ORF_ID e_value Gene_name EC_number CAZy COGs Description
CMMOHOCF_00001 5.6e-18 yjcE P Sodium/hydrogen exchanger family
CMMOHOCF_00002 8.6e-34 dcd 3.5.4.13 F Belongs to the dCTP deaminase family
CMMOHOCF_00003 9.5e-20 dcd 3.5.4.13 F Belongs to the dCTP deaminase family
CMMOHOCF_00004 0.0 3.2.1.22 G Glycosyl hydrolase family 36 N-terminal domain
CMMOHOCF_00005 0.0 pacL2 3.6.3.8 P Cation transporter/ATPase, N-terminus
CMMOHOCF_00006 2.9e-10 pacL2 3.6.3.8 P Cation transporter/ATPase, N-terminus
CMMOHOCF_00008 3.6e-132 rlmB 2.1.1.185 J Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
CMMOHOCF_00009 5.9e-174 KLT Domain of unknown function (DUF4032)
CMMOHOCF_00010 2.9e-56 KLT Domain of unknown function (DUF4032)
CMMOHOCF_00011 1.6e-149
CMMOHOCF_00012 2.7e-86 3.4.22.70 M Sortase family
CMMOHOCF_00013 1.4e-135 M LPXTG-motif cell wall anchor domain protein
CMMOHOCF_00014 1.4e-47 M LPXTG-motif cell wall anchor domain protein
CMMOHOCF_00015 0.0 S LPXTG-motif cell wall anchor domain protein
CMMOHOCF_00016 0.0 S LPXTG-motif cell wall anchor domain protein
CMMOHOCF_00017 1.4e-174 S LPXTG-motif cell wall anchor domain protein
CMMOHOCF_00018 3.4e-100 L Helix-turn-helix domain
CMMOHOCF_00019 1.6e-17 ugpC E Belongs to the ABC transporter superfamily
CMMOHOCF_00020 1.9e-161 ugpC E Belongs to the ABC transporter superfamily
CMMOHOCF_00021 3.4e-174 K Psort location Cytoplasmic, score
CMMOHOCF_00022 1.1e-87 KLT Protein tyrosine kinase
CMMOHOCF_00023 4e-81 KLT Protein tyrosine kinase
CMMOHOCF_00024 3.7e-168 KLT Protein tyrosine kinase
CMMOHOCF_00025 8.4e-151 O Thioredoxin
CMMOHOCF_00027 1.1e-169 S G5
CMMOHOCF_00028 6.3e-171 ksgA 2.1.1.182, 2.1.1.184 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
CMMOHOCF_00029 1.4e-23 ispE 2.1.1.182, 2.7.1.148 F Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol
CMMOHOCF_00030 5.9e-126 ispE 2.1.1.182, 2.7.1.148 F Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol
CMMOHOCF_00031 9.6e-89 S LytR cell envelope-related transcriptional attenuator
CMMOHOCF_00032 2.8e-279 cca 2.7.7.19, 2.7.7.72 J Probable RNA and SrmB- binding site of polymerase A
CMMOHOCF_00033 5.2e-124 deoC 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 L Belongs to the Nudix hydrolase family
CMMOHOCF_00034 0.0 M Conserved repeat domain
CMMOHOCF_00035 3.7e-15 murJ KLT MviN-like protein
CMMOHOCF_00036 0.0 murJ KLT MviN-like protein
CMMOHOCF_00037 6.5e-29 murJ KLT MviN-like protein
CMMOHOCF_00038 4.5e-50 murJ KLT MviN-like protein
CMMOHOCF_00039 3.8e-202 trxB 1.8.1.9, 4.3.1.9 C Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family
CMMOHOCF_00040 1.8e-243 parB K Belongs to the ParB family
CMMOHOCF_00041 8.5e-179 parA D CobQ CobB MinD ParA nucleotide binding domain protein
CMMOHOCF_00042 2.5e-124 rsmG 2.1.1.170 J Specifically methylates the N7 position of a guanine in 16S rRNA
CMMOHOCF_00043 6.5e-93 jag S Putative single-stranded nucleic acids-binding domain
CMMOHOCF_00044 2.9e-56 yidC U Membrane protein insertase, YidC Oxa1 family
CMMOHOCF_00045 3.6e-84 yidC U Membrane protein insertase, YidC Oxa1 family
CMMOHOCF_00046 4.5e-14 rpmH J Belongs to the bacterial ribosomal protein bL34 family
CMMOHOCF_00047 1.8e-70 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
CMMOHOCF_00048 2.8e-196 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
CMMOHOCF_00049 4.6e-161 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
CMMOHOCF_00050 2e-32 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
CMMOHOCF_00051 4e-240 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
CMMOHOCF_00052 3.2e-93 S Protein of unknown function (DUF721)
CMMOHOCF_00053 1.3e-52 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
CMMOHOCF_00054 4.3e-114 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
CMMOHOCF_00055 1.3e-196 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
CMMOHOCF_00056 1.2e-134 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
CMMOHOCF_00057 3.4e-99 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
CMMOHOCF_00058 1.5e-17 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
CMMOHOCF_00059 4.6e-73 S Transmembrane domain of unknown function (DUF3566)
CMMOHOCF_00060 1.7e-14 abfA1 3.2.1.55 GH51 G arabinose metabolic process
CMMOHOCF_00063 9.2e-28 G Glycosyl hydrolases family 43
CMMOHOCF_00064 2.5e-112 G Glycosyl hydrolases family 43
CMMOHOCF_00065 2.2e-189 K Periplasmic binding protein domain
CMMOHOCF_00066 6.1e-229 I Serine aminopeptidase, S33
CMMOHOCF_00067 6.7e-09 K helix_turn _helix lactose operon repressor
CMMOHOCF_00071 1.8e-121 S PAC2 family
CMMOHOCF_00072 3.7e-24 S PAC2 family
CMMOHOCF_00073 1.1e-167 uppP 3.6.1.27 V Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin
CMMOHOCF_00074 6e-159 G Fructosamine kinase
CMMOHOCF_00075 1.5e-68 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
CMMOHOCF_00076 3.9e-108 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
CMMOHOCF_00077 3.3e-54 hrcA K Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons
CMMOHOCF_00078 1.5e-134 hrcA K Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons
CMMOHOCF_00079 1.3e-124 tkt 2.2.1.1 H Belongs to the transketolase family
CMMOHOCF_00080 9.8e-123 tkt 2.2.1.1 H Belongs to the transketolase family
CMMOHOCF_00081 1.4e-169 tal 2.2.1.2 H Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway
CMMOHOCF_00082 3.1e-142 yoaK S Protein of unknown function (DUF1275)
CMMOHOCF_00083 2.1e-132 brnQ U Component of the transport system for branched-chain amino acids
CMMOHOCF_00084 1.2e-104 brnQ U Component of the transport system for branched-chain amino acids
CMMOHOCF_00086 8.5e-183 mepA_6 V MatE
CMMOHOCF_00087 1.7e-30 mepA_6 V MatE
CMMOHOCF_00088 8e-162 S Sucrose-6F-phosphate phosphohydrolase
CMMOHOCF_00089 3.2e-141 ldh 1.1.1.27 C Belongs to the LDH MDH superfamily
CMMOHOCF_00090 8e-33 secG U Preprotein translocase SecG subunit
CMMOHOCF_00091 5.3e-147 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)
CMMOHOCF_00092 4.7e-186 pgk 2.7.2.3, 5.3.1.1 F Phosphoglycerate kinase
CMMOHOCF_00093 9e-173 whiA K May be required for sporulation
CMMOHOCF_00094 1.1e-169 rapZ S Displays ATPase and GTPase activities
CMMOHOCF_00095 3e-181 aroE 1.1.1.25 E Shikimate dehydrogenase substrate binding domain
CMMOHOCF_00096 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
CMMOHOCF_00097 5.4e-308 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
CMMOHOCF_00098 3.5e-199 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
CMMOHOCF_00099 1.2e-77
CMMOHOCF_00100 4.7e-32 V MacB-like periplasmic core domain
CMMOHOCF_00102 3.3e-118 K Transcriptional regulatory protein, C terminal
CMMOHOCF_00103 3.7e-47 qseC 2.7.13.3 T HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain
CMMOHOCF_00104 1.7e-85 qseC 2.7.13.3 T HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain
CMMOHOCF_00105 2.4e-62 vanY 3.4.17.14 M D-alanyl-D-alanine carboxypeptidase
CMMOHOCF_00106 1.8e-145 ybiT S ABC transporter
CMMOHOCF_00107 1.4e-133 ybiT S ABC transporter
CMMOHOCF_00108 7.2e-197 galE 5.1.3.2 M Belongs to the NAD(P)-dependent epimerase dehydratase family
CMMOHOCF_00109 1.4e-51 galT 2.7.7.12 G UDP-glucose--hexose-1-phosphate uridylyltransferase
CMMOHOCF_00110 3.7e-128 galT 2.7.7.12 G UDP-glucose--hexose-1-phosphate uridylyltransferase
CMMOHOCF_00111 2.8e-105 mdsC 2.7.1.162, 2.7.1.39 S Phosphotransferase enzyme family
CMMOHOCF_00112 1e-75 mdsC 2.7.1.162, 2.7.1.39 S Phosphotransferase enzyme family
CMMOHOCF_00113 1.2e-202 GK ROK family
CMMOHOCF_00114 1.5e-177 2.7.1.2 GK ROK family
CMMOHOCF_00115 0.0 gnpA 2.4.1.211 S Lacto-N-biose phosphorylase C-terminal domain
CMMOHOCF_00116 1.5e-09 G ABC transporter permease
CMMOHOCF_00117 1.6e-17 G ABC transporter permease
CMMOHOCF_00118 8.7e-93 G ABC transporter permease
CMMOHOCF_00119 3.7e-67 G Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00120 4.1e-75 G Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00121 4.9e-227 G Bacterial extracellular solute-binding protein
CMMOHOCF_00122 2e-222 trpE 4.1.3.27 E 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
CMMOHOCF_00123 1.8e-75 trpE 4.1.3.27 E 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
CMMOHOCF_00124 1e-75 hisI 3.5.4.19, 3.6.1.31 E Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP
CMMOHOCF_00125 1.4e-139 hisF 4.1.3.27 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
CMMOHOCF_00126 5e-226 rlmN 2.1.1.192 J Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
CMMOHOCF_00127 1.8e-176 cdsA 2.7.7.41, 2.7.7.67 I Cytidylyltransferase family
CMMOHOCF_00128 1.4e-11 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
CMMOHOCF_00129 8.8e-21 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
CMMOHOCF_00130 3.4e-127 pyrH 2.7.4.22 F Catalyzes the reversible phosphorylation of UMP to UDP
CMMOHOCF_00131 3.3e-126 3.2.1.8 S alpha beta
CMMOHOCF_00132 4.8e-146 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
CMMOHOCF_00133 6.9e-120 rpsB J Belongs to the universal ribosomal protein uS2 family
CMMOHOCF_00134 1.7e-87 def 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
CMMOHOCF_00135 0.0 fadD3 6.2.1.3 I long-chain-fatty acid CoA ligase
CMMOHOCF_00136 5.7e-91
CMMOHOCF_00137 1.6e-11 guaB 1.1.1.205 F IMP dehydrogenase family protein
CMMOHOCF_00138 2.1e-162 S Sucrose-6F-phosphate phosphohydrolase
CMMOHOCF_00139 5.1e-09 S Sucrose-6F-phosphate phosphohydrolase
CMMOHOCF_00141 1.5e-97 3.4.22.70 M Sortase family
CMMOHOCF_00142 3.6e-67 3.4.22.70 M Sortase family
CMMOHOCF_00143 8.2e-86 M chlorophyll binding
CMMOHOCF_00144 2.9e-93 M chlorophyll binding
CMMOHOCF_00145 9.2e-196 M chlorophyll binding
CMMOHOCF_00146 1.8e-157 M LPXTG cell wall anchor motif
CMMOHOCF_00147 5e-57 M LPXTG cell wall anchor motif
CMMOHOCF_00148 9.8e-56 M LPXTG cell wall anchor motif
CMMOHOCF_00149 1.3e-09
CMMOHOCF_00150 1.2e-48 K Winged helix DNA-binding domain
CMMOHOCF_00151 3.8e-10 K Winged helix DNA-binding domain
CMMOHOCF_00152 2.4e-301 V ABC transporter, ATP-binding protein
CMMOHOCF_00153 0.0 V ABC transporter transmembrane region
CMMOHOCF_00154 4.1e-70
CMMOHOCF_00155 1.1e-91 XK26_04485 P Cobalt transport protein
CMMOHOCF_00157 2.8e-39 pepD E Peptidase family C69
CMMOHOCF_00158 1.7e-251 pepD E Peptidase family C69
CMMOHOCF_00159 1e-170 S Glycosyl hydrolases related to GH101 family, GH129
CMMOHOCF_00160 1.3e-204 S Glycosyl hydrolases related to GH101 family, GH129
CMMOHOCF_00161 6.6e-198 XK27_01805 M Glycosyltransferase like family 2
CMMOHOCF_00162 7.6e-67 icaR K Bacterial regulatory proteins, tetR family
CMMOHOCF_00164 6.5e-136 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)
CMMOHOCF_00165 9.3e-56 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)
CMMOHOCF_00166 1.7e-11 amt U Ammonium Transporter Family
CMMOHOCF_00167 1.3e-186 amt U Ammonium Transporter Family
CMMOHOCF_00168 1e-54 glnB K Nitrogen regulatory protein P-II
CMMOHOCF_00169 0.0 2.7.7.19, 2.7.7.59 O Nucleotidyltransferase domain
CMMOHOCF_00170 5.6e-95 dinF V MatE
CMMOHOCF_00171 4.3e-54 dinF V MatE
CMMOHOCF_00172 7.7e-36 dinF V MatE
CMMOHOCF_00173 7.1e-87 dnaB 3.6.4.12 L Participates in initiation and elongation during chromosome replication
CMMOHOCF_00174 3e-139 dnaB 3.6.4.12 L Participates in initiation and elongation during chromosome replication
CMMOHOCF_00175 1.3e-274 murD 3.4.21.10, 6.3.2.13, 6.3.2.9 M Domain of unknown function (DUF1727)
CMMOHOCF_00176 7.5e-143 cobQ S CobB/CobQ-like glutamine amidotransferase domain
CMMOHOCF_00177 1.8e-47 ubiB S ABC1 family
CMMOHOCF_00178 2.7e-266 ubiB S ABC1 family
CMMOHOCF_00179 8.2e-25 pacS 3.6.3.54 P E1-E2 ATPase
CMMOHOCF_00180 3e-67 pacS 3.6.3.54 P E1-E2 ATPase
CMMOHOCF_00181 7.1e-187 pacS 3.6.3.54 P E1-E2 ATPase
CMMOHOCF_00182 1.1e-47 pacS 3.6.3.54 P E1-E2 ATPase
CMMOHOCF_00183 1.5e-40 pacS 3.6.3.54 P E1-E2 ATPase
CMMOHOCF_00184 8.8e-54 pacS 3.6.3.54 P E1-E2 ATPase
CMMOHOCF_00185 5.3e-19 csoR S Metal-sensitive transcriptional repressor
CMMOHOCF_00186 5.8e-13 csoR S Metal-sensitive transcriptional repressor
CMMOHOCF_00187 2.9e-214 rmuC S RmuC family
CMMOHOCF_00188 7.7e-129 pyrE 2.4.2.10 F Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP)
CMMOHOCF_00189 3.6e-26 spoU 2.1.1.185 J RNA methyltransferase TrmH family
CMMOHOCF_00190 6e-118 spoU 2.1.1.185 J RNA methyltransferase TrmH family
CMMOHOCF_00191 1.9e-29 V ABC transporter
CMMOHOCF_00192 9.1e-63 V ABC transporter
CMMOHOCF_00193 5.3e-14 V ABC transporter
CMMOHOCF_00194 6.2e-48 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)
CMMOHOCF_00195 8.1e-94 gatA 6.3.5.6, 6.3.5.7 F 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)
CMMOHOCF_00196 3.6e-165 gatA 6.3.5.6, 6.3.5.7 F 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)
CMMOHOCF_00197 1.4e-286 gatB 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)
CMMOHOCF_00198 3.1e-144 2.3.1.57 J Acetyltransferase (GNAT) domain
CMMOHOCF_00199 1.4e-44 2.3.1.57 J Acetyltransferase (GNAT) domain
CMMOHOCF_00200 3.3e-52 S Protein of unknown function (DUF2469)
CMMOHOCF_00201 2.9e-158 5.4.99.9 H Flavin containing amine oxidoreductase
CMMOHOCF_00202 2.8e-119 5.4.99.9 H Flavin containing amine oxidoreductase
CMMOHOCF_00203 8.2e-14 rho K Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template
CMMOHOCF_00204 8.3e-33 rho K Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template
CMMOHOCF_00205 1.4e-228 rho K Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template
CMMOHOCF_00206 4.2e-61 E Aminotransferase class I and II
CMMOHOCF_00207 6.7e-80 E Aminotransferase class I and II
CMMOHOCF_00208 1.2e-68 lrp_3 K helix_turn_helix ASNC type
CMMOHOCF_00209 2.3e-63 tyrA 5.4.99.5 E Chorismate mutase type II
CMMOHOCF_00210 1.8e-174 S domain protein
CMMOHOCF_00211 1.4e-72 S domain protein
CMMOHOCF_00212 1.9e-47 S domain protein
CMMOHOCF_00213 3.4e-59 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
CMMOHOCF_00214 2.3e-49 deaD 3.6.4.13 JKL helicase superfamily c-terminal domain
CMMOHOCF_00215 1.4e-140 3.5.2.6 V Beta-lactamase enzyme family
CMMOHOCF_00216 3.8e-53 yeaD 4.2.1.9, 5.1.3.15 G Aldose 1-epimerase
CMMOHOCF_00217 5e-94 yeaD 4.2.1.9, 5.1.3.15 G Aldose 1-epimerase
CMMOHOCF_00218 1.4e-106
CMMOHOCF_00220 8.5e-156 cma 2.1.1.79 M Mycolic acid cyclopropane synthetase
CMMOHOCF_00221 1.9e-115 iolG 1.1.1.18, 1.1.1.369 S Oxidoreductase family, C-terminal alpha/beta domain
CMMOHOCF_00222 7.8e-38 iolG 1.1.1.18, 1.1.1.369 S Oxidoreductase family, C-terminal alpha/beta domain
CMMOHOCF_00223 2.6e-163 glcU G Sugar transport protein
CMMOHOCF_00224 1.2e-186 K helix_turn_helix, arabinose operon control protein
CMMOHOCF_00226 3.9e-36 rpmE J Binds the 23S rRNA
CMMOHOCF_00227 2.6e-189 prfA J Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA
CMMOHOCF_00228 1.6e-188 prmC 2.1.1.297 J Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif
CMMOHOCF_00229 2.1e-54 2.3.1.79 S Bacterial transferase hexapeptide repeat protein
CMMOHOCF_00230 2.6e-54 ywlC 2.7.7.87 J Belongs to the SUA5 family
CMMOHOCF_00231 9e-191 tagO 2.7.8.33, 2.7.8.35 M Glycosyl transferase family 4
CMMOHOCF_00232 8.9e-265 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
CMMOHOCF_00233 0.0 3.2.1.10, 3.2.1.20, 3.2.1.93 GH13,GH31 G Alpha-amylase domain
CMMOHOCF_00234 4.8e-51 orn L 3'-to-5' exoribonuclease specific for small oligoribonucleotides
CMMOHOCF_00235 3.3e-30 orn L 3'-to-5' exoribonuclease specific for small oligoribonucleotides
CMMOHOCF_00236 7.6e-160 supH S Sucrose-6F-phosphate phosphohydrolase
CMMOHOCF_00237 2.2e-215 recD2 3.6.4.12 L PIF1-like helicase
CMMOHOCF_00238 2.8e-46 recD2 3.6.4.12 L PIF1-like helicase
CMMOHOCF_00240 3.3e-268 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
CMMOHOCF_00241 6.2e-26
CMMOHOCF_00242 8.2e-117 L Single-strand binding protein family
CMMOHOCF_00243 1.2e-70 pepO 3.4.24.71 O Peptidase family M13
CMMOHOCF_00244 2.3e-284 pepO 3.4.24.71 O Peptidase family M13
CMMOHOCF_00245 7.7e-26 S Short repeat of unknown function (DUF308)
CMMOHOCF_00246 2e-73 S Short repeat of unknown function (DUF308)
CMMOHOCF_00247 1.1e-149 map 3.4.11.18 E Methionine aminopeptidase
CMMOHOCF_00248 5.4e-36 gltA 2.3.3.1 C Citrate synthase, C-terminal domain
CMMOHOCF_00249 1.6e-28 gltA 2.3.3.1 C Citrate synthase, C-terminal domain
CMMOHOCF_00250 1.4e-77 gltA 2.3.3.1 C Citrate synthase, C-terminal domain
CMMOHOCF_00251 1.9e-100 dnaQ 2.7.7.7 L Exonuclease, DNA polymerase III, epsilon subunit family
CMMOHOCF_00252 4.9e-41 yghZ C Aldo/keto reductase family
CMMOHOCF_00253 7.3e-98 yghZ C Aldo/keto reductase family
CMMOHOCF_00254 2.9e-54 racA K MerR, DNA binding
CMMOHOCF_00255 5.8e-124 ctpE P E1-E2 ATPase
CMMOHOCF_00256 1.2e-79 ctpE P E1-E2 ATPase
CMMOHOCF_00257 1e-187 MA20_16500 1.1.1.399, 1.1.1.95 EH Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family
CMMOHOCF_00258 2.6e-62 sapF E ATPases associated with a variety of cellular activities
CMMOHOCF_00259 7.5e-53 sapF E ATPases associated with a variety of cellular activities
CMMOHOCF_00260 6.8e-116 oppD EP oligopeptide transport protein of the ABC superfamily, ATP-binding component
CMMOHOCF_00261 1.1e-15 oppD EP oligopeptide transport protein of the ABC superfamily, ATP-binding component
CMMOHOCF_00262 7e-145 EP Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00263 3.1e-154 P Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00264 4.1e-158 E ABC transporter, substrate-binding protein, family 5
CMMOHOCF_00265 1e-132 E ABC transporter, substrate-binding protein, family 5
CMMOHOCF_00266 1.1e-142 coaX 2.7.1.33 H Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis
CMMOHOCF_00267 1.4e-140 G Bacterial extracellular solute-binding protein
CMMOHOCF_00268 1.2e-29 G Bacterial extracellular solute-binding protein
CMMOHOCF_00269 5.7e-58 G carbohydrate transport
CMMOHOCF_00270 3.9e-66 lacZ5 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_00271 7.3e-88 lacZ5 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_00272 1.5e-160 lacZ5 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_00273 1.8e-69 lacZ5 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_00274 2.3e-62 G ABC transporter permease
CMMOHOCF_00275 7.7e-43 G ABC transporter permease
CMMOHOCF_00276 1.6e-42 K Periplasmic binding protein domain
CMMOHOCF_00277 7.2e-135 K Periplasmic binding protein domain
CMMOHOCF_00278 9.4e-11 ghrA EH D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain
CMMOHOCF_00279 1.5e-31 3.2.1.51 GH29 G Alpha-L-fucosidase
CMMOHOCF_00280 0.0 3.2.1.51 GH29 G Alpha-L-fucosidase
CMMOHOCF_00281 0.0 3.2.1.51 GH29 G Alpha-L-fucosidase
CMMOHOCF_00283 3.6e-46 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)
CMMOHOCF_00284 8e-56 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)
CMMOHOCF_00285 6.5e-242 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)
CMMOHOCF_00286 2e-102 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)
CMMOHOCF_00287 6.8e-114 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)
CMMOHOCF_00288 8.5e-55 yvlD S Mycobacterial 4 TMS phage holin, superfamily IV
CMMOHOCF_00289 1.1e-122 aldH 1.2.1.3, 1.2.1.5 C Aldehyde dehydrogenase family
CMMOHOCF_00290 1.3e-75 aldH 1.2.1.3, 1.2.1.5 C Aldehyde dehydrogenase family
CMMOHOCF_00292 3.8e-51 bcgIB 2.1.1.72, 3.1.21.3 V Type I restriction modification DNA specificity domain
CMMOHOCF_00293 1.9e-251 V Type I restriction-modification system methyltransferase subunit()
CMMOHOCF_00294 1.1e-23 relB L RelB antitoxin
CMMOHOCF_00295 4.3e-28 L Transposase
CMMOHOCF_00296 9.2e-127 XK27_08050 O prohibitin homologues
CMMOHOCF_00297 4.5e-244 2.5.1.49 E Cys/Met metabolism PLP-dependent enzyme
CMMOHOCF_00298 2.4e-220 metC 4.4.1.8 E Cys/Met metabolism PLP-dependent enzyme
CMMOHOCF_00299 1.4e-259 nox 1.6.3.4 C Pyridine nucleotide-disulphide oxidoreductase
CMMOHOCF_00300 7e-26 glxK 2.7.1.165 G Belongs to the glycerate kinase type-1 family
CMMOHOCF_00301 7.5e-92 glxK 2.7.1.165 G Belongs to the glycerate kinase type-1 family
CMMOHOCF_00302 7.3e-13 M Parallel beta-helix repeats
CMMOHOCF_00303 4e-47 M Parallel beta-helix repeats
CMMOHOCF_00304 6.6e-109 M Parallel beta-helix repeats
CMMOHOCF_00305 1.2e-227 M Glycosyl transferase 4-like domain
CMMOHOCF_00306 5.9e-199 ltaE 4.1.2.48 E Beta-eliminating lyase
CMMOHOCF_00308 9.3e-62 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
CMMOHOCF_00309 3.3e-80 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
CMMOHOCF_00310 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
CMMOHOCF_00311 5.6e-36 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
CMMOHOCF_00312 8.1e-232 tuf J This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis
CMMOHOCF_00313 1.3e-55 S Esterase-like activity of phytase
CMMOHOCF_00314 8e-147 S Esterase-like activity of phytase
CMMOHOCF_00315 1e-151 S Esterase-like activity of phytase
CMMOHOCF_00316 1.1e-210 EGP Transmembrane secretion effector
CMMOHOCF_00318 1.1e-75 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
CMMOHOCF_00319 6.1e-88 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
CMMOHOCF_00320 2.2e-237 carA 6.3.5.5 F Belongs to the CarA family
CMMOHOCF_00321 1.6e-197 carB 6.3.5.5 EF Carbamoyl-phosphate synthetase large chain, oligomerisation domain
CMMOHOCF_00322 3.5e-172 carB 6.3.5.5 EF Carbamoyl-phosphate synthetase large chain, oligomerisation domain
CMMOHOCF_00323 6.5e-70 carB 6.3.5.5 EF Carbamoyl-phosphate synthetase large chain, oligomerisation domain
CMMOHOCF_00324 1.1e-61 carB 6.3.5.5 EF Carbamoyl-phosphate synthetase large chain, oligomerisation domain
CMMOHOCF_00325 1.8e-69 carB 6.3.5.5 EF Carbamoyl-phosphate synthetase large chain, oligomerisation domain
CMMOHOCF_00326 1.1e-54 gmk 2.4.2.10, 2.7.4.8, 4.1.1.23 F Essential for recycling GMP and indirectly, cGMP
CMMOHOCF_00327 1.6e-42 gmk 2.4.2.10, 2.7.4.8, 4.1.1.23 F Essential for recycling GMP and indirectly, cGMP
CMMOHOCF_00328 1.9e-86 gmk 2.7.4.8, 4.1.1.23 F Essential for recycling GMP and indirectly, cGMP
CMMOHOCF_00329 7e-286 S Protein of unknown function DUF262
CMMOHOCF_00330 8e-106 S Protein of unknown function DUF262
CMMOHOCF_00331 9.4e-104 K helix_turn_helix, Lux Regulon
CMMOHOCF_00332 1.6e-123 T Histidine kinase
CMMOHOCF_00333 2.5e-125 T Histidine kinase
CMMOHOCF_00334 9.8e-96 S Domain of unknown function (DUF5067)
CMMOHOCF_00335 3.8e-141 ybhL S Belongs to the BI1 family
CMMOHOCF_00336 2.9e-171 ydeD EG EamA-like transporter family
CMMOHOCF_00337 1.2e-35 relA2 2.7.6.5 S Region found in RelA / SpoT proteins
CMMOHOCF_00338 8.4e-39 relA2 2.7.6.5 S Region found in RelA / SpoT proteins
CMMOHOCF_00339 7.4e-280 miaB 2.8.4.3 H Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine
CMMOHOCF_00340 1.8e-161 miaA 2.5.1.75 F Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A)
CMMOHOCF_00341 3.9e-36 fic D Fic/DOC family
CMMOHOCF_00342 1.8e-32 fic D Fic/DOC family
CMMOHOCF_00343 2.1e-26 fic D Fic/DOC family
CMMOHOCF_00344 3.2e-105 ftsK D FtsK SpoIIIE family protein
CMMOHOCF_00345 1.9e-36 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
CMMOHOCF_00346 5.3e-97 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
CMMOHOCF_00347 1.7e-96 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
CMMOHOCF_00348 6.9e-114 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
CMMOHOCF_00349 1.1e-53 rpoZ 2.7.7.6 K Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits
CMMOHOCF_00350 0.0 ilvD 4.2.1.9 H Belongs to the IlvD Edd family
CMMOHOCF_00351 9.2e-172 gmk 1.1.1.23, 2.7.4.8 S Protein conserved in bacteria
CMMOHOCF_00352 4.2e-112 acnA 4.2.1.3 C Catalyzes the isomerization of citrate to isocitrate via cis-aconitate
CMMOHOCF_00353 2.5e-144 acnA 4.2.1.3 C Catalyzes the isomerization of citrate to isocitrate via cis-aconitate
CMMOHOCF_00354 4.5e-81 acnA 4.2.1.3 C Catalyzes the isomerization of citrate to isocitrate via cis-aconitate
CMMOHOCF_00355 2.6e-146 acnA 4.2.1.3 C Catalyzes the isomerization of citrate to isocitrate via cis-aconitate
CMMOHOCF_00356 1.1e-104 ctpE P E1-E2 ATPase
CMMOHOCF_00357 6.9e-274 ctpE P E1-E2 ATPase
CMMOHOCF_00358 1.3e-21 ctpE P E1-E2 ATPase
CMMOHOCF_00359 2.7e-31
CMMOHOCF_00360 2.2e-14
CMMOHOCF_00361 6.1e-257 trmA 2.1.1.190, 2.1.1.35 J Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family
CMMOHOCF_00362 7.8e-61 S Protein of unknown function (DUF3159)
CMMOHOCF_00363 3.3e-28 S Protein of unknown function (DUF3159)
CMMOHOCF_00364 1.2e-138 S Protein of unknown function (DUF3710)
CMMOHOCF_00365 3.7e-170 exoA 3.1.11.2 L Endonuclease/Exonuclease/phosphatase family
CMMOHOCF_00366 8.7e-270 pepC 3.4.22.40 E Peptidase C1-like family
CMMOHOCF_00367 1.2e-258 oppA E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_00368 1e-18 oppA E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_00369 7.9e-282 oppD P Belongs to the ABC transporter superfamily
CMMOHOCF_00370 4.7e-133 dppC EP N-terminal TM domain of oligopeptide transport permease C
CMMOHOCF_00371 7.9e-177 appB EP Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00372 4.7e-185 xerC D Belongs to the 'phage' integrase family. XerC subfamily
CMMOHOCF_00373 7.3e-42
CMMOHOCF_00374 7.1e-187 tyrA 1.3.1.12, 1.3.1.43 E Prephenate dehydrogenase
CMMOHOCF_00375 6.5e-198 pheA 1.3.1.12, 4.2.1.51, 5.4.99.5 E Prephenate dehydratase
CMMOHOCF_00376 4.4e-51
CMMOHOCF_00377 1.6e-40 typA T Elongation factor G C-terminus
CMMOHOCF_00378 5.5e-30 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
CMMOHOCF_00379 5.7e-211 mrp D Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP
CMMOHOCF_00380 1.9e-91 gmk 1.1.1.23, 2.7.4.8 S Protein conserved in bacteria
CMMOHOCF_00381 2e-86 int L Phage integrase, N-terminal SAM-like domain
CMMOHOCF_00382 1.5e-66 L Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell
CMMOHOCF_00383 7.8e-33 3.1.21.4 L Recognizes the double-stranded sequence CTCGAG and cleaves after C-1
CMMOHOCF_00384 1.6e-44 S GIY-YIG catalytic domain
CMMOHOCF_00385 4.5e-19 S GIY-YIG catalytic domain
CMMOHOCF_00390 4.5e-33 traSA D FtsK/SpoIIIE family
CMMOHOCF_00393 3.1e-286 glnA 6.3.1.2 E glutamine synthetase
CMMOHOCF_00394 1.4e-95 S Domain of unknown function (DUF4191)
CMMOHOCF_00395 5.5e-158 lpdA 1.16.1.1, 1.8.1.4 C Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
CMMOHOCF_00396 8.2e-48 lpdA 1.16.1.1, 1.8.1.4 C Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
CMMOHOCF_00397 2.7e-103 S Protein of unknown function (DUF3043)
CMMOHOCF_00398 6.8e-174 argE E Peptidase dimerisation domain
CMMOHOCF_00399 9.3e-14 argE E Peptidase dimerisation domain
CMMOHOCF_00400 3.9e-171 V N-Acetylmuramoyl-L-alanine amidase
CMMOHOCF_00401 1.9e-136 ytrE V ATPases associated with a variety of cellular activities
CMMOHOCF_00402 3.1e-12
CMMOHOCF_00403 1.9e-175
CMMOHOCF_00404 7.4e-231 ybbD 3.2.1.52 G Glycosyl hydrolase family 3 N-terminal domain protein
CMMOHOCF_00405 0.0 S Uncharacterised protein family (UPF0182)
CMMOHOCF_00406 1.3e-13 S Uncharacterised protein family (UPF0182)
CMMOHOCF_00407 1.4e-131 S Uncharacterised protein family (UPF0182)
CMMOHOCF_00408 2.3e-212 tagB 2.7.8.14, 2.7.8.44, 2.7.8.47 M CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase
CMMOHOCF_00409 1.3e-173 2.7.8.14, 2.7.8.47 M CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase
CMMOHOCF_00410 2.6e-149 2.7.8.14, 2.7.8.47 M CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase
CMMOHOCF_00411 2.7e-126 pspC KT PspC domain
CMMOHOCF_00412 1.1e-150 pspC KT PspC domain
CMMOHOCF_00413 7.4e-116
CMMOHOCF_00414 1.6e-111 S Protein of unknown function (DUF4125)
CMMOHOCF_00415 1.3e-79 S Domain of unknown function (DUF4037)
CMMOHOCF_00416 1e-196 S Domain of unknown function (DUF4037)
CMMOHOCF_00417 5.5e-56 araJ EGP Major facilitator Superfamily
CMMOHOCF_00418 1e-104 araJ EGP Major facilitator Superfamily
CMMOHOCF_00420 4.4e-40 lysS 6.1.1.6 J Belongs to the class-II aminoacyl-tRNA synthetase family
CMMOHOCF_00421 9.1e-275 lysS 6.1.1.6 J Belongs to the class-II aminoacyl-tRNA synthetase family
CMMOHOCF_00422 9.5e-175 menA 2.5.1.74 H Belongs to the MenA family. Type 1 subfamily
CMMOHOCF_00423 4.3e-115 gpmA 5.4.2.11 G Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate
CMMOHOCF_00424 1.8e-09 EGP Major facilitator Superfamily
CMMOHOCF_00425 1.3e-117 phoU P Plays a role in the regulation of phosphate uptake
CMMOHOCF_00426 2.3e-190 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_00427 2.6e-39
CMMOHOCF_00428 3.7e-57 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
CMMOHOCF_00429 1.9e-125 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
CMMOHOCF_00430 9.4e-164 usp 3.5.1.28 CBM50 S CHAP domain
CMMOHOCF_00431 3.2e-107 M NlpC/P60 family
CMMOHOCF_00432 4.6e-191 T Universal stress protein family
CMMOHOCF_00433 1e-72 attW O OsmC-like protein
CMMOHOCF_00434 6.6e-175 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
CMMOHOCF_00435 8.7e-30 folA 1.5.1.3 H dihydrofolate reductase
CMMOHOCF_00436 6.3e-84 folA 1.5.1.3 H dihydrofolate reductase
CMMOHOCF_00437 4e-95 ptpA 3.1.3.48 T low molecular weight
CMMOHOCF_00439 5.7e-180 afr_2 S Oxidoreductase family, NAD-binding Rossmann fold
CMMOHOCF_00440 2.2e-45 azlD E Branched-chain amino acid transport protein (AzlD)
CMMOHOCF_00441 1.3e-111 vex2 V ABC transporter, ATP-binding protein
CMMOHOCF_00442 8.1e-86 vex1 V Efflux ABC transporter, permease protein
CMMOHOCF_00443 2.6e-42 vex1 V Efflux ABC transporter, permease protein
CMMOHOCF_00444 2.9e-70 vex3 V ABC transporter permease
CMMOHOCF_00445 1.2e-137 vex3 V ABC transporter permease
CMMOHOCF_00446 9.8e-12 S Psort location CytoplasmicMembrane, score 9.99
CMMOHOCF_00447 5.4e-181 lacR K Transcriptional regulator, LacI family
CMMOHOCF_00448 9e-59 nagA 3.5.1.25 G Amidohydrolase family
CMMOHOCF_00450 1.7e-84 S Short C-terminal domain
CMMOHOCF_00451 1.2e-16 L Helix-turn-helix domain
CMMOHOCF_00452 3.3e-62 cbh 3.5.1.24 M Linear amide C-N hydrolase, choloylglycine hydrolase family protein
CMMOHOCF_00453 6e-114 cbh 3.5.1.24 M Linear amide C-N hydrolase, choloylglycine hydrolase family protein
CMMOHOCF_00454 7.9e-117 ybeM S Carbon-nitrogen hydrolase
CMMOHOCF_00455 4.7e-182 modF 3.6.3.21, 3.6.3.34 P ATPases associated with a variety of cellular activities
CMMOHOCF_00456 3.6e-51 glgA 2.4.1.342 GT4 G Starch synthase catalytic domain
CMMOHOCF_00457 2.9e-176 glgA 2.4.1.342 GT4 G Starch synthase catalytic domain
CMMOHOCF_00458 3.6e-82
CMMOHOCF_00459 1e-303 gltD 1.4.1.13, 1.4.1.14 C Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster
CMMOHOCF_00460 0.0 gltB 1.4.1.13, 1.4.1.14, 1.4.7.1 E glutamate synthase NADPH large subunit
CMMOHOCF_00461 1e-122 gltB 1.4.1.13, 1.4.1.14, 1.4.7.1 E glutamate synthase NADPH large subunit
CMMOHOCF_00462 8e-94 gltB 1.4.1.13, 1.4.1.14, 1.4.7.1 E glutamate synthase NADPH large subunit
CMMOHOCF_00463 1.8e-38 gltB 1.4.1.13, 1.4.1.14, 1.4.7.1 E glutamate synthase NADPH large subunit
CMMOHOCF_00464 8.3e-59 gltB 1.4.1.13, 1.4.1.14, 1.4.7.1 E glutamate synthase NADPH large subunit
CMMOHOCF_00465 1.7e-123 gltB 1.4.1.13, 1.4.1.14, 1.4.7.1 E glutamate synthase NADPH large subunit
CMMOHOCF_00466 6.5e-77 tetP J Elongation factor G, domain IV
CMMOHOCF_00467 7.2e-179 tetP J Elongation factor G, domain IV
CMMOHOCF_00468 3.4e-103 tetP J Elongation factor G, domain IV
CMMOHOCF_00469 8.2e-293 alaA 2.6.1.2, 2.6.1.66 E Aminotransferase, class I II
CMMOHOCF_00470 4e-13 S Membrane
CMMOHOCF_00471 8.2e-244 hemN H Involved in the biosynthesis of porphyrin-containing compound
CMMOHOCF_00472 5.2e-209 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
CMMOHOCF_00473 1.1e-112 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
CMMOHOCF_00474 9.9e-34 rpsT J Binds directly to 16S ribosomal RNA
CMMOHOCF_00475 1.9e-121 S UPF0126 domain
CMMOHOCF_00476 3.1e-15 3.1.4.37 T RNA ligase
CMMOHOCF_00477 1e-110 3.1.4.37 T RNA ligase
CMMOHOCF_00478 2.4e-225 ilvE 2.6.1.42 E Amino-transferase class IV
CMMOHOCF_00479 3.3e-91 ctc J This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance
CMMOHOCF_00480 8.2e-190 S alpha beta
CMMOHOCF_00481 4.5e-94 pntB 1.6.1.2 C The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane
CMMOHOCF_00482 0.0
CMMOHOCF_00483 2.9e-148 QT PucR C-terminal helix-turn-helix domain
CMMOHOCF_00484 1.5e-129 nucS L Cleaves both 3' and 5' ssDNA extremities of branched DNA structures
CMMOHOCF_00485 8.8e-50 atpC C Produces ATP from ADP in the presence of a proton gradient across the membrane
CMMOHOCF_00486 1.5e-283 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
CMMOHOCF_00487 6e-166 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
CMMOHOCF_00488 0.0 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
CMMOHOCF_00489 1.4e-150 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
CMMOHOCF_00490 5.2e-36 atpF C Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0)
CMMOHOCF_00491 1.2e-30 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
CMMOHOCF_00492 6e-146 atpB C it plays a direct role in the translocation of protons across the membrane
CMMOHOCF_00493 3.5e-207 metAA 2.3.1.46 E Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine
CMMOHOCF_00495 3e-34
CMMOHOCF_00496 1e-40 K RNA polymerase II activating transcription factor binding
CMMOHOCF_00497 3.6e-145 K RNA polymerase II activating transcription factor binding
CMMOHOCF_00498 1.4e-140 K RNA polymerase II activating transcription factor binding
CMMOHOCF_00499 9.5e-70 glgE 2.4.99.16 GH13 G Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB
CMMOHOCF_00500 2.4e-291 glgE 2.4.99.16 GH13 G Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB
CMMOHOCF_00501 5.2e-92 ppa 3.6.1.1 C Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions
CMMOHOCF_00503 3e-96 mntP P Probably functions as a manganese efflux pump
CMMOHOCF_00504 1.4e-125
CMMOHOCF_00505 4e-122 KT Transcriptional regulatory protein, C terminal
CMMOHOCF_00506 3e-127 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
CMMOHOCF_00507 9.5e-25 E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_00508 1.1e-220 E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_00509 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
CMMOHOCF_00510 1.4e-172 dkgA 1.1.1.346 C Aldo/keto reductase family
CMMOHOCF_00511 1.3e-156 yvgN 1.1.1.346 S Aldo/keto reductase family
CMMOHOCF_00512 3.4e-202 K WYL domain
CMMOHOCF_00514 0.0 4.2.1.53 S MCRA family
CMMOHOCF_00515 2e-46 yhbY J CRS1_YhbY
CMMOHOCF_00516 4.5e-96 S zinc-ribbon domain
CMMOHOCF_00517 0.0 dnaE 2.7.7.7 L DNA polymerase III alpha subunit
CMMOHOCF_00518 0.0 dnaE 2.7.7.7 L DNA polymerase III alpha subunit
CMMOHOCF_00519 3e-39 cscA 3.2.1.26 GH32 G Belongs to the glycosyl hydrolase 32 family
CMMOHOCF_00520 1.2e-17 cscA 3.2.1.26 GH32 G Belongs to the glycosyl hydrolase 32 family
CMMOHOCF_00521 3.2e-90 ywqG S Domain of unknown function (DUF1963)
CMMOHOCF_00522 3e-89 ywqG S Domain of unknown function (DUF1963)
CMMOHOCF_00523 1.8e-155 uppS 2.5.1.31, 2.5.1.86, 2.5.1.88 H Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids
CMMOHOCF_00524 2.7e-143 recO L Involved in DNA repair and RecF pathway recombination
CMMOHOCF_00525 1e-12 I acetylesterase activity
CMMOHOCF_00526 4.1e-243 I acetylesterase activity
CMMOHOCF_00527 8.4e-122 ispG 1.17.7.1, 1.17.7.3 I Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate
CMMOHOCF_00528 1.9e-74 ispG 1.17.7.1, 1.17.7.3 I Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate
CMMOHOCF_00529 1.5e-222 dxr 1.1.1.267 I Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP)
CMMOHOCF_00530 3.1e-68 2.7.11.1 NU Tfp pilus assembly protein FimV
CMMOHOCF_00531 5.7e-96 2.7.11.1 NU Tfp pilus assembly protein FimV
CMMOHOCF_00533 1e-81
CMMOHOCF_00534 1.9e-146 rluA 5.4.99.28, 5.4.99.29 J RNA pseudouridylate synthase
CMMOHOCF_00535 3e-76 smpB J the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA
CMMOHOCF_00536 3.7e-92 usp 3.5.1.28 CBM50 D CHAP domain protein
CMMOHOCF_00537 4.7e-71 ftsX D Part of the ABC transporter FtsEX involved in cellular division
CMMOHOCF_00538 1.1e-64 ftsX D Part of the ABC transporter FtsEX involved in cellular division
CMMOHOCF_00539 1.4e-66 rlrG K Bacterial regulatory helix-turn-helix protein, lysR family
CMMOHOCF_00540 4.2e-118 3.1.3.27 E haloacid dehalogenase-like hydrolase
CMMOHOCF_00541 8.9e-40 F Nucleoside 2-deoxyribosyltransferase
CMMOHOCF_00542 1.5e-186 2.4.1.166 GT2 M Glycosyltransferase like family 2
CMMOHOCF_00545 6.7e-64 pbpB 2.7.11.1, 3.4.16.4 S PASTA domain
CMMOHOCF_00546 4.5e-294 pbpB 2.7.11.1, 3.4.16.4 S PASTA domain
CMMOHOCF_00547 1.6e-79 ypfH S Phospholipase/Carboxylesterase
CMMOHOCF_00548 2.7e-73 def2 3.5.1.31, 3.5.1.88 J Removes the formyl group from the N-terminal Met of newly synthesized proteins
CMMOHOCF_00549 9.5e-24
CMMOHOCF_00550 1.2e-34 yhcC S Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082)
CMMOHOCF_00551 2.8e-66 S Zincin-like metallopeptidase
CMMOHOCF_00552 1.2e-89 S Helix-turn-helix
CMMOHOCF_00553 1.7e-122 S Short C-terminal domain
CMMOHOCF_00554 5.6e-23 S Short C-terminal domain
CMMOHOCF_00555 2.7e-22
CMMOHOCF_00556 2.9e-191
CMMOHOCF_00558 1.1e-43 K Psort location Cytoplasmic, score
CMMOHOCF_00559 1.7e-89 KLT Protein tyrosine kinase
CMMOHOCF_00560 2e-139 KLT Protein tyrosine kinase
CMMOHOCF_00561 3.7e-48 S Cupin 2, conserved barrel domain protein
CMMOHOCF_00562 4.7e-09 S Cupin 2, conserved barrel domain protein
CMMOHOCF_00563 6.7e-75 ksgA 2.1.1.182 J Methyltransferase domain
CMMOHOCF_00564 2e-68 ksgA 2.1.1.182 J Methyltransferase domain
CMMOHOCF_00565 5.6e-59 yccF S Inner membrane component domain
CMMOHOCF_00566 1.3e-78 E Psort location Cytoplasmic, score 8.87
CMMOHOCF_00567 6.8e-248 XK27_00240 K Fic/DOC family
CMMOHOCF_00568 2.4e-192 ychF J ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner
CMMOHOCF_00569 2.4e-33 mtnE 2.6.1.83 E Aminotransferase class I and II
CMMOHOCF_00570 2.5e-43 mtnE 2.6.1.83 E Aminotransferase class I and II
CMMOHOCF_00571 9.5e-95 mtnE 2.6.1.83 E Aminotransferase class I and II
CMMOHOCF_00572 5.5e-85 metI P Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00574 3e-204 metN P Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system
CMMOHOCF_00575 1.8e-178 metE 2.1.1.14 E Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation
CMMOHOCF_00576 3.6e-31 sixA T Phosphoglycerate mutase family
CMMOHOCF_00577 9.6e-59 sixA T Phosphoglycerate mutase family
CMMOHOCF_00578 9.4e-83 trmI 2.1.1.219, 2.1.1.220 J Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA
CMMOHOCF_00579 4.8e-54 trmI 2.1.1.219, 2.1.1.220 J Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA
CMMOHOCF_00580 8.8e-178 I alpha/beta hydrolase fold
CMMOHOCF_00581 8e-24 rarD S EamA-like transporter family
CMMOHOCF_00582 7.9e-75 rarD 3.4.17.13 E Rard protein
CMMOHOCF_00583 1e-27
CMMOHOCF_00584 4.7e-185 mcrB L Restriction endonuclease
CMMOHOCF_00585 5.6e-10
CMMOHOCF_00586 1.6e-91 O ATPase family associated with various cellular activities (AAA)
CMMOHOCF_00587 2.3e-253 O Subtilase family
CMMOHOCF_00588 7.6e-08 O Subtilase family
CMMOHOCF_00589 5.9e-144 L helicase
CMMOHOCF_00590 3.9e-299 L helicase
CMMOHOCF_00591 1.7e-125 L helicase
CMMOHOCF_00592 1.9e-119 S Domain of unknown function (DUF4391)
CMMOHOCF_00593 2e-75 2.1.1.72 L DNA methylase
CMMOHOCF_00594 3e-101 2.1.1.72 L DNA methylase
CMMOHOCF_00595 8.8e-18 res 3.1.21.5 V Type III restriction enzyme, res subunit
CMMOHOCF_00597 1.3e-79 res 3.1.21.5 V Type III restriction enzyme, res subunit
CMMOHOCF_00598 2.4e-18 res 3.1.21.5 V Type III restriction enzyme, res subunit
CMMOHOCF_00599 0.0 res 3.1.21.5 V Type III restriction enzyme, res subunit
CMMOHOCF_00600 8e-21 prrC S AAA domain
CMMOHOCF_00601 6.7e-14 prrC S AAA domain
CMMOHOCF_00602 4e-22 XK26_04895
CMMOHOCF_00603 5.9e-102 XK26_04895
CMMOHOCF_00604 3.9e-12 V Abi-like protein
CMMOHOCF_00605 1.9e-77 L Transposase
CMMOHOCF_00606 9.5e-18 E Transglutaminase-like superfamily
CMMOHOCF_00607 6.3e-110 E Transglutaminase-like superfamily
CMMOHOCF_00608 8e-182 S Protein of unknown function DUF58
CMMOHOCF_00609 2.5e-31 S Protein of unknown function DUF58
CMMOHOCF_00610 8.2e-230 S ATPase family associated with various cellular activities (AAA)
CMMOHOCF_00611 5.8e-305 S Fibronectin type 3 domain
CMMOHOCF_00612 0.0 S Fibronectin type 3 domain
CMMOHOCF_00613 2.2e-232 KLT Protein tyrosine kinase
CMMOHOCF_00614 0.0 uvrD 3.6.4.12 L PD-(D/E)XK nuclease superfamily
CMMOHOCF_00615 8.6e-115 uvrD2 3.6.4.12 L Belongs to the helicase family. UvrD subfamily
CMMOHOCF_00616 0.0 uvrD2 3.6.4.12 L Belongs to the helicase family. UvrD subfamily
CMMOHOCF_00617 3.7e-18 K -acetyltransferase
CMMOHOCF_00618 9.9e-117 K -acetyltransferase
CMMOHOCF_00619 4.7e-130 G Major Facilitator Superfamily
CMMOHOCF_00620 1.7e-88 G Major Facilitator Superfamily
CMMOHOCF_00621 2.3e-18 appF P Belongs to the ABC transporter superfamily
CMMOHOCF_00622 6.4e-24 relB L RelB antitoxin
CMMOHOCF_00623 7.9e-34 L Transposase
CMMOHOCF_00624 1.6e-32 dapB 1.17.1.8 E Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate
CMMOHOCF_00625 6.4e-85 L Helix-turn-helix domain
CMMOHOCF_00626 7.2e-15 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_00627 4.5e-49 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_00628 2.2e-16 ykiI
CMMOHOCF_00629 2.7e-25 ykiI
CMMOHOCF_00630 2.5e-27 ykiI
CMMOHOCF_00631 5.3e-42 ykiI
CMMOHOCF_00632 8.1e-13 ykiI
CMMOHOCF_00633 0.0 glgX 3.2.1.68 CBM48,GH13 G Belongs to the glycosyl hydrolase 13 family
CMMOHOCF_00634 9.3e-119 3.6.1.13 L NUDIX domain
CMMOHOCF_00635 1.4e-170 yqfO 3.5.4.16 L NIF3 (NGG1p interacting factor 3)
CMMOHOCF_00636 5.8e-17 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
CMMOHOCF_00637 8e-50 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
CMMOHOCF_00638 5e-60 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
CMMOHOCF_00639 1.4e-149 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
CMMOHOCF_00640 3.3e-94 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
CMMOHOCF_00641 9.5e-43 polA 2.7.7.7 L In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
CMMOHOCF_00642 6.1e-116 pdtaR T Response regulator receiver domain protein
CMMOHOCF_00644 5.6e-109 aspA 3.6.1.13 L NUDIX domain
CMMOHOCF_00645 2.5e-272 pyk 2.7.1.40 G Pyruvate kinase
CMMOHOCF_00646 5.6e-178 terC P Integral membrane protein, TerC family
CMMOHOCF_00647 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
CMMOHOCF_00648 5e-100 coaE 2.7.1.24 H Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A
CMMOHOCF_00649 2.7e-156 rpsA J Ribosomal protein S1
CMMOHOCF_00650 4.6e-64 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
CMMOHOCF_00651 1.8e-65 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
CMMOHOCF_00652 3.7e-172 P Zinc-uptake complex component A periplasmic
CMMOHOCF_00653 2.5e-72 znuC P ATPases associated with a variety of cellular activities
CMMOHOCF_00654 3.2e-49 znuC P ATPases associated with a variety of cellular activities
CMMOHOCF_00655 7.3e-69 znuB U ABC 3 transport family
CMMOHOCF_00656 7.9e-59 znuB U ABC 3 transport family
CMMOHOCF_00657 1.5e-26 ispF 2.1.1.228, 2.7.7.60, 4.6.1.12 H Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP)
CMMOHOCF_00658 5.1e-102 carD K CarD-like/TRCF domain
CMMOHOCF_00659 2.8e-188 nusA K Participates in both transcription termination and antitermination
CMMOHOCF_00660 1.4e-113
CMMOHOCF_00661 1.6e-26
CMMOHOCF_00662 7.2e-145 L Transposase and inactivated derivatives
CMMOHOCF_00664 1.3e-153 E Transglutaminase/protease-like homologues
CMMOHOCF_00665 1.6e-148 gcs2 S A circularly permuted ATPgrasp
CMMOHOCF_00666 4.1e-272 gcs2 S A circularly permuted ATPgrasp
CMMOHOCF_00667 6.4e-173 truA 5.4.99.12 J Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs
CMMOHOCF_00668 4.3e-184 3.2.1.52 GH20 G hydrolase family 20, catalytic
CMMOHOCF_00669 1.5e-279 3.2.1.52 GH20 G hydrolase family 20, catalytic
CMMOHOCF_00670 2.7e-292 3.2.1.52 GH20 G hydrolase family 20, catalytic
CMMOHOCF_00671 4.6e-65 rplQ J Ribosomal protein L17
CMMOHOCF_00672 8.9e-184 rpoA 2.7.7.6 K DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates
CMMOHOCF_00673 2.9e-41 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
CMMOHOCF_00674 6.6e-61 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
CMMOHOCF_00675 6.5e-14 rpmJ J Belongs to the bacterial ribosomal protein bL36 family
CMMOHOCF_00676 1.6e-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
CMMOHOCF_00677 1e-72 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
CMMOHOCF_00678 4.7e-249 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
CMMOHOCF_00679 7.6e-59 rplO J binds to the 23S rRNA
CMMOHOCF_00680 1e-24 rpmD J Ribosomal protein L30p/L7e
CMMOHOCF_00681 8.3e-94 rpsE J Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body
CMMOHOCF_00683 3.6e-72 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
CMMOHOCF_00684 2.5e-13 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
CMMOHOCF_00685 9.2e-18 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
CMMOHOCF_00686 2.3e-43 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
CMMOHOCF_00687 2.6e-34 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
CMMOHOCF_00688 3.5e-52 rplX J One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit
CMMOHOCF_00689 6.6e-60 rplN J Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome
CMMOHOCF_00690 3.5e-42 rpsQ J One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA
CMMOHOCF_00691 5e-38 rpmC J Belongs to the universal ribosomal protein uL29 family
CMMOHOCF_00692 4.5e-39 rplP J Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs
CMMOHOCF_00693 3.5e-13 plyA3 3.2.1.18 GH33 M Parallel beta-helix repeats
CMMOHOCF_00694 5.8e-89 K MarR family
CMMOHOCF_00695 1.5e-66 V ABC transporter, ATP-binding protein
CMMOHOCF_00696 1.6e-258 V ABC transporter, ATP-binding protein
CMMOHOCF_00697 1.1e-181 V ABC transporter transmembrane region
CMMOHOCF_00698 6.7e-184 V ABC transporter transmembrane region
CMMOHOCF_00699 1.1e-102 S Patatin-like phospholipase
CMMOHOCF_00700 1.5e-152 murI 5.1.1.3 M Provides the (R)-glutamate required for cell wall biosynthesis
CMMOHOCF_00701 4.5e-85 dapF 5.1.1.7 E Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine
CMMOHOCF_00703 7.3e-56 dapF 5.1.1.7 E Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine
CMMOHOCF_00704 3.4e-115 S Vitamin K epoxide reductase
CMMOHOCF_00705 2.5e-166 PPA1328 3.1.3.97 S DNA polymerase alpha chain like domain
CMMOHOCF_00706 6.1e-32 S Protein of unknown function (DUF3107)
CMMOHOCF_00707 9.9e-207 mphA S Aminoglycoside phosphotransferase
CMMOHOCF_00708 2.6e-274 uvrD2 3.6.4.12 L DNA helicase
CMMOHOCF_00709 1.7e-287 S Zincin-like metallopeptidase
CMMOHOCF_00710 2.1e-66 lon T Belongs to the peptidase S16 family
CMMOHOCF_00711 7.3e-29 lon T Belongs to the peptidase S16 family
CMMOHOCF_00712 3.5e-12 lon T Belongs to the peptidase S16 family
CMMOHOCF_00713 5.7e-47 S Protein of unknown function (DUF3052)
CMMOHOCF_00714 8.1e-196 K helix_turn _helix lactose operon repressor
CMMOHOCF_00715 1.2e-61 S Thiamine-binding protein
CMMOHOCF_00716 3.5e-163 thiD 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 H Phosphomethylpyrimidine kinase
CMMOHOCF_00717 1.1e-201 O AAA domain (Cdc48 subfamily)
CMMOHOCF_00718 1.3e-54
CMMOHOCF_00719 4.3e-19
CMMOHOCF_00720 1.4e-10 thiC 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 H Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction
CMMOHOCF_00721 0.0 thiC 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 H Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction
CMMOHOCF_00722 2.4e-38 tmk 2.7.4.9 F Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis
CMMOHOCF_00723 6.2e-47 tmk 2.7.4.9 F Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis
CMMOHOCF_00724 2e-195 holB 2.7.7.7 L DNA polymerase III
CMMOHOCF_00725 4.2e-195 K helix_turn _helix lactose operon repressor
CMMOHOCF_00726 1.9e-37 ptsH G PTS HPr component phosphorylation site
CMMOHOCF_00727 2.9e-47 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)
CMMOHOCF_00728 3e-177 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)
CMMOHOCF_00729 2.9e-163 L Transposase, Mutator family
CMMOHOCF_00730 3.8e-76 S Fic/DOC family
CMMOHOCF_00731 1.8e-37 S Fic/DOC family
CMMOHOCF_00732 7.2e-197 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
CMMOHOCF_00733 4.5e-22 G MFS/sugar transport protein
CMMOHOCF_00734 1.9e-306 efeU_1 P Iron permease FTR1 family
CMMOHOCF_00735 1.9e-63 tpd P Fe2+ transport protein
CMMOHOCF_00736 5.8e-14 tpd P Fe2+ transport protein
CMMOHOCF_00737 1.3e-232 S Predicted membrane protein (DUF2318)
CMMOHOCF_00738 1.1e-221 macB_2 V ABC transporter permease
CMMOHOCF_00739 3.9e-108 Z012_06715 V FtsX-like permease family
CMMOHOCF_00740 5.7e-149 macB V ABC transporter, ATP-binding protein
CMMOHOCF_00741 3.8e-70 S FMN_bind
CMMOHOCF_00742 3.6e-131 yydK K UTRA
CMMOHOCF_00744 6.6e-72 S haloacid dehalogenase-like hydrolase
CMMOHOCF_00745 4e-81 gmuC 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
CMMOHOCF_00746 1.2e-11 gmuC 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
CMMOHOCF_00747 5.3e-107 gmuC 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
CMMOHOCF_00748 1.2e-48 celA 2.7.1.196, 2.7.1.205 G PTS system, Lactose/Cellobiose specific IIB subunit
CMMOHOCF_00749 2e-39 celC 2.7.1.196, 2.7.1.205 G PTS system, Lactose/Cellobiose specific IIA subunit
CMMOHOCF_00750 1.2e-209 bglA 3.2.1.86 GT1 G Glycosyl hydrolase family 1
CMMOHOCF_00751 1e-09 5.2.1.8 S haloacid dehalogenase-like hydrolase
CMMOHOCF_00752 7.3e-82 fthC 6.3.3.2 H 5-formyltetrahydrofolate cyclo-ligase family
CMMOHOCF_00753 3.7e-33 fmdB S Putative regulatory protein
CMMOHOCF_00754 3.6e-109 flgA NO SAF
CMMOHOCF_00755 9.6e-42
CMMOHOCF_00756 1.7e-249 L Superfamily I DNA and RNA helicases and helicase subunits
CMMOHOCF_00757 0.0 L Superfamily I DNA and RNA helicases and helicase subunits
CMMOHOCF_00758 1.7e-72 T Forkhead associated domain
CMMOHOCF_00759 2.9e-163 T Forkhead associated domain
CMMOHOCF_00760 2.2e-17 rplL J Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation
CMMOHOCF_00761 1.4e-07 rplJ J Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors
CMMOHOCF_00762 8.3e-58 rplJ J Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors
CMMOHOCF_00763 1.1e-184 xynB2 1.1.1.169 E lipolytic protein G-D-S-L family
CMMOHOCF_00764 5.5e-185 guxA1 3.2.1.18, 3.2.1.91 GH33,GH6 G BNR repeat-like domain
CMMOHOCF_00765 6.3e-308 guxA1 3.2.1.18, 3.2.1.91 GH33,GH6 G BNR repeat-like domain
CMMOHOCF_00766 2.6e-49 guxA1 3.2.1.18, 3.2.1.91 GH33,GH6 G BNR repeat-like domain
CMMOHOCF_00767 0.0 guxA1 3.2.1.18, 3.2.1.91 GH33,GH6 G BNR repeat-like domain
CMMOHOCF_00769 3.9e-147 pbuO S Permease family
CMMOHOCF_00770 3.5e-12 pbuO S Permease family
CMMOHOCF_00771 5.6e-133 gmk 1.1.1.23, 2.7.4.8 S Protein conserved in bacteria
CMMOHOCF_00772 3.6e-148 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
CMMOHOCF_00773 1.2e-40 pstA P Phosphate transport system permease
CMMOHOCF_00774 1.4e-128 pstA P Phosphate transport system permease
CMMOHOCF_00775 3.8e-171 pstC P probably responsible for the translocation of the substrate across the membrane
CMMOHOCF_00776 2.1e-101 pstS P Part of the ABC transporter complex PstSACB involved in phosphate import
CMMOHOCF_00777 9.4e-47 pstS P Part of the ABC transporter complex PstSACB involved in phosphate import
CMMOHOCF_00778 1.1e-98 KT Transcriptional regulatory protein, C terminal
CMMOHOCF_00780 6.8e-74 pstP 3.1.3.16 T Sigma factor PP2C-like phosphatases
CMMOHOCF_00781 1.6e-200 rodA D Belongs to the SEDS family
CMMOHOCF_00782 2.5e-53 rodA D Belongs to the SEDS family
CMMOHOCF_00783 4.3e-50 pbpA M penicillin-binding protein
CMMOHOCF_00784 2.3e-171 pbpA M penicillin-binding protein
CMMOHOCF_00785 3.9e-154 T Protein tyrosine kinase
CMMOHOCF_00786 3.9e-55 pknB 2.7.11.1 KLT Protein tyrosine kinase
CMMOHOCF_00787 5.4e-123 pknB 2.7.11.1 KLT Protein tyrosine kinase
CMMOHOCF_00788 4.1e-26 pknB 2.7.11.1 KLT Protein tyrosine kinase
CMMOHOCF_00789 1.9e-108 pknB 2.7.11.1 KLT Protein tyrosine kinase
CMMOHOCF_00790 3.4e-120 trpG 2.6.1.85 EH para-aminobenzoate synthase glutamine amidotransferase component II
CMMOHOCF_00791 4.8e-196 srtA 3.4.22.70 M Sortase family
CMMOHOCF_00792 4.5e-127 S Bacterial protein of unknown function (DUF881)
CMMOHOCF_00793 6.9e-67 crgA D Involved in cell division
CMMOHOCF_00794 1.7e-254 L ribosomal rna small subunit methyltransferase
CMMOHOCF_00795 2e-76 L HTH-like domain
CMMOHOCF_00796 7.1e-144 gluP 3.4.21.105 S Rhomboid family
CMMOHOCF_00797 3.4e-35
CMMOHOCF_00798 1.9e-155 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
CMMOHOCF_00799 3.7e-105 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
CMMOHOCF_00800 6.3e-77 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
CMMOHOCF_00801 3.3e-43 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
CMMOHOCF_00802 2e-73 I Sterol carrier protein
CMMOHOCF_00803 8.7e-46 L Transposase
CMMOHOCF_00804 2.4e-43 L IstB-like ATP binding protein
CMMOHOCF_00805 1.7e-42 tnp7109-21 L Integrase core domain
CMMOHOCF_00806 5e-154 cysB 4.2.1.22 EGP Major facilitator Superfamily
CMMOHOCF_00807 6.9e-54 cysB 4.2.1.22 EGP Major facilitator Superfamily
CMMOHOCF_00808 1.5e-33 cysB 4.2.1.22 EGP Major facilitator Superfamily
CMMOHOCF_00809 4.5e-12
CMMOHOCF_00811 2.1e-29 M Glycosyl hydrolases family 25
CMMOHOCF_00812 7.2e-141 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
CMMOHOCF_00813 3.2e-135 3.8.1.2 S Haloacid dehalogenase-like hydrolase
CMMOHOCF_00814 4.3e-183 fmt 2.1.1.176, 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
CMMOHOCF_00815 6.6e-139 serB 3.1.3.3 E haloacid dehalogenase-like hydrolase
CMMOHOCF_00816 2.1e-197 arc O AAA ATPase forming ring-shaped complexes
CMMOHOCF_00817 1.3e-105 arc O AAA ATPase forming ring-shaped complexes
CMMOHOCF_00818 4.2e-51 dop 3.5.1.119, 6.3.1.19 S Pup-ligase protein
CMMOHOCF_00819 2.6e-252 dop 3.5.1.119, 6.3.1.19 S Pup-ligase protein
CMMOHOCF_00820 2e-157 hisN 3.1.3.25 G Inositol monophosphatase family
CMMOHOCF_00821 1.6e-10 pup S Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation
CMMOHOCF_00822 4.7e-188 pafA 6.3.1.19 O Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine
CMMOHOCF_00823 7.8e-70 pafA 6.3.1.19 O Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine
CMMOHOCF_00824 8.1e-42 hup L Belongs to the bacterial histone-like protein family
CMMOHOCF_00825 0.0 S Lysylphosphatidylglycerol synthase TM region
CMMOHOCF_00826 3.4e-122 S Lysylphosphatidylglycerol synthase TM region
CMMOHOCF_00827 1.1e-280 purB 4.3.2.2 F Adenylosuccinate lyase C-terminal
CMMOHOCF_00828 6.1e-111 S PGAP1-like protein
CMMOHOCF_00829 5.3e-134 S PGAP1-like protein
CMMOHOCF_00831 4.2e-75
CMMOHOCF_00832 3.6e-148 S von Willebrand factor (vWF) type A domain
CMMOHOCF_00833 6.8e-190 S von Willebrand factor (vWF) type A domain
CMMOHOCF_00834 1.7e-60
CMMOHOCF_00835 1.5e-92 S Protein of unknown function DUF58
CMMOHOCF_00836 1.1e-81 moxR S ATPase family associated with various cellular activities (AAA)
CMMOHOCF_00837 9.9e-89 moxR S ATPase family associated with various cellular activities (AAA)
CMMOHOCF_00838 1.5e-32 3.5.1.28 M NLP P60 protein
CMMOHOCF_00839 6.5e-67 S SPP1 phage holin
CMMOHOCF_00841 3e-69
CMMOHOCF_00842 8.4e-26 L DNA integration
CMMOHOCF_00844 5.5e-57
CMMOHOCF_00846 1.4e-193 S Psort location Cytoplasmic, score
CMMOHOCF_00847 1.4e-117 NT phage tail tape measure protein
CMMOHOCF_00849 4.8e-18
CMMOHOCF_00850 1.5e-51 eae N domain, Protein
CMMOHOCF_00851 9.7e-16
CMMOHOCF_00853 1.6e-14 S Phage protein Gp19/Gp15/Gp42
CMMOHOCF_00854 4.7e-33
CMMOHOCF_00855 3.1e-12 S Phage capsid family
CMMOHOCF_00856 1e-53 S Phage capsid family
CMMOHOCF_00858 2.2e-50
CMMOHOCF_00859 2.3e-72 S Phage portal protein, SPP1 Gp6-like
CMMOHOCF_00860 2.8e-46 S Terminase
CMMOHOCF_00861 3.3e-50 S Terminase
CMMOHOCF_00862 1.2e-13
CMMOHOCF_00865 3.3e-11
CMMOHOCF_00866 2e-65 1.8.4.10, 1.8.4.8 EH sulfate reduction
CMMOHOCF_00867 7.4e-13 S Phage plasmid primase, P4 family domain protein
CMMOHOCF_00869 5.5e-101
CMMOHOCF_00873 7e-43 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
CMMOHOCF_00874 1.7e-38 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
CMMOHOCF_00875 5.3e-12 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
CMMOHOCF_00877 2.6e-107 M Bacterial capsule synthesis protein PGA_cap
CMMOHOCF_00878 3.2e-91 M Bacterial capsule synthesis protein PGA_cap
CMMOHOCF_00879 2.4e-113 yigZ 2.1.1.45, 3.4.13.9 S Uncharacterized protein family UPF0029
CMMOHOCF_00880 6.8e-69
CMMOHOCF_00881 4.9e-38 malQ 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 CBM48,GH13,GH77 G 4-alpha-glucanotransferase
CMMOHOCF_00882 8.6e-223 malQ 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 CBM48,GH13,GH77 G 4-alpha-glucanotransferase
CMMOHOCF_00883 6.1e-16 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
CMMOHOCF_00884 8.8e-68 rpsI J Belongs to the universal ribosomal protein uS9 family
CMMOHOCF_00885 6.2e-279 glgX 3.2.1.196, 3.2.1.68 CBM48,GH13 G Belongs to the glycosyl hydrolase 13 family
CMMOHOCF_00886 1.1e-120 glgX 3.2.1.196, 3.2.1.68 CBM48,GH13 G Belongs to the glycosyl hydrolase 13 family
CMMOHOCF_00887 5.8e-173 2.7.1.2 GK transcriptional repressor of nag (N-acetylglucosamine) operon K02565
CMMOHOCF_00888 1.4e-248 adhE 1.1.1.1, 1.2.1.10 C belongs to the iron- containing alcohol dehydrogenase family
CMMOHOCF_00889 1e-270 adhE 1.1.1.1, 1.2.1.10 C belongs to the iron- containing alcohol dehydrogenase family
CMMOHOCF_00890 8.7e-167 budA 4.1.1.5 H Alpha-acetolactate decarboxylase
CMMOHOCF_00891 4.2e-08 ywiC S YwiC-like protein
CMMOHOCF_00892 1.4e-18 ywiC S YwiC-like protein
CMMOHOCF_00893 5.2e-50 rpsJ J Involved in the binding of tRNA to the ribosomes
CMMOHOCF_00894 4.2e-118 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
CMMOHOCF_00895 1.8e-27 rplD J Forms part of the polypeptide exit tunnel
CMMOHOCF_00896 3.7e-41 rplD J Forms part of the polypeptide exit tunnel
CMMOHOCF_00897 2.6e-46 rplW J One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome
CMMOHOCF_00898 4.2e-155 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
CMMOHOCF_00899 3.7e-47 rpsS J Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA
CMMOHOCF_00900 4.3e-56 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
CMMOHOCF_00901 1.1e-56
CMMOHOCF_00902 1.2e-65
CMMOHOCF_00903 1.6e-103 ytlD1 2.7.1.50 P Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00904 1e-17 ytlD1 2.7.1.50 P Binding-protein-dependent transport system inner membrane component
CMMOHOCF_00905 8.6e-201 P NMT1/THI5 like
CMMOHOCF_00906 4.9e-122 S HAD hydrolase, family IA, variant 3
CMMOHOCF_00908 1.7e-254 gltX 6.1.1.17 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)
CMMOHOCF_00909 3.7e-11 gltX 6.1.1.17 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)
CMMOHOCF_00910 5.9e-93 S Domain of unknown function (DUF4143)
CMMOHOCF_00913 5.8e-252 S Calcineurin-like phosphoesterase
CMMOHOCF_00914 2.2e-138 ltbR K Transcriptional regulator, IclR family, C-terminal domain protein
CMMOHOCF_00915 5.6e-56 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
CMMOHOCF_00916 9.1e-107 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
CMMOHOCF_00917 2.5e-74 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
CMMOHOCF_00918 3.8e-133 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
CMMOHOCF_00919 0.0 snf 2.7.11.1 KL Psort location Cytoplasmic, score 8.87
CMMOHOCF_00920 0.0 snf 2.7.11.1 KL Psort location Cytoplasmic, score 8.87
CMMOHOCF_00923 5.1e-180 S CAAX protease self-immunity
CMMOHOCF_00924 1.8e-209 S Glycosyltransferase, group 2 family protein
CMMOHOCF_00925 5.7e-29 ureD O Required for maturation of urease via the functional incorporation of the urease nickel metallocenter
CMMOHOCF_00926 4.2e-80
CMMOHOCF_00927 2.6e-204 mutT 3.6.1.13, 3.6.1.55 LT Phosphoglycerate mutase family
CMMOHOCF_00928 0.0 ppk 2.7.4.1 P Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP)
CMMOHOCF_00930 8.4e-127 cpaE D bacterial-type flagellum organization
CMMOHOCF_00931 2.8e-190 cpaF U Type II IV secretion system protein
CMMOHOCF_00932 5.1e-122 U Type ii secretion system
CMMOHOCF_00933 9.2e-14 gspF NU Type II secretion system (T2SS), protein F
CMMOHOCF_00934 3.2e-15 gspF NU Type II secretion system (T2SS), protein F
CMMOHOCF_00935 1.7e-26 S Protein of unknown function (DUF4244)
CMMOHOCF_00936 6.9e-57 S TIGRFAM helicase secretion neighborhood TadE-like protein
CMMOHOCF_00937 6.4e-215 dagK 2.7.1.107 I Diacylglycerol kinase catalytic domain protein
CMMOHOCF_00938 3.3e-256 dnaX 2.7.7.7 L DNA polymerase III subunit gamma tau
CMMOHOCF_00939 3e-74 dnaX 2.7.7.7 L DNA polymerase III subunit gamma tau
CMMOHOCF_00940 3.4e-28 dnaX 2.7.7.7 L DNA polymerase III subunit gamma tau
CMMOHOCF_00941 6.7e-110 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
CMMOHOCF_00942 8.9e-131 ask 1.1.1.3, 2.7.2.4 E Amino acid kinase family
CMMOHOCF_00943 2.1e-97 askB 1.1.1.3, 2.7.2.4 E ACT domain
CMMOHOCF_00945 1.7e-212 asd 1.2.1.11, 1.2.1.12 E Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate
CMMOHOCF_00946 8.5e-105
CMMOHOCF_00947 1e-88 G Transmembrane secretion effector
CMMOHOCF_00948 2.6e-202 rfbB 4.2.1.46 M Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily
CMMOHOCF_00949 1e-49
CMMOHOCF_00950 1.7e-08
CMMOHOCF_00951 7.4e-43 3.6.1.13 L NUDIX domain
CMMOHOCF_00952 1.1e-228 glf 5.4.99.9 M UDP-galactopyranose mutase
CMMOHOCF_00953 3.9e-99 glfT 2.4.1.288 GT2 S Glycosyltransferase like family 2
CMMOHOCF_00954 5.1e-32 glfT 2.4.1.288 GT2 S Glycosyltransferase like family 2
CMMOHOCF_00955 2.7e-116 glfT 2.4.1.288 GT2 S Glycosyltransferase like family 2
CMMOHOCF_00956 1.1e-98 rgpD 3.6.3.38 GM ABC transporter, ATP-binding protein
CMMOHOCF_00957 2.9e-36 rgpD 3.6.3.38 GM ABC transporter, ATP-binding protein
CMMOHOCF_00958 3.2e-150 rgpC U Transport permease protein
CMMOHOCF_00959 3.7e-180 GM GDP-mannose 4,6 dehydratase
CMMOHOCF_00960 1e-136 ispD 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 I Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP)
CMMOHOCF_00961 7.5e-211 M LicD family
CMMOHOCF_00962 0.0 2.4.1.288 GT2 S Glycosyltransferase like family 2
CMMOHOCF_00963 3e-86 cps3I G Psort location CytoplasmicMembrane, score 9.99
CMMOHOCF_00964 2.3e-25 3.1.1.5, 3.2.1.97 GH101 E GDSL-like Lipase/Acylhydrolase family
CMMOHOCF_00965 1.1e-16 ykoT 2.4.1.83 GT2 M Glycosyl transferase family 2
CMMOHOCF_00968 2e-13
CMMOHOCF_00970 8.3e-55 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
CMMOHOCF_00971 2.5e-21 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
CMMOHOCF_00972 3.4e-71 S LytR cell envelope-related transcriptional attenuator
CMMOHOCF_00973 2.2e-44 cspA K 'Cold-shock' DNA-binding domain
CMMOHOCF_00974 1.4e-287 groL O Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions
CMMOHOCF_00975 4e-173
CMMOHOCF_00976 1.5e-244 2.7.13.3 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_00977 1e-66 cspB K 'Cold-shock' DNA-binding domain
CMMOHOCF_00978 5.7e-175 S Protein of unknown function (DUF3027)
CMMOHOCF_00979 1.4e-30 uspA T Belongs to the universal stress protein A family
CMMOHOCF_00980 8.4e-129 uspA T Belongs to the universal stress protein A family
CMMOHOCF_00981 0.0 clpC O ATPase family associated with various cellular activities (AAA)
CMMOHOCF_00982 2.5e-67 clpC O ATPase family associated with various cellular activities (AAA)
CMMOHOCF_00986 6.6e-217 3.1.26.12, 3.2.1.8 S Domain of Unknown Function (DUF349)
CMMOHOCF_00987 5.2e-142 hisS 6.1.1.21 J Histidyl-tRNA synthetase
CMMOHOCF_00988 1.3e-96 hisS 6.1.1.21 J Histidyl-tRNA synthetase
CMMOHOCF_00989 3e-81 aspS 6.1.1.12 J Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn)
CMMOHOCF_00990 2.4e-72 aspS 6.1.1.12 J Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn)
CMMOHOCF_00991 8.9e-124 aspS 6.1.1.12 J Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn)
CMMOHOCF_00992 1.2e-91 V VanZ like family
CMMOHOCF_00993 4.7e-79 V VanZ like family
CMMOHOCF_00994 2.3e-110 ycaK 1.6.5.2 S NADPH-dependent FMN reductase
CMMOHOCF_00995 1.2e-97 ypjC S Putative ABC-transporter type IV
CMMOHOCF_00996 6.6e-41
CMMOHOCF_00997 5.5e-71 3.6.4.12
CMMOHOCF_00999 1.6e-96 EGP Major facilitator Superfamily
CMMOHOCF_01000 2.2e-163 rpoC M heme binding
CMMOHOCF_01001 2.7e-75 MA20_22310 4.4.1.5 E Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily
CMMOHOCF_01002 1.3e-125
CMMOHOCF_01003 1.7e-37 S SOS response associated peptidase (SRAP)
CMMOHOCF_01004 7.9e-83 S SOS response associated peptidase (SRAP)
CMMOHOCF_01005 1.9e-75 qseC 2.7.13.3 T Histidine kinase
CMMOHOCF_01006 1.3e-184 S Acetyltransferase (GNAT) domain
CMMOHOCF_01008 1.2e-68
CMMOHOCF_01009 2.4e-43 2.7.7.1, 3.6.1.13, 3.6.1.55 F Hydrolase of X-linked nucleoside diphosphate N terminal
CMMOHOCF_01010 1.1e-15 K Transcriptional regulator
CMMOHOCF_01011 1.4e-80 MA20_25245 K FR47-like protein
CMMOHOCF_01012 4.4e-120 ydaF_1 J Acetyltransferase (GNAT) domain
CMMOHOCF_01013 1.5e-64 yeaO K Protein of unknown function, DUF488
CMMOHOCF_01014 2.5e-163 nfo 3.1.21.2 L Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin
CMMOHOCF_01015 3.9e-30 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_01016 2.9e-204 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_01017 1.3e-114 S Domain of unknown function (DUF4194)
CMMOHOCF_01018 3.9e-46 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_01019 5e-24 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_01020 7.3e-37 yjjP S Threonine/Serine exporter, ThrE
CMMOHOCF_01021 4.4e-43 yjjP S Threonine/Serine exporter, ThrE
CMMOHOCF_01022 0.0 ppc 4.1.1.31 H Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle
CMMOHOCF_01023 3.1e-94 ppc 4.1.1.31 H Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle
CMMOHOCF_01024 1e-81 yhjX EGP Major facilitator Superfamily
CMMOHOCF_01025 8.2e-115 yhjX EGP Major facilitator Superfamily
CMMOHOCF_01026 1.1e-18 yhjX EGP Major facilitator Superfamily
CMMOHOCF_01027 0.0 trxB1 1.8.1.9 C Thioredoxin domain
CMMOHOCF_01028 2.9e-107 ahpC 1.11.1.15 O C-terminal domain of 1-Cys peroxiredoxin
CMMOHOCF_01029 1.5e-80 cah 4.2.1.1 P Reversible hydration of carbon dioxide
CMMOHOCF_01030 4e-47 K helix_turn _helix lactose operon repressor
CMMOHOCF_01031 1.2e-241 ytfL P Transporter associated domain
CMMOHOCF_01032 1.4e-130 yddG EG EamA-like transporter family
CMMOHOCF_01033 7.5e-50 yddG EG EamA-like transporter family
CMMOHOCF_01034 1.9e-83 dps P Belongs to the Dps family
CMMOHOCF_01035 4e-86 S Protein of unknown function DUF45
CMMOHOCF_01036 1.3e-35 S Protein of unknown function DUF45
CMMOHOCF_01037 1.2e-138 ulaA 2.7.1.194 S PTS system sugar-specific permease component
CMMOHOCF_01038 3.2e-84 ulaA 2.7.1.194 S PTS system sugar-specific permease component
CMMOHOCF_01039 2.3e-13 ulaA 2.7.1.194 S PTS system sugar-specific permease component
CMMOHOCF_01040 3.3e-40 ulaC 2.7.1.194 G PTS system, Lactose/Cellobiose specific IIB subunit
CMMOHOCF_01041 1.6e-32 ulaC 2.7.1.194, 2.7.1.197, 2.7.1.202 G Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2
CMMOHOCF_01042 6.9e-23 ulaC 2.7.1.194, 2.7.1.197, 2.7.1.202 G Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2
CMMOHOCF_01043 1.9e-81 K helix_turn _helix lactose operon repressor
CMMOHOCF_01044 6e-97 K helix_turn _helix lactose operon repressor
CMMOHOCF_01045 2.9e-41 G Glycosyl hydrolase family 20, domain 2
CMMOHOCF_01046 2.4e-305 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
CMMOHOCF_01047 4.6e-28 S Tetratricopeptide repeat
CMMOHOCF_01048 5.7e-142 S Tetratricopeptide repeat
CMMOHOCF_01049 4.2e-31 S Tetratricopeptide repeat
CMMOHOCF_01050 1.4e-251 S Tetratricopeptide repeat
CMMOHOCF_01051 9.4e-99 S Tetratricopeptide repeat
CMMOHOCF_01052 9e-154 M 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family
CMMOHOCF_01053 1.5e-33 M 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family
CMMOHOCF_01054 2.1e-196 M 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family
CMMOHOCF_01055 4.9e-75 2.8.2.22 S Arylsulfotransferase Ig-like domain
CMMOHOCF_01056 2.3e-35 bioM P ATPases associated with a variety of cellular activities
CMMOHOCF_01057 1.8e-63 bioM P ATPases associated with a variety of cellular activities
CMMOHOCF_01058 4.8e-105 E Aminotransferase class I and II
CMMOHOCF_01059 9.5e-39 E Aminotransferase class I and II
CMMOHOCF_01060 1.5e-83 ppgK 2.7.1.2, 2.7.1.63 GK ROK family
CMMOHOCF_01061 1.3e-27 ppgK 2.7.1.2, 2.7.1.63 GK ROK family
CMMOHOCF_01062 1.1e-104 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
CMMOHOCF_01063 1.6e-60 ecfA GP ABC transporter, ATP-binding protein
CMMOHOCF_01064 8.3e-54 ecfA GP ABC transporter, ATP-binding protein
CMMOHOCF_01065 6.9e-106 ecfA GP ABC transporter, ATP-binding protein
CMMOHOCF_01066 3.2e-122 ecfA GP ABC transporter, ATP-binding protein
CMMOHOCF_01067 5.2e-257 EGP Major facilitator Superfamily
CMMOHOCF_01069 2e-124 rarA L Recombination factor protein RarA
CMMOHOCF_01070 4.4e-62 rarA L Recombination factor protein RarA
CMMOHOCF_01071 4.7e-27 rarA L Recombination factor protein RarA
CMMOHOCF_01072 8.9e-68 helY L DEAD DEAH box helicase
CMMOHOCF_01073 2.6e-172
CMMOHOCF_01074 8.7e-27 thiS 2.8.1.10 H ThiS family
CMMOHOCF_01075 9.2e-164 thiG 2.8.1.10 H Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S
CMMOHOCF_01076 0.0 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_01077 1.4e-51 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 H Protein of unknown function (DUF4012)
CMMOHOCF_01078 3.4e-52 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 H Protein of unknown function (DUF4012)
CMMOHOCF_01079 8.7e-219 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 H Protein of unknown function (DUF4012)
CMMOHOCF_01080 6.1e-116 V ABC transporter permease
CMMOHOCF_01081 1.4e-106 V ABC transporter permease
CMMOHOCF_01082 4.2e-181 V ABC transporter
CMMOHOCF_01083 4.6e-137 T HD domain
CMMOHOCF_01084 1.3e-162 S Glutamine amidotransferase domain
CMMOHOCF_01086 3.8e-244 kup P Transport of potassium into the cell
CMMOHOCF_01087 1.6e-143 kup P Transport of potassium into the cell
CMMOHOCF_01088 5.9e-185 tatD L TatD related DNase
CMMOHOCF_01089 2.5e-16 G MFS/sugar transport protein
CMMOHOCF_01090 1.2e-117 xylR 5.3.1.12 G MFS/sugar transport protein
CMMOHOCF_01091 7.2e-101 sdhA 1.3.5.1, 1.3.5.4 C Succinate dehydrogenase flavoprotein subunit
CMMOHOCF_01092 7.8e-58 pdxK 2.7.1.35 H Phosphomethylpyrimidine kinase
CMMOHOCF_01093 4.5e-94 pdxK 2.7.1.35 H Phosphomethylpyrimidine kinase
CMMOHOCF_01094 1.6e-157 S Putative ABC-transporter type IV
CMMOHOCF_01095 6.8e-232 metY 2.5.1.49 E Aminotransferase class-V
CMMOHOCF_01096 8.9e-163 V ABC transporter, ATP-binding protein
CMMOHOCF_01097 0.0 MV MacB-like periplasmic core domain
CMMOHOCF_01098 3.6e-46 MV MacB-like periplasmic core domain
CMMOHOCF_01099 0.0 phoN I PAP2 superfamily
CMMOHOCF_01100 6.1e-132 K helix_turn_helix, Lux Regulon
CMMOHOCF_01101 0.0 tcsS2 T Histidine kinase
CMMOHOCF_01102 6.7e-24 tcsS2 T Histidine kinase
CMMOHOCF_01103 3.6e-263 pip 3.4.11.5 S alpha/beta hydrolase fold
CMMOHOCF_01104 7.7e-102 proC 1.5.1.2 E Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline
CMMOHOCF_01105 3.9e-23 proC 1.5.1.2 E Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline
CMMOHOCF_01106 7.8e-11 iaaA 3.4.19.5, 3.5.1.1 E Asparaginase
CMMOHOCF_01107 3.1e-137 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)
CMMOHOCF_01108 7.8e-235 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)
CMMOHOCF_01109 8.3e-147 3.2.1.52 GH20 M Glycosyl hydrolase family 20, catalytic domain
CMMOHOCF_01110 2.5e-293 3.2.1.52 GH20 M Glycosyl hydrolase family 20, catalytic domain
CMMOHOCF_01111 1e-131 yebC K transcriptional regulatory protein
CMMOHOCF_01112 1.8e-99 ruvC 3.1.22.4 L Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group
CMMOHOCF_01114 2.3e-39 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
CMMOHOCF_01115 1.8e-201 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
CMMOHOCF_01116 2.6e-44 yajC U Preprotein translocase subunit
CMMOHOCF_01117 7.2e-101 apt 2.4.2.7 F Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis
CMMOHOCF_01118 9.6e-225 sucC 6.2.1.5 F Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit
CMMOHOCF_01119 3.1e-167 sucD 6.2.1.5 C Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit
CMMOHOCF_01120 8.1e-122
CMMOHOCF_01121 5.8e-83
CMMOHOCF_01122 1.4e-37 purH 2.1.2.3, 3.5.4.10 F Bifunctional purine biosynthesis protein PurH
CMMOHOCF_01123 1.1e-87 purH 2.1.2.3, 3.5.4.10 F Bifunctional purine biosynthesis protein PurH
CMMOHOCF_01124 2.3e-153 purH 2.1.2.3, 3.5.4.10 F Bifunctional purine biosynthesis protein PurH
CMMOHOCF_01125 5.7e-30
CMMOHOCF_01126 4.1e-103 glpF U Belongs to the MIP aquaporin (TC 1.A.8) family
CMMOHOCF_01127 6.7e-125 rluB 5.4.99.19, 5.4.99.22 J Belongs to the pseudouridine synthase RsuA family
CMMOHOCF_01128 3.3e-47 der 1.1.1.399, 1.1.1.95, 2.7.4.25 F GTPase that plays an essential role in the late steps of ribosome biogenesis
CMMOHOCF_01129 2.2e-84 uvrA3 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
CMMOHOCF_01130 9.1e-16 KLT Protein tyrosine kinase
CMMOHOCF_01131 1.5e-17 K Psort location Cytoplasmic, score
CMMOHOCF_01132 7.2e-148
CMMOHOCF_01133 6.2e-117 1.1.1.1, 1.1.1.14 C Zinc-binding dehydrogenase
CMMOHOCF_01134 1.2e-47 1.1.1.1, 1.1.1.14 C Zinc-binding dehydrogenase
CMMOHOCF_01135 9.9e-68 K MerR family regulatory protein
CMMOHOCF_01136 2.5e-124 pyrE 2.4.2.10 F Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP)
CMMOHOCF_01137 9.6e-180 pyrD 1.3.1.14 F Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily
CMMOHOCF_01138 4.6e-34 pyrK 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 C Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B
CMMOHOCF_01139 1.5e-112 pyrK 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 C Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B
CMMOHOCF_01140 3.2e-26 pyrF 2.4.2.10, 4.1.1.23 F Belongs to the OMP decarboxylase family. Type 2 subfamily
CMMOHOCF_01141 3.9e-113 pyrF 2.4.2.10, 4.1.1.23 F Belongs to the OMP decarboxylase family. Type 2 subfamily
CMMOHOCF_01142 4.7e-279 pyrC 3.5.2.3 F Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily
CMMOHOCF_01143 2e-73 pyrI 2.1.3.2 F Aspartate carbamoyltransferase regulatory chain, allosteric domain protein
CMMOHOCF_01144 9.5e-141 pyrB 2.1.3.2 F Belongs to the ATCase OTCase family
CMMOHOCF_01145 3.2e-23 pyrB 2.1.3.2 F Belongs to the ATCase OTCase family
CMMOHOCF_01146 1.9e-272 glnE 2.7.7.42, 2.7.7.89 H Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell
CMMOHOCF_01147 8.3e-238 glnE 2.7.7.42, 2.7.7.89 H Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell
CMMOHOCF_01149 9.6e-163 metF 1.5.1.20 E Methylenetetrahydrofolate reductase
CMMOHOCF_01150 1.9e-42 metE 2.1.1.14 E Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation
CMMOHOCF_01151 1.8e-147 metE 2.1.1.14 E Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation
CMMOHOCF_01152 1.1e-30 L Transposase
CMMOHOCF_01153 1.3e-17
CMMOHOCF_01154 1.8e-161
CMMOHOCF_01155 1e-24
CMMOHOCF_01156 6.7e-33 guaA 6.3.5.2 F Catalyzes the synthesis of GMP from XMP
CMMOHOCF_01157 4.5e-228 guaA 6.3.5.2 F Catalyzes the synthesis of GMP from XMP
CMMOHOCF_01158 2e-192 xfp 4.1.2.22, 4.1.2.9 G D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase
CMMOHOCF_01159 5.3e-164 xfp 4.1.2.22, 4.1.2.9 G D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase
CMMOHOCF_01160 1e-161 pit P Phosphate transporter family
CMMOHOCF_01161 1.1e-115 MA20_27875 P Protein of unknown function DUF47
CMMOHOCF_01162 6.3e-120 K helix_turn_helix, Lux Regulon
CMMOHOCF_01163 5.3e-130 T Histidine kinase
CMMOHOCF_01164 1.2e-42 pacL 3.6.3.8, 3.6.3.9 P ATPase, P-type transporting, HAD superfamily, subfamily IC
CMMOHOCF_01165 7.9e-185 V ATPases associated with a variety of cellular activities
CMMOHOCF_01166 3.8e-224 V ABC-2 family transporter protein
CMMOHOCF_01167 4.2e-251 V ABC-2 family transporter protein
CMMOHOCF_01168 2e-285 3.6.4.12 K Putative ATP-dependent DNA helicase recG C-terminal
CMMOHOCF_01169 1.1e-36 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_01171 4.3e-242 yxiO S Vacuole effluxer Atg22 like
CMMOHOCF_01172 2e-132 K helix_turn_helix, mercury resistance
CMMOHOCF_01173 2.9e-66 T Toxic component of a toxin-antitoxin (TA) module
CMMOHOCF_01174 1.9e-21 relB L RelB antitoxin
CMMOHOCF_01175 3e-74
CMMOHOCF_01176 4.8e-100 hpaIM 2.1.1.72 L Belongs to the N(4) N(6)-methyltransferase family
CMMOHOCF_01177 8.6e-21 relB L RelB antitoxin
CMMOHOCF_01178 3.9e-190 L Transposase
CMMOHOCF_01179 3.2e-33 3.4.11.5 I carboxylic ester hydrolase activity
CMMOHOCF_01180 7.3e-155 K Helix-turn-helix XRE-family like proteins
CMMOHOCF_01181 3.7e-31 K Helix-turn-helix XRE-family like proteins
CMMOHOCF_01182 3.6e-132 tam 2.1.1.144, 2.1.1.197 S Methyltransferase domain
CMMOHOCF_01187 1.6e-32
CMMOHOCF_01189 0.0 fadD 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_01190 2e-41 K Transcriptional regulator
CMMOHOCF_01192 8.7e-08 M Belongs to the glycosyl hydrolase 28 family
CMMOHOCF_01193 2.3e-15
CMMOHOCF_01194 1.6e-52
CMMOHOCF_01195 2.2e-57 V FtsX-like permease family
CMMOHOCF_01196 1.4e-22 V FtsX-like permease family
CMMOHOCF_01197 6.4e-81 V ABC transporter
CMMOHOCF_01198 9.3e-36 V ABC transporter
CMMOHOCF_01199 7e-101 K Transcriptional regulator C-terminal region
CMMOHOCF_01200 1.3e-274 aroP E aromatic amino acid transport protein AroP K03293
CMMOHOCF_01201 0.0 lacZ 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01202 1.7e-176 lacZ 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01203 2.6e-183 gmk 1.1.1.23, 2.7.4.8 S Protein of unknown function (DUF559)
CMMOHOCF_01204 4e-83 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
CMMOHOCF_01205 6.3e-92 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
CMMOHOCF_01206 3.1e-83 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
CMMOHOCF_01207 2.9e-98 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
CMMOHOCF_01208 1.4e-40 yhjE EGP Sugar (and other) transporter
CMMOHOCF_01209 1.5e-89 yhjE EGP Sugar (and other) transporter
CMMOHOCF_01210 1.8e-89 yhjE EGP Sugar (and other) transporter
CMMOHOCF_01211 4e-179 scrT G Transporter major facilitator family protein
CMMOHOCF_01212 2.3e-39 scrT G Transporter major facilitator family protein
CMMOHOCF_01213 7.1e-25 crr G pts system, glucose-specific IIABC component
CMMOHOCF_01214 7.2e-92 crr G pts system, glucose-specific IIABC component
CMMOHOCF_01215 1.7e-67 crr G pts system, glucose-specific IIABC component
CMMOHOCF_01216 2.1e-42 M Spy0128-like isopeptide containing domain
CMMOHOCF_01217 1.3e-54 M Spy0128-like isopeptide containing domain
CMMOHOCF_01220 6.5e-109 pgm 5.4.2.2 G Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II
CMMOHOCF_01221 3.6e-82 pgm 5.4.2.2 G Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II
CMMOHOCF_01222 7.7e-91 pgm 5.4.2.2 G Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II
CMMOHOCF_01223 3.8e-227 merA 1.16.1.1, 1.8.1.7 C Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
CMMOHOCF_01224 1.3e-16 merA 1.16.1.1, 1.8.1.7 C Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
CMMOHOCF_01225 2.9e-42 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01226 2e-258 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01227 2.8e-177 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01228 7e-91 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01229 1.9e-189 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01230 1.3e-138 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01231 1.6e-202 rnhA 3.1.26.4 L Endonuclease that specifically degrades the RNA of RNA- DNA hybrids
CMMOHOCF_01232 5.4e-127 rpiA 2.7.1.12, 5.3.1.6 G Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate
CMMOHOCF_01234 1.3e-102
CMMOHOCF_01235 3.5e-91
CMMOHOCF_01237 5.4e-16 XK27_00500 KL Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair
CMMOHOCF_01238 5.2e-19 XK27_00500 KL Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair
CMMOHOCF_01240 1e-27 XK27_00500 KL Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair
CMMOHOCF_01241 1.9e-197 XK27_00500 KL Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair
CMMOHOCF_01242 3.2e-39
CMMOHOCF_01243 9.3e-31
CMMOHOCF_01244 1.4e-246 U Type IV secretory system Conjugative DNA transfer
CMMOHOCF_01245 9.2e-59 U Type IV secretory system Conjugative DNA transfer
CMMOHOCF_01248 1.5e-69 K Helix-turn-helix domain protein
CMMOHOCF_01250 4.4e-51
CMMOHOCF_01251 6.2e-23
CMMOHOCF_01253 3.6e-14 U Type IV secretory system Conjugative DNA transfer
CMMOHOCF_01254 2.6e-117 isp2 3.2.1.96 M CHAP domain
CMMOHOCF_01255 2.5e-130 natA V ATPases associated with a variety of cellular activities
CMMOHOCF_01256 9.1e-64 epsG M Glycosyl transferase family 21
CMMOHOCF_01257 6e-34 epsG M Glycosyl transferase family 21
CMMOHOCF_01258 8.1e-97 epsG M Glycosyl transferase family 21
CMMOHOCF_01259 9.6e-273 S AI-2E family transporter
CMMOHOCF_01260 6.2e-160 3.4.14.13 M Glycosyltransferase like family 2
CMMOHOCF_01261 8.1e-205 fucO 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 C Iron-containing alcohol dehydrogenase
CMMOHOCF_01264 3e-18 S Domain of unknown function (DUF4190)
CMMOHOCF_01265 1.8e-42 S Domain of unknown function (DUF4190)
CMMOHOCF_01266 6.9e-200 galE 5.1.3.2 M Belongs to the NAD(P)-dependent epimerase dehydratase family
CMMOHOCF_01267 5.1e-76 trmB 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 GT30 J Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA
CMMOHOCF_01268 2.2e-78 trmB 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 GT30 J Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA
CMMOHOCF_01270 7.8e-17 S Transcription factor WhiB
CMMOHOCF_01271 1.4e-99 lacS G Psort location CytoplasmicMembrane, score 10.00
CMMOHOCF_01272 3.2e-36 lacS G Psort location CytoplasmicMembrane, score 10.00
CMMOHOCF_01273 7e-47 lacS G Psort location CytoplasmicMembrane, score 10.00
CMMOHOCF_01274 4.4e-100 lacL 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01275 2e-210 lacL 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01276 1.1e-45 lacL 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01277 1.1e-47 lysX S Uncharacterised conserved protein (DUF2156)
CMMOHOCF_01278 2.1e-26 S Putative esterase
CMMOHOCF_01279 1.2e-47 S Putative esterase
CMMOHOCF_01280 7.1e-78 S Putative esterase
CMMOHOCF_01281 0.0 XK27_08315 M Psort location CytoplasmicMembrane, score 9.26
CMMOHOCF_01282 4.6e-174 purD 6.3.4.13 F Belongs to the GARS family
CMMOHOCF_01283 6.7e-23 purD 6.3.4.13 F Belongs to the GARS family
CMMOHOCF_01284 6.8e-76 purM 6.3.3.1, 6.3.4.13 F Phosphoribosylformylglycinamidine cyclo-ligase
CMMOHOCF_01285 1.1e-55 purM 6.3.3.1, 6.3.4.13 F Phosphoribosylformylglycinamidine cyclo-ligase
CMMOHOCF_01286 4.9e-102 purF 2.4.2.14 F Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine
CMMOHOCF_01287 4.4e-90 purF 2.4.2.14 F Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine
CMMOHOCF_01288 5.4e-42 purF 2.4.2.14 F Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine
CMMOHOCF_01289 4.4e-302 umuC 2.7.7.7 L DNA-damage repair protein (DNA polymerase IV) K00961
CMMOHOCF_01290 2e-32
CMMOHOCF_01291 1.8e-68 MA20_22310 4.4.1.5 E Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily
CMMOHOCF_01292 1.7e-31 K DNA-binding transcription factor activity
CMMOHOCF_01293 7.6e-149 mug 3.2.2.28 L Uracil DNA glycosylase superfamily
CMMOHOCF_01294 9e-97 S Protein of unknown function (DUF4230)
CMMOHOCF_01295 3.7e-109
CMMOHOCF_01296 0.0 purL 6.3.5.3 F CobB/CobQ-like glutamine amidotransferase domain
CMMOHOCF_01303 5.9e-86 S KilA-N
CMMOHOCF_01304 8e-35
CMMOHOCF_01305 2.9e-68
CMMOHOCF_01306 7.1e-61
CMMOHOCF_01307 2.5e-113 int8 L Phage integrase family
CMMOHOCF_01308 1e-220 3.5.1.104 G Polysaccharide deacetylase
CMMOHOCF_01309 9.8e-194 fbaA 4.1.2.13 G Fructose-bisphosphate aldolase class-II
CMMOHOCF_01310 1.8e-68 S AAA ATPase domain
CMMOHOCF_01311 2.3e-10 V endonuclease activity
CMMOHOCF_01312 1.7e-251 purA 6.3.4.4 F Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP
CMMOHOCF_01313 2.5e-164 U Important for reducing fluoride concentration in the cell, thus reducing its toxicity
CMMOHOCF_01314 1.5e-59 crcB U Important for reducing fluoride concentration in the cell, thus reducing its toxicity
CMMOHOCF_01315 2e-107 K helix_turn _helix lactose operon repressor
CMMOHOCF_01316 4.2e-71 K helix_turn _helix lactose operon repressor
CMMOHOCF_01317 3.1e-44 gtfA 2.4.1.329, 2.4.1.7 GH13 G Domain of unknown function (DUF1964)
CMMOHOCF_01319 1.6e-150 spoU 2.1.1.185 J SpoU rRNA Methylase family
CMMOHOCF_01320 4.7e-243 glgC 2.7.7.27 H Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans
CMMOHOCF_01321 5.2e-17 yitW S Iron-sulfur cluster assembly protein
CMMOHOCF_01322 5.2e-69 yitW S Iron-sulfur cluster assembly protein
CMMOHOCF_01323 3.4e-80 iscU C SUF system FeS assembly protein, NifU family
CMMOHOCF_01324 7.7e-241 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
CMMOHOCF_01325 1e-84 sufC O FeS assembly ATPase SufC
CMMOHOCF_01326 1.6e-48 sufD O FeS assembly protein SufD
CMMOHOCF_01327 3.4e-163 sufD O FeS assembly protein SufD
CMMOHOCF_01328 4e-289 sufB O FeS assembly protein SufB
CMMOHOCF_01329 1.8e-152 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
CMMOHOCF_01330 7.7e-46 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
CMMOHOCF_01331 6.8e-08 3.4.22.70 M Sortase family
CMMOHOCF_01332 8.1e-120 K helix_turn_helix, Lux Regulon
CMMOHOCF_01333 3.2e-13
CMMOHOCF_01334 2.2e-78 aroQ 4.2.1.10 E Catalyzes a trans-dehydration via an enolate intermediate
CMMOHOCF_01335 2.7e-185 aroK 2.7.1.71, 4.2.3.4 H Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ)
CMMOHOCF_01336 2.9e-66 aroK 2.7.1.71, 4.2.3.4 H Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ)
CMMOHOCF_01337 8.8e-35 aroK 2.7.1.71, 4.2.3.4 H Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ)
CMMOHOCF_01338 2.5e-56 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
CMMOHOCF_01339 3e-54 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
CMMOHOCF_01340 9.2e-25 proB 2.7.2.11 E Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate
CMMOHOCF_01341 2.1e-174 aspC E DegT/DnrJ/EryC1/StrS aminotransferase family
CMMOHOCF_01342 4.8e-31 aspC E DegT/DnrJ/EryC1/StrS aminotransferase family
CMMOHOCF_01344 2.1e-32 secE U Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation
CMMOHOCF_01345 3.8e-81 nusG K Participates in transcription elongation, termination and antitermination
CMMOHOCF_01346 9.3e-163 plsC2 2.3.1.51 I Phosphate acyltransferases
CMMOHOCF_01347 9.1e-122 gpsA 1.1.1.94 I NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus
CMMOHOCF_01348 8.9e-23 gpsA 1.1.1.94 I NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus
CMMOHOCF_01349 1.3e-218 ddl 6.3.2.4 F Belongs to the D-alanine--D-alanine ligase family
CMMOHOCF_01350 3.7e-201 ugpQ 3.1.4.46 C Glycerophosphoryl diester phosphodiesterase family
CMMOHOCF_01351 7.4e-230 3.2.1.97 GH101 G Glycosyl hydrolase 101 beta sandwich domain
CMMOHOCF_01352 0.0 3.2.1.97 GH101 G Glycosyl hydrolase 101 beta sandwich domain
CMMOHOCF_01353 6e-169 3.2.1.97 GH101 G Glycosyl hydrolase 101 beta sandwich domain
CMMOHOCF_01354 6e-223 3.2.1.97 GH101 G Glycosyl hydrolase 101 beta sandwich domain
CMMOHOCF_01355 1.3e-38 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)
CMMOHOCF_01356 4.5e-143 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)
CMMOHOCF_01357 7.4e-175 D Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides
CMMOHOCF_01358 4e-104 3.4.22.70 M Sortase family
CMMOHOCF_01359 3.3e-80 3.4.22.70 M Sortase family
CMMOHOCF_01360 3.7e-205 M LPXTG cell wall anchor motif
CMMOHOCF_01361 1.1e-50 M LPXTG cell wall anchor motif
CMMOHOCF_01362 0.0 inlJ M domain protein
CMMOHOCF_01363 2e-18 inlJ M domain protein
CMMOHOCF_01364 3.6e-53 acyP 3.6.1.7 C Acylphosphatase
CMMOHOCF_01365 1.1e-33 yggS S Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis
CMMOHOCF_01366 4.7e-87 yggS S Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis
CMMOHOCF_01367 7.4e-166 gluQ 6.1.1.17 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_01368 1.3e-81 M Protein of unknown function (DUF3152)
CMMOHOCF_01369 1.1e-130 gla U Belongs to the MIP aquaporin (TC 1.A.8) family
CMMOHOCF_01373 1e-66 E Domain of unknown function (DUF5011)
CMMOHOCF_01374 1e-27 S Parallel beta-helix repeats
CMMOHOCF_01375 3.2e-11 rplI J Binds to the 23S rRNA
CMMOHOCF_01376 2e-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
CMMOHOCF_01377 5.4e-149 pepD E Peptidase family C69
CMMOHOCF_01378 5.5e-22 pepD E Peptidase family C69
CMMOHOCF_01379 1.3e-107 S Phosphatidylethanolamine-binding protein
CMMOHOCF_01380 1.8e-32 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01381 2e-43 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01382 1e-65 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01383 0.0 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01384 2.2e-145 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01385 1.1e-192 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01386 9.3e-11 3.2.1.51 GH95 G Glycosyl hydrolase family 65, N-terminal domain
CMMOHOCF_01387 0.0 lmrA2 V ABC transporter transmembrane region
CMMOHOCF_01388 0.0 lmrA1 V ABC transporter, ATP-binding protein
CMMOHOCF_01389 3.3e-52 ydgJ K helix_turn_helix multiple antibiotic resistance protein
CMMOHOCF_01390 3.5e-32 ydgJ K helix_turn_helix multiple antibiotic resistance protein
CMMOHOCF_01391 6.4e-42 S Protein of unknown function (DUF1778)
CMMOHOCF_01392 1.6e-23 yitI S Acetyltransferase (GNAT) domain
CMMOHOCF_01393 3.2e-189 1.1.1.65 C Aldo/keto reductase family
CMMOHOCF_01394 2.1e-164 pknL 2.7.11.1 KLT PASTA
CMMOHOCF_01395 1.8e-63 plsC2 2.3.1.51 I Phosphate acyltransferases
CMMOHOCF_01396 1.5e-109
CMMOHOCF_01397 2.6e-100 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)
CMMOHOCF_01398 4.5e-71 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)
CMMOHOCF_01399 2.6e-184 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
CMMOHOCF_01400 9.3e-293 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
CMMOHOCF_01401 6.7e-111 hpf J Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase
CMMOHOCF_01402 1.4e-07
CMMOHOCF_01403 1.1e-86 recX S Modulates RecA activity
CMMOHOCF_01404 5.7e-155 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
CMMOHOCF_01405 3.7e-40 S Protein of unknown function (DUF3046)
CMMOHOCF_01406 5.6e-47 K Helix-turn-helix XRE-family like proteins
CMMOHOCF_01407 2.5e-15 K Helix-turn-helix XRE-family like proteins
CMMOHOCF_01408 5.4e-34 cinA 3.5.1.42 S Belongs to the CinA family
CMMOHOCF_01409 1.5e-109 pgsA 2.7.8.41, 2.7.8.5 I Belongs to the CDP-alcohol phosphatidyltransferase class-I family
CMMOHOCF_01410 1.2e-266 ftsK D FtsK SpoIIIE family protein
CMMOHOCF_01411 1.7e-174 smc D Required for chromosome condensation and partitioning
CMMOHOCF_01412 3.7e-87 racD 5.1.1.13 G Belongs to the aspartate glutamate racemases family
CMMOHOCF_01413 5.2e-27 racD 5.1.1.13 G Belongs to the aspartate glutamate racemases family
CMMOHOCF_01414 5.1e-59 yxbA 6.3.1.12 S ATP-grasp
CMMOHOCF_01415 7.7e-132 yxbA 6.3.1.12 S ATP-grasp
CMMOHOCF_01416 2.2e-229 2.6.1.33 M DegT/DnrJ/EryC1/StrS aminotransferase family
CMMOHOCF_01417 2e-191 V Acetyltransferase (GNAT) domain
CMMOHOCF_01418 6.3e-296 murE 6.3.2.13, 6.3.2.7 M Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan
CMMOHOCF_01419 4.9e-126 sigH K Belongs to the sigma-70 factor family. ECF subfamily
CMMOHOCF_01420 2e-64
CMMOHOCF_01421 9.5e-08
CMMOHOCF_01422 6.3e-70 galM 5.1.3.3 G Aldose 1-epimerase
CMMOHOCF_01423 2.2e-179 ispH 1.17.7.4, 2.7.4.25 IM Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis
CMMOHOCF_01425 1.3e-81 ybaK J Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily
CMMOHOCF_01426 7.6e-103 gap 1.2.1.12 G Belongs to the glyceraldehyde-3-phosphate dehydrogenase family
CMMOHOCF_01427 2.9e-37 gap 1.2.1.12 G Belongs to the glyceraldehyde-3-phosphate dehydrogenase family
CMMOHOCF_01428 8e-134 2.7.6.2 H Thiamin pyrophosphokinase, vitamin B1 binding domain
CMMOHOCF_01430 2.1e-41 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
CMMOHOCF_01431 5.3e-48 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
CMMOHOCF_01432 8.8e-177 yvnB 3.1.4.53 S Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes
CMMOHOCF_01433 3.9e-222 yvnB 3.1.4.53 S Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes
CMMOHOCF_01435 3e-248 bga1 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01436 6e-121 bga1 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01437 7.5e-28 bga1 3.2.1.23 G Psort location Cytoplasmic, score 8.87
CMMOHOCF_01438 4.6e-111 L HNH endonuclease
CMMOHOCF_01439 6.7e-14 3.6.4.12 K Putative ATP-dependent DNA helicase recG C-terminal
CMMOHOCF_01440 2.1e-255 3.6.4.12 K Putative ATP-dependent DNA helicase recG C-terminal
CMMOHOCF_01441 1.8e-53
CMMOHOCF_01442 7.5e-135 EGP Major Facilitator Superfamily
CMMOHOCF_01443 8.9e-69 EGP Major Facilitator Superfamily
CMMOHOCF_01444 8.4e-42 EGP Major Facilitator Superfamily
CMMOHOCF_01445 2e-32 1.3.3.6, 2.3.1.39 IQ [acyl-carrier-protein] S-malonyltransferase activity
CMMOHOCF_01446 1.9e-115 K WHG domain
CMMOHOCF_01447 1.7e-70 pptA 6.3.2.14 Q 4'-phosphopantetheinyl transferase superfamily
CMMOHOCF_01449 2.9e-50
CMMOHOCF_01450 2e-20 M Belongs to the glycosyl hydrolase 30 family
CMMOHOCF_01451 2e-62 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
CMMOHOCF_01452 1.2e-184 mltG S Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation
CMMOHOCF_01453 2.1e-79 yqgF L Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA
CMMOHOCF_01454 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
CMMOHOCF_01455 1.1e-36
CMMOHOCF_01456 2.5e-135 pgm3 G Phosphoglycerate mutase family
CMMOHOCF_01457 6.6e-229 oatA I Psort location CytoplasmicMembrane, score 9.99
CMMOHOCF_01458 6.4e-132 oatA I Psort location CytoplasmicMembrane, score 9.99
CMMOHOCF_01459 1e-108 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
CMMOHOCF_01460 3.1e-71 lolD V ABC transporter
CMMOHOCF_01461 3.2e-51 V FtsX-like permease family
CMMOHOCF_01462 5e-85 V FtsX-like permease family
CMMOHOCF_01463 2.9e-11 V FtsX-like permease family
CMMOHOCF_01464 1.9e-20 V FtsX-like permease family
CMMOHOCF_01465 8.2e-64 S Domain of unknown function (DUF4418)
CMMOHOCF_01466 1.5e-301 pcrA 3.6.4.12 L DNA helicase
CMMOHOCF_01467 1.3e-190 I transferase activity, transferring acyl groups other than amino-acyl groups
CMMOHOCF_01469 1.8e-130 ispD 2.7.7.60, 4.6.1.12 I Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP)
CMMOHOCF_01470 1.9e-197 GM GDP-mannose 4,6 dehydratase
CMMOHOCF_01471 2.3e-150 GM ABC-2 type transporter
CMMOHOCF_01472 4.9e-145 tagH 3.6.3.38, 3.6.3.40 GM ABC transporter
CMMOHOCF_01473 1.1e-95 2.3.1.183 M Acetyltransferase (GNAT) domain
CMMOHOCF_01474 7.6e-114 pth 3.1.1.29 J The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis
CMMOHOCF_01475 3.1e-265 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
CMMOHOCF_01476 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
CMMOHOCF_01477 9e-297 pabB 2.6.1.85, 4.1.3.27, 4.1.3.38 EH chorismate binding enzyme
CMMOHOCF_01478 6.4e-153 pabC 2.6.1.42, 2.6.1.85, 4.1.3.38 E branched-chain-amino-acid transaminase activity
CMMOHOCF_01479 6.9e-245 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
CMMOHOCF_01480 3.2e-101 divIC D Septum formation initiator
CMMOHOCF_01481 2.6e-121 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)
CMMOHOCF_01482 7.7e-128 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)
CMMOHOCF_01484 6.3e-60 yjcF Q Acetyltransferase (GNAT) domain
CMMOHOCF_01485 6e-154 I Serine aminopeptidase, S33
CMMOHOCF_01486 2.1e-31 ybjQ S Putative heavy-metal-binding
CMMOHOCF_01488 2.1e-24 D DivIVA domain protein
CMMOHOCF_01489 3.4e-59 nudG 3.6.1.55, 3.6.1.65 L NUDIX domain
CMMOHOCF_01490 4.4e-286 KL Domain of unknown function (DUF3427)
CMMOHOCF_01491 1.5e-310 KL Domain of unknown function (DUF3427)
CMMOHOCF_01493 2.1e-196 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
CMMOHOCF_01495 2.6e-103
CMMOHOCF_01496 2e-164 yicL EG EamA-like transporter family
CMMOHOCF_01497 1.9e-158 pldB 3.1.1.5 I Serine aminopeptidase, S33
CMMOHOCF_01498 8.2e-37 pldB 3.1.1.5 I Serine aminopeptidase, S33
CMMOHOCF_01499 0.0 helY L DEAD DEAH box helicase
CMMOHOCF_01500 3e-62 rbpA K Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters
CMMOHOCF_01501 2e-20 pgp 3.1.3.18 S HAD-hyrolase-like
CMMOHOCF_01502 2e-27 pgp 3.1.3.18 S HAD-hyrolase-like
CMMOHOCF_01504 1.9e-62
CMMOHOCF_01505 2.8e-64 K helix_turn_helix, mercury resistance
CMMOHOCF_01506 9.6e-74 garA T Inner membrane component of T3SS, cytoplasmic domain
CMMOHOCF_01507 3.6e-110 S Bacterial protein of unknown function (DUF881)
CMMOHOCF_01508 2.6e-31 sbp S Protein of unknown function (DUF1290)
CMMOHOCF_01509 7e-47 S Bacterial protein of unknown function (DUF881)
CMMOHOCF_01510 3.3e-100 S Bacterial protein of unknown function (DUF881)
CMMOHOCF_01511 1.8e-116 pgsA 2.7.8.41, 2.7.8.5 I Belongs to the CDP-alcohol phosphatidyltransferase class-I family
CMMOHOCF_01512 1.8e-156 hisG 2.4.2.17 F ATP phosphoribosyltransferase
CMMOHOCF_01513 6.4e-41 hisE 3.5.4.19, 3.6.1.31, 5.3.1.16 E Phosphoribosyl-ATP pyrophosphohydrolase
CMMOHOCF_01514 6.3e-101 rpe 5.1.3.1 G Ribulose-phosphate 3-epimerase
CMMOHOCF_01515 4.2e-55 lgt 2.1.1.199 M Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins
CMMOHOCF_01516 3.8e-78 lgt 2.1.1.199 M Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins
CMMOHOCF_01517 1.3e-162 trpA 4.2.1.20 E The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate
CMMOHOCF_01518 1e-15 trpB 4.1.1.48, 4.2.1.20 E The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine
CMMOHOCF_01519 1.2e-62 trpB 4.1.1.48, 4.2.1.20 E The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine
CMMOHOCF_01520 1.8e-221 trpB 4.1.1.48, 4.2.1.20 E The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine
CMMOHOCF_01521 4.4e-87 yjjP S Threonine/Serine exporter, ThrE
CMMOHOCF_01522 7.9e-77 yjjP S Threonine/Serine exporter, ThrE
CMMOHOCF_01523 6.5e-180 S Amidohydrolase family
CMMOHOCF_01524 3.4e-58 gmk 1.1.1.23, 2.7.4.8 S Protein conserved in bacteria
CMMOHOCF_01525 7.5e-123 gmk 1.1.1.23, 2.7.4.8 S Protein conserved in bacteria
CMMOHOCF_01526 9.4e-203 trpS 6.1.1.2 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_01527 1.2e-37 S Protein of unknown function (DUF3073)
CMMOHOCF_01529 1.3e-88 K LytTr DNA-binding domain
CMMOHOCF_01530 2e-61 T protein histidine kinase activity
CMMOHOCF_01531 1.5e-23 rfbB 4.2.1.46 M Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily
CMMOHOCF_01532 1e-38 rfbB 4.2.1.46 M Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily
CMMOHOCF_01533 6.5e-101 rfbB 4.2.1.46 M Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily
CMMOHOCF_01534 3.5e-29 I transferase activity, transferring acyl groups other than amino-acyl groups
CMMOHOCF_01535 1.5e-241 lytC 2.1.1.197, 3.2.1.17, 3.2.1.96 M Glycosyl hydrolases family 25
CMMOHOCF_01536 6.4e-36 lytC 2.1.1.197, 3.2.1.17, 3.2.1.96 M Glycosyl hydrolases family 25
CMMOHOCF_01537 1.9e-22 yfdH 2.4.2.53 GT2 M Glycosyltransferase like family 2
CMMOHOCF_01538 3.3e-21 yfdH 2.4.2.53 GT2 M Glycosyltransferase like family 2
CMMOHOCF_01539 7.6e-35 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_01540 1e-35 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_01541 3.7e-58 guaB 1.1.1.205 F IMP dehydrogenase family protein
CMMOHOCF_01542 2.2e-123 icd 1.1.1.42 C Belongs to the isocitrate and isopropylmalate dehydrogenases family
CMMOHOCF_01543 1.9e-100 icd 1.1.1.42 C Belongs to the isocitrate and isopropylmalate dehydrogenases family
CMMOHOCF_01544 1.7e-128 G ABC transporter substrate-binding protein
CMMOHOCF_01545 3e-133 G ABC transporter substrate-binding protein
CMMOHOCF_01546 1.1e-186 fadD1 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_01547 1.3e-132 fadD1 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_01548 2.5e-65 M Peptidase family M23
CMMOHOCF_01550 1.4e-195 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
CMMOHOCF_01551 2e-93 rimI 2.3.1.128, 2.3.1.234 K FR47-like protein
CMMOHOCF_01552 3.8e-145 yeaZ 2.3.1.234 O Glycoprotease family
CMMOHOCF_01553 1.2e-111 ydiB 2.7.1.221, 5.1.1.1 S Threonylcarbamoyl adenosine biosynthesis protein TsaE
CMMOHOCF_01554 1.1e-181 holA 2.7.7.7 L DNA polymerase III delta subunit
CMMOHOCF_01555 1.5e-264 comE S Competence protein
CMMOHOCF_01556 5.3e-08 pbpB 2.7.11.1, 3.4.16.4 S PASTA domain
CMMOHOCF_01557 3e-87 gmk 1.1.1.23, 2.7.4.8 S Protein conserved in bacteria
CMMOHOCF_01558 3.9e-67 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
CMMOHOCF_01559 1.5e-171 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
CMMOHOCF_01560 1.4e-206 hisC 2.6.1.9 E Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily
CMMOHOCF_01561 3.2e-112 hisB 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 E Imidazoleglycerol-phosphate dehydratase
CMMOHOCF_01562 7.3e-27
CMMOHOCF_01563 8.2e-73
CMMOHOCF_01564 1.6e-30 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
CMMOHOCF_01565 1e-66 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
CMMOHOCF_01566 4.9e-93 hisA 5.3.1.16, 5.3.1.24 E Histidine biosynthesis protein
CMMOHOCF_01567 1.7e-28 hisA 5.3.1.16, 5.3.1.24 E Histidine biosynthesis protein
CMMOHOCF_01568 2.6e-274 S Uncharacterized protein conserved in bacteria (DUF2252)
CMMOHOCF_01569 1.1e-176 glnA2 6.3.1.2 E glutamine synthetase
CMMOHOCF_01570 1.6e-48 glnA2 6.3.1.2 E glutamine synthetase
CMMOHOCF_01571 6e-139 S Domain of unknown function (DUF5067)
CMMOHOCF_01572 6.5e-150 M Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses
CMMOHOCF_01573 9.9e-16 ddpA E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_01574 8.7e-18 ddpA E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_01575 5.6e-198 ddpA E Bacterial extracellular solute-binding proteins, family 5 Middle
CMMOHOCF_01576 6.7e-185 dppB EP Binding-protein-dependent transport system inner membrane component
CMMOHOCF_01578 7.6e-125 dppC EP Binding-protein-dependent transport system inner membrane component
CMMOHOCF_01579 2.9e-35 dppC EP Binding-protein-dependent transport system inner membrane component
CMMOHOCF_01580 2.1e-260 P Belongs to the ABC transporter superfamily
CMMOHOCF_01581 6.7e-238 pepP 3.4.11.9 E Aminopeptidase P, N-terminal domain
CMMOHOCF_01582 2.5e-32 pepP 3.4.11.9 E Aminopeptidase P, N-terminal domain
CMMOHOCF_01583 3e-74 3.6.1.55 F NUDIX domain
CMMOHOCF_01585 1.4e-282 folC 6.3.2.12, 6.3.2.17 H Mur ligase middle domain
CMMOHOCF_01586 5.7e-194 smc D Required for chromosome condensation and partitioning
CMMOHOCF_01587 8.8e-96 smc D Required for chromosome condensation and partitioning
CMMOHOCF_01588 1.1e-160 hgdC I CoA enzyme activase uncharacterised domain (DUF2229)
CMMOHOCF_01589 9.6e-49 hgdC I CoA enzyme activase uncharacterised domain (DUF2229)
CMMOHOCF_01590 1.7e-25 hgdC I CoA enzyme activase uncharacterised domain (DUF2229)
CMMOHOCF_01591 2.5e-76 hgdC I CoA enzyme activase uncharacterised domain (DUF2229)
CMMOHOCF_01593 4.3e-140 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
CMMOHOCF_01594 3.1e-131 nrdD 1.1.98.6 F Anaerobic ribonucleoside-triphosphate reductase
CMMOHOCF_01595 6.9e-36 nrdD 1.1.98.6 F Anaerobic ribonucleoside-triphosphate reductase
CMMOHOCF_01596 2e-67 nrdD 1.1.98.6 F Anaerobic ribonucleoside-triphosphate reductase
CMMOHOCF_01597 3.1e-18 nrdD 1.1.98.6 F Anaerobic ribonucleoside-triphosphate reductase
CMMOHOCF_01598 6.2e-56 nrdD 1.1.98.6 F Anaerobic ribonucleoside-triphosphate reductase
CMMOHOCF_01599 1.1e-272 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
CMMOHOCF_01600 7.8e-43 xseB 3.1.11.6 L Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides
CMMOHOCF_01601 6.6e-159 S Endonuclease/Exonuclease/phosphatase family
CMMOHOCF_01603 2.8e-182 iunH1 3.2.2.1 F Inosine-uridine preferring nucleoside hydrolase
CMMOHOCF_01604 2.8e-76 cdr OP Sulfurtransferase TusA
CMMOHOCF_01605 9.7e-76 yjjK S ATP-binding cassette protein, ChvD family
CMMOHOCF_01606 4.6e-212 yjjK S ATP-binding cassette protein, ChvD family
CMMOHOCF_01607 1.2e-35 M domain, Protein
CMMOHOCF_01608 7.9e-116 M domain, Protein
CMMOHOCF_01609 2e-126
CMMOHOCF_01610 4.4e-115 pcp 3.4.19.3 O Removes 5-oxoproline from various penultimate amino acid residues except L-proline
CMMOHOCF_01611 5e-13 S Protein of unknown function (DUF979)
CMMOHOCF_01612 6.6e-34 S DUF218 domain
CMMOHOCF_01613 8.2e-57 S DUF218 domain
CMMOHOCF_01615 1.4e-18 S Pyridoxamine 5'-phosphate oxidase
CMMOHOCF_01616 1.2e-85 S Pyridoxamine 5'-phosphate oxidase
CMMOHOCF_01617 8e-129 I alpha/beta hydrolase fold
CMMOHOCF_01618 3.7e-16 EGP Major facilitator Superfamily
CMMOHOCF_01619 3.5e-299 S ATPases associated with a variety of cellular activities
CMMOHOCF_01620 1.5e-35 pepN 3.4.11.2 E Peptidase family M1 domain
CMMOHOCF_01621 2.8e-186 O Subtilase family
CMMOHOCF_01622 7.2e-58 O Subtilase family
CMMOHOCF_01623 3.7e-39 glmM 5.4.2.10 G Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate
CMMOHOCF_01624 1.9e-200 glmM 5.4.2.10 G Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate
CMMOHOCF_01625 2.1e-105 def 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
CMMOHOCF_01626 9.7e-127 S zinc finger
CMMOHOCF_01627 3.1e-38 S zinc finger
CMMOHOCF_01628 5.8e-68 S zinc finger
CMMOHOCF_01629 1.5e-112 vsr L May nick specific sequences that contain T G mispairs resulting from m5C-deamination
CMMOHOCF_01630 3.5e-61 aspB E Aminotransferase class-V
CMMOHOCF_01631 1.5e-157 aspB E Aminotransferase class-V
CMMOHOCF_01632 1.4e-21 ppx 3.6.1.11, 3.6.1.40 FP Ppx/GppA phosphatase family
CMMOHOCF_01633 5.4e-71 ppx 3.6.1.11, 3.6.1.40 FP Ppx/GppA phosphatase family
CMMOHOCF_01634 1e-131 tmp1 S Domain of unknown function (DUF4391)
CMMOHOCF_01635 9.1e-36 moeB 2.7.7.80 H ThiF family
CMMOHOCF_01636 1.6e-57 moeB 2.7.7.80 H ThiF family
CMMOHOCF_01638 2.1e-57
CMMOHOCF_01639 1.3e-63 D MobA/MobL family
CMMOHOCF_01640 3.5e-42 L Transposase
CMMOHOCF_01641 2.4e-80 tnp7109-21 L Integrase core domain
CMMOHOCF_01642 1.7e-27 2.1.1.72 S Adenine-specific methyltransferase EcoRI
CMMOHOCF_01644 9e-40
CMMOHOCF_01645 3.6e-111 pncA 2.7.11.1, 3.5.1.19 Q Isochorismatase family
CMMOHOCF_01647 6.7e-90 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
CMMOHOCF_01648 1.2e-11 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
CMMOHOCF_01649 1.4e-11 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
CMMOHOCF_01651 6.3e-241 pbuX F Permease family
CMMOHOCF_01652 8.7e-107 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
CMMOHOCF_01653 1.8e-233 yrhL I Psort location CytoplasmicMembrane, score 9.99
CMMOHOCF_01654 2.5e-83 XK27_09800 I Psort location CytoplasmicMembrane, score 9.99
CMMOHOCF_01655 1.9e-37 pcrA 3.6.4.12 L DNA helicase
CMMOHOCF_01656 7.4e-48 pcrA 3.6.4.12 L DNA helicase
CMMOHOCF_01657 0.0 dnaK O Heat shock 70 kDa protein
CMMOHOCF_01658 6.7e-09 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
CMMOHOCF_01659 6.3e-33 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
CMMOHOCF_01660 1.4e-173 dnaJ1 O DnaJ molecular chaperone homology domain
CMMOHOCF_01661 1.2e-86 hspR K transcriptional regulator, MerR family
CMMOHOCF_01662 0.0 3.2.1.18, 3.2.1.51 GH29,GH33 G BNR repeat-like domain
CMMOHOCF_01663 2.2e-224 3.2.1.18, 3.2.1.51 GH29,GH33 G BNR Asp-box repeat
CMMOHOCF_01664 3.2e-270 3.2.1.18, 3.2.1.51 GH29,GH33 G BNR repeat-like domain
CMMOHOCF_01665 1.5e-155 3.2.1.18, 3.2.1.51 GH29,GH33 G BNR Asp-box repeat
CMMOHOCF_01666 4.1e-17 3.2.1.52, 3.2.1.83 GH16,GH20 G hydrolase family 20, catalytic
CMMOHOCF_01667 3.5e-89 3.2.1.52, 3.2.1.83 GH16,GH20 G hydrolase family 20, catalytic
CMMOHOCF_01668 9.8e-223 3.2.1.52, 3.2.1.83 GH16,GH20 G hydrolase family 20, catalytic
CMMOHOCF_01669 5e-177 3.2.1.52, 3.2.1.83 GH16,GH20 G hydrolase family 20, catalytic
CMMOHOCF_01670 3.9e-45 tesB I Thioesterase-like superfamily
CMMOHOCF_01671 6.7e-110 tesB I Thioesterase-like superfamily
CMMOHOCF_01672 1.9e-76 S Protein of unknown function (DUF3180)
CMMOHOCF_01673 4.4e-106 folK 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 H Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin
CMMOHOCF_01674 7.7e-150 folK 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 H Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin
CMMOHOCF_01675 4.9e-135 folP 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 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
CMMOHOCF_01676 1e-38 folE 2.7.6.3, 3.5.4.16 H GTP cyclohydrolase
CMMOHOCF_01677 1.1e-49 folE 2.7.6.3, 3.5.4.16 H GTP cyclohydrolase
CMMOHOCF_01678 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
CMMOHOCF_01679 9.4e-98 hpt 2.4.2.8, 6.3.4.19 F Belongs to the purine pyrimidine phosphoribosyltransferase family
CMMOHOCF_01680 1.5e-129 tilS 2.4.2.8, 6.3.4.19 J Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine
CMMOHOCF_01681 8.2e-83 yjjK S ABC transporter
CMMOHOCF_01682 1.2e-81 yjjK S ABC transporter
CMMOHOCF_01683 7.4e-95 yjjK S ABC transporter
CMMOHOCF_01684 2e-58 S Protein of unknown function (DUF3039)
CMMOHOCF_01685 1.1e-72 coaD 2.7.7.3 H Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate
CMMOHOCF_01686 1.7e-95
CMMOHOCF_01687 1e-113 yceD S Uncharacterized ACR, COG1399
CMMOHOCF_01689 8.8e-82 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
CMMOHOCF_01690 2.4e-09 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
CMMOHOCF_01691 3.7e-71 ilvB 2.2.1.6 H Thiamine pyrophosphate enzyme, central domain
CMMOHOCF_01692 3.3e-32 ilvB 2.2.1.6 H Thiamine pyrophosphate enzyme, central domain
CMMOHOCF_01693 2.6e-42 ilvB 2.2.1.6 H Thiamine pyrophosphate enzyme, central domain
CMMOHOCF_01694 9.5e-100 ilvB 2.2.1.6 H Thiamine pyrophosphate enzyme, central domain
CMMOHOCF_01695 5.8e-59 ilvN 2.2.1.6 E ACT domain
CMMOHOCF_01698 5.7e-247 pncB 6.3.4.21 F Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP
CMMOHOCF_01699 3.5e-140 rph 2.7.7.56, 3.6.1.66 J Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates
CMMOHOCF_01700 7.1e-43 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
CMMOHOCF_01701 2.8e-38 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
CMMOHOCF_01702 1.5e-123 3.8.1.2 S Haloacid dehalogenase-like hydrolase
CMMOHOCF_01703 1.2e-171 cpsY K Bacterial regulatory helix-turn-helix protein, lysR family
CMMOHOCF_01704 4.7e-85 T Domain of unknown function (DUF4234)
CMMOHOCF_01705 4.2e-101 K Bacterial regulatory proteins, tetR family
CMMOHOCF_01706 3.5e-18
CMMOHOCF_01707 7.1e-17 tam 2.1.1.144, 2.1.1.197 FG trans-aconitate 2-methyltransferase activity
CMMOHOCF_01708 3.1e-26 K Helix-turn-helix
CMMOHOCF_01709 7e-225 hipA 2.7.11.1 S HipA N-terminal domain
CMMOHOCF_01710 8.1e-66 4.1.1.44 S Cupin domain
CMMOHOCF_01711 1.1e-75 S Membrane transport protein
CMMOHOCF_01712 3.6e-81 S Membrane transport protein
CMMOHOCF_01713 1.7e-93 laaE K Transcriptional regulator PadR-like family
CMMOHOCF_01714 1.2e-33 magIII L endonuclease III
CMMOHOCF_01715 1.9e-66 magIII L endonuclease III
CMMOHOCF_01716 1.6e-131 S Enoyl-(Acyl carrier protein) reductase
CMMOHOCF_01717 3.1e-204 vbsD V MatE
CMMOHOCF_01718 4.4e-269 uvrA3 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
CMMOHOCF_01719 1.1e-33 murC 6.3.2.8 M Belongs to the MurCDEF family
CMMOHOCF_01720 2.6e-92 ftsQ 6.3.2.4 D Cell division protein FtsQ
CMMOHOCF_01721 4.6e-35
CMMOHOCF_01723 1.2e-85 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
CMMOHOCF_01724 1.3e-227 G Major Facilitator Superfamily
CMMOHOCF_01725 1e-119 2.7.1.4 G pfkB family carbohydrate kinase
CMMOHOCF_01726 2.5e-26 2.7.1.4 G pfkB family carbohydrate kinase
CMMOHOCF_01727 2.5e-65 GK ROK family
CMMOHOCF_01728 1.3e-124 GK ROK family
CMMOHOCF_01729 1.2e-116 cutC P Participates in the control of copper homeostasis
CMMOHOCF_01730 1e-215 GK ROK family
CMMOHOCF_01731 6.6e-153 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
CMMOHOCF_01732 3.1e-59 nagA 3.5.1.25 G Amidohydrolase family
CMMOHOCF_01733 9e-68 nagA 3.5.1.25 G Amidohydrolase family
CMMOHOCF_01734 2.7e-133 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
CMMOHOCF_01735 4.3e-95 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
CMMOHOCF_01736 2.9e-34 S Endonuclease/Exonuclease/phosphatase family
CMMOHOCF_01737 3e-87 S Endonuclease/Exonuclease/phosphatase family
CMMOHOCF_01738 2.2e-93 argO S LysE type translocator
CMMOHOCF_01739 2.9e-295 ydfD EK Alanine-glyoxylate amino-transferase
CMMOHOCF_01740 1e-54 rpsP J Belongs to the bacterial ribosomal protein bS16 family
CMMOHOCF_01741 1.8e-34 CP_0960 S Belongs to the UPF0109 family
CMMOHOCF_01742 7.6e-106 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
CMMOHOCF_01743 1.4e-165 trmD 2.1.1.228, 4.6.1.12 J Belongs to the RNA methyltransferase TrmD family
CMMOHOCF_01744 8.9e-56 hsp20 O Hsp20/alpha crystallin family
CMMOHOCF_01745 2e-20 XK27_02070 S Nitroreductase family
CMMOHOCF_01746 4.1e-107 XK27_02070 S Nitroreductase family
CMMOHOCF_01747 2.5e-95 rsmD 2.1.1.171 L Conserved hypothetical protein 95
CMMOHOCF_01748 2.7e-186 MA20_14895 S Conserved hypothetical protein 698
CMMOHOCF_01749 2.7e-11 estB S Phospholipase/Carboxylesterase
CMMOHOCF_01750 5.2e-108 3.1.3.73 G Phosphoglycerate mutase family
CMMOHOCF_01751 1.1e-208 rutG F Permease family
CMMOHOCF_01752 1.7e-78 K AraC-like ligand binding domain
CMMOHOCF_01753 3.7e-51 IQ oxidoreductase activity
CMMOHOCF_01754 4.2e-136 ybbM V Uncharacterised protein family (UPF0014)
CMMOHOCF_01755 8.9e-81 ybbL V ATPases associated with a variety of cellular activities
CMMOHOCF_01756 1.1e-43 ybbL V ATPases associated with a variety of cellular activities
CMMOHOCF_01757 4.5e-94 IV02_28330 2.1.1.185, 2.1.1.34 J Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
CMMOHOCF_01758 4.6e-63 pheS 6.1.1.20 J Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily
CMMOHOCF_01759 1.4e-129 pheS 6.1.1.20 J Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily
CMMOHOCF_01760 0.0 pheT 6.1.1.20 J Phenylalanyl-tRNA synthetase beta
CMMOHOCF_01761 1.1e-43 adh3 C Zinc-binding dehydrogenase
CMMOHOCF_01762 4.7e-85 purE 5.4.99.18 F Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR)
CMMOHOCF_01763 6.6e-53 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)
CMMOHOCF_01764 2.4e-135 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)
CMMOHOCF_01765 4.3e-73 zur P Belongs to the Fur family
CMMOHOCF_01766 5.8e-45
CMMOHOCF_01767 2.6e-154 S TIGRFAM TIGR03943 family protein
CMMOHOCF_01768 9.5e-113 ycgR S Predicted permease
CMMOHOCF_01769 1.7e-63 ycgR S Predicted permease
CMMOHOCF_01770 4.3e-22 J Ribosomal L32p protein family
CMMOHOCF_01771 8.2e-15 rpmJ J Ribosomal protein L36
CMMOHOCF_01772 2.2e-41 rpmE2 J Ribosomal protein L31
CMMOHOCF_01773 7.5e-49 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
CMMOHOCF_01774 5.3e-41 rpmB J Ribosomal L28 family
CMMOHOCF_01775 3.1e-136 S cobalamin synthesis protein
CMMOHOCF_01776 1.1e-161 P Zinc-uptake complex component A periplasmic
CMMOHOCF_01777 9.3e-197 lysX S Uncharacterised conserved protein (DUF2156)
CMMOHOCF_01778 1.7e-129 lysX S Uncharacterised conserved protein (DUF2156)
CMMOHOCF_01779 6.7e-48 lysX S Uncharacterised conserved protein (DUF2156)
CMMOHOCF_01780 4.6e-25 pyrD 1.3.1.14 F Dihydroorotate dehydrogenase
CMMOHOCF_01781 9.8e-255 murA 2.5.1.7 M Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine
CMMOHOCF_01782 9.6e-147 G Transmembrane secretion effector
CMMOHOCF_01783 2.4e-63 G Transmembrane secretion effector
CMMOHOCF_01784 2.1e-131 K Bacterial regulatory proteins, tetR family
CMMOHOCF_01785 2.5e-132
CMMOHOCF_01786 2.3e-72 rplK J Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors
CMMOHOCF_01787 1.1e-39 rplA J Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release
CMMOHOCF_01788 1.3e-54 rplA J Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release
CMMOHOCF_01789 9.8e-167 fkbB 5.2.1.8 M FKBP-type peptidyl-prolyl cis-trans isomerase
CMMOHOCF_01790 2.2e-188
CMMOHOCF_01791 7.9e-180
CMMOHOCF_01792 1.7e-83 trxA2 O Tetratricopeptide repeat
CMMOHOCF_01793 2.3e-50 nadE 6.3.1.5, 6.3.5.1 H Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source
CMMOHOCF_01794 2.8e-117 nadE 6.3.1.5, 6.3.5.1 H Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source
CMMOHOCF_01795 3.7e-96 nadE 6.3.1.5, 6.3.5.1 H Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source
CMMOHOCF_01796 2.8e-96 S Peptidase dimerisation domain
CMMOHOCF_01797 5.6e-42 S Peptidase dimerisation domain
CMMOHOCF_01799 2.6e-28 P ABC-type metal ion transport system permease component
CMMOHOCF_01800 3.9e-15 S Sucrose-6F-phosphate phosphohydrolase
CMMOHOCF_01801 5.8e-134 S Sucrose-6F-phosphate phosphohydrolase
CMMOHOCF_01802 9.7e-115 ppiA 5.2.1.8 G PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides
CMMOHOCF_01803 1.8e-54
CMMOHOCF_01804 3.3e-23
CMMOHOCF_01805 2.3e-98
CMMOHOCF_01806 1.6e-74
CMMOHOCF_01807 1.1e-29
CMMOHOCF_01808 9.4e-16
CMMOHOCF_01809 1.6e-11 S Helix-turn-helix domain
CMMOHOCF_01810 6.8e-152 S Helix-turn-helix domain
CMMOHOCF_01811 2.1e-41
CMMOHOCF_01812 2.6e-91 S Transcription factor WhiB
CMMOHOCF_01813 7.2e-136 rsmH 2.1.1.199 J Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA
CMMOHOCF_01814 2.7e-37 mraZ K Belongs to the MraZ family
CMMOHOCF_01815 5.7e-36 L DNA helicase
CMMOHOCF_01816 2.4e-32 L DNA helicase
CMMOHOCF_01817 2.3e-262 L DNA helicase
CMMOHOCF_01818 2.9e-229 serA 1.1.1.399, 1.1.1.95 EH D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain
CMMOHOCF_01819 4.6e-62 nrdR K Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes
CMMOHOCF_01820 3.2e-33 M Lysin motif
CMMOHOCF_01821 1e-118 lexA 3.4.21.88 K Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair
CMMOHOCF_01822 2.3e-165 czcD P Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family
CMMOHOCF_01823 4.6e-177 ldh 1.1.1.27, 1.1.1.37 C Belongs to the LDH MDH superfamily. LDH family
CMMOHOCF_01824 1e-78 hflX S GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis
CMMOHOCF_01825 1.6e-07 senX3 2.7.13.3 T His Kinase A (phosphoacceptor) domain
CMMOHOCF_01826 1.2e-86 senX3 2.7.13.3 T His Kinase A (phosphoacceptor) domain
CMMOHOCF_01827 2.5e-65 senX3 2.7.13.3 T His Kinase A (phosphoacceptor) domain
CMMOHOCF_01828 4.3e-124 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
CMMOHOCF_01829 1.2e-32 aroG 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)
CMMOHOCF_01830 4.8e-155 aroG 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)
CMMOHOCF_01831 3.6e-36 K helix_turn_helix, Arsenical Resistance Operon Repressor
CMMOHOCF_01832 1e-23 K helix_turn_helix, Arsenical Resistance Operon Repressor
CMMOHOCF_01833 4.7e-189 EGP Major facilitator Superfamily
CMMOHOCF_01834 1.7e-54 aroG 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)
CMMOHOCF_01835 2.5e-23 aroG 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)
CMMOHOCF_01836 2.8e-83 aroG 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)
CMMOHOCF_01837 7.8e-167 L Excalibur calcium-binding domain
CMMOHOCF_01838 3.5e-93 pepC 3.4.22.40 E Peptidase C1-like family
CMMOHOCF_01839 1.1e-164 pepC 3.4.22.40 E Peptidase C1-like family
CMMOHOCF_01840 2.8e-202 yhdG E aromatic amino acid transport protein AroP K03293
CMMOHOCF_01841 5.2e-53 yhdG E aromatic amino acid transport protein AroP K03293
CMMOHOCF_01842 2.9e-101 cysE 2.3.1.178 J COG1670 acetyltransferases, including N-acetylases of ribosomal proteins
CMMOHOCF_01843 2.1e-31 J Acetyltransferase (GNAT) domain
CMMOHOCF_01844 3.9e-92 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)
CMMOHOCF_01845 5.9e-90 recQ 3.6.4.12 L ATP-dependent DNA helicase RecQ
CMMOHOCF_01846 1.5e-43 recQ 3.6.4.12 L ATP-dependent DNA helicase RecQ
CMMOHOCF_01847 1.8e-74 recQ 3.6.4.12 L ATP-dependent DNA helicase RecQ
CMMOHOCF_01848 5.4e-19 metB 2.5.1.48, 4.4.1.1, 4.4.1.8 E Cys/Met metabolism PLP-dependent enzyme
CMMOHOCF_01849 3.4e-49 metB 2.5.1.48, 4.4.1.1, 4.4.1.8 E Cys/Met metabolism PLP-dependent enzyme
CMMOHOCF_01850 9.5e-109 metB 2.5.1.48, 4.4.1.1, 4.4.1.8 E Cys/Met metabolism PLP-dependent enzyme
CMMOHOCF_01851 4.9e-173 cbs 2.5.1.47, 4.2.1.22 E Pyridoxal-phosphate dependent enzyme
CMMOHOCF_01852 4.4e-109
CMMOHOCF_01853 2.4e-118 gnpA 2.4.1.211 S Lacto-N-biose phosphorylase C-terminal domain
CMMOHOCF_01854 5.2e-63 psp1 3.5.99.10 J Endoribonuclease L-PSP
CMMOHOCF_01855 5.6e-92 3.1.4.46 C Glycerophosphoryl diester phosphodiesterase family
CMMOHOCF_01856 3.7e-96 3.1.4.46 C Glycerophosphoryl diester phosphodiesterase family
CMMOHOCF_01857 6.4e-85 argS 6.1.1.19 J Arginyl-tRNA synthetase
CMMOHOCF_01858 7.9e-123 argS 6.1.1.19 J Arginyl-tRNA synthetase
CMMOHOCF_01859 5.7e-305 lysA 4.1.1.20 E Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine
CMMOHOCF_01860 1.9e-81 2.7.1.208 G phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1
CMMOHOCF_01861 1.9e-161 nagE 2.7.1.193, 2.7.1.199 G phosphotransferase system, EIIB
CMMOHOCF_01862 1.9e-94 nagE 2.7.1.193, 2.7.1.199 G phosphotransferase system, EIIB
CMMOHOCF_01863 2e-40 hom 1.1.1.3 E Homoserine dehydrogenase
CMMOHOCF_01864 6.5e-16 hom 1.1.1.3 E Homoserine dehydrogenase
CMMOHOCF_01865 1.3e-17 nucH 3.1.3.5 F 5'-nucleotidase, C-terminal domain
CMMOHOCF_01866 3.9e-286 nucH 3.1.3.5 F 5'-nucleotidase, C-terminal domain
CMMOHOCF_01867 6.9e-225 nucH 3.1.3.5 F 5'-nucleotidase, C-terminal domain
CMMOHOCF_01868 1.7e-12 nucH 3.1.3.5 F 5'-nucleotidase, C-terminal domain
CMMOHOCF_01869 2.6e-19 nucH 3.1.3.5 F 5'-nucleotidase, C-terminal domain
CMMOHOCF_01870 8.9e-48 nucH 3.1.3.5 F 5'-nucleotidase, C-terminal domain
CMMOHOCF_01871 5.6e-229 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)
CMMOHOCF_01873 6.1e-95 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_01874 5e-144 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_01875 2.1e-20 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_01876 5.6e-49 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_01877 1.4e-37 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_01878 8.8e-22 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_01879 1.7e-134 S Glycosyl transferase, family 2
CMMOHOCF_01880 3.6e-219 S Glycosyl transferase, family 2
CMMOHOCF_01881 1.2e-136
CMMOHOCF_01882 5.8e-71
CMMOHOCF_01883 6.3e-66 MA20_43655 2.7.2.8 S Zincin-like metallopeptidase
CMMOHOCF_01884 5e-72 cof 5.2.1.8 T Eukaryotic phosphomannomutase
CMMOHOCF_01885 7.5e-132 ctsW S Phosphoribosyl transferase domain
CMMOHOCF_01886 2.8e-114 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_01887 9.4e-73 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_01888 1.9e-127 T Response regulator receiver domain protein
CMMOHOCF_01889 6.1e-72 glgB 2.4.1.18 CBM48,GH13 G Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position
CMMOHOCF_01890 1.5e-269 glgB 2.4.1.18 CBM48,GH13 G Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position
CMMOHOCF_01891 2.7e-70 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_01893 1.1e-212 E Serine carboxypeptidase
CMMOHOCF_01894 1.1e-64 E Serine carboxypeptidase
CMMOHOCF_01895 4e-161 3.1.3.85, 5.4.2.11, 5.4.2.12 G Phosphoglycerate mutase family
CMMOHOCF_01896 3.7e-171 corA P CorA-like Mg2+ transporter protein
CMMOHOCF_01897 2.7e-166 ET Bacterial periplasmic substrate-binding proteins
CMMOHOCF_01898 1.6e-242 leuS 6.1.1.4 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_01899 2.8e-298 leuS 6.1.1.4 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_01900 7.4e-96 comEA 2.4.1.21 GT5 L Helix-hairpin-helix motif
CMMOHOCF_01901 9.8e-144 tcsS3 KT PspC domain
CMMOHOCF_01902 6e-83 tcsS3 KT PspC domain
CMMOHOCF_01903 2e-19 degU K helix_turn_helix, Lux Regulon
CMMOHOCF_01904 1.5e-95 degU K helix_turn_helix, Lux Regulon
CMMOHOCF_01905 1.5e-259 gnd 1.1.1.343, 1.1.1.44 H Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH
CMMOHOCF_01906 1.2e-135 pgl 3.1.1.31 G Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase
CMMOHOCF_01907 2.1e-301 zwf 1.1.1.363, 1.1.1.49 G Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone
CMMOHOCF_01908 1.7e-99
CMMOHOCF_01910 2e-67 galK 2.7.1.6, 2.7.7.12 G Belongs to the GHMP kinase family. GalK subfamily
CMMOHOCF_01911 5.9e-52 galK 2.7.1.6, 2.7.7.12 G Belongs to the GHMP kinase family. GalK subfamily
CMMOHOCF_01912 8.6e-243 EGP Sugar (and other) transporter
CMMOHOCF_01913 4.2e-43 gcvR T Belongs to the UPF0237 family
CMMOHOCF_01914 7e-176 S UPF0210 protein
CMMOHOCF_01915 1.3e-47 S UPF0210 protein
CMMOHOCF_01916 3.2e-130 S Membrane
CMMOHOCF_01917 9e-11 S Membrane
CMMOHOCF_01918 3.1e-25 S Membrane
CMMOHOCF_01919 6.3e-122 trmL 2.1.1.207 J Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily
CMMOHOCF_01920 8e-67 exsH 3.2.1.178, 3.2.1.18, 3.2.1.52 GH16,GH20,GH33 G Putative cell wall binding repeat
CMMOHOCF_01921 4.5e-39 pnp 2.7.7.8 J Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction
CMMOHOCF_01922 5.2e-41 pnp 2.7.7.8 J Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction
CMMOHOCF_01923 4.2e-245 pnp 2.7.7.8 J Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction
CMMOHOCF_01924 7.4e-40 rpsO J Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome
CMMOHOCF_01925 8.9e-119
CMMOHOCF_01926 1e-95 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01927 3e-143 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01928 2.8e-144 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01929 4.7e-110 nagH 3.2.1.35, 3.2.1.52 GH20 G beta-N-acetylglucosaminidase
CMMOHOCF_01931 6.2e-61 birA 2.7.1.33, 6.3.4.15 H Biotin/lipoate A/B protein ligase family
CMMOHOCF_01932 1.1e-43 birA 2.7.1.33, 6.3.4.15 H Biotin/lipoate A/B protein ligase family
CMMOHOCF_01933 3.4e-92 acpS 2.7.8.7, 3.2.1.52 I Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein
CMMOHOCF_01934 1.4e-172 gdhA 1.4.1.4 E Belongs to the Glu Leu Phe Val dehydrogenases family
CMMOHOCF_01935 7.8e-73 gdhA 1.4.1.4 E Belongs to the Glu Leu Phe Val dehydrogenases family
CMMOHOCF_01936 1.9e-95 gntR K FCD
CMMOHOCF_01937 2.4e-48 mscL M Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell
CMMOHOCF_01938 0.0 3.2.1.55 GH51 G arabinose metabolic process
CMMOHOCF_01941 2e-39 G Glycosyl hydrolase family 20, domain 2
CMMOHOCF_01942 1.6e-172 G Glycosyl hydrolase family 20, domain 2
CMMOHOCF_01943 4.1e-58 L Integrase core domain
CMMOHOCF_01944 8.1e-102 rfbP 2.7.8.6 M Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase
CMMOHOCF_01945 5.8e-305 EGP Major facilitator Superfamily
CMMOHOCF_01946 1.5e-223 mntH P H( )-stimulated, divalent metal cation uptake system
CMMOHOCF_01947 5.2e-59 L Protein of unknown function (DUF1524)
CMMOHOCF_01948 8.5e-147 dkgA 1.1.1.346 S Oxidoreductase, aldo keto reductase family protein
CMMOHOCF_01949 2.4e-11 E Domain of unknown function (DUF5011)
CMMOHOCF_01950 7e-176 K helix_turn _helix lactose operon repressor
CMMOHOCF_01951 4.4e-53 L Phage integrase family
CMMOHOCF_01952 9.1e-115 L Phage integrase family
CMMOHOCF_01954 3.1e-206 E Belongs to the peptidase S1B family
CMMOHOCF_01955 6e-32
CMMOHOCF_01957 1.7e-27
CMMOHOCF_01958 1.1e-56 relA 2.7.6.5, 3.1.7.2 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
CMMOHOCF_01959 3.4e-101 relA 2.7.6.5, 3.1.7.2 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
CMMOHOCF_01960 1.1e-248 relA 2.7.6.5, 3.1.7.2 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
CMMOHOCF_01961 9.5e-49 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
CMMOHOCF_01962 1.4e-47 S Domain of unknown function (DUF4193)
CMMOHOCF_01963 4.9e-101 S Protein of unknown function (DUF3071)
CMMOHOCF_01964 9.8e-231 S HipA-like C-terminal domain
CMMOHOCF_01965 3.2e-46
CMMOHOCF_01966 4.4e-60
CMMOHOCF_01967 1.1e-81
CMMOHOCF_01968 4.7e-14 topB 5.99.1.2 L DNA topoisomerase
CMMOHOCF_01969 2.9e-250 topB 5.99.1.2 L DNA topoisomerase
CMMOHOCF_01970 2e-106
CMMOHOCF_01971 3e-55
CMMOHOCF_01972 3.9e-40 S Protein of unknown function (DUF2442)
CMMOHOCF_01973 2.5e-62 S Bacterial mobilisation protein (MobC)
CMMOHOCF_01974 2.2e-81 ltrBE1 U Relaxase/Mobilisation nuclease domain
CMMOHOCF_01975 2e-73 ltrBE1 U Relaxase/Mobilisation nuclease domain
CMMOHOCF_01976 3.2e-44 pheT 6.1.1.20 J Phenylalanyl-tRNA synthetase beta
CMMOHOCF_01977 4.4e-36
CMMOHOCF_01978 6.5e-58 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
CMMOHOCF_01979 1.8e-136 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
CMMOHOCF_01980 1.3e-215 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
CMMOHOCF_01981 4.5e-87 argB 2.7.2.8 E Belongs to the acetylglutamate kinase family. ArgB subfamily
CMMOHOCF_01982 2.2e-41 argB 2.7.2.8 E Belongs to the acetylglutamate kinase family. ArgB subfamily
CMMOHOCF_01983 1.5e-17 argB 2.7.2.8 E Belongs to the acetylglutamate kinase family. ArgB subfamily
CMMOHOCF_01984 1.7e-44 argD 2.6.1.11, 2.6.1.17 E Aminotransferase class-III
CMMOHOCF_01985 2.1e-117 argD 2.6.1.11, 2.6.1.17 E Aminotransferase class-III
CMMOHOCF_01986 2.3e-123 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
CMMOHOCF_01987 8.1e-44 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
CMMOHOCF_01988 1.4e-84 argR K Regulates arginine biosynthesis genes
CMMOHOCF_01989 3.3e-36 argG 6.3.4.5 E Belongs to the argininosuccinate synthase family. Type 1 subfamily
CMMOHOCF_01990 1.1e-107 argG 6.3.4.5 E Belongs to the argininosuccinate synthase family. Type 1 subfamily
CMMOHOCF_01991 2.7e-51 argG 6.3.4.5 E Belongs to the argininosuccinate synthase family. Type 1 subfamily
CMMOHOCF_01992 1.5e-119 rimJ 2.3.1.128 J Acetyltransferase (GNAT) domain
CMMOHOCF_01993 1.3e-71
CMMOHOCF_01994 6.3e-58
CMMOHOCF_01995 1.5e-46 groS O Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter
CMMOHOCF_01996 5.1e-131 bla1 3.5.2.6 V Beta-lactamase enzyme family
CMMOHOCF_01997 3.3e-18 KLT Associated with various cellular activities
CMMOHOCF_01998 5.4e-27 KLT Associated with various cellular activities
CMMOHOCF_02002 1.9e-25 rpmG J Ribosomal protein L33
CMMOHOCF_02003 6.9e-215 murB 1.3.1.98 M Cell wall formation
CMMOHOCF_02004 9e-61 fdxA C 4Fe-4S binding domain
CMMOHOCF_02005 4.3e-109 dapC E Aminotransferase class I and II
CMMOHOCF_02006 2.4e-40 dapC E Aminotransferase class I and II
CMMOHOCF_02007 2.1e-48 dapC E Aminotransferase class I and II
CMMOHOCF_02008 2.3e-176 gyrA 5.99.1.3 L DNA topoisomerase (ATP-hydrolyzing)
CMMOHOCF_02009 2e-100 lhr L DEAD DEAH box helicase
CMMOHOCF_02010 6.8e-284 lhr L DEAD DEAH box helicase
CMMOHOCF_02011 3.2e-84 lhr L DEAD DEAH box helicase
CMMOHOCF_02012 5.8e-187 lhr L DEAD DEAH box helicase
CMMOHOCF_02013 4.9e-146 lhr L DEAD DEAH box helicase
CMMOHOCF_02014 1.7e-11 K Transcriptional regulator
CMMOHOCF_02015 1.1e-15 K Transcriptional regulator
CMMOHOCF_02016 8e-27 S Protein of unknown function (DUF2975)
CMMOHOCF_02017 3.7e-26 aspA 4.3.1.1 E Fumarase C C-terminus
CMMOHOCF_02018 8.2e-105 aspA 4.3.1.1 E Fumarase C C-terminus
CMMOHOCF_02019 1.1e-60 K helix_turn_helix, Lux Regulon
CMMOHOCF_02020 2.7e-15 S Aminoacyl-tRNA editing domain
CMMOHOCF_02021 1.1e-59 S Aminoacyl-tRNA editing domain
CMMOHOCF_02022 3.9e-139 gluA 3.6.3.21 E ATP-binding protein of ABC transporter for glutamate K02028
CMMOHOCF_02023 9.5e-147 gluB ET Belongs to the bacterial solute-binding protein 3 family
CMMOHOCF_02024 6.8e-111 gluC E Binding-protein-dependent transport system inner membrane component
CMMOHOCF_02025 3.9e-193 gluD E Binding-protein-dependent transport system inner membrane component
CMMOHOCF_02026 1.2e-108 2.7.4.1 S Polyphosphate kinase 2 (PPK2)
CMMOHOCF_02027 2.9e-56 2.7.4.1 S Polyphosphate kinase 2 (PPK2)
CMMOHOCF_02028 1.1e-29 L DEAD DEAH box helicase
CMMOHOCF_02029 4.8e-199 L DEAD DEAH box helicase
CMMOHOCF_02030 3.3e-08 L DEAD DEAH box helicase
CMMOHOCF_02031 8.8e-22 3.5.1.28 M NLP P60 protein
CMMOHOCF_02035 6.9e-170 htpX O Belongs to the peptidase M48B family
CMMOHOCF_02036 2.3e-168 fprA 1.18.1.2, 1.19.1.1 C Pyridine nucleotide-disulphide oxidoreductase
CMMOHOCF_02037 1.2e-27 cadA P E1-E2 ATPase
CMMOHOCF_02038 2.7e-180 cadA P E1-E2 ATPase
CMMOHOCF_02039 4.8e-25 cadA P E1-E2 ATPase
CMMOHOCF_02040 3.7e-126 cadA P E1-E2 ATPase
CMMOHOCF_02041 1.1e-211 degP O Domain present in PSD-95, Dlg, and ZO-1/2.
CMMOHOCF_02042 7.8e-144 glpR K DeoR C terminal sensor domain
CMMOHOCF_02043 1.3e-19 pyrD 1.3.1.14, 1.3.5.2, 1.3.98.1 F Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor
CMMOHOCF_02044 1.7e-28 pyrD 1.3.1.14, 1.3.5.2, 1.3.98.1 F Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor
CMMOHOCF_02045 9e-71 pyrD 1.3.1.14, 1.3.5.2, 1.3.98.1 F Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor
CMMOHOCF_02046 4.5e-39 pyrD 1.3.1.14, 1.3.5.2, 1.3.98.1 F Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor
CMMOHOCF_02047 1.9e-219 namA 1.6.99.1 C NADH:flavin oxidoreductase / NADH oxidase family
CMMOHOCF_02048 2e-159 pon1 2.4.1.129, 3.4.16.4 GT51 M Transglycosylase
CMMOHOCF_02049 4.7e-161 pon1 2.4.1.129, 3.4.16.4 GT51 M Transglycosylase
CMMOHOCF_02050 6.4e-55 pon1 2.4.1.129, 3.4.16.4 GT51 M Transglycosylase
CMMOHOCF_02051 4.4e-133 glxR K helix_turn_helix, cAMP Regulatory protein
CMMOHOCF_02052 2.2e-125 lplA 6.3.1.20 H Biotin/lipoate A/B protein ligase family
CMMOHOCF_02053 2.8e-236 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
CMMOHOCF_02054 1.1e-80 rnd 3.1.13.5 J 3'-5' exonuclease
CMMOHOCF_02055 1.3e-132 rnd 3.1.13.5 J 3'-5' exonuclease
CMMOHOCF_02056 4.4e-114 S Protein of unknown function (DUF3000)
CMMOHOCF_02057 1.6e-81 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
CMMOHOCF_02058 1.3e-74 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
CMMOHOCF_02059 2.1e-225 pflB 2.3.1.54 C Pyruvate formate lyase-like
CMMOHOCF_02060 5.2e-85 pflB 2.3.1.54 C Pyruvate formate lyase-like
CMMOHOCF_02061 6.4e-40
CMMOHOCF_02062 1.2e-36 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
CMMOHOCF_02063 2e-58 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
CMMOHOCF_02064 8.3e-44 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
CMMOHOCF_02065 1.9e-177 trkB P Cation transport protein
CMMOHOCF_02066 1.8e-44 trkB P Cation transport protein
CMMOHOCF_02067 6.8e-116 trkA P TrkA-N domain
CMMOHOCF_02068 2.1e-35
CMMOHOCF_02069 3.6e-58
CMMOHOCF_02070 1e-122 tlyA 2.1.1.226, 2.1.1.227 J Ribosomal RNA large subunit methyltransferase J
CMMOHOCF_02072 8.6e-190 yutF 3.1.3.41 G Haloacid dehalogenase-like hydrolase
CMMOHOCF_02073 4.4e-133 L Tetratricopeptide repeat
CMMOHOCF_02074 1.2e-35 sdhA 1.3.5.1, 1.3.5.4 C Succinate dehydrogenase flavoprotein subunit
CMMOHOCF_02075 3.8e-30 sdhA 1.3.5.1, 1.3.5.4 C Succinate dehydrogenase flavoprotein subunit
CMMOHOCF_02076 9.7e-82 sdhA 1.3.5.1, 1.3.5.4 C Succinate dehydrogenase flavoprotein subunit
CMMOHOCF_02077 1.3e-57 ybaZ 2.1.1.63 L 6-O-methylguanine DNA methyltransferase, DNA binding domain
CMMOHOCF_02078 6.7e-284 dprA 5.99.1.2 LU DNA recombination-mediator protein A
CMMOHOCF_02079 1.2e-97 comM O Magnesium chelatase, subunit ChlI C-terminal
CMMOHOCF_02080 1.5e-12 comM O Magnesium chelatase, subunit ChlI C-terminal
CMMOHOCF_02081 3.7e-51 comM O Magnesium chelatase, subunit ChlI C-terminal
CMMOHOCF_02082 1.4e-74 yraN L Belongs to the UPF0102 family
CMMOHOCF_02083 3.7e-29 sdhB 1.3.5.1, 1.3.5.4 C 4Fe-4S dicluster domain
CMMOHOCF_02084 1.7e-90 sdhB 1.3.5.1, 1.3.5.4 C 4Fe-4S dicluster domain
CMMOHOCF_02085 1e-23 sdhB 1.3.5.1, 1.3.5.4 C 4Fe-4S dicluster domain
CMMOHOCF_02086 5.7e-118 safC S O-methyltransferase
CMMOHOCF_02087 2.9e-84 fmt2 3.2.2.10 S Belongs to the LOG family
CMMOHOCF_02088 1.2e-61 L Integrase core domain
CMMOHOCF_02090 9.5e-63 S Protein of unknown function DUF262
CMMOHOCF_02091 5.9e-56 S Protein of unknown function (DUF1524)
CMMOHOCF_02092 3.9e-13 S Protein of unknown function (DUF1524)
CMMOHOCF_02093 3.7e-117 S Protein of unknown function (DUF3800)
CMMOHOCF_02095 7.9e-23
CMMOHOCF_02096 4.3e-37 recB 3.6.4.12 L UvrD/REP helicase N-terminal domain
CMMOHOCF_02097 8.6e-17 S AAA ATPase domain
CMMOHOCF_02098 8.8e-11 L AAA ATPase domain
CMMOHOCF_02099 1.3e-298 V FtsX-like permease family
CMMOHOCF_02100 8.6e-84 rlmH 2.1.1.177 J Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA
CMMOHOCF_02101 5.1e-116 upp 2.4.2.9 F Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate
CMMOHOCF_02102 2.9e-38 E ABC transporter
CMMOHOCF_02103 1.9e-98 bcp 1.11.1.15 O Redoxin
CMMOHOCF_02104 1e-155 S Virulence factor BrkB
CMMOHOCF_02105 2.1e-41 XAC3035 O Glutaredoxin
CMMOHOCF_02106 6.1e-101 S AIPR protein
CMMOHOCF_02107 4.9e-86 L Transposase
CMMOHOCF_02108 4.7e-55 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_02109 1.1e-108 pta 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 C phosphate acetyltransferase
CMMOHOCF_02110 3.6e-35 pta 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 C phosphate acetyltransferase
CMMOHOCF_02111 5.4e-95 ackA 2.7.2.1, 2.7.2.15 H Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction
CMMOHOCF_02112 4.1e-98 ackA 2.7.2.1, 2.7.2.15 H Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction
CMMOHOCF_02113 3e-253 aroA 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
CMMOHOCF_02114 9.7e-65 3.4.13.21 E Peptidase family S51
CMMOHOCF_02115 3.1e-121 L Phage integrase family
CMMOHOCF_02117 6.7e-37 lemA S LemA family
CMMOHOCF_02118 6.3e-95 S Predicted membrane protein (DUF2207)
CMMOHOCF_02119 2.6e-234 S Predicted membrane protein (DUF2207)
CMMOHOCF_02120 1.3e-73 megL 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 E Cys/Met metabolism PLP-dependent enzyme
CMMOHOCF_02121 6.3e-128 nrdF 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
CMMOHOCF_02122 3.2e-40 nrdF 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
CMMOHOCF_02123 3.7e-69 nrdE 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
CMMOHOCF_02124 1e-44 nrdE 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
CMMOHOCF_02125 2.6e-179 nrdE 1.17.4.1 F Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
CMMOHOCF_02126 1.9e-72 nrdI F Probably involved in ribonucleotide reductase function
CMMOHOCF_02127 2.6e-94
CMMOHOCF_02128 8.2e-59 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
CMMOHOCF_02129 5.7e-73 fkbP 5.2.1.8 G Peptidyl-prolyl cis-trans
CMMOHOCF_02130 8.8e-281 sdaA 4.3.1.17 E Serine dehydratase alpha chain
CMMOHOCF_02131 1.4e-16
CMMOHOCF_02132 1.2e-21
CMMOHOCF_02133 2.3e-38
CMMOHOCF_02135 4.4e-169 ppx 3.6.1.11, 3.6.1.40 FP Ppx/GppA phosphatase family
CMMOHOCF_02136 5.8e-70 ppx2 3.6.1.11, 3.6.1.40 S Protein of unknown function (DUF501)
CMMOHOCF_02137 8e-78 lepB 3.4.21.89 U Belongs to the peptidase S26 family
CMMOHOCF_02138 1.3e-54 lepB 3.4.21.89 U Belongs to the peptidase S26 family
CMMOHOCF_02139 1e-59 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
CMMOHOCF_02140 1.1e-129 araD 4.1.2.17, 5.1.3.4 G Class II Aldolase and Adducin N-terminal domain
CMMOHOCF_02141 1.2e-171 ulaE 5.1.3.22 G Xylose isomerase-like TIM barrel
CMMOHOCF_02142 3.8e-10 2.7.1.53 G FGGY family of carbohydrate kinases, C-terminal domain
CMMOHOCF_02143 1.2e-261 2.7.1.53 G FGGY family of carbohydrate kinases, C-terminal domain
CMMOHOCF_02144 6.3e-15 gatC G PTS system sugar-specific permease component
CMMOHOCF_02145 1.6e-131 gatC G PTS system sugar-specific permease component
CMMOHOCF_02146 9.9e-23 gatC G PTS system sugar-specific permease component
CMMOHOCF_02147 3e-90 K Putative sugar-binding domain
CMMOHOCF_02148 5.8e-233 hgdC I CoA enzyme activase uncharacterised domain (DUF2229)
CMMOHOCF_02149 5.9e-39 hgdC I CoA enzyme activase uncharacterised domain (DUF2229)
CMMOHOCF_02150 1.3e-97
CMMOHOCF_02151 3.1e-38
CMMOHOCF_02152 9.4e-106 gshA 6.3.2.2 H Glutamate-cysteine ligase family 2(GCS2)
CMMOHOCF_02153 5.8e-29 gshA 6.3.2.2 H Glutamate-cysteine ligase family 2(GCS2)
CMMOHOCF_02154 3.1e-98 gshA 6.3.2.2 H Glutamate-cysteine ligase family 2(GCS2)
CMMOHOCF_02155 0.0 plyA3 M Parallel beta-helix repeats
CMMOHOCF_02156 3.2e-86 plyA3 3.2.1.18 GH33 M Parallel beta-helix repeats
CMMOHOCF_02157 1.6e-52 plyA3 3.2.1.18 GH33 M Parallel beta-helix repeats
CMMOHOCF_02158 3.9e-20 plyA3 3.2.1.18 GH33 M Parallel beta-helix repeats
CMMOHOCF_02159 1.7e-263 gyrB2 5.99.1.3 L DNA topoisomerase (ATP-hydrolyzing)
CMMOHOCF_02160 3.6e-111 gyrB2 5.99.1.3 L DNA topoisomerase (ATP-hydrolyzing)
CMMOHOCF_02161 1e-24 gyrB2 5.99.1.3 L DNA topoisomerase (ATP-hydrolyzing)
CMMOHOCF_02162 6.3e-181 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
CMMOHOCF_02163 1.7e-122
CMMOHOCF_02164 1.5e-200 crtE 2.5.1.1, 2.5.1.10, 2.5.1.29 H Belongs to the FPP GGPP synthase family
CMMOHOCF_02165 1.7e-50 pknL 2.7.11.1 KLT PASTA
CMMOHOCF_02166 2e-73 pknL 2.7.11.1 KLT PASTA
CMMOHOCF_02167 2.3e-29 M Glycosyl hydrolases family 25
CMMOHOCF_02169 1e-17 S Protein of unknown function (DUF2806)
CMMOHOCF_02171 3.5e-119 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_02172 1.7e-39 L Transposase and inactivated derivatives IS30 family
CMMOHOCF_02173 3e-73 comF S competence protein
CMMOHOCF_02174 2.1e-71 dprA LU DNA recombination-mediator protein A
CMMOHOCF_02175 3.7e-15 dprA LU DNA recombination-mediator protein A
CMMOHOCF_02176 1.6e-14 int L Phage integrase, N-terminal SAM-like domain
CMMOHOCF_02177 0.0 hrpA 3.6.4.13 L Helicase associated domain (HA2) Add an annotation
CMMOHOCF_02178 2e-250 hrpA 3.6.4.13 L Helicase associated domain (HA2) Add an annotation
CMMOHOCF_02179 9.9e-70 rsmC 2.1.1.172 J Ribosomal protein L11 methyltransferase (PrmA)
CMMOHOCF_02180 3.3e-36 rsmC 2.1.1.172 J Ribosomal protein L11 methyltransferase (PrmA)
CMMOHOCF_02181 1.2e-171
CMMOHOCF_02182 5.3e-49 hflX S GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis
CMMOHOCF_02183 2.9e-266 clpB O Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE
CMMOHOCF_02184 4.7e-137 clpB O Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE
CMMOHOCF_02185 1.8e-131 M Mechanosensitive ion channel
CMMOHOCF_02186 3.8e-119 K Bacterial regulatory proteins, tetR family
CMMOHOCF_02187 8.9e-69 MA20_36090 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_02188 3.3e-129 MA20_36090 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_02189 1.4e-231 yhdR 2.6.1.1 E Psort location Cytoplasmic, score 8.87
CMMOHOCF_02190 1.2e-103 mhpC I Alpha/beta hydrolase family
CMMOHOCF_02191 1.1e-206 nudC 1.3.7.1, 3.6.1.22 L NADH pyrophosphatase zinc ribbon domain
CMMOHOCF_02192 2.9e-85 enhA_2 S L,D-transpeptidase catalytic domain
CMMOHOCF_02193 3.1e-167 enhA_2 S L,D-transpeptidase catalytic domain
CMMOHOCF_02194 3.7e-72 gcvH E The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein
CMMOHOCF_02195 3.9e-121 S Uncharacterized conserved protein (DUF2183)
CMMOHOCF_02196 2.3e-107 S Uncharacterized conserved protein (DUF2183)
CMMOHOCF_02197 1e-66 ptrB 3.4.21.83 E Peptidase, S9A B C family, catalytic domain protein
CMMOHOCF_02198 6.9e-39 ptrB 3.4.21.83 E Peptidase, S9A B C family, catalytic domain protein
CMMOHOCF_02199 2.1e-310 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
CMMOHOCF_02200 4.7e-84 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
CMMOHOCF_02201 2e-149 truB 5.4.99.25 J Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs
CMMOHOCF_02202 5.9e-125 ribF 2.7.1.26, 2.7.7.2 H riboflavin kinase
CMMOHOCF_02203 4.2e-86 ribF 2.7.1.26, 2.7.7.2 H riboflavin kinase
CMMOHOCF_02204 5.3e-201 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
CMMOHOCF_02205 8.2e-51
CMMOHOCF_02208 2.5e-141
CMMOHOCF_02209 9.6e-22
CMMOHOCF_02210 1.5e-40 pgi 5.3.1.9 G Belongs to the GPI family
CMMOHOCF_02211 2.8e-132 pgi 5.3.1.9 G Belongs to the GPI family
CMMOHOCF_02215 5.4e-173 S Auxin Efflux Carrier
CMMOHOCF_02216 8.1e-31 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
CMMOHOCF_02217 1.7e-52 E Transglutaminase-like superfamily
CMMOHOCF_02218 1.3e-165 3.1.3.16 T Sigma factor PP2C-like phosphatases
CMMOHOCF_02219 1.4e-67 B Belongs to the OprB family
CMMOHOCF_02220 2.9e-96 T Forkhead associated domain
CMMOHOCF_02221 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
CMMOHOCF_02222 2.9e-106 rpoC 2.7.7.6 K DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates
CMMOHOCF_02223 3.9e-119 phoH T PhoH-like protein
CMMOHOCF_02224 7.4e-100 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
CMMOHOCF_02225 2.4e-251 corC S CBS domain
CMMOHOCF_02226 6.7e-156 era S An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism
CMMOHOCF_02227 4.2e-53 fadD 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_02228 1.1e-284 fadD 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_02229 8.2e-45 pntA 1.6.1.2 C NAD(P) transhydrogenase subunit alpha part 1 K00324
CMMOHOCF_02230 3.9e-51 trxA2 O Tetratricopeptide repeat
CMMOHOCF_02231 1.2e-54 cyaA 4.6.1.1 S CYTH
CMMOHOCF_02232 3.5e-51 cyaA 4.6.1.1 S CYTH
CMMOHOCF_02234 1.9e-112 K Bacterial regulatory proteins, lacI family
CMMOHOCF_02235 1.3e-33 K Bacterial regulatory proteins, lacI family
CMMOHOCF_02236 1.6e-17 4.2.1.68 M carboxylic acid catabolic process
CMMOHOCF_02237 7.9e-40 4.2.1.68 M Enolase C-terminal domain-like
CMMOHOCF_02238 6.7e-118 IQ KR domain
CMMOHOCF_02240 7.2e-299 gnpA 2.4.1.211 S Lacto-N-biose phosphorylase C-terminal domain
CMMOHOCF_02241 7.9e-46 rsmI 2.1.1.198 H Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA
CMMOHOCF_02242 5.2e-31 rsmI 2.1.1.198 H Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA
CMMOHOCF_02243 1.5e-58
CMMOHOCF_02244 3.6e-130
CMMOHOCF_02245 1.5e-212 metG 6.1.1.10 J Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation
CMMOHOCF_02246 5.9e-46 metG 6.1.1.10 J Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation
CMMOHOCF_02247 1.2e-80 K Transcriptional regulator
CMMOHOCF_02248 5.4e-42 xylR 5.3.1.12 G MFS/sugar transport protein
CMMOHOCF_02249 9.9e-62 xylR 5.3.1.12 G MFS/sugar transport protein
CMMOHOCF_02250 2.5e-46 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
CMMOHOCF_02251 8.8e-72 sepF D Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA
CMMOHOCF_02252 3.7e-42 yggT S YGGT family
CMMOHOCF_02253 9.6e-36 tccB2 V DivIVA protein
CMMOHOCF_02254 3.4e-44 3.1.21.3 V DivIVA protein
CMMOHOCF_02255 1.4e-100 lspA 3.4.23.36 MU This protein specifically catalyzes the removal of signal peptides from prolipoproteins
CMMOHOCF_02256 3.4e-177 rluD 5.4.99.23, 5.4.99.28, 5.4.99.29 J Responsible for synthesis of pseudouridine from uracil
CMMOHOCF_02258 6e-63
CMMOHOCF_02259 6.7e-56 dapD 2.3.1.117 E Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA
CMMOHOCF_02260 1.4e-31 pip S YhgE Pip domain protein
CMMOHOCF_02261 3.1e-27 pip S YhgE Pip domain protein
CMMOHOCF_02262 4.4e-21 pip S YhgE Pip domain protein
CMMOHOCF_02263 2.7e-35 pip S YhgE Pip domain protein
CMMOHOCF_02264 2.8e-62 pip S YhgE Pip domain protein
CMMOHOCF_02265 5.4e-41 pip S YhgE Pip domain protein
CMMOHOCF_02266 7.3e-27 pip S YhgE Pip domain protein
CMMOHOCF_02267 0.0 dpp4 3.4.14.5 E Dipeptidyl peptidase IV (DPP IV) N-terminal region
CMMOHOCF_02268 1e-130 fhaA T Protein of unknown function (DUF2662)
CMMOHOCF_02269 3.7e-18 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)
CMMOHOCF_02270 5e-44 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)
CMMOHOCF_02272 1.2e-263 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
CMMOHOCF_02273 9.3e-69 rsfS 2.7.7.18 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
CMMOHOCF_02274 1.5e-79 3.1.3.85, 5.4.2.11, 5.4.2.12 G Phosphoglycerate mutase family
CMMOHOCF_02275 1.3e-78 S Bacterial PH domain
CMMOHOCF_02276 1e-19 nplT 3.2.1.1 GH13 G Alpha amylase, catalytic domain
CMMOHOCF_02277 5.5e-70 nplT 3.2.1.1 GH13 G Alpha amylase, catalytic domain
CMMOHOCF_02278 2.3e-127 nplT 3.2.1.1 GH13 G Alpha amylase, catalytic domain
CMMOHOCF_02280 5.7e-24
CMMOHOCF_02281 3.5e-242 lacZ 3.2.1.23 G Domain of unknown function (DUF4982)
CMMOHOCF_02282 3.6e-233 lacZ 3.2.1.23 G Domain of unknown function (DUF4982)
CMMOHOCF_02283 8.8e-300 glyQS 6.1.1.14 J Catalyzes the attachment of glycine to tRNA(Gly)
CMMOHOCF_02284 2.1e-225 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
CMMOHOCF_02285 2e-252 thrC 4.2.3.1 E Threonine synthase N terminus
CMMOHOCF_02286 4e-122 S ABC-2 family transporter protein
CMMOHOCF_02287 1e-123 S ABC-2 family transporter protein
CMMOHOCF_02288 8.6e-142 V ATPases associated with a variety of cellular activities
CMMOHOCF_02289 1e-15 V ATPases associated with a variety of cellular activities
CMMOHOCF_02290 2.4e-23 K helix_turn_helix gluconate operon transcriptional repressor
CMMOHOCF_02291 1.6e-24 K helix_turn_helix gluconate operon transcriptional repressor
CMMOHOCF_02292 5.8e-123 S Haloacid dehalogenase-like hydrolase
CMMOHOCF_02293 5.2e-99 recN L May be involved in recombinational repair of damaged DNA
CMMOHOCF_02294 2.3e-292 yegQ O Peptidase family U32 C-terminal domain
CMMOHOCF_02295 8.7e-187 yfiH Q Multi-copper polyphenol oxidoreductase laccase
CMMOHOCF_02296 6.5e-145 ispD 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 I Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP)
CMMOHOCF_02297 8e-128 pcp 3.4.19.3 O Removes 5-oxoproline from various penultimate amino acid residues except L-proline
CMMOHOCF_02298 1.5e-30 D nuclear chromosome segregation
CMMOHOCF_02299 5e-10 D nuclear chromosome segregation
CMMOHOCF_02300 1.7e-102 clpP 3.4.21.92 O Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins
CMMOHOCF_02301 4e-90 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
CMMOHOCF_02302 1.8e-36 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
CMMOHOCF_02303 3.5e-52 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
CMMOHOCF_02306 1.9e-233 patB 4.4.1.8 E Aminotransferase, class I II
CMMOHOCF_02307 6.2e-123 nhaA P Na( ) H( ) antiporter that extrudes sodium in exchange for external protons
CMMOHOCF_02308 2.5e-93 nhaA P Na( ) H( ) antiporter that extrudes sodium in exchange for external protons
CMMOHOCF_02310 1.1e-36 rne 3.1.26.12 J Ribonuclease E/G family
CMMOHOCF_02311 2.4e-84 rne 3.1.26.12 J Ribonuclease E/G family
CMMOHOCF_02312 1.1e-160 rne 3.1.26.12 J Ribonuclease E/G family
CMMOHOCF_02313 1.2e-36 rplU J This protein binds to 23S rRNA in the presence of protein L20
CMMOHOCF_02314 3.1e-40 rpmA J Ribosomal L27 protein
CMMOHOCF_02315 1.4e-151 K Psort location Cytoplasmic, score
CMMOHOCF_02316 5.2e-30 dapB 1.17.1.8 E Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate
CMMOHOCF_02317 1.9e-161 dapA 4.3.3.7 E Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA)
CMMOHOCF_02318 0.0 rnj J An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay
CMMOHOCF_02319 7.4e-164 pepN 3.4.11.2 E Peptidase family M1 domain
CMMOHOCF_02320 1.6e-216 pepN 3.4.11.2 E Peptidase family M1 domain
CMMOHOCF_02321 6.8e-144 cobB2 K Sir2 family
CMMOHOCF_02322 2.2e-234 tdcB 4.3.1.19 E Pyridoxal-phosphate dependent enzyme
CMMOHOCF_02323 1.1e-83 tadA 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 FJ Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2)
CMMOHOCF_02324 5.4e-135 ypfH S Phospholipase/Carboxylesterase
CMMOHOCF_02325 1.2e-255 yjcE P Sodium/hydrogen exchanger family
CMMOHOCF_02326 1.9e-35 yjcE P Sodium/hydrogen exchanger family
CMMOHOCF_02329 3.7e-287 ugpA 2.7.7.9 G UTP-glucose-1-phosphate uridylyltransferase
CMMOHOCF_02330 1.3e-23 pafB K WYL domain
CMMOHOCF_02331 3.7e-152 pafB K WYL domain
CMMOHOCF_02332 1e-50 pafB K WYL domain
CMMOHOCF_02333 1.1e-47
CMMOHOCF_02334 8.7e-122 helY L DEAD DEAH box helicase
CMMOHOCF_02335 0.0 vpr M PA domain
CMMOHOCF_02336 0.0 vpr M PA domain
CMMOHOCF_02337 1.4e-41 L Psort location Cytoplasmic, score 8.87
CMMOHOCF_02338 2.4e-223
CMMOHOCF_02339 3.9e-179 S G5
CMMOHOCF_02340 3e-13 trxA 1.8.1.8, 1.8.1.9 O Belongs to the thioredoxin family
CMMOHOCF_02341 3.4e-35 trxA 1.8.1.8, 1.8.1.9 O Belongs to the thioredoxin family
CMMOHOCF_02342 1.3e-13 F Domain of unknown function (DUF4916)
CMMOHOCF_02343 9.5e-45 F Domain of unknown function (DUF4916)
CMMOHOCF_02344 0.0 hsdR 3.1.21.3 V Subunit R is required for both nuclease and ATPase activities, but not for modification
CMMOHOCF_02345 8.7e-236 hsdR 3.1.21.3 V Subunit R is required for both nuclease and ATPase activities, but not for modification
CMMOHOCF_02346 9.9e-236 K Putative DNA-binding domain
CMMOHOCF_02348 8.4e-75 yplQ S Haemolysin-III related
CMMOHOCF_02349 5.1e-57 yplQ S Haemolysin-III related
CMMOHOCF_02350 5e-131 pdtaS 2.7.13.3 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_02351 5.3e-41 pdtaS 2.7.13.3 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_02352 4.1e-89 pdtaS 2.7.13.3 T ATPase histidine kinase DNA gyrase B HSP90 domain protein
CMMOHOCF_02353 5.4e-46 whiB K Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA
CMMOHOCF_02354 1.8e-107 D FtsK/SpoIIIE family
CMMOHOCF_02355 3.2e-186 D FtsK/SpoIIIE family
CMMOHOCF_02356 9e-26 sprF 4.6.1.1 M Cell surface antigen C-terminus
CMMOHOCF_02357 2.5e-58 XK27_00515 D Cell surface antigen C-terminus
CMMOHOCF_02358 7e-180 XK27_00515 D Cell surface antigen C-terminus
CMMOHOCF_02359 3.5e-87 XK27_00515 D Cell surface antigen C-terminus
CMMOHOCF_02360 8.9e-26 sprF 4.6.1.1 M Cell surface antigen C-terminus
CMMOHOCF_02361 2.2e-79 sprF 4.6.1.1 M Cell surface antigen C-terminus
CMMOHOCF_02362 1.2e-09 phoA 3.1.3.1, 3.1.3.39 P Alkaline phosphatase homologues
CMMOHOCF_02363 2.3e-38 phoA 3.1.3.1, 3.1.3.39 P Alkaline phosphatase homologues
CMMOHOCF_02364 7e-180 phoA 3.1.3.1, 3.1.3.39 P Alkaline phosphatase homologues
CMMOHOCF_02365 2.9e-190 K Psort location Cytoplasmic, score
CMMOHOCF_02366 5.4e-08 traX S TraX protein
CMMOHOCF_02368 6.4e-53 G Phosphoglycerate mutase family
CMMOHOCF_02369 8.3e-40 G Phosphoglycerate mutase family
CMMOHOCF_02370 7.1e-64 S Protein of unknown function (DUF4235)
CMMOHOCF_02371 3e-287 pbpB 2.7.11.1, 3.4.16.4 S PASTA domain
CMMOHOCF_02372 8.6e-11 pbpB 2.7.11.1, 3.4.16.4 S PASTA domain
CMMOHOCF_02373 5.1e-278 S Calcineurin-like phosphoesterase
CMMOHOCF_02374 9.4e-152 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)
CMMOHOCF_02375 1.8e-32 lacZ 3.2.1.23 G Domain of unknown function (DUF4982)
CMMOHOCF_02376 5.5e-10 lacZ 3.2.1.23 G Domain of unknown function (DUF4982)
CMMOHOCF_02377 6.7e-46 lacZ 3.2.1.23 G Domain of unknown function (DUF4982)
CMMOHOCF_02378 0.0 lacZ 3.2.1.23 G Domain of unknown function (DUF4982)
CMMOHOCF_02379 5.3e-116 thiM 2.7.1.50 H Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ)
CMMOHOCF_02380 8.8e-34 thiM 2.7.1.50 H Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ)
CMMOHOCF_02381 1.7e-86 thiC 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 H Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction
CMMOHOCF_02382 2.8e-38 V ATPases associated with a variety of cellular activities
CMMOHOCF_02383 2.6e-56
CMMOHOCF_02384 2.7e-64
CMMOHOCF_02385 1.1e-151 maf 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 DF Maf-like protein
CMMOHOCF_02386 1.9e-48 maf 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 DF Maf-like protein
CMMOHOCF_02387 1.8e-177 thrB 2.7.1.39 E Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate
CMMOHOCF_02388 2.9e-48 hom 1.1.1.3 E Homoserine dehydrogenase
CMMOHOCF_02389 0.0 trsE U type IV secretory pathway VirB4
CMMOHOCF_02390 1e-62 S PrgI family protein
CMMOHOCF_02391 8.2e-138
CMMOHOCF_02392 8.9e-26
CMMOHOCF_02393 4e-10 K Winged helix DNA-binding domain
CMMOHOCF_02394 6.8e-53 1.1.1.122, 1.1.1.65 C Aldo/keto reductase family
CMMOHOCF_02395 3.4e-252 metY 2.5.1.49 H Psort location Cytoplasmic, score 9.98
CMMOHOCF_02396 1.6e-28 MA20_36090 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_02397 2.7e-111 MA20_36090 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_02398 2.3e-216 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)
CMMOHOCF_02399 4.6e-143 S Putative ABC-transporter type IV
CMMOHOCF_02400 1e-107 6.1.1.14 S Metal dependent phosphohydrolases with conserved 'HD' motif.
CMMOHOCF_02401 5.2e-209 argH 4.3.2.1 E argininosuccinate lyase
CMMOHOCF_02402 4.9e-39 adh3 C Zinc-binding dehydrogenase
CMMOHOCF_02403 0.0 dxs 2.2.1.7 H Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP)
CMMOHOCF_02405 1.4e-44 S Memo-like protein
CMMOHOCF_02406 1.2e-24 K Putative ATP-dependent DNA helicase recG C-terminal
CMMOHOCF_02407 7.9e-20 K Putative ATP-dependent DNA helicase recG C-terminal
CMMOHOCF_02408 1.7e-38 deaD 3.6.4.13 JKL helicase superfamily c-terminal domain
CMMOHOCF_02409 5.1e-31 EG EamA-like transporter family
CMMOHOCF_02410 2e-83 EG EamA-like transporter family
CMMOHOCF_02412 1.9e-71 V FtsX-like permease family
CMMOHOCF_02413 1.3e-60 S Sulfite exporter TauE/SafE
CMMOHOCF_02414 1e-78 yegV G pfkB family carbohydrate kinase
CMMOHOCF_02415 3.9e-26 rpmB J Ribosomal L28 family
CMMOHOCF_02416 6e-247 recG 3.6.4.12 L helicase superfamily c-terminal domain
CMMOHOCF_02417 3.3e-78 recG 3.6.4.12 L helicase superfamily c-terminal domain
CMMOHOCF_02418 5.5e-104 recG 3.6.4.12 L helicase superfamily c-terminal domain
CMMOHOCF_02419 3.6e-198 3.2.1.18 GH33 E GDSL-like Lipase/Acylhydrolase
CMMOHOCF_02420 7.7e-74 S HAD hydrolase, family IA, variant 3
CMMOHOCF_02422 2.7e-126 dedA S SNARE associated Golgi protein
CMMOHOCF_02423 4.1e-36 rsmI 2.1.1.198 H Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA
CMMOHOCF_02424 0.0 accA 6.3.4.14, 6.4.1.2, 6.4.1.3 I Carbamoyl-phosphate synthase L chain, ATP binding domain protein
CMMOHOCF_02425 2e-68 pccB I Carboxyl transferase domain
CMMOHOCF_02426 9.8e-174 alr 5.1.1.1 M Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids
CMMOHOCF_02427 1.4e-85 dgt 3.1.5.1 F Phosphohydrolase-associated domain
CMMOHOCF_02428 2.7e-137 dgt 3.1.5.1 F Phosphohydrolase-associated domain
CMMOHOCF_02429 2.1e-157 dnaG L RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication
CMMOHOCF_02430 4.6e-90 dnaG L RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication
CMMOHOCF_02431 5.8e-91 macB_2 V ATPases associated with a variety of cellular activities
CMMOHOCF_02432 4.2e-249 macB_2 V ATPases associated with a variety of cellular activities
CMMOHOCF_02433 2.4e-128 macB_2 V ATPases associated with a variety of cellular activities
CMMOHOCF_02434 2.1e-108 ctpE P E1-E2 ATPase
CMMOHOCF_02435 2.9e-265 typA T Elongation factor G C-terminus
CMMOHOCF_02436 3.5e-106 iscS1 2.8.1.7 E Aminotransferase class-V
CMMOHOCF_02437 1.7e-37 iscS1 2.8.1.7 E Aminotransferase class-V
CMMOHOCF_02438 1.2e-42 iscS1 2.8.1.7 E Aminotransferase class-V
CMMOHOCF_02439 2.4e-164 nadC 1.4.3.16, 2.4.2.19 H Quinolinate phosphoribosyl transferase, N-terminal domain
CMMOHOCF_02440 7.2e-29 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
CMMOHOCF_02441 7.4e-72 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
CMMOHOCF_02442 2.2e-105 soj D CobQ CobB MinD ParA nucleotide binding domain protein
CMMOHOCF_02443 3.3e-175 xerD D recombinase XerD
CMMOHOCF_02444 9.6e-62 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
CMMOHOCF_02445 2.1e-25 rpmI J Ribosomal protein L35
CMMOHOCF_02446 3e-90 abcT3 P ATPases associated with a variety of cellular activities
CMMOHOCF_02447 1.8e-111 mgtA 3.6.3.2 P Cation transporting ATPase, C-terminus
CMMOHOCF_02448 2e-125 mgtA 3.6.3.2 P Cation transporting ATPase, C-terminus
CMMOHOCF_02449 3.1e-245 mgtA 3.6.3.2 P Cation transporting ATPase, C-terminus
CMMOHOCF_02450 6.1e-48 rpsF J Binds together with S18 to 16S ribosomal RNA
CMMOHOCF_02451 1.5e-163 T Pfam Adenylate and Guanylate cyclase catalytic domain
CMMOHOCF_02452 3.1e-117
CMMOHOCF_02453 7.7e-15 ftsK 2.7.11.1, 2.7.7.7, 3.4.21.110, 4.2.1.2 D Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides
CMMOHOCF_02454 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
CMMOHOCF_02455 3.3e-126 murD 6.3.2.9 M Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA)
CMMOHOCF_02456 4.4e-200 mraY 2.7.8.13 M First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan
CMMOHOCF_02457 6.7e-220 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
CMMOHOCF_02458 3.2e-34
CMMOHOCF_02459 3e-71 S Domain of unknown function (DUF4357)
CMMOHOCF_02460 1.3e-26 S Domain of unknown function (DUF4357)
CMMOHOCF_02461 7.3e-21 S Domain of unknown function (DUF4357)
CMMOHOCF_02462 4.8e-169 hsdM 2.1.1.72 V modification (methylase) protein of type I restriction-modification system K03427
CMMOHOCF_02463 8.2e-282 hsdM 2.1.1.72 V modification (methylase) protein of type I restriction-modification system K03427
CMMOHOCF_02464 1.2e-111
CMMOHOCF_02465 4.8e-102
CMMOHOCF_02466 5.8e-09
CMMOHOCF_02469 2.1e-104 U Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family
CMMOHOCF_02470 8.5e-44 U Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family
CMMOHOCF_02471 2e-29 U Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family
CMMOHOCF_02472 1.1e-113 pdxS 4.3.3.6 H Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively
CMMOHOCF_02473 9e-110 pdxT 4.3.3.6 H Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS
CMMOHOCF_02476 9.4e-121 G Glycosyl hydrolases family 43
CMMOHOCF_02477 2e-43
CMMOHOCF_02478 6.7e-240
CMMOHOCF_02479 1e-36 dacB 3.4.16.4 M D-Ala-D-Ala carboxypeptidase 3 (S13) family
CMMOHOCF_02480 9.3e-209 dacB 3.4.16.4 M D-Ala-D-Ala carboxypeptidase 3 (S13) family
CMMOHOCF_02481 1.2e-61 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)
CMMOHOCF_02482 1.1e-23 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)
CMMOHOCF_02483 3.1e-217 mrcB 2.4.1.129, 3.4.16.4 GT51 M Transglycosylase
CMMOHOCF_02484 6.6e-23 mrcB 2.4.1.129, 3.4.16.4 GT51 M Transglycosylase
CMMOHOCF_02485 5e-19 fhs 1.5.1.5, 3.5.4.9, 6.3.4.3 F Formate-tetrahydrofolate ligase
CMMOHOCF_02486 1.8e-178 fhs 1.5.1.5, 3.5.4.9, 6.3.4.3 F Formate-tetrahydrofolate ligase
CMMOHOCF_02487 1.1e-61 S Macrophage migration inhibitory factor (MIF)
CMMOHOCF_02488 2.6e-97 S GtrA-like protein
CMMOHOCF_02489 3e-116 EGP Major facilitator Superfamily
CMMOHOCF_02490 1.7e-131 gyrA 5.99.1.3 L DNA topoisomerase (ATP-hydrolyzing)
CMMOHOCF_02491 1.8e-48 gyrA 5.99.1.3 L DNA topoisomerase (ATP-hydrolyzing)
CMMOHOCF_02492 5.9e-87 S Type I phosphodiesterase / nucleotide pyrophosphatase
CMMOHOCF_02493 2.2e-93 S Type I phosphodiesterase / nucleotide pyrophosphatase
CMMOHOCF_02494 1.1e-37 S Domain of unknown function (DUF4854)
CMMOHOCF_02495 3.7e-18 fahA Q Fumarylacetoacetate (FAA) hydrolase family
CMMOHOCF_02496 4.1e-118 fahA Q Fumarylacetoacetate (FAA) hydrolase family
CMMOHOCF_02497 8.1e-17 2.1.1.72 S Protein conserved in bacteria
CMMOHOCF_02498 1.1e-24 clpB O Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE
CMMOHOCF_02499 1.4e-104 clpP 3.4.21.92 O Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins
CMMOHOCF_02502 1.6e-16 clcA_2 P Voltage gated chloride channel
CMMOHOCF_02503 2.6e-77 clcA_2 P Voltage gated chloride channel
CMMOHOCF_02504 7.5e-47 clcA_2 P Voltage gated chloride channel
CMMOHOCF_02505 1e-73 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)
CMMOHOCF_02506 8.1e-145 nadD 2.7.7.18, 3.6.1.55 H Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD)
CMMOHOCF_02507 1.8e-60
CMMOHOCF_02508 6.9e-18
CMMOHOCF_02509 5.1e-81 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
CMMOHOCF_02510 4.3e-47 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
CMMOHOCF_02511 3.1e-87 ftsE D Cell division ATP-binding protein FtsE
CMMOHOCF_02512 3.7e-202 prfB J Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA
CMMOHOCF_02513 8.3e-13
CMMOHOCF_02514 1.1e-19 ftsL D Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic
CMMOHOCF_02515 1.3e-16 ftsI 3.4.16.4 M Penicillin-binding protein, transpeptidase domain protein
CMMOHOCF_02516 0.0 ftsI 3.4.16.4 M Penicillin-binding protein, transpeptidase domain protein
CMMOHOCF_02517 1.5e-70 yqeC 6.3.2.10, 6.3.2.13 M Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan
CMMOHOCF_02518 4.1e-15 yqeC 6.3.2.10, 6.3.2.13 M Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan
CMMOHOCF_02519 2.8e-38 guaA1 6.3.5.2 F Peptidase C26
CMMOHOCF_02520 4.8e-83 guaA1 6.3.5.2 F Peptidase C26
CMMOHOCF_02521 1.3e-72 cysS 6.1.1.16 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_02522 1.3e-44 cysS 6.1.1.16 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_02523 1.6e-12 cysS 6.1.1.16 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_02524 1.3e-38 cysS 6.1.1.16 J Belongs to the class-I aminoacyl-tRNA synthetase family
CMMOHOCF_02525 1.3e-41 purL 6.3.5.3 F CobB/CobQ-like glutamine amidotransferase domain
CMMOHOCF_02526 2.6e-30 purL 6.3.5.3 F CobB/CobQ-like glutamine amidotransferase domain
CMMOHOCF_02527 8.7e-61 purL 6.3.5.3 F CobB/CobQ-like glutamine amidotransferase domain
CMMOHOCF_02528 3.9e-139 purC 4.1.1.21, 4.3.2.2, 6.3.2.6 F Belongs to the SAICAR synthetase family
CMMOHOCF_02530 1.6e-215 glf 5.4.99.9 M UDP-galactopyranose mutase
CMMOHOCF_02531 1.4e-101 yplQ S Haemolysin-III related
CMMOHOCF_02532 4.7e-272 opuAB P Binding-protein-dependent transport system inner membrane component
CMMOHOCF_02533 5.2e-25 opuAB P Binding-protein-dependent transport system inner membrane component
CMMOHOCF_02534 6.5e-22 abcT3 P ATPases associated with a variety of cellular activities
CMMOHOCF_02536 9e-224 ftsW 2.4.1.227 GT28 D Belongs to the SEDS family
CMMOHOCF_02537 1.3e-33 murD 6.3.2.9 M Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA)
CMMOHOCF_02538 1.8e-51 pip S YhgE Pip domain protein
CMMOHOCF_02539 1.4e-21 pip S YhgE Pip domain protein
CMMOHOCF_02540 5.4e-189 pip S YhgE Pip domain protein
CMMOHOCF_02541 8.4e-177 V Efflux ABC transporter, permease protein
CMMOHOCF_02542 2.7e-97 mdcF S Transporter, auxin efflux carrier (AEC) family protein
CMMOHOCF_02543 1.3e-40 mdcF S Transporter, auxin efflux carrier (AEC) family protein
CMMOHOCF_02544 1.4e-43 dapE 3.5.1.18 E Peptidase dimerisation domain
CMMOHOCF_02545 9.9e-183 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
CMMOHOCF_02546 2e-40 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
CMMOHOCF_02547 1.4e-57 3.6.1.27 I PAP2 superfamily
CMMOHOCF_02548 3.9e-242 L PFAM Integrase catalytic
CMMOHOCF_02549 1.1e-33 L PFAM Integrase catalytic
CMMOHOCF_02550 4.1e-144 L IstB-like ATP binding protein
CMMOHOCF_02551 1e-126 M Parallel beta-helix repeats
CMMOHOCF_02552 2.3e-56 M Parallel beta-helix repeats
CMMOHOCF_02553 2.2e-63 M Parallel beta-helix repeats
CMMOHOCF_02554 1.4e-60 M Parallel beta-helix repeats
CMMOHOCF_02555 8.7e-167 fas 2.3.1.179 I Beta-ketoacyl synthase, C-terminal domain
CMMOHOCF_02556 2.3e-60 fas 2.3.1.179 I Beta-ketoacyl synthase, C-terminal domain
CMMOHOCF_02557 1.9e-109 rnhB 3.1.26.4 L Endonuclease that specifically degrades the RNA of RNA- DNA hybrids
CMMOHOCF_02558 8e-88 K helix_turn _helix lactose operon repressor
CMMOHOCF_02559 4.2e-33 K helix_turn _helix lactose operon repressor
CMMOHOCF_02560 3.8e-60 K helix_turn _helix lactose operon repressor
CMMOHOCF_02561 3.7e-20 ltrBE1 U Relaxase/Mobilisation nuclease domain
CMMOHOCF_02562 7.1e-122 S Protein of unknown function (DUF3801)
CMMOHOCF_02563 4.6e-58
CMMOHOCF_02564 2.6e-25
CMMOHOCF_02565 5.3e-169 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
CMMOHOCF_02566 1e-87 ptrB 3.4.21.83 E Peptidase, S9A B C family, catalytic domain protein
CMMOHOCF_02567 1.2e-15 iaaA 3.4.19.5, 3.5.1.1 E Asparaginase
CMMOHOCF_02568 5.1e-110 P NLPA lipoprotein
CMMOHOCF_02569 0.0 fadD 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_02570 2.8e-45 fadD 6.2.1.3 I AMP-binding enzyme
CMMOHOCF_02571 7.9e-50 steT E amino acid
CMMOHOCF_02572 2.8e-89 steT E Amino acid permease
CMMOHOCF_02576 1e-147 I Diacylglycerol kinase catalytic domain
CMMOHOCF_02577 1.9e-65 arbG K CAT RNA binding domain
CMMOHOCF_02578 4.7e-49 arbG K CAT RNA binding domain
CMMOHOCF_02579 7.9e-58 crr G pts system, glucose-specific IIABC component
CMMOHOCF_02580 1.2e-76 yijF S Domain of unknown function (DUF1287)
CMMOHOCF_02581 2.7e-70 pdxH S Pfam:Pyridox_oxidase
CMMOHOCF_02582 4.8e-82 KT RESPONSE REGULATOR receiver
CMMOHOCF_02583 8.8e-24 O Bacterial Ig-like domain (group 3)
CMMOHOCF_02584 7.1e-221
CMMOHOCF_02585 2e-123 1.1.1.65 C Oxidoreductase, aldo keto reductase family protein
CMMOHOCF_02586 2.1e-13 1.1.1.65 C Oxidoreductase, aldo keto reductase family protein
CMMOHOCF_02587 2.2e-41 nrdH O Glutaredoxin
CMMOHOCF_02588 1.3e-187 S Putative ABC-transporter type IV
CMMOHOCF_02589 5.6e-14 S Putative ABC-transporter type IV
CMMOHOCF_02590 7e-81
CMMOHOCF_02591 7.9e-17 dnaG L RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication
CMMOHOCF_02592 2.3e-159 K Helix-turn-helix domain, rpiR family
CMMOHOCF_02593 3.6e-55 K Putative ATP-dependent DNA helicase recG C-terminal
CMMOHOCF_02594 1.2e-25 lemA S LemA family
CMMOHOCF_02595 7.2e-116 xylR K purine nucleotide biosynthetic process
CMMOHOCF_02596 4.5e-15 pnp 2.7.7.8 J Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction
CMMOHOCF_02597 3.2e-35 G Transmembrane secretion effector
CMMOHOCF_02598 4.5e-53 G Transmembrane secretion effector
CMMOHOCF_02599 2.8e-70 K Bacterial regulatory proteins, tetR family
CMMOHOCF_02600 2.7e-16 K Bacterial regulatory proteins, tetR family
CMMOHOCF_02601 7.8e-191 S Psort location Cytoplasmic, score 8.87
CMMOHOCF_02602 1.1e-208 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_02603 7.3e-59 nagLU 3.1.4.53, 3.2.1.21, 3.2.1.50 GH3 G Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain
CMMOHOCF_02604 2e-74 nadA 2.5.1.72 H Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate
CMMOHOCF_02605 5.2e-161 nadA 2.5.1.72 H Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate
CMMOHOCF_02606 5.1e-60 S Glycosyl transferase, family 2
CMMOHOCF_02607 6.6e-20 whiB K Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA
CMMOHOCF_02608 1.2e-110 4.1.1.44 S Carboxymuconolactone decarboxylase family
CMMOHOCF_02609 1.2e-38 dkgB S Oxidoreductase, aldo keto reductase family protein
CMMOHOCF_02610 6.8e-51 pntA 1.6.1.2 C NAD(P) transhydrogenase subunit alpha part 1 K00324
CMMOHOCF_02611 9.7e-29 pntA 1.6.1.2 C NAD(P) transhydrogenase subunit alpha part 1 K00324
CMMOHOCF_02612 4.4e-44 pntA 1.6.1.2 C 4TM region of pyridine nucleotide transhydrogenase, mitoch
CMMOHOCF_02613 9.2e-94 pntB 1.6.1.2 C The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane
CMMOHOCF_02614 3.1e-21 pntB 1.6.1.2 C The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane
CMMOHOCF_02615 9e-60 mgtC S MgtC family
CMMOHOCF_02617 2.8e-57
CMMOHOCF_02618 3.2e-175 fas 2.3.1.179 I Beta-ketoacyl synthase, C-terminal domain
CMMOHOCF_02619 1.8e-33 fas 2.3.1.179 I Beta-ketoacyl synthase, C-terminal domain
CMMOHOCF_02620 3.1e-14 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
CMMOHOCF_02621 5.1e-66 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
CMMOHOCF_02622 7.6e-100 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
CMMOHOCF_02623 5e-287 der 1.1.1.399, 1.1.1.95, 2.7.4.25 F GTPase that plays an essential role in the late steps of ribosome biogenesis
CMMOHOCF_02624 2.8e-67 L PFAM Integrase catalytic
CMMOHOCF_02625 4e-40 L PFAM Integrase catalytic
CMMOHOCF_02626 6.5e-84 murC 6.3.2.8 M Belongs to the MurCDEF family
CMMOHOCF_02627 1.3e-68 murC 6.3.2.8 M Belongs to the MurCDEF family
CMMOHOCF_02628 7.1e-98 murG 2.4.1.227, 6.3.2.8 GT28 M Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II)
CMMOHOCF_02629 4.2e-164 P Cation efflux family
CMMOHOCF_02630 1.1e-104 acoA 1.2.4.1 C Dehydrogenase E1 component
CMMOHOCF_02631 1.3e-27 1.2.4.1 C Pyruvate 2-oxoglutarate dehydrogenase complex dehydrogenase (E1) component eukaryotic type beta subunit
CMMOHOCF_02632 3.1e-26 1.2.4.1 C Pyruvate 2-oxoglutarate dehydrogenase complex dehydrogenase (E1) component eukaryotic type beta subunit
CMMOHOCF_02633 3.9e-163 K Cell envelope-related transcriptional attenuator domain
CMMOHOCF_02634 1.3e-48 K Cell envelope-related transcriptional attenuator domain
CMMOHOCF_02635 3e-164 dapE 3.5.1.18 E Peptidase dimerisation domain
CMMOHOCF_02637 5.8e-126 mutY 2.1.1.37, 2.1.3.15, 6.4.1.2 L FES
CMMOHOCF_02638 4.7e-30
CMMOHOCF_02639 1.9e-40
CMMOHOCF_02640 1.1e-14 A 3'-to-5' exoribonuclease specific for small oligoribonucleotides
CMMOHOCF_02643 8.1e-39 ftsK 2.7.11.1, 2.7.7.7, 3.4.21.110, 4.2.1.2 D Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides
CMMOHOCF_02644 8e-28 D Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides
CMMOHOCF_02645 3.4e-43 U Sodium:dicarboxylate symporter family
CMMOHOCF_02646 9.2e-60 U Sodium:dicarboxylate symporter family
CMMOHOCF_02649 2.5e-132 C Putative TM nitroreductase
CMMOHOCF_02650 1.5e-143 fic D Fic/DOC family
CMMOHOCF_02651 3.3e-26
CMMOHOCF_02652 4.7e-140 nfrA 1.5.1.38, 1.5.1.39 C Nitroreductase family
CMMOHOCF_02653 1.1e-45
CMMOHOCF_02654 1.6e-83 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
CMMOHOCF_02655 4.4e-58 hinT 2.1.1.226, 2.1.1.227 FG Scavenger mRNA decapping enzyme C-term binding
CMMOHOCF_02656 1.2e-159 neo 2.7.1.87, 2.7.1.95 F Phosphotransferase enzyme family
CMMOHOCF_02657 2e-148 fas 2.3.1.179 I Beta-ketoacyl synthase, C-terminal domain
CMMOHOCF_02658 7.1e-50 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
CMMOHOCF_02659 4.6e-126 nrtR 3.6.1.55 F NUDIX hydrolase
CMMOHOCF_02660 4.3e-103 fas 2.3.1.179 I Beta-ketoacyl synthase, C-terminal domain
CMMOHOCF_02661 3.1e-32 K Putative sugar-binding domain
CMMOHOCF_02663 2.5e-174 galT 2.7.7.12 C Galactose-1-phosphate uridyl transferase, N-terminal domain
CMMOHOCF_02664 5.6e-39 fhaB T Inner membrane component of T3SS, cytoplasmic domain
CMMOHOCF_02665 1.4e-71 pstP 3.1.3.16 T Sigma factor PP2C-like phosphatases
CMMOHOCF_02666 6.6e-41 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
CMMOHOCF_02667 2.2e-51 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
CMMOHOCF_02668 1.6e-72 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
CMMOHOCF_02669 1.4e-113 birA 2.7.1.33, 6.3.4.15 H Biotin/lipoate A/B protein ligase family
CMMOHOCF_02670 2.3e-40 int L Phage integrase, N-terminal SAM-like domain
CMMOHOCF_02671 1e-32 int L Phage integrase, N-terminal SAM-like domain
CMMOHOCF_02672 1.8e-107 nadB 1.3.5.4, 1.4.3.16, 2.4.2.19 H Catalyzes the oxidation of L-aspartate to iminoaspartate
CMMOHOCF_02673 1.1e-18
CMMOHOCF_02674 1.6e-47
CMMOHOCF_02675 4.8e-13
CMMOHOCF_02676 5.4e-20 L Phage integrase family
CMMOHOCF_02678 3.6e-131 L Phage integrase family
CMMOHOCF_02679 5.4e-144 L IstB-like ATP binding protein
CMMOHOCF_02680 4.3e-68 EGP Major facilitator Superfamily
CMMOHOCF_02682 8.6e-27 L Transposase
CMMOHOCF_02683 1.3e-80 plyA3 3.2.1.18 GH33 M Parallel beta-helix repeats
CMMOHOCF_02684 1.3e-28 plyA3 M Parallel beta-helix repeats
CMMOHOCF_02685 1.1e-124 3.1.3.3, 3.1.3.73 G Phosphoglycerate mutase family
CMMOHOCF_02686 9.2e-60 recN L May be involved in recombinational repair of damaged DNA
CMMOHOCF_02687 6.5e-66 G Glycosyl hydrolases family 43
CMMOHOCF_02688 1.2e-29 E Transglutaminase-like superfamily
CMMOHOCF_02689 5.2e-17 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
CMMOHOCF_02690 4.6e-52 V Efflux ABC transporter, permease protein
CMMOHOCF_02691 1.6e-32 pepD E Peptidase family C69

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