4e-11 ulaG S L-ascorbate 6-phosphate lactonase
NJMBNHFK_00348 1.4e-121 ktrA P COG0569 K transport systems, NAD-binding component
NJMBNHFK_00349 1.2e-244 P COG0168 Trk-type K transport systems, membrane components
NJMBNHFK_00350 1.1e-130 rsmG 2.1.1.170 J Ribosomal RNA small subunit methyltransferase G
NJMBNHFK_00351 2.4e-90 yceD K metal-binding, possibly nucleic acid-binding protein
NJMBNHFK_00352 3e-122 T Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain
NJMBNHFK_00353 2.8e-282 T PhoQ Sensor
NJMBNHFK_00354 4.7e-82 nrdR K Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes
NJMBNHFK_00355 6.5e-218 dnaB L Replication initiation and membrane attachment
NJMBNHFK_00356 4.4e-166 dnaI L Primosomal protein DnaI
NJMBNHFK_00357 2.6e-247 der 1.1.1.399, 1.1.1.95 S GTPase that plays an essential role in the late steps of ribosome biogenesis
NJMBNHFK_00359 1.2e-34
NJMBNHFK_00360 6.7e-14 yrdC 3.5.1.19 Q isochorismatase
NJMBNHFK_00361 3e-27 L Integrase core domain protein
NJMBNHFK_00362 3.4e-50 L transposition
NJMBNHFK_00363 5.7e-23 L Transposase
NJMBNHFK_00364 7.8e-28 L transposase activity
NJMBNHFK_00365 8.6e-232 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)
NJMBNHFK_00366 4.2e-62 manO S protein conserved in bacteria
NJMBNHFK_00367 6.2e-168 manN G PTS system mannose fructose sorbose family IID component
NJMBNHFK_00368 2.3e-116 manM G pts system
NJMBNHFK_00369 1.1e-181 manL 2.7.1.191 G pts system
NJMBNHFK_00370 1.5e-140 XK27_00940 1.2.1.70, 3.5.1.9 S Metal-dependent hydrolase
NJMBNHFK_00371 1e-153 yitU 3.1.3.104 S hydrolases of the HAD superfamily
NJMBNHFK_00372 1.9e-248 pbuO S permease
NJMBNHFK_00373 1.4e-77 ydiB 2.7.1.221, 5.1.1.1 M ATPase or kinase
NJMBNHFK_00374 2.4e-92 XK27_05885 2.3.1.82 M Acetyltransferase GNAT Family
NJMBNHFK_00375 2.5e-220 brpA K Transcriptional
NJMBNHFK_00376 3.9e-81 rimP S Required for maturation of 30S ribosomal subunits
NJMBNHFK_00377 3.1e-212 nusA K Participates in both transcription termination and antitermination
NJMBNHFK_00378 1e-47 ylxR K Nucleic-acid-binding protein implicated in transcription termination
NJMBNHFK_00379 2e-46 ylxQ J ribosomal protein
NJMBNHFK_00380 0.0 infB J One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex
NJMBNHFK_00381 1.7e-57 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
NJMBNHFK_00382 2e-22 yvdD 3.2.2.10 S Belongs to the LOG family
NJMBNHFK_00383 1.5e-25 yvdD 3.2.2.10 S cytokinin biosynthetic process
NJMBNHFK_00384 3.6e-48 femA 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 V protein involved in methicillin resistance
NJMBNHFK_00385 6.2e-85 femA 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 V protein involved in methicillin resistance
NJMBNHFK_00386 3.2e-49 femA 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 V protein involved in methicillin resistance
NJMBNHFK_00387 4.9e-276 murE 6.3.2.13, 6.3.2.7 M to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan
NJMBNHFK_00388 4.5e-283 ytgP S Membrane protein involved in the export of O-antigen and teichoic acid
NJMBNHFK_00389 3.3e-96 pacL 3.6.3.8, 3.6.3.9 P cation transport ATPase
NJMBNHFK_00390 4.7e-202 metB 2.5.1.48, 4.4.1.8 E cystathionine
NJMBNHFK_00391 1e-223 malY 4.4.1.8 E COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities
NJMBNHFK_00393 4.4e-112 upp 2.4.2.9 F Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate
NJMBNHFK_00394 2.9e-105 clpP 3.4.21.92 OU 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
NJMBNHFK_00395 1.2e-74 ylbF S Belongs to the UPF0342 family
NJMBNHFK_00396 7.1e-46 ylbG S UPF0298 protein
NJMBNHFK_00397 1.3e-210 livJ E COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component
NJMBNHFK_00398 1.9e-145 livH E Belongs to the binding-protein-dependent transport system permease family
NJMBNHFK_00399 1.4e-138 livM E Belongs to the binding-protein-dependent transport system permease family
NJMBNHFK_00400 9.6e-138 livG E COG0411 ABC-type branched-chain amino acid transport systems, ATPase component
NJMBNHFK_00401 4.8e-123 livF E COG0410 ABC-type branched-chain amino acid transport systems, ATPase component
NJMBNHFK_00402 6.8e-69 acuB S IMP dehydrogenase activity
NJMBNHFK_00403 8.9e-41 acuB S IMP dehydrogenase activity
NJMBNHFK_00404 3.7e-168 cysK 2.5.1.47 E Belongs to the cysteine synthase cystathionine beta- synthase family
NJMBNHFK_00405 1.1e-110 yvyE 3.4.13.9 S YigZ family
NJMBNHFK_00406 4.5e-252 comFA L Superfamily II DNA RNA helicase required for DNA uptake (late competence protein)
NJMBNHFK_00407 1.7e-122 comFC S Competence protein
NJMBNHFK_00408 2.1e-94 hpf J Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase
NJMBNHFK_00416 2.1e-166 ppaC 3.6.1.1 C inorganic pyrophosphatase
NJMBNHFK_00417 6.4e-108 S Domain of unknown function (DUF1803)
NJMBNHFK_00418 7.8e-102 ygaC J Belongs to the UPF0374 family
NJMBNHFK_00419 1.2e-130 recX 2.4.1.337 GT4 S Regulatory protein RecX
NJMBNHFK_00420 6.7e-259 rumA 2.1.1.190, 2.1.1.35 J Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family
NJMBNHFK_00421 8e-193 asnA 6.3.1.1 E aspartate--ammonia ligase
NJMBNHFK_00422 2.6e-255 lysC 2.7.2.4 E Belongs to the aspartokinase family
NJMBNHFK_00423 1.9e-115 S Haloacid dehalogenase-like hydrolase
NJMBNHFK_00424 2.4e-139 phaB 5.3.3.14, 5.3.3.18 I Belongs to the enoyl-CoA hydratase isomerase family
NJMBNHFK_00425 4e-72 marR K Transcriptional regulator, MarR family
NJMBNHFK_00426 2.3e-173 fabH 2.3.1.180 I Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids
NJMBNHFK_00427 3.3e-30 acpP IQ Carrier of the growing fatty acid chain in fatty acid biosynthesis
NJMBNHFK_00428 5.8e-172 fabK 1.3.1.9 S 2-Nitropropane dioxygenase
NJMBNHFK_00429 8.5e-165 fabD 2.3.1.39 I Malonyl CoA-acyl carrier protein transacylase
NJMBNHFK_00430 1.6e-126 IQ reductase
NJMBNHFK_00431 2.6e-233 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
NJMBNHFK_00432 7.7e-56 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
NJMBNHFK_00433 1.5e-71 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
NJMBNHFK_00434 1.7e-257 accC 6.3.4.14, 6.4.1.2 I An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism
NJMBNHFK_00435 1.6e-160 accD 2.1.3.15, 6.4.1.2 I Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA
NJMBNHFK_00436 1.1e-138 accA 2.1.3.15, 6.4.1.2 I Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA
NJMBNHFK_00437 4.7e-90 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)
NJMBNHFK_00438 1.1e-65 tnp L Transposase
NJMBNHFK_00439 2.3e-214 gadB 4.1.1.15 E Belongs to the group II decarboxylase family
NJMBNHFK_00440 9.8e-176 gadC E Psort location CytoplasmicMembrane, score 10.00
NJMBNHFK_00441 4.7e-27 L Transposase and inactivated derivatives, TnpA family
NJMBNHFK_00442 3.4e-126 tnp L Transposase
NJMBNHFK_00444 8e-277 S Protein of unknown function (DUF3114)
NJMBNHFK_00445 2.2e-38 2.3.1.128 K Acetyltransferase GNAT Family
NJMBNHFK_00446 7.7e-198 V (ABC) transporter
NJMBNHFK_00447 1.4e-74 C Arylsulfatase regulator (Fe-S oxidoreductase)
NJMBNHFK_00448 6.4e-85 C Arylsulfatase regulator (Fe-S oxidoreductase)
NJMBNHFK_00449 1.1e-113 K sequence-specific DNA binding
NJMBNHFK_00450 8.4e-155 L COG2801 Transposase and inactivated derivatives
NJMBNHFK_00451 6.6e-38 L transposase activity
NJMBNHFK_00452 1.3e-205 rny D Endoribonuclease that initiates mRNA decay
NJMBNHFK_00453 1.8e-84 L Transposase
NJMBNHFK_00454 5.5e-122 fruR K transcriptional
NJMBNHFK_00455 3.8e-165 pfkB 2.7.1.11, 2.7.1.56 H Belongs to the carbohydrate kinase PfkB family. LacC subfamily
NJMBNHFK_00456 0.0 fruA 2.7.1.202 G phosphotransferase system
NJMBNHFK_00457 2.7e-260 gor 1.8.1.7 C Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
NJMBNHFK_00458 2.6e-241 folC 6.3.2.12, 6.3.2.17 H Belongs to the folylpolyglutamate synthase family
NJMBNHFK_00460 6.1e-213 iscS2 2.8.1.7 E Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes
NJMBNHFK_00461 6.5e-229 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
NJMBNHFK_00462 4.9e-295 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
NJMBNHFK_00463 7.2e-258 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
NJMBNHFK_00464 6.4e-29 2.3.1.128 K acetyltransferase
NJMBNHFK_00465 4.5e-49 rplU J This protein binds to 23S rRNA in the presence of protein L20
NJMBNHFK_00466 1.5e-46 rpmA J Belongs to the bacterial ribosomal protein bL27 family
NJMBNHFK_00467 7.7e-134 ydaF_2 J COG1670 acetyltransferases, including N-acetylases of ribosomal proteins
NJMBNHFK_00468 2.6e-64 WQ51_03320 S cog cog4835
NJMBNHFK_00469 9.8e-91 XK27_08360 S EDD domain protein, DegV family
NJMBNHFK_00470 3e-139 dapB 1.17.1.8 E Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate
NJMBNHFK_00471 9.6e-225 cca 2.7.7.19, 2.7.7.72 J Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
NJMBNHFK_00472 0.0 yfmR S abc transporter atp-binding protein
NJMBNHFK_00473 1.6e-24 U response to pH
NJMBNHFK_00474 1.1e-141 3.6.1.13, 3.6.1.55 F AdP-ribose pyrophosphatase
NJMBNHFK_00475 1.7e-212 nadD 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 H adenylyltransferase
NJMBNHFK_00476 1.8e-256 gdhA 1.4.1.4 E Belongs to the Glu Leu Phe Val dehydrogenases family
NJMBNHFK_00477 1e-69 def_1 3.5.1.31, 3.5.1.88 J Removes the formyl group from the N-terminal Met of newly synthesized proteins
NJMBNHFK_00478 9.4e-77 K DNA-binding transcription factor activity
NJMBNHFK_00479 0.0 lmrA1 V abc transporter atp-binding protein
NJMBNHFK_00480 0.0 lmrA2 V abc transporter atp-binding protein
NJMBNHFK_00481 5.4e-45 K Acetyltransferase (GNAT) family
NJMBNHFK_00482 3.2e-78 sptS 2.7.13.3 T Histidine kinase
NJMBNHFK_00483 4.9e-131 pyrH 2.7.4.22 F Catalyzes the reversible phosphorylation of UMP to UDP
NJMBNHFK_00484 1.3e-91 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
NJMBNHFK_00485 5.3e-161 cvfB S Protein conserved in bacteria
NJMBNHFK_00486 7.4e-35 yozE S Belongs to the UPF0346 family
NJMBNHFK_00487 6.7e-124 usp 3.5.1.104, 3.5.1.28 CBM50 S pathogenesis
NJMBNHFK_00488 2.3e-61 rlpA M LysM domain protein
NJMBNHFK_00489 2.3e-190 phoH T phosphate starvation-inducible protein PhoH
NJMBNHFK_00493 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
NJMBNHFK_00494 1.8e-164 K transcriptional regulator (lysR family)
NJMBNHFK_00495 1.4e-186 coiA 3.6.4.12 S Competence protein
NJMBNHFK_00496 0.0 pepF E oligoendopeptidase F
NJMBNHFK_00497 5.4e-127 yrrM 2.1.1.104 S O-Methyltransferase
NJMBNHFK_00498 1.3e-167 prsA 3.1.3.16, 5.2.1.8 O peptidyl-prolyl cis-trans isomerase activity
NJMBNHFK_00499 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
NJMBNHFK_00500 7.9e-24 3.4.17.14, 3.5.1.28 M GBS Bsp-like repeat
NJMBNHFK_00501 6.9e-179 3.4.17.14, 3.5.1.28 M GBS Bsp-like repeat
NJMBNHFK_00502 3.9e-120 3.4.17.14, 3.5.1.28 NU amidase activity
NJMBNHFK_00503 4.9e-145 cnhA 3.5.1.3 S Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase
NJMBNHFK_00504 1.7e-226 mtnE 2.6.1.83 E mutations do not affect methionine salvage in vivo however
NJMBNHFK_00505 1.4e-189 argC 1.2.1.38 E Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde
NJMBNHFK_00506 1.5e-222 argJ 2.3.1.1, 2.3.1.35, 2.7.2.8 E Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate
NJMBNHFK_00507 7.9e-129 argB 2.7.2.8 E Belongs to the acetylglutamate kinase family. ArgB subfamily
NJMBNHFK_00508 1.6e-210 argD 2.6.1.11, 2.6.1.17 E acetylornithine aminotransferase
NJMBNHFK_00509 2.2e-130 yxkH G deacetylase
NJMBNHFK_00510 2.3e-237 hom 1.1.1.3, 2.7.2.4 E homoserine dehydrogenase
NJMBNHFK_00511 2.8e-154 thrB 2.7.1.39 E Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate
NJMBNHFK_00512 5.5e-153 rarD S Transporter
NJMBNHFK_00513 2.2e-15 T peptidase
NJMBNHFK_00514 8.9e-14 coiA 3.6.4.12 S Competence protein
NJMBNHFK_00515 4.1e-112 S COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family
NJMBNHFK_00516 1.9e-46 2.3.1.128, 5.2.1.8 J COG1670 acetyltransferases, including N-acetylases of ribosomal proteins
NJMBNHFK_00517 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
NJMBNHFK_00518 3.2e-16 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
NJMBNHFK_00519 4.3e-124 atpB C it plays a direct role in the translocation of protons across the membrane
NJMBNHFK_00520 3.3e-78 atpF C ATP synthase F(0) sector subunit b
NJMBNHFK_00521 9.3e-87 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
NJMBNHFK_00522 3.8e-279 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
NJMBNHFK_00523 7.4e-158 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
NJMBNHFK_00524 2.7e-263 atpD 3.6.3.14 C Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits
NJMBNHFK_00525 5.2e-67 atpC C Produces ATP from ADP in the presence of a proton gradient across the membrane
NJMBNHFK_00526 2.8e-230 ftsW D Belongs to the SEDS family
NJMBNHFK_00527 9.5e-225 tuf J This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis
NJMBNHFK_00528 1.4e-136 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)
NJMBNHFK_00529 2.8e-111 tmk 2.7.4.9 F Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis
NJMBNHFK_00530 1.9e-161 holB 2.7.7.7 L dna polymerase iii
NJMBNHFK_00531 2.1e-135 yaaT S stage 0 sporulation protein
NJMBNHFK_00532 9.5e-55 yabA L Involved in initiation control of chromosome replication
NJMBNHFK_00533 3.9e-159 rsmI 2.1.1.198 H Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA
NJMBNHFK_00534 7.5e-233 amt P Ammonium Transporter
NJMBNHFK_00535 1.1e-53 glnB K Belongs to the P(II) protein family
NJMBNHFK_00536 4.9e-106 mur1 NU mannosyl-glycoprotein
NJMBNHFK_00537 1.7e-148 XK27_04800 S Sucrose-6F-phosphate phosphohydrolase
NJMBNHFK_00538 2.9e-68 nptA P sodium-dependent phosphate transmembrane transporter activity
NJMBNHFK_00539 2.1e-221 nagA 3.5.1.25 G Belongs to the metallo-dependent hydrolases superfamily. NagA family
NJMBNHFK_00540 1.8e-53
NJMBNHFK_00541 7.5e-26
NJMBNHFK_00542 1.5e-59
NJMBNHFK_00543 6.1e-63 S membrane
NJMBNHFK_00544 4.8e-176 glyQ 6.1.1.14 J glycyl-tRNA synthetase alpha subunit
NJMBNHFK_00545 0.0 glyS 6.1.1.14 J Glycyl-tRNA synthetase beta subunit
NJMBNHFK_00546 4.5e-39 ynzC S UPF0291 protein
NJMBNHFK_00547 1.8e-254 cycA E permease
NJMBNHFK_00548 1.1e-09 uvrX 2.7.7.7 L ImpB mucB samB family
NJMBNHFK_00549 2.8e-24 2.7.1.208, 2.7.1.211 G protein-N(PI)-phosphohistidine-sugar phosphotransferase activity
NJMBNHFK_00550 5.8e-71 pts33BCA G pts system
NJMBNHFK_00551 9e-96 pts33BCA G pts system
NJMBNHFK_00552 9.7e-77 2.7.1.199, 2.7.1.211 G PTS glucose transporter subunit IIA
NJMBNHFK_00553 3.2e-141 ppiA 5.2.1.8 O PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides
NJMBNHFK_00554 1.2e-165 L integrase core domain
NJMBNHFK_00555 3.9e-122 L Transposase
NJMBNHFK_00560 1.4e-167 fhuR K transcriptional regulator (lysR family)
NJMBNHFK_00561 1.5e-77 lspA 3.4.23.36 MU This protein specifically catalyzes the removal of signal peptides from prolipoproteins
NJMBNHFK_00562 4.5e-163 rluD 5.4.99.23 J Responsible for synthesis of pseudouridine from uracil
NJMBNHFK_00563 3.7e-88 pyrR 2.4.2.9 F Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant
NJMBNHFK_00564 4.9e-227 pyrP F uracil Permease
NJMBNHFK_00565 1e-173 pyrB 2.1.3.2 F Belongs to the ATCase OTCase family
NJMBNHFK_00566 1.1e-211 carA 6.3.5.5 F carbamoyl-phosphate synthetase glutamine chain
NJMBNHFK_00567 0.0 carB 6.3.5.5 F carbamoyl-phosphate synthetase ammonia chain
NJMBNHFK_00568 2.2e-134 2.1.1.223 S Putative SAM-dependent methyltransferase
NJMBNHFK_00569 4e-37 acrA M Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family
NJMBNHFK_00570 1.6e-33 V permease protein
NJMBNHFK_00571 1e-09 V permease protein
NJMBNHFK_00572 8.8e-21 V permease protein
NJMBNHFK_00573 1.7e-07 V efflux transmembrane transporter activity
NJMBNHFK_00574 1.1e-24 ytrF V efflux transmembrane transporter activity
NJMBNHFK_00575 5.6e-78 rplJ J Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors
NJMBNHFK_00576 3.9e-52 rplL J Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation
NJMBNHFK_00577 8.8e-223 L Transposase
NJMBNHFK_00579 0.0 mdlB V abc transporter atp-binding protein
NJMBNHFK_00580 0.0 lmrA V abc transporter atp-binding protein
NJMBNHFK_00581 4.6e-199 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)
NJMBNHFK_00582 5.8e-121 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
NJMBNHFK_00583 6.3e-214 2.7.13.3 T signal transduction protein with a C-terminal ATPase domain
NJMBNHFK_00584 2.5e-132 rr02 KT response regulator
NJMBNHFK_00585 3.5e-202 2.7.7.73, 2.7.7.80 H Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2
NJMBNHFK_00586 4.8e-168 V ABC transporter
NJMBNHFK_00587 5.4e-122 sagI S ABC-2 type transporter
NJMBNHFK_00588 4.5e-196 yceA S Belongs to the UPF0176 family
NJMBNHFK_00589 8e-28 XK27_00085 K Transcriptional
NJMBNHFK_00590 1.7e-23
NJMBNHFK_00591 1.2e-143 deoD_1 2.4.2.3 F Phosphorylase superfamily
NJMBNHFK_00592 2.8e-112 S VIT family
NJMBNHFK_00593 7.4e-132 rsuA 5.4.99.19, 5.4.99.22 J Belongs to the pseudouridine synthase RsuA family
NJMBNHFK_00594 2.4e-217 hipO 3.5.1.47 E COG1473 Metal-dependent amidase aminoacylase carboxypeptidase
NJMBNHFK_00595 3.4e-17 ald 1.4.1.1 E alanine dehydrogenase activity
NJMBNHFK_00596 2e-47 ald 1.4.1.1 C Belongs to the AlaDH PNT family
NJMBNHFK_00597 5.7e-247 merA 1.16.1.1 C Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
NJMBNHFK_00598 8.8e-104 GBS0088 J protein conserved in bacteria
NJMBNHFK_00599 2.5e-142 mvk 1.1.1.88, 2.3.3.10, 2.7.1.36 I mevalonate kinase
NJMBNHFK_00600 1.5e-172 mvaD 4.1.1.33 I diphosphomevalonate decarboxylase
NJMBNHFK_00601 1.6e-177 mvaK2 2.7.1.36, 2.7.1.43, 2.7.4.2 I GHMP kinases N terminal domain
NJMBNHFK_00602 7.6e-191 fni 1.1.1.88, 5.3.3.2 C Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP)
NJMBNHFK_00603 1.5e-253 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
NJMBNHFK_00604 1e-96 nudF 3.6.1.13 L AdP-ribose pyrophosphatase
NJMBNHFK_00605 2.5e-21
NJMBNHFK_00606 2e-118 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
NJMBNHFK_00608 3.5e-07 U protein secretion
NJMBNHFK_00609 2.5e-51 U protein secretion
NJMBNHFK_00610 7.4e-08 M Pilin isopeptide linkage domain protein
NJMBNHFK_00611 7.6e-191 dgs 2.4.1.208 GT4 M Glycosyltransferase, group 1 family protein
NJMBNHFK_00612 1.5e-247 mgs 2.4.1.337 GT4 M Glycosyltransferase, group 1 family protein
NJMBNHFK_00613 3.5e-49 XK27_13030
NJMBNHFK_00614 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)
NJMBNHFK_00615 8.3e-55 S hydrolase activity, acting on ester bonds
NJMBNHFK_00616 9.4e-71 S hydrolases or acyltransferases (alpha beta hydrolase superfamily)
NJMBNHFK_00617 6.8e-164 S Protein of unknown function (DUF3114)
NJMBNHFK_00618 1.2e-22 S Protein of unknown function (DUF3114)
NJMBNHFK_00619 1.5e-118 yqfA K protein, Hemolysin III
NJMBNHFK_00620 1e-25 K hmm pf08876
NJMBNHFK_00621 2.7e-233 mvaA 1.1.1.34, 1.1.1.88, 2.3.1.9 C Belongs to the HMG-CoA reductase family
NJMBNHFK_00622 1.7e-218 mvaS 2.3.3.10 I synthase
NJMBNHFK_00623 2.2e-167 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
NJMBNHFK_00624 3.4e-91 folA 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 H Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis
NJMBNHFK_00625 9.7e-22
NJMBNHFK_00626 2e-225 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
NJMBNHFK_00627 3e-110 engB D Necessary for normal cell division and for the maintenance of normal septation
NJMBNHFK_00628 1.5e-250 mmuP E amino acid
NJMBNHFK_00629 1.2e-177 mmuM 1.5.1.20, 2.1.1.10 H Homocysteine
NJMBNHFK_00630 1.4e-29 S Domain of unknown function (DUF1912)
NJMBNHFK_00631 4.9e-15 L Helix-hairpin-helix DNA-binding motif class 1
NJMBNHFK_00632 7.1e-102 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
NJMBNHFK_00633 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
NJMBNHFK_00634 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
NJMBNHFK_00635 2.4e-200 ilvE 2.6.1.42 E Aminotransferase
NJMBNHFK_00636 4.8e-16 S Protein of unknown function (DUF2969)
NJMBNHFK_00639 8.4e-205 rpsA 1.17.7.4 J ribosomal protein S1
NJMBNHFK_00642 1.1e-44 S Domain of Unknown Function with PDB structure (DUF3862)
NJMBNHFK_00643 1.3e-29 S Domain of Unknown Function with PDB structure (DUF3862)
NJMBNHFK_00644 3.7e-70 M Pfam SNARE associated Golgi protein
NJMBNHFK_00645 3.4e-233 murN 2.3.2.10, 2.3.2.16 V FemAB family
NJMBNHFK_00646 1.6e-08 S oxidoreductase
NJMBNHFK_00647 9.3e-59 S oxidoreductase
NJMBNHFK_00648 9.7e-66 S oxidoreductase
NJMBNHFK_00649 3.7e-48 XK27_09445 S Domain of unknown function (DUF1827)
NJMBNHFK_00650 1.8e-86 mutT 3.5.4.33, 3.6.1.13, 3.6.1.55 L Belongs to the Nudix hydrolase family
NJMBNHFK_00651 0.0 clpE O Belongs to the ClpA ClpB family
NJMBNHFK_00652 1.2e-180 argF 2.1.3.3 E Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline
NJMBNHFK_00653 1.3e-34 ykuJ S protein conserved in bacteria
NJMBNHFK_00654 7.5e-118 WQ51_01820 P Binding-protein-dependent transport system inner membrane component
NJMBNHFK_00655 2.2e-131 glnQ 3.6.3.21 E abc transporter atp-binding protein
NJMBNHFK_00656 3.1e-78 feoA P FeoA domain protein
NJMBNHFK_00657 0.0 feoB P transporter of a GTP-driven Fe(2 ) uptake system
NJMBNHFK_00658 1.5e-07
NJMBNHFK_00659 2.4e-104 1.1.1.133, 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
NJMBNHFK_00660 2.2e-45 K sequence-specific DNA binding
NJMBNHFK_00661 1.5e-35 yugF I carboxylic ester hydrolase activity
NJMBNHFK_00662 7.5e-23 I Alpha/beta hydrolase family
NJMBNHFK_00663 3.9e-156 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
NJMBNHFK_00664 7.8e-149 nnrD 4.2.1.136, 5.1.99.6 H Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration
NJMBNHFK_00665 0.0 pbp2b 3.4.16.4 M penicillin-binding protein
NJMBNHFK_00666 4.9e-105 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
NJMBNHFK_00667 5.8e-64 licT K transcriptional antiterminator
NJMBNHFK_00668 6.8e-53 licT K transcriptional antiterminator
NJMBNHFK_00669 5.9e-88 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
NJMBNHFK_00670 1.7e-64 dgkA 2.7.1.107, 2.7.1.66 M Diacylglycerol kinase
NJMBNHFK_00671 1.3e-165 era M 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
NJMBNHFK_00672 1.9e-155 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
NJMBNHFK_00673 1.1e-104 coaE 2.7.1.24, 3.2.2.23, 4.2.99.18 GH23 H Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A
NJMBNHFK_00674 2.5e-220 mdtG EGP Major facilitator Superfamily
NJMBNHFK_00675 2e-33 secG U Preprotein translocase subunit SecG
NJMBNHFK_00676 0.0 rnr J 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs
NJMBNHFK_00677 1.1e-80 smpB O 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
NJMBNHFK_00678 9.6e-277 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
NJMBNHFK_00679 1.7e-63 yugI 5.3.1.9 J RNA binding protein, contains ribosomal protein S1 domain
NJMBNHFK_00680 4.2e-211 pepQ 3.4.13.9 E Belongs to the peptidase M24B family
NJMBNHFK_00681 4.4e-183 ccpA K Catabolite control protein A
NJMBNHFK_00682 2.8e-28 yyaQ S YjbR
NJMBNHFK_00683 6.6e-101 yyaQ V Protein conserved in bacteria
NJMBNHFK_00684 1.3e-207 glxK 2.7.1.165 G Belongs to the glycerate kinase type-1 family
NJMBNHFK_00685 1e-78 yueI S Protein of unknown function (DUF1694)
NJMBNHFK_00686 9.6e-247 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
NJMBNHFK_00687 2e-25 WQ51_00785
NJMBNHFK_00688 0.0 ltaS 2.7.8.20 M Belongs to the LTA synthase family
NJMBNHFK_00689 2e-219 ywbD 2.1.1.191 J Methyltransferase
NJMBNHFK_00690 8.6e-122 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
NJMBNHFK_00691 1.7e-162 aroE 1.1.1.25 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)
NJMBNHFK_00692 3.5e-202 aroB 2.7.1.71, 4.2.3.4 E Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ)
NJMBNHFK_00693 4.5e-219 aroC 4.2.3.5 E Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system
NJMBNHFK_00694 2.2e-207 tyrA 1.3.1.12, 1.3.1.43 E prephenate dehydrogenase
NJMBNHFK_00695 3.2e-53 yheA S Belongs to the UPF0342 family
NJMBNHFK_00696 3e-173 ldh 1.1.1.27 C Belongs to the LDH MDH superfamily
NJMBNHFK_00697 2.6e-236 aroA 1.3.1.12, 1.3.1.43, 2.5.1.19 E Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate
NJMBNHFK_00698 1.7e-87 aroK 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 F Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate
NJMBNHFK_00699 6.7e-153 pheA 4.2.1.51 E Prephenate dehydratase
NJMBNHFK_00700 6.4e-252 msrR K Transcriptional regulator
NJMBNHFK_00701 2.2e-149 ydiA P C4-dicarboxylate transporter malic acid transport protein
NJMBNHFK_00702 2.4e-203 I acyl-CoA dehydrogenase
NJMBNHFK_00703 4.5e-97 mip S hydroperoxide reductase activity
NJMBNHFK_00704 1.7e-257 rumA 2.1.1.190 J Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family
NJMBNHFK_00705 8.9e-20
NJMBNHFK_00706 3.2e-46
NJMBNHFK_00707 1e-31 K Cro/C1-type HTH DNA-binding domain
NJMBNHFK_00708 7.8e-50 dam 2.1.1.72 L D12 class N6 adenine-specific DNA methyltransferase
NJMBNHFK_00709 9.7e-34 estA E GDSL-like Lipase/Acylhydrolase
NJMBNHFK_00710 1.1e-94
NJMBNHFK_00711 0.0 cas9 L CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer
NJMBNHFK_00712 4.2e-172 cas1 L CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette
NJMBNHFK_00713 3.1e-53 cas2 L CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette
NJMBNHFK_00714 2.6e-194 S CRISPR-associated protein Csn2 subfamily St
NJMBNHFK_00715 2.7e-146 ycgQ S TIGR03943 family
NJMBNHFK_00716 4.6e-155 XK27_03015 S permease
NJMBNHFK_00718 0.0 yhgF K Transcriptional accessory protein
NJMBNHFK_00719 9.9e-42 pspC KT PspC domain
NJMBNHFK_00720 2e-169 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
NJMBNHFK_00721 4e-147 lgt 2.1.1.199 M Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins
NJMBNHFK_00723 5.5e-69 ytxH S General stress protein
NJMBNHFK_00725 2e-177 yegQ O Peptidase U32
NJMBNHFK_00726 3.4e-252 yegQ O Peptidase U32
NJMBNHFK_00727 8.1e-46 S CHY zinc finger
NJMBNHFK_00728 8.4e-88 bioY S biotin synthase
NJMBNHFK_00730 1.1e-33 XK27_12190 S protein conserved in bacteria
NJMBNHFK_00731 1.1e-234 mntH P H( )-stimulated, divalent metal cation uptake system
NJMBNHFK_00732 4.8e-11
NJMBNHFK_00733 6e-209 dcm 2.1.1.37 H C-5 cytosine-specific DNA methylase
NJMBNHFK_00734 4.1e-225 mutH L DNA mismatch repair enzyme MutH
NJMBNHFK_00735 5.2e-29 S SIR2-like domain
NJMBNHFK_00736 1.2e-33 S SIR2-like domain
NJMBNHFK_00737 9.2e-286 lysS 6.1.1.6 J Belongs to the class-II aminoacyl-tRNA synthetase family
NJMBNHFK_00738 6.4e-158 M LysM domain
NJMBNHFK_00739 7.6e-16
NJMBNHFK_00740 2.3e-175 S hydrolase
NJMBNHFK_00741 1.9e-115 pgm6 5.4.2.11, 5.4.2.12 G Phosphoglycerate mutase
NJMBNHFK_00742 7.9e-82 ybaK S Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily
NJMBNHFK_00743 1.6e-145 XK27_00880 3.5.1.28 M Glycosyl hydrolase, family 25
NJMBNHFK_00744 2.7e-27 P Hemerythrin HHE cation binding domain protein
NJMBNHFK_00745 2.3e-113 1.14.14.5 C COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases
NJMBNHFK_00746 1.7e-10 MA20_36090 S Protein of unknown function (DUF2974)
NJMBNHFK_00747 1.1e-33 MA20_36090 S Protein of unknown function (DUF2974)
NJMBNHFK_00748 0.0 hsdR 3.1.21.3 V Type I restriction enzyme R protein N terminus (HSDR_N)
NJMBNHFK_00749 3.9e-290 hsdM 2.1.1.72 V N-6 DNA Methylase
NJMBNHFK_00750 2.2e-147 3.1.21.3 V type I restriction modification DNA specificity domain
NJMBNHFK_00752 2.5e-44
NJMBNHFK_00753 3e-38
NJMBNHFK_00754 2.3e-171 spd F DNA RNA non-specific endonuclease
NJMBNHFK_00755 1.5e-92 lemA S LemA family
NJMBNHFK_00756 1.8e-135 htpX O Belongs to the peptidase M48B family
NJMBNHFK_00757 4.2e-75 S Psort location CytoplasmicMembrane, score
NJMBNHFK_00758 6.2e-56 S Domain of unknown function (DUF4430)
NJMBNHFK_00759 0.0 ppc 4.1.1.31 H Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle
NJMBNHFK_00760 1.2e-183 holA 2.7.7.7 L DNA polymerase III delta subunit
NJMBNHFK_00761 8.5e-113 sodA 1.15.1.1 C radicals which are normally produced within the cells and which are toxic to biological systems
NJMBNHFK_00762 2.7e-160 L Transposase
NJMBNHFK_00763 3e-50 L Transposase
NJMBNHFK_00764 2.6e-189 3.5.2.6 V D-alanyl-D-alanine carboxypeptidase
NJMBNHFK_00765 4.4e-115 pilD 3.4.23.43 NOU Bacterial Peptidase A24 N-terminal domain
NJMBNHFK_00766 3.5e-91 dps P Belongs to the Dps family
NJMBNHFK_00767 1.1e-80 perR P Belongs to the Fur family
NJMBNHFK_00768 8.4e-28 yqgQ S protein conserved in bacteria
NJMBNHFK_00769 2.2e-179 glk 2.7.1.2 G Glucokinase
NJMBNHFK_00770 0.0 typA T GTP-binding protein TypA
NJMBNHFK_00772 1.6e-252 murD 6.3.2.9 M Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA)
NJMBNHFK_00773 1e-201 murG 2.4.1.227 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)
NJMBNHFK_00774 1.8e-177 divIB D Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex
NJMBNHFK_00775 8e-252 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
NJMBNHFK_00776 5.4e-237 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
NJMBNHFK_00777 2.3e-122 ylmE S Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis
NJMBNHFK_00778 6.8e-96 sepF D cell septum assembly
NJMBNHFK_00779 2.6e-34 yggT D integral membrane protein
NJMBNHFK_00780 4.2e-144 ylmH T S4 RNA-binding domain
NJMBNHFK_00781 1.8e-135 divIVA D Cell division protein DivIVA
NJMBNHFK_00782 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)
NJMBNHFK_00783 5.5e-30
NJMBNHFK_00784 8.4e-10
NJMBNHFK_00785 3.2e-231 mntH P Mn2 and Fe2 transporters of the NRAMP family
NJMBNHFK_00786 2e-45 rpmE2 J 50S ribosomal protein L31
NJMBNHFK_00787 8.3e-176 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
NJMBNHFK_00788 1e-184 nrnA 3.1.13.3, 3.1.3.7 S domain protein
NJMBNHFK_00789 8.9e-155 gst O Glutathione S-transferase
NJMBNHFK_00790 4.6e-188 add 3.5.4.4 F Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism
NJMBNHFK_00791 4.5e-111 tdk 2.7.1.21 F thymidine kinase
NJMBNHFK_00792 3e-193 prfA J Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA
NJMBNHFK_00793 1.2e-154 prmB 2.1.1.297, 2.1.1.298 J Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif
NJMBNHFK_00794 9.7e-109 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
NJMBNHFK_00795 1.8e-234 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
NJMBNHFK_00796 1.2e-177 ndpA S 37-kD nucleoid-associated bacterial protein
NJMBNHFK_00797 8e-100 pvaA M lytic transglycosylase activity
NJMBNHFK_00798 0.0 yfiB1 V abc transporter atp-binding protein
NJMBNHFK_00799 0.0 XK27_10035 V abc transporter atp-binding protein
NJMBNHFK_00800 1.7e-09 S D-Ala-teichoic acid biosynthesis protein
NJMBNHFK_00801 1.4e-297 dltA 6.1.1.13 Q 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
NJMBNHFK_00802 3.9e-237 dltB M Membrane protein involved in D-alanine export
NJMBNHFK_00803 1.7e-35 dltC 6.1.1.13 IQ Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall
NJMBNHFK_00804 3.6e-230 dltD M Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein)
NJMBNHFK_00805 4.5e-233 L Transposase
NJMBNHFK_00806 9.8e-32 L Integrase core domain protein
NJMBNHFK_00807 9.6e-32 L transposition
NJMBNHFK_00808 6.5e-54 L transposition
NJMBNHFK_00809 7.7e-19 L transposase activity
NJMBNHFK_00810 2.5e-40 L Transposase
NJMBNHFK_00811 0.0 3.6.3.8 P cation transport ATPase
NJMBNHFK_00812 0.0 pabB 2.6.1.85, 4.1.3.27, 4.1.3.38 EH component I
NJMBNHFK_00813 1.9e-105 V Abi-like protein
NJMBNHFK_00815 2.3e-12
NJMBNHFK_00817 2e-296 S DNA primase
NJMBNHFK_00818 3e-164 KL Phage plasmid primase P4 family
NJMBNHFK_00819 2.4e-22
NJMBNHFK_00820 1.2e-14
NJMBNHFK_00824 1.8e-19 K Cro/C1-type HTH DNA-binding domain
NJMBNHFK_00825 1e-21 xre K transcriptional
NJMBNHFK_00826 6.9e-220 sip L Belongs to the 'phage' integrase family
NJMBNHFK_00828 0.0 metE 2.1.1.14 E Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation
NJMBNHFK_00829 7.3e-166 metF 1.5.1.20 E reductase
NJMBNHFK_00830 0.0 pgm 5.4.2.2, 5.4.2.8 G Phosphoglucomutase
NJMBNHFK_00831 1.7e-94 panT S ECF transporter, substrate-specific component
NJMBNHFK_00832 4.8e-94 coaBC 4.1.1.36, 6.3.2.5 H Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine
NJMBNHFK_00833 1.2e-120 coaB 4.1.1.36, 6.3.2.5 H Phosphopantothenate-cysteine ligase
NJMBNHFK_00834 0.0 fhs 6.3.4.3 F Belongs to the formate--tetrahydrofolate ligase family
NJMBNHFK_00835 6.4e-66 T Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain
NJMBNHFK_00836 2.8e-40 T PhoQ Sensor
NJMBNHFK_00837 1.7e-43 T PhoQ Sensor
NJMBNHFK_00838 5.8e-79 T PhoQ Sensor
NJMBNHFK_00839 6.7e-122 L Helix-turn-helix domain
NJMBNHFK_00840 1.2e-165 L integrase core domain
NJMBNHFK_00841 2.1e-30 rpsT J rRNA binding
NJMBNHFK_00842 1.9e-172 coaA 2.7.1.33 F Pantothenic acid kinase
NJMBNHFK_00843 1.8e-107 rsmC 2.1.1.172 J Methyltransferase small domain protein
NJMBNHFK_00844 1.2e-57 pdp 2.4.2.2, 2.4.2.4 F Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate
NJMBNHFK_00845 6e-98 pdp 2.4.2.2, 2.4.2.4 F Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate
NJMBNHFK_00846 1.4e-22 deoC 4.1.2.4, 5.4.2.8 F Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate
NJMBNHFK_00847 4e-63 deoC 4.1.2.4, 5.4.2.8 F Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate
NJMBNHFK_00848 1.3e-69 cdd 2.4.2.2, 3.5.4.5 F This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis
NJMBNHFK_00849 9.5e-192 tcsA S ABC-type transport system, periplasmic component surface lipoprotein
NJMBNHFK_00850 3.7e-282 xylG 3.6.3.17 S ABC transporter, ATP-binding protein
NJMBNHFK_00851 4.7e-191 yufP S Belongs to the binding-protein-dependent transport system permease family
NJMBNHFK_00852 4.8e-171 yufQ S Belongs to the binding-protein-dependent transport system permease family
NJMBNHFK_00853 8.9e-121 ycbL 3.1.2.6 S COG0491 Zn-dependent hydrolases, including glyoxylases
NJMBNHFK_00854 0.0 dinG 2.7.7.7, 3.6.4.12 L helicase involved in DNA repair and perhaps also replication
NJMBNHFK_00855 3.1e-81 ypmB S Protein conserved in bacteria
NJMBNHFK_00856 6.5e-218 aspB 2.6.1.1, 2.6.1.14 E Aminotransferase
NJMBNHFK_00857 1.7e-262 asnS 6.1.1.22 J Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA
NJMBNHFK_00858 1.5e-07
NJMBNHFK_00859 2.4e-30
NJMBNHFK_00860 3e-13
NJMBNHFK_00861 3e-63 tdcF 3.5.99.10 J endoribonuclease L-PSP
NJMBNHFK_00862 2e-123 queC 6.3.4.20 F Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0))
NJMBNHFK_00863 2.2e-81 queD 4.1.2.50, 4.2.3.12 H synthase
NJMBNHFK_00864 3.9e-133 queE 1.97.1.4, 4.3.99.3 H Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds
NJMBNHFK_00865 2.5e-94 queF 1.7.1.13 S Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily
NJMBNHFK_00866 4.2e-18 D nuclear chromosome segregation
NJMBNHFK_00867 1.5e-135 yejC S cyclic nucleotide-binding protein
NJMBNHFK_00868 1.2e-163 rapZ S Displays ATPase and GTPase activities
NJMBNHFK_00869 1.8e-181 ybhK S Required for morphogenesis under gluconeogenic growth conditions
NJMBNHFK_00870 8.7e-162 whiA K May be required for sporulation
NJMBNHFK_00871 8e-90 pepD E Dipeptidase
NJMBNHFK_00872 5.8e-41 pepD E dipeptidase activity
NJMBNHFK_00873 5.4e-32 cspD K Cold shock protein domain
NJMBNHFK_00874 1.6e-249 L Transposase
NJMBNHFK_00875 9.4e-43 K Cold-Shock Protein
NJMBNHFK_00876 3.6e-224 L Transposase, Mutator family
NJMBNHFK_00877 0.0 copB 3.6.3.4 P P-type ATPase
NJMBNHFK_00878 1.6e-88 L Transposase
NJMBNHFK_00879 6.6e-94 L Transposase
NJMBNHFK_00880 1.5e-194 3.1.21.3 L Subunit R is required for both nuclease and ATPase activities, but not for modification
NJMBNHFK_00881 2.3e-170 mccA 2.5.1.134, 2.5.1.47 E Belongs to the cysteine synthase cystathionine beta- synthase family
NJMBNHFK_00882 2.7e-219 metC 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 E cystathionine
NJMBNHFK_00883 1.5e-95 cysE 2.3.1.30 E Bacterial transferase hexapeptide (six repeats)
NJMBNHFK_00884 8.8e-223 L Transposase
NJMBNHFK_00885 4.8e-157 glcU U Glucose uptake
NJMBNHFK_00886 1.8e-08 4.2.1.53 S Myosin-crossreactive antigen
NJMBNHFK_00887 5.9e-79 hsdM 2.1.1.72 V HsdM N-terminal domain
NJMBNHFK_00888 2.2e-101 XK27_10720 D peptidase activity
NJMBNHFK_00889 3.1e-292 adcA P Belongs to the bacterial solute-binding protein 9 family
NJMBNHFK_00890 1.7e-08
NJMBNHFK_00892 1.2e-172 yeiH S Membrane
NJMBNHFK_00893 5.5e-119 mur1 NU muramidase
NJMBNHFK_00894 1.9e-83 L transposition
NJMBNHFK_00895 2.6e-166 cpsY K Transcriptional regulator
NJMBNHFK_00896 0.0 glmS 2.6.1.16 M Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source
NJMBNHFK_00897 1.2e-57 phnA P Alkylphosphonate utilization operon protein PhnA
NJMBNHFK_00898 2e-104 artQ P ABC transporter (Permease
NJMBNHFK_00899 1.8e-113 glnQ 3.6.3.21 E abc transporter atp-binding protein
NJMBNHFK_00900 1.1e-158 aatB ET ABC transporter substrate-binding protein
NJMBNHFK_00901 3.5e-40 uvrX 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
NJMBNHFK_00902 2.5e-139 uvrX 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
NJMBNHFK_00903 1.7e-57 adhP 1.1.1.1 C alcohol dehydrogenase
NJMBNHFK_00904 1.3e-106 adhP 1.1.1.1 C alcohol dehydrogenase
NJMBNHFK_00905 9.3e-20 sthIM 2.1.1.72 L Adenine specific DNA methylase Mod
NJMBNHFK_00906 3.9e-303 guaA 2.3.1.128, 6.3.5.2 F Catalyzes the synthesis of GMP from XMP
NJMBNHFK_00907 4.5e-126 gntR1 K transcriptional
NJMBNHFK_00908 1.1e-53 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
NJMBNHFK_00909 1.3e-269 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
NJMBNHFK_00910 4.1e-87 niaX
NJMBNHFK_00911 8.6e-90 niaR S small molecule binding protein (contains 3H domain)
NJMBNHFK_00912 6.9e-127 K DNA-binding helix-turn-helix protein
NJMBNHFK_00913 1.4e-158 ylqF S Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity
NJMBNHFK_00914 1.5e-135 rnhB 3.1.26.4 L Endonuclease that specifically degrades the RNA of RNA- DNA hybrids
NJMBNHFK_00915 4.1e-167 GK ROK family
NJMBNHFK_00916 8.3e-159 dprA LU DNA protecting protein DprA
NJMBNHFK_00917 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
NJMBNHFK_00918 1.4e-150 S TraX protein
NJMBNHFK_00919 2.2e-122 KT Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain
NJMBNHFK_00920 2.4e-251 T PhoQ Sensor
NJMBNHFK_00921 6.6e-259 trmFO 2.1.1.74 J Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs
NJMBNHFK_00922 1.1e-152 XK27_05470 E Methionine synthase
NJMBNHFK_00923 1.7e-75 ndk 2.7.4.6 F Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate
NJMBNHFK_00924 2.7e-48 pspE P 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
NJMBNHFK_00925 1.8e-51 IQ Acetoin reductase
NJMBNHFK_00926 3.9e-19 IQ Acetoin reductase
NJMBNHFK_00927 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
NJMBNHFK_00928 1.8e-156 Z012_04635 K Transcriptional activator, Rgg GadR MutR family
NJMBNHFK_00931 1.3e-212 pqqE C radical SAM domain protein
NJMBNHFK_00932 3.9e-136 speB 3.5.3.11 E hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines
NJMBNHFK_00933 6.6e-61 EGP Major facilitator Superfamily
NJMBNHFK_00934 0.0 alsS 2.2.1.6 EH Belongs to the TPP enzyme family
NJMBNHFK_00935 3e-133 budA 4.1.1.5 H Belongs to the alpha-acetolactate decarboxylase family
NJMBNHFK_00936 8.6e-196 L Transposase
NJMBNHFK_00937 6.4e-104 V ABC transporter (Permease
NJMBNHFK_00938 4.1e-114 IQ Belongs to the short-chain dehydrogenases reductases (SDR) family
NJMBNHFK_00939 1.6e-10
NJMBNHFK_00940 1.2e-97 K Transcriptional regulator, TetR family
NJMBNHFK_00941 1.2e-158 czcD P cation diffusion facilitator family transporter
NJMBNHFK_00942 2.7e-210 hemH 4.99.1.1, 4.99.1.9 H Catalyzes the ferrous insertion into protoporphyrin IX
NJMBNHFK_00943 6.2e-196 adhB 1.1.1.1, 1.1.1.14 E Dehydrogenase
NJMBNHFK_00944 6e-08 S Hydrolases of the alpha beta superfamily
NJMBNHFK_00945 7.9e-17 S Alpha/beta hydrolase of unknown function (DUF915)
NJMBNHFK_00946 3.8e-78 S Alpha/beta hydrolase of unknown function (DUF915)
NJMBNHFK_00947 1.6e-249 L Transposase
NJMBNHFK_00950 2.6e-143 2.4.2.3 F Phosphorylase superfamily
NJMBNHFK_00951 4.1e-118 gph 3.1.3.18 S HAD hydrolase, family IA, variant 1
NJMBNHFK_00952 9.4e-15 yclQ P ABC-type enterochelin transport system, periplasmic component
NJMBNHFK_00953 3.3e-19 yclQ P ABC-type enterochelin transport system, periplasmic component
NJMBNHFK_00954 6.6e-73 dinF V Mate efflux family protein
NJMBNHFK_00955 4.8e-41 dinF V Mate efflux family protein
NJMBNHFK_00957 2.3e-309 FbpA K RNA-binding protein homologous to eukaryotic snRNP
NJMBNHFK_00958 3.7e-190
NJMBNHFK_00959 3.1e-89 FNV0100 F Belongs to the Nudix hydrolase family
NJMBNHFK_00960 3.5e-28 3.4.13.21 I Protein conserved in bacteria
NJMBNHFK_00962 5.7e-118 S TraX protein
NJMBNHFK_00963 1.3e-96 thiJ 2.7.11.1, 3.5.1.124 S DJ-1 family
NJMBNHFK_00964 1.3e-148 pyrK C Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( )
NJMBNHFK_00965 3.2e-175 pyrD 1.3.1.14, 1.3.98.1 F Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily
NJMBNHFK_00966 4.7e-143 cas1 L CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette
NJMBNHFK_00967 3.7e-54 cas2 L CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette
NJMBNHFK_00968 6.8e-133 cas6 S Pfam:DUF2276
NJMBNHFK_00969 0.0 csm1 S CRISPR-associated protein Csm1 family
NJMBNHFK_00970 5.6e-62 csm2 L Pfam:DUF310
NJMBNHFK_00971 1.1e-116 csm3 L RAMP superfamily
NJMBNHFK_00972 5.8e-166 csm4 L CRISPR-associated RAMP protein, Csm4 family
NJMBNHFK_00973 4.4e-205 csm5 L CRISPR-associated RAMP protein, Csm5 family
NJMBNHFK_00974 2.1e-14 csm6 S Psort location Cytoplasmic, score
NJMBNHFK_00975 5.2e-74 csm6 S Psort location Cytoplasmic, score
NJMBNHFK_00976 7e-127 pyrF 4.1.1.23 F Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP)
NJMBNHFK_00977 7.5e-112 pyrE 2.4.2.10, 4.1.1.23 F Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP)
NJMBNHFK_00978 1.2e-63 nylA 3.5.1.4 J Belongs to the amidase family
NJMBNHFK_00980 2.5e-267 dtpT E transporter
NJMBNHFK_00981 1e-103 nylA 3.5.1.4 J Belongs to the amidase family
NJMBNHFK_00982 8.8e-134 yckB ET Belongs to the bacterial solute-binding protein 3 family
NJMBNHFK_00983 1.8e-67 yecS P ABC transporter (Permease
NJMBNHFK_00985 8.1e-114 sasH 3.1.3.5, 3.6.1.45 F Belongs to the 5'-nucleotidase family
NJMBNHFK_00986 9.8e-35 3.1.3.6, 3.1.4.16 F nucleotide catabolic process
NJMBNHFK_00987 5.4e-104 yfiF3 K sequence-specific DNA binding
NJMBNHFK_00988 1.9e-147 L Transposase
NJMBNHFK_00989 1.6e-247 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
NJMBNHFK_00990 1.8e-240 agcS E (Alanine) symporter
NJMBNHFK_00991 0.0 pcrA 3.6.4.12 L ATP-dependent DNA helicase
NJMBNHFK_00992 4.6e-241 metY 2.5.1.49 E o-acetylhomoserine
NJMBNHFK_00993 1.8e-59 Q phosphatase activity
NJMBNHFK_00994 9.3e-62 S haloacid dehalogenase-like hydrolase
NJMBNHFK_00995 3.5e-88 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
NJMBNHFK_00996 1.1e-110 hsdS2 2.1.1.72 V Type I restriction modification DNA specificity domain
NJMBNHFK_00997 1.7e-96 XK27_04775 S hemerythrin HHE cation binding domain
NJMBNHFK_00998 2.6e-49 XK27_04775 S hemerythrin HHE cation binding domain
NJMBNHFK_00999 4.9e-151 truB 5.4.99.25 J Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs
NJMBNHFK_01000 5.3e-175 ribF 2.7.1.26, 2.7.7.2 H Belongs to the ribF family
NJMBNHFK_01001 1.4e-71 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
NJMBNHFK_01002 1.9e-43 yktA S Belongs to the UPF0223 family
NJMBNHFK_01003 5e-142 suhB 3.1.3.25 G Belongs to the inositol monophosphatase superfamily
NJMBNHFK_01004 3e-256 rsmF 2.1.1.176, 2.1.1.178 J NOL1 NOP2 sun family protein
NJMBNHFK_01005 3.3e-158 pstS P phosphate
NJMBNHFK_01006 1.8e-154 pstC P probably responsible for the translocation of the substrate across the membrane
NJMBNHFK_01007 2e-155 pstA P phosphate transport system permease
NJMBNHFK_01008 5.2e-150 pstB 3.6.3.27 P Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system
NJMBNHFK_01009 1.7e-139 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
NJMBNHFK_01010 2.4e-113 phoU P Plays a role in the regulation of phosphate uptake
NJMBNHFK_01011 0.0 pepN 3.4.11.2 E aminopeptidase
NJMBNHFK_01012 7e-195 xerS D Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division
NJMBNHFK_01013 1.3e-187 lplA 6.3.1.20 H Lipoate-protein ligase
NJMBNHFK_01014 1.1e-17
NJMBNHFK_01015 3.7e-09
NJMBNHFK_01016 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
NJMBNHFK_01017 3.4e-304 malQ 2.4.1.25 GH77 G 4-alpha-glucanotransferase
NJMBNHFK_01018 2.3e-23 L Transposase
NJMBNHFK_01019 4.6e-25 tatA U protein secretion
NJMBNHFK_01020 5.8e-121 tatC U Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes
NJMBNHFK_01021 1.1e-300 ywbL P COG0672 High-affinity Fe2 Pb2 permease
NJMBNHFK_01022 5.6e-233 ycdB P peroxidase
NJMBNHFK_01023 7.1e-153 ycdO P periplasmic lipoprotein involved in iron transport
NJMBNHFK_01024 3e-34 pulA 3.2.1.1, 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01025 3.7e-85 pulA 3.2.1.1, 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01026 1.7e-60 pulA 3.2.1.1, 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01027 1.5e-65 pulA 3.2.1.1, 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01028 2.4e-134 pulA 3.2.1.1, 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01029 1.9e-37 3.5.1.28 NU amidase activity
NJMBNHFK_01030 8.5e-266 3.5.1.28 NU amidase activity
NJMBNHFK_01031 3.6e-82 3.4.17.14, 3.5.1.28 M GBS Bsp-like repeat
NJMBNHFK_01032 2.6e-20 3.4.17.14, 3.5.1.28 M GBS Bsp-like repeat
NJMBNHFK_01033 0.0 lpdA 1.8.1.4 C Dehydrogenase
NJMBNHFK_01034 1.8e-198 acoC 2.3.1.12 C Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex
NJMBNHFK_01035 3.7e-182 acoB 1.2.4.1, 1.2.4.4 C COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit
NJMBNHFK_01036 6e-185 acoA 1.2.4.1, 1.2.4.4 C Dehydrogenase E1 component
NJMBNHFK_01037 5e-38 P membrane protein (DUF2207)
NJMBNHFK_01038 2.8e-65 S the current gene model (or a revised gene model) may contain a frame shift
NJMBNHFK_01039 3.7e-235 pyrC 3.5.2.3 F Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily
NJMBNHFK_01040 2.9e-127 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
NJMBNHFK_01041 8.6e-218 yeaB K Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family
NJMBNHFK_01042 1.2e-157 rssA S Phospholipase, patatin family
NJMBNHFK_01043 3.9e-78 estA E GDSL-like protein
NJMBNHFK_01044 2.6e-15 estA E Lysophospholipase L1 and related esterases
NJMBNHFK_01045 3.7e-293 S unusual protein kinase
NJMBNHFK_01046 4.9e-39 S granule-associated protein
NJMBNHFK_01047 7.9e-138 bglH 3.2.1.86 GT1 G Belongs to the glycosyl hydrolase 1 family
NJMBNHFK_01048 5.8e-28 bglH 3.2.1.86 GT1 G beta-glucosidase activity
NJMBNHFK_01049 1.3e-199 S hmm pf01594
NJMBNHFK_01050 1.6e-44 G alpha-ribazole phosphatase activity
NJMBNHFK_01051 2e-33 G Belongs to the phosphoglycerate mutase family
NJMBNHFK_01052 1.1e-25 G Belongs to the phosphoglycerate mutase family
NJMBNHFK_01053 8.8e-66 pgm G Belongs to the phosphoglycerate mutase family
NJMBNHFK_01054 1.7e-80 supH 3.1.3.102, 3.1.3.104 S Sucrose-6F-phosphate phosphohydrolase
NJMBNHFK_01055 4.9e-94 V VanZ like family
NJMBNHFK_01056 8.1e-23 L Transposase
NJMBNHFK_01057 3.2e-92 L Transposase
NJMBNHFK_01058 6.4e-33 cpsJ S Glycosyltransferase like family 2
NJMBNHFK_01059 3e-15
NJMBNHFK_01060 1.1e-71 M Glycosyltransferase sugar-binding region containing DXD motif
NJMBNHFK_01061 1.9e-41 pssE S Glycosyltransferase family 28 C-terminal domain
NJMBNHFK_01062 1.4e-72 cpsF M Oligosaccharide biosynthesis protein Alg14 like
NJMBNHFK_01063 1.2e-70 rfbP 2.7.8.6 M Bacterial sugar transferase
NJMBNHFK_01064 3.3e-37 L transposase activity
NJMBNHFK_01065 4e-60 L COG2801 Transposase and inactivated derivatives
NJMBNHFK_01066 2.4e-30 tra981A L Integrase core domain
NJMBNHFK_01067 8.1e-52 tnp L DDE domain
NJMBNHFK_01068 1.4e-235 cps1C S Polysaccharide biosynthesis protein
NJMBNHFK_01069 9.1e-110 L Transposase
NJMBNHFK_01070 2.4e-93 L Transposase
NJMBNHFK_01071 6.9e-96 2.7.8.12 GT2 S Glycosyltransferase like family 2
NJMBNHFK_01072 3e-139 L Integrase core domain
NJMBNHFK_01073 2.2e-22 L Transposase
NJMBNHFK_01074 1.7e-27 tnp L DDE domain
NJMBNHFK_01075 8.5e-23 rgpAc GT4 M group 1 family protein
NJMBNHFK_01076 5.7e-250 cpsE M Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase
NJMBNHFK_01077 5.3e-112 cpsD D COG0489 ATPases involved in chromosome partitioning
NJMBNHFK_01078 2.6e-105 cps4C M biosynthesis protein
NJMBNHFK_01079 3e-136 cpsB 3.1.3.48 GM Capsular polysaccharide biosynthesis protein
NJMBNHFK_01080 3.8e-252 cps4A K Cell envelope-like function transcriptional attenuator common domain protein
NJMBNHFK_01081 2.4e-130 deoD 2.4.2.1, 2.4.2.28 F purine nucleoside phosphorylase
NJMBNHFK_01082 1.7e-48 yfeJ 6.3.5.2 F glutamine amidotransferase
NJMBNHFK_01083 2.5e-43 yfeJ 6.3.5.2 F glutamine amidotransferase
NJMBNHFK_01084 3.6e-40 clcA_2 P chloride
NJMBNHFK_01085 3.8e-42 clcA_2 P chloride channel
NJMBNHFK_01086 7.5e-149 punA 2.4.2.1 F The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate
NJMBNHFK_01087 9.3e-236 deoB 5.4.2.7 G Phosphotransfer between the C1 and C5 carbon atoms of pentose
NJMBNHFK_01088 6.6e-122 rpiA 2.7.1.12, 2.7.1.15, 5.3.1.6 G Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate
NJMBNHFK_01090 4e-21 V Glucan-binding protein C
NJMBNHFK_01091 1e-110 ung2 3.2.2.27 L Uracil-DNA glycosylase
NJMBNHFK_01092 2.4e-275 pepV 3.5.1.18 E Dipeptidase
NJMBNHFK_01093 3.2e-26 dmpI 5.3.2.6 G Belongs to the 4-oxalocrotonate tautomerase family
NJMBNHFK_01094 6.9e-86 XK27_03610 K Gnat family
NJMBNHFK_01095 9.1e-10 L COG1943 Transposase and inactivated derivatives
NJMBNHFK_01096 1.5e-56 rplT J Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit
NJMBNHFK_01097 2.1e-28 rpmI J Belongs to the bacterial ribosomal protein bL35 family
NJMBNHFK_01098 3.5e-86 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
NJMBNHFK_01099 2.8e-120 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
NJMBNHFK_01100 3.9e-15 M LysM domain
NJMBNHFK_01101 2.9e-90 ebsA S Family of unknown function (DUF5322)
NJMBNHFK_01102 1.8e-234 pepT 3.4.11.4 E Cleaves the N-terminal amino acid of tripeptides
NJMBNHFK_01103 4.2e-98 lepB 3.4.21.89 U Belongs to the peptidase S26 family
NJMBNHFK_01104 4.9e-224 G COG0457 FOG TPR repeat
NJMBNHFK_01105 1.1e-175 yubA S permease
NJMBNHFK_01106 3.5e-93 mutX 3.6.1.55 F NTP pyrophosphohydrolases including oxidative damage repair enzymes
NJMBNHFK_01107 3.6e-163 ftsX D Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation
NJMBNHFK_01108 2.5e-124 ftsE D cell division ATP-binding protein FtsE
NJMBNHFK_01109 1.8e-181 prfB J Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA
NJMBNHFK_01110 1.2e-202 queG 1.17.99.6 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)
NJMBNHFK_01111 4.3e-180 yjjH S Calcineurin-like phosphoesterase
NJMBNHFK_01112 5.2e-136 nfrA 1.5.1.38, 1.5.1.39 C nitroreductase
NJMBNHFK_01113 0.0 pacL 3.6.3.8 P cation transport ATPase
NJMBNHFK_01114 2.6e-67 ywiB S Domain of unknown function (DUF1934)
NJMBNHFK_01115 6.3e-51 XK27_00115 2.3.1.128 K acetyltransferase
NJMBNHFK_01116 9.2e-147 yidA S hydrolases of the HAD superfamily
NJMBNHFK_01117 9e-231 murM 2.3.2.10, 2.3.2.16 V protein involved in methicillin resistance
NJMBNHFK_01118 5e-35 F Protein of unknown function (DUF454)
NJMBNHFK_01119 2.1e-154 vicX 3.1.26.11 S Metal-dependent hydrolases of the beta-lactamase superfamily I
NJMBNHFK_01120 1.5e-247 vicK 2.7.13.3 T Histidine kinase
NJMBNHFK_01121 9.9e-129 KT Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain
NJMBNHFK_01122 1e-139 glnQ 3.6.3.21 E abc transporter atp-binding protein
NJMBNHFK_01123 3.5e-149 peb1A ET ABC-type amino acid transport signal transduction systems, periplasmic component domain
NJMBNHFK_01124 8e-115 gltJ P ABC transporter (Permease
NJMBNHFK_01125 4.2e-110 tcyB_2 P ABC transporter (permease)
NJMBNHFK_01126 1.4e-124 endA F DNA RNA non-specific endonuclease
NJMBNHFK_01127 1.2e-25 epuA S DNA-directed RNA polymerase subunit beta
NJMBNHFK_01128 7.2e-231 murA 2.5.1.7 M Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine
NJMBNHFK_01130 3.7e-193 galE 5.1.3.2 M Belongs to the NAD(P)-dependent epimerase dehydratase family
NJMBNHFK_01131 4.9e-21 G Domain of unknown function (DUF4832)
NJMBNHFK_01132 8.4e-53 G Domain of unknown function (DUF4832)
NJMBNHFK_01133 1.5e-211 cotH M CotH kinase protein
NJMBNHFK_01134 6.8e-185 pelG M Putative exopolysaccharide Exporter (EPS-E)
NJMBNHFK_01135 1.9e-109 pelF GT4 M Domain of unknown function (DUF3492)
NJMBNHFK_01136 7.6e-160 pelF GT4 M Domain of unknown function (DUF3492)
NJMBNHFK_01137 0.0 S Uncharacterised protein conserved in bacteria (DUF2194)
NJMBNHFK_01138 4.1e-143
NJMBNHFK_01139 7.6e-134 5.1.3.2 GM Psort location CytoplasmicMembrane, score
NJMBNHFK_01140 2.9e-196 L Transposase
NJMBNHFK_01141 2.2e-63 L Transposase
NJMBNHFK_01142 1.2e-88 L Transposase
NJMBNHFK_01143 2.1e-203 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
NJMBNHFK_01144 4.2e-175 birA 6.3.4.15 HK Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor
NJMBNHFK_01145 3.2e-295 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
NJMBNHFK_01146 1.6e-88 ytsP 1.8.4.14 T GAF domain-containing protein
NJMBNHFK_01147 1.9e-164 miaA 2.5.1.75 J 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)
NJMBNHFK_01148 1.2e-19 WQ51_02665 S Protein of unknown function (DUF3042)
NJMBNHFK_01150 7.7e-35
NJMBNHFK_01153 7.8e-202 S Phage integrase family
NJMBNHFK_01155 8.5e-57 rplS J This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site
NJMBNHFK_01156 4.3e-133 XK27_05110 P chloride
NJMBNHFK_01157 1.2e-61 XK27_05110 P chloride
NJMBNHFK_01158 8.7e-41 pheA 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 E Chorismate mutase
NJMBNHFK_01159 1.3e-282 clcA P Chloride transporter, ClC family
NJMBNHFK_01160 6.7e-75 fld C Flavodoxin
NJMBNHFK_01162 4.7e-126 XK27_08875 O Zinc-dependent metalloprotease
NJMBNHFK_01163 3.5e-151 estA CE1 S Putative esterase
NJMBNHFK_01164 1e-309 rnjB S 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
NJMBNHFK_01165 1.2e-135 XK27_08845 S abc transporter atp-binding protein
NJMBNHFK_01166 4e-148 XK27_08840 S Belongs to the binding-protein-dependent transport system permease family
NJMBNHFK_01167 3.3e-178 XK27_08835 S ABC transporter substrate binding protein
NJMBNHFK_01168 3.2e-17 S Domain of unknown function (DUF4649)
NJMBNHFK_01170 6.9e-30 Q the current gene model (or a revised gene model) may contain a frame shift
NJMBNHFK_01171 1.1e-22 Q the current gene model (or a revised gene model) may contain a frame shift
NJMBNHFK_01172 3.2e-09 Q the current gene model (or a revised gene model) may contain a frame shift
NJMBNHFK_01173 8.8e-223 L Transposase
NJMBNHFK_01175 1.6e-249 L Transposase
NJMBNHFK_01176 1.3e-276 pyk 2.7.1.40, 2.7.7.4 G Belongs to the pyruvate kinase family
NJMBNHFK_01177 1.2e-188 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
NJMBNHFK_01178 0.0 dnaE 2.7.7.7 L DNA polymerase
NJMBNHFK_01179 1.4e-152 sua5 2.7.7.87 J Belongs to the SUA5 family
NJMBNHFK_01180 3.1e-112 leuD 4.2.1.33, 4.2.1.35 E Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate
NJMBNHFK_01181 6.8e-275 leuC 4.2.1.33, 4.2.1.35 E Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate
NJMBNHFK_01182 2.5e-43 ysdA L Membrane
NJMBNHFK_01183 6.6e-190 leuB 1.1.1.85 CE Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate
NJMBNHFK_01184 3.4e-291 leuA 2.3.3.13 E Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate)
NJMBNHFK_01185 3e-130 gpmA 5.4.2.11 G Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate
NJMBNHFK_01186 3.6e-179 pyrD 1.3.1.14, 1.3.98.1 F Catalyzes the conversion of dihydroorotate to orotate
NJMBNHFK_01188 2.8e-39 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
NJMBNHFK_01189 1.7e-83 ypmS S Protein conserved in bacteria
NJMBNHFK_01190 6e-144 ypmR E lipolytic protein G-D-S-L family
NJMBNHFK_01191 1e-148 DegV S DegV family
NJMBNHFK_01192 5.8e-305 recN L May be involved in recombinational repair of damaged DNA
NJMBNHFK_01193 1.8e-72 argR K Regulates arginine biosynthesis genes
NJMBNHFK_01194 5e-159 rrmJ 2.1.1.226, 2.1.1.227 J Ribosomal RNA large subunit methyltransferase J
NJMBNHFK_01195 3e-159 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
NJMBNHFK_01196 3.5e-29 xseB 3.1.11.6 L exodeoxyribonuclease VII activity
NJMBNHFK_01197 1.2e-247 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
NJMBNHFK_01200 3.4e-120 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
NJMBNHFK_01201 2.9e-125 dnaD
NJMBNHFK_01202 9.3e-183 metA 2.3.1.46 E Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine
NJMBNHFK_01203 2e-94 apt 2.4.2.22, 2.4.2.7 F Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis
NJMBNHFK_01204 0.0 recJ L Single-strand DNA-specific exonuclease, C terminal domain
NJMBNHFK_01205 6.7e-139 XK27_05435 1.1.1.100 S Belongs to the short-chain dehydrogenases reductases (SDR) family
NJMBNHFK_01206 9.2e-175 rnz 3.1.26.11 S Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA
NJMBNHFK_01207 4.2e-118 galT 2.7.7.12 G UDPglucose--hexose-1-phosphate uridylyltransferase
NJMBNHFK_01208 7.1e-223 hflX S GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis
NJMBNHFK_01209 1.6e-239 rodA D Belongs to the SEDS family
NJMBNHFK_01210 4.5e-49 hisE 3.5.4.19, 3.6.1.31, 5.3.1.16 E phosphoribosyl-ATP diphosphatase activity
NJMBNHFK_01211 5.5e-61 hisI 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 E Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP
NJMBNHFK_01212 1.9e-133 hisF 3.5.4.19, 3.6.1.31 E IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit
NJMBNHFK_01213 5e-128 hisA 5.3.1.16 E 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase
NJMBNHFK_01214 1.2e-109 hisH E IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR
NJMBNHFK_01215 1.5e-106 hisB 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 E imidazoleglycerol-phosphate dehydratase
NJMBNHFK_01216 1.1e-234 hisD 1.1.1.23, 1.1.1.308 E Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine
NJMBNHFK_01217 2.3e-116 hisG 2.4.2.17 E Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity
NJMBNHFK_01218 5.7e-183 hisZ 2.4.2.17, 6.1.1.21 E Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine
NJMBNHFK_01219 2.1e-196 hisC 2.6.1.9 E Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily
NJMBNHFK_01221 4.2e-86 L Integrase core domain protein
NJMBNHFK_01222 1.1e-53 L transposition
NJMBNHFK_01223 1.8e-21 L Transposase
NJMBNHFK_01224 5.2e-36 L transposase activity
NJMBNHFK_01225 1.3e-22 XK27_08085
NJMBNHFK_01226 5.6e-92 XK27_08080 3.1.1.53 G Exopolysaccharide biosynthesis protein
NJMBNHFK_01227 2.3e-09 XK27_08080 3.1.1.53 G Exopolysaccharide biosynthesis protein
NJMBNHFK_01228 2e-140 hisK 3.1.3.15 E Histidinol phosphatase and related hydrolases of the PHP family
NJMBNHFK_01229 1.1e-121 ylfI S tigr01906
NJMBNHFK_01230 5.9e-143 nagD 2.7.1.25, 3.1.3.41 G Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro
NJMBNHFK_01231 1.5e-143 fat 3.1.2.21 I Acyl-ACP thioesterase
NJMBNHFK_01232 4.1e-217 hemN H Involved in the biosynthesis of porphyrin-containing compound
NJMBNHFK_01235 1.9e-205 rfbB 4.2.1.46 M Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily
NJMBNHFK_01236 8.3e-113 rmlC 1.1.1.133, 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
NJMBNHFK_01237 1.9e-161 rfbA 2.7.7.24 M Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis
NJMBNHFK_01238 1.1e-206 yurR 1.4.5.1 E oxidoreductase
NJMBNHFK_01239 5.7e-102 zupT P Mediates zinc uptake. May also transport other divalent cations
NJMBNHFK_01240 9.6e-149 yqfO 3.5.4.16 S Belongs to the GTP cyclohydrolase I type 2 NIF3 family
NJMBNHFK_01241 2.7e-123 trmK 2.1.1.217 S SAM-dependent methyltransferase
NJMBNHFK_01242 1.7e-70 gtrA S GtrA-like protein
NJMBNHFK_01243 1.5e-250 glmM 5.4.2.10 G Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate
NJMBNHFK_01244 6e-169 ybbR S Protein conserved in bacteria
NJMBNHFK_01245 5.6e-124 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
NJMBNHFK_01246 7.5e-255 murD 3.4.21.10, 6.3.2.13, 6.3.2.9 M Mur ligase, middle domain protein
NJMBNHFK_01247 8.7e-150 cobQ S glutamine amidotransferase
NJMBNHFK_01248 0.0 mprF 2.3.2.3 J 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
NJMBNHFK_01249 2.2e-131 pip 1.11.1.10 S Alpha beta hydrolase
NJMBNHFK_01250 0.0 uup S abc transporter atp-binding protein
NJMBNHFK_01251 2.1e-114 udk 2.7.1.48 F Cytidine monophosphokinase
NJMBNHFK_01252 2.1e-178 yfmL 3.6.4.13 L DEAD DEAH box helicase
NJMBNHFK_01253 2.1e-28 6.3.2.2, 6.3.2.4 F Belongs to the D-alanine--D-alanine ligase family
NJMBNHFK_01254 8.6e-265 gapN 1.2.1.9 C Belongs to the aldehyde dehydrogenase family
NJMBNHFK_01255 6.2e-249 L Transposase
NJMBNHFK_01256 0.0 ptsI 2.7.3.9 G General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr)
NJMBNHFK_01257 7.9e-39 ptsH G phosphocarrier protein Hpr
NJMBNHFK_01258 3.3e-222 icd 1.1.1.42 C Isocitrate dehydrogenase
NJMBNHFK_01259 5.1e-212 citZ 2.3.3.1 C Belongs to the citrate synthase family
NJMBNHFK_01260 0.0 acnA 4.2.1.3 C Catalyzes the isomerization of citrate to isocitrate via cis-aconitate
NJMBNHFK_01261 2.2e-34 nrdH O Glutaredoxin
NJMBNHFK_01262 0.0 nrdE 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
NJMBNHFK_01263 1.7e-184 nrdF 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
NJMBNHFK_01265 4.2e-71 L Transposase (IS116 IS110 IS902 family)
NJMBNHFK_01266 3.3e-26 L Transposase (IS116 IS110 IS902 family)
NJMBNHFK_01267 1.2e-164 ypuA S secreted protein
NJMBNHFK_01268 1.1e-55 yaeR E COG0346 LactoylglutaTHIone lyase and related lyases
NJMBNHFK_01269 5.1e-131 srtA 3.4.22.70 M Sortase (surface protein transpeptidase)
NJMBNHFK_01270 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
NJMBNHFK_01271 1.1e-181 ldh 1.1.1.27 C Belongs to the LDH MDH superfamily. LDH family
NJMBNHFK_01272 3.4e-258 noxE P NADH oxidase
NJMBNHFK_01273 1.9e-294 yfmM S abc transporter atp-binding protein
NJMBNHFK_01274 3.3e-82 XK27_01265 S ECF-type riboflavin transporter, S component
NJMBNHFK_01275 8.7e-85 pdxK 2.7.1.35 H Belongs to the pyridoxine kinase family
NJMBNHFK_01276 4.5e-44 pdxK 2.7.1.35 H Belongs to the pyridoxine kinase family
NJMBNHFK_01277 2e-86 S ECF-type riboflavin transporter, S component
NJMBNHFK_01279 5e-240 XK27_08130 K Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs
NJMBNHFK_01280 2e-55 nrdD_1 1.1.98.6, 1.17.4.1 F Ribonucleoside-triphosphate reductase
NJMBNHFK_01283 0.0 pheT 6.1.1.20 J Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily
NJMBNHFK_01284 9.9e-94 paiA 2.3.1.57 K COG0454 Histone acetyltransferase HPA2 and related acetyltransferases
NJMBNHFK_01285 1.1e-197 pheS 6.1.1.20 J Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily
NJMBNHFK_01286 0.0 smc D Required for chromosome condensation and partitioning
NJMBNHFK_01287 8.4e-125 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
NJMBNHFK_01288 6.6e-173 dapA 4.3.3.7 E Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA)
NJMBNHFK_01289 1.1e-198 asd 1.2.1.11 E Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate
NJMBNHFK_01290 2.4e-92 pat 2.3.1.183 M acetyltransferase
NJMBNHFK_01291 1.1e-12
NJMBNHFK_01292 8.9e-30
NJMBNHFK_01293 9e-278 cls I Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol
NJMBNHFK_01294 0.0 uvrC L The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision
NJMBNHFK_01295 3.1e-127 yjjG 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 E hydrolase
NJMBNHFK_01296 1.2e-62 bioY S biotin transmembrane transporter activity
NJMBNHFK_01297 9.8e-88 proW P Binding-protein-dependent transport system inner membrane component
NJMBNHFK_01298 1.5e-138 proV E abc transporter atp-binding protein
NJMBNHFK_01299 4.4e-169 proX M ABC transporter, substrate-binding protein, QAT family
NJMBNHFK_01300 3e-111 proWZ P ABC transporter (Permease
NJMBNHFK_01301 1.2e-280 hutH 4.3.1.3 E Histidine ammonia-lyase
NJMBNHFK_01302 1.6e-205 S Protein of unknown function (DUF917)
NJMBNHFK_01303 1.3e-309 hutU 4.2.1.49 E Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate
NJMBNHFK_01304 1.6e-59 sdaAB 4.3.1.17 E L-serine dehydratase
NJMBNHFK_01305 4.4e-101 desR K COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain
NJMBNHFK_01306 1.5e-192 desK 2.7.13.3 T Histidine kinase
NJMBNHFK_01307 1.4e-133 yvfS V ABC-2 type transporter
NJMBNHFK_01308 8.7e-159 XK27_09825 V abc transporter atp-binding protein
NJMBNHFK_01311 8.1e-163 yocS S Transporter
NJMBNHFK_01312 1.2e-82 cdd 2.4.2.4, 3.5.4.5 F cytidine deaminase activity
NJMBNHFK_01313 7.5e-115 yvfS V Transporter
NJMBNHFK_01314 3.9e-151 XK27_09825 V abc transporter atp-binding protein
NJMBNHFK_01315 2.7e-14 liaI KT membrane
NJMBNHFK_01316 2.6e-30 liaI KT membrane
NJMBNHFK_01317 6e-99 XK27_05000 S Fe-S-cluster oxidoreductase
NJMBNHFK_01318 0.0 V ABC transporter (permease)
NJMBNHFK_01319 1.9e-133 macB2 V ABC transporter, ATP-binding protein
NJMBNHFK_01320 3.1e-165 T Histidine kinase
NJMBNHFK_01321 4.6e-123 KT Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain
NJMBNHFK_01322 2e-77 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
NJMBNHFK_01323 3.3e-69 pbuX F xanthine permease
NJMBNHFK_01324 9.2e-119 pbuX F xanthine permease
NJMBNHFK_01325 1.5e-247 norM V Multidrug efflux pump
NJMBNHFK_01326 4.3e-188 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
NJMBNHFK_01327 1.3e-235 brnQ E Component of the transport system for branched-chain amino acids
NJMBNHFK_01328 9.4e-65 manA 5.3.1.8 G mannose-6-phosphate isomerase
NJMBNHFK_01329 8.2e-57 manA 5.3.1.8 G mannose-6-phosphate isomerase
NJMBNHFK_01330 4.8e-25 csbD K CsbD-like
NJMBNHFK_01331 6.2e-228 yfnA E amino acid
NJMBNHFK_01332 5.1e-110 XK27_02070 S nitroreductase
NJMBNHFK_01333 9.5e-150 1.13.11.2 S glyoxalase
NJMBNHFK_01334 5.6e-77 ywnA K Transcriptional regulator
NJMBNHFK_01335 9.5e-158 E Alpha/beta hydrolase of unknown function (DUF915)
NJMBNHFK_01336 1.9e-231 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
NJMBNHFK_01337 1.4e-110 drgA C Nitroreductase
NJMBNHFK_01338 3e-102 yoaK S Protein of unknown function (DUF1275)
NJMBNHFK_01340 6.8e-161 yvgN C reductase
NJMBNHFK_01341 1.7e-179 galE 5.1.3.2 M Belongs to the NAD(P)-dependent epimerase dehydratase family
NJMBNHFK_01342 3.6e-282 XK27_07020 S Belongs to the UPF0371 family
NJMBNHFK_01344 1.1e-37 BP1961 P nitric oxide dioxygenase activity
NJMBNHFK_01345 1.4e-54 K response regulator
NJMBNHFK_01346 9.3e-72 S Signal peptide protein, YSIRK family
NJMBNHFK_01348 4.5e-61
NJMBNHFK_01349 1.8e-270 uvrX 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
NJMBNHFK_01350 1e-137
NJMBNHFK_01351 5.3e-12 IQ PFAM AMP-dependent synthetase and ligase
NJMBNHFK_01352 2.7e-12 IQ PFAM AMP-dependent synthetase and ligase
NJMBNHFK_01353 5.8e-109 MA20_06410 E LysE type translocator
NJMBNHFK_01354 5.6e-08
NJMBNHFK_01355 2.7e-09
NJMBNHFK_01356 0.0 M family 8
NJMBNHFK_01358 1.5e-162 hrtB V MacB-like periplasmic core domain
NJMBNHFK_01359 3.1e-116 devA 3.6.3.25 V abc transporter atp-binding protein
NJMBNHFK_01360 1.1e-151 V MatE
NJMBNHFK_01362 3.9e-110 C Fe-S oxidoreductases
NJMBNHFK_01363 1.2e-176 EGP Major Facilitator Superfamily
NJMBNHFK_01364 5.5e-258 I radical SAM domain protein
NJMBNHFK_01366 6.5e-159 Z012_04635 K Transcriptional activator, Rgg GadR MutR family
NJMBNHFK_01367 1.4e-150 L Integrase core domain protein
NJMBNHFK_01368 1.8e-87 L transposase activity
NJMBNHFK_01370 2.8e-85
NJMBNHFK_01371 0.0 sbcC L ATPase involved in DNA repair
NJMBNHFK_01372 6.9e-231 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
NJMBNHFK_01373 0.0 lacL 3.2.1.23 G -beta-galactosidase
NJMBNHFK_01374 0.0 lacS G transporter
NJMBNHFK_01375 6.4e-201 galM 5.1.3.3 G Catalyzes the interconversion of alpha and beta anomers of maltose
NJMBNHFK_01376 6.6e-195 galE 5.1.3.2 M Belongs to the NAD(P)-dependent epimerase dehydratase family
NJMBNHFK_01377 4e-289 galT 2.7.7.12 G UDPglucose--hexose-1-phosphate uridylyltransferase
NJMBNHFK_01378 1.6e-221 galK 2.7.1.6 G Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P)
NJMBNHFK_01379 2.3e-184 galR K Transcriptional regulator
NJMBNHFK_01380 2.7e-08 L Integrase core domain protein
NJMBNHFK_01381 1.2e-25 L transposition
NJMBNHFK_01382 3.5e-228 zmpB M M26 IgA1-specific Metallo-endopeptidase C-terminal region
NJMBNHFK_01383 6.7e-17 rtxA M M26 IgA1-specific Metallo-endopeptidase C-terminal region
NJMBNHFK_01384 2.5e-101 V abc transporter atp-binding protein
NJMBNHFK_01385 4.3e-40 V abc transporter atp-binding protein
NJMBNHFK_01386 0.0 gshF 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 H Belongs to the glutamate--cysteine ligase type 1 family
NJMBNHFK_01387 6.4e-62 L Transposase
NJMBNHFK_01388 7e-150 pulA 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01389 1.8e-33 pulA 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01390 1.7e-120 pulA 3.2.1.41 CBM48,GH13 G belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01391 0.0 ftsK D Belongs to the FtsK SpoIIIE SftA family
NJMBNHFK_01392 5.9e-188 trxB1 1.18.1.2, 1.19.1.1 C Ferredoxin--NADP reductase
NJMBNHFK_01393 1.4e-135 trmD 2.1.1.228, 4.6.1.12 J Belongs to the RNA methyltransferase TrmD family
NJMBNHFK_01394 5.8e-94 rimM J An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes
NJMBNHFK_01397 2.2e-114 vraR K Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain
NJMBNHFK_01398 5.8e-175 vraS 2.7.13.3 T Histidine kinase
NJMBNHFK_01399 3.7e-120 yvqF KT membrane
NJMBNHFK_01400 0.0 prkC 2.7.11.1 KLT serine threonine protein kinase
NJMBNHFK_01401 2e-132 stp 3.1.3.16 T phosphatase
NJMBNHFK_01402 4.4e-247 sun 2.1.1.176 J Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA
NJMBNHFK_01403 2.5e-172 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
NJMBNHFK_01404 0.0 priA L Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA
NJMBNHFK_01405 2.7e-46 rpoZ 2.7.7.6 K DNA-directed 5'-3' RNA polymerase activity
NJMBNHFK_01406 9.8e-112 gmk 2.7.4.8 F Essential for recycling GMP and indirectly, cGMP
NJMBNHFK_01407 2.8e-212 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)
NJMBNHFK_01408 3.4e-149 XK27_02985 S overlaps another CDS with the same product name
NJMBNHFK_01409 2.1e-148 supH S overlaps another CDS with the same product name
NJMBNHFK_01410 8.6e-63 yvoA_1 K Transcriptional
NJMBNHFK_01411 2.8e-120 skfE V abc transporter atp-binding protein
NJMBNHFK_01412 3.3e-133 V ATPase activity
NJMBNHFK_01413 4.3e-172 oppF P Belongs to the ABC transporter superfamily
NJMBNHFK_01414 2.2e-204 oppD P Belongs to the ABC transporter superfamily
NJMBNHFK_01415 4.9e-168 amiD P ABC transporter (Permease
NJMBNHFK_01416 4.2e-278 amiC P ABC transporter (Permease
NJMBNHFK_01417 0.0 amiA E ABC transporter, substrate-binding protein, family 5
NJMBNHFK_01418 1.5e-65
NJMBNHFK_01419 7.3e-130 L Transposase
NJMBNHFK_01420 0.0 amiA E ABC transporter, substrate-binding protein, family 5
NJMBNHFK_01421 8.1e-45 L Transposase
NJMBNHFK_01422 4.1e-158 L COG2801 Transposase and inactivated derivatives
NJMBNHFK_01423 1.2e-24 oppF P Belongs to the ABC transporter superfamily
NJMBNHFK_01424 3.8e-45 oppF P Belongs to the ABC transporter superfamily
NJMBNHFK_01425 1.4e-40 tatD L Hydrolase, tatd
NJMBNHFK_01426 6.7e-218 oxlT P COG0477 Permeases of the major facilitator superfamily
NJMBNHFK_01427 1e-110 L Integrase core domain protein
NJMBNHFK_01428 1.1e-23 L transposase activity
NJMBNHFK_01429 8.9e-18 L transposase activity
NJMBNHFK_01430 1.4e-181 pta 2.3.1.8, 3.6.3.21 C phosphate acetyltransferase
NJMBNHFK_01431 9.8e-174 rluD 5.4.99.23, 5.4.99.28, 5.4.99.29 J Responsible for synthesis of pseudouridine from uracil
NJMBNHFK_01432 5.4e-150 nadK 2.7.1.23 H 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
NJMBNHFK_01433 5.5e-121 yjbM 2.7.6.5 S Gtp pyrophosphokinase
NJMBNHFK_01434 1.5e-103 yjbK S Adenylate cyclase
NJMBNHFK_01435 2.1e-177 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)
NJMBNHFK_01436 7e-206 iscS 2.8.1.7 E Cysteine desulfurase
NJMBNHFK_01437 2e-58 XK27_04120 S Putative amino acid metabolism
NJMBNHFK_01438 5.7e-118 rex K Modulates transcription in response to changes in cellular NADH NAD( ) redox state
NJMBNHFK_01439 1.6e-131 puuD T peptidase C26
NJMBNHFK_01440 6.2e-120 radC E Belongs to the UPF0758 family
NJMBNHFK_01441 4.9e-272 rgpF M Rhamnan synthesis protein F
NJMBNHFK_01442 9e-223 rgpD 3.6.3.38 P Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system
NJMBNHFK_01443 6.4e-140 rgpC GM Transport permease protein
NJMBNHFK_01444 2e-169 rgpB GT2 M Glycosyltransferase, group 2 family protein
NJMBNHFK_01445 1.1e-222 rgpA GT4 M Domain of unknown function (DUF1972)
NJMBNHFK_01446 5e-174 S Glucosyl transferase GtrII
NJMBNHFK_01447 1.8e-28 S Glucosyl transferase GtrII
NJMBNHFK_01448 1.6e-219 GT4 M transferase activity, transferring glycosyl groups
NJMBNHFK_01449 2e-217 M Psort location CytoplasmicMembrane, score
NJMBNHFK_01450 0.0 rgpF GT2,GT4 M Glycosyltransferase like family 2
NJMBNHFK_01451 5.9e-151 2.4.1.60 S Glycosyltransferase group 2 family protein
NJMBNHFK_01452 4.6e-42 S Uncharacterized conserved protein (DUF2304)
NJMBNHFK_01453 4.5e-129 arnC M group 2 family protein
NJMBNHFK_01454 1.1e-181 cpsIaJ S Glycosyltransferase like family 2
NJMBNHFK_01455 1e-184 S Glycosyltransferase like family 2
NJMBNHFK_01456 9.4e-223 amrA S membrane protein involved in the export of O-antigen and teichoic acid
NJMBNHFK_01457 1.5e-160 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
NJMBNHFK_01458 2.9e-235 S Predicted membrane protein (DUF2142)
NJMBNHFK_01459 1.7e-173 yfdH GT2 M COG0463, glycosyltransferases involved in cell wall biogenesis
NJMBNHFK_01460 3.4e-55 yitW K metal-sulfur cluster biosynthetic enzyme
NJMBNHFK_01461 1.1e-201 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
NJMBNHFK_01462 0.0 dnaG L RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication
NJMBNHFK_01463 5.5e-20 rpsU J Belongs to the bacterial ribosomal protein bS21 family
NJMBNHFK_01464 1.1e-136 gltS ET Belongs to the bacterial solute-binding protein 3 family
NJMBNHFK_01465 2.1e-202 arcT 2.6.1.1 E Aminotransferase
NJMBNHFK_01466 9.4e-136 ET ABC transporter
NJMBNHFK_01467 1.1e-142 ET Belongs to the bacterial solute-binding protein 3 family
NJMBNHFK_01468 2.9e-84 mutT 3.6.1.55 F Nudix family
NJMBNHFK_01469 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
NJMBNHFK_01471 1.2e-55 V CAAX protease self-immunity
NJMBNHFK_01472 2.6e-32 S CAAX amino terminal protease family protein
NJMBNHFK_01473 0.0 glnP P ABC-type amino acid transport signal transduction systems periplasmic component domain
NJMBNHFK_01474 1e-136 glnQ 3.6.3.21 E abc transporter atp-binding protein
NJMBNHFK_01475 2.4e-16 XK27_00735
NJMBNHFK_01476 1.4e-248 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
NJMBNHFK_01478 7.3e-135 rsuA 5.4.99.19, 5.4.99.22 J Belongs to the pseudouridine synthase RsuA family
NJMBNHFK_01481 5.5e-65 paaI Q protein possibly involved in aromatic compounds catabolism
NJMBNHFK_01482 6.6e-30 ycaO O OsmC-like protein
NJMBNHFK_01484 1.7e-154 EG Permeases of the drug metabolite transporter (DMT) superfamily
NJMBNHFK_01486 5.6e-110 csn2 S CRISPR-associated protein (Cas_Csn2)
NJMBNHFK_01487 3.5e-52 cas2 L CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette
NJMBNHFK_01488 1.5e-163 cas1 L CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette
NJMBNHFK_01489 0.0 cas9 L CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer
NJMBNHFK_01490 6.7e-116 serB 3.1.3.3 E phosphoserine phosphatase
NJMBNHFK_01491 3.2e-298 ezrA D modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization
NJMBNHFK_01492 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
NJMBNHFK_01493 2.6e-109 3.1.3.18 S IA, variant 1
NJMBNHFK_01494 2.2e-117 lrgB M effector of murein hydrolase
NJMBNHFK_01495 2.2e-58 lrgA S Effector of murein hydrolase LrgA
NJMBNHFK_01497 5.4e-59 arsC 1.20.4.1 P Belongs to the ArsC family
NJMBNHFK_01498 1.5e-52 ogt 2.1.1.63, 3.2.2.20 L methylated-DNA-[protein]-cysteine S-methyltransferase activity
NJMBNHFK_01499 7e-220 serA 1.1.1.399, 1.1.1.95 EH Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family
NJMBNHFK_01500 3.9e-104 wecD M Acetyltransferase GNAT family
NJMBNHFK_01501 1.3e-209 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
NJMBNHFK_01502 5.1e-96 GK ROK family
NJMBNHFK_01503 8.1e-72 gloA 4.4.1.5 E Lactoylglutathione lyase
NJMBNHFK_01504 1.7e-47 XK27_08050 O stress-induced mitochondrial fusion
NJMBNHFK_01505 1.3e-19 XK27_08050 O HflC and HflK could regulate a protease
NJMBNHFK_01506 2.3e-206 potD P spermidine putrescine ABC transporter
NJMBNHFK_01507 3e-134 potC P ABC-type spermidine putrescine transport system, permease component II
NJMBNHFK_01508 3.7e-140 potB P ABC-type spermidine putrescine transport system, permease component I
NJMBNHFK_01509 1.2e-213 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
NJMBNHFK_01510 7.8e-171 murB 1.3.1.98 M cell wall formation
NJMBNHFK_01511 2.9e-87 folK 2.7.6.3, 4.1.2.25 H 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
NJMBNHFK_01512 1.2e-61 folB 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 H Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin
NJMBNHFK_01513 1.2e-298 amy 3.2.1.1 GH13 G Belongs to the glycosyl hydrolase 13 family
NJMBNHFK_01514 7e-147 folP 2.5.1.15, 2.7.6.3 H Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives
NJMBNHFK_01515 1e-99 folE 3.5.4.16 F gtp cyclohydrolase
NJMBNHFK_01516 0.0 ydaO E amino acid
NJMBNHFK_01517 1.1e-239 folC 6.3.2.12, 6.3.2.17 H Belongs to the folylpolyglutamate synthase family
NJMBNHFK_01518 4.1e-37 ylqC L Belongs to the UPF0109 family
NJMBNHFK_01519 2.4e-43 rpsP J Belongs to the bacterial ribosomal protein bS16 family
NJMBNHFK_01520 6.9e-172 tehB 2.1.1.265 PQ tellurite resistance protein tehb
NJMBNHFK_01521 8.2e-159 xth 3.1.11.2 L exodeoxyribonuclease III
NJMBNHFK_01522 2.1e-74 S QueT transporter
NJMBNHFK_01523 1.9e-55 L Transposase
NJMBNHFK_01524 5.7e-186 yegS 2.7.1.107 I Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase
NJMBNHFK_01525 0.0 ligA 6.5.1.2 L DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA
NJMBNHFK_01526 3.7e-85 ccl S cog cog4708
NJMBNHFK_01527 7.4e-164 rbn E Belongs to the UPF0761 family
NJMBNHFK_01528 1.5e-166 map 3.4.11.18 E Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed
NJMBNHFK_01529 3.3e-231 ytoI K transcriptional regulator containing CBS domains
NJMBNHFK_01530 2.4e-98 XK27_07830 2.3.1.128 J Acetyltransferase GNAT Family
NJMBNHFK_01531 1e-232 murA 2.5.1.7 M Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine
NJMBNHFK_01532 0.0 comEC S Competence protein ComEC
NJMBNHFK_01533 2.2e-96 comEA L COG1555 DNA uptake protein and related DNA-binding proteins
NJMBNHFK_01534 1.3e-142 plsC 2.3.1.51 I Acyltransferase
NJMBNHFK_01535 1.7e-77 nodB3 G polysaccharide deacetylase
NJMBNHFK_01536 4.1e-22 nodB3 G polysaccharide deacetylase
NJMBNHFK_01537 2.3e-139 yabB 2.1.1.223 L Methyltransferase
NJMBNHFK_01538 1e-41 yazA L endonuclease containing a URI domain
NJMBNHFK_01539 3.2e-252 cshA 3.6.4.13 JKL DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity
NJMBNHFK_01540 2.3e-154 corA P CorA-like protein
NJMBNHFK_01541 1.9e-62 yjqA S Bacterial PH domain
NJMBNHFK_01542 7.8e-100 thiT S Thiamine transporter
NJMBNHFK_01543 2.1e-157 Z012_04635 K Transcriptional activator, Rgg GadR MutR family
NJMBNHFK_01544 1.9e-201 yjbB G Permeases of the major facilitator superfamily
NJMBNHFK_01545 3.1e-300 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
NJMBNHFK_01546 1.4e-121 ywaF S Integral membrane protein (intg_mem_TP0381)
NJMBNHFK_01547 3e-259 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
NJMBNHFK_01551 1.1e-155 cjaA ET ABC transporter substrate-binding protein
NJMBNHFK_01552 1.7e-134 glnQ 3.6.3.21 E abc transporter atp-binding protein
NJMBNHFK_01553 3e-106 P ABC transporter (Permease
NJMBNHFK_01554 6e-115 papP P ABC transporter (Permease
NJMBNHFK_01555 1.7e-193 ddl 6.3.2.4 F Belongs to the D-alanine--D-alanine ligase family
NJMBNHFK_01556 4.7e-31 copZ 2.7.7.77 P Heavy metal-associated domain protein
NJMBNHFK_01557 0.0 copA 3.6.3.54 P P-type ATPase
NJMBNHFK_01558 2.7e-73 copY K Copper transport repressor, CopY TcrY family
NJMBNHFK_01559 2.1e-143 trpA 4.2.1.20 E The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate
NJMBNHFK_01560 1.1e-228 trpB 4.2.1.20, 5.3.1.24 E The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine
NJMBNHFK_01561 3.3e-98 trpF 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 E belongs to the TrpF family
NJMBNHFK_01562 2.5e-133 trpC 4.1.1.48, 5.3.1.24 E Belongs to the TrpC family
NJMBNHFK_01563 7.8e-180 trpD 2.4.2.18, 4.1.3.27 F Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA)
NJMBNHFK_01564 8e-105 trpG 2.4.2.18, 2.6.1.85, 4.1.3.27 EH anthranilate
NJMBNHFK_01565 2.8e-257 trpE 4.1.3.27 EH Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia
NJMBNHFK_01566 3.7e-42 pchB 2.5.1.19, 4.2.1.10, 4.2.99.21, 5.4.99.5 E Chorismate mutase
NJMBNHFK_01567 3.2e-56
NJMBNHFK_01568 0.0 ctpE P E1-E2 ATPase
NJMBNHFK_01569 2e-25
NJMBNHFK_01570 1.2e-43 yaaK S Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection
NJMBNHFK_01571 9.7e-28 L transposase activity
NJMBNHFK_01572 2.7e-129 K transcriptional regulator, MerR family
NJMBNHFK_01573 1.4e-104 dnaQ 2.7.7.7 L DNA polymerase III
NJMBNHFK_01574 1.2e-41 WQ51_02910 S Protein of unknown function, DUF536
NJMBNHFK_01575 7.4e-64 XK27_02560 S cog cog2151
NJMBNHFK_01576 0.0 ilvD 4.2.1.9 E Belongs to the IlvD Edd family
NJMBNHFK_01577 7.7e-227 ytfP S Flavoprotein
NJMBNHFK_01579 3.1e-121 trmB 2.1.1.297, 2.1.1.33 J Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA
NJMBNHFK_01580 1.2e-151 ytmP 2.7.1.89 M Phosphotransferase
NJMBNHFK_01581 2.7e-183 ecsB U ABC transporter
NJMBNHFK_01582 2.3e-133 ecsA V abc transporter atp-binding protein
NJMBNHFK_01583 3.9e-72 hit FG Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases
NJMBNHFK_01584 5.6e-12
NJMBNHFK_01585 2.6e-55 S CD20-like family
NJMBNHFK_01586 2.1e-106
NJMBNHFK_01587 0.0 clpL O ATP-dependent Clp protease ATP-binding subunit
NJMBNHFK_01588 6.9e-206 ylbM S Belongs to the UPF0348 family
NJMBNHFK_01589 2e-140 yqeM Q Methyltransferase domain protein
NJMBNHFK_01590 6e-58 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
NJMBNHFK_01591 1.4e-107 nadD 2.7.6.3, 2.7.7.18 H HD superfamily hydrolase involved in NAD metabolism
NJMBNHFK_01592 3.1e-118 nadD 2.7.7.18, 3.6.1.55 H Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD)
NJMBNHFK_01593 3.5e-49 yhbY J RNA-binding protein
NJMBNHFK_01594 1.7e-215 yqeH S in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis
NJMBNHFK_01595 1.8e-98 yqeG S hydrolase of the HAD superfamily
NJMBNHFK_01596 2.6e-153 yicL EG COG0697 Permeases of the drug metabolite transporter (DMT) superfamily
NJMBNHFK_01597 1.3e-57
NJMBNHFK_01598 2.3e-273 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)
NJMBNHFK_01599 3.5e-269 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)
NJMBNHFK_01600 1.4e-47 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)
NJMBNHFK_01601 1.8e-23 2.4.1.52 GT4 M transferase activity, transferring glycosyl groups
NJMBNHFK_01602 6.3e-31 M lipopolysaccharide 3-alpha-galactosyltransferase activity
NJMBNHFK_01603 1e-148 ascB 3.2.1.86 GT1 G Belongs to the glycosyl hydrolase 1 family
NJMBNHFK_01604 5.1e-77 ascB 3.2.1.86 GT1 G Belongs to the glycosyl hydrolase 1 family
NJMBNHFK_01605 3.6e-96 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
NJMBNHFK_01606 3.7e-154 hlpA M Belongs to the NlpA lipoprotein family
NJMBNHFK_01607 6.8e-101 pncA Q isochorismatase
NJMBNHFK_01608 1.2e-140 codY K DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor
NJMBNHFK_01609 3.7e-240 alaA 2.6.1.2, 2.6.1.66 E Aminotransferase
NJMBNHFK_01610 2.4e-75 XK27_03180 T universal stress protein
NJMBNHFK_01613 2e-157 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
NJMBNHFK_01614 2e-239 hlyX S COG1253 Hemolysins and related proteins containing CBS domains
NJMBNHFK_01615 2.4e-144 modF 3.6.3.21, 3.6.3.34 P abc transporter atp-binding protein
NJMBNHFK_01616 0.0 yjcE P NhaP-type Na H and K H antiporters
NJMBNHFK_01618 1.4e-98 ytqB 2.1.1.176 J (SAM)-dependent
NJMBNHFK_01619 1.3e-184 yhcC S radical SAM protein
NJMBNHFK_01620 2.2e-196 ylbL T Belongs to the peptidase S16 family
NJMBNHFK_01621 2.7e-88 coaD 2.7.7.3 H Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate
NJMBNHFK_01622 5.1e-93 rsmD 2.1.1.171 L Methyltransferase
NJMBNHFK_01623 1.9e-172 trxB 1.8.1.9 C Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family
NJMBNHFK_01624 1.5e-09 S Protein of unknown function (DUF4059)
NJMBNHFK_01625 6.5e-131 tcyN 3.6.3.21 E abc transporter atp-binding protein
NJMBNHFK_01626 4.7e-163 yxeN P ABC transporter (Permease
NJMBNHFK_01627 1.5e-152 yxeM ET ABC-type amino acid transport signal transduction systems, periplasmic component domain
NJMBNHFK_01629 3.1e-206 dinB 2.7.7.7 L Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII
NJMBNHFK_01630 0.0 pflB 2.3.1.54 C formate acetyltransferase'
NJMBNHFK_01631 1.8e-147 cah 4.2.1.1 P carbonic anhydrase
NJMBNHFK_01632 2.1e-85 yjcF S COG0454 Histone acetyltransferase HPA2 and related acetyltransferases
NJMBNHFK_01633 1e-44 hsdS_1 3.1.21.3 V type I restriction modification DNA specificity domain
NJMBNHFK_01634 2.9e-87 D nuclear chromosome segregation
NJMBNHFK_01635 1.5e-127 ybbM S transport system, permease component
NJMBNHFK_01636 1.2e-117 ybbL S abc transporter atp-binding protein
NJMBNHFK_01637 4.5e-185 ampC V COG1680 Beta-lactamase class C and other penicillin binding proteins
NJMBNHFK_01638 4.6e-140 cppA E CppA N-terminal
NJMBNHFK_01639 5e-44 V CAAX protease self-immunity
NJMBNHFK_01640 2.3e-164 gla U Belongs to the MIP aquaporin (TC 1.A.8) family
NJMBNHFK_01641 0.0 pepX 3.4.14.11 E Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline
NJMBNHFK_01644 3e-47 spiA K sequence-specific DNA binding
NJMBNHFK_01645 2.9e-28 blpT
NJMBNHFK_01646 6.7e-98 blpT
NJMBNHFK_01647 3.9e-122 L Transposase
NJMBNHFK_01648 1.2e-165 L integrase core domain
NJMBNHFK_01653 4.3e-25 S Bacteriocin class II with double-glycine leader peptide
NJMBNHFK_01656 8.9e-133 agrA KT phosphorelay signal transduction system
NJMBNHFK_01657 3e-235 blpH 2.7.13.3 T protein histidine kinase activity
NJMBNHFK_01659 7.3e-237 mesE M Transport protein ComB
NJMBNHFK_01660 0.0 comA V ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain
NJMBNHFK_01661 0.0 mdlB V abc transporter atp-binding protein
NJMBNHFK_01662 0.0 mdlA V abc transporter atp-binding protein
NJMBNHFK_01664 1.7e-93 XK27_09885 V Glycopeptide antibiotics resistance protein
NJMBNHFK_01665 7.9e-224 rlmN 2.1.1.192 J Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
NJMBNHFK_01666 2.3e-72 yutD J protein conserved in bacteria
NJMBNHFK_01667 4.3e-269 yunD 3.1.3.5 F Belongs to the 5'-nucleotidase family
NJMBNHFK_01669 7.2e-221 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
NJMBNHFK_01670 6.3e-185 mraY 2.7.8.13 M First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan
NJMBNHFK_01671 0.0 ftsI 3.4.16.4 M penicillin-binding protein
NJMBNHFK_01672 8.1e-46 ftsL D cell division protein FtsL
NJMBNHFK_01673 3.9e-173 rsmH 2.1.1.199 J Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA
NJMBNHFK_01674 3e-128
NJMBNHFK_01675 9.7e-32 yhaI J Protein of unknown function (DUF805)
NJMBNHFK_01676 1.3e-08 D nuclear chromosome segregation
NJMBNHFK_01677 2e-225 proA 1.2.1.41 E Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate
NJMBNHFK_01678 5.7e-141 proB 2.7.2.11 E Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate
NJMBNHFK_01679 2.2e-285 XK27_00765
NJMBNHFK_01680 8.1e-134 ecsA_2 V abc transporter atp-binding protein
NJMBNHFK_01681 5.2e-125 S Protein of unknown function (DUF554)
NJMBNHFK_01682 0.0 addA 3.6.4.12 L ATP-dependent helicase nuclease subunit A
NJMBNHFK_01683 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
NJMBNHFK_01684 9.8e-57 liaI S membrane
NJMBNHFK_01685 7e-10 XK27_02470 K LytTr DNA-binding domain protein
NJMBNHFK_01686 1.8e-65 KT response to antibiotic
NJMBNHFK_01687 5.2e-81 yebC M Membrane
NJMBNHFK_01688 2.9e-18 yebC M Membrane
NJMBNHFK_01689 4.3e-261 XK27_03190 5.2.1.8 S hydrolases of the HAD superfamily
NJMBNHFK_01690 1.8e-181 ansA 3.5.1.1 EJ COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D
NJMBNHFK_01691 0.0 recG 3.6.4.12 L Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA)
NJMBNHFK_01692 1.9e-182 alr 5.1.1.1, 5.1.1.5 E Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids
NJMBNHFK_01693 4.1e-62 acpS 2.7.6.3, 2.7.8.7, 5.1.1.1 I Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein
NJMBNHFK_01694 1.1e-197 aroF 2.5.1.54 E Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP)
NJMBNHFK_01695 3.8e-198 aroF 2.5.1.54 E Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP)
NJMBNHFK_01696 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
NJMBNHFK_01698 3e-189 manA 5.3.1.8 G mannose-6-phosphate isomerase
NJMBNHFK_01699 4.1e-172 scrK 2.7.1.2, 2.7.1.4 GK Fructokinase
NJMBNHFK_01700 0.0 scrA 2.7.1.211 G pts system
NJMBNHFK_01701 4.1e-291 scrB 3.2.1.26 GH32 G invertase
NJMBNHFK_01702 7.5e-180 scrR K Transcriptional
NJMBNHFK_01703 2.1e-73 nusB K Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons
NJMBNHFK_01704 3.4e-62 yqhY S protein conserved in bacteria
NJMBNHFK_01705 1.2e-97 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
NJMBNHFK_01706 3.7e-84 comEB 3.5.4.12 F ComE operon protein 2
NJMBNHFK_01707 5e-193 pepP 3.4.11.9, 3.4.13.9 E Belongs to the peptidase M24B family
NJMBNHFK_01709 8e-44 V 'abc transporter, ATP-binding protein
NJMBNHFK_01710 1e-58 V 'abc transporter, ATP-binding protein
NJMBNHFK_01713 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
NJMBNHFK_01714 2e-169 corA P COG0598 Mg2 and Co2 transporters
NJMBNHFK_01715 3.1e-124 XK27_01040 S Pfam PF06570
NJMBNHFK_01717 9.7e-36 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
NJMBNHFK_01718 2.7e-91 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
NJMBNHFK_01719 3.9e-47 rpsF J Binds together with S18 to 16S ribosomal RNA
NJMBNHFK_01720 2.8e-31 XK27_05745
NJMBNHFK_01721 2.5e-230 mutY L A G-specific adenine glycosylase
NJMBNHFK_01726 0.0 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
NJMBNHFK_01727 0.0 mutS2 L Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity
NJMBNHFK_01728 1e-93 cvpA S toxin biosynthetic process
NJMBNHFK_01729 2.3e-13 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
NJMBNHFK_01730 4.7e-160 rnhC 3.1.26.4 L Endonuclease that specifically degrades the RNA of RNA- DNA hybrids
NJMBNHFK_01731 1.3e-113 lepB 3.4.21.89 U Belongs to the peptidase S26 family
NJMBNHFK_01732 0.0 recD2 3.1.11.5 L DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity
NJMBNHFK_01733 2e-47 azlD E branched-chain amino acid
NJMBNHFK_01734 1.8e-114 azlC E AzlC protein
NJMBNHFK_01735 1.9e-186 tsaD 2.3.1.234 O 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
NJMBNHFK_01736 4.8e-73 rimI 2.3.1.128 K This enzyme acetylates the N-terminal alanine of ribosomal protein S18
NJMBNHFK_01737 5.6e-121 yeaZ 2.3.1.234 O COG1214, inactive homolog of metal-dependent proteases
NJMBNHFK_01738 2.5e-33 ykzG S Belongs to the UPF0356 family
NJMBNHFK_01739 0.0 rnjA S 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
NJMBNHFK_01740 2.7e-40 pscB M CHAP domain protein
NJMBNHFK_01741 1.5e-263 glnA 6.3.1.2 E glutamine synthetase
NJMBNHFK_01742 8.5e-63 glnR K Transcriptional regulator
NJMBNHFK_01743 1.3e-87 S Fusaric acid resistance protein-like
NJMBNHFK_01744 1.1e-12
NJMBNHFK_01745 8.9e-30
NJMBNHFK_01746 2e-222 pgk 2.7.2.3, 5.3.1.1 F Belongs to the phosphoglycerate kinase family
NJMBNHFK_01747 3.2e-42 L Transposase
NJMBNHFK_01748 1.9e-46 L transposase activity
NJMBNHFK_01749 7.4e-23 L Transposase
NJMBNHFK_01750 1.8e-56 L transposition
NJMBNHFK_01751 9.1e-83 L Integrase core domain protein
NJMBNHFK_01752 1e-102 L Transposase
NJMBNHFK_01753 2.6e-112 L Transposase
NJMBNHFK_01754 1.4e-189 gap 1.2.1.12 G Belongs to the glyceraldehyde-3-phosphate dehydrogenase family
NJMBNHFK_01755 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
NJMBNHFK_01756 6.7e-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
NJMBNHFK_01757 2.3e-69 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
NJMBNHFK_01758 1.1e-142 purR 2.4.2.7 F operon repressor
NJMBNHFK_01759 3.6e-179 cbf S 3'-5' exoribonuclease yhaM
NJMBNHFK_01760 6.9e-173 rmuC S RmuC domain protein
NJMBNHFK_01761 3.1e-118 thiN 2.7.6.2 H thiamine pyrophosphokinase
NJMBNHFK_01762 8.6e-119 rpe 5.1.3.1 G Belongs to the ribulose-phosphate 3-epimerase family
NJMBNHFK_01763 6.4e-162 rsgA 3.1.3.100 G 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
NJMBNHFK_01765 8.9e-156 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
NJMBNHFK_01766 1.1e-98 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
NJMBNHFK_01767 1.6e-143 tatD L Hydrolase, tatd
NJMBNHFK_01768 7.2e-74 yccU S CoA-binding protein
NJMBNHFK_01769 4.8e-51 trxA O Belongs to the thioredoxin family
NJMBNHFK_01770 1.9e-141 S Macro domain protein
NJMBNHFK_01771 2e-09 L thioesterase
NJMBNHFK_01772 2.2e-54 bta 1.8.1.8 CO cell redox homeostasis
NJMBNHFK_01776 1.7e-226 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)
NJMBNHFK_01777 2.7e-62 L Transposase
NJMBNHFK_01778 1e-13 rpmH J Ribosomal protein L34
NJMBNHFK_01779 2e-186 jag S RNA-binding protein
NJMBNHFK_01780 7.5e-141 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
NJMBNHFK_01781 5.9e-55 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
NJMBNHFK_01782 4.1e-264 argH 4.3.2.1 E Argininosuccinate lyase
NJMBNHFK_01783 2e-230 argG 6.3.4.5 E Belongs to the argininosuccinate synthase family. Type 1 subfamily
NJMBNHFK_01784 2.1e-282 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)
NJMBNHFK_01785 6.7e-81 amiA E transmembrane transport
NJMBNHFK_01786 4.2e-74 amiA E transmembrane transport
NJMBNHFK_01787 4.8e-120 rplA J Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release
NJMBNHFK_01788 3.7e-70 rplK J Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors
NJMBNHFK_01789 3.5e-50 S Protein of unknown function (DUF3397)
NJMBNHFK_01790 2e-88 cah 4.2.1.1 P Reversible hydration of carbon dioxide
NJMBNHFK_01791 7.3e-59 WQ51_05710 S Mitochondrial biogenesis AIM24
NJMBNHFK_01792 6.2e-12 WQ51_05710 S Mitochondrial biogenesis AIM24
NJMBNHFK_01793 1.4e-226 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
NJMBNHFK_01794 1.1e-80 dut 3.6.1.23, 4.1.1.36, 6.3.2.5 F This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA
NJMBNHFK_01795 1.8e-19 XK27_09620 S FMN reductase (NADPH) activity
NJMBNHFK_01796 4.3e-77 XK27_09620 S reductase
NJMBNHFK_01797 2.1e-32 XK27_09615 S FMN reductase (NADPH) activity
NJMBNHFK_01798 1.2e-131 XK27_09615 S PAS domain
NJMBNHFK_01799 1.9e-07 fnt P Formate nitrite transporter
NJMBNHFK_01800 6.4e-54 fnt P Formate nitrite transporter
NJMBNHFK_01801 7.2e-64 XK27_08585 S Psort location CytoplasmicMembrane, score
NJMBNHFK_01802 2.8e-185 gpsA 1.1.1.94 I Glycerol-3-phosphate dehydrogenase
NJMBNHFK_01803 1.8e-170 galU 2.7.7.9 M UTP-glucose-1-phosphate uridylyltransferase
NJMBNHFK_01804 1.2e-165 L integrase core domain
NJMBNHFK_01805 1.1e-121 L Transposase
NJMBNHFK_01806 2.8e-117 gluP 3.4.21.105 O membrane protein (homolog of Drosophila rhomboid)
NJMBNHFK_01807 3.5e-94 ygfA 6.3.3.2 H Belongs to the 5-formyltetrahydrofolate cyclo-ligase family
NJMBNHFK_01808 3e-220 hipO 3.5.1.47 E Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate
NJMBNHFK_01809 8.1e-59 dapD 2.3.1.117, 2.3.1.89 E Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate
NJMBNHFK_01810 1.6e-21 S glycolate biosynthetic process
NJMBNHFK_01811 1.5e-64 S phosphatase activity
NJMBNHFK_01812 2e-157 rrmA 2.1.1.187 Q methyltransferase
NJMBNHFK_01815 2.7e-91 tadA 3.5.4.1, 3.5.4.33 FJ Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2)
NJMBNHFK_01816 1.9e-65 ssb_2 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
NJMBNHFK_01817 2.4e-36 yeeD O sulfur carrier activity
NJMBNHFK_01818 1.8e-187 yeeE S Sulphur transport
NJMBNHFK_01819 7.9e-114 pheT 6.1.1.20 J Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily
NJMBNHFK_01820 4.2e-55 ytpP 2.7.1.180, 5.3.4.1 CO Thioredoxin
NJMBNHFK_01821 4.1e-09 S Domain of unknown function (DUF4651)
NJMBNHFK_01822 2e-205 pepA 3.4.11.7 G COG1363 Cellulase M and related proteins
NJMBNHFK_01823 3.9e-131 proC 1.5.1.2 E Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline
NJMBNHFK_01824 1.8e-111 S CAAX amino terminal protease family protein
NJMBNHFK_01826 5e-67 V CAAX protease self-immunity
NJMBNHFK_01827 1.4e-33 V CAAX protease self-immunity
NJMBNHFK_01828 8.8e-27 lanR K sequence-specific DNA binding
NJMBNHFK_01829 2.9e-221 ackA 2.7.2.1 F Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction
NJMBNHFK_01830 7.7e-177 ytxK 2.1.1.72 L DNA methylase
NJMBNHFK_01831 6.8e-13 comGF U Putative Competence protein ComGF
NJMBNHFK_01832 4e-72 comGF U Competence protein ComGF
NJMBNHFK_01833 1.4e-15 NU Type II secretory pathway pseudopilin
NJMBNHFK_01834 1.8e-57 cglD NU Competence protein
NJMBNHFK_01835 8.5e-43 comGC U Required for transformation and DNA binding
NJMBNHFK_01836 9.2e-153 cglB NU type II secretion system
NJMBNHFK_01837 1.9e-175 comGA NU Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB
NJMBNHFK_01838 2.9e-68 S cog cog4699
NJMBNHFK_01839 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
NJMBNHFK_01840 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
NJMBNHFK_01841 0.0 pbp1B 2.4.1.129, 3.4.16.4 GT51 M penicillin-binding protein
NJMBNHFK_01842 1.2e-238 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)
NJMBNHFK_01843 1.6e-196 ilvC 1.1.1.86 H Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate
NJMBNHFK_01844 7.7e-77 ilvN 2.2.1.6 E Acetolactate synthase
NJMBNHFK_01845 0.0 ilvB 2.2.1.6 EH Acetolactate synthase
NJMBNHFK_01846 8.8e-281 ilvD 4.2.1.9 E Belongs to the IlvD Edd family
NJMBNHFK_01847 8.4e-09 ilvD 4.2.1.9 E Belongs to the IlvD Edd family
NJMBNHFK_01848 1.7e-304 yloV S kinase related to dihydroxyacetone kinase
NJMBNHFK_01849 1.8e-57 asp S cog cog1302
NJMBNHFK_01850 3.2e-226 norN V Mate efflux family protein
NJMBNHFK_01851 1.9e-278 thrC 4.2.3.1 E Threonine synthase
NJMBNHFK_01852 1.9e-65 adhE 1.1.1.1, 1.2.1.10 C belongs to the iron- containing alcohol dehydrogenase family
NJMBNHFK_01853 1.2e-35 adhE 1.1.1.1, 1.2.1.10 C hydroxyacid-oxoacid transhydrogenase activity
NJMBNHFK_01854 3.5e-76 adhE 1.1.1.1, 1.2.1.10 C belongs to the iron- containing alcohol dehydrogenase family
NJMBNHFK_01855 1.3e-135 adhE 1.1.1.1, 1.2.1.10 C belongs to the iron- containing alcohol dehydrogenase family
NJMBNHFK_01856 1.4e-63 adhE 1.1.1.1, 1.2.1.10 C Dehydrogenase
NJMBNHFK_01857 0.0 pepO 3.4.24.71 O Peptidase family M13
NJMBNHFK_01858 2.8e-38 treC 3.2.1.93 GH13 G COG0366 Glycosidases
NJMBNHFK_01859 1.2e-69 treC 3.2.1.93 GH13 G COG0366 Glycosidases
NJMBNHFK_01860 1.3e-65 treC 3.2.1.93 GH13 G COG0366 Glycosidases
NJMBNHFK_01861 1.4e-54 treB 2.7.1.201 G PTS System
NJMBNHFK_01862 5.8e-21 treR K DNA-binding transcription factor activity
NJMBNHFK_01863 1.2e-85 treR K trehalose operon
NJMBNHFK_01864 3.3e-95 ywlG S Belongs to the UPF0340 family
NJMBNHFK_01867 2e-35 L PFAM Integrase, catalytic core
NJMBNHFK_01868 2e-94 L PFAM Integrase, catalytic core
NJMBNHFK_01869 3.3e-46 K Putative DNA-binding domain
NJMBNHFK_01870 2.5e-13 2.3.1.82 M Acetyltransferase GNAT Family
NJMBNHFK_01871 1.2e-126 gltT C Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family
NJMBNHFK_01872 6.4e-136 HJ the current gene model (or a revised gene model) may contain a frame shift
NJMBNHFK_01877 1e-39
NJMBNHFK_01878 6.5e-31
NJMBNHFK_01879 5e-31 S Hypothetical protein (DUF2513)
NJMBNHFK_01880 7.7e-13
NJMBNHFK_01882 3.7e-216 S MvaI/BcnI restriction endonuclease family
NJMBNHFK_01884 2.2e-282 dcm 2.1.1.37 H C-5 cytosine-specific DNA methylase
NJMBNHFK_01885 9e-164 fba 4.1.2.13, 4.1.2.29 G aldolase
NJMBNHFK_01887 6.7e-110 6.3.2.2 H ergothioneine biosynthetic process
NJMBNHFK_01888 1.5e-65 6.3.2.2 H gamma-glutamylcysteine synthetase
NJMBNHFK_01889 3.2e-12 6.3.2.2 H gamma-glutamylcysteine synthetase
NJMBNHFK_01890 3.3e-09 L PFAM Integrase, catalytic core
NJMBNHFK_01891 1.8e-111 L PFAM Integrase, catalytic core
NJMBNHFK_01892 3.3e-62 rplQ J ribosomal protein l17
NJMBNHFK_01893 4.8e-171 rpoA 2.7.7.6 K DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates
NJMBNHFK_01894 9.6e-62 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
NJMBNHFK_01895 4e-57 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
NJMBNHFK_01896 6e-15 rpmJ J Belongs to the bacterial ribosomal protein bL36 family
NJMBNHFK_01897 2.7e-32 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
NJMBNHFK_01898 9.2e-121 adk 2.7.4.3 F Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism
NJMBNHFK_01899 2.1e-230 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
NJMBNHFK_01900 4.4e-58 rplO J binds to the 23S rRNA
NJMBNHFK_01901 2.5e-23 rpmD J ribosomal protein l30
NJMBNHFK_01902 1.7e-79 rpsE J Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body
NJMBNHFK_01903 1.9e-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
NJMBNHFK_01904 2.3e-93 rplF J This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center
NJMBNHFK_01905 1.2e-67 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
NJMBNHFK_01906 1.5e-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
NJMBNHFK_01907 1.6e-94 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
NJMBNHFK_01908 1.4e-47 rplX J One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit
NJMBNHFK_01909 1.1e-59 rplN J Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome
NJMBNHFK_01910 6e-39 rpsQ J One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA
NJMBNHFK_01911 2.7e-26 rpmC J Belongs to the universal ribosomal protein uL29 family
NJMBNHFK_01912 7.2e-71 rplP J Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs
NJMBNHFK_01913 2.1e-117 rpsC J Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation
NJMBNHFK_01914 7.3e-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
NJMBNHFK_01915 4.9e-47 rpsS J Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA
NJMBNHFK_01916 8.8e-153 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
NJMBNHFK_01917 2.4e-44 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
NJMBNHFK_01918 5.7e-104 rplD J Forms part of the polypeptide exit tunnel
NJMBNHFK_01919 1.1e-110 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
NJMBNHFK_01920 1.3e-48 rpsJ J Involved in the binding of tRNA to the ribosomes
NJMBNHFK_01921 7.8e-188 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
NJMBNHFK_01922 0.0 XK27_09800 I Acyltransferase
NJMBNHFK_01923 1.7e-35 XK27_09805 S MORN repeat protein
NJMBNHFK_01924 1e-80 ptpA 3.1.3.48 T Belongs to the low molecular weight phosphotyrosine protein phosphatase family
NJMBNHFK_01925 4.1e-250 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
NJMBNHFK_01926 1.5e-89 adk 2.7.4.3 F topology modulation protein
NJMBNHFK_01927 8.6e-127 Z012_04635 K sequence-specific DNA binding
NJMBNHFK_01929 6.3e-16 C Radical SAM
NJMBNHFK_01930 3.4e-191 C Radical SAM
NJMBNHFK_01931 3.9e-287 V ABC transporter transmembrane region
NJMBNHFK_01932 2.5e-89 K sequence-specific DNA binding
NJMBNHFK_01933 1.3e-36 L Replication initiation factor
NJMBNHFK_01934 1.4e-107 L Replication initiation factor
NJMBNHFK_01935 1.9e-18 S Domain of unknown function (DUF3173)
NJMBNHFK_01936 3.5e-216 int L Belongs to the 'phage' integrase family
NJMBNHFK_01938 5.2e-237 rarA L ATPase related to the helicase subunit of the Holliday junction resolvase
NJMBNHFK_01939 8.4e-27 rpmB J Belongs to the bacterial ribosomal protein bL28 family
NJMBNHFK_01940 2.8e-44 yrzL S Belongs to the UPF0297 family
NJMBNHFK_01941 1.2e-70 yqgF L Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA
NJMBNHFK_01942 4.2e-44 yrzB S Belongs to the UPF0473 family
NJMBNHFK_01943 6.6e-301 ccs S the current gene model (or a revised gene model) may contain a frame shift
NJMBNHFK_01944 0.0 nrdD 1.1.98.6 F Ribonucleoside-triphosphate reductase
NJMBNHFK_01945 7.5e-14
NJMBNHFK_01946 2.6e-91 XK27_10930 K acetyltransferase
NJMBNHFK_01947 3.7e-116 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
NJMBNHFK_01948 2.3e-41 yaaA S Belongs to the UPF0246 family
NJMBNHFK_01949 1.2e-50 yaaA S Belongs to the UPF0246 family
NJMBNHFK_01950 9.9e-169 XK27_01785 S cog cog1284
NJMBNHFK_01951 0.0 aspS 6.1.1.12 J Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp)
NJMBNHFK_01953 1.6e-241 hisS 6.1.1.21 J histidyl-tRNA synthetase
NJMBNHFK_01954 5.7e-52 metE 2.1.1.14 E Methionine synthase
NJMBNHFK_01955 7.6e-64 metE 2.1.1.14 E Methionine synthase
NJMBNHFK_01956 9.2e-36 metE 2.1.1.14 E Methionine synthase
NJMBNHFK_01957 2e-25 rpmF J Belongs to the bacterial ribosomal protein bL32 family
NJMBNHFK_01958 6.7e-19 rpmG J Belongs to the bacterial ribosomal protein bL33 family
NJMBNHFK_01960 3.1e-20 yegS 2.7.1.107 I lipid kinase activity
NJMBNHFK_01961 2.7e-95 S Hydrophobic domain protein
NJMBNHFK_01963 3.7e-27 S Membrane
NJMBNHFK_01964 3.1e-101
NJMBNHFK_01965 1.8e-23 S Small integral membrane protein
NJMBNHFK_01966 1.1e-71 M Protein conserved in bacteria
NJMBNHFK_01967 4.9e-12 K CsbD-like
NJMBNHFK_01968 3.5e-97 nudL L hydrolase
NJMBNHFK_01969 3.4e-13 nudL L hydrolase
NJMBNHFK_01970 4e-19 K negative regulation of transcription, DNA-templated
NJMBNHFK_01971 1.7e-23 K negative regulation of transcription, DNA-templated
NJMBNHFK_01973 1.8e-19 XK27_06920 S Protein of unknown function (DUF1700)
NJMBNHFK_01974 1.8e-88 S Putative adhesin
NJMBNHFK_01975 3.9e-161 XK27_06930 V domain protein
NJMBNHFK_01976 6.4e-96 XK27_06935 K transcriptional regulator
NJMBNHFK_01977 4.8e-55 ypaA M Membrane
NJMBNHFK_01978 2.7e-08
NJMBNHFK_01979 9.8e-109 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
NJMBNHFK_01980 8.2e-48 veg S Biofilm formation stimulator VEG
NJMBNHFK_01981 1.5e-245 dnaB 3.6.4.12 L Participates in initiation and elongation during chromosome replication
NJMBNHFK_01982 3.9e-70 rplI J binds to the 23S rRNA
NJMBNHFK_01983 0.0 yybT T signaling protein consisting of a modified GGDEF domain and a DHH domain
NJMBNHFK_01984 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
NJMBNHFK_01985 1.5e-77 F NUDIX domain
NJMBNHFK_01986 8.6e-220 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
NJMBNHFK_01987 0.0 S Bacterial membrane protein, YfhO
NJMBNHFK_01988 1.5e-88 isaA GH23 M Immunodominant staphylococcal antigen A
NJMBNHFK_01989 5.3e-85 lytE M LysM domain protein
NJMBNHFK_01990 2e-138 ecfT P 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
NJMBNHFK_01991 5.2e-153 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
NJMBNHFK_01992 1.5e-152 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
NJMBNHFK_01993 3.1e-90 pgsA 2.7.8.41, 2.7.8.5 I Belongs to the CDP-alcohol phosphatidyltransferase class-I family
NJMBNHFK_01994 6.3e-138 ymfM S sequence-specific DNA binding
NJMBNHFK_01995 3.1e-242 ymfH S Peptidase M16
NJMBNHFK_01996 4.8e-235 ymfF S Peptidase M16
NJMBNHFK_01997 1.6e-45 yaaA S S4 domain protein YaaA
NJMBNHFK_01998 5.9e-205 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
NJMBNHFK_01999 4.3e-275 guaB 1.1.1.205 F Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth
NJMBNHFK_02000 6.3e-193 trpS 6.1.1.2 J Tryptophanyl-tRNA synthetase
NJMBNHFK_02001 4.2e-153 yvjA S membrane
NJMBNHFK_02002 6.7e-306 ybiT S abc transporter atp-binding protein
NJMBNHFK_02003 0.0 XK27_10405 S Bacterial membrane protein YfhO
NJMBNHFK_02007 6.2e-120 yoaK S Psort location CytoplasmicMembrane, score
NJMBNHFK_02008 1.1e-86 rlmH 2.1.1.177 J Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA
NJMBNHFK_02009 2.6e-193 htrA 3.4.21.107 O Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain'
NJMBNHFK_02010 8.5e-134 parB K Belongs to the ParB family

eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)