ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AHMNLFMI_00001 | 7.1e-102 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_00002 | 1.2e-97 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_00003 | 6.7e-58 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_00004 | 2.4e-87 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHMNLFMI_00005 | 2.8e-38 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHMNLFMI_00006 | 2.4e-26 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHMNLFMI_00007 | 9.3e-107 | vicK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_00008 | 2.6e-75 | S | peptidoglycan catabolic process | |||
AHMNLFMI_00009 | 4.8e-48 | K | AraC-like ligand binding domain | |||
AHMNLFMI_00010 | 6e-42 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
AHMNLFMI_00011 | 1.6e-227 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
AHMNLFMI_00012 | 1e-108 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
AHMNLFMI_00013 | 3.1e-31 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_00014 | 3.9e-120 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_00015 | 8.2e-61 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_00016 | 1.9e-75 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AHMNLFMI_00017 | 8.9e-235 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AHMNLFMI_00018 | 7.2e-31 | S | peptidoglycan catabolic process | |||
AHMNLFMI_00019 | 1.6e-30 | S | peptidoglycan catabolic process | |||
AHMNLFMI_00020 | 1.5e-21 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_00021 | 1e-55 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_00022 | 4.2e-68 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_00023 | 4.3e-118 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
AHMNLFMI_00024 | 1.7e-144 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_00025 | 1.4e-21 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_00026 | 4.5e-35 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHMNLFMI_00027 | 2.4e-55 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
AHMNLFMI_00028 | 2.2e-10 | 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 | ||
AHMNLFMI_00029 | 2.4e-76 | 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 | ||
AHMNLFMI_00030 | 2.2e-205 | 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 | ||
AHMNLFMI_00031 | 3.1e-78 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHMNLFMI_00032 | 5.5e-52 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHMNLFMI_00033 | 1.3e-102 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AHMNLFMI_00034 | 1.8e-89 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AHMNLFMI_00035 | 4.6e-64 | glnR | K | Transcriptional regulator | ||
AHMNLFMI_00036 | 9.1e-49 | 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) | |
AHMNLFMI_00037 | 1.1e-87 | F | DNA/RNA non-specific endonuclease | |||
AHMNLFMI_00038 | 1.1e-104 | F | DNA/RNA non-specific endonuclease | |||
AHMNLFMI_00039 | 3.9e-57 | |||||
AHMNLFMI_00040 | 4e-44 | |||||
AHMNLFMI_00041 | 5.2e-13 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_00042 | 1.1e-08 | hol | S | Bacteriophage holin | ||
AHMNLFMI_00044 | 5.6e-10 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_00045 | 8.1e-93 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_00046 | 1.6e-23 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_00047 | 1e-51 | argO | S | LysE type translocator | ||
AHMNLFMI_00048 | 1.5e-22 | argO | S | LysE type translocator | ||
AHMNLFMI_00049 | 9.5e-63 | EG | EamA-like transporter family | |||
AHMNLFMI_00050 | 3.1e-77 | EG | EamA-like transporter family | |||
AHMNLFMI_00051 | 1.2e-21 | EG | EamA-like transporter family | |||
AHMNLFMI_00052 | 4.5e-36 | ubiB | S | ABC1 family | ||
AHMNLFMI_00053 | 2.4e-37 | ubiB | S | ABC1 family | ||
AHMNLFMI_00054 | 2.5e-37 | ubiB | S | ABC1 family | ||
AHMNLFMI_00055 | 1.2e-49 | pstA | P | Phosphate transport system permease protein PstA | ||
AHMNLFMI_00056 | 4.8e-104 | pstA | P | Phosphate transport system permease protein PstA | ||
AHMNLFMI_00057 | 2e-40 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AHMNLFMI_00058 | 6e-32 | pstA | P | Phosphate transport system permease protein PstA | ||
AHMNLFMI_00059 | 5.2e-53 | E | ABC transporter, substratebinding protein | |||
AHMNLFMI_00060 | 2e-26 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_00061 | 5.5e-75 | E | ABC transporter, substratebinding protein | |||
AHMNLFMI_00062 | 4e-214 | |||||
AHMNLFMI_00063 | 5.1e-259 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
AHMNLFMI_00064 | 1.2e-103 | |||||
AHMNLFMI_00065 | 7.7e-45 | ykiI | ||||
AHMNLFMI_00066 | 8.6e-218 | ykiI | ||||
AHMNLFMI_00067 | 3.6e-117 | GM | NAD(P)H-binding | |||
AHMNLFMI_00068 | 2.5e-138 | IQ | reductase | |||
AHMNLFMI_00069 | 6.7e-53 | IQ | reductase | |||
AHMNLFMI_00070 | 4.6e-17 | C | C4-dicarboxylate transmembrane transporter activity | |||
AHMNLFMI_00071 | 9.5e-42 | 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) | |
AHMNLFMI_00072 | 1.3e-63 | 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) | |
AHMNLFMI_00073 | 4.7e-100 | 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) | |
AHMNLFMI_00077 | 3e-62 | ytrB | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_00078 | 9.5e-65 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
AHMNLFMI_00081 | 4.2e-44 | ybiT | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_00082 | 4.9e-138 | ybiT | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_00083 | 2.8e-29 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
AHMNLFMI_00084 | 9.4e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
AHMNLFMI_00085 | 3.3e-217 | nusA | K | Participates in both transcription termination and antitermination | ||
AHMNLFMI_00086 | 9.5e-49 | ylxR | K | Protein of unknown function (DUF448) | ||
AHMNLFMI_00087 | 1.1e-47 | ylxQ | J | ribosomal protein | ||
AHMNLFMI_00088 | 1.8e-69 | 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 | |
AHMNLFMI_00089 | 1.3e-133 | |||||
AHMNLFMI_00090 | 5.8e-51 | |||||
AHMNLFMI_00091 | 1.2e-54 | KLT | Protein tyrosine kinase | |||
AHMNLFMI_00092 | 7.5e-57 | KLT | Protein tyrosine kinase | |||
AHMNLFMI_00093 | 2.2e-34 | |||||
AHMNLFMI_00094 | 3e-31 | |||||
AHMNLFMI_00095 | 1.2e-76 | 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 | |
AHMNLFMI_00096 | 7.7e-63 | 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 | |
AHMNLFMI_00097 | 3.4e-39 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_00098 | 1.6e-87 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_00099 | 7.9e-21 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_00100 | 2.6e-37 | |||||
AHMNLFMI_00101 | 1.3e-120 | |||||
AHMNLFMI_00102 | 4.3e-08 | |||||
AHMNLFMI_00103 | 5.3e-17 | 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 | |
AHMNLFMI_00104 | 3.7e-36 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
AHMNLFMI_00105 | 5.9e-39 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_00106 | 1.5e-157 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
AHMNLFMI_00107 | 7.8e-103 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
AHMNLFMI_00108 | 3.4e-23 | dnaB | L | replication initiation and membrane attachment | ||
AHMNLFMI_00109 | 4.4e-146 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_00110 | 9.5e-43 | 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) | |
AHMNLFMI_00111 | 4.8e-36 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHMNLFMI_00112 | 8.4e-131 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHMNLFMI_00113 | 4.7e-33 | |||||
AHMNLFMI_00114 | 1.2e-32 | amtB | P | ammonium transporter | ||
AHMNLFMI_00115 | 1.2e-32 | amtB | P | ammonium transporter | ||
AHMNLFMI_00116 | 1.2e-43 | S | Cupin domain | |||
AHMNLFMI_00117 | 1.4e-90 | 5.3.3.19 | S | Cupin 2, conserved barrel domain protein | ||
AHMNLFMI_00118 | 1.6e-165 | K | Transcriptional regulator | |||
AHMNLFMI_00121 | 5.3e-41 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_00122 | 9e-22 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_00123 | 1.8e-180 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
AHMNLFMI_00124 | 8.9e-109 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_00125 | 1.6e-34 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_00126 | 5.9e-24 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_00127 | 2.2e-41 | sufD | O | FeS assembly protein SufD | ||
AHMNLFMI_00128 | 9e-94 | sufC | O | FeS assembly ATPase SufC | ||
AHMNLFMI_00129 | 6.3e-20 | sufD | O | FeS assembly protein SufD | ||
AHMNLFMI_00130 | 5.6e-62 | sufD | O | FeS assembly protein SufD | ||
AHMNLFMI_00131 | 6.3e-20 | sufD | O | FeS assembly protein SufD | ||
AHMNLFMI_00132 | 2.4e-57 | ctpA | 3.6.3.54 | P | P-type ATPase | |
AHMNLFMI_00133 | 2.1e-210 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
AHMNLFMI_00134 | 1.1e-32 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
AHMNLFMI_00135 | 1.8e-76 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_00136 | 1.7e-57 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
AHMNLFMI_00137 | 3.4e-33 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHMNLFMI_00138 | 2.6e-258 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHMNLFMI_00139 | 1.2e-39 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHMNLFMI_00140 | 6.8e-125 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00141 | 1e-70 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00142 | 3.9e-99 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00143 | 1.8e-16 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00144 | 2.3e-21 | cps3F | ||||
AHMNLFMI_00145 | 1.5e-107 | cps3F | ||||
AHMNLFMI_00146 | 3e-121 | cps3F | ||||
AHMNLFMI_00147 | 1.4e-110 | cps3E | ||||
AHMNLFMI_00148 | 5.9e-163 | cps3D | ||||
AHMNLFMI_00149 | 5.6e-30 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_00150 | 7.3e-36 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_00151 | 1.6e-74 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_00152 | 7.9e-130 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AHMNLFMI_00153 | 4.9e-102 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
AHMNLFMI_00154 | 8.3e-110 | ypsA | S | Belongs to the UPF0398 family | ||
AHMNLFMI_00155 | 2e-62 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
AHMNLFMI_00157 | 3.1e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
AHMNLFMI_00158 | 1.2e-38 | C | Aldo/keto reductase family | |||
AHMNLFMI_00160 | 2.2e-16 | hol | S | Bacteriophage holin | ||
AHMNLFMI_00161 | 1.7e-10 | hol | S | Bacteriophage holin | ||
AHMNLFMI_00162 | 7.8e-24 | hol | S | Bacteriophage holin | ||
AHMNLFMI_00163 | 2.6e-46 | |||||
AHMNLFMI_00164 | 2.1e-21 | M | hydrolase, family 25 | |||
AHMNLFMI_00165 | 1.3e-25 | |||||
AHMNLFMI_00166 | 2.2e-47 | K | Helix-turn-helix domain, rpiR family | |||
AHMNLFMI_00167 | 1.5e-80 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_00168 | 7.3e-53 | ppaX_1 | 3.1.3.18, 3.6.1.1 | S | haloacid dehalogenase-like hydrolase | |
AHMNLFMI_00169 | 2.5e-83 | ppaX_1 | 3.1.3.18, 3.6.1.1 | S | haloacid dehalogenase-like hydrolase | |
AHMNLFMI_00170 | 1.4e-40 | ppaX_1 | 3.1.3.18, 3.6.1.1 | S | haloacid dehalogenase-like hydrolase | |
AHMNLFMI_00171 | 3.9e-52 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_00172 | 6.1e-34 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_00175 | 1.7e-22 | N | domain, Protein | |||
AHMNLFMI_00179 | 9.7e-12 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_00180 | 8e-22 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_00181 | 1.1e-23 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_00182 | 1e-13 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_00183 | 6.7e-19 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00184 | 4.3e-95 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00185 | 1.6e-16 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00186 | 2.2e-13 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
AHMNLFMI_00187 | 8.1e-38 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
AHMNLFMI_00188 | 2.3e-40 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
AHMNLFMI_00189 | 1.6e-73 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
AHMNLFMI_00190 | 4.2e-228 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
AHMNLFMI_00191 | 4.2e-70 | S | Pyrimidine dimer DNA glycosylase | |||
AHMNLFMI_00192 | 2.2e-70 | frlB | M | SIS domain | ||
AHMNLFMI_00193 | 5.8e-11 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_00194 | 1.1e-144 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_00195 | 2.5e-56 | phnE1 | 3.6.1.63 | U | ABC transporter permease | |
AHMNLFMI_00196 | 1.7e-115 | 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 | |
AHMNLFMI_00197 | 6.4e-19 | yaaA | S | S4 domain protein YaaA | ||
AHMNLFMI_00198 | 3.7e-28 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
AHMNLFMI_00199 | 5.6e-37 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
AHMNLFMI_00200 | 6e-106 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
AHMNLFMI_00202 | 1.2e-140 | |||||
AHMNLFMI_00203 | 4.3e-186 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_00204 | 1.9e-23 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
AHMNLFMI_00205 | 5.6e-96 | 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 | |
AHMNLFMI_00206 | 1.9e-66 | 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 | |
AHMNLFMI_00207 | 8.1e-32 | K | Transcriptional regulator | |||
AHMNLFMI_00208 | 4.9e-32 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_00209 | 6e-37 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
AHMNLFMI_00210 | 2.2e-21 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
AHMNLFMI_00211 | 3.1e-179 | K | AI-2E family transporter | |||
AHMNLFMI_00212 | 4.6e-166 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
AHMNLFMI_00213 | 8.2e-134 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_00214 | 6.2e-12 | K | AI-2E family transporter | |||
AHMNLFMI_00215 | 1e-64 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHMNLFMI_00216 | 1e-39 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHMNLFMI_00217 | 1.4e-59 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHMNLFMI_00218 | 1.2e-48 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHMNLFMI_00219 | 1.6e-59 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHMNLFMI_00220 | 1.6e-36 | S | Protein of unknown function (DUF1211) | |||
AHMNLFMI_00221 | 3.4e-300 | ydgH | S | MMPL family | ||
AHMNLFMI_00222 | 2.6e-27 | ydgH | S | MMPL family | ||
AHMNLFMI_00223 | 9.5e-43 | pepF2 | E | Oligopeptidase F | ||
AHMNLFMI_00224 | 5.7e-82 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHMNLFMI_00225 | 1.2e-60 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHMNLFMI_00226 | 3.9e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
AHMNLFMI_00227 | 4.7e-66 | 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 | |
AHMNLFMI_00228 | 1.4e-22 | 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 | ||
AHMNLFMI_00229 | 2.7e-61 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_00230 | 2.9e-70 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_00231 | 9.1e-50 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_00232 | 3.2e-161 | fhuD | P | Periplasmic binding protein | ||
AHMNLFMI_00235 | 5.5e-33 | 3.1.3.16 | L | DnaD domain protein | ||
AHMNLFMI_00236 | 2.5e-16 | |||||
AHMNLFMI_00237 | 1.5e-07 | |||||
AHMNLFMI_00239 | 1.7e-18 | E | IrrE N-terminal-like domain | |||
AHMNLFMI_00240 | 4.5e-23 | yvaO | K | Helix-turn-helix domain | ||
AHMNLFMI_00241 | 6.4e-16 | yvaO | K | Helix-turn-helix domain | ||
AHMNLFMI_00246 | 1.3e-15 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AHMNLFMI_00247 | 2.7e-33 | ywkB | S | Membrane transport protein | ||
AHMNLFMI_00249 | 5.4e-08 | |||||
AHMNLFMI_00250 | 1.2e-51 | |||||
AHMNLFMI_00251 | 2.1e-32 | |||||
AHMNLFMI_00252 | 3.3e-10 | |||||
AHMNLFMI_00255 | 7e-69 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
AHMNLFMI_00256 | 4.3e-200 | S | DUF218 domain | |||
AHMNLFMI_00257 | 1.5e-169 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
AHMNLFMI_00258 | 1.2e-129 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
AHMNLFMI_00259 | 2.2e-28 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
AHMNLFMI_00260 | 3.4e-175 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_00261 | 3.7e-303 | ubiB | S | ABC1 family | ||
AHMNLFMI_00262 | 1.2e-42 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_00263 | 1.8e-108 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_00264 | 9.6e-16 | 3.1.3.1 | S | associated with various cellular activities | ||
AHMNLFMI_00266 | 5.7e-31 | 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 | |
AHMNLFMI_00267 | 2.1e-132 | 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 | |
AHMNLFMI_00268 | 1.3e-45 | mleR | K | LysR substrate binding domain | ||
AHMNLFMI_00269 | 1.3e-88 | mleR | K | LysR substrate binding domain | ||
AHMNLFMI_00270 | 3.9e-15 | mleR | K | LysR substrate binding domain | ||
AHMNLFMI_00271 | 1.5e-35 | copR | K | Copper transport repressor CopY TcrY | ||
AHMNLFMI_00272 | 1.7e-111 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_00273 | 9.4e-74 | copR | K | Copper transport repressor CopY TcrY | ||
AHMNLFMI_00274 | 1.5e-11 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_00275 | 1.4e-24 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_00276 | 8.2e-183 | pts30BCA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_00277 | 1.3e-154 | licT | K | CAT RNA binding domain | ||
AHMNLFMI_00278 | 2.6e-49 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
AHMNLFMI_00279 | 2.8e-35 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
AHMNLFMI_00280 | 1.3e-40 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHMNLFMI_00281 | 2.8e-121 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHMNLFMI_00282 | 5.3e-42 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHMNLFMI_00283 | 1.9e-119 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_00284 | 2.5e-206 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_00285 | 1.4e-124 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_00286 | 1.1e-38 | ypbG | 2.7.1.2 | GK | ROK family | |
AHMNLFMI_00287 | 3.9e-34 | norB | EGP | Major Facilitator | ||
AHMNLFMI_00288 | 1.7e-188 | norB | EGP | Major Facilitator | ||
AHMNLFMI_00289 | 1.4e-28 | f42a | O | Band 7 protein | ||
AHMNLFMI_00290 | 3.4e-13 | f42a | O | Band 7 protein | ||
AHMNLFMI_00291 | 2.3e-125 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_00292 | 5.9e-22 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_00293 | 5.9e-22 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_00294 | 2.6e-64 | |||||
AHMNLFMI_00295 | 5.6e-58 | |||||
AHMNLFMI_00296 | 2.3e-44 | |||||
AHMNLFMI_00297 | 1.1e-35 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_00298 | 7.1e-104 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_00299 | 1e-70 | E | glutamate:sodium symporter activity | |||
AHMNLFMI_00300 | 2.2e-47 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_00301 | 1.4e-26 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
AHMNLFMI_00302 | 2.6e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
AHMNLFMI_00303 | 3.4e-57 | 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 | ||
AHMNLFMI_00304 | 4.3e-20 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
AHMNLFMI_00305 | 5.7e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
AHMNLFMI_00306 | 1.5e-47 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
AHMNLFMI_00307 | 1.7e-15 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
AHMNLFMI_00308 | 1.4e-87 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHMNLFMI_00309 | 3.6e-13 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AHMNLFMI_00310 | 4.1e-110 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AHMNLFMI_00311 | 4.1e-181 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AHMNLFMI_00312 | 1.9e-07 | asnB | 6.3.5.4 | E | Protein of unknown function (DUF3923) | |
AHMNLFMI_00313 | 1.9e-57 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
AHMNLFMI_00314 | 1.4e-84 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
AHMNLFMI_00315 | 3.1e-101 | livF | E | ABC transporter | ||
AHMNLFMI_00316 | 2.6e-81 | sip | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_00317 | 5.1e-44 | sip | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_00318 | 9.2e-74 | pgm1 | G | phosphoglycerate mutase | ||
AHMNLFMI_00319 | 5.7e-55 | int | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_00321 | 8.9e-30 | |||||
AHMNLFMI_00323 | 2e-38 | |||||
AHMNLFMI_00324 | 1.4e-43 | |||||
AHMNLFMI_00325 | 3.9e-34 | K | MarR family | |||
AHMNLFMI_00326 | 3.9e-131 | int | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_00328 | 1.7e-123 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
AHMNLFMI_00329 | 1.9e-189 | comGB | NU | type II secretion system | ||
AHMNLFMI_00330 | 2.1e-21 | comGA | NU | Type II IV secretion system protein | ||
AHMNLFMI_00331 | 9.2e-35 | comGB | NU | type II secretion system | ||
AHMNLFMI_00332 | 8.7e-22 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
AHMNLFMI_00333 | 4.2e-121 | K | Crp-like helix-turn-helix domain | |||
AHMNLFMI_00334 | 1.2e-35 | |||||
AHMNLFMI_00335 | 4.2e-71 | gtcA | S | Teichoic acid glycosylation protein | ||
AHMNLFMI_00336 | 4.3e-88 | |||||
AHMNLFMI_00337 | 2.1e-49 | |||||
AHMNLFMI_00338 | 1.6e-37 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_00339 | 2.5e-39 | luxT | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_00341 | 2.8e-29 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_00342 | 6e-61 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_00343 | 2.3e-75 | T | Universal stress protein family | |||
AHMNLFMI_00344 | 6e-61 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_00345 | 2.3e-51 | S | Threonine/Serine exporter, ThrE | |||
AHMNLFMI_00346 | 2.6e-152 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_00347 | 9.1e-166 | ybeC | E | amino acid | ||
AHMNLFMI_00348 | 5.3e-74 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_00349 | 5.8e-77 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_00350 | 2.6e-48 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
AHMNLFMI_00351 | 2.5e-84 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
AHMNLFMI_00352 | 1.6e-24 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
AHMNLFMI_00365 | 5.1e-08 | |||||
AHMNLFMI_00372 | 4.6e-78 | ybiR | P | Citrate transporter | ||
AHMNLFMI_00373 | 5.4e-190 | ybiR | P | Citrate transporter | ||
AHMNLFMI_00374 | 2.1e-38 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
AHMNLFMI_00375 | 6.6e-18 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_00376 | 1.1e-43 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_00377 | 8.5e-37 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_00378 | 8.3e-46 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_00379 | 1e-199 | bla2 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
AHMNLFMI_00380 | 1.1e-19 | usp6 | T | universal stress protein | ||
AHMNLFMI_00381 | 2.1e-82 | usp6 | T | universal stress protein | ||
AHMNLFMI_00382 | 1e-44 | usp6 | T | universal stress protein | ||
AHMNLFMI_00383 | 1.5e-38 | |||||
AHMNLFMI_00384 | 1.9e-121 | rarA | L | recombination factor protein RarA | ||
AHMNLFMI_00385 | 1.5e-58 | rarA | L | recombination factor protein RarA | ||
AHMNLFMI_00386 | 8.1e-68 | yebR | 1.8.4.14 | T | L-methionine-(R)-S-oxide reductase activity | |
AHMNLFMI_00387 | 2.8e-202 | yebS | S | response to heat | ||
AHMNLFMI_00388 | 8e-24 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHMNLFMI_00389 | 1.4e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHMNLFMI_00390 | 1.5e-166 | yobV1 | K | WYL domain | ||
AHMNLFMI_00391 | 2.8e-20 | EGP | the major facilitator superfamily | |||
AHMNLFMI_00392 | 2.5e-248 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_00393 | 4.4e-37 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_00394 | 2.1e-11 | S | COG NOG18757 non supervised orthologous group | |||
AHMNLFMI_00395 | 7.7e-73 | S | COG NOG18757 non supervised orthologous group | |||
AHMNLFMI_00396 | 1.4e-52 | S | COG NOG18757 non supervised orthologous group | |||
AHMNLFMI_00397 | 7.4e-40 | |||||
AHMNLFMI_00398 | 1.1e-33 | copR | K | Copper transport repressor CopY TcrY | ||
AHMNLFMI_00399 | 3.3e-47 | ywkB | S | Membrane transport protein | ||
AHMNLFMI_00400 | 2.1e-52 | ywkB | S | Membrane transport protein | ||
AHMNLFMI_00401 | 9.6e-30 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
AHMNLFMI_00402 | 2.9e-53 | |||||
AHMNLFMI_00403 | 5.9e-43 | |||||
AHMNLFMI_00404 | 2.9e-53 | |||||
AHMNLFMI_00406 | 1.3e-37 | K | Helix-turn-helix | |||
AHMNLFMI_00407 | 2.6e-07 | E | IrrE N-terminal-like domain | |||
AHMNLFMI_00408 | 2e-32 | E | IrrE N-terminal-like domain | |||
AHMNLFMI_00409 | 1.7e-26 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
AHMNLFMI_00410 | 4.9e-114 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
AHMNLFMI_00411 | 1.3e-120 | S | CAAX protease self-immunity | |||
AHMNLFMI_00412 | 1.7e-52 | M | Lysin motif | |||
AHMNLFMI_00413 | 6.4e-19 | lytE | M | LysM domain protein | ||
AHMNLFMI_00414 | 1.2e-29 | lytE | M | LysM domain protein | ||
AHMNLFMI_00415 | 3.4e-29 | M | LysM domain protein | |||
AHMNLFMI_00416 | 2.2e-54 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_00417 | 4.1e-84 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_00418 | 2.7e-18 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_00419 | 9.1e-66 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
AHMNLFMI_00420 | 4.7e-36 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
AHMNLFMI_00421 | 3.3e-38 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
AHMNLFMI_00422 | 1.2e-219 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
AHMNLFMI_00423 | 4.3e-59 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
AHMNLFMI_00424 | 3.2e-21 | 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 | |
AHMNLFMI_00425 | 6.1e-18 | 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 | |
AHMNLFMI_00426 | 1.2e-49 | 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 | |
AHMNLFMI_00427 | 5.6e-68 | 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 | |
AHMNLFMI_00428 | 1.2e-89 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_00429 | 2.6e-30 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_00430 | 2.9e-14 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_00431 | 4.6e-27 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AHMNLFMI_00432 | 3.3e-80 | 2.7.8.7 | H | Belongs to the P-Pant transferase superfamily | ||
AHMNLFMI_00433 | 9.2e-98 | 2.7.8.7 | H | Belongs to the P-Pant transferase superfamily | ||
AHMNLFMI_00434 | 1.3e-115 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
AHMNLFMI_00435 | 8.3e-33 | KT | helix_turn_helix, mercury resistance | |||
AHMNLFMI_00436 | 9.1e-40 | KT | helix_turn_helix, mercury resistance | |||
AHMNLFMI_00437 | 5e-13 | KT | helix_turn_helix, mercury resistance | |||
AHMNLFMI_00438 | 2.1e-44 | KT | helix_turn_helix, mercury resistance | |||
AHMNLFMI_00439 | 8.2e-102 | XK27_07075 | V | CAAX protease self-immunity | ||
AHMNLFMI_00440 | 0.0 | L | AAA domain | |||
AHMNLFMI_00441 | 1.1e-40 | L | AAA domain | |||
AHMNLFMI_00445 | 6e-32 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
AHMNLFMI_00446 | 3.7e-27 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
AHMNLFMI_00447 | 8.7e-139 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
AHMNLFMI_00448 | 4.8e-99 | gshR | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_00449 | 3.1e-101 | proV | E | ABC transporter, ATP-binding protein | ||
AHMNLFMI_00450 | 2.3e-48 | proV | E | ABC transporter, ATP-binding protein | ||
AHMNLFMI_00451 | 4.7e-174 | P | ABC transporter | |||
AHMNLFMI_00452 | 3.8e-38 | P | ABC transporter | |||
AHMNLFMI_00453 | 3.8e-38 | P | ABC transporter | |||
AHMNLFMI_00454 | 3.8e-38 | P | ABC transporter | |||
AHMNLFMI_00455 | 1.1e-66 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_00456 | 1.4e-217 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_00457 | 4.3e-26 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHMNLFMI_00458 | 1.5e-38 | frlB | M | SIS domain | ||
AHMNLFMI_00459 | 1.2e-57 | frlB | M | SIS domain | ||
AHMNLFMI_00460 | 1.3e-139 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_00461 | 1.8e-27 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_00462 | 5.7e-133 | 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 | ||
AHMNLFMI_00463 | 1.7e-33 | 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 | ||
AHMNLFMI_00464 | 2.1e-104 | pbpX2 | V | Beta-lactamase | ||
AHMNLFMI_00466 | 1e-84 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHMNLFMI_00467 | 3e-44 | T | diguanylate cyclase | |||
AHMNLFMI_00468 | 4.7e-75 | desK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_00469 | 3.3e-164 | desK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_00470 | 1.2e-103 | desR | K | helix_turn_helix, Lux Regulon | ||
AHMNLFMI_00471 | 2e-12 | S | Domain of unknown function (DUF4767) | |||
AHMNLFMI_00472 | 1.4e-43 | malT | G | Major Facilitator | ||
AHMNLFMI_00473 | 1.2e-67 | malT | G | Major Facilitator | ||
AHMNLFMI_00474 | 6.9e-162 | sirB | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHMNLFMI_00475 | 4.8e-32 | N | domain, Protein | |||
AHMNLFMI_00476 | 1.8e-44 | N | domain, Protein | |||
AHMNLFMI_00477 | 4.9e-42 | N | domain, Protein | |||
AHMNLFMI_00478 | 7.8e-85 | S | (CBS) domain | |||
AHMNLFMI_00479 | 3.3e-116 | S | Putative peptidoglycan binding domain | |||
AHMNLFMI_00480 | 9.2e-30 | S | Putative peptidoglycan binding domain | |||
AHMNLFMI_00481 | 8.2e-31 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
AHMNLFMI_00482 | 8.2e-31 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
AHMNLFMI_00483 | 2.7e-52 | 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 | |
AHMNLFMI_00484 | 2.4e-87 | 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 | |
AHMNLFMI_00485 | 2.3e-48 | pts20B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_00486 | 2.3e-48 | pts20B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_00487 | 1e-23 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
AHMNLFMI_00488 | 3e-58 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_00489 | 1.7e-45 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_00490 | 1.2e-30 | |||||
AHMNLFMI_00491 | 4.8e-09 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_00492 | 7e-38 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AHMNLFMI_00493 | 2e-50 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
AHMNLFMI_00494 | 1.7e-105 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AHMNLFMI_00495 | 1.3e-40 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
AHMNLFMI_00496 | 1.1e-42 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
AHMNLFMI_00497 | 3.9e-41 | S | hydrolase activity, acting on ester bonds | |||
AHMNLFMI_00498 | 2.8e-19 | S | hydrolase activity, acting on ester bonds | |||
AHMNLFMI_00499 | 3.2e-11 | yphH | S | Cupin domain | ||
AHMNLFMI_00500 | 1.7e-78 | K | transcriptional regulator, MerR family | |||
AHMNLFMI_00502 | 1.3e-29 | celB | 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 | ||
AHMNLFMI_00503 | 7e-35 | |||||
AHMNLFMI_00505 | 1.5e-18 | celB | 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 | ||
AHMNLFMI_00507 | 1.9e-16 | celB | 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 | ||
AHMNLFMI_00508 | 6.3e-16 | |||||
AHMNLFMI_00509 | 6.5e-41 | aroD | S | Alpha/beta hydrolase family | ||
AHMNLFMI_00510 | 3.2e-37 | |||||
AHMNLFMI_00511 | 2.4e-28 | aroD | S | Alpha/beta hydrolase family | ||
AHMNLFMI_00512 | 4e-14 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_00513 | 6.1e-54 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_00514 | 8.7e-83 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_00515 | 1.1e-46 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00516 | 6.7e-63 | tagE6 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_00517 | 7.8e-47 | M | domain protein | |||
AHMNLFMI_00518 | 1.5e-22 | M | domain protein | |||
AHMNLFMI_00519 | 1.9e-32 | |||||
AHMNLFMI_00520 | 1.9e-165 | yghZ | C | Aldo keto reductase family protein | ||
AHMNLFMI_00521 | 9.4e-36 | pgm1 | G | phosphoglycerate mutase | ||
AHMNLFMI_00522 | 1.6e-78 | S | Bacterial protein of unknown function (DUF871) | |||
AHMNLFMI_00523 | 3.9e-40 | S | Sterol carrier protein domain | |||
AHMNLFMI_00524 | 3.9e-40 | S | Sterol carrier protein domain | |||
AHMNLFMI_00525 | 1.1e-15 | S | Sterol carrier protein domain | |||
AHMNLFMI_00526 | 2.8e-21 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHMNLFMI_00527 | 2e-79 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHMNLFMI_00528 | 8.9e-48 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHMNLFMI_00530 | 1.5e-103 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
AHMNLFMI_00531 | 1.6e-157 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
AHMNLFMI_00532 | 2.7e-97 | drgA | C | Nitroreductase family | ||
AHMNLFMI_00533 | 3.1e-78 | S | Polyphosphate kinase 2 (PPK2) | |||
AHMNLFMI_00534 | 1.4e-133 | S | Polyphosphate kinase 2 (PPK2) | |||
AHMNLFMI_00535 | 4e-57 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
AHMNLFMI_00536 | 8.9e-111 | 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 | ||
AHMNLFMI_00537 | 2e-26 | 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 | ||
AHMNLFMI_00538 | 3.5e-36 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_00539 | 3.1e-58 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_00540 | 6.1e-21 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_00541 | 8.3e-69 | yiaC | K | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_00542 | 2.7e-23 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_00543 | 4.4e-30 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_00544 | 1.5e-45 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_00545 | 4.1e-31 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_00546 | 2e-157 | 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 | ||
AHMNLFMI_00547 | 3.8e-16 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
AHMNLFMI_00548 | 1.1e-147 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
AHMNLFMI_00549 | 3.6e-52 | rsmC | 2.1.1.172 | J | Methyltransferase | |
AHMNLFMI_00550 | 5e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
AHMNLFMI_00551 | 1.2e-162 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_00552 | 6.4e-35 | 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 | |
AHMNLFMI_00553 | 5.4e-56 | 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 | |
AHMNLFMI_00554 | 3.1e-199 | 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 | |
AHMNLFMI_00555 | 4.3e-183 | 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 | |
AHMNLFMI_00556 | 1.1e-68 | 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 | |
AHMNLFMI_00557 | 2.4e-15 | 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 | ||
AHMNLFMI_00558 | 1.6e-62 | 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 | ||
AHMNLFMI_00559 | 1.4e-17 | 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 |
AHMNLFMI_00560 | 1.6e-115 | S | Protein of unknown function (DUF554) | |||
AHMNLFMI_00561 | 6.4e-148 | KT | helix_turn_helix, mercury resistance | |||
AHMNLFMI_00562 | 4e-25 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
AHMNLFMI_00563 | 3.9e-53 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_00564 | 3.1e-10 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
AHMNLFMI_00565 | 8.9e-173 | 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 | ||
AHMNLFMI_00566 | 2.2e-38 | 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 | ||
AHMNLFMI_00567 | 3.9e-27 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AHMNLFMI_00568 | 2.8e-77 | 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 | ||
AHMNLFMI_00569 | 2.1e-60 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_00570 | 4e-10 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
AHMNLFMI_00571 | 3.6e-23 | 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 | ||
AHMNLFMI_00572 | 1.2e-11 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
AHMNLFMI_00573 | 4.4e-29 | 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 | ||
AHMNLFMI_00574 | 1.2e-11 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
AHMNLFMI_00575 | 2.3e-128 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHMNLFMI_00576 | 1.6e-60 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_00577 | 2.1e-115 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_00578 | 7.2e-54 | patA | 1.1.1.28, 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHMNLFMI_00579 | 1.5e-27 | patA | 1.1.1.28, 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHMNLFMI_00580 | 1e-130 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
AHMNLFMI_00581 | 1.3e-47 | trxA | O | Belongs to the thioredoxin family | ||
AHMNLFMI_00582 | 1.9e-29 | trxA | O | Belongs to the thioredoxin family | ||
AHMNLFMI_00583 | 4.9e-44 | trxA | O | Belongs to the thioredoxin family | ||
AHMNLFMI_00584 | 6.5e-46 | yslB | S | Protein of unknown function (DUF2507) | ||
AHMNLFMI_00585 | 7.6e-32 | trxA | O | Belongs to the thioredoxin family | ||
AHMNLFMI_00586 | 1e-154 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00587 | 4.8e-35 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00589 | 6.3e-103 | yfgQ | P | E1-E2 ATPase | ||
AHMNLFMI_00590 | 8.5e-94 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_00591 | 2.6e-277 | pipD | E | Dipeptidase | ||
AHMNLFMI_00592 | 4.8e-53 | pipD | E | Dipeptidase | ||
AHMNLFMI_00593 | 6.2e-36 | pipD | E | Dipeptidase | ||
AHMNLFMI_00594 | 1e-63 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
AHMNLFMI_00595 | 1e-64 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
AHMNLFMI_00596 | 3.7e-18 | ybiR | P | Citrate transporter | ||
AHMNLFMI_00597 | 1.1e-19 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHMNLFMI_00598 | 1.7e-76 | GM | epimerase | |||
AHMNLFMI_00599 | 2.7e-210 | CP_1020 | S | Zinc finger, swim domain protein | ||
AHMNLFMI_00600 | 9.3e-57 | CP_1020 | S | Zinc finger, swim domain protein | ||
AHMNLFMI_00601 | 9.4e-35 | CP_1020 | S | Zinc finger, swim domain protein | ||
AHMNLFMI_00602 | 1.5e-22 | CP_1020 | S | Zinc finger, swim domain protein | ||
AHMNLFMI_00603 | 5.4e-168 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_00604 | 1.2e-36 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_00605 | 4.3e-109 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_00606 | 1.9e-125 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_00607 | 7.7e-30 | 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) | |
AHMNLFMI_00608 | 4.1e-63 | K | Transcriptional regulator | |||
AHMNLFMI_00609 | 1.4e-209 | pepF2 | E | Oligopeptidase F | ||
AHMNLFMI_00610 | 1.5e-33 | K | Transcriptional regulator | |||
AHMNLFMI_00611 | 1.4e-59 | pepF2 | E | Oligopeptidase F | ||
AHMNLFMI_00615 | 8.6e-69 | dnaI | L | Primosomal protein DnaI | ||
AHMNLFMI_00616 | 1.4e-26 | 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) | |
AHMNLFMI_00617 | 2.1e-55 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
AHMNLFMI_00618 | 4.6e-213 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
AHMNLFMI_00619 | 2.4e-65 | malT | G | Major Facilitator | ||
AHMNLFMI_00620 | 2.7e-50 | malT | G | Major Facilitator | ||
AHMNLFMI_00621 | 2.9e-35 | malT | G | Major Facilitator | ||
AHMNLFMI_00622 | 1e-37 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_00624 | 7.7e-55 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_00625 | 2.3e-71 | 3.6.4.13 | S | domain, Protein | ||
AHMNLFMI_00627 | 9.3e-294 | tagE1 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_00628 | 5.6e-118 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AHMNLFMI_00629 | 3.1e-111 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
AHMNLFMI_00630 | 2.2e-101 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_00631 | 7.7e-39 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_00632 | 6.3e-96 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
AHMNLFMI_00633 | 1.2e-58 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
AHMNLFMI_00634 | 4.4e-43 | terC | P | membrane | ||
AHMNLFMI_00635 | 4.1e-44 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
AHMNLFMI_00636 | 7.3e-101 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
AHMNLFMI_00637 | 1.2e-30 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
AHMNLFMI_00638 | 9.1e-30 | dps | P | Ferritin-like domain | ||
AHMNLFMI_00639 | 2.9e-85 | dps | P | Belongs to the Dps family | ||
AHMNLFMI_00640 | 3.4e-216 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_00641 | 1.9e-92 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_00642 | 5.8e-20 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_00643 | 2e-49 | 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 | |
AHMNLFMI_00645 | 1.6e-11 | 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 | |
AHMNLFMI_00647 | 7.7e-154 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
AHMNLFMI_00648 | 1.6e-64 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_00649 | 3.5e-117 | GM | NAD(P)H-binding | |||
AHMNLFMI_00650 | 9.3e-159 | ypaH | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
AHMNLFMI_00653 | 5e-119 | drgA | C | Nitroreductase family | ||
AHMNLFMI_00654 | 2.9e-21 | drgA | C | Nitroreductase family | ||
AHMNLFMI_00655 | 4.5e-42 | drgA | C | Nitroreductase family | ||
AHMNLFMI_00656 | 1.6e-10 | ysaA | V | RDD family | ||
AHMNLFMI_00657 | 1.2e-20 | ysaA | V | RDD family | ||
AHMNLFMI_00658 | 4e-53 | corA | P | CorA-like Mg2+ transporter protein | ||
AHMNLFMI_00659 | 1.3e-116 | ysaA | V | RDD family | ||
AHMNLFMI_00660 | 1.2e-20 | ysaA | V | RDD family | ||
AHMNLFMI_00661 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_00662 | 1.6e-140 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_00663 | 6.2e-58 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_00664 | 6.5e-51 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_00665 | 2.3e-54 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
AHMNLFMI_00666 | 1.3e-47 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
AHMNLFMI_00667 | 8.5e-92 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
AHMNLFMI_00668 | 1.2e-47 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_00669 | 8.5e-82 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_00670 | 1.7e-15 | htrA | 3.4.21.107 | O | serine protease | |
AHMNLFMI_00671 | 8.6e-103 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_00672 | 1.4e-68 | f42a | O | Band 7 protein | ||
AHMNLFMI_00673 | 4.4e-139 | f42a | O | Band 7 protein | ||
AHMNLFMI_00674 | 2.2e-39 | L | Pfam:Integrase_AP2 | |||
AHMNLFMI_00675 | 1.2e-25 | L | Phage integrase, N-terminal SAM-like domain | |||
AHMNLFMI_00677 | 2.2e-41 | gutM | K | Glucitol operon activator protein (GutM) | ||
AHMNLFMI_00678 | 8.2e-22 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
AHMNLFMI_00679 | 6.2e-21 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_00680 | 1.1e-86 | gutM | K | Glucitol operon activator protein (GutM) | ||
AHMNLFMI_00681 | 2.3e-31 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
AHMNLFMI_00682 | 2.3e-25 | S | ATPases associated with a variety of cellular activities | |||
AHMNLFMI_00683 | 6e-44 | S | ATPases associated with a variety of cellular activities | |||
AHMNLFMI_00684 | 2.8e-27 | S | ATPases associated with a variety of cellular activities | |||
AHMNLFMI_00685 | 6.8e-11 | S | ATPases associated with a variety of cellular activities | |||
AHMNLFMI_00686 | 8.7e-47 | S | Bacteriophage Mu Gam like protein | |||
AHMNLFMI_00687 | 2.6e-24 | S | Bacteriophage Mu Gam like protein | |||
AHMNLFMI_00689 | 7.9e-21 | |||||
AHMNLFMI_00691 | 6.7e-16 | |||||
AHMNLFMI_00692 | 1e-26 | |||||
AHMNLFMI_00693 | 3.2e-70 | S | Phage tail tube protein | |||
AHMNLFMI_00694 | 1.4e-21 | |||||
AHMNLFMI_00695 | 6.7e-25 | |||||
AHMNLFMI_00696 | 7.4e-23 | |||||
AHMNLFMI_00697 | 2.3e-92 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
AHMNLFMI_00698 | 4.6e-64 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
AHMNLFMI_00699 | 1.1e-34 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHMNLFMI_00700 | 8.2e-51 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHMNLFMI_00701 | 3e-58 | perR | P | Belongs to the Fur family | ||
AHMNLFMI_00702 | 1.5e-87 | |||||
AHMNLFMI_00703 | 6.4e-87 | perR | P | Belongs to the Fur family | ||
AHMNLFMI_00704 | 4.9e-102 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_00705 | 1.9e-90 | K | Transcriptional regulator | |||
AHMNLFMI_00706 | 9.5e-35 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_00707 | 3.4e-57 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHMNLFMI_00708 | 6.2e-29 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHMNLFMI_00709 | 2.1e-29 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHMNLFMI_00710 | 8e-37 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_00711 | 2.2e-51 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AHMNLFMI_00712 | 1.6e-159 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AHMNLFMI_00713 | 6.4e-66 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_00714 | 4.6e-78 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_00715 | 2.4e-49 | lysP | E | amino acid | ||
AHMNLFMI_00716 | 1.3e-145 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_00717 | 4.6e-34 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
AHMNLFMI_00718 | 1.7e-44 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
AHMNLFMI_00719 | 2.4e-65 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
AHMNLFMI_00720 | 2.3e-115 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_00721 | 1.1e-51 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
AHMNLFMI_00722 | 9.9e-49 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
AHMNLFMI_00723 | 1.6e-38 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
AHMNLFMI_00724 | 1e-15 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
AHMNLFMI_00725 | 8.7e-31 | S | Phage minor structural protein | |||
AHMNLFMI_00726 | 3.9e-24 | S | Phage minor structural protein | |||
AHMNLFMI_00727 | 1.6e-85 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHMNLFMI_00728 | 8.2e-56 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHMNLFMI_00729 | 3.9e-17 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
AHMNLFMI_00730 | 3.5e-85 | msmK | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_00731 | 3.2e-32 | msmK | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_00732 | 1.2e-30 | terL | S | overlaps another CDS with the same product name | ||
AHMNLFMI_00733 | 6.2e-207 | terL | S | overlaps another CDS with the same product name | ||
AHMNLFMI_00735 | 3.6e-202 | S | Phage portal protein | |||
AHMNLFMI_00736 | 1.1e-46 | K | Helix-turn-helix domain | |||
AHMNLFMI_00737 | 3e-57 | K | Transcriptional regulator | |||
AHMNLFMI_00738 | 2.2e-11 | K | Helix-turn-helix domain | |||
AHMNLFMI_00739 | 2.2e-11 | K | Helix-turn-helix domain | |||
AHMNLFMI_00740 | 2e-118 | S | hydrolase activity, acting on ester bonds | |||
AHMNLFMI_00741 | 9.8e-59 | |||||
AHMNLFMI_00742 | 5.2e-54 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
AHMNLFMI_00743 | 1.4e-53 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
AHMNLFMI_00744 | 1.2e-26 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
AHMNLFMI_00745 | 8e-25 | S | Protein of unknown function (DUF554) | |||
AHMNLFMI_00746 | 1.1e-07 | K | LysR substrate binding domain | |||
AHMNLFMI_00747 | 3e-34 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_00748 | 2.1e-32 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHMNLFMI_00749 | 1.7e-145 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_00750 | 2e-66 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
AHMNLFMI_00751 | 3.7e-77 | uspA | T | Belongs to the universal stress protein A family | ||
AHMNLFMI_00752 | 1.9e-135 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_00753 | 1.1e-70 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_00754 | 1.3e-07 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_00755 | 1.5e-48 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_00758 | 1.5e-97 | yjjH | S | Calcineurin-like phosphoesterase | ||
AHMNLFMI_00759 | 4.8e-55 | yjjH | S | Calcineurin-like phosphoesterase | ||
AHMNLFMI_00760 | 5.2e-49 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
AHMNLFMI_00761 | 3.1e-81 | ydiC1 | EGP | Major facilitator Superfamily | ||
AHMNLFMI_00762 | 1e-40 | |||||
AHMNLFMI_00763 | 1.7e-40 | |||||
AHMNLFMI_00764 | 1.5e-115 | |||||
AHMNLFMI_00765 | 6.5e-233 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHMNLFMI_00766 | 4.3e-121 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_00767 | 1.8e-72 | K | Transcriptional regulator | |||
AHMNLFMI_00768 | 2e-80 | K | LytTr DNA-binding domain | |||
AHMNLFMI_00769 | 1e-52 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_00770 | 7.1e-43 | K | LytTr DNA-binding domain | |||
AHMNLFMI_00771 | 1.8e-57 | K | LytTr DNA-binding domain | |||
AHMNLFMI_00772 | 2e-36 | Q | Methyltransferase | |||
AHMNLFMI_00773 | 2.1e-140 | Q | Methyltransferase | |||
AHMNLFMI_00774 | 1.9e-10 | rihC | 3.2.2.1 | F | Nucleoside | |
AHMNLFMI_00775 | 4e-93 | rihC | 3.2.2.1 | F | Nucleoside | |
AHMNLFMI_00776 | 2.5e-38 | vdlC | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
AHMNLFMI_00777 | 1.1e-49 | rihC | 3.2.2.1 | F | Nucleoside | |
AHMNLFMI_00778 | 5.2e-79 | 1.6.5.2 | GM | NmrA-like family | ||
AHMNLFMI_00779 | 0.0 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_00780 | 2.9e-145 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AHMNLFMI_00781 | 4.8e-79 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
AHMNLFMI_00782 | 7.2e-197 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
AHMNLFMI_00783 | 1e-62 | hxlR | K | Transcriptional regulator, HxlR family | ||
AHMNLFMI_00784 | 4.2e-121 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
AHMNLFMI_00785 | 5.5e-55 | C | Aldo/keto reductase family | |||
AHMNLFMI_00786 | 1.4e-69 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AHMNLFMI_00787 | 1.2e-13 | ymfF | S | Peptidase M16 inactive domain protein | ||
AHMNLFMI_00788 | 5.9e-52 | S | ABC-2 family transporter protein | |||
AHMNLFMI_00789 | 1.4e-35 | S | ABC-2 family transporter protein | |||
AHMNLFMI_00790 | 2.5e-248 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00791 | 7.9e-48 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00792 | 1.2e-38 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_00793 | 2.4e-37 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_00794 | 1.1e-197 | yhhX | 1.1.1.371 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
AHMNLFMI_00795 | 2.5e-175 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
AHMNLFMI_00796 | 8.1e-117 | K | Helix-turn-helix domain, rpiR family | |||
AHMNLFMI_00797 | 1e-66 | aatB | ET | ABC transporter substrate-binding protein | ||
AHMNLFMI_00798 | 2.5e-115 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_00799 | 4.6e-109 | glnP | P | ABC transporter permease | ||
AHMNLFMI_00800 | 2.3e-15 | glnP | P | ABC transporter permease | ||
AHMNLFMI_00801 | 1.2e-146 | minD | D | Belongs to the ParA family | ||
AHMNLFMI_00802 | 1.9e-116 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
AHMNLFMI_00803 | 2.3e-57 | 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) | |
AHMNLFMI_00804 | 2.2e-154 | S | DUF218 domain | |||
AHMNLFMI_00805 | 2.7e-68 | lemA | S | LemA family | ||
AHMNLFMI_00806 | 4.3e-56 | lemA | S | LemA family | ||
AHMNLFMI_00807 | 1.2e-28 | lemA | S | LemA family | ||
AHMNLFMI_00808 | 5.3e-37 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AHMNLFMI_00809 | 5.6e-85 | drrA | V | ABC transporter | ||
AHMNLFMI_00812 | 6.6e-156 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_00813 | 6.5e-30 | 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 | |||
AHMNLFMI_00814 | 4.8e-16 | 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 | |||
AHMNLFMI_00815 | 4.2e-50 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AHMNLFMI_00816 | 5.6e-37 | 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 | |||
AHMNLFMI_00817 | 1.2e-34 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_00818 | 4.5e-30 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_00819 | 3.7e-32 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHMNLFMI_00820 | 4.1e-42 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHMNLFMI_00821 | 5.8e-43 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHMNLFMI_00822 | 2.5e-86 | mmuP | E | amino acid | ||
AHMNLFMI_00823 | 2.9e-27 | mmuP | E | amino acid | ||
AHMNLFMI_00824 | 9.6e-08 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
AHMNLFMI_00825 | 1.1e-21 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
AHMNLFMI_00826 | 6.7e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
AHMNLFMI_00827 | 1.8e-80 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
AHMNLFMI_00828 | 2.3e-124 | L | AAA domain | |||
AHMNLFMI_00829 | 1.3e-48 | L | AAA domain | |||
AHMNLFMI_00830 | 3.2e-26 | spr | 3.4.17.13 | M | NlpC/P60 family | |
AHMNLFMI_00831 | 3.2e-32 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
AHMNLFMI_00832 | 5.8e-10 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
AHMNLFMI_00833 | 1.5e-24 | gutM | K | Glucitol operon activator protein (GutM) | ||
AHMNLFMI_00834 | 7.6e-27 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_00835 | 1.2e-12 | gutM | K | Glucitol operon activator protein (GutM) | ||
AHMNLFMI_00836 | 1.1e-62 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_00837 | 8.9e-28 | gutM | K | Glucitol operon activator protein (GutM) | ||
AHMNLFMI_00838 | 6.8e-278 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
AHMNLFMI_00839 | 9.4e-87 | 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 | |
AHMNLFMI_00840 | 1.1e-46 | 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 | |
AHMNLFMI_00841 | 1.7e-159 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHMNLFMI_00842 | 3.7e-13 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_00843 | 1.2e-46 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_00844 | 2.4e-18 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_00846 | 3.2e-133 | XK27_00765 | ||||
AHMNLFMI_00848 | 5.7e-30 | XK27_00765 | ||||
AHMNLFMI_00850 | 2.3e-79 | |||||
AHMNLFMI_00851 | 5.5e-119 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_00852 | 7.3e-27 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_00853 | 6.8e-75 | 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 | |
AHMNLFMI_00854 | 3.1e-150 | lacR | K | Transcriptional regulator | ||
AHMNLFMI_00855 | 1.5e-31 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | ||
AHMNLFMI_00856 | 1.2e-40 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHMNLFMI_00857 | 1.6e-123 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHMNLFMI_00858 | 6.9e-152 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AHMNLFMI_00859 | 2.9e-54 | XK27_00670 | S | ABC transporter | ||
AHMNLFMI_00860 | 1.9e-28 | XK27_00670 | S | ABC transporter | ||
AHMNLFMI_00861 | 1e-24 | GM | NAD(P)H-binding | |||
AHMNLFMI_00862 | 6.3e-91 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AHMNLFMI_00863 | 1.2e-103 | GM | NAD(P)H-binding | |||
AHMNLFMI_00864 | 7e-31 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
AHMNLFMI_00865 | 2.9e-78 | KT | response to antibiotic | |||
AHMNLFMI_00866 | 5.6e-137 | lys | M | Glycosyl hydrolases family 25 | ||
AHMNLFMI_00869 | 1.9e-83 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
AHMNLFMI_00870 | 1.7e-51 | rplQ | J | Ribosomal protein L17 | ||
AHMNLFMI_00871 | 2.1e-61 | rplQ | J | Ribosomal protein L17 | ||
AHMNLFMI_00872 | 4.7e-118 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_00873 | 1.2e-22 | ftpA | P | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_00874 | 7.6e-43 | uspA | T | Universal stress protein family | ||
AHMNLFMI_00875 | 2.7e-26 | ftpA | P | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_00876 | 1.2e-48 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHMNLFMI_00877 | 3.3e-96 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHMNLFMI_00878 | 4.1e-25 | S | AAA domain | |||
AHMNLFMI_00879 | 5.9e-70 | S | Protein of unknown function (DUF669) | |||
AHMNLFMI_00880 | 2.1e-26 | S | AAA domain | |||
AHMNLFMI_00881 | 1.3e-78 | S | Protein of unknown function (DUF669) | |||
AHMNLFMI_00882 | 7e-26 | S | AAA domain | |||
AHMNLFMI_00883 | 4.2e-11 | S | Protein of unknown function (DUF669) | |||
AHMNLFMI_00884 | 3.1e-30 | S | AAA domain | |||
AHMNLFMI_00887 | 4.2e-36 | S | UPF0397 protein | |||
AHMNLFMI_00888 | 5.2e-15 | S | UPF0397 protein | |||
AHMNLFMI_00889 | 3.1e-295 | ykoD | P | ABC transporter, ATP-binding protein | ||
AHMNLFMI_00890 | 4.9e-151 | cbiQ | P | cobalt transport | ||
AHMNLFMI_00891 | 4.3e-40 | |||||
AHMNLFMI_00892 | 1.3e-61 | S | Cell surface protein | |||
AHMNLFMI_00893 | 2e-101 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_00894 | 1.8e-50 | |||||
AHMNLFMI_00895 | 2.6e-41 | |||||
AHMNLFMI_00896 | 2.8e-111 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00897 | 6.9e-18 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
AHMNLFMI_00898 | 4.6e-25 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
AHMNLFMI_00899 | 2.1e-123 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_00900 | 2e-65 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_00901 | 3.1e-28 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
AHMNLFMI_00902 | 4.1e-30 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
AHMNLFMI_00903 | 3.1e-28 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
AHMNLFMI_00904 | 2.5e-201 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
AHMNLFMI_00905 | 5.6e-43 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
AHMNLFMI_00906 | 2.4e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_00907 | 9.8e-146 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
AHMNLFMI_00909 | 6.3e-105 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
AHMNLFMI_00910 | 1.8e-19 | |||||
AHMNLFMI_00911 | 1.8e-19 | |||||
AHMNLFMI_00912 | 1.3e-82 | galR | K | Transcriptional regulator | ||
AHMNLFMI_00913 | 9e-33 | |||||
AHMNLFMI_00914 | 5.2e-47 | |||||
AHMNLFMI_00915 | 4.5e-12 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
AHMNLFMI_00916 | 3.1e-29 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
AHMNLFMI_00917 | 4.9e-23 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_00918 | 1.1e-36 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_00919 | 3.6e-136 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_00920 | 1.6e-41 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_00921 | 8e-28 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_00922 | 6.1e-105 | yxjI | ||||
AHMNLFMI_00923 | 1.2e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_00924 | 2.9e-90 | glnP | P | ABC transporter | ||
AHMNLFMI_00925 | 8.7e-52 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_00926 | 4e-44 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_00927 | 8.3e-33 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_00928 | 1.7e-130 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_00929 | 2.9e-33 | 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 | ||
AHMNLFMI_00930 | 3.7e-33 | 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 | ||
AHMNLFMI_00931 | 8.9e-24 | 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 | ||
AHMNLFMI_00932 | 5e-33 | 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 | ||
AHMNLFMI_00933 | 1.1e-14 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_00934 | 8.9e-48 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_00935 | 1.5e-152 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
AHMNLFMI_00936 | 8.7e-162 | K | LysR substrate binding domain | |||
AHMNLFMI_00937 | 9.9e-24 | 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 | ||
AHMNLFMI_00938 | 7.3e-127 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
AHMNLFMI_00939 | 2.2e-11 | S | Enterocin A Immunity | |||
AHMNLFMI_00940 | 9.1e-40 | C | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_00941 | 9.4e-41 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_00942 | 4.2e-42 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_00943 | 2.9e-86 | 1.6.5.5 | C | Alcohol dehydrogenase GroES-like domain | ||
AHMNLFMI_00944 | 5.3e-57 | 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 | ||
AHMNLFMI_00945 | 1.1e-66 | 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 | ||
AHMNLFMI_00946 | 5.5e-83 | 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 | ||
AHMNLFMI_00947 | 3.6e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
AHMNLFMI_00948 | 1.6e-07 | D | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_00950 | 5.4e-88 | |||||
AHMNLFMI_00951 | 3.9e-189 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_00952 | 4.8e-208 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_00953 | 1.6e-102 | uvrA3 | L | excinuclease ABC | ||
AHMNLFMI_00954 | 1.2e-49 | uvrA3 | L | excinuclease ABC | ||
AHMNLFMI_00955 | 7.7e-120 | 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 | |
AHMNLFMI_00956 | 1.3e-21 | 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 | |
AHMNLFMI_00957 | 4e-38 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_00958 | 3.9e-148 | glnH | ET | ABC transporter substrate-binding protein | ||
AHMNLFMI_00959 | 1.6e-109 | gluC | P | ABC transporter permease | ||
AHMNLFMI_00960 | 4e-108 | glnP | P | ABC transporter permease | ||
AHMNLFMI_00961 | 4.4e-83 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |||
AHMNLFMI_00962 | 3.1e-153 | K | CAT RNA binding domain | |||
AHMNLFMI_00963 | 7.5e-158 | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
AHMNLFMI_00964 | 7.1e-48 | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
AHMNLFMI_00965 | 2.2e-92 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_00966 | 3.6e-54 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_00967 | 1.8e-39 | G | Transmembrane secretion effector | |||
AHMNLFMI_00968 | 4e-125 | EGP | Transmembrane secretion effector | |||
AHMNLFMI_00969 | 3.2e-07 | EGP | Transmembrane secretion effector | |||
AHMNLFMI_00971 | 1.5e-123 | yliE | T | EAL domain | ||
AHMNLFMI_00972 | 1.9e-50 | yliE | T | EAL domain | ||
AHMNLFMI_00973 | 2e-75 | |||||
AHMNLFMI_00974 | 2.3e-67 | yhaO | L | Ser Thr phosphatase family protein | ||
AHMNLFMI_00975 | 1.2e-94 | yhaO | L | Ser Thr phosphatase family protein | ||
AHMNLFMI_00976 | 8.6e-51 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_00977 | 1.4e-53 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_00978 | 3.5e-39 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_00979 | 4.6e-48 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_00980 | 4.9e-49 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_00981 | 8e-17 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_00982 | 1.5e-109 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_00983 | 8.9e-79 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_00984 | 6.1e-15 | S | Haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_00985 | 1.8e-198 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AHMNLFMI_00986 | 2.9e-93 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
AHMNLFMI_00987 | 9.8e-91 | srtA | 3.4.22.70 | M | sortase family | |
AHMNLFMI_00988 | 2.9e-38 | srtA | 3.4.22.70 | M | sortase family | |
AHMNLFMI_00989 | 2.7e-213 | J | translation release factor activity | |||
AHMNLFMI_00990 | 8.1e-67 | |||||
AHMNLFMI_00991 | 3.2e-101 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_00992 | 4.1e-51 | |||||
AHMNLFMI_00993 | 1.3e-48 | cps3D | ||||
AHMNLFMI_00994 | 1.3e-57 | cps3D | ||||
AHMNLFMI_00995 | 1.5e-222 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
AHMNLFMI_00996 | 2.5e-74 | cps3B | S | Glycosyltransferase like family 2 | ||
AHMNLFMI_00997 | 4.6e-08 | |||||
AHMNLFMI_00998 | 3.2e-15 | |||||
AHMNLFMI_00999 | 1.2e-07 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_01000 | 4.3e-09 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_01003 | 2.3e-158 | 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 | |
AHMNLFMI_01004 | 4e-75 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
AHMNLFMI_01005 | 2.9e-96 | rmaB | K | Transcriptional regulator, MarR family | ||
AHMNLFMI_01006 | 3e-32 | rmaB | K | Transcriptional regulator, MarR family | ||
AHMNLFMI_01007 | 3e-63 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
AHMNLFMI_01008 | 2e-36 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
AHMNLFMI_01009 | 3.5e-97 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHMNLFMI_01010 | 6e-13 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_01011 | 1e-96 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_01012 | 1.4e-28 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_01013 | 1.5e-157 | galR | K | Transcriptional regulator | ||
AHMNLFMI_01014 | 3.2e-60 | lacS | G | Transporter | ||
AHMNLFMI_01015 | 2.8e-15 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_01016 | 5.4e-36 | S | Prolyl oligopeptidase family | |||
AHMNLFMI_01017 | 4.2e-74 | 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 | |
AHMNLFMI_01018 | 1.1e-95 | 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 | |
AHMNLFMI_01019 | 1.6e-19 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01020 | 5.9e-163 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01021 | 2.8e-122 | mngA | 2.7.1.195, 2.7.1.202 | U | Phosphotransferase system, EIIC | |
AHMNLFMI_01022 | 2.4e-26 | mngA | 2.7.1.195, 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_01023 | 1.7e-20 | fryA | 2.7.1.202 | G | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
AHMNLFMI_01024 | 2.2e-90 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_01025 | 2e-77 | merR | K | MerR family regulatory protein | ||
AHMNLFMI_01026 | 1.7e-99 | 1.6.5.2 | GM | NmrA-like family | ||
AHMNLFMI_01027 | 1.2e-30 | merR | K | MerR family regulatory protein | ||
AHMNLFMI_01028 | 1.8e-15 | 1.6.5.2 | GM | NmrA-like family | ||
AHMNLFMI_01029 | 9.7e-35 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01030 | 4e-19 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_01032 | 1.2e-18 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
AHMNLFMI_01033 | 1.1e-42 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
AHMNLFMI_01034 | 3.7e-91 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
AHMNLFMI_01035 | 1.4e-186 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
AHMNLFMI_01036 | 8.1e-99 | 1.5.1.3 | H | RibD C-terminal domain | ||
AHMNLFMI_01037 | 7.4e-19 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHMNLFMI_01039 | 5.6e-10 | S | Minor capsid protein from bacteriophage | |||
AHMNLFMI_01040 | 2.1e-10 | N | domain, Protein | |||
AHMNLFMI_01041 | 5.7e-25 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_01042 | 1.1e-36 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_01043 | 3.4e-16 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_01044 | 2.1e-22 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_01045 | 5.2e-81 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_01046 | 8.9e-66 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_01047 | 3.8e-60 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_01049 | 2.8e-30 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_01050 | 8.8e-10 | S | Cell surface protein | |||
AHMNLFMI_01051 | 5.5e-95 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
AHMNLFMI_01052 | 1.5e-64 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
AHMNLFMI_01053 | 2.7e-69 | |||||
AHMNLFMI_01054 | 5.6e-57 | |||||
AHMNLFMI_01055 | 0.0 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | ||
AHMNLFMI_01056 | 4.3e-15 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01057 | 4.1e-18 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01058 | 5e-19 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01059 | 1e-10 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01060 | 2.8e-15 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01061 | 2.7e-17 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01062 | 1.4e-21 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01063 | 3.2e-75 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01064 | 2.9e-149 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01065 | 1.3e-158 | cadA | P | P-type ATPase | ||
AHMNLFMI_01066 | 3.3e-116 | cadA | P | P-type ATPase | ||
AHMNLFMI_01067 | 6.5e-22 | cadA | P | P-type ATPase | ||
AHMNLFMI_01068 | 8.5e-111 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AHMNLFMI_01069 | 2.2e-35 | 3.6.1.55 | F | NUDIX domain | ||
AHMNLFMI_01070 | 3.9e-71 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AHMNLFMI_01071 | 1.3e-74 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AHMNLFMI_01072 | 2.8e-53 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AHMNLFMI_01073 | 1.4e-22 | 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 | ||
AHMNLFMI_01074 | 1.1e-59 | 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 | ||
AHMNLFMI_01075 | 2.1e-23 | 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 | ||
AHMNLFMI_01076 | 3.3e-22 | 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 | |
AHMNLFMI_01077 | 9.4e-144 | 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 | |
AHMNLFMI_01078 | 7.1e-54 | glpQ3 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
AHMNLFMI_01079 | 5.4e-214 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
AHMNLFMI_01080 | 2.3e-63 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
AHMNLFMI_01081 | 2.7e-46 | 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 | |
AHMNLFMI_01082 | 1.3e-117 | K | Transcriptional regulator | |||
AHMNLFMI_01083 | 3e-70 | V | ABC transporter | |||
AHMNLFMI_01084 | 7.1e-80 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_01085 | 1.7e-78 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_01086 | 9.2e-108 | tag | 3.2.2.20 | L | glycosylase | |
AHMNLFMI_01087 | 1.4e-79 | yycH | S | YycH protein | ||
AHMNLFMI_01088 | 1.3e-42 | yycH | S | YycH protein | ||
AHMNLFMI_01089 | 2.8e-65 | yycH | S | YycH protein | ||
AHMNLFMI_01090 | 2.2e-14 | 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) | ||
AHMNLFMI_01091 | 2.6e-58 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
AHMNLFMI_01092 | 2.2e-14 | 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) | ||
AHMNLFMI_01093 | 5.6e-149 | |||||
AHMNLFMI_01094 | 1.2e-100 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
AHMNLFMI_01095 | 5e-52 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
AHMNLFMI_01096 | 5.4e-130 | emrY | EGP | Major facilitator Superfamily | ||
AHMNLFMI_01097 | 6.8e-36 | |||||
AHMNLFMI_01098 | 4.1e-39 | |||||
AHMNLFMI_01099 | 3.2e-147 | sepS16B | ||||
AHMNLFMI_01100 | 2.2e-66 | gcvH | E | Glycine cleavage H-protein | ||
AHMNLFMI_01101 | 5.7e-24 | lytE | M | LysM domain protein | ||
AHMNLFMI_01102 | 2.3e-41 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_01103 | 7.4e-70 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_01104 | 8.1e-18 | K | Helix-turn-helix domain | |||
AHMNLFMI_01105 | 2.6e-35 | K | Helix-turn-helix domain | |||
AHMNLFMI_01106 | 1e-91 | K | Helix-turn-helix domain | |||
AHMNLFMI_01107 | 2.2e-20 | fhuC | 3.6.3.34 | HP | ABC transporter | |
AHMNLFMI_01108 | 2.8e-44 | fhuC | 3.6.3.34 | HP | ABC transporter | |
AHMNLFMI_01109 | 8e-29 | P | Concanavalin A-like lectin/glucanases superfamily | |||
AHMNLFMI_01110 | 1.4e-194 | P | Concanavalin A-like lectin/glucanases superfamily | |||
AHMNLFMI_01111 | 5.8e-229 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHMNLFMI_01112 | 1.9e-38 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHMNLFMI_01113 | 5.4e-14 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHMNLFMI_01114 | 2.1e-85 | pts29C | 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 | ||
AHMNLFMI_01115 | 2.1e-85 | pts29C | 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 | ||
AHMNLFMI_01116 | 6.9e-145 | ysaA | V | RDD family | ||
AHMNLFMI_01117 | 7.9e-31 | lacR | K | Transcriptional regulator | ||
AHMNLFMI_01118 | 1.1e-61 | lacR | K | Transcriptional regulator | ||
AHMNLFMI_01119 | 1.6e-40 | lacR | K | Transcriptional regulator | ||
AHMNLFMI_01120 | 1.2e-18 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_01121 | 1.7e-27 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_01122 | 1.4e-33 | nupG | F | Nucleoside | ||
AHMNLFMI_01123 | 4.3e-26 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_01124 | 6.9e-47 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_01125 | 1e-94 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_01126 | 7.2e-89 | ywnB | S | NAD(P)H-binding | ||
AHMNLFMI_01127 | 2.5e-49 | XK27_04080 | H | RibD C-terminal domain | ||
AHMNLFMI_01129 | 7.7e-21 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_01130 | 2.9e-38 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_01131 | 2.7e-20 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_01132 | 1.8e-53 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_01133 | 1.6e-22 | V | ABC transporter | |||
AHMNLFMI_01134 | 4e-42 | V | ABC transporter | |||
AHMNLFMI_01135 | 2.7e-38 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AHMNLFMI_01136 | 9.9e-108 | 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 | ||
AHMNLFMI_01137 | 4.8e-69 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AHMNLFMI_01138 | 8.4e-49 | 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 | ||
AHMNLFMI_01139 | 3.2e-24 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01140 | 5.8e-37 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01141 | 7e-26 | 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 | ||
AHMNLFMI_01142 | 3.3e-33 | yfbR | S | HD containing hydrolase-like enzyme | ||
AHMNLFMI_01143 | 3.2e-113 | 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 | ||
AHMNLFMI_01144 | 1e-93 | 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 | ||
AHMNLFMI_01145 | 1.1e-29 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
AHMNLFMI_01146 | 2e-37 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
AHMNLFMI_01147 | 1.5e-76 | flhF | N | Uncharacterized conserved protein (DUF2075) | ||
AHMNLFMI_01148 | 8.8e-95 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHMNLFMI_01149 | 6.1e-40 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHMNLFMI_01150 | 2.2e-151 | celB | 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 | ||
AHMNLFMI_01151 | 5.3e-17 | celB | 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 | ||
AHMNLFMI_01152 | 1.9e-45 | dedA | S | SNARE associated Golgi protein | ||
AHMNLFMI_01153 | 3.6e-59 | pva2 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
AHMNLFMI_01154 | 2.5e-90 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AHMNLFMI_01155 | 1.7e-185 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AHMNLFMI_01156 | 4.7e-100 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_01157 | 5.5e-56 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_01158 | 2.3e-187 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_01159 | 4.4e-206 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHMNLFMI_01165 | 2.2e-17 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AHMNLFMI_01166 | 1.3e-72 | 3.6.1.55 | F | NUDIX domain | ||
AHMNLFMI_01167 | 1.3e-48 | sugE | U | Multidrug resistance protein | ||
AHMNLFMI_01168 | 2.4e-19 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_01169 | 1.3e-199 | cps4F | 2.4.1.306 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01170 | 2.7e-123 | tuaA | M | Bacterial sugar transferase | ||
AHMNLFMI_01171 | 1.1e-175 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
AHMNLFMI_01172 | 3.9e-142 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
AHMNLFMI_01173 | 2.2e-102 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
AHMNLFMI_01174 | 8.4e-77 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
AHMNLFMI_01175 | 1e-131 | epsB | M | biosynthesis protein | ||
AHMNLFMI_01176 | 1.4e-22 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
AHMNLFMI_01177 | 6.5e-15 | |||||
AHMNLFMI_01178 | 3.8e-119 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
AHMNLFMI_01179 | 4.1e-44 | V | ABC transporter | |||
AHMNLFMI_01180 | 1.6e-204 | rhaB | 2.7.1.12, 2.7.1.16, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
AHMNLFMI_01181 | 5.3e-83 | K | response regulator | |||
AHMNLFMI_01182 | 1.3e-95 | phoR | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_01183 | 2.1e-194 | |||||
AHMNLFMI_01184 | 1.9e-40 | 3.6.3.35 | P | ATPases associated with a variety of cellular activities | ||
AHMNLFMI_01185 | 8.1e-92 | L | restriction endonuclease | |||
AHMNLFMI_01186 | 2e-22 | L | restriction endonuclease | |||
AHMNLFMI_01187 | 2.3e-103 | 3.6.4.13 | S | domain, Protein | ||
AHMNLFMI_01188 | 3.3e-21 | L | HNH nucleases | |||
AHMNLFMI_01189 | 1.1e-12 | V | HNH nucleases | |||
AHMNLFMI_01190 | 6.4e-10 | S | Phage terminase, small subunit | |||
AHMNLFMI_01191 | 3.3e-33 | L | HNH nucleases | |||
AHMNLFMI_01193 | 4e-65 | gatC | G | PTS system sugar-specific permease component | ||
AHMNLFMI_01194 | 4.4e-86 | K | DeoR C terminal sensor domain | |||
AHMNLFMI_01195 | 1.5e-80 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_01197 | 0.0 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHMNLFMI_01198 | 1.1e-71 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01199 | 1.2e-124 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01200 | 3.5e-18 | ycgX | S | Protein of unknown function (DUF1398) | ||
AHMNLFMI_01201 | 4.3e-39 | ycgX | S | Protein of unknown function (DUF1398) | ||
AHMNLFMI_01202 | 4.2e-49 | |||||
AHMNLFMI_01203 | 3.4e-25 | |||||
AHMNLFMI_01204 | 1.7e-59 | dedA | S | SNARE-like domain protein | ||
AHMNLFMI_01205 | 1.1e-74 | dedA | S | SNARE-like domain protein | ||
AHMNLFMI_01206 | 4.6e-117 | S | Protein of unknown function (DUF1461) | |||
AHMNLFMI_01207 | 1.5e-146 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
AHMNLFMI_01208 | 1.5e-80 | yutD | S | Protein of unknown function (DUF1027) | ||
AHMNLFMI_01209 | 5.1e-43 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
AHMNLFMI_01210 | 1e-123 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_01211 | 7.7e-141 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_01212 | 1.1e-48 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01213 | 2.9e-70 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01214 | 5.7e-77 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01215 | 9.3e-13 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01216 | 1.1e-35 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01217 | 9.3e-13 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01218 | 3.7e-35 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01219 | 9.5e-22 | cps4F | 2.4.1.306 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01220 | 5.3e-37 | cps4F | 2.4.1.306 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01221 | 4.3e-189 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_01222 | 1.2e-36 | |||||
AHMNLFMI_01223 | 2.8e-104 | akr5f | 1.1.1.346 | S | reductase | |
AHMNLFMI_01224 | 2e-78 | K | Transcriptional regulator | |||
AHMNLFMI_01227 | 3.2e-28 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHMNLFMI_01228 | 3.1e-93 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHMNLFMI_01229 | 4e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
AHMNLFMI_01230 | 4.3e-28 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
AHMNLFMI_01231 | 1e-95 | 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 | |
AHMNLFMI_01232 | 3.3e-30 | 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 | |
AHMNLFMI_01233 | 3.3e-30 | 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 | |
AHMNLFMI_01234 | 4.2e-32 | S | YozE SAM-like fold | |||
AHMNLFMI_01235 | 2.1e-59 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
AHMNLFMI_01236 | 3.4e-45 | hchA | S | DJ-1/PfpI family | ||
AHMNLFMI_01237 | 1.2e-72 | MA20_25245 | K | FR47-like protein | ||
AHMNLFMI_01238 | 5e-50 | hchA | S | DJ-1/PfpI family | ||
AHMNLFMI_01239 | 1.6e-85 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_01240 | 2.8e-211 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
AHMNLFMI_01241 | 3.7e-56 | XK27_05470 | E | Methionine synthase | ||
AHMNLFMI_01242 | 5e-142 | XK27_05470 | E | Methionine synthase | ||
AHMNLFMI_01243 | 2.3e-170 | cpsY | K | Transcriptional regulator, LysR family | ||
AHMNLFMI_01244 | 1.8e-98 | L | restriction endonuclease | |||
AHMNLFMI_01245 | 1.1e-43 | L | restriction endonuclease | |||
AHMNLFMI_01246 | 1.1e-66 | nikMN | P | PDGLE domain | ||
AHMNLFMI_01247 | 4.8e-182 | nikMN | P | PDGLE domain | ||
AHMNLFMI_01248 | 4.6e-112 | P | Cobalt transport protein | |||
AHMNLFMI_01249 | 6.3e-52 | P | Cobalt transport protein | |||
AHMNLFMI_01250 | 3.2e-89 | P | Cobalt transport protein | |||
AHMNLFMI_01251 | 2.8e-126 | cbiO | P | ABC transporter | ||
AHMNLFMI_01252 | 1.2e-59 | cbiO | P | ABC transporter | ||
AHMNLFMI_01253 | 4.8e-40 | |||||
AHMNLFMI_01254 | 1.3e-62 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
AHMNLFMI_01256 | 2.2e-46 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_01257 | 1.2e-69 | ctpA | 3.6.3.54 | P | P-type ATPase | |
AHMNLFMI_01258 | 2e-176 | ctpA | 3.6.3.54 | P | P-type ATPase | |
AHMNLFMI_01259 | 3e-21 | ctpA | 3.6.3.54 | P | P-type ATPase | |
AHMNLFMI_01260 | 5e-31 | S | membrane transporter protein | |||
AHMNLFMI_01261 | 1.5e-14 | S | membrane transporter protein | |||
AHMNLFMI_01262 | 2.1e-12 | S | membrane transporter protein | |||
AHMNLFMI_01263 | 2e-49 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_01264 | 6.2e-154 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_01265 | 2.2e-129 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
AHMNLFMI_01266 | 7e-113 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
AHMNLFMI_01267 | 8.5e-284 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
AHMNLFMI_01268 | 5.5e-127 | S | hydrolase | |||
AHMNLFMI_01269 | 6.5e-182 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AHMNLFMI_01270 | 2e-19 | EG | EamA-like transporter family | |||
AHMNLFMI_01271 | 2e-55 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AHMNLFMI_01273 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AHMNLFMI_01274 | 7.2e-64 | mdtG | EGP | Major facilitator Superfamily | ||
AHMNLFMI_01275 | 6e-38 | GM | NAD(P)H-binding | |||
AHMNLFMI_01276 | 5.2e-20 | GM | NAD(P)H-binding | |||
AHMNLFMI_01277 | 1.9e-121 | nox | C | NADH oxidase | ||
AHMNLFMI_01278 | 7.9e-50 | nox | C | NADH oxidase | ||
AHMNLFMI_01279 | 7.8e-44 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
AHMNLFMI_01280 | 9.1e-138 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
AHMNLFMI_01281 | 1.4e-31 | P | Major Facilitator Superfamily | |||
AHMNLFMI_01282 | 1.5e-203 | P | Major Facilitator Superfamily | |||
AHMNLFMI_01283 | 1.2e-46 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_01284 | 3.5e-26 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
AHMNLFMI_01285 | 4.4e-46 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_01286 | 2.1e-10 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01287 | 5.3e-60 | S | membrane transporter protein | |||
AHMNLFMI_01288 | 3.2e-37 | |||||
AHMNLFMI_01291 | 7.4e-38 | S | zinc-ribbon domain | |||
AHMNLFMI_01293 | 9e-57 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
AHMNLFMI_01294 | 6.8e-30 | dhaL | 2.7.1.121 | S | Dak2 | |
AHMNLFMI_01295 | 1.9e-59 | M1-874 | K | Domain of unknown function (DUF1836) | ||
AHMNLFMI_01296 | 1.2e-74 | rrp8 | K | LytTr DNA-binding domain | ||
AHMNLFMI_01297 | 4.8e-111 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_01298 | 8.7e-72 | K | Transcriptional regulator | |||
AHMNLFMI_01299 | 1.6e-65 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_01300 | 5.6e-33 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_01301 | 1.8e-32 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_01302 | 8.4e-65 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_01303 | 3.1e-16 | pbuG | S | permease | ||
AHMNLFMI_01304 | 3.1e-31 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_01305 | 1.3e-113 | gph | 3.1.3.18 | S | Haloacid dehalogenase-like hydrolase | |
AHMNLFMI_01306 | 4.1e-165 | gutB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
AHMNLFMI_01307 | 1.1e-231 | gatC | G | PTS system sugar-specific permease component | ||
AHMNLFMI_01308 | 1.1e-44 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
AHMNLFMI_01309 | 6.6e-31 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_01310 | 3.3e-158 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_01311 | 6.5e-16 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_01312 | 1.6e-19 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_01313 | 8e-56 | yfmR | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_01314 | 7.3e-95 | yfmR | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_01316 | 1.5e-49 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHMNLFMI_01317 | 8.8e-95 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHMNLFMI_01318 | 1.2e-23 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01319 | 7.7e-36 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01320 | 4.5e-29 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01321 | 5.3e-86 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01322 | 2.8e-20 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01323 | 2.8e-53 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01324 | 2.7e-70 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
AHMNLFMI_01325 | 3.3e-118 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
AHMNLFMI_01326 | 4e-31 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
AHMNLFMI_01327 | 5.6e-18 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHMNLFMI_01328 | 4.5e-33 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHMNLFMI_01329 | 5.9e-52 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHMNLFMI_01330 | 2.7e-120 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
AHMNLFMI_01331 | 6e-36 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
AHMNLFMI_01332 | 4.5e-37 | yviA | S | Protein of unknown function (DUF421) | ||
AHMNLFMI_01333 | 8.2e-15 | S | Protein of unknown function (DUF3290) | |||
AHMNLFMI_01334 | 7.5e-75 | yviA | S | Protein of unknown function (DUF421) | ||
AHMNLFMI_01335 | 1.6e-97 | typA | T | GTP-binding protein TypA | ||
AHMNLFMI_01336 | 3.8e-49 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
AHMNLFMI_01337 | 5.3e-20 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
AHMNLFMI_01338 | 5.3e-101 | uvrA3 | L | excinuclease ABC | ||
AHMNLFMI_01339 | 1e-151 | 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 | ||
AHMNLFMI_01340 | 2e-54 | 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 | ||
AHMNLFMI_01341 | 3.1e-81 | 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 | |
AHMNLFMI_01342 | 1.4e-114 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_01343 | 4.9e-162 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
AHMNLFMI_01344 | 1.1e-79 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
AHMNLFMI_01345 | 1.1e-65 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
AHMNLFMI_01346 | 2e-46 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHMNLFMI_01347 | 2.9e-85 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHMNLFMI_01348 | 2e-38 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHMNLFMI_01349 | 3.9e-26 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHMNLFMI_01350 | 2e-25 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHMNLFMI_01351 | 2e-41 | GM | NAD(P)H-binding | |||
AHMNLFMI_01352 | 1.6e-26 | IQ | reductase | |||
AHMNLFMI_01353 | 7.1e-103 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
AHMNLFMI_01354 | 1.4e-34 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
AHMNLFMI_01355 | 1.2e-57 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_01356 | 2.3e-57 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHMNLFMI_01357 | 8.6e-84 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHMNLFMI_01358 | 5.7e-33 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHMNLFMI_01359 | 1.8e-130 | gntR | K | UTRA | ||
AHMNLFMI_01360 | 4.2e-47 | pts20B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_01361 | 1e-28 | 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 | |
AHMNLFMI_01362 | 7.5e-20 | ymdB | S | YmdB-like protein | ||
AHMNLFMI_01363 | 4.8e-81 | ymdB | S | YmdB-like protein | ||
AHMNLFMI_01364 | 8.8e-28 | |||||
AHMNLFMI_01365 | 3.3e-46 | T | Belongs to the universal stress protein A family | |||
AHMNLFMI_01366 | 5.7e-22 | S | Haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_01367 | 4.1e-89 | S | Haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_01368 | 4.9e-34 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_01369 | 8.4e-87 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_01370 | 4e-34 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_01371 | 2.3e-33 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_01372 | 2e-24 | S | Phage major capsid protein E | |||
AHMNLFMI_01373 | 6.5e-43 | S | Phage major capsid protein E | |||
AHMNLFMI_01374 | 1.2e-181 | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
AHMNLFMI_01375 | 2e-74 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
AHMNLFMI_01376 | 4.2e-92 | yrvN | L | AAA C-terminal domain | ||
AHMNLFMI_01377 | 2.2e-41 | cof | S | haloacid dehalogenase-like hydrolase | ||
AHMNLFMI_01378 | 6.8e-11 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01379 | 8.2e-36 | cof | S | haloacid dehalogenase-like hydrolase | ||
AHMNLFMI_01380 | 1.1e-71 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01381 | 2e-46 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01382 | 6e-48 | P | Major Facilitator Superfamily | |||
AHMNLFMI_01383 | 2.6e-171 | P | Major Facilitator Superfamily | |||
AHMNLFMI_01384 | 7.2e-236 | EK | Aminotransferase, class I | |||
AHMNLFMI_01385 | 6.1e-168 | K | LysR substrate binding domain | |||
AHMNLFMI_01386 | 5e-20 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
AHMNLFMI_01387 | 1.6e-24 | gutM | K | Glucitol operon activator protein (GutM) | ||
AHMNLFMI_01388 | 2e-100 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
AHMNLFMI_01389 | 1e-174 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
AHMNLFMI_01390 | 4.7e-36 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
AHMNLFMI_01391 | 2.5e-181 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AHMNLFMI_01392 | 1.2e-97 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01393 | 4.7e-91 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_01394 | 1.8e-21 | luxT | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_01395 | 2.8e-49 | pstS | P | Phosphate | ||
AHMNLFMI_01396 | 3e-151 | pstS | P | Phosphate | ||
AHMNLFMI_01398 | 4.2e-51 | sufB | O | assembly protein SufB | ||
AHMNLFMI_01399 | 1.2e-137 | sufB | O | assembly protein SufB | ||
AHMNLFMI_01400 | 1.6e-23 | sufB | O | assembly protein SufB | ||
AHMNLFMI_01401 | 5.8e-22 | opuCA | 3.6.3.32 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_01402 | 7.4e-54 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
AHMNLFMI_01403 | 6.5e-93 | opuCB | E | ABC transporter permease | ||
AHMNLFMI_01404 | 5.7e-222 | opuCA | 3.6.3.32 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_01405 | 7.9e-269 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AHMNLFMI_01406 | 3.2e-37 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AHMNLFMI_01407 | 2.4e-77 | 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 | |
AHMNLFMI_01408 | 7.5e-175 | 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 | |
AHMNLFMI_01409 | 7.4e-27 | S | QueT transporter | |||
AHMNLFMI_01410 | 1.2e-83 | S | QueT transporter | |||
AHMNLFMI_01411 | 1.1e-38 | S | (CBS) domain | |||
AHMNLFMI_01412 | 3.7e-205 | yacL | S | domain protein | ||
AHMNLFMI_01413 | 1.3e-257 | 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 | ||
AHMNLFMI_01414 | 1.1e-10 | L | Domain of unknown function (DUF4373) | |||
AHMNLFMI_01415 | 1.2e-48 | |||||
AHMNLFMI_01416 | 7.9e-65 | ps308 | K | AntA/AntB antirepressor | ||
AHMNLFMI_01417 | 6.9e-63 | |||||
AHMNLFMI_01418 | 7.1e-65 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
AHMNLFMI_01419 | 1.2e-20 | |||||
AHMNLFMI_01420 | 5.7e-64 | K | LysR substrate binding domain | |||
AHMNLFMI_01421 | 1.2e-12 | |||||
AHMNLFMI_01422 | 3.5e-26 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
AHMNLFMI_01423 | 2.7e-23 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
AHMNLFMI_01424 | 9.4e-40 | yghZ | C | Aldo keto reductase family protein | ||
AHMNLFMI_01425 | 9.2e-26 | yghZ | C | Aldo keto reductase family protein | ||
AHMNLFMI_01426 | 1.6e-11 | pgm1 | G | phosphoglycerate mutase | ||
AHMNLFMI_01427 | 1.1e-09 | pgm1 | G | phosphoglycerate mutase | ||
AHMNLFMI_01428 | 1.1e-63 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_01429 | 2.7e-177 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_01430 | 3e-21 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_01432 | 8.4e-116 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHMNLFMI_01433 | 3.9e-15 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_01434 | 1.8e-32 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHMNLFMI_01435 | 1.8e-74 | 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 | ||
AHMNLFMI_01436 | 1.6e-09 | 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 | ||
AHMNLFMI_01437 | 3.7e-32 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AHMNLFMI_01438 | 1.1e-78 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AHMNLFMI_01439 | 1.6e-146 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
AHMNLFMI_01440 | 2e-142 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
AHMNLFMI_01441 | 7.8e-16 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AHMNLFMI_01442 | 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) | |
AHMNLFMI_01443 | 5.2e-153 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AHMNLFMI_01444 | 8.3e-179 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
AHMNLFMI_01445 | 7.3e-86 | 2.7.7.1, 3.6.1.55 | F | belongs to the nudix hydrolase family | ||
AHMNLFMI_01446 | 6e-48 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
AHMNLFMI_01447 | 7.9e-41 | |||||
AHMNLFMI_01448 | 4.3e-67 | tspO | T | TspO/MBR family | ||
AHMNLFMI_01449 | 1.4e-75 | uspA | T | Belongs to the universal stress protein A family | ||
AHMNLFMI_01450 | 8e-66 | S | Protein of unknown function (DUF805) | |||
AHMNLFMI_01451 | 1.8e-164 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
AHMNLFMI_01452 | 3.5e-36 | |||||
AHMNLFMI_01453 | 3.1e-14 | |||||
AHMNLFMI_01454 | 6.5e-41 | S | transglycosylase associated protein | |||
AHMNLFMI_01455 | 4.8e-29 | S | CsbD-like | |||
AHMNLFMI_01456 | 9.4e-40 | |||||
AHMNLFMI_01457 | 1.9e-17 | S | CsbD-like | |||
AHMNLFMI_01458 | 2e-23 | |||||
AHMNLFMI_01459 | 3.7e-16 | yfcC | S | C4-dicarboxylate anaerobic | ||
AHMNLFMI_01460 | 4.7e-25 | yfcC | S | C4-dicarboxylate anaerobic | ||
AHMNLFMI_01461 | 1.1e-21 | yfcC | S | C4-dicarboxylate anaerobic | ||
AHMNLFMI_01462 | 5e-19 | yfcC | S | C4-dicarboxylate anaerobic | ||
AHMNLFMI_01463 | 5.1e-49 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
AHMNLFMI_01464 | 1.2e-191 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
AHMNLFMI_01465 | 1.6e-54 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
AHMNLFMI_01466 | 2.1e-55 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
AHMNLFMI_01467 | 2e-65 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_01468 | 1.6e-49 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_01469 | 1.1e-106 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_01470 | 3.5e-34 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_01474 | 1.8e-24 | S | Protein of unknown function (DUF2829) | |||
AHMNLFMI_01475 | 7.8e-62 | ps333 | L | Terminase small subunit | ||
AHMNLFMI_01476 | 4.9e-240 | ps334 | S | Terminase-like family | ||
AHMNLFMI_01477 | 5.1e-151 | holB | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_01478 | 2.4e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
AHMNLFMI_01479 | 8.6e-69 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHMNLFMI_01480 | 1.1e-08 | |||||
AHMNLFMI_01481 | 6.9e-66 | |||||
AHMNLFMI_01482 | 8.8e-24 | |||||
AHMNLFMI_01483 | 1.8e-40 | 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 | |
AHMNLFMI_01484 | 7.8e-49 | qacC | P | Small Multidrug Resistance protein | ||
AHMNLFMI_01485 | 6.3e-71 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
AHMNLFMI_01486 | 1.4e-198 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
AHMNLFMI_01487 | 2.7e-13 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01488 | 1.9e-100 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01489 | 3.2e-56 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01490 | 4e-78 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
AHMNLFMI_01492 | 2.2e-82 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AHMNLFMI_01493 | 1.8e-178 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AHMNLFMI_01494 | 8.7e-99 | pgm5 | G | Phosphoglycerate mutase family | ||
AHMNLFMI_01495 | 5.8e-70 | frataxin | S | Domain of unknown function (DU1801) | ||
AHMNLFMI_01496 | 8.2e-18 | frataxin | S | Domain of unknown function (DU1801) | ||
AHMNLFMI_01497 | 3e-22 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_01498 | 3e-248 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_01499 | 6.1e-41 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_01500 | 7.1e-89 | pgm5 | G | Phosphoglycerate mutase family | ||
AHMNLFMI_01501 | 4.3e-31 | ymfF | S | Peptidase M16 inactive domain protein | ||
AHMNLFMI_01502 | 9.6e-25 | ymfF | S | Peptidase M16 inactive domain protein | ||
AHMNLFMI_01503 | 1.1e-32 | ymfF | S | Peptidase M16 inactive domain protein | ||
AHMNLFMI_01504 | 7.4e-60 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AHMNLFMI_01506 | 1.1e-26 | S | Membrane | |||
AHMNLFMI_01507 | 5.8e-54 | |||||
AHMNLFMI_01508 | 2e-74 | |||||
AHMNLFMI_01509 | 5.9e-64 | S | Haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_01510 | 6.4e-100 | S | Haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_01511 | 2e-61 | K | Transcriptional regulator, HxlR family | |||
AHMNLFMI_01512 | 4.9e-91 | P | ABC transporter | |||
AHMNLFMI_01513 | 3.4e-40 | P | ABC transporter | |||
AHMNLFMI_01514 | 3.1e-101 | S | ABC transporter permease | |||
AHMNLFMI_01515 | 6.9e-89 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
AHMNLFMI_01516 | 2e-129 | cof | S | haloacid dehalogenase-like hydrolase | ||
AHMNLFMI_01517 | 5.6e-43 | qorB | 1.6.5.2 | GM | NmrA-like family | |
AHMNLFMI_01518 | 2.5e-89 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
AHMNLFMI_01519 | 2.2e-20 | yacL | S | domain protein | ||
AHMNLFMI_01521 | 2.9e-20 | yacL | S | domain protein | ||
AHMNLFMI_01522 | 6.3e-96 | int | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_01523 | 1.3e-24 | ybjQ | S | Belongs to the UPF0145 family | ||
AHMNLFMI_01524 | 6.7e-31 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_01525 | 1.8e-41 | ybjQ | S | Belongs to the UPF0145 family | ||
AHMNLFMI_01526 | 1.3e-25 | ybjQ | S | Belongs to the UPF0145 family | ||
AHMNLFMI_01527 | 3.2e-20 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_01528 | 1.5e-22 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_01529 | 1.5e-22 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_01530 | 1.5e-128 | yejC | S | Protein of unknown function (DUF1003) | ||
AHMNLFMI_01531 | 2.8e-154 | ccpA | K | catabolite control protein A | ||
AHMNLFMI_01532 | 6.5e-191 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
AHMNLFMI_01533 | 7e-57 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_01534 | 5e-20 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_01535 | 2.5e-168 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_01536 | 2.7e-160 | rbsU | U | ribose uptake protein RbsU | ||
AHMNLFMI_01537 | 6.7e-23 | IQ | NAD dependent epimerase/dehydratase family | |||
AHMNLFMI_01538 | 9.5e-147 | mdtH | P | Sugar (and other) transporter | ||
AHMNLFMI_01539 | 7.9e-304 | ram2 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | |
AHMNLFMI_01540 | 1.2e-24 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_01541 | 1e-19 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01542 | 1.6e-46 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01543 | 4.5e-252 | gor | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_01544 | 2.7e-34 | S | Domain of unknown function (DUF4811) | |||
AHMNLFMI_01545 | 2.1e-102 | rimL | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_01546 | 9.3e-173 | S | Conserved hypothetical protein 698 | |||
AHMNLFMI_01547 | 3.7e-151 | rlrG | K | Transcriptional regulator | ||
AHMNLFMI_01548 | 2e-43 | |||||
AHMNLFMI_01549 | 2.9e-151 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_01550 | 2.5e-72 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_01551 | 1.7e-194 | yclI | V | MacB-like periplasmic core domain | ||
AHMNLFMI_01552 | 4.5e-32 | yclI | V | MacB-like periplasmic core domain | ||
AHMNLFMI_01553 | 2.6e-71 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHMNLFMI_01554 | 2.6e-26 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
AHMNLFMI_01555 | 1.2e-95 | cadD | P | Cadmium resistance transporter | ||
AHMNLFMI_01556 | 2e-49 | K | Transcriptional regulator, ArsR family | |||
AHMNLFMI_01557 | 6.8e-106 | S | SNARE associated Golgi protein | |||
AHMNLFMI_01558 | 1.5e-33 | |||||
AHMNLFMI_01559 | 6.1e-45 | S | SNARE associated Golgi protein | |||
AHMNLFMI_01560 | 1.8e-51 | L | DNA replication protein | |||
AHMNLFMI_01561 | 1.2e-84 | L | DNA replication protein | |||
AHMNLFMI_01562 | 1.9e-111 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
AHMNLFMI_01563 | 1.1e-10 | S | lytic transglycosylase activity | |||
AHMNLFMI_01564 | 3.1e-79 | S | membrane | |||
AHMNLFMI_01565 | 1.3e-88 | S | membrane | |||
AHMNLFMI_01566 | 1.5e-16 | S | membrane | |||
AHMNLFMI_01567 | 6.1e-73 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01568 | 2.5e-62 | celD | 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 | ||
AHMNLFMI_01569 | 1.1e-59 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01570 | 4.2e-190 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01571 | 2.9e-39 | darA | C | Flavodoxin | ||
AHMNLFMI_01573 | 2.5e-76 | darA | C | Flavodoxin | ||
AHMNLFMI_01574 | 1.7e-73 | IQ | reductase | |||
AHMNLFMI_01575 | 4.1e-78 | C | nadph quinone reductase | |||
AHMNLFMI_01576 | 1.5e-87 | C | nadph quinone reductase | |||
AHMNLFMI_01577 | 3.3e-66 | 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) | |
AHMNLFMI_01578 | 2e-35 | 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) | |
AHMNLFMI_01579 | 3e-38 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHMNLFMI_01582 | 5.1e-96 | |||||
AHMNLFMI_01583 | 2.5e-218 | pacL1 | P | P-type ATPase | ||
AHMNLFMI_01584 | 9.9e-149 | pacL1 | P | P-type ATPase | ||
AHMNLFMI_01585 | 2.1e-12 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_01586 | 4.7e-132 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_01587 | 8.7e-89 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01588 | 3.5e-140 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHMNLFMI_01589 | 4.4e-43 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHMNLFMI_01590 | 2.7e-23 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHMNLFMI_01591 | 8.4e-78 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHMNLFMI_01592 | 9.1e-23 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AHMNLFMI_01593 | 3.4e-77 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AHMNLFMI_01594 | 1.3e-45 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
AHMNLFMI_01595 | 1.2e-28 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01596 | 2.2e-61 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01597 | 1.7e-113 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01598 | 4.6e-21 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01599 | 1.5e-26 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_01600 | 6.9e-174 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_01601 | 1.4e-82 | macB | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_01602 | 1.1e-89 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
AHMNLFMI_01603 | 2.2e-57 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_01604 | 7e-15 | |||||
AHMNLFMI_01605 | 6.5e-66 | fic | D | Fic/DOC family | ||
AHMNLFMI_01606 | 1.6e-76 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_01607 | 1.8e-37 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
AHMNLFMI_01608 | 6.2e-36 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
AHMNLFMI_01609 | 5.5e-22 | yliE | T | Putative diguanylate phosphodiesterase | ||
AHMNLFMI_01610 | 5.2e-150 | nox | C | NADH oxidase | ||
AHMNLFMI_01611 | 3.9e-96 | yliE | T | Putative diguanylate phosphodiesterase | ||
AHMNLFMI_01612 | 1.3e-122 | yliE | T | Putative diguanylate phosphodiesterase | ||
AHMNLFMI_01613 | 2.1e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
AHMNLFMI_01614 | 3.4e-77 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AHMNLFMI_01615 | 8e-28 | GM | NmrA-like family | |||
AHMNLFMI_01616 | 2.2e-35 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_01617 | 2.3e-130 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_01618 | 4e-38 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_01619 | 5.3e-36 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_01620 | 1.4e-28 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_01621 | 4.3e-37 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_01622 | 1.4e-116 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01623 | 1.1e-147 | lysP | E | amino acid | ||
AHMNLFMI_01624 | 1e-70 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
AHMNLFMI_01625 | 2.3e-22 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
AHMNLFMI_01626 | 2.1e-35 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01627 | 2.3e-26 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01628 | 1.9e-22 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_01631 | 8.4e-36 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01632 | 4e-22 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01633 | 3.3e-19 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_01634 | 2.2e-19 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_01635 | 7.3e-72 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_01636 | 8.2e-48 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_01637 | 4.1e-240 | gshR1 | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_01638 | 9e-50 | |||||
AHMNLFMI_01639 | 1.1e-16 | |||||
AHMNLFMI_01640 | 1.7e-38 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_01641 | 7.3e-101 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_01642 | 5e-27 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_01644 | 2.4e-59 | I | sulfurtransferase activity | |||
AHMNLFMI_01645 | 2.3e-77 | yphH | S | Cupin domain | ||
AHMNLFMI_01646 | 1.1e-48 | S | Phosphatidylethanolamine-binding protein | |||
AHMNLFMI_01650 | 1.8e-10 | |||||
AHMNLFMI_01651 | 2.5e-48 | S | Transcriptional regulator, RinA family | |||
AHMNLFMI_01652 | 3.9e-49 | S | Transcriptional regulator, RinA family | |||
AHMNLFMI_01653 | 1.4e-26 | hxlR | K | HxlR-like helix-turn-helix | ||
AHMNLFMI_01654 | 8.3e-63 | hxlR | K | HxlR-like helix-turn-helix | ||
AHMNLFMI_01655 | 2.9e-131 | ydfG | S | KR domain | ||
AHMNLFMI_01656 | 3.6e-97 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01657 | 3.5e-42 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_01658 | 3.2e-113 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_01659 | 2e-83 | uspA | T | Universal stress protein family | ||
AHMNLFMI_01660 | 3.4e-25 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
AHMNLFMI_01661 | 5.1e-09 | uspA | T | Universal stress protein family | ||
AHMNLFMI_01662 | 6.1e-18 | uspA | T | Universal stress protein family | ||
AHMNLFMI_01663 | 3.3e-59 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
AHMNLFMI_01664 | 1.1e-110 | yebC | K | Transcriptional regulatory protein | ||
AHMNLFMI_01665 | 3.3e-63 | yebC | K | Transcriptional regulatory protein | ||
AHMNLFMI_01666 | 1.1e-42 | yebC | K | Transcriptional regulatory protein | ||
AHMNLFMI_01667 | 6.7e-105 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
AHMNLFMI_01668 | 5.3e-86 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
AHMNLFMI_01669 | 5.4e-149 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
AHMNLFMI_01670 | 2.4e-19 | yknV | V | ABC transporter | ||
AHMNLFMI_01671 | 4.4e-47 | yknV | V | ABC transporter | ||
AHMNLFMI_01672 | 1e-132 | yknV | V | ABC transporter | ||
AHMNLFMI_01673 | 1.6e-19 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
AHMNLFMI_01674 | 1.1e-33 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_01675 | 2e-46 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
AHMNLFMI_01677 | 8.1e-109 | cmpC | S | ATPases associated with a variety of cellular activities | ||
AHMNLFMI_01678 | 2.2e-81 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
AHMNLFMI_01679 | 2.2e-61 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_01680 | 9.4e-16 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_01681 | 3.5e-41 | V | VanZ like family | |||
AHMNLFMI_01682 | 3.4e-40 | V | VanZ like family | |||
AHMNLFMI_01683 | 1.1e-48 | S | membrane | |||
AHMNLFMI_01684 | 1e-85 | S | VIT family | |||
AHMNLFMI_01685 | 1.5e-26 | S | VIT family | |||
AHMNLFMI_01686 | 4.4e-18 | S | VIT family | |||
AHMNLFMI_01687 | 1.6e-151 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHMNLFMI_01688 | 6.5e-88 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AHMNLFMI_01689 | 7.8e-79 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AHMNLFMI_01690 | 1.1e-34 | S | aldo-keto reductase (NADP) activity | |||
AHMNLFMI_01691 | 9.1e-49 | GM | NAD(P)H-binding | |||
AHMNLFMI_01692 | 1.4e-16 | S | aldo-keto reductase (NADP) activity | |||
AHMNLFMI_01693 | 1.7e-91 | yrvN | L | AAA C-terminal domain | ||
AHMNLFMI_01694 | 8.9e-86 | yrvN | L | AAA C-terminal domain | ||
AHMNLFMI_01695 | 4.2e-77 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
AHMNLFMI_01696 | 1.4e-33 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
AHMNLFMI_01697 | 4.4e-167 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
AHMNLFMI_01698 | 6e-301 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
AHMNLFMI_01699 | 2.7e-75 | clpE | O | Belongs to the ClpA ClpB family | ||
AHMNLFMI_01700 | 3e-54 | clpE | O | Belongs to the ClpA ClpB family | ||
AHMNLFMI_01701 | 2.5e-166 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
AHMNLFMI_01702 | 3.5e-183 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_01703 | 8.2e-105 | cps4F | 2.4.1.21, 2.4.1.306 | GT4,GT5 | M | Glycosyl transferases group 1 |
AHMNLFMI_01704 | 1.1e-25 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_01706 | 6.4e-45 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHMNLFMI_01709 | 3e-55 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_01710 | 2.2e-35 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHMNLFMI_01711 | 4.6e-86 | 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 | |
AHMNLFMI_01712 | 1e-23 | KT | PspC domain | |||
AHMNLFMI_01713 | 4.1e-77 | S | NADPH-dependent FMN reductase | |||
AHMNLFMI_01714 | 1.7e-46 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01715 | 2.2e-215 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01716 | 3.1e-14 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AHMNLFMI_01717 | 1.2e-108 | tdk | 2.7.1.21 | F | thymidine kinase | |
AHMNLFMI_01718 | 1.5e-08 | S | Bacteriophage Gp15 protein | |||
AHMNLFMI_01719 | 3.7e-07 | M | Phage tail tape measure protein TP901 | |||
AHMNLFMI_01720 | 2.4e-27 | S | Domain of unknown function (DUF4828) | |||
AHMNLFMI_01722 | 2e-51 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHMNLFMI_01723 | 4e-85 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHMNLFMI_01725 | 1.9e-53 | |||||
AHMNLFMI_01726 | 3.5e-55 | yifK | E | Amino acid permease | ||
AHMNLFMI_01727 | 3.2e-120 | |||||
AHMNLFMI_01728 | 4.3e-126 | ydjP | I | Alpha/beta hydrolase family | ||
AHMNLFMI_01729 | 2.7e-73 | ydjP | I | Alpha/beta hydrolase family | ||
AHMNLFMI_01730 | 2e-43 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
AHMNLFMI_01731 | 4.1e-116 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
AHMNLFMI_01732 | 3e-84 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
AHMNLFMI_01733 | 1.3e-36 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
AHMNLFMI_01734 | 1.9e-69 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_01735 | 3.2e-129 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_01736 | 4.7e-24 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_01737 | 2.6e-31 | ypbD | S | CAAX protease self-immunity | ||
AHMNLFMI_01738 | 1.3e-120 | ypbD | S | CAAX protease self-immunity | ||
AHMNLFMI_01740 | 1.7e-141 | E | ABC transporter, substratebinding protein | |||
AHMNLFMI_01741 | 4.9e-17 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | ||
AHMNLFMI_01742 | 6.8e-36 | mdtH | P | Sugar (and other) transporter | ||
AHMNLFMI_01743 | 5.8e-69 | mdtH | P | Sugar (and other) transporter | ||
AHMNLFMI_01744 | 1.8e-31 | mdtH | P | Sugar (and other) transporter | ||
AHMNLFMI_01745 | 3.8e-108 | scrA | 2.7.1.193, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AHMNLFMI_01746 | 4e-123 | scrA | 2.7.1.193, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AHMNLFMI_01747 | 1.5e-183 | ywhK | S | Membrane | ||
AHMNLFMI_01748 | 2.1e-160 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
AHMNLFMI_01749 | 6.8e-45 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
AHMNLFMI_01750 | 2.7e-76 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_01751 | 3.2e-184 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_01752 | 1.6e-42 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_01753 | 1.6e-42 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_01754 | 3e-32 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
AHMNLFMI_01755 | 1.5e-18 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
AHMNLFMI_01756 | 3.9e-99 | S | SdpI/YhfL protein family | |||
AHMNLFMI_01757 | 6.4e-95 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_01758 | 1.9e-17 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
AHMNLFMI_01759 | 1.9e-204 | cytX | U | Belongs to the purine-cytosine permease (2.A.39) family | ||
AHMNLFMI_01760 | 5.1e-136 | S | peptidase C26 | |||
AHMNLFMI_01761 | 2e-167 | L | HIRAN domain | |||
AHMNLFMI_01762 | 2.3e-23 | L | HIRAN domain | |||
AHMNLFMI_01763 | 7.4e-19 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_01764 | 4.2e-43 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_01765 | 2.5e-60 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_01766 | 5.9e-52 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AHMNLFMI_01767 | 1.2e-72 | 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 | ||
AHMNLFMI_01768 | 7.7e-126 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AHMNLFMI_01769 | 4.6e-24 | 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 | ||
AHMNLFMI_01773 | 5.1e-15 | |||||
AHMNLFMI_01774 | 5.5e-97 | 3.6.4.12 | L | UvrD/REP helicase N-terminal domain | ||
AHMNLFMI_01775 | 8.6e-50 | L | AAA ATPase domain | |||
AHMNLFMI_01776 | 1.3e-58 | L | AAA ATPase domain | |||
AHMNLFMI_01777 | 1.8e-50 | yoaK | S | Protein of unknown function (DUF1275) | ||
AHMNLFMI_01778 | 3.1e-82 | prsA | 3.1.3.16, 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AHMNLFMI_01779 | 5.7e-67 | prsA | 3.1.3.16, 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AHMNLFMI_01781 | 1.1e-95 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
AHMNLFMI_01782 | 1.9e-64 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_01783 | 1.1e-197 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_01784 | 7.6e-83 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_01785 | 2.1e-28 | celE | 3.2.1.4 | GH5,GH9 | E | GDSL-like Lipase/Acylhydrolase family |
AHMNLFMI_01786 | 2.6e-126 | ydcF | S | Gram-negative-bacterium-type cell wall biogenesis | ||
AHMNLFMI_01787 | 1.7e-136 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AHMNLFMI_01788 | 3.3e-39 | yfeX | P | Peroxidase | ||
AHMNLFMI_01789 | 2.1e-37 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AHMNLFMI_01790 | 7.1e-43 | yfeX | P | Peroxidase | ||
AHMNLFMI_01791 | 8.7e-31 | EG | EamA-like transporter family | |||
AHMNLFMI_01792 | 3.6e-69 | EG | EamA-like transporter family | |||
AHMNLFMI_01793 | 4.7e-114 | ampC | V | Beta-lactamase | ||
AHMNLFMI_01795 | 1.4e-12 | |||||
AHMNLFMI_01797 | 1.6e-46 | |||||
AHMNLFMI_01798 | 6.1e-58 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_01799 | 1.2e-42 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_01800 | 4.9e-84 | merR | K | MerR HTH family regulatory protein | ||
AHMNLFMI_01801 | 2.8e-12 | L | Belongs to the 'phage' integrase family | |||
AHMNLFMI_01802 | 8e-46 | L | Belongs to the 'phage' integrase family | |||
AHMNLFMI_01805 | 1.6e-31 | |||||
AHMNLFMI_01806 | 1.6e-282 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_01807 | 6.6e-58 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_01808 | 3.9e-162 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_01809 | 5.2e-48 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_01810 | 4.8e-15 | S | Protein of unknown function (DUF1093) | |||
AHMNLFMI_01811 | 4.1e-168 | ycfI | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_01812 | 2.4e-26 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
AHMNLFMI_01813 | 9e-09 | L | transposase activity | |||
AHMNLFMI_01814 | 4.7e-51 | S | Phage terminase, large subunit, PBSX family | |||
AHMNLFMI_01815 | 1.4e-23 | L | transposase activity | |||
AHMNLFMI_01816 | 1.5e-39 | 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 | |
AHMNLFMI_01817 | 1.5e-39 | 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 | |
AHMNLFMI_01818 | 3.1e-203 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHMNLFMI_01819 | 1.2e-151 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_01820 | 2.4e-50 | P | ABC transporter, substratebinding protein | |||
AHMNLFMI_01821 | 3.3e-43 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_01822 | 3.1e-41 | U | Binding-protein-dependent transport system inner membrane component | |||
AHMNLFMI_01823 | 5.2e-181 | U | Binding-protein-dependent transport system inner membrane component | |||
AHMNLFMI_01824 | 1.5e-161 | lplC | U | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_01825 | 4.5e-123 | G | Domain of unknown function (DUF3502) | |||
AHMNLFMI_01826 | 3.5e-60 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AHMNLFMI_01827 | 3.9e-55 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AHMNLFMI_01828 | 1.9e-42 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AHMNLFMI_01829 | 1.4e-82 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
AHMNLFMI_01830 | 2.9e-57 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
AHMNLFMI_01831 | 3.6e-44 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
AHMNLFMI_01832 | 9.2e-45 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
AHMNLFMI_01833 | 9.4e-175 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
AHMNLFMI_01834 | 1.4e-14 | V | ABC-type multidrug transport system, ATPase component | |||
AHMNLFMI_01835 | 1.4e-27 | S | DNA binding | |||
AHMNLFMI_01836 | 2.6e-50 | S | sequence-specific DNA binding | |||
AHMNLFMI_01837 | 2.3e-34 | S | sequence-specific DNA binding | |||
AHMNLFMI_01838 | 1.9e-68 | S | DNA binding | |||
AHMNLFMI_01839 | 3.3e-58 | S | Domain of unknown function (DUF771) | |||
AHMNLFMI_01840 | 9.3e-32 | K | Peptidase S24-like | |||
AHMNLFMI_01841 | 4.1e-158 | tagE6 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_01842 | 1.6e-113 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01843 | 2.3e-67 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_01844 | 5.8e-81 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
AHMNLFMI_01845 | 7.6e-61 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
AHMNLFMI_01846 | 6.2e-50 | |||||
AHMNLFMI_01847 | 1.7e-63 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_01848 | 1.6e-129 | L | AAA domain | |||
AHMNLFMI_01849 | 1.9e-25 | sidC | GT2,GT4 | LM | DNA recombination | |
AHMNLFMI_01850 | 1.8e-27 | |||||
AHMNLFMI_01851 | 1.1e-07 | pts10B | 2.7.1.191, 2.7.1.202 | G | PTS system sorbose subfamily IIB component | |
AHMNLFMI_01852 | 6.6e-22 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_01853 | 3.4e-86 | pts10B | 2.7.1.191, 2.7.1.202 | G | PTS system sorbose subfamily IIB component | |
AHMNLFMI_01854 | 8.6e-72 | pts10A | 2.7.1.191 | G | PTS system fructose IIA component | |
AHMNLFMI_01855 | 2.3e-81 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_01856 | 1.2e-62 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_01857 | 1e-72 | C | FMN binding | |||
AHMNLFMI_01858 | 4.3e-77 | K | Transcriptional regulator | |||
AHMNLFMI_01859 | 2.8e-76 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_01860 | 1.1e-10 | 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 | ||
AHMNLFMI_01861 | 1.1e-36 | 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 | ||
AHMNLFMI_01862 | 1.3e-42 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
AHMNLFMI_01863 | 5.4e-37 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
AHMNLFMI_01864 | 6.5e-57 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
AHMNLFMI_01865 | 1.1e-43 | yniA | G | Fructosamine kinase | ||
AHMNLFMI_01866 | 6.9e-33 | yvbK | 3.1.3.25 | K | GNAT family | |
AHMNLFMI_01867 | 7.3e-21 | |||||
AHMNLFMI_01868 | 1.9e-86 | yvbK | 3.1.3.25 | K | GNAT family | |
AHMNLFMI_01869 | 7e-37 | |||||
AHMNLFMI_01870 | 8.2e-48 | |||||
AHMNLFMI_01871 | 1.2e-112 | pgm8 | G | Histidine phosphatase superfamily (branch 1) | ||
AHMNLFMI_01872 | 1e-139 | K | DeoR C terminal sensor domain | |||
AHMNLFMI_01873 | 3e-176 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_01874 | 7.8e-244 | iolF | EGP | Major facilitator Superfamily | ||
AHMNLFMI_01875 | 1e-27 | ynfM | EGP | Major facilitator Superfamily | ||
AHMNLFMI_01876 | 4.7e-33 | J | Acetyltransferase (GNAT) domain | |||
AHMNLFMI_01877 | 2.1e-83 | J | Acetyltransferase (GNAT) domain | |||
AHMNLFMI_01878 | 3.4e-58 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
AHMNLFMI_01879 | 1e-63 | ptlF | S | KR domain | ||
AHMNLFMI_01880 | 1.7e-94 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
AHMNLFMI_01881 | 1.7e-84 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AHMNLFMI_01882 | 3e-23 | |||||
AHMNLFMI_01883 | 2.4e-46 | 4.1.1.46 | S | Amidohydrolase | ||
AHMNLFMI_01884 | 2.5e-52 | S | Uncharacterized protein conserved in bacteria (DUF2316) | |||
AHMNLFMI_01885 | 8.1e-108 | |||||
AHMNLFMI_01887 | 2.1e-61 | |||||
AHMNLFMI_01888 | 1.1e-53 | |||||
AHMNLFMI_01889 | 2.7e-10 | ykuL | S | (CBS) domain | ||
AHMNLFMI_01890 | 6.5e-87 | ykuL | S | (CBS) domain | ||
AHMNLFMI_01891 | 2.6e-76 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
AHMNLFMI_01892 | 1e-34 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01893 | 1.7e-37 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01894 | 4.1e-49 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01895 | 6.6e-104 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01896 | 5.5e-201 | pbuG | S | Permease family | ||
AHMNLFMI_01897 | 8.4e-87 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
AHMNLFMI_01898 | 7.5e-111 | S | Putative adhesin | |||
AHMNLFMI_01899 | 4.2e-23 | S | Putative adhesin | |||
AHMNLFMI_01900 | 6.8e-114 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
AHMNLFMI_01901 | 3.2e-189 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
AHMNLFMI_01902 | 1.4e-144 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_01903 | 7.4e-74 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
AHMNLFMI_01904 | 5.7e-30 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_01905 | 9.1e-35 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_01906 | 4.3e-60 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_01907 | 2.7e-22 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_01908 | 5.4e-130 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
AHMNLFMI_01909 | 1e-139 | S | Belongs to the UPF0246 family | |||
AHMNLFMI_01910 | 9.7e-24 | S | Belongs to the UPF0246 family | |||
AHMNLFMI_01911 | 4.8e-42 | S | Belongs to the UPF0246 family | |||
AHMNLFMI_01912 | 2.6e-26 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_01913 | 5.8e-63 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_01914 | 5e-111 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
AHMNLFMI_01915 | 5.2e-78 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_01916 | 8.8e-108 | pgaC | GT2 | M | Glycosyl transferase | |
AHMNLFMI_01917 | 8.2e-70 | pgaC | GT2 | M | Glycosyl transferase | |
AHMNLFMI_01918 | 1.8e-116 | pgaC | GT2 | M | Glycosyl transferase | |
AHMNLFMI_01920 | 4.1e-16 | relB | L | bacterial-type proximal promoter sequence-specific DNA binding | ||
AHMNLFMI_01921 | 4.5e-77 | cps2J | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_01922 | 1.4e-46 | yxaB | GM | Polysaccharide pyruvyl transferase | ||
AHMNLFMI_01923 | 7.4e-119 | cps4I | M | Glycosyltransferase like family 2 | ||
AHMNLFMI_01924 | 2.1e-169 | |||||
AHMNLFMI_01925 | 4.8e-39 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_01927 | 3e-131 | K | LytTr DNA-binding domain | |||
AHMNLFMI_01928 | 3.4e-92 | K | LytTr DNA-binding domain | |||
AHMNLFMI_01929 | 9.3e-87 | V | ABC transporter | |||
AHMNLFMI_01930 | 5.5e-95 | V | ABC transporter | |||
AHMNLFMI_01931 | 7.3e-11 | V | ABC transporter | |||
AHMNLFMI_01932 | 1.7e-60 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHMNLFMI_01933 | 1.8e-42 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHMNLFMI_01934 | 1.7e-227 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
AHMNLFMI_01935 | 6.6e-95 | S | Protein of unknown function (DUF1440) | |||
AHMNLFMI_01936 | 5.2e-174 | hrtB | V | ABC transporter permease | ||
AHMNLFMI_01937 | 2.9e-33 | fhuC | 3.6.3.34 | HP | ABC transporter | |
AHMNLFMI_01938 | 4.2e-89 | fhuC | 3.6.3.34 | HP | ABC transporter | |
AHMNLFMI_01939 | 6.2e-57 | sirB | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHMNLFMI_01940 | 2.8e-63 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
AHMNLFMI_01941 | 4.2e-74 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
AHMNLFMI_01942 | 1.2e-158 | ypbG | 2.7.1.2 | GK | ROK family | |
AHMNLFMI_01943 | 7.8e-99 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01944 | 1.1e-28 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_01945 | 1.9e-37 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_01946 | 9.8e-105 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_01947 | 1.9e-10 | S | Domain of unknown function (DU1801) | |||
AHMNLFMI_01948 | 6.1e-19 | |||||
AHMNLFMI_01949 | 4.9e-34 | |||||
AHMNLFMI_01950 | 8.7e-60 | S | Domain of unknown function (DU1801) | |||
AHMNLFMI_01951 | 3.8e-27 | P | ABC transporter | |||
AHMNLFMI_01952 | 1.5e-115 | P | cobalt transport | |||
AHMNLFMI_01953 | 1.9e-33 | |||||
AHMNLFMI_01955 | 2.2e-66 | 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 | |
AHMNLFMI_01956 | 2.8e-12 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AHMNLFMI_01957 | 3.7e-12 | 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 | |
AHMNLFMI_01958 | 5e-15 | |||||
AHMNLFMI_01959 | 3.3e-48 | 2.6.1.2, 2.6.1.66 | K | Bacteriophage CI repressor helix-turn-helix domain | ||
AHMNLFMI_01960 | 1.6e-35 | 2.6.1.2, 2.6.1.66 | K | Bacteriophage CI repressor helix-turn-helix domain | ||
AHMNLFMI_01961 | 1.6e-38 | degV | S | DegV family | ||
AHMNLFMI_01962 | 1.2e-157 | degV | S | DegV family | ||
AHMNLFMI_01963 | 1e-48 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_01964 | 2.3e-220 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_01965 | 2.2e-47 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_01966 | 8.9e-60 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
AHMNLFMI_01967 | 4.7e-72 | |||||
AHMNLFMI_01968 | 2.6e-48 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
AHMNLFMI_01969 | 1.2e-47 | dnaD | L | Replication initiation and membrane attachment | ||
AHMNLFMI_01970 | 7.3e-56 | dnaD | L | Replication initiation and membrane attachment | ||
AHMNLFMI_01971 | 2.4e-57 | dnaD | L | Replication initiation and membrane attachment | ||
AHMNLFMI_01972 | 3.3e-74 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
AHMNLFMI_01973 | 3.7e-79 | ptsG | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |
AHMNLFMI_01974 | 1.3e-137 | yleF | K | Helix-turn-helix domain, rpiR family | ||
AHMNLFMI_01975 | 7.2e-246 | sacX | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_01976 | 5.4e-156 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
AHMNLFMI_01977 | 5.6e-23 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01978 | 6e-36 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01979 | 1.1e-92 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_01980 | 3.4e-28 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_01981 | 5.7e-22 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHMNLFMI_01982 | 1.6e-106 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHMNLFMI_01983 | 2.1e-50 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHMNLFMI_01984 | 1.2e-33 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_01985 | 6.6e-19 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_01986 | 2.8e-17 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_01987 | 2.8e-179 | S | Aldo keto reductase | |||
AHMNLFMI_01988 | 1.7e-55 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_01989 | 6.5e-15 | S | sequence-specific DNA binding | |||
AHMNLFMI_01990 | 1.2e-78 | K | Peptidase S24-like | |||
AHMNLFMI_01991 | 8.3e-11 | tcdC | ||||
AHMNLFMI_01993 | 5.3e-68 | GM | NmrA-like family | |||
AHMNLFMI_01994 | 3.8e-50 | GM | NmrA-like family | |||
AHMNLFMI_01995 | 2.1e-40 | |||||
AHMNLFMI_01996 | 2.1e-14 | |||||
AHMNLFMI_01997 | 6.2e-79 | S | Phosphoesterase | |||
AHMNLFMI_01998 | 2.6e-79 | S | Phosphoesterase | |||
AHMNLFMI_01999 | 8.5e-176 | clcA | P | chloride | ||
AHMNLFMI_02000 | 2e-115 | comEC | S | Competence protein ComEC | ||
AHMNLFMI_02001 | 9.2e-63 | comEC | S | Competence protein ComEC | ||
AHMNLFMI_02002 | 1.5e-49 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AHMNLFMI_02003 | 2e-230 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AHMNLFMI_02004 | 4.3e-31 | mdlA2 | V | ABC transporter | ||
AHMNLFMI_02005 | 4.2e-44 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
AHMNLFMI_02006 | 1.5e-77 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
AHMNLFMI_02007 | 5.3e-176 | XK27_08835 | S | ABC transporter | ||
AHMNLFMI_02008 | 8.7e-154 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AHMNLFMI_02009 | 2.7e-55 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_02010 | 6e-123 | cadA | P | P-type ATPase | ||
AHMNLFMI_02011 | 5.8e-40 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_02012 | 2.7e-34 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_02016 | 9.2e-212 | norA | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02017 | 5.7e-44 | XK27_09800 | I | Acyltransferase family | ||
AHMNLFMI_02018 | 4.1e-38 | XK27_09800 | I | Acyltransferase family | ||
AHMNLFMI_02019 | 1.9e-46 | XK27_09800 | I | Acyltransferase family | ||
AHMNLFMI_02020 | 1.3e-54 | XK27_09800 | I | Acyltransferase family | ||
AHMNLFMI_02021 | 2e-208 | |||||
AHMNLFMI_02022 | 1.6e-215 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
AHMNLFMI_02023 | 9e-22 | V | ABC transporter | |||
AHMNLFMI_02024 | 0.0 | V | ABC transporter | |||
AHMNLFMI_02025 | 5.1e-51 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AHMNLFMI_02026 | 9.1e-20 | 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 | ||
AHMNLFMI_02027 | 3.8e-70 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_02028 | 7e-28 | yfjF | U | Sugar (and other) transporter | ||
AHMNLFMI_02029 | 7.2e-33 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_02030 | 2.6e-51 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_02031 | 2.6e-51 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_02032 | 7.2e-33 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_02033 | 5e-54 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_02034 | 6.4e-257 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
AHMNLFMI_02035 | 1e-145 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHMNLFMI_02036 | 3.1e-30 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHMNLFMI_02037 | 3.1e-30 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHMNLFMI_02038 | 1.7e-28 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHMNLFMI_02039 | 1.7e-100 | ydaO | E | amino acid | ||
AHMNLFMI_02040 | 6.7e-72 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
AHMNLFMI_02041 | 4.9e-78 | S | Uncharacterized protein conserved in bacteria (DUF2255) | |||
AHMNLFMI_02042 | 1.4e-113 | GM | NmrA-like family | |||
AHMNLFMI_02043 | 1.2e-08 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_02044 | 4e-13 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHMNLFMI_02045 | 3.6e-25 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHMNLFMI_02046 | 1.9e-33 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHMNLFMI_02047 | 4.5e-12 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_02048 | 1.5e-30 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHMNLFMI_02049 | 5.5e-37 | lacS | G | Transporter | ||
AHMNLFMI_02050 | 1.7e-16 | lacS | G | Transporter | ||
AHMNLFMI_02051 | 6.4e-57 | |||||
AHMNLFMI_02052 | 4.3e-130 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_02053 | 7.8e-252 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_02054 | 1.9e-43 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_02055 | 7.5e-35 | mmuP | E | amino acid | ||
AHMNLFMI_02056 | 3.2e-61 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AHMNLFMI_02057 | 2.6e-28 | D | Alpha beta | |||
AHMNLFMI_02058 | 3.1e-78 | M1-874 | K | Domain of unknown function (DUF1836) | ||
AHMNLFMI_02059 | 1.3e-74 | S | DUF218 domain | |||
AHMNLFMI_02060 | 3.2e-26 | |||||
AHMNLFMI_02061 | 5.8e-49 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
AHMNLFMI_02062 | 6.3e-82 | K | response regulator | |||
AHMNLFMI_02063 | 2.6e-97 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
AHMNLFMI_02064 | 1.6e-38 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
AHMNLFMI_02068 | 6.8e-209 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
AHMNLFMI_02069 | 5.8e-24 | pbpX1 | V | Beta-lactamase | ||
AHMNLFMI_02070 | 7.2e-20 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
AHMNLFMI_02071 | 1.3e-60 | pbpX1 | V | Beta-lactamase | ||
AHMNLFMI_02072 | 1.4e-107 | yycI | S | YycH protein | ||
AHMNLFMI_02073 | 4.9e-55 | yycI | S | YycH protein | ||
AHMNLFMI_02074 | 8.9e-158 | vicX | 3.1.26.11 | S | domain protein | |
AHMNLFMI_02075 | 6.8e-173 | htrA | 3.4.21.107 | O | serine protease | |
AHMNLFMI_02076 | 2.9e-17 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AHMNLFMI_02077 | 1.3e-36 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AHMNLFMI_02078 | 9.6e-39 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AHMNLFMI_02079 | 2.1e-64 | malD | P | ABC transporter permease | ||
AHMNLFMI_02080 | 6.4e-227 | malC | P | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_02081 | 1.5e-65 | mdxE | G | Bacterial extracellular solute-binding protein | ||
AHMNLFMI_02082 | 9.6e-50 | S | Protein of unknown function (DUF1211) | |||
AHMNLFMI_02083 | 1.8e-26 | S | Aldo keto reductase | |||
AHMNLFMI_02084 | 2.3e-41 | S | Protein of unknown function (DUF1211) | |||
AHMNLFMI_02085 | 3.2e-48 | 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 | |
AHMNLFMI_02086 | 5.4e-23 | 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 | |
AHMNLFMI_02087 | 4.1e-30 | 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 | |
AHMNLFMI_02088 | 4.3e-33 | 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 | |
AHMNLFMI_02089 | 4.9e-29 | S | Protein of unknown function (DUF2922) | |||
AHMNLFMI_02090 | 2.3e-32 | S | Protein of unknown function (DUF2922) | |||
AHMNLFMI_02091 | 7.3e-33 | S | Protein of unknown function (DUF2922) | |||
AHMNLFMI_02092 | 1.1e-52 | |||||
AHMNLFMI_02093 | 1.4e-51 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
AHMNLFMI_02094 | 1.1e-47 | pts15B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_02095 | 3.9e-175 | pts15C | 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 | ||
AHMNLFMI_02096 | 3.4e-107 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
AHMNLFMI_02097 | 1.3e-52 | oatA | I | Acyltransferase | ||
AHMNLFMI_02098 | 1.1e-34 | oatA | I | Acyltransferase | ||
AHMNLFMI_02099 | 1.7e-86 | lssY | 3.6.1.27 | I | phosphatase | |
AHMNLFMI_02100 | 1.7e-42 | S | Cell surface protein | |||
AHMNLFMI_02101 | 7.2e-178 | S | Cell surface protein | |||
AHMNLFMI_02102 | 4.7e-57 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_02103 | 1e-200 | 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 | |
AHMNLFMI_02104 | 5.4e-09 | 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 | |
AHMNLFMI_02105 | 3e-20 | K | MarR family | |||
AHMNLFMI_02106 | 2.4e-72 | K | MarR family | |||
AHMNLFMI_02107 | 3.7e-149 | XK27_00825 | S | Sulfite exporter TauE/SafE | ||
AHMNLFMI_02108 | 5.7e-74 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_02110 | 3.1e-30 | |||||
AHMNLFMI_02112 | 2.3e-215 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AHMNLFMI_02113 | 1.1e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
AHMNLFMI_02114 | 3.3e-95 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
AHMNLFMI_02115 | 8.6e-63 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
AHMNLFMI_02116 | 5.3e-09 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
AHMNLFMI_02119 | 3.1e-64 | M | Phage tail tape measure protein TP901 | |||
AHMNLFMI_02120 | 1.6e-42 | M | Phage tail tape measure protein TP901 | |||
AHMNLFMI_02121 | 1.5e-31 | M | Phage tail tape measure protein TP901 | |||
AHMNLFMI_02123 | 1.1e-55 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_02124 | 8.3e-18 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_02125 | 6e-39 | xerC | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_02126 | 1.4e-76 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02127 | 1.6e-260 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02128 | 4.5e-30 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02129 | 1.4e-39 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02130 | 2.5e-56 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
AHMNLFMI_02131 | 6.7e-92 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02132 | 1.5e-40 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02133 | 3.1e-22 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_02134 | 1.9e-70 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_02135 | 4.1e-45 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_02136 | 2.2e-33 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
AHMNLFMI_02137 | 4.5e-80 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
AHMNLFMI_02138 | 3.5e-101 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
AHMNLFMI_02139 | 4.2e-92 | K | Transcriptional regulator | |||
AHMNLFMI_02140 | 9.5e-47 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_02141 | 1.9e-52 | ubiB | H | Is probably a protein kinase regulator of UbiI activity which is involved in aerobic coenzyme Q (ubiquinone) biosynthesis | ||
AHMNLFMI_02142 | 5.9e-79 | ubiB | H | Is probably a protein kinase regulator of UbiI activity which is involved in aerobic coenzyme Q (ubiquinone) biosynthesis | ||
AHMNLFMI_02143 | 1.3e-97 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AHMNLFMI_02144 | 1.7e-61 | S | YheO-like PAS domain | |||
AHMNLFMI_02145 | 2.4e-30 | S | YheO-like PAS domain | |||
AHMNLFMI_02146 | 5.1e-27 | |||||
AHMNLFMI_02147 | 1.4e-289 | mdlA2 | V | ABC transporter | ||
AHMNLFMI_02148 | 1.5e-97 | mdlA2 | V | ABC transporter | ||
AHMNLFMI_02149 | 1.7e-26 | yknV | V | ABC transporter | ||
AHMNLFMI_02150 | 9.3e-37 | yfnA | E | Amino Acid | ||
AHMNLFMI_02151 | 3.9e-93 | K | LytTr DNA-binding domain | |||
AHMNLFMI_02152 | 9.1e-22 | 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) | |
AHMNLFMI_02153 | 2e-48 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
AHMNLFMI_02154 | 5.7e-69 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHMNLFMI_02155 | 1.9e-34 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHMNLFMI_02156 | 1.6e-52 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHMNLFMI_02157 | 1.3e-14 | S | Repeat protein | |||
AHMNLFMI_02158 | 4.5e-133 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
AHMNLFMI_02159 | 7e-68 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_02160 | 7e-68 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_02161 | 8.6e-53 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_02162 | 7e-68 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_02163 | 3.7e-36 | arpU | S | Transcriptional regulator, ArpU family | ||
AHMNLFMI_02165 | 1.3e-20 | |||||
AHMNLFMI_02166 | 6.7e-22 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_02167 | 5.4e-59 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
AHMNLFMI_02168 | 6.7e-22 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_02169 | 4.6e-52 | S | CAAX protease self-immunity | |||
AHMNLFMI_02170 | 9.9e-46 | S | CAAX protease self-immunity | |||
AHMNLFMI_02171 | 8.3e-154 | S | CAAX protease self-immunity | |||
AHMNLFMI_02172 | 9.7e-58 | V | ABC transporter, ATP-binding protein | |||
AHMNLFMI_02173 | 1e-55 | |||||
AHMNLFMI_02174 | 1.2e-142 | ytrB | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_02175 | 1.1e-66 | yfiC | V | ABC transporter | ||
AHMNLFMI_02176 | 2.2e-73 | yfiC | V | ABC transporter | ||
AHMNLFMI_02177 | 1.2e-34 | yfiC | V | ABC transporter | ||
AHMNLFMI_02178 | 2.2e-20 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHMNLFMI_02179 | 2e-22 | lacL | 3.2.1.23 | G | hydrolase activity, hydrolyzing O-glycosyl compounds | |
AHMNLFMI_02180 | 6.6e-139 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHMNLFMI_02182 | 1.3e-260 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_02186 | 6.2e-84 | |||||
AHMNLFMI_02187 | 4e-184 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
AHMNLFMI_02188 | 8.9e-77 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
AHMNLFMI_02189 | 7.7e-108 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
AHMNLFMI_02190 | 2.6e-224 | S | Phage minor structural protein | |||
AHMNLFMI_02191 | 3.4e-63 | S | Phage tail protein | |||
AHMNLFMI_02192 | 6.7e-11 | S | Phage tail protein | |||
AHMNLFMI_02193 | 7.5e-25 | S | Phage minor structural protein | |||
AHMNLFMI_02194 | 4.1e-238 | |||||
AHMNLFMI_02195 | 9.5e-211 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
AHMNLFMI_02196 | 1e-20 | G | Xylose isomerase-like TIM barrel | |||
AHMNLFMI_02197 | 4.9e-34 | EGP | Major Facilitator Superfamily | |||
AHMNLFMI_02198 | 2.1e-79 | K | Transcriptional regulator, LysR family | |||
AHMNLFMI_02199 | 7e-51 | EGP | Major Facilitator Superfamily | |||
AHMNLFMI_02200 | 5.1e-64 | EGP | Major Facilitator Superfamily | |||
AHMNLFMI_02201 | 7.6e-64 | |||||
AHMNLFMI_02202 | 1.8e-155 | estA | S | Putative esterase | ||
AHMNLFMI_02203 | 4.2e-87 | K | UTRA domain | |||
AHMNLFMI_02204 | 1.2e-33 | gntR1 | K | Transcriptional regulator, GntR family | ||
AHMNLFMI_02205 | 7.9e-61 | gntR1 | K | Transcriptional regulator, GntR family | ||
AHMNLFMI_02206 | 6.9e-164 | V | ABC transporter, ATP-binding protein | |||
AHMNLFMI_02207 | 8.9e-23 | pbuX | F | xanthine permease | ||
AHMNLFMI_02209 | 3.9e-73 | pbuX | F | xanthine permease | ||
AHMNLFMI_02210 | 4.4e-11 | pbuX | F | xanthine permease | ||
AHMNLFMI_02211 | 1.5e-98 | smc | D | Required for chromosome condensation and partitioning | ||
AHMNLFMI_02212 | 9.6e-81 | smc | D | Required for chromosome condensation and partitioning | ||
AHMNLFMI_02213 | 5e-38 | yclK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_02214 | 3.9e-37 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
AHMNLFMI_02215 | 6.4e-64 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
AHMNLFMI_02216 | 1.5e-51 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHMNLFMI_02217 | 7.6e-52 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHMNLFMI_02218 | 1.1e-56 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHMNLFMI_02219 | 1.3e-39 | 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 | ||
AHMNLFMI_02220 | 3e-42 | 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 | ||
AHMNLFMI_02221 | 3.4e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
AHMNLFMI_02222 | 1.8e-84 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_02223 | 1.1e-153 | mccF | 3.4.17.13 | V | LD-carboxypeptidase | |
AHMNLFMI_02224 | 9.8e-61 | mccF | 3.4.17.13 | V | LD-carboxypeptidase | |
AHMNLFMI_02225 | 1.7e-73 | XK27_05710 | K | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_02226 | 7.3e-122 | |||||
AHMNLFMI_02227 | 3.3e-121 | 3.6.3.35 | P | ATPases associated with a variety of cellular activities | ||
AHMNLFMI_02228 | 1.3e-119 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_02229 | 4.2e-29 | |||||
AHMNLFMI_02230 | 1.1e-39 | V | FtsX-like permease family | |||
AHMNLFMI_02231 | 1.3e-71 | V | FtsX-like permease family | |||
AHMNLFMI_02232 | 1.3e-27 | V | FtsX-like permease family | |||
AHMNLFMI_02233 | 5.9e-26 | V | FtsX-like permease family | |||
AHMNLFMI_02234 | 2.1e-65 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
AHMNLFMI_02235 | 1e-44 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
AHMNLFMI_02236 | 4.1e-56 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
AHMNLFMI_02237 | 9.5e-110 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
AHMNLFMI_02238 | 2.3e-43 | comGA | NU | Type II IV secretion system protein | ||
AHMNLFMI_02239 | 2.9e-11 | comGA | NU | Type II IV secretion system protein | ||
AHMNLFMI_02240 | 3.8e-40 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
AHMNLFMI_02241 | 1.8e-53 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
AHMNLFMI_02243 | 3.4e-278 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
AHMNLFMI_02244 | 4.5e-76 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHMNLFMI_02245 | 4.5e-140 | dkgB | S | reductase | ||
AHMNLFMI_02246 | 5.6e-39 | S | Cytochrome B5 | |||
AHMNLFMI_02247 | 2.2e-88 | pts21A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
AHMNLFMI_02248 | 1e-190 | malR | K | Transcriptional regulator, LacI family | ||
AHMNLFMI_02249 | 4.4e-175 | yvdE | K | helix_turn _helix lactose operon repressor | ||
AHMNLFMI_02250 | 1e-24 | yvdE | K | helix_turn _helix lactose operon repressor | ||
AHMNLFMI_02251 | 2.1e-25 | yvdE | K | helix_turn _helix lactose operon repressor | ||
AHMNLFMI_02252 | 1.8e-25 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_02253 | 3.4e-294 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_02255 | 2.4e-30 | |||||
AHMNLFMI_02256 | 1.7e-62 | S | Phage Mu protein F like protein | |||
AHMNLFMI_02257 | 3.8e-265 | S | Phage Mu protein F like protein | |||
AHMNLFMI_02258 | 3.9e-66 | lysM | M | LysM domain | ||
AHMNLFMI_02259 | 2.7e-129 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
AHMNLFMI_02260 | 1.3e-65 | |||||
AHMNLFMI_02261 | 2.7e-100 | |||||
AHMNLFMI_02262 | 1.2e-36 | mtsB | U | ABC 3 transport family | ||
AHMNLFMI_02263 | 7.9e-60 | mtsB | U | ABC 3 transport family | ||
AHMNLFMI_02264 | 1.2e-43 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_02265 | 3.7e-99 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
AHMNLFMI_02266 | 6.8e-29 | 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 | ||
AHMNLFMI_02267 | 6.5e-22 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AHMNLFMI_02268 | 2.4e-101 | sigH | K | Sigma-70 region 2 | ||
AHMNLFMI_02270 | 2e-291 | yfbS | P | Sodium:sulfate symporter transmembrane region | ||
AHMNLFMI_02271 | 3.4e-50 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AHMNLFMI_02272 | 1.6e-47 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
AHMNLFMI_02273 | 3.6e-19 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
AHMNLFMI_02274 | 3.4e-15 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AHMNLFMI_02275 | 5.5e-12 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AHMNLFMI_02276 | 3.9e-37 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
AHMNLFMI_02277 | 1.9e-13 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AHMNLFMI_02278 | 7.6e-88 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
AHMNLFMI_02279 | 2.4e-12 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
AHMNLFMI_02280 | 1.4e-43 | S | hydrolase | |||
AHMNLFMI_02281 | 2.8e-13 | |||||
AHMNLFMI_02282 | 4.2e-40 | S | hydrolase | |||
AHMNLFMI_02283 | 4.9e-43 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
AHMNLFMI_02284 | 8.4e-90 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
AHMNLFMI_02285 | 1.7e-55 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
AHMNLFMI_02286 | 3.2e-53 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
AHMNLFMI_02287 | 7.6e-35 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
AHMNLFMI_02289 | 1.6e-21 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AHMNLFMI_02290 | 3.9e-17 | tarJ | 1.1.1.137, 1.1.1.303, 1.1.1.4, 1.1.1.405 | E | Catalyzes the NADPH dependent reduction of D-ribulose 5- phosphate to D-ribitol 5-phosphate | |
AHMNLFMI_02291 | 3.9e-17 | tarJ | 1.1.1.137, 1.1.1.303, 1.1.1.4, 1.1.1.405 | E | Catalyzes the NADPH dependent reduction of D-ribulose 5- phosphate to D-ribitol 5-phosphate | |
AHMNLFMI_02294 | 1.7e-67 | yqhL | P | Rhodanese-like protein | ||
AHMNLFMI_02295 | 1.2e-109 | pepE | 3.4.13.21 | E | Belongs to the peptidase S51 family | |
AHMNLFMI_02296 | 4.4e-28 | pepE | 3.4.13.21 | E | Belongs to the peptidase S51 family | |
AHMNLFMI_02297 | 1.8e-57 | pepE | 3.4.13.21 | E | Belongs to the peptidase S51 family | |
AHMNLFMI_02298 | 2.7e-25 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_02299 | 2.7e-25 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_02300 | 4.6e-39 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
AHMNLFMI_02301 | 1.8e-43 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_02302 | 9.8e-70 | L | Phage-associated protein | |||
AHMNLFMI_02303 | 2.3e-59 | T | Universal stress protein family | |||
AHMNLFMI_02304 | 9.6e-37 | T | Universal stress protein family | |||
AHMNLFMI_02305 | 1.9e-48 | T | Universal stress protein family | |||
AHMNLFMI_02306 | 4.6e-28 | padR | K | Virulence activator alpha C-term | ||
AHMNLFMI_02307 | 9.8e-20 | T | Universal stress protein family | |||
AHMNLFMI_02308 | 5e-57 | padR | K | Virulence activator alpha C-term | ||
AHMNLFMI_02310 | 3.8e-23 | |||||
AHMNLFMI_02311 | 1.9e-138 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
AHMNLFMI_02312 | 3.2e-23 | yceI | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02313 | 3.4e-34 | comGB | NU | type II secretion system | ||
AHMNLFMI_02314 | 3.8e-64 | comGA | NU | Type II IV secretion system protein | ||
AHMNLFMI_02315 | 1.5e-24 | comGB | NU | type II secretion system | ||
AHMNLFMI_02316 | 1.9e-167 | comGA | NU | Type II IV secretion system protein | ||
AHMNLFMI_02317 | 2.1e-25 | comGA | NU | Type II IV secretion system protein | ||
AHMNLFMI_02318 | 3.1e-40 | S | Metal-independent alpha-mannosidase (GH125) | |||
AHMNLFMI_02319 | 3.6e-108 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_02320 | 4.5e-52 | S | Metal-independent alpha-mannosidase (GH125) | |||
AHMNLFMI_02321 | 1.5e-43 | yliE | T | EAL domain | ||
AHMNLFMI_02322 | 4.8e-205 | 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 | |
AHMNLFMI_02323 | 8.5e-141 | 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 | |
AHMNLFMI_02324 | 7.3e-86 | 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 | |
AHMNLFMI_02325 | 2.6e-21 | 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 | |
AHMNLFMI_02326 | 1.7e-92 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_02327 | 2.6e-37 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_02328 | 1e-47 | S | Domain of unknown function (DUF1905) | |||
AHMNLFMI_02329 | 1e-47 | S | Domain of unknown function (DUF1905) | |||
AHMNLFMI_02330 | 1.2e-38 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHMNLFMI_02331 | 8.7e-48 | pmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02332 | 7.9e-41 | pmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02333 | 2.1e-65 | pmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02334 | 2.7e-11 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
AHMNLFMI_02335 | 2.4e-62 | S | Domain of unknown function (DUF3284) | |||
AHMNLFMI_02336 | 5.1e-44 | K | PRD domain | |||
AHMNLFMI_02338 | 6.6e-128 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_02339 | 2.3e-52 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_02340 | 1.3e-144 | S | Cell surface protein | |||
AHMNLFMI_02341 | 1.1e-43 | S | Cell surface protein | |||
AHMNLFMI_02342 | 7.4e-150 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_02343 | 3.3e-94 | AtpB | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | |
AHMNLFMI_02344 | 8e-68 | 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 | |
AHMNLFMI_02346 | 4.2e-44 | S | zinc-ribbon domain | |||
AHMNLFMI_02347 | 3.7e-69 | S | response to antibiotic | |||
AHMNLFMI_02348 | 1.7e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
AHMNLFMI_02349 | 5.6e-21 | S | Protein of unknown function (DUF2929) | |||
AHMNLFMI_02350 | 2.1e-15 | K | Cro/C1-type HTH DNA-binding domain | |||
AHMNLFMI_02351 | 4.8e-11 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_02352 | 3.4e-143 | yclK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_02353 | 1.5e-139 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHMNLFMI_02355 | 3.5e-49 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
AHMNLFMI_02356 | 1.1e-65 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_02357 | 4.2e-28 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
AHMNLFMI_02358 | 3.4e-43 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHMNLFMI_02359 | 5.7e-114 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AHMNLFMI_02360 | 1.1e-49 | 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 | |
AHMNLFMI_02361 | 1.9e-27 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_02362 | 1.8e-101 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
AHMNLFMI_02363 | 2.7e-12 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_02364 | 1.2e-23 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_02365 | 1.6e-44 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AHMNLFMI_02366 | 7.9e-52 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AHMNLFMI_02367 | 3e-150 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AHMNLFMI_02368 | 1.2e-277 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHMNLFMI_02369 | 9.9e-48 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHMNLFMI_02370 | 5.5e-40 | yvdE | K | helix_turn _helix lactose operon repressor | ||
AHMNLFMI_02371 | 6.1e-57 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHMNLFMI_02372 | 2.4e-124 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHMNLFMI_02373 | 9.5e-47 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_02374 | 3.2e-85 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_02375 | 2.2e-111 | akr5f | 1.1.1.346 | S | reductase | |
AHMNLFMI_02376 | 7.5e-152 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
AHMNLFMI_02377 | 8e-18 | L | Transposase | |||
AHMNLFMI_02378 | 9.3e-77 | S | Alpha beta hydrolase | |||
AHMNLFMI_02379 | 1.7e-44 | S | Alpha beta hydrolase | |||
AHMNLFMI_02380 | 2.8e-16 | ytrB | V | ABC transporter | ||
AHMNLFMI_02381 | 1.1e-46 | ytrB | V | ABC transporter | ||
AHMNLFMI_02382 | 1.9e-23 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
AHMNLFMI_02383 | 2e-163 | ytrB | V | ABC transporter | ||
AHMNLFMI_02384 | 1.1e-75 | |||||
AHMNLFMI_02385 | 3.1e-18 | XK27_09620 | 1.3.5.4 | S | NADPH-dependent FMN reductase | |
AHMNLFMI_02386 | 5.6e-116 | XK27_09615 | 1.3.5.4 | S | reductase | |
AHMNLFMI_02387 | 1.8e-110 | XK27_09620 | 1.3.5.4 | S | NADPH-dependent FMN reductase | |
AHMNLFMI_02388 | 4e-27 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
AHMNLFMI_02389 | 9e-23 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
AHMNLFMI_02390 | 6.2e-131 | K | response regulator | |||
AHMNLFMI_02391 | 1e-07 | S | Phage minor capsid protein 2 | |||
AHMNLFMI_02394 | 2.1e-26 | S | Phage minor capsid protein 2 | |||
AHMNLFMI_02396 | 2.3e-79 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_02397 | 1.2e-161 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_02400 | 1.3e-44 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHMNLFMI_02402 | 1.3e-81 | yiiE | S | Protein of unknown function (DUF1211) | ||
AHMNLFMI_02403 | 5.8e-104 | 1.3.5.4 | S | NADPH-dependent FMN reductase | ||
AHMNLFMI_02404 | 5.5e-190 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_02405 | 6.2e-208 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_02406 | 2.2e-70 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_02407 | 7.5e-104 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_02411 | 2.2e-117 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHMNLFMI_02412 | 6.9e-156 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
AHMNLFMI_02414 | 2.4e-164 | G | Peptidase_C39 like family | |||
AHMNLFMI_02415 | 1.3e-168 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
AHMNLFMI_02416 | 1e-43 | manY | G | PTS system | ||
AHMNLFMI_02417 | 1.8e-11 | L | Helix-turn-helix domain | |||
AHMNLFMI_02418 | 7.3e-12 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_02419 | 4.2e-47 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_02420 | 5e-162 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_02421 | 1.2e-219 | ydiN | EGP | Major Facilitator Superfamily | ||
AHMNLFMI_02422 | 9.2e-175 | K | Transcriptional regulator, LysR family | |||
AHMNLFMI_02423 | 1.1e-77 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_02428 | 4.3e-56 | S | Protein conserved in bacteria | |||
AHMNLFMI_02429 | 2.6e-168 | |||||
AHMNLFMI_02430 | 3.9e-87 | yqeG | S | HAD phosphatase, family IIIA | ||
AHMNLFMI_02431 | 2.2e-57 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AHMNLFMI_02432 | 1.1e-272 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AHMNLFMI_02433 | 7.2e-48 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_02434 | 1.9e-96 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_02435 | 3.8e-38 | J | Cysteine protease Prp | |||
AHMNLFMI_02436 | 8.8e-64 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
AHMNLFMI_02437 | 9.8e-25 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
AHMNLFMI_02438 | 2.3e-33 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
AHMNLFMI_02439 | 5.9e-64 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_02440 | 4e-56 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_02441 | 3.2e-49 | K | Acetyltransferase (GNAT) domain | |||
AHMNLFMI_02442 | 6e-48 | |||||
AHMNLFMI_02443 | 1.8e-15 | sufC | O | FeS assembly ATPase SufC | ||
AHMNLFMI_02444 | 4.1e-113 | sufC | O | FeS assembly ATPase SufC | ||
AHMNLFMI_02445 | 4.2e-56 | sufC | O | FeS assembly ATPase SufC | ||
AHMNLFMI_02446 | 1.9e-51 | sufC | O | FeS assembly ATPase SufC | ||
AHMNLFMI_02447 | 2.3e-28 | S | Cysteine-rich secretory protein family | |||
AHMNLFMI_02448 | 1.4e-234 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_02449 | 3.8e-57 | hxlR | K | HxlR-like helix-turn-helix | ||
AHMNLFMI_02450 | 1.2e-29 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AHMNLFMI_02451 | 7.4e-11 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AHMNLFMI_02452 | 7.4e-64 | yodB | K | Transcriptional regulator, HxlR family | ||
AHMNLFMI_02453 | 1.3e-93 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
AHMNLFMI_02454 | 7.9e-140 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_02455 | 5.3e-76 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_02456 | 5.6e-35 | S | Cysteine-rich secretory protein family | |||
AHMNLFMI_02458 | 2.4e-101 | phnD | P | Phosphonate ABC transporter | ||
AHMNLFMI_02459 | 2.1e-14 | phnD | P | Phosphonate ABC transporter | ||
AHMNLFMI_02460 | 9.5e-30 | phnD | P | Phosphonate ABC transporter | ||
AHMNLFMI_02461 | 7.6e-24 | phnD | P | Phosphonate ABC transporter | ||
AHMNLFMI_02462 | 1.7e-59 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_02463 | 7.7e-36 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_02464 | 2.8e-41 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_02465 | 4.2e-47 | galR | K | Transcriptional regulator | ||
AHMNLFMI_02466 | 7.9e-160 | galR | K | Transcriptional regulator | ||
AHMNLFMI_02467 | 1.4e-33 | galR | K | Transcriptional regulator | ||
AHMNLFMI_02468 | 1e-72 | yfnA | E | Amino Acid | ||
AHMNLFMI_02469 | 1.5e-88 | yfnA | E | Amino Acid | ||
AHMNLFMI_02470 | 4.4e-16 | 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 | |
AHMNLFMI_02471 | 4e-44 | 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 | |
AHMNLFMI_02472 | 3.2e-63 | 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 | |
AHMNLFMI_02473 | 4.5e-32 | 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 | |
AHMNLFMI_02474 | 1.2e-61 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AHMNLFMI_02475 | 7.2e-74 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AHMNLFMI_02476 | 2.7e-35 | trxA1 | O | Belongs to the thioredoxin family | ||
AHMNLFMI_02477 | 6.2e-57 | trxA1 | O | Belongs to the thioredoxin family | ||
AHMNLFMI_02478 | 6.1e-49 | |||||
AHMNLFMI_02479 | 6.6e-96 | |||||
AHMNLFMI_02480 | 2.4e-28 | K | UTRA | |||
AHMNLFMI_02481 | 2.2e-45 | K | UTRA | |||
AHMNLFMI_02482 | 7.8e-56 | L | Transposase | |||
AHMNLFMI_02483 | 5e-19 | |||||
AHMNLFMI_02484 | 5e-42 | |||||
AHMNLFMI_02485 | 1.2e-42 | S | Putative metallopeptidase domain | |||
AHMNLFMI_02486 | 6.9e-84 | S | Putative metallopeptidase domain | |||
AHMNLFMI_02487 | 1.5e-49 | |||||
AHMNLFMI_02488 | 5.4e-104 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_02489 | 1.3e-41 | S | Putative metallopeptidase domain | |||
AHMNLFMI_02491 | 3.1e-51 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
AHMNLFMI_02492 | 3e-75 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
AHMNLFMI_02493 | 3.3e-60 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_02494 | 5.8e-150 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_02495 | 4.7e-21 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_02496 | 3.2e-13 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_02497 | 8.8e-23 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_02498 | 1.8e-80 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
AHMNLFMI_02499 | 6.1e-290 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
AHMNLFMI_02500 | 3.5e-86 | pts15C | 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 | ||
AHMNLFMI_02501 | 2.1e-39 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
AHMNLFMI_02502 | 8.1e-08 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AHMNLFMI_02503 | 4.4e-21 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AHMNLFMI_02504 | 2.6e-21 | 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 | |
AHMNLFMI_02505 | 1.7e-37 | 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 | |
AHMNLFMI_02506 | 8.7e-34 | glnPH2 | P | ABC transporter permease | ||
AHMNLFMI_02508 | 1.8e-90 | glnPH2 | P | ABC transporter permease | ||
AHMNLFMI_02509 | 1.3e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_02510 | 9.5e-106 | 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 | ||
AHMNLFMI_02511 | 2.1e-98 | 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 | ||
AHMNLFMI_02512 | 5.5e-99 | epsB | M | biosynthesis protein | ||
AHMNLFMI_02513 | 3.1e-173 | 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 | ||
AHMNLFMI_02514 | 9.7e-40 | 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 | ||
AHMNLFMI_02515 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_02516 | 2.6e-70 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_02517 | 9.6e-103 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_02518 | 7.8e-266 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
AHMNLFMI_02519 | 4.9e-69 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
AHMNLFMI_02520 | 1e-45 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
AHMNLFMI_02521 | 2e-15 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
AHMNLFMI_02522 | 8.5e-41 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
AHMNLFMI_02523 | 5.2e-41 | yesM | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_02524 | 5.7e-135 | yesM | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_02525 | 3.3e-161 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_02526 | 4.8e-61 | EG | EamA-like transporter family | |||
AHMNLFMI_02527 | 3e-64 | EG | EamA-like transporter family | |||
AHMNLFMI_02529 | 4.1e-52 | L | Integrase core domain | |||
AHMNLFMI_02530 | 1e-27 | celB | 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 | ||
AHMNLFMI_02531 | 1.6e-143 | celB | 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 | ||
AHMNLFMI_02532 | 1.5e-113 | yidA | K | Helix-turn-helix domain, rpiR family | ||
AHMNLFMI_02533 | 8.6e-47 | yidA | K | Helix-turn-helix domain, rpiR family | ||
AHMNLFMI_02534 | 1.2e-45 | yidA | K | Helix-turn-helix domain, rpiR family | ||
AHMNLFMI_02535 | 1.2e-57 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHMNLFMI_02536 | 7e-37 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHMNLFMI_02537 | 8.2e-151 | yhcA | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_02538 | 1.2e-24 | S | Cytochrome B5 | |||
AHMNLFMI_02539 | 1.1e-31 | S | Cytochrome B5 | |||
AHMNLFMI_02540 | 2.3e-20 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
AHMNLFMI_02541 | 4.6e-91 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
AHMNLFMI_02542 | 4.8e-46 | dnaB | L | replication initiation and membrane attachment | ||
AHMNLFMI_02543 | 8.6e-38 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_02544 | 1.7e-44 | L | Integrase | |||
AHMNLFMI_02545 | 1.1e-99 | L | Integrase | |||
AHMNLFMI_02546 | 9.6e-154 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
AHMNLFMI_02547 | 5.1e-93 | M | Parallel beta-helix repeats | |||
AHMNLFMI_02548 | 5.1e-44 | rfbX | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
AHMNLFMI_02549 | 1.7e-55 | dedA | S | SNARE associated Golgi protein | ||
AHMNLFMI_02550 | 1e-232 | pyrP | F | Permease | ||
AHMNLFMI_02551 | 5.1e-66 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_02552 | 1.9e-77 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_02553 | 1.7e-99 | |||||
AHMNLFMI_02554 | 3.5e-32 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
AHMNLFMI_02555 | 5.1e-35 | S | Cell surface protein | |||
AHMNLFMI_02556 | 4.1e-83 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_02557 | 3.4e-29 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_02558 | 7.4e-64 | |||||
AHMNLFMI_02559 | 9.1e-28 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_02560 | 2e-20 | |||||
AHMNLFMI_02561 | 7.7e-97 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
AHMNLFMI_02562 | 3.1e-294 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_02563 | 9.1e-138 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_02564 | 6.8e-13 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
AHMNLFMI_02565 | 1.9e-161 | L | Belongs to the 'phage' integrase family | |||
AHMNLFMI_02566 | 4.4e-45 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AHMNLFMI_02567 | 1.6e-53 | 3.1.21.3 | V | PFAM restriction modification system DNA specificity domain | ||
AHMNLFMI_02568 | 1e-229 | hsdM | 2.1.1.72 | V | PFAM N-6 DNA methylase | |
AHMNLFMI_02569 | 6.6e-78 | S | Pyridoxamine 5'-phosphate oxidase | |||
AHMNLFMI_02570 | 1.6e-31 | cspA | K | Cold shock protein domain | ||
AHMNLFMI_02571 | 1.7e-37 | |||||
AHMNLFMI_02572 | 5.1e-26 | D | protein tyrosine kinase activity | |||
AHMNLFMI_02573 | 2.7e-35 | wcoI | 2.7.10.1, 2.7.10.2 | M | biosynthesis protein | |
AHMNLFMI_02574 | 3.1e-217 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
AHMNLFMI_02575 | 9.7e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_02576 | 5.8e-153 | yihY | S | Belongs to the UPF0761 family | ||
AHMNLFMI_02577 | 1.2e-61 | S | CAAX protease self-immunity | |||
AHMNLFMI_02578 | 2.3e-67 | V | CAAX protease self-immunity | |||
AHMNLFMI_02579 | 2.1e-09 | V | ABC transporter | |||
AHMNLFMI_02580 | 6.2e-19 | V | ABC transporter | |||
AHMNLFMI_02582 | 5.6e-40 | yyaQ | S | YjbR | ||
AHMNLFMI_02583 | 4e-116 | yyaQ | S | YjbR | ||
AHMNLFMI_02584 | 4.8e-221 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AHMNLFMI_02585 | 8.2e-29 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AHMNLFMI_02586 | 3.5e-34 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
AHMNLFMI_02587 | 5.5e-44 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
AHMNLFMI_02588 | 5.5e-44 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
AHMNLFMI_02589 | 1.9e-44 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
AHMNLFMI_02590 | 6e-11 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
AHMNLFMI_02591 | 4.1e-32 | M | O-Antigen ligase | |||
AHMNLFMI_02592 | 1.1e-22 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
AHMNLFMI_02593 | 8.8e-139 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
AHMNLFMI_02594 | 2.1e-31 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
AHMNLFMI_02596 | 2.8e-17 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_02597 | 1e-42 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_02598 | 1.8e-96 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_02600 | 7e-40 | |||||
AHMNLFMI_02601 | 5.6e-61 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_02602 | 8.8e-124 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AHMNLFMI_02603 | 1.5e-62 | 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 | ||
AHMNLFMI_02604 | 1.5e-72 | 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 | ||
AHMNLFMI_02605 | 2.5e-43 | 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 | ||
AHMNLFMI_02606 | 2.3e-59 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
AHMNLFMI_02607 | 2.7e-118 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
AHMNLFMI_02608 | 1.4e-20 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
AHMNLFMI_02609 | 1.8e-44 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
AHMNLFMI_02610 | 2.7e-85 | 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 | |
AHMNLFMI_02611 | 2.9e-223 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_02612 | 3.3e-47 | azlC | E | branched-chain amino acid | ||
AHMNLFMI_02613 | 6.4e-60 | azlC | E | branched-chain amino acid | ||
AHMNLFMI_02614 | 7.2e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
AHMNLFMI_02615 | 7.2e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
AHMNLFMI_02616 | 2.4e-164 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
AHMNLFMI_02617 | 3.1e-113 | acmA | 3.2.1.17 | NU | mannosyl-glycoprotein | |
AHMNLFMI_02618 | 2e-20 | 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 | |
AHMNLFMI_02619 | 4.6e-41 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_02620 | 7.8e-69 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
AHMNLFMI_02621 | 1.1e-12 | V | HNH nucleases | |||
AHMNLFMI_02623 | 1.5e-74 | S | Transcriptional regulator, RinA family | |||
AHMNLFMI_02624 | 2.6e-14 | |||||
AHMNLFMI_02626 | 5.5e-09 | |||||
AHMNLFMI_02627 | 1.9e-26 | S | YopX protein | |||
AHMNLFMI_02630 | 4.8e-15 | |||||
AHMNLFMI_02631 | 2.9e-48 | |||||
AHMNLFMI_02633 | 1.1e-58 | pi346 | L | IstB-like ATP binding protein | ||
AHMNLFMI_02634 | 5.3e-100 | 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 | ||
AHMNLFMI_02635 | 1.6e-91 | pbpX2 | V | Beta-lactamase | ||
AHMNLFMI_02636 | 1.9e-95 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
AHMNLFMI_02637 | 4.4e-63 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
AHMNLFMI_02638 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
AHMNLFMI_02639 | 3e-86 | 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) | |
AHMNLFMI_02641 | 5.9e-08 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_02642 | 5.9e-08 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_02644 | 3.7e-53 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_02645 | 7e-84 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AHMNLFMI_02646 | 2.4e-33 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
AHMNLFMI_02647 | 2.8e-63 | |||||
AHMNLFMI_02648 | 5.3e-125 | |||||
AHMNLFMI_02649 | 1.7e-151 | yfiC | V | ABC transporter | ||
AHMNLFMI_02650 | 8.6e-123 | yfiC | V | ABC transporter | ||
AHMNLFMI_02651 | 1.8e-17 | yfiC | V | ABC transporter | ||
AHMNLFMI_02652 | 1.4e-145 | K | PRD domain | |||
AHMNLFMI_02653 | 3.4e-66 | 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 | |
AHMNLFMI_02654 | 8.7e-54 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AHMNLFMI_02655 | 7.9e-57 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AHMNLFMI_02656 | 2.3e-40 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AHMNLFMI_02657 | 1.3e-30 | yneE | K | Transcriptional regulator | ||
AHMNLFMI_02658 | 6.7e-148 | yneE | K | Transcriptional regulator | ||
AHMNLFMI_02659 | 3e-145 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_02660 | 2.7e-58 | S | Protein of unknown function (DUF1648) | |||
AHMNLFMI_02661 | 2.5e-12 | S | Protein of unknown function (DUF1648) | |||
AHMNLFMI_02662 | 1.6e-12 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHMNLFMI_02663 | 2.2e-30 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_02664 | 6.6e-142 | uup | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_02665 | 7.6e-38 | |||||
AHMNLFMI_02666 | 1.5e-92 | |||||
AHMNLFMI_02667 | 2.7e-09 | |||||
AHMNLFMI_02668 | 1.9e-46 | yifK | E | Amino acid permease | ||
AHMNLFMI_02669 | 1.1e-119 | yifK | E | Amino acid permease | ||
AHMNLFMI_02670 | 3e-22 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_02671 | 8.4e-24 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_02672 | 1.5e-16 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_02673 | 3e-22 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_02674 | 8.5e-15 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_02675 | 9.1e-84 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_02676 | 4.9e-36 | yitW | S | Pfam:DUF59 | ||
AHMNLFMI_02677 | 1.3e-46 | yitW | S | Pfam:DUF59 | ||
AHMNLFMI_02678 | 6.7e-48 | yitW | S | Pfam:DUF59 | ||
AHMNLFMI_02679 | 1.5e-49 | yitW | S | Pfam:DUF59 | ||
AHMNLFMI_02680 | 2.6e-93 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_02681 | 2.3e-80 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
AHMNLFMI_02682 | 9.2e-54 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
AHMNLFMI_02683 | 2e-49 | pspC | KT | positive regulation of macromolecule biosynthetic process | ||
AHMNLFMI_02684 | 5.2e-63 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AHMNLFMI_02685 | 6e-29 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_02686 | 2.9e-238 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_02687 | 2.4e-25 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_02688 | 2.3e-94 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AHMNLFMI_02689 | 1.9e-15 | |||||
AHMNLFMI_02690 | 7.2e-53 | |||||
AHMNLFMI_02691 | 1.6e-28 | |||||
AHMNLFMI_02692 | 2.5e-52 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_02693 | 4.6e-12 | |||||
AHMNLFMI_02694 | 4.2e-59 | hit | FG | histidine triad | ||
AHMNLFMI_02695 | 9.5e-36 | |||||
AHMNLFMI_02696 | 1.4e-30 | hit | FG | histidine triad | ||
AHMNLFMI_02697 | 2.6e-13 | 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 | ||
AHMNLFMI_02698 | 6.2e-83 | fadR | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_02699 | 6.8e-35 | GM | NmrA-like family | |||
AHMNLFMI_02700 | 3.1e-148 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AHMNLFMI_02701 | 5.8e-45 | pstS | P | Phosphate | ||
AHMNLFMI_02702 | 1.3e-62 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AHMNLFMI_02703 | 4.4e-172 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AHMNLFMI_02704 | 4.2e-169 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
AHMNLFMI_02705 | 1e-10 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
AHMNLFMI_02707 | 8.4e-08 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
AHMNLFMI_02708 | 1.5e-144 | 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 | |
AHMNLFMI_02709 | 4.8e-53 | |||||
AHMNLFMI_02710 | 4.1e-38 | 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 | |
AHMNLFMI_02711 | 4.6e-163 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
AHMNLFMI_02712 | 1.8e-18 | ugpA | U | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_02713 | 1.6e-35 | ugpB | G | Bacterial extracellular solute-binding protein | ||
AHMNLFMI_02714 | 7.4e-35 | S | Prolyl oligopeptidase family | |||
AHMNLFMI_02715 | 2.6e-79 | S | Prolyl oligopeptidase family | |||
AHMNLFMI_02716 | 4.7e-91 | S | Prolyl oligopeptidase family | |||
AHMNLFMI_02717 | 4.7e-57 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
AHMNLFMI_02718 | 8.5e-57 | S | SdpI/YhfL protein family | |||
AHMNLFMI_02719 | 1.8e-173 | C | Zinc-binding dehydrogenase | |||
AHMNLFMI_02720 | 2.8e-61 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_02721 | 4.9e-20 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
AHMNLFMI_02722 | 7.1e-52 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
AHMNLFMI_02723 | 2.8e-73 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_02724 | 3.7e-47 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_02725 | 5.5e-17 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_02726 | 7e-21 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_02727 | 2.6e-109 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_02728 | 5.9e-15 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_02729 | 1.3e-76 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_02731 | 1.8e-205 | S | Pfam Methyltransferase | |||
AHMNLFMI_02732 | 3.2e-77 | pipD | E | Dipeptidase | ||
AHMNLFMI_02733 | 6.4e-27 | pipD | E | Dipeptidase | ||
AHMNLFMI_02734 | 4.5e-67 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_02735 | 9.1e-217 | msmX | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_02736 | 1.4e-89 | ypdD | G | Glycosyl hydrolase family 92 | ||
AHMNLFMI_02737 | 7.2e-23 | ypdD | G | Glycosyl hydrolase family 92 | ||
AHMNLFMI_02738 | 8.4e-17 | |||||
AHMNLFMI_02739 | 3.1e-13 | |||||
AHMNLFMI_02740 | 3.6e-46 | |||||
AHMNLFMI_02741 | 1.1e-11 | |||||
AHMNLFMI_02742 | 1.6e-14 | |||||
AHMNLFMI_02743 | 2.1e-80 | |||||
AHMNLFMI_02744 | 1.8e-170 | |||||
AHMNLFMI_02746 | 3.5e-22 | S | Barstar (barnase inhibitor) | |||
AHMNLFMI_02748 | 3e-60 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_02749 | 3.8e-54 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_02750 | 9e-26 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_02751 | 1.9e-40 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_02752 | 4.1e-72 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
AHMNLFMI_02753 | 5e-176 | |||||
AHMNLFMI_02754 | 4.6e-93 | cobB | K | SIR2 family | ||
AHMNLFMI_02755 | 9.9e-82 | cobB | K | SIR2 family | ||
AHMNLFMI_02757 | 3.3e-54 | yneR | S | Belongs to the HesB IscA family | ||
AHMNLFMI_02758 | 3.7e-20 | XK27_02470 | K | LytTr DNA-binding domain | ||
AHMNLFMI_02759 | 4.4e-54 | S | Membrane | |||
AHMNLFMI_02760 | 9.6e-171 | S | Membrane | |||
AHMNLFMI_02761 | 2.7e-90 | K | response regulator | |||
AHMNLFMI_02762 | 1.6e-22 | 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 | ||
AHMNLFMI_02763 | 1.4e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
AHMNLFMI_02764 | 1.8e-63 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_02765 | 2.1e-19 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_02766 | 1e-38 | GK | ROK family | |||
AHMNLFMI_02767 | 1.3e-84 | GK | ROK family | |||
AHMNLFMI_02768 | 5.5e-139 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
AHMNLFMI_02769 | 8.3e-129 | yjjC | V | ABC transporter | ||
AHMNLFMI_02770 | 4.7e-47 | cvfB | S | S1 domain | ||
AHMNLFMI_02771 | 2.6e-35 | yitW | S | Pfam:DUF59 | ||
AHMNLFMI_02773 | 1.6e-42 | XK27_06930 | V | domain protein | ||
AHMNLFMI_02774 | 6.4e-59 | XK27_06930 | V | domain protein | ||
AHMNLFMI_02776 | 6.1e-58 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AHMNLFMI_02777 | 1.3e-34 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AHMNLFMI_02778 | 3.9e-25 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_02779 | 1.2e-97 | yacP | S | YacP-like NYN domain | ||
AHMNLFMI_02780 | 6.9e-51 | EG | EamA-like transporter family | |||
AHMNLFMI_02781 | 1.3e-81 | elaA | S | GNAT family | ||
AHMNLFMI_02782 | 6e-103 | yunF | F | Protein of unknown function DUF72 | ||
AHMNLFMI_02783 | 1.8e-130 | nupG | F | Nucleoside | ||
AHMNLFMI_02784 | 4.1e-82 | nupG | F | Nucleoside | ||
AHMNLFMI_02785 | 5.3e-33 | nupG | F | Nucleoside | ||
AHMNLFMI_02786 | 4.7e-23 | |||||
AHMNLFMI_02787 | 2.4e-25 | xerC | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_02789 | 2e-64 | sat | 2.7.7.4 | H | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
AHMNLFMI_02790 | 2.2e-48 | cysC | 2.7.1.25, 2.7.7.4 | F | Catalyzes the synthesis of activated sulfate | |
AHMNLFMI_02791 | 5.3e-57 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_02792 | 3.4e-132 | ytbD | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02793 | 2.5e-42 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
AHMNLFMI_02794 | 8.6e-141 | 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 | |
AHMNLFMI_02795 | 4.3e-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 | |
AHMNLFMI_02796 | 1.1e-30 | 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 | |
AHMNLFMI_02797 | 3.8e-159 | licT | K | CAT RNA binding domain | ||
AHMNLFMI_02798 | 3.9e-140 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_02799 | 7.8e-100 | mdxE | G | Bacterial extracellular solute-binding protein | ||
AHMNLFMI_02800 | 2e-126 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
AHMNLFMI_02801 | 2.1e-51 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
AHMNLFMI_02803 | 1.1e-104 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
AHMNLFMI_02804 | 1.3e-60 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHMNLFMI_02805 | 8.8e-40 | |||||
AHMNLFMI_02807 | 6.8e-33 | L | transposase activity | |||
AHMNLFMI_02809 | 2.9e-57 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
AHMNLFMI_02810 | 4.7e-70 | 1.14.14.9 | Q | 4-hydroxyphenylacetate | ||
AHMNLFMI_02811 | 2.9e-81 | 6.3.3.2 | S | ASCH | ||
AHMNLFMI_02812 | 7.4e-08 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHMNLFMI_02813 | 6.3e-36 | 3.5.1.10 | C | nadph quinone reductase | ||
AHMNLFMI_02814 | 9.6e-150 | 3.5.1.10 | C | nadph quinone reductase | ||
AHMNLFMI_02815 | 2.1e-103 | 3.5.1.10 | C | nadph quinone reductase | ||
AHMNLFMI_02816 | 8.6e-45 | 3.5.1.10 | C | nadph quinone reductase | ||
AHMNLFMI_02817 | 1.7e-42 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
AHMNLFMI_02818 | 1.7e-42 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
AHMNLFMI_02819 | 2.7e-181 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
AHMNLFMI_02820 | 2.8e-144 | pstS | P | Phosphate | ||
AHMNLFMI_02821 | 1.7e-114 | yvyE | 3.4.13.9 | S | YigZ family | |
AHMNLFMI_02822 | 1.4e-170 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_02823 | 7.5e-10 | L | Transposase | |||
AHMNLFMI_02825 | 1.4e-46 | pts4ABC | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHMNLFMI_02826 | 2.7e-222 | pts4ABC | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHMNLFMI_02827 | 1.1e-25 | mocA | S | Oxidoreductase | ||
AHMNLFMI_02828 | 1.5e-132 | mocA | S | Oxidoreductase | ||
AHMNLFMI_02829 | 1.7e-40 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHMNLFMI_02830 | 1.7e-42 | pltR | K | LytTr DNA-binding domain | ||
AHMNLFMI_02831 | 4.1e-23 | pltR | K | LytTr DNA-binding domain | ||
AHMNLFMI_02832 | 1e-40 | S | CAAX protease self-immunity | |||
AHMNLFMI_02833 | 3e-114 | S | CAAX protease self-immunity | |||
AHMNLFMI_02834 | 2.5e-46 | |||||
AHMNLFMI_02835 | 5.3e-38 | S | CAAX protease self-immunity | |||
AHMNLFMI_02836 | 1.2e-19 | K | LytTr DNA-binding domain | |||
AHMNLFMI_02837 | 2.7e-50 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_02838 | 4.6e-115 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_02839 | 5.7e-200 | K | PRD domain | |||
AHMNLFMI_02840 | 1.3e-25 | K | PRD domain | |||
AHMNLFMI_02841 | 4.4e-20 | K | PRD domain | |||
AHMNLFMI_02842 | 2.8e-28 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
AHMNLFMI_02843 | 1.9e-46 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
AHMNLFMI_02844 | 2e-40 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
AHMNLFMI_02845 | 2.1e-88 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
AHMNLFMI_02846 | 5e-81 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
AHMNLFMI_02847 | 8.1e-88 | 2.3.1.128, 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_02848 | 7.2e-32 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_02849 | 1.2e-28 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_02850 | 1.5e-58 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AHMNLFMI_02851 | 1e-15 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
AHMNLFMI_02852 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AHMNLFMI_02853 | 1e-47 | P | Rhodanese Homology Domain | |||
AHMNLFMI_02854 | 1.9e-62 | P | Rhodanese Homology Domain | |||
AHMNLFMI_02855 | 2e-18 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_02856 | 1.2e-36 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_02857 | 2.4e-40 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_02858 | 3e-102 | C | Zinc-binding dehydrogenase | |||
AHMNLFMI_02859 | 2.5e-245 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_02860 | 2.6e-43 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_02861 | 1.6e-255 | araP | U | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
AHMNLFMI_02862 | 3.1e-206 | araR | K | Transcriptional regulator | ||
AHMNLFMI_02863 | 7.7e-65 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
AHMNLFMI_02864 | 2.5e-58 | G | YdjC-like protein | |||
AHMNLFMI_02865 | 8.3e-246 | steT | E | amino acid | ||
AHMNLFMI_02866 | 9.6e-13 | steT | E | amino acid | ||
AHMNLFMI_02867 | 1.4e-57 | steT | E | amino acid | ||
AHMNLFMI_02868 | 1e-158 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AHMNLFMI_02869 | 5.9e-167 | 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) | |
AHMNLFMI_02870 | 1.5e-104 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Peptidase C26 | |
AHMNLFMI_02871 | 2.9e-127 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_02872 | 1.1e-33 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Peptidase C26 | |
AHMNLFMI_02873 | 9.4e-124 | gshR | 1.8.1.7 | C | Pyridine nucleotide-disulphide oxidoreductase | |
AHMNLFMI_02874 | 4.2e-75 | gshR | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_02875 | 4.3e-36 | GM | NAD(P)H-binding | |||
AHMNLFMI_02876 | 2.6e-91 | S | Phosphatidylethanolamine-binding protein | |||
AHMNLFMI_02877 | 3.5e-38 | GM | NAD(P)H-binding | |||
AHMNLFMI_02878 | 8.6e-28 | cadA | P | P-type ATPase | ||
AHMNLFMI_02880 | 2.6e-49 | yyaQ | S | YjbR | ||
AHMNLFMI_02881 | 5.4e-248 | ftpA | P | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_02882 | 1.2e-39 | ftpA | P | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_02883 | 2.1e-76 | macB3 | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_02884 | 1.2e-37 | pgm3 | G | Phosphoglycerate mutase family | ||
AHMNLFMI_02886 | 5.1e-19 | yjbQ | P | TrkA C-terminal domain protein | ||
AHMNLFMI_02887 | 1.1e-19 | |||||
AHMNLFMI_02888 | 3.8e-165 | |||||
AHMNLFMI_02890 | 6.2e-156 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_02891 | 6.9e-93 | S | Cell surface protein | |||
AHMNLFMI_02892 | 7e-50 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_02893 | 3.1e-25 | T | Universal stress protein family | |||
AHMNLFMI_02894 | 3.5e-233 | pts14C | 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 | ||
AHMNLFMI_02895 | 6.6e-60 | pts14C | 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 | ||
AHMNLFMI_02896 | 6e-12 | patA | 1.1.1.28, 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHMNLFMI_02897 | 1.1e-57 | patA | 1.1.1.28, 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHMNLFMI_02898 | 3.1e-124 | T | Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain | |||
AHMNLFMI_02899 | 3.5e-88 | K | Winged helix DNA-binding domain | |||
AHMNLFMI_02900 | 4.9e-111 | luxT | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_02901 | 5.9e-28 | |||||
AHMNLFMI_02902 | 1.7e-127 | ypuA | S | Protein of unknown function (DUF1002) | ||
AHMNLFMI_02903 | 5.7e-180 | glk | 2.7.1.2 | G | Glucokinase | |
AHMNLFMI_02904 | 1.4e-33 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
AHMNLFMI_02905 | 1.9e-26 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
AHMNLFMI_02906 | 1.2e-53 | glk | 2.7.1.2 | G | Glucokinase | |
AHMNLFMI_02907 | 1.1e-41 | glk | 2.7.1.2 | G | Glucokinase | |
AHMNLFMI_02908 | 4.8e-39 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
AHMNLFMI_02909 | 1.7e-137 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
AHMNLFMI_02910 | 6.3e-28 | cad | S | FMN_bind | ||
AHMNLFMI_02911 | 6e-132 | cad | S | FMN_bind | ||
AHMNLFMI_02912 | 6.8e-12 | cad | S | FMN_bind | ||
AHMNLFMI_02913 | 6.9e-147 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_02914 | 1.6e-16 | uhpT | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02915 | 2.3e-100 | uhpT | EGP | Major facilitator Superfamily | ||
AHMNLFMI_02916 | 1.3e-51 | gntP | EG | Gluconate | ||
AHMNLFMI_02917 | 1.5e-57 | gntP | EG | Gluconate | ||
AHMNLFMI_02918 | 2.9e-60 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
AHMNLFMI_02919 | 4.5e-36 | pepN | 3.4.11.2 | E | aminopeptidase | |
AHMNLFMI_02920 | 6.5e-272 | pepN | 3.4.11.2 | E | aminopeptidase | |
AHMNLFMI_02921 | 1.9e-37 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
AHMNLFMI_02922 | 2.7e-28 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHMNLFMI_02923 | 1.2e-52 | K | Transcriptional regulator | |||
AHMNLFMI_02924 | 1.1e-83 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHMNLFMI_02925 | 3.7e-68 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHMNLFMI_02926 | 5e-48 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHMNLFMI_02927 | 1.4e-77 | |||||
AHMNLFMI_02928 | 1.8e-121 | E | GDSL-like Lipase/Acylhydrolase family | |||
AHMNLFMI_02929 | 1.7e-20 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
AHMNLFMI_02930 | 5.3e-150 | malA | S | maltodextrose utilization protein MalA | ||
AHMNLFMI_02931 | 9.6e-141 | malD | P | ABC transporter permease | ||
AHMNLFMI_02932 | 8.1e-11 | malA | S | maltodextrose utilization protein MalA | ||
AHMNLFMI_02933 | 5.1e-51 | malA | S | maltodextrose utilization protein MalA | ||
AHMNLFMI_02934 | 1e-31 | malD | P | ABC transporter permease | ||
AHMNLFMI_02935 | 4.2e-73 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
AHMNLFMI_02936 | 7.4e-225 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
AHMNLFMI_02937 | 1.1e-37 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
AHMNLFMI_02938 | 4.8e-28 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
AHMNLFMI_02939 | 8.6e-232 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_02940 | 2.2e-182 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
AHMNLFMI_02941 | 3.1e-82 | fic | D | Fic/DOC family | ||
AHMNLFMI_02943 | 2.7e-10 | sigH | K | Sigma-70 region 2 | ||
AHMNLFMI_02944 | 5.4e-15 | sigH | K | Sigma-70 region 2 | ||
AHMNLFMI_02945 | 5.4e-15 | sigH | K | Sigma-70 region 2 | ||
AHMNLFMI_02947 | 2.4e-96 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
AHMNLFMI_02948 | 2.3e-32 | ymfM | S | Helix-turn-helix domain | ||
AHMNLFMI_02950 | 1.2e-130 | yvfR | V | ABC transporter | ||
AHMNLFMI_02951 | 3e-37 | yvfR | V | ABC transporter | ||
AHMNLFMI_02952 | 9.7e-18 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_02953 | 3.3e-21 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_02954 | 3.3e-65 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_02955 | 1.8e-95 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_02956 | 3.1e-33 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_02957 | 9.8e-28 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHMNLFMI_02958 | 2e-133 | |||||
AHMNLFMI_02959 | 4.4e-34 | |||||
AHMNLFMI_02960 | 2.1e-11 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHMNLFMI_02961 | 3.2e-08 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHMNLFMI_02962 | 1.3e-134 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHMNLFMI_02963 | 1.2e-13 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_02964 | 3.6e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AHMNLFMI_02965 | 1.5e-95 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_02966 | 1.4e-25 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_02967 | 4.6e-35 | ywfO | S | HD domain protein | ||
AHMNLFMI_02968 | 5e-58 | ywfO | S | HD domain protein | ||
AHMNLFMI_02969 | 4.6e-25 | |||||
AHMNLFMI_02970 | 2.9e-43 | sirR | K | iron dependent repressor | ||
AHMNLFMI_02971 | 6.5e-37 | |||||
AHMNLFMI_02972 | 2.2e-30 | yqeG | S | HAD phosphatase, family IIIA | ||
AHMNLFMI_02973 | 4.5e-216 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_02974 | 1.7e-37 | yhbY | J | RNA-binding protein | ||
AHMNLFMI_02975 | 1.4e-173 | |||||
AHMNLFMI_02976 | 4.9e-38 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
AHMNLFMI_02977 | 4.4e-132 | 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 | |
AHMNLFMI_02978 | 4.7e-182 | 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 | |
AHMNLFMI_02979 | 8.7e-16 | 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 | |
AHMNLFMI_02980 | 1.2e-155 | mleP3 | S | Membrane transport protein | ||
AHMNLFMI_02981 | 9.8e-110 | S | Membrane | |||
AHMNLFMI_02982 | 1.2e-176 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHMNLFMI_02983 | 1.7e-17 | 1.5.1.3 | H | RibD C-terminal domain | ||
AHMNLFMI_02984 | 1.2e-36 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
AHMNLFMI_02985 | 6.2e-36 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
AHMNLFMI_02986 | 1.9e-45 | tdcC | E | amino acid | ||
AHMNLFMI_02987 | 9.8e-51 | tdcC | E | amino acid | ||
AHMNLFMI_02988 | 1.8e-212 | tdcC | E | amino acid | ||
AHMNLFMI_02989 | 3.6e-41 | 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) | |
AHMNLFMI_02990 | 1.9e-63 | soj | D | Sporulation initiation inhibitor | ||
AHMNLFMI_02991 | 2.7e-149 | noc | K | Belongs to the ParB family | ||
AHMNLFMI_02992 | 1.8e-64 | noc | K | Belongs to the ParB family | ||
AHMNLFMI_02993 | 1.1e-65 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
AHMNLFMI_02994 | 5.3e-27 | ymfF | S | Peptidase M16 inactive domain protein | ||
AHMNLFMI_02995 | 2.5e-163 | ymfH | S | Peptidase M16 | ||
AHMNLFMI_02996 | 2.7e-25 | ymfH | S | Peptidase M16 | ||
AHMNLFMI_02997 | 3.1e-197 | |||||
AHMNLFMI_02998 | 2.9e-30 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_02999 | 9.9e-26 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
AHMNLFMI_03000 | 9.2e-42 | 2.7.1.191 | G | PTS system fructose IIA component | ||
AHMNLFMI_03001 | 3.3e-16 | G | PTS system mannose/fructose/sorbose family IID component | |||
AHMNLFMI_03002 | 1.3e-90 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
AHMNLFMI_03003 | 1.3e-135 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
AHMNLFMI_03005 | 7.5e-58 | GBS0088 | S | Nucleotidyltransferase | ||
AHMNLFMI_03006 | 1.3e-75 | GBS0088 | S | Nucleotidyltransferase | ||
AHMNLFMI_03007 | 1.6e-120 | S | Repeat protein | |||
AHMNLFMI_03008 | 5.5e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
AHMNLFMI_03009 | 4e-71 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_03010 | 5e-56 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
AHMNLFMI_03011 | 1.2e-36 | rhaB | 2.7.1.12, 2.7.1.16, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
AHMNLFMI_03012 | 2e-34 | cps3B | S | Glycosyltransferase like family 2 | ||
AHMNLFMI_03013 | 1.2e-32 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
AHMNLFMI_03014 | 1.9e-95 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
AHMNLFMI_03015 | 4.6e-28 | |||||
AHMNLFMI_03016 | 3e-57 | 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 | |
AHMNLFMI_03017 | 1.1e-54 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AHMNLFMI_03018 | 4.6e-101 | ccpB | 5.1.1.1 | K | lacI family | |
AHMNLFMI_03019 | 2.4e-76 | ccpB | 5.1.1.1 | K | lacI family | |
AHMNLFMI_03020 | 1.4e-43 | S | Prophage endopeptidase tail | |||
AHMNLFMI_03023 | 2.2e-122 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_03024 | 6.1e-54 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_03025 | 9.1e-56 | fadR | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_03026 | 2.8e-55 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_03027 | 2.6e-38 | 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 | |
AHMNLFMI_03028 | 5e-116 | yfmR | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03029 | 2.7e-29 | ktrB | P | Potassium uptake protein | ||
AHMNLFMI_03030 | 2.6e-63 | ktrA | P | domain protein | ||
AHMNLFMI_03031 | 9e-13 | ytgB | S | Transglycosylase associated protein | ||
AHMNLFMI_03032 | 3.6e-11 | |||||
AHMNLFMI_03033 | 4.5e-89 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
AHMNLFMI_03034 | 1.1e-11 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
AHMNLFMI_03035 | 1.2e-30 | N | domain, Protein | |||
AHMNLFMI_03037 | 6.3e-10 | N | domain, Protein | |||
AHMNLFMI_03038 | 2e-208 | G | Major Facilitator | |||
AHMNLFMI_03039 | 7.2e-49 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AHMNLFMI_03040 | 2.8e-48 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AHMNLFMI_03041 | 2.1e-75 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
AHMNLFMI_03042 | 3.2e-50 | 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) | |
AHMNLFMI_03043 | 2.6e-198 | camS | S | sex pheromone | ||
AHMNLFMI_03044 | 4.1e-40 | 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 | |
AHMNLFMI_03046 | 5.5e-13 | comGC | U | competence protein ComGC | ||
AHMNLFMI_03047 | 2.7e-82 | gspG | NU | general secretion pathway protein | ||
AHMNLFMI_03048 | 8.6e-20 | |||||
AHMNLFMI_03049 | 4.5e-88 | S | Prokaryotic N-terminal methylation motif | |||
AHMNLFMI_03051 | 1.4e-109 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AHMNLFMI_03052 | 1e-60 | K | MarR family | |||
AHMNLFMI_03053 | 5.3e-37 | bztC | D | nuclear chromosome segregation | ||
AHMNLFMI_03054 | 2.6e-28 | bztC | D | nuclear chromosome segregation | ||
AHMNLFMI_03055 | 1.8e-46 | 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 | |
AHMNLFMI_03056 | 2.1e-106 | 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 | |
AHMNLFMI_03061 | 1.7e-74 | V | CAAX protease self-immunity | |||
AHMNLFMI_03062 | 1.5e-30 | yejC | S | Protein of unknown function (DUF1003) | ||
AHMNLFMI_03063 | 6.2e-51 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
AHMNLFMI_03064 | 6.2e-51 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
AHMNLFMI_03065 | 4.6e-12 | |||||
AHMNLFMI_03066 | 1.2e-104 | pmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_03067 | 1.5e-51 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHMNLFMI_03068 | 4.4e-121 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHMNLFMI_03069 | 8.4e-38 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHMNLFMI_03071 | 2.1e-146 | S | Cell surface protein | |||
AHMNLFMI_03072 | 2.5e-13 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AHMNLFMI_03073 | 1.7e-122 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AHMNLFMI_03074 | 3.6e-31 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AHMNLFMI_03075 | 9.2e-118 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_03076 | 3.8e-268 | N | domain, Protein | |||
AHMNLFMI_03077 | 3.9e-53 | N | domain, Protein | |||
AHMNLFMI_03078 | 5.1e-46 | K | response regulator | |||
AHMNLFMI_03079 | 2.3e-79 | phoR | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_03080 | 4.3e-31 | phoR | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_03081 | 8.5e-83 | phoR | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_03082 | 2.3e-177 | arlS | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_03083 | 7.4e-150 | K | AI-2E family transporter | |||
AHMNLFMI_03084 | 5.4e-63 | K | AI-2E family transporter | |||
AHMNLFMI_03085 | 3.4e-49 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHMNLFMI_03086 | 3.4e-124 | |||||
AHMNLFMI_03087 | 1.2e-26 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_03088 | 4.7e-152 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_03089 | 3.7e-48 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_03090 | 7.8e-153 | ydgH | S | MMPL family | ||
AHMNLFMI_03091 | 2.8e-67 | msbA2 | 3.6.3.44 | P | ABC transporter transmembrane region | |
AHMNLFMI_03092 | 1.6e-16 | |||||
AHMNLFMI_03093 | 1.9e-18 | |||||
AHMNLFMI_03094 | 1.6e-16 | |||||
AHMNLFMI_03095 | 1.6e-16 | |||||
AHMNLFMI_03096 | 1.6e-16 | |||||
AHMNLFMI_03097 | 1.1e-18 | |||||
AHMNLFMI_03098 | 5.2e-15 | |||||
AHMNLFMI_03099 | 7.2e-17 | |||||
AHMNLFMI_03100 | 2.7e-16 | |||||
AHMNLFMI_03101 | 7e-46 | M | MucBP domain | |||
AHMNLFMI_03102 | 6.3e-28 | 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 | ||
AHMNLFMI_03103 | 1.6e-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 | ||
AHMNLFMI_03104 | 7.9e-90 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_03105 | 1.5e-90 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_03106 | 3e-81 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AHMNLFMI_03107 | 1.9e-92 | |||||
AHMNLFMI_03108 | 2.3e-20 | 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 | |
AHMNLFMI_03109 | 2.3e-20 | 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 | |
AHMNLFMI_03110 | 1e-46 | |||||
AHMNLFMI_03111 | 1.1e-72 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_03112 | 6.6e-25 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
AHMNLFMI_03113 | 2.1e-48 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AHMNLFMI_03114 | 4.1e-116 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AHMNLFMI_03115 | 3.1e-33 | ykzG | S | Belongs to the UPF0356 family | ||
AHMNLFMI_03116 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
AHMNLFMI_03117 | 2.6e-29 | |||||
AHMNLFMI_03118 | 7.4e-101 | S | CAAX protease self-immunity | |||
AHMNLFMI_03119 | 1.2e-95 | |||||
AHMNLFMI_03120 | 9.1e-32 | |||||
AHMNLFMI_03121 | 8.1e-54 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHMNLFMI_03122 | 3.9e-50 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHMNLFMI_03123 | 2.1e-54 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHMNLFMI_03124 | 3.3e-62 | 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) | |
AHMNLFMI_03125 | 3.3e-62 | 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) | |
AHMNLFMI_03126 | 3.7e-107 | pncA | Q | Isochorismatase family | ||
AHMNLFMI_03127 | 2.7e-132 | |||||
AHMNLFMI_03128 | 5.1e-125 | skfE | V | ABC transporter | ||
AHMNLFMI_03129 | 3.7e-61 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
AHMNLFMI_03130 | 3.3e-28 | skfE | V | ABC transporter | ||
AHMNLFMI_03131 | 6.3e-12 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_03132 | 3.6e-73 | larC | 4.99.1.12 | S | Protein of unknown function DUF111 | |
AHMNLFMI_03133 | 1.1e-74 | larC | 4.99.1.12 | S | Protein of unknown function DUF111 | |
AHMNLFMI_03134 | 7.7e-12 | larC | 4.99.1.12 | S | Protein of unknown function DUF111 | |
AHMNLFMI_03135 | 9.1e-13 | mbl | D | Cell shape determining protein MreB Mrl | ||
AHMNLFMI_03136 | 2.8e-58 | mbl | D | Cell shape determining protein MreB Mrl | ||
AHMNLFMI_03137 | 2.6e-117 | mbl | D | Cell shape determining protein MreB Mrl | ||
AHMNLFMI_03138 | 3.8e-18 | G | response to abiotic stimulus | |||
AHMNLFMI_03139 | 2.1e-31 | |||||
AHMNLFMI_03140 | 2.8e-125 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHMNLFMI_03141 | 3.1e-50 | |||||
AHMNLFMI_03142 | 3.9e-64 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_03143 | 2.8e-93 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_03144 | 1.3e-35 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
AHMNLFMI_03145 | 1.7e-120 | yfnA | E | Amino Acid | ||
AHMNLFMI_03146 | 7.1e-13 | yitU | 3.1.3.104 | S | hydrolase | |
AHMNLFMI_03147 | 3.3e-68 | msbA2 | 3.6.3.44 | P | ABC transporter transmembrane region | |
AHMNLFMI_03148 | 9.4e-31 | msbA2 | 3.6.3.44 | P | ABC transporter transmembrane region | |
AHMNLFMI_03149 | 9.3e-105 | msbA2 | 3.6.3.44 | P | ABC transporter transmembrane region | |
AHMNLFMI_03150 | 1.8e-50 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_03151 | 3.7e-111 | S | Alpha beta hydrolase | |||
AHMNLFMI_03152 | 2.7e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
AHMNLFMI_03153 | 1.6e-48 | yrzB | S | Belongs to the UPF0473 family | ||
AHMNLFMI_03154 | 7.3e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
AHMNLFMI_03155 | 2.4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
AHMNLFMI_03156 | 5.6e-115 | 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 | |
AHMNLFMI_03157 | 1.4e-252 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_03158 | 2.8e-173 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_03159 | 2.3e-71 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHMNLFMI_03160 | 7e-104 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03161 | 6.4e-148 | 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_03162 | 2.5e-46 | 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_03163 | 8.3e-60 | S | UPF0397 protein | |||
AHMNLFMI_03164 | 2e-113 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_03165 | 1.1e-24 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_03166 | 1.8e-41 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
AHMNLFMI_03167 | 4e-111 | 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 | |
AHMNLFMI_03168 | 7e-53 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_03169 | 3.5e-269 | pts23C | 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 | ||
AHMNLFMI_03170 | 2.3e-65 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_03171 | 2.7e-97 | 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 | |
AHMNLFMI_03172 | 3.8e-49 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_03173 | 3.1e-59 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_03174 | 1.6e-39 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_03175 | 1.5e-55 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_03176 | 1.3e-25 | |||||
AHMNLFMI_03177 | 7e-30 | |||||
AHMNLFMI_03178 | 6.6e-10 | |||||
AHMNLFMI_03179 | 1.2e-52 | V | ABC transporter | |||
AHMNLFMI_03180 | 1.7e-19 | V | ABC transporter | |||
AHMNLFMI_03181 | 6.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
AHMNLFMI_03182 | 6.5e-89 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
AHMNLFMI_03183 | 1.1e-96 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_03184 | 4e-30 | |||||
AHMNLFMI_03185 | 7.2e-42 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_03186 | 2.1e-93 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_03187 | 4.5e-72 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_03188 | 1.3e-36 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_03189 | 7.6e-28 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
AHMNLFMI_03190 | 2.2e-37 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AHMNLFMI_03191 | 4e-90 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHMNLFMI_03192 | 5e-24 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
AHMNLFMI_03193 | 1.5e-109 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03194 | 1.6e-31 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_03195 | 2.5e-179 | 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 | ||
AHMNLFMI_03196 | 5.8e-39 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_03197 | 7.9e-70 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_03198 | 1.8e-15 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_03199 | 6e-13 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_03200 | 4.8e-105 | rapZ | S | Displays ATPase and GTPase activities | ||
AHMNLFMI_03201 | 6.4e-111 | rapZ | S | Displays ATPase and GTPase activities | ||
AHMNLFMI_03202 | 1.5e-15 | rapZ | S | Displays ATPase and GTPase activities | ||
AHMNLFMI_03203 | 1e-64 | rapZ | S | Displays ATPase and GTPase activities | ||
AHMNLFMI_03204 | 3.7e-20 | V | FtsX-like permease family | |||
AHMNLFMI_03205 | 9.8e-27 | V | FtsX-like permease family | |||
AHMNLFMI_03206 | 1.1e-53 | V | FtsX-like permease family | |||
AHMNLFMI_03207 | 1.3e-129 | V | FtsX-like permease family | |||
AHMNLFMI_03208 | 2.3e-63 | cysA | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03209 | 1.1e-38 | ubiB | S | ABC1 family | ||
AHMNLFMI_03210 | 6.9e-22 | acm2 | 3.2.1.17 | NU | Bacterial SH3 domain | |
AHMNLFMI_03211 | 1e-221 | acm2 | 3.2.1.17 | NU | Bacterial SH3 domain | |
AHMNLFMI_03212 | 1.6e-119 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
AHMNLFMI_03213 | 5.8e-46 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AHMNLFMI_03214 | 1.2e-35 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AHMNLFMI_03215 | 6.5e-60 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHMNLFMI_03216 | 1.3e-58 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHMNLFMI_03217 | 2.4e-27 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHMNLFMI_03218 | 9e-156 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
AHMNLFMI_03219 | 6.9e-87 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AHMNLFMI_03220 | 2.9e-20 | murE | 6.3.2.10, 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 | |
AHMNLFMI_03221 | 1e-43 | murE | 6.3.2.10, 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 | |
AHMNLFMI_03222 | 1.1e-57 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHMNLFMI_03223 | 1.8e-101 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHMNLFMI_03225 | 3.8e-176 | QT | PucR C-terminal helix-turn-helix domain | |||
AHMNLFMI_03226 | 3.3e-43 | QT | PucR C-terminal helix-turn-helix domain | |||
AHMNLFMI_03227 | 1.3e-74 | QT | PucR C-terminal helix-turn-helix domain | |||
AHMNLFMI_03228 | 3.7e-146 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_03229 | 8.7e-270 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHMNLFMI_03230 | 3.2e-47 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHMNLFMI_03231 | 3.5e-18 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03232 | 3.3e-218 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03233 | 6.1e-41 | norB | EGP | Major Facilitator | ||
AHMNLFMI_03234 | 6.3e-109 | norB | EGP | Major Facilitator | ||
AHMNLFMI_03235 | 1.1e-26 | K | transcriptional regulator | |||
AHMNLFMI_03236 | 1.8e-47 | K | transcriptional regulator | |||
AHMNLFMI_03237 | 1.2e-188 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
AHMNLFMI_03238 | 1.2e-45 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
AHMNLFMI_03239 | 9.4e-51 | ydgH | S | MMPL family | ||
AHMNLFMI_03240 | 1.5e-66 | ydgH | S | MMPL family | ||
AHMNLFMI_03241 | 3.9e-110 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
AHMNLFMI_03243 | 1.3e-241 | ktrB | P | Potassium uptake protein | ||
AHMNLFMI_03244 | 3.8e-53 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
AHMNLFMI_03245 | 2e-197 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
AHMNLFMI_03246 | 7.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
AHMNLFMI_03248 | 2.7e-35 | argR | K | Regulates arginine biosynthesis genes | ||
AHMNLFMI_03249 | 1.7e-68 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AHMNLFMI_03250 | 1.6e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03251 | 2.9e-69 | hit | FG | histidine triad | ||
AHMNLFMI_03252 | 3.5e-39 | |||||
AHMNLFMI_03253 | 5.8e-141 | S | module of peptide synthetase | |||
AHMNLFMI_03254 | 1.1e-76 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
AHMNLFMI_03255 | 1.7e-36 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHMNLFMI_03256 | 7.1e-50 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHMNLFMI_03257 | 8.1e-33 | pucR | QT | Purine catabolism regulatory protein-like family | ||
AHMNLFMI_03258 | 9.1e-108 | pucR | QT | Purine catabolism regulatory protein-like family | ||
AHMNLFMI_03259 | 3.6e-45 | yktA | S | Belongs to the UPF0223 family | ||
AHMNLFMI_03260 | 9.7e-10 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
AHMNLFMI_03261 | 1.9e-43 | pgaC | GT2 | M | Glycosyl transferase | |
AHMNLFMI_03262 | 4.2e-32 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
AHMNLFMI_03263 | 1.5e-153 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
AHMNLFMI_03264 | 1.1e-32 | S | Phospholipase_D-nuclease N-terminal | |||
AHMNLFMI_03265 | 1e-30 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
AHMNLFMI_03266 | 9.5e-23 | S | Phospholipase_D-nuclease N-terminal | |||
AHMNLFMI_03267 | 1.1e-22 | S | Phospholipase_D-nuclease N-terminal | |||
AHMNLFMI_03268 | 2.6e-27 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
AHMNLFMI_03269 | 1.5e-69 | apt | 2.4.2.22, 2.4.2.7 | F | Phosphoribosyl transferase domain | |
AHMNLFMI_03270 | 2.8e-102 | mdtG | EGP | Major facilitator Superfamily | ||
AHMNLFMI_03271 | 2.3e-64 | bztC | D | nuclear chromosome segregation | ||
AHMNLFMI_03272 | 2.3e-59 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHMNLFMI_03273 | 3.8e-75 | |||||
AHMNLFMI_03274 | 5.7e-77 | S | Cell surface protein | |||
AHMNLFMI_03275 | 9.7e-54 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_03276 | 2.9e-64 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_03277 | 8e-11 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_03278 | 7.5e-149 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_03279 | 1.5e-180 | ansA | 3.5.1.1 | EJ | Asparaginase | |
AHMNLFMI_03280 | 1.7e-139 | cysA | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03281 | 1.7e-25 | V | FtsX-like permease family | |||
AHMNLFMI_03282 | 9.7e-17 | pva2 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
AHMNLFMI_03283 | 2.3e-290 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_03284 | 1.1e-36 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_03285 | 1.6e-13 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_03286 | 1.7e-37 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_03287 | 1.1e-67 | acuB | S | Domain in cystathionine beta-synthase and other proteins. | ||
AHMNLFMI_03288 | 2.1e-129 | |||||
AHMNLFMI_03289 | 2e-46 | |||||
AHMNLFMI_03290 | 4.6e-75 | |||||
AHMNLFMI_03291 | 4e-181 | 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) | |
AHMNLFMI_03292 | 1.4e-42 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
AHMNLFMI_03293 | 1.5e-71 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
AHMNLFMI_03294 | 1e-47 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
AHMNLFMI_03295 | 9e-26 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHMNLFMI_03296 | 1.1e-18 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHMNLFMI_03297 | 5.1e-52 | 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 | |
AHMNLFMI_03298 | 2.7e-12 | 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 | |
AHMNLFMI_03299 | 1.4e-110 | 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 | |
AHMNLFMI_03300 | 7.4e-70 | 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 | |
AHMNLFMI_03301 | 1.4e-27 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AHMNLFMI_03302 | 2.4e-40 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_03303 | 1.4e-27 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AHMNLFMI_03304 | 2.5e-29 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_03305 | 3.4e-231 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AHMNLFMI_03306 | 4.5e-12 | rrmA | 2.1.1.187 | H | Methyltransferase | |
AHMNLFMI_03307 | 4.5e-12 | rrmA | 2.1.1.187 | H | Methyltransferase | |
AHMNLFMI_03309 | 1.5e-94 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_03310 | 4.1e-74 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_03311 | 7e-18 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_03312 | 4.2e-36 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_03313 | 7e-18 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_03314 | 7e-18 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_03315 | 7e-18 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_03316 | 1.5e-29 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AHMNLFMI_03317 | 1.9e-168 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AHMNLFMI_03319 | 1.4e-50 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
AHMNLFMI_03320 | 5.1e-173 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
AHMNLFMI_03321 | 1.1e-21 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_03322 | 1.9e-43 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
AHMNLFMI_03323 | 1.2e-110 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_03324 | 2.9e-39 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_03325 | 6.8e-50 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_03326 | 1.2e-68 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_03327 | 1.8e-32 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_03328 | 8.9e-36 | |||||
AHMNLFMI_03329 | 1.6e-106 | celD | 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 | ||
AHMNLFMI_03332 | 1.4e-21 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_03333 | 1.4e-18 | 1.3.5.4 | C | FAD binding domain | ||
AHMNLFMI_03335 | 1.2e-172 | xylP1 | G | MFS/sugar transport protein | ||
AHMNLFMI_03336 | 1e-53 | xylP1 | G | MFS/sugar transport protein | ||
AHMNLFMI_03337 | 3.5e-36 | S | membrane | |||
AHMNLFMI_03338 | 8.6e-43 | S | membrane | |||
AHMNLFMI_03339 | 1.7e-46 | S | membrane | |||
AHMNLFMI_03340 | 9.4e-15 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03341 | 2.5e-142 | S | membrane | |||
AHMNLFMI_03342 | 9.4e-16 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03343 | 2.4e-17 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03344 | 3.4e-142 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_03345 | 2.4e-48 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_03346 | 3.6e-51 | 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 | ||
AHMNLFMI_03347 | 2.2e-70 | 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 | ||
AHMNLFMI_03348 | 5.9e-63 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
AHMNLFMI_03349 | 3e-33 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
AHMNLFMI_03350 | 6.3e-31 | K | AI-2E family transporter | |||
AHMNLFMI_03352 | 6.9e-66 | 3.5.1.28 | M | Glycosyl hydrolases family 25 | ||
AHMNLFMI_03353 | 1.9e-31 | S | Haemolysin XhlA | |||
AHMNLFMI_03354 | 3.3e-37 | S | Haemolysin XhlA | |||
AHMNLFMI_03355 | 1.9e-189 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
AHMNLFMI_03356 | 5.1e-21 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
AHMNLFMI_03357 | 7.9e-48 | |||||
AHMNLFMI_03358 | 1e-97 | yfnA | E | Amino Acid | ||
AHMNLFMI_03361 | 3.5e-20 | S | peptidoglycan catabolic process | |||
AHMNLFMI_03363 | 2e-64 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
AHMNLFMI_03364 | 2.4e-125 | larB | S | AIR carboxylase | ||
AHMNLFMI_03365 | 3.2e-40 | larB | S | AIR carboxylase | ||
AHMNLFMI_03366 | 5.3e-21 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
AHMNLFMI_03367 | 1.8e-147 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
AHMNLFMI_03368 | 2.5e-82 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
AHMNLFMI_03369 | 8e-16 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
AHMNLFMI_03370 | 1.3e-80 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
AHMNLFMI_03371 | 1.5e-62 | S | membrane | |||
AHMNLFMI_03372 | 2.9e-158 | mutS | L | MutS domain V | ||
AHMNLFMI_03373 | 1.9e-44 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_03374 | 2.4e-19 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_03375 | 1.7e-122 | yfiC | V | ABC transporter | ||
AHMNLFMI_03376 | 1.8e-14 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_03377 | 1.3e-27 | |||||
AHMNLFMI_03378 | 1.3e-27 | |||||
AHMNLFMI_03379 | 1.3e-27 | |||||
AHMNLFMI_03380 | 1.4e-69 | accB | 2.3.1.12 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
AHMNLFMI_03381 | 1.4e-92 | rihC | 3.2.2.1 | F | Nucleoside | |
AHMNLFMI_03382 | 1.1e-71 | ydfD | K | Alanine-glyoxylate amino-transferase | ||
AHMNLFMI_03383 | 1.1e-32 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_03384 | 4e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_03385 | 2.7e-114 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_03386 | 3.1e-56 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_03387 | 7.3e-96 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_03388 | 1.3e-178 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHMNLFMI_03389 | 2.9e-157 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
AHMNLFMI_03390 | 2.5e-106 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
AHMNLFMI_03391 | 8.6e-98 | J | glyoxalase III activity | |||
AHMNLFMI_03392 | 5.6e-40 | GM | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_03393 | 1.4e-147 | GM | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_03394 | 5.9e-91 | rmeB | K | transcriptional regulator, MerR family | ||
AHMNLFMI_03395 | 2.1e-55 | S | Domain of unknown function (DU1801) | |||
AHMNLFMI_03396 | 1e-149 | corA | P | CorA-like Mg2+ transporter protein | ||
AHMNLFMI_03397 | 3.9e-38 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_03398 | 4.6e-39 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_03399 | 2e-40 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_03400 | 6.5e-156 | phnW | 2.5.1.49, 2.6.1.37, 3.11.1.1 | E | Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. PhnW subfamily | |
AHMNLFMI_03401 | 4e-95 | phnW | 2.5.1.49, 2.6.1.37, 3.11.1.1 | E | Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. PhnW subfamily | |
AHMNLFMI_03402 | 3.2e-182 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
AHMNLFMI_03403 | 5.7e-36 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
AHMNLFMI_03404 | 2.3e-65 | M | LysM domain | |||
AHMNLFMI_03405 | 5.5e-37 | M | Lysin motif | |||
AHMNLFMI_03406 | 8.4e-17 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_03407 | 8.9e-23 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_03408 | 2.4e-26 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_03409 | 1e-50 | L | Transposase | |||
AHMNLFMI_03410 | 5.3e-86 | L | Transposase | |||
AHMNLFMI_03411 | 1.5e-89 | L | Transposase | |||
AHMNLFMI_03412 | 2.6e-47 | maa | S | transferase hexapeptide repeat | ||
AHMNLFMI_03413 | 1.3e-68 | maa | S | transferase hexapeptide repeat | ||
AHMNLFMI_03414 | 2.5e-130 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_03415 | 2.7e-163 | GM | NmrA-like family | |||
AHMNLFMI_03416 | 5.4e-92 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03417 | 5.5e-28 | S | haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_03419 | 1.1e-115 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
AHMNLFMI_03420 | 4.4e-68 | pheP | E | Amino acid permease | ||
AHMNLFMI_03421 | 5.2e-45 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AHMNLFMI_03422 | 3.1e-192 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AHMNLFMI_03423 | 6.5e-25 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
AHMNLFMI_03424 | 6.2e-58 | rliB | K | helix_turn_helix gluconate operon transcriptional repressor | ||
AHMNLFMI_03425 | 2.2e-193 | rliB | K | helix_turn_helix gluconate operon transcriptional repressor | ||
AHMNLFMI_03426 | 3.2e-39 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AHMNLFMI_03427 | 2.2e-121 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AHMNLFMI_03428 | 4.9e-63 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AHMNLFMI_03429 | 3.4e-111 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AHMNLFMI_03430 | 1.8e-57 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
AHMNLFMI_03431 | 1.2e-24 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AHMNLFMI_03432 | 2.2e-107 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_03433 | 8.3e-63 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
AHMNLFMI_03434 | 3.8e-19 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
AHMNLFMI_03435 | 9.3e-58 | prsA | 3.1.3.16, 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AHMNLFMI_03436 | 1.1e-147 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
AHMNLFMI_03437 | 7e-172 | C | Zinc-binding dehydrogenase | |||
AHMNLFMI_03438 | 2e-54 | yceD | S | Uncharacterized ACR, COG1399 | ||
AHMNLFMI_03439 | 4.7e-115 | pts30BCA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_03440 | 1.2e-140 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
AHMNLFMI_03441 | 1.7e-188 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
AHMNLFMI_03442 | 5e-173 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHMNLFMI_03443 | 1.5e-44 | 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 | ||
AHMNLFMI_03444 | 1.5e-124 | |||||
AHMNLFMI_03445 | 2.1e-16 | |||||
AHMNLFMI_03446 | 3.4e-37 | metQ | M | Belongs to the nlpA lipoprotein family | ||
AHMNLFMI_03447 | 5.8e-66 | metI | U | ABC transporter permease | ||
AHMNLFMI_03448 | 2.6e-107 | metQ | M | Belongs to the nlpA lipoprotein family | ||
AHMNLFMI_03449 | 3e-11 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
AHMNLFMI_03450 | 3e-145 | yxeH | S | hydrolase | ||
AHMNLFMI_03451 | 1.3e-174 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHMNLFMI_03452 | 2.6e-111 | 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
AHMNLFMI_03453 | 1.1e-83 | 6.3.3.2 | S | ASCH | ||
AHMNLFMI_03454 | 1e-84 | K | GNAT family | |||
AHMNLFMI_03455 | 9.7e-10 | K | acetyltransferase | |||
AHMNLFMI_03456 | 1.8e-53 | K | GNAT family | |||
AHMNLFMI_03457 | 5.6e-141 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_03458 | 6.7e-23 | |||||
AHMNLFMI_03459 | 3e-19 | celB | 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 | ||
AHMNLFMI_03460 | 3.1e-102 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AHMNLFMI_03461 | 6.8e-25 | |||||
AHMNLFMI_03462 | 4.7e-122 | ykuT | M | mechanosensitive ion channel | ||
AHMNLFMI_03463 | 1.9e-23 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
AHMNLFMI_03464 | 2.8e-56 | |||||
AHMNLFMI_03465 | 1.6e-19 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_03466 | 9.4e-27 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_03467 | 1.1e-80 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_03468 | 1.7e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_03470 | 5.9e-28 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_03471 | 1.2e-08 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_03472 | 1.7e-54 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
AHMNLFMI_03473 | 0.0 | M | Bacterial surface protein 26-residue PARCEL repeat (3 repeats) | |||
AHMNLFMI_03474 | 1e-30 | M | Bacterial surface protein 26-residue PARCEL repeat (3 repeats) | |||
AHMNLFMI_03475 | 3.7e-142 | 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) | |
AHMNLFMI_03476 | 1.5e-67 | 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) | |
AHMNLFMI_03477 | 1.2e-22 | K | Transcriptional regulator | |||
AHMNLFMI_03478 | 4.5e-106 | V | ABC transporter | |||
AHMNLFMI_03479 | 3.9e-69 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
AHMNLFMI_03480 | 7.3e-36 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_03481 | 4.6e-72 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_03482 | 7.8e-58 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_03483 | 8.8e-13 | lmrA | 3.6.3.44 | V | ABC transporter | |
AHMNLFMI_03484 | 9.2e-35 | S | Domain of unknown function (DUF771) | |||
AHMNLFMI_03489 | 4.8e-98 | C | Aldo keto reductase | |||
AHMNLFMI_03490 | 1.5e-142 | akr5f | 1.1.1.346 | S | reductase | |
AHMNLFMI_03491 | 1.3e-142 | EGP | Major Facilitator Superfamily | |||
AHMNLFMI_03492 | 5.7e-83 | GM | NAD(P)H-binding | |||
AHMNLFMI_03493 | 6.1e-76 | T | Belongs to the universal stress protein A family | |||
AHMNLFMI_03494 | 3.9e-15 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
AHMNLFMI_03495 | 5.1e-19 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
AHMNLFMI_03503 | 1.8e-15 | |||||
AHMNLFMI_03504 | 2.3e-66 | K | IrrE N-terminal-like domain | |||
AHMNLFMI_03505 | 1.5e-144 | IQ | NAD dependent epimerase/dehydratase family | |||
AHMNLFMI_03506 | 5.1e-91 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
AHMNLFMI_03507 | 1e-30 | IQ | NAD dependent epimerase/dehydratase family | |||
AHMNLFMI_03508 | 4.8e-12 | celD | 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 | ||
AHMNLFMI_03509 | 4.4e-30 | celD | 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 | ||
AHMNLFMI_03510 | 2.9e-31 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_03511 | 2.3e-23 | |||||
AHMNLFMI_03512 | 6.7e-26 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_03513 | 4.8e-28 | |||||
AHMNLFMI_03514 | 8.8e-62 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_03515 | 7.5e-41 | cggR | K | Putative sugar-binding domain | ||
AHMNLFMI_03516 | 5.7e-97 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_03517 | 1e-122 | comEC | S | Competence protein ComEC | ||
AHMNLFMI_03518 | 1.8e-97 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AHMNLFMI_03519 | 1.6e-129 | manY | G | PTS system | ||
AHMNLFMI_03520 | 1e-126 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHMNLFMI_03521 | 1.2e-185 | G | Domain of unknown function (DUF3502) | |||
AHMNLFMI_03522 | 2.4e-87 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
AHMNLFMI_03523 | 3.2e-59 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
AHMNLFMI_03524 | 2e-41 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
AHMNLFMI_03525 | 6.9e-50 | mreD | M | rod shape-determining protein MreD | ||
AHMNLFMI_03526 | 3.3e-37 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
AHMNLFMI_03527 | 4e-87 | mreD | M | rod shape-determining protein MreD | ||
AHMNLFMI_03528 | 2.6e-144 | mreC | M | Involved in formation and maintenance of cell shape | ||
AHMNLFMI_03529 | 2.9e-25 | mreC | M | Involved in formation and maintenance of cell shape | ||
AHMNLFMI_03531 | 2.1e-123 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AHMNLFMI_03532 | 3.1e-47 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AHMNLFMI_03533 | 2.1e-15 | tcyB | E | ABC transporter | ||
AHMNLFMI_03534 | 1.2e-80 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
AHMNLFMI_03535 | 1.3e-57 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AHMNLFMI_03536 | 9.2e-159 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHMNLFMI_03537 | 4.3e-33 | 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 | |
AHMNLFMI_03538 | 1.1e-14 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHMNLFMI_03539 | 5.3e-26 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
AHMNLFMI_03540 | 2.2e-137 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
AHMNLFMI_03541 | 2e-29 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
AHMNLFMI_03542 | 4.2e-33 | ymfM | S | Helix-turn-helix domain | ||
AHMNLFMI_03543 | 4.3e-87 | ymfM | S | Helix-turn-helix domain | ||
AHMNLFMI_03544 | 6.8e-54 | ymfM | S | Helix-turn-helix domain | ||
AHMNLFMI_03545 | 2.2e-33 | ymfM | S | Helix-turn-helix domain | ||
AHMNLFMI_03546 | 6.9e-15 | S | Psort location CytoplasmicMembrane, score | |||
AHMNLFMI_03547 | 5.4e-113 | S | Psort location CytoplasmicMembrane, score | |||
AHMNLFMI_03548 | 6.2e-73 | K | MarR family | |||
AHMNLFMI_03549 | 6e-82 | K | Acetyltransferase (GNAT) domain | |||
AHMNLFMI_03550 | 7.1e-81 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AHMNLFMI_03551 | 1.1e-26 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AHMNLFMI_03552 | 1.1e-17 | argR | K | Regulates arginine biosynthesis genes | ||
AHMNLFMI_03553 | 5.1e-139 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
AHMNLFMI_03554 | 2.6e-78 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
AHMNLFMI_03555 | 3.5e-95 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
AHMNLFMI_03556 | 2.6e-33 | 2.7.7.1, 3.6.1.55 | F | belongs to the nudix hydrolase family | ||
AHMNLFMI_03557 | 3.5e-97 | |||||
AHMNLFMI_03558 | 8.2e-44 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
AHMNLFMI_03559 | 6.7e-90 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
AHMNLFMI_03560 | 8.4e-78 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
AHMNLFMI_03561 | 1.1e-23 | K | helix_turn_helix, arabinose operon control protein | |||
AHMNLFMI_03562 | 1.6e-12 | L | Transposase | |||
AHMNLFMI_03563 | 1.7e-13 | L | Transposase | |||
AHMNLFMI_03564 | 2.8e-21 | L | Transposase | |||
AHMNLFMI_03565 | 2.4e-22 | L | Transposase | |||
AHMNLFMI_03566 | 1.3e-61 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
AHMNLFMI_03567 | 1.2e-205 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
AHMNLFMI_03568 | 8.3e-44 | potB | P | ABC transporter permease | ||
AHMNLFMI_03569 | 3e-41 | potB | P | ABC transporter permease | ||
AHMNLFMI_03570 | 1.9e-53 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHMNLFMI_03571 | 5.4e-116 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AHMNLFMI_03572 | 3.6e-169 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AHMNLFMI_03573 | 1.1e-71 | yviA | S | Protein of unknown function (DUF421) | ||
AHMNLFMI_03574 | 3.7e-148 | yxeH | S | hydrolase | ||
AHMNLFMI_03575 | 1e-112 | |||||
AHMNLFMI_03576 | 3.9e-113 | pgaC | GT2 | M | Glycosyl transferase | |
AHMNLFMI_03577 | 3.1e-72 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
AHMNLFMI_03578 | 5.4e-19 | |||||
AHMNLFMI_03581 | 1.7e-30 | |||||
AHMNLFMI_03582 | 8.1e-22 | |||||
AHMNLFMI_03583 | 8e-91 | K | acetyltransferase | |||
AHMNLFMI_03584 | 1.5e-27 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
AHMNLFMI_03585 | 4.7e-31 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
AHMNLFMI_03586 | 1e-81 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
AHMNLFMI_03587 | 6.7e-161 | 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 | |
AHMNLFMI_03588 | 3.8e-105 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
AHMNLFMI_03589 | 5.7e-77 | entB | 3.5.1.19 | Q | Isochorismatase family | |
AHMNLFMI_03590 | 2.7e-32 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
AHMNLFMI_03591 | 4.8e-20 | |||||
AHMNLFMI_03592 | 2.3e-201 | rpoN | K | Sigma-54 factor, core binding domain | ||
AHMNLFMI_03593 | 2.9e-131 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
AHMNLFMI_03594 | 1.2e-23 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
AHMNLFMI_03595 | 1e-40 | glcU | U | sugar transport | ||
AHMNLFMI_03596 | 4.9e-82 | glcU | U | sugar transport | ||
AHMNLFMI_03597 | 2.3e-69 | tnp2PF3 | L | manually curated | ||
AHMNLFMI_03598 | 1.7e-34 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_03599 | 9.2e-65 | S | Domain of unknown function (DUF4440) | |||
AHMNLFMI_03600 | 7.2e-259 | qacA | EGP | Fungal trichothecene efflux pump (TRI12) | ||
AHMNLFMI_03601 | 3.2e-77 | 3.5.4.1 | GM | SnoaL-like domain | ||
AHMNLFMI_03602 | 3.5e-10 | |||||
AHMNLFMI_03603 | 1.1e-53 | |||||
AHMNLFMI_03605 | 3.7e-42 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_03606 | 3.5e-28 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_03607 | 1.4e-44 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_03608 | 1.5e-88 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_03609 | 1.8e-69 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
AHMNLFMI_03610 | 1.6e-25 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
AHMNLFMI_03611 | 1e-117 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHMNLFMI_03612 | 8.3e-24 | T | Belongs to the universal stress protein A family | |||
AHMNLFMI_03613 | 9.8e-71 | ecsB | U | ABC transporter | ||
AHMNLFMI_03614 | 2.1e-23 | ecsA | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03615 | 2.3e-48 | rplQ | J | Ribosomal protein L17 | ||
AHMNLFMI_03616 | 2.8e-25 | rplQ | J | Ribosomal protein L17 | ||
AHMNLFMI_03617 | 7e-37 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHMNLFMI_03618 | 2.6e-146 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHMNLFMI_03619 | 1.5e-38 | XK27_09615 | 1.3.5.4 | S | reductase | |
AHMNLFMI_03620 | 2e-88 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
AHMNLFMI_03621 | 1.3e-33 | 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 | |
AHMNLFMI_03622 | 7.6e-11 | 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 | |
AHMNLFMI_03623 | 2.3e-57 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_03624 | 1.2e-123 | 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 | |
AHMNLFMI_03625 | 3e-40 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_03626 | 5.6e-94 | pipD | E | Dipeptidase | ||
AHMNLFMI_03627 | 1.1e-29 | |||||
AHMNLFMI_03629 | 1.2e-51 | pipD | E | Dipeptidase | ||
AHMNLFMI_03630 | 9.1e-112 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
AHMNLFMI_03631 | 2.2e-104 | 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 | |
AHMNLFMI_03632 | 3.1e-127 | yliE | T | EAL domain | ||
AHMNLFMI_03633 | 1.5e-216 | 2.7.7.65 | T | Diguanylate cyclase, GGDEF domain | ||
AHMNLFMI_03634 | 2.4e-39 | G | PTS system sorbose-specific iic component | |||
AHMNLFMI_03635 | 2.1e-53 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
AHMNLFMI_03636 | 5.9e-95 | cytR | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | |
AHMNLFMI_03637 | 2e-91 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_03638 | 1.5e-84 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_03639 | 2.3e-117 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_03640 | 3.8e-107 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_03641 | 2.2e-72 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_03642 | 1.1e-260 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
AHMNLFMI_03643 | 9.9e-47 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_03644 | 4.1e-23 | S | Protein of unknown function (DUF2922) | |||
AHMNLFMI_03645 | 1.8e-221 | rfbX | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
AHMNLFMI_03646 | 3.4e-25 | spx4 | 1.20.4.1 | P | ArsC family | |
AHMNLFMI_03647 | 5.7e-49 | spx4 | 1.20.4.1 | P | ArsC family | |
AHMNLFMI_03648 | 5.4e-66 | K | Winged helix DNA-binding domain | |||
AHMNLFMI_03649 | 3.4e-31 | S | Domain of unknown function (DUF4352) | |||
AHMNLFMI_03650 | 4.8e-100 | KLT | Protein tyrosine kinase | |||
AHMNLFMI_03651 | 6.8e-25 | S | Protein of unknown function (DUF4064) | |||
AHMNLFMI_03652 | 6e-97 | S | Domain of unknown function (DUF4352) | |||
AHMNLFMI_03653 | 3.9e-75 | S | Psort location Cytoplasmic, score | |||
AHMNLFMI_03655 | 4.1e-54 | |||||
AHMNLFMI_03656 | 1.8e-109 | S | membrane transporter protein | |||
AHMNLFMI_03657 | 2.3e-54 | azlD | S | branched-chain amino acid | ||
AHMNLFMI_03658 | 5.1e-131 | azlC | E | branched-chain amino acid | ||
AHMNLFMI_03659 | 1e-78 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
AHMNLFMI_03660 | 1.5e-37 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
AHMNLFMI_03661 | 1.1e-26 | K | MarR family | |||
AHMNLFMI_03662 | 6.4e-210 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_03663 | 1.5e-14 | S | membrane transporter protein | |||
AHMNLFMI_03664 | 2.9e-168 | ftpB | P | Bacterial extracellular solute-binding protein | ||
AHMNLFMI_03665 | 5.1e-64 | lrgA | S | LrgA family | ||
AHMNLFMI_03666 | 7.3e-127 | lrgB | M | LrgB-like family | ||
AHMNLFMI_03667 | 2.5e-145 | DegV | S | EDD domain protein, DegV family | ||
AHMNLFMI_03668 | 1.1e-48 | EG | EamA-like transporter family | |||
AHMNLFMI_03669 | 4.3e-56 | EG | EamA-like transporter family | |||
AHMNLFMI_03670 | 4.3e-56 | EG | EamA-like transporter family | |||
AHMNLFMI_03671 | 1e-78 | scrR | K | Transcriptional regulator, LacI family | ||
AHMNLFMI_03672 | 3.3e-64 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_03673 | 8.1e-26 | scrR | K | Transcriptional regulator, LacI family | ||
AHMNLFMI_03674 | 4e-19 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_03675 | 3.3e-161 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
AHMNLFMI_03676 | 6.2e-117 | glpQ3 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
AHMNLFMI_03677 | 4e-78 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
AHMNLFMI_03678 | 3e-78 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
AHMNLFMI_03679 | 2e-16 | M | domain protein | |||
AHMNLFMI_03683 | 3.3e-65 | S | Protein of unknown function (DUF1093) | |||
AHMNLFMI_03684 | 1.3e-09 | hisS | 6.1.1.21 | J | histidyl-tRNA aminoacylation | |
AHMNLFMI_03685 | 4.2e-122 | hisS | 6.1.1.21 | J | histidyl-tRNA aminoacylation | |
AHMNLFMI_03686 | 5.8e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
AHMNLFMI_03687 | 1.1e-32 | 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 | ||
AHMNLFMI_03688 | 8e-36 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
AHMNLFMI_03689 | 8.7e-73 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
AHMNLFMI_03690 | 5e-122 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AHMNLFMI_03691 | 3.3e-30 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AHMNLFMI_03692 | 5.8e-20 | C | Aldo keto reductase | |||
AHMNLFMI_03693 | 1.9e-79 | C | Aldo keto reductase | |||
AHMNLFMI_03694 | 2.5e-114 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_03695 | 4.8e-20 | adhR | K | helix_turn_helix, mercury resistance | ||
AHMNLFMI_03696 | 3e-25 | fldA | C | Flavodoxin | ||
AHMNLFMI_03697 | 3.7e-305 | S | peptidoglycan catabolic process | |||
AHMNLFMI_03698 | 1.2e-23 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_03699 | 2.2e-60 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_03700 | 3.3e-30 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_03701 | 2.4e-51 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_03702 | 1.8e-24 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_03703 | 1.9e-42 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_03704 | 2.1e-30 | S | Elongation factor G-binding protein, N-terminal | |||
AHMNLFMI_03705 | 8.1e-27 | S | Elongation factor G-binding protein, N-terminal | |||
AHMNLFMI_03706 | 6.3e-66 | yeaO | S | Protein of unknown function, DUF488 | ||
AHMNLFMI_03707 | 9.3e-29 | |||||
AHMNLFMI_03708 | 9.6e-124 | hpk9 | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_03709 | 5.1e-44 | S | TfoX C-terminal domain | |||
AHMNLFMI_03710 | 6e-140 | K | Helix-turn-helix domain | |||
AHMNLFMI_03711 | 4.7e-15 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_03712 | 7.4e-250 | yjjP | S | Putative threonine/serine exporter | ||
AHMNLFMI_03713 | 1.1e-194 | pva1 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHMNLFMI_03714 | 3e-66 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHMNLFMI_03715 | 6.5e-75 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | S | MucBP domain | |
AHMNLFMI_03716 | 1.3e-118 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | S | MucBP domain | |
AHMNLFMI_03717 | 2e-56 | S | NUDIX domain | |||
AHMNLFMI_03718 | 4.1e-266 | 3.6.4.13 | M | domain protein | ||
AHMNLFMI_03719 | 3.1e-108 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
AHMNLFMI_03720 | 2.8e-52 | 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 | ||
AHMNLFMI_03722 | 3.4e-57 | fliD | N | Required for morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
AHMNLFMI_03723 | 7.1e-94 | fliD | N | Required for morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
AHMNLFMI_03724 | 8.5e-39 | M | Exporter of polyketide antibiotics | |||
AHMNLFMI_03725 | 6.1e-62 | M | Exporter of polyketide antibiotics | |||
AHMNLFMI_03726 | 6.4e-26 | M | Exporter of polyketide antibiotics | |||
AHMNLFMI_03727 | 1.2e-213 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
AHMNLFMI_03728 | 6.5e-96 | tag | 3.2.2.20 | L | glycosylase | |
AHMNLFMI_03730 | 2.1e-21 | |||||
AHMNLFMI_03731 | 3.6e-31 | 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
AHMNLFMI_03732 | 3.7e-74 | S | Tetratricopeptide repeat protein | |||
AHMNLFMI_03733 | 7.4e-55 | S | Tetratricopeptide repeat protein | |||
AHMNLFMI_03734 | 1.3e-51 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_03735 | 1.1e-43 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_03736 | 5.6e-39 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_03737 | 3.9e-72 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
AHMNLFMI_03738 | 1.2e-224 | 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 | |
AHMNLFMI_03739 | 5.8e-52 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
AHMNLFMI_03740 | 6.3e-241 | lacS | G | Transporter | ||
AHMNLFMI_03741 | 1.9e-181 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03742 | 3.1e-33 | V | ABC transporter | |||
AHMNLFMI_03743 | 1.5e-25 | V | ABC transporter | |||
AHMNLFMI_03744 | 4e-134 | pbuG | S | permease | ||
AHMNLFMI_03745 | 9.4e-138 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03746 | 3.2e-225 | malY | 4.4.1.8 | E | Aminotransferase class I and II | |
AHMNLFMI_03747 | 3.8e-257 | frvB | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_03748 | 6.2e-13 | E | glutamate:sodium symporter activity | |||
AHMNLFMI_03749 | 2.6e-16 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_03750 | 2.7e-37 | E | glutamate:sodium symporter activity | |||
AHMNLFMI_03751 | 4.2e-112 | E | glutamate:sodium symporter activity | |||
AHMNLFMI_03752 | 1.4e-59 | ybbJ | K | Acetyltransferase (GNAT) family | ||
AHMNLFMI_03753 | 1.4e-32 | ybbJ | K | Acetyltransferase (GNAT) family | ||
AHMNLFMI_03754 | 2.5e-26 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_03755 | 1.1e-32 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_03756 | 1e-53 | entB | 3.5.1.19 | Q | Isochorismatase family | |
AHMNLFMI_03757 | 3.8e-162 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_03758 | 1.5e-69 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_03759 | 1.5e-191 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AHMNLFMI_03760 | 9e-164 | S | Virulence-associated protein E | |||
AHMNLFMI_03761 | 8.5e-63 | |||||
AHMNLFMI_03762 | 7.2e-71 | |||||
AHMNLFMI_03763 | 1.5e-54 | oppF | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_03764 | 8.1e-32 | oppF | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_03765 | 2e-92 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_03766 | 3e-15 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHMNLFMI_03767 | 2.2e-38 | yaaL | S | Protein of unknown function (DUF2508) | ||
AHMNLFMI_03768 | 9e-107 | 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 | ||
AHMNLFMI_03770 | 1.2e-40 | ccpB | 5.1.1.1 | K | lacI family | |
AHMNLFMI_03771 | 8.8e-123 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AHMNLFMI_03772 | 2e-26 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
AHMNLFMI_03773 | 3.9e-36 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
AHMNLFMI_03774 | 2.5e-156 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
AHMNLFMI_03775 | 6.9e-267 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03776 | 4.7e-45 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03777 | 4.2e-57 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03778 | 2.2e-18 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_03779 | 6.2e-54 | K | response regulator | |||
AHMNLFMI_03780 | 1.1e-16 | M | domain protein | |||
AHMNLFMI_03781 | 5.8e-165 | M | domain protein | |||
AHMNLFMI_03782 | 1.1e-152 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHMNLFMI_03783 | 3.6e-57 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHMNLFMI_03784 | 2e-07 | S | zinc-ribbon domain | |||
AHMNLFMI_03785 | 5.7e-20 | |||||
AHMNLFMI_03786 | 1.7e-77 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_03787 | 2.8e-39 | hsdM | 2.1.1.72 | V | PFAM N-6 DNA methylase | |
AHMNLFMI_03788 | 0.0 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
AHMNLFMI_03789 | 1.2e-15 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
AHMNLFMI_03790 | 9.1e-54 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
AHMNLFMI_03791 | 3.5e-54 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
AHMNLFMI_03792 | 1.3e-21 | S | Putative esterase | |||
AHMNLFMI_03793 | 1.5e-124 | S | Putative esterase | |||
AHMNLFMI_03794 | 2.3e-32 | S | Putative esterase | |||
AHMNLFMI_03795 | 5.9e-09 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_03796 | 6.6e-186 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
AHMNLFMI_03797 | 1.2e-36 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
AHMNLFMI_03798 | 7.5e-10 | L | Transposase | |||
AHMNLFMI_03799 | 5.5e-109 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
AHMNLFMI_03800 | 1.4e-74 | yugI | 5.3.1.9 | J | general stress protein | |
AHMNLFMI_03801 | 3.5e-64 | |||||
AHMNLFMI_03802 | 1.2e-104 | |||||
AHMNLFMI_03804 | 9e-13 | |||||
AHMNLFMI_03805 | 3.8e-28 | K | response regulator | |||
AHMNLFMI_03806 | 3.3e-20 | K | response regulator | |||
AHMNLFMI_03807 | 3.1e-133 | K | response regulator | |||
AHMNLFMI_03808 | 3.4e-27 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
AHMNLFMI_03809 | 3.2e-250 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
AHMNLFMI_03810 | 6.4e-57 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
AHMNLFMI_03811 | 1.6e-80 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AHMNLFMI_03812 | 8.2e-96 | 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 | ||
AHMNLFMI_03813 | 8.5e-28 | ylqC | S | Belongs to the UPF0109 family | ||
AHMNLFMI_03814 | 2.6e-39 | ylqC | S | Belongs to the UPF0109 family | ||
AHMNLFMI_03815 | 2.9e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
AHMNLFMI_03816 | 8.5e-60 | 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 | |
AHMNLFMI_03817 | 3.8e-219 | 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 | |
AHMNLFMI_03818 | 1.1e-15 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
AHMNLFMI_03819 | 2e-132 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHMNLFMI_03820 | 2e-62 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHMNLFMI_03821 | 1.6e-122 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_03822 | 2.8e-82 | gtrA | S | GtrA-like protein | ||
AHMNLFMI_03823 | 6e-103 | zmp3 | O | Zinc-dependent metalloprotease | ||
AHMNLFMI_03824 | 2.9e-56 | yibE | S | overlaps another CDS with the same product name | ||
AHMNLFMI_03825 | 6.6e-30 | S | SMI1-KNR4 cell-wall | |||
AHMNLFMI_03826 | 4.2e-17 | |||||
AHMNLFMI_03827 | 9.7e-25 | S | Barstar (barnase inhibitor) | |||
AHMNLFMI_03829 | 1.9e-236 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_03830 | 3.8e-177 | pepN | 3.4.11.2 | E | aminopeptidase | |
AHMNLFMI_03831 | 1.9e-43 | G | Glycogen debranching enzyme | |||
AHMNLFMI_03832 | 1.9e-28 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_03834 | 2.2e-96 | metI | P | ABC transporter permease | ||
AHMNLFMI_03835 | 6.8e-44 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
AHMNLFMI_03836 | 5.5e-158 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
AHMNLFMI_03837 | 7.6e-16 | uspA | T | Universal stress protein family | ||
AHMNLFMI_03838 | 5.2e-23 | ctsR | K | Belongs to the CtsR family | ||
AHMNLFMI_03839 | 1.1e-12 | ctsR | K | Belongs to the CtsR family | ||
AHMNLFMI_03840 | 3.1e-136 | yvfS | V | ABC-2 type transporter | ||
AHMNLFMI_03841 | 2.1e-92 | yvfR | V | ABC transporter | ||
AHMNLFMI_03842 | 1.2e-51 | 1.5.1.39 | C | nitroreductase | ||
AHMNLFMI_03843 | 2.8e-35 | L | transposase activity | |||
AHMNLFMI_03845 | 2.2e-10 | L | HTH-like domain | |||
AHMNLFMI_03846 | 2.3e-187 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_03847 | 5.2e-29 | |||||
AHMNLFMI_03848 | 2.3e-56 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
AHMNLFMI_03849 | 3.7e-38 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
AHMNLFMI_03850 | 2.5e-19 | ybbL | S | abc transporter atp-binding protein | ||
AHMNLFMI_03851 | 8.7e-85 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHMNLFMI_03852 | 1.4e-116 | ybbL | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_03853 | 8.9e-27 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
AHMNLFMI_03854 | 9.8e-42 | S | ABC transporter, ATP-binding protein | |||
AHMNLFMI_03855 | 1.1e-30 | 2.7.7.65 | T | diguanylate cyclase | ||
AHMNLFMI_03856 | 4.4e-37 | S | ABC transporter, ATP-binding protein | |||
AHMNLFMI_03857 | 7.2e-36 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHMNLFMI_03859 | 8.5e-84 | |||||
AHMNLFMI_03861 | 4.6e-39 | S | Bacterial protein of unknown function (DUF871) | |||
AHMNLFMI_03862 | 1.5e-126 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_03863 | 4.3e-25 | aRA11 | 1.1.1.346 | S | reductase | |
AHMNLFMI_03864 | 2.1e-10 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_03865 | 2.8e-17 | aRA11 | 1.1.1.346 | S | reductase | |
AHMNLFMI_03866 | 2.8e-33 | mleP | S | Sodium Bile acid symporter family | ||
AHMNLFMI_03867 | 1.5e-54 | yfnA | E | Amino Acid | ||
AHMNLFMI_03868 | 2e-09 | mleP | S | Sodium Bile acid symporter family | ||
AHMNLFMI_03869 | 2e-09 | mleP | S | Sodium Bile acid symporter family | ||
AHMNLFMI_03870 | 2.1e-18 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_03871 | 4.3e-49 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_03872 | 4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHMNLFMI_03873 | 3.6e-48 | gcsH2 | E | glycine cleavage | ||
AHMNLFMI_03874 | 5.1e-96 | rodA | D | Belongs to the SEDS family | ||
AHMNLFMI_03875 | 4e-42 | rodA | D | Belongs to the SEDS family | ||
AHMNLFMI_03876 | 2.8e-21 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_03877 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
AHMNLFMI_03878 | 9.6e-36 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
AHMNLFMI_03879 | 4.1e-36 | sat | 2.7.7.4 | H | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
AHMNLFMI_03880 | 6e-83 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHMNLFMI_03881 | 1.4e-49 | |||||
AHMNLFMI_03882 | 2.1e-22 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
AHMNLFMI_03885 | 5.8e-176 | tanA | S | alpha beta | ||
AHMNLFMI_03886 | 2.5e-88 | |||||
AHMNLFMI_03887 | 9.1e-38 | ecsB | U | ABC transporter | ||
AHMNLFMI_03888 | 3.2e-152 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
AHMNLFMI_03889 | 1.7e-120 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
AHMNLFMI_03890 | 4.6e-28 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AHMNLFMI_03891 | 4.6e-28 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AHMNLFMI_03892 | 1.7e-45 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
AHMNLFMI_03893 | 1.4e-66 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AHMNLFMI_03894 | 3e-21 | L | leucine-zipper of insertion element IS481 | |||
AHMNLFMI_03895 | 1e-41 | |||||
AHMNLFMI_03897 | 1.1e-77 | 3.1.26.4 | L | RNA-DNA hybrid ribonuclease activity | ||
AHMNLFMI_03900 | 1.1e-141 | L | Belongs to the 'phage' integrase family | |||
AHMNLFMI_03904 | 7.7e-49 | |||||
AHMNLFMI_03905 | 1.2e-103 | |||||
AHMNLFMI_03907 | 2.6e-14 | pipD | E | Dipeptidase | ||
AHMNLFMI_03908 | 4.8e-48 | pipD | E | Dipeptidase | ||
AHMNLFMI_03909 | 3e-40 | |||||
AHMNLFMI_03910 | 6.9e-96 | bioY | S | BioY family | ||
AHMNLFMI_03911 | 2.9e-42 | bioY | S | BioY family | ||
AHMNLFMI_03912 | 5e-34 | bioY | S | BioY family | ||
AHMNLFMI_03913 | 1.6e-41 | yieF | S | NADPH-dependent FMN reductase | ||
AHMNLFMI_03914 | 3.9e-72 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
AHMNLFMI_03915 | 1.3e-42 | |||||
AHMNLFMI_03916 | 3.9e-50 | |||||
AHMNLFMI_03917 | 1.4e-136 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | U | Ion channel | |
AHMNLFMI_03918 | 1e-170 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
AHMNLFMI_03919 | 2.8e-148 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AHMNLFMI_03920 | 2.1e-62 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AHMNLFMI_03921 | 2.3e-120 | cggR | K | Putative sugar-binding domain | ||
AHMNLFMI_03922 | 6.4e-26 | yhdG | E | C-terminus of AA_permease | ||
AHMNLFMI_03923 | 1.3e-41 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_03924 | 7.3e-13 | yhdG | E | C-terminus of AA_permease | ||
AHMNLFMI_03926 | 1.1e-83 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_03927 | 9e-161 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_03928 | 6e-32 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_03929 | 1.5e-112 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_03930 | 1.3e-19 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHMNLFMI_03931 | 6.3e-16 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_03932 | 1.6e-137 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_03933 | 7e-244 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_03934 | 5.7e-21 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_03935 | 1.8e-67 | P | Major Facilitator Superfamily | |||
AHMNLFMI_03936 | 1.8e-61 | ypuA | S | Protein of unknown function (DUF1002) | ||
AHMNLFMI_03937 | 2.2e-101 | ypuA | S | Protein of unknown function (DUF1002) | ||
AHMNLFMI_03938 | 4.3e-23 | lldP | C | L-lactate permease | ||
AHMNLFMI_03939 | 4.7e-53 | lldP | C | L-lactate permease | ||
AHMNLFMI_03940 | 1.2e-43 | lldP | C | L-lactate permease | ||
AHMNLFMI_03941 | 3.7e-53 | lldP | C | L-lactate permease | ||
AHMNLFMI_03942 | 3e-23 | lldP | C | L-lactate permease | ||
AHMNLFMI_03943 | 2.2e-32 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
AHMNLFMI_03945 | 8.9e-147 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
AHMNLFMI_03946 | 3.1e-48 | P | secondary active sulfate transmembrane transporter activity | |||
AHMNLFMI_03947 | 1.9e-173 | P | secondary active sulfate transmembrane transporter activity | |||
AHMNLFMI_03948 | 4.7e-11 | P | secondary active sulfate transmembrane transporter activity | |||
AHMNLFMI_03949 | 5e-37 | yaaA | S | S4 domain protein YaaA | ||
AHMNLFMI_03950 | 1.9e-206 | 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 | ||
AHMNLFMI_03951 | 7.2e-09 | J | translation release factor activity | |||
AHMNLFMI_03952 | 7.1e-40 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
AHMNLFMI_03953 | 1.9e-124 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
AHMNLFMI_03954 | 6.5e-29 | |||||
AHMNLFMI_03955 | 1.9e-60 | S | ATPases associated with a variety of cellular activities | |||
AHMNLFMI_03956 | 3.2e-79 | argO | S | LysE type translocator | ||
AHMNLFMI_03957 | 1.3e-121 | G | Xylose isomerase-like TIM barrel | |||
AHMNLFMI_03958 | 9.8e-97 | G | Xylose isomerase-like TIM barrel | |||
AHMNLFMI_03959 | 7e-81 | ddpX | 3.4.13.22 | S | protein conserved in bacteria | |
AHMNLFMI_03960 | 2.8e-45 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHMNLFMI_03961 | 9.8e-20 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
AHMNLFMI_03962 | 5.1e-116 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
AHMNLFMI_03963 | 1.7e-52 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
AHMNLFMI_03964 | 4.1e-17 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_03967 | 6.6e-81 | K | AsnC family | |||
AHMNLFMI_03968 | 2e-35 | |||||
AHMNLFMI_03969 | 5.1e-34 | |||||
AHMNLFMI_03970 | 1.2e-112 | yhdG | E | C-terminus of AA_permease | ||
AHMNLFMI_03971 | 1.1e-138 | yhdG | E | C-terminus of AA_permease | ||
AHMNLFMI_03972 | 2.2e-87 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_03973 | 4.4e-141 | tesE | Q | hydratase | ||
AHMNLFMI_03974 | 1.7e-104 | padC | Q | Phenolic acid decarboxylase | ||
AHMNLFMI_03975 | 2e-79 | dprA | LU | DNA protecting protein DprA | ||
AHMNLFMI_03976 | 8.4e-30 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_03977 | 2.2e-78 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_03978 | 5.9e-104 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
AHMNLFMI_03979 | 2e-07 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_03980 | 3.3e-23 | 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 | ||
AHMNLFMI_03981 | 1.3e-92 | 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 | ||
AHMNLFMI_03982 | 1.4e-56 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
AHMNLFMI_03983 | 6.3e-296 | 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 | ||
AHMNLFMI_03984 | 9.9e-64 | 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 | ||
AHMNLFMI_03986 | 5.2e-25 | S | Phage head-tail joining protein | |||
AHMNLFMI_03987 | 3.4e-50 | S | Phage gp6-like head-tail connector protein | |||
AHMNLFMI_03988 | 7.4e-11 | S | Phage capsid family | |||
AHMNLFMI_03989 | 1.2e-33 | S | Phage gp6-like head-tail connector protein | |||
AHMNLFMI_03990 | 1.5e-39 | S | phage major capsid protein, HK97 | |||
AHMNLFMI_03991 | 1.8e-183 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_03992 | 4e-59 | yfnA | E | Amino Acid | ||
AHMNLFMI_03993 | 2.8e-178 | gabT | 2.6.1.19, 5.1.1.21 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
AHMNLFMI_03994 | 6.9e-251 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
AHMNLFMI_03995 | 9.3e-68 | S | Iron-sulphur cluster biosynthesis | |||
AHMNLFMI_03996 | 3.3e-47 | S | GyrI-like small molecule binding domain | |||
AHMNLFMI_03997 | 6.6e-116 | S | GyrI-like small molecule binding domain | |||
AHMNLFMI_03998 | 3.8e-108 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_03999 | 9.6e-13 | sat | 2.7.7.4 | H | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
AHMNLFMI_04000 | 1.4e-72 | S | Protein conserved in bacteria | |||
AHMNLFMI_04001 | 9.6e-13 | sat | 2.7.7.4 | H | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
AHMNLFMI_04002 | 1.6e-100 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
AHMNLFMI_04003 | 3.3e-177 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AHMNLFMI_04004 | 5.6e-62 | citP | P | Sodium:sulfate symporter transmembrane region | ||
AHMNLFMI_04005 | 1e-113 | citR | K | sugar-binding domain protein | ||
AHMNLFMI_04006 | 2.4e-153 | citR | K | sugar-binding domain protein | ||
AHMNLFMI_04007 | 3e-207 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
AHMNLFMI_04008 | 1.4e-75 | M | domain protein | |||
AHMNLFMI_04009 | 6.2e-31 | M | dTDP-4-dehydrorhamnose reductase activity | |||
AHMNLFMI_04010 | 2.7e-35 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
AHMNLFMI_04011 | 3.1e-138 | cps3H | ||||
AHMNLFMI_04012 | 1e-201 | cps3I | G | Acyltransferase family | ||
AHMNLFMI_04013 | 1.9e-112 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_04014 | 2.7e-79 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_04015 | 6.7e-136 | K | helix_turn_helix, arabinose operon control protein | |||
AHMNLFMI_04016 | 8.5e-61 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
AHMNLFMI_04017 | 6.1e-244 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
AHMNLFMI_04018 | 2.4e-76 | M | Glycosyl transferase family group 2 | |||
AHMNLFMI_04019 | 1.4e-118 | endA | F | DNA RNA non-specific endonuclease | ||
AHMNLFMI_04020 | 4.1e-46 | speG | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_04021 | 9.3e-53 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
AHMNLFMI_04022 | 1.5e-19 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_04023 | 3.9e-33 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_04024 | 7.1e-30 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_04025 | 1.8e-93 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_04026 | 1.6e-64 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_04027 | 7.5e-152 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_04028 | 6.7e-111 | bmr3 | EGP | Major facilitator Superfamily | ||
AHMNLFMI_04029 | 2.7e-20 | N | Cell shape-determining protein MreB | |||
AHMNLFMI_04030 | 2.3e-43 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04031 | 7.3e-25 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AHMNLFMI_04032 | 1.6e-47 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AHMNLFMI_04033 | 9.2e-29 | 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 | |
AHMNLFMI_04034 | 1.2e-149 | yitU | 3.1.3.104 | S | hydrolase | |
AHMNLFMI_04035 | 8.8e-21 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
AHMNLFMI_04036 | 1e-125 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_04037 | 2e-63 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_04038 | 8.9e-40 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_04039 | 2e-115 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_04040 | 6.3e-81 | ydcK | S | Belongs to the SprT family | ||
AHMNLFMI_04041 | 8.5e-196 | yhgF | K | Tex-like protein N-terminal domain protein | ||
AHMNLFMI_04042 | 2.5e-24 | yhgF | K | Tex-like protein N-terminal domain protein | ||
AHMNLFMI_04043 | 1.7e-184 | D | Alpha beta | |||
AHMNLFMI_04044 | 7.4e-166 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
AHMNLFMI_04045 | 5.9e-35 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
AHMNLFMI_04046 | 2.9e-28 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
AHMNLFMI_04047 | 1e-19 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
AHMNLFMI_04048 | 1.4e-169 | macB3 | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_04050 | 1.6e-88 | gtcA | S | Teichoic acid glycosylation protein | ||
AHMNLFMI_04051 | 3.6e-58 | S | Protein of unknown function (DUF1516) | |||
AHMNLFMI_04052 | 6.5e-93 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_04053 | 2e-137 | 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 | ||
AHMNLFMI_04054 | 7.4e-40 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
AHMNLFMI_04055 | 7.4e-40 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
AHMNLFMI_04056 | 3.1e-92 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
AHMNLFMI_04057 | 1.3e-45 | 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) | |
AHMNLFMI_04058 | 3.7e-39 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_04059 | 0.0 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_04060 | 1.1e-38 | mleP | S | Sodium Bile acid symporter family | ||
AHMNLFMI_04061 | 5.1e-59 | L | AAA domain | |||
AHMNLFMI_04062 | 4.7e-55 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
AHMNLFMI_04063 | 2.3e-28 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
AHMNLFMI_04064 | 1.9e-57 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
AHMNLFMI_04065 | 5.7e-23 | ydiL | S | CAAX protease self-immunity | ||
AHMNLFMI_04066 | 3.8e-31 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
AHMNLFMI_04067 | 8.6e-60 | ybiT | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_04068 | 1.5e-107 | yugP | S | Putative neutral zinc metallopeptidase | ||
AHMNLFMI_04069 | 3.6e-68 | yugP | S | Putative neutral zinc metallopeptidase | ||
AHMNLFMI_04070 | 2.2e-140 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
AHMNLFMI_04071 | 2.9e-76 | |||||
AHMNLFMI_04072 | 1.7e-67 | 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 | ||
AHMNLFMI_04073 | 3.5e-74 | yqhY | S | Asp23 family, cell envelope-related function | ||
AHMNLFMI_04074 | 2.2e-99 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
AHMNLFMI_04075 | 4.6e-30 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_04076 | 5.5e-55 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04077 | 4.7e-22 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AHMNLFMI_04078 | 5.6e-26 | metQ | M | Belongs to the nlpA lipoprotein family | ||
AHMNLFMI_04079 | 4.7e-32 | hicD1 | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHMNLFMI_04080 | 1.3e-83 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
AHMNLFMI_04081 | 1e-20 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
AHMNLFMI_04082 | 1.6e-163 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
AHMNLFMI_04083 | 2.1e-37 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AHMNLFMI_04084 | 9.6e-75 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AHMNLFMI_04085 | 1.5e-14 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AHMNLFMI_04086 | 1.7e-108 | |||||
AHMNLFMI_04087 | 2.1e-83 | pltK | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_04088 | 6.4e-12 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_04089 | 1.7e-107 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_04090 | 1.9e-142 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_04091 | 2e-80 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
AHMNLFMI_04092 | 7.2e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
AHMNLFMI_04093 | 3.2e-21 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
AHMNLFMI_04094 | 7.6e-52 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
AHMNLFMI_04095 | 3.8e-59 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
AHMNLFMI_04096 | 6.6e-99 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
AHMNLFMI_04099 | 1.6e-51 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_04100 | 2.5e-28 | S | Bacterial membrane protein YfhO | |||
AHMNLFMI_04101 | 7.8e-29 | |||||
AHMNLFMI_04102 | 6.1e-16 | zmp2 | O | Zinc-dependent metalloprotease | ||
AHMNLFMI_04103 | 3.9e-40 | zmp2 | O | Zinc-dependent metalloprotease | ||
AHMNLFMI_04104 | 1.8e-113 | zmp2 | O | Zinc-dependent metalloprotease | ||
AHMNLFMI_04105 | 1.1e-144 | cps3H | ||||
AHMNLFMI_04106 | 1e-52 | cps3F | ||||
AHMNLFMI_04107 | 2e-28 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_04108 | 1.2e-69 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_04109 | 1.7e-21 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_04110 | 3.4e-106 | helD | 3.6.4.12 | L | DNA helicase | |
AHMNLFMI_04111 | 1.5e-41 | helD | 3.6.4.12 | L | DNA helicase | |
AHMNLFMI_04112 | 2.5e-28 | helD | 3.6.4.12 | L | DNA helicase | |
AHMNLFMI_04113 | 5.5e-30 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
AHMNLFMI_04114 | 9.4e-194 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
AHMNLFMI_04115 | 3.4e-15 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
AHMNLFMI_04116 | 5.3e-46 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
AHMNLFMI_04117 | 4.4e-73 | S | SnoaL-like domain | |||
AHMNLFMI_04118 | 1.1e-19 | M | Glycosyltransferase group 2 family protein | |||
AHMNLFMI_04119 | 1.1e-127 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04120 | 2.5e-79 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04121 | 4.8e-109 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
AHMNLFMI_04122 | 3.3e-33 | yeaN | P | Transporter, major facilitator family protein | ||
AHMNLFMI_04123 | 3.4e-185 | yeaN | P | Transporter, major facilitator family protein | ||
AHMNLFMI_04124 | 7.2e-91 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_04125 | 3.1e-115 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_04126 | 2.5e-31 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_04127 | 2.5e-31 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_04129 | 8.2e-09 | S | Domain of unknown function (DUF4767) | |||
AHMNLFMI_04130 | 2.9e-90 | S | Domain of unknown function (DUF4767) | |||
AHMNLFMI_04131 | 1.4e-31 | K | PRD domain | |||
AHMNLFMI_04132 | 2.2e-54 | |||||
AHMNLFMI_04133 | 9.1e-79 | K | PRD domain | |||
AHMNLFMI_04134 | 4.3e-75 | gntP | EG | Gluconate | ||
AHMNLFMI_04135 | 8.4e-103 | gntP | EG | Gluconate | ||
AHMNLFMI_04136 | 1.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
AHMNLFMI_04137 | 2.2e-106 | yueF | S | AI-2E family transporter | ||
AHMNLFMI_04138 | 8.1e-99 | yueF | S | AI-2E family transporter | ||
AHMNLFMI_04139 | 5.2e-90 | yueF | S | AI-2E family transporter | ||
AHMNLFMI_04140 | 3.4e-169 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHMNLFMI_04141 | 8.7e-22 | pbpX | V | Beta-lactamase | ||
AHMNLFMI_04142 | 1.7e-142 | pbpX | V | Beta-lactamase | ||
AHMNLFMI_04143 | 1.3e-27 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
AHMNLFMI_04144 | 2.9e-33 | K | sequence-specific DNA binding | |||
AHMNLFMI_04145 | 1.3e-27 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
AHMNLFMI_04146 | 4.4e-30 | yloV | S | DAK2 domain fusion protein YloV | ||
AHMNLFMI_04147 | 1.8e-57 | asp | S | Asp23 family, cell envelope-related function | ||
AHMNLFMI_04148 | 1e-38 | yloV | S | DAK2 domain fusion protein YloV | ||
AHMNLFMI_04149 | 0.0 | yloV | S | DAK2 domain fusion protein YloV | ||
AHMNLFMI_04150 | 2.4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHMNLFMI_04151 | 3.8e-54 | metI | P | ABC transporter permease | ||
AHMNLFMI_04152 | 2.9e-12 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHMNLFMI_04153 | 7.3e-162 | 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 | ||
AHMNLFMI_04154 | 1.2e-26 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
AHMNLFMI_04156 | 4.7e-83 | cvpA | S | Colicin V production protein | ||
AHMNLFMI_04157 | 6e-121 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_04158 | 5.3e-147 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHMNLFMI_04159 | 1.3e-72 | |||||
AHMNLFMI_04160 | 6.4e-43 | ankB | S | ankyrin repeats | ||
AHMNLFMI_04161 | 3.3e-23 | |||||
AHMNLFMI_04162 | 6.6e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
AHMNLFMI_04163 | 1.2e-207 | 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 | |
AHMNLFMI_04164 | 6.3e-38 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
AHMNLFMI_04165 | 7.3e-27 | S | Cell surface protein | |||
AHMNLFMI_04166 | 8.4e-67 | S | Cell surface protein | |||
AHMNLFMI_04167 | 4.4e-139 | S | Cell surface protein | |||
AHMNLFMI_04168 | 1.7e-101 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_04169 | 4e-28 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_04170 | 2.4e-51 | |||||
AHMNLFMI_04171 | 3.6e-89 | |||||
AHMNLFMI_04172 | 3e-101 | K | DNA-templated transcription, initiation | |||
AHMNLFMI_04173 | 4.1e-98 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
AHMNLFMI_04174 | 8.2e-33 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
AHMNLFMI_04175 | 1.1e-98 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHMNLFMI_04176 | 6.5e-122 | 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 | |
AHMNLFMI_04177 | 3.6e-88 | niaR | S | 3H domain | ||
AHMNLFMI_04178 | 1.3e-34 | S | Sterol carrier protein domain | |||
AHMNLFMI_04179 | 2.2e-69 | S | Sterol carrier protein domain | |||
AHMNLFMI_04180 | 5.9e-88 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
AHMNLFMI_04181 | 8.6e-46 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
AHMNLFMI_04182 | 3e-113 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
AHMNLFMI_04183 | 1.2e-114 | |||||
AHMNLFMI_04184 | 3.8e-53 | tarL | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_04185 | 5e-210 | tarL | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_04186 | 6.7e-68 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04187 | 8.1e-63 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04188 | 2.5e-26 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04189 | 6.1e-79 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_04190 | 4.9e-201 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AHMNLFMI_04191 | 1.9e-76 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
AHMNLFMI_04192 | 1.7e-42 | 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 | |
AHMNLFMI_04193 | 3e-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 | |
AHMNLFMI_04194 | 5e-40 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
AHMNLFMI_04195 | 4.1e-32 | L | leucine-zipper of insertion element IS481 | |||
AHMNLFMI_04196 | 9.6e-53 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AHMNLFMI_04197 | 2.6e-71 | yqeY | S | YqeY-like protein | ||
AHMNLFMI_04198 | 7.7e-171 | phoH | T | phosphate starvation-inducible protein PhoH | ||
AHMNLFMI_04199 | 6.2e-79 | 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 | |
AHMNLFMI_04200 | 1e-72 | 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 | |
AHMNLFMI_04201 | 2.7e-34 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
AHMNLFMI_04202 | 3.9e-112 | mdtG | EGP | Major Facilitator Superfamily | ||
AHMNLFMI_04203 | 1.9e-27 | mdtG | EGP | Major Facilitator Superfamily | ||
AHMNLFMI_04204 | 4.2e-18 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_04205 | 1.2e-144 | |||||
AHMNLFMI_04206 | 3e-128 | pts4ABC | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHMNLFMI_04207 | 1.3e-127 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_04208 | 4.1e-90 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_04209 | 8e-137 | K | DeoR C terminal sensor domain | |||
AHMNLFMI_04210 | 1.7e-108 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
AHMNLFMI_04211 | 9.1e-71 | yneH | 1.20.4.1 | P | ArsC family | |
AHMNLFMI_04212 | 1.4e-68 | S | Protein of unknown function (DUF1722) | |||
AHMNLFMI_04213 | 2.9e-12 | |||||
AHMNLFMI_04214 | 4.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
AHMNLFMI_04215 | 1.6e-10 | arcT | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_04216 | 1.2e-143 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
AHMNLFMI_04217 | 2.9e-30 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
AHMNLFMI_04218 | 1.2e-188 | dtpT | U | amino acid peptide transporter | ||
AHMNLFMI_04219 | 1.1e-63 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AHMNLFMI_04220 | 2.6e-183 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
AHMNLFMI_04221 | 2.9e-199 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AHMNLFMI_04222 | 5.9e-39 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
AHMNLFMI_04223 | 5e-107 | |||||
AHMNLFMI_04225 | 7e-203 | 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 | |
AHMNLFMI_04226 | 3.7e-28 | 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 | |
AHMNLFMI_04227 | 2.5e-23 | 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 | |
AHMNLFMI_04228 | 1.1e-212 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_04229 | 1.5e-11 | |||||
AHMNLFMI_04230 | 9.4e-41 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
AHMNLFMI_04231 | 1.3e-23 | rmeD | K | helix_turn_helix, mercury resistance | ||
AHMNLFMI_04232 | 7.6e-64 | S | Protein of unknown function (DUF1093) | |||
AHMNLFMI_04233 | 4.2e-158 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHMNLFMI_04234 | 8.3e-31 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
AHMNLFMI_04235 | 5.9e-87 | K | Transcriptional regulator, LacI family | |||
AHMNLFMI_04236 | 5.8e-291 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_04237 | 1.5e-28 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04238 | 7e-25 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04239 | 1e-205 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04240 | 8.8e-13 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHMNLFMI_04241 | 2.6e-40 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04242 | 9.3e-35 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04243 | 6.3e-204 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHMNLFMI_04244 | 1.7e-54 | |||||
AHMNLFMI_04245 | 1.1e-77 | fld | C | Flavodoxin | ||
AHMNLFMI_04246 | 5.7e-69 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_04247 | 1.7e-159 | clcA | P | chloride | ||
AHMNLFMI_04248 | 5.5e-68 | |||||
AHMNLFMI_04249 | 2.2e-243 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AHMNLFMI_04250 | 8.1e-17 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AHMNLFMI_04251 | 4.1e-131 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04252 | 5.2e-80 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04253 | 3.3e-217 | nhaC | C | Na H antiporter NhaC | ||
AHMNLFMI_04254 | 3.8e-21 | |||||
AHMNLFMI_04255 | 8.8e-30 | |||||
AHMNLFMI_04256 | 7.8e-103 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04257 | 9.6e-197 | ylbL | T | Belongs to the peptidase S16 family | ||
AHMNLFMI_04258 | 4.1e-26 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
AHMNLFMI_04259 | 2.5e-113 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_04261 | 6.2e-09 | |||||
AHMNLFMI_04262 | 1.5e-130 | yhgE | V | domain protein | ||
AHMNLFMI_04263 | 1.4e-33 | yhgE | V | domain protein | ||
AHMNLFMI_04264 | 8.1e-42 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04265 | 7.1e-35 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04266 | 2.8e-173 | ykfC | 3.4.14.13 | M | NlpC/P60 family | |
AHMNLFMI_04267 | 4.4e-26 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AHMNLFMI_04268 | 6.1e-249 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AHMNLFMI_04269 | 1.2e-14 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_04270 | 1.1e-43 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_04271 | 1.8e-25 | |||||
AHMNLFMI_04272 | 1.3e-51 | |||||
AHMNLFMI_04274 | 4.1e-59 | |||||
AHMNLFMI_04275 | 2e-135 | qorB | 1.6.5.2 | GM | NmrA-like family | |
AHMNLFMI_04276 | 5.1e-59 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHMNLFMI_04277 | 5.8e-125 | IQ | reductase | |||
AHMNLFMI_04278 | 7.2e-28 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
AHMNLFMI_04279 | 4.6e-67 | hom1 | 1.1.1.3 | E | Homoserine dehydrogenase | |
AHMNLFMI_04280 | 5.8e-25 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
AHMNLFMI_04281 | 2.2e-210 | thrC | 4.2.3.1 | E | Threonine synthase | |
AHMNLFMI_04282 | 1.4e-08 | |||||
AHMNLFMI_04283 | 2e-100 | S | NADPH-dependent FMN reductase | |||
AHMNLFMI_04284 | 9.8e-31 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AHMNLFMI_04285 | 5e-191 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
AHMNLFMI_04287 | 2.4e-82 | F | DNA/RNA non-specific endonuclease | |||
AHMNLFMI_04288 | 1.2e-38 | L | nuclease | |||
AHMNLFMI_04289 | 1.1e-78 | glnP | P | ABC transporter | ||
AHMNLFMI_04290 | 4.6e-50 | 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 | ||
AHMNLFMI_04291 | 1.7e-25 | 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 | ||
AHMNLFMI_04292 | 1.5e-30 | 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 | ||
AHMNLFMI_04293 | 6.3e-102 | zmp1 | O | Zinc-dependent metalloprotease | ||
AHMNLFMI_04294 | 3.7e-44 | |||||
AHMNLFMI_04295 | 5.2e-81 | K | Helix-turn-helix domain | |||
AHMNLFMI_04296 | 4.1e-21 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
AHMNLFMI_04297 | 4.3e-100 | K | Helix-turn-helix domain | |||
AHMNLFMI_04298 | 1.1e-159 | S | Tetratricopeptide repeat | |||
AHMNLFMI_04299 | 3.8e-232 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AHMNLFMI_04300 | 9.2e-98 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
AHMNLFMI_04301 | 7.8e-32 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
AHMNLFMI_04302 | 1.2e-85 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
AHMNLFMI_04303 | 2.6e-222 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
AHMNLFMI_04304 | 1.1e-73 | yjfP | S | Dienelactone hydrolase family | ||
AHMNLFMI_04305 | 9.1e-130 | yjfP | S | Dienelactone hydrolase family | ||
AHMNLFMI_04306 | 1e-11 | yjfP | S | Dienelactone hydrolase family | ||
AHMNLFMI_04307 | 1.5e-08 | yjfP | S | Dienelactone hydrolase family | ||
AHMNLFMI_04308 | 2.3e-56 | dsbJ | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
AHMNLFMI_04309 | 1.9e-37 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
AHMNLFMI_04310 | 3e-276 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04311 | 6e-154 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHMNLFMI_04312 | 7.2e-46 | yieF | S | NADPH-dependent FMN reductase | ||
AHMNLFMI_04313 | 6.1e-94 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
AHMNLFMI_04314 | 8.6e-69 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
AHMNLFMI_04315 | 1.5e-40 | yhfI | S | Metallo-beta-lactamase superfamily | ||
AHMNLFMI_04316 | 1.5e-26 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
AHMNLFMI_04317 | 4e-22 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
AHMNLFMI_04318 | 1.8e-104 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
AHMNLFMI_04319 | 4.8e-249 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHMNLFMI_04320 | 2.6e-103 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
AHMNLFMI_04321 | 2.8e-93 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
AHMNLFMI_04322 | 1e-43 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
AHMNLFMI_04323 | 1.5e-46 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
AHMNLFMI_04324 | 1.2e-62 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
AHMNLFMI_04325 | 3.8e-37 | cvpA | S | Colicin V production protein | ||
AHMNLFMI_04326 | 2.1e-32 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_04327 | 1.2e-36 | S | Fn3-like domain | |||
AHMNLFMI_04328 | 4e-103 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_04329 | 2.3e-88 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_04330 | 9.3e-19 | S | Bacterial membrane protein, YfhO | |||
AHMNLFMI_04331 | 7.7e-106 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHMNLFMI_04332 | 3e-21 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
AHMNLFMI_04333 | 1.4e-30 | M | domain protein | |||
AHMNLFMI_04334 | 0.0 | M | domain protein | |||
AHMNLFMI_04335 | 2.6e-22 | M | domain protein | |||
AHMNLFMI_04336 | 1.1e-15 | S | Alpha beta | |||
AHMNLFMI_04337 | 7.8e-13 | S | ECF transporter, substrate-specific component | |||
AHMNLFMI_04338 | 6e-21 | S | ECF transporter, substrate-specific component | |||
AHMNLFMI_04339 | 3e-99 | S | ECF transporter, substrate-specific component | |||
AHMNLFMI_04340 | 1.8e-23 | |||||
AHMNLFMI_04341 | 1.4e-74 | S | Alpha beta | |||
AHMNLFMI_04342 | 5.7e-36 | S | Alpha beta | |||
AHMNLFMI_04343 | 1.1e-43 | S | Alpha beta | |||
AHMNLFMI_04345 | 3.2e-118 | yxkH | G | Polysaccharide deacetylase | ||
AHMNLFMI_04346 | 3.7e-38 | yxkH | G | Polysaccharide deacetylase | ||
AHMNLFMI_04347 | 6.9e-36 | 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 | |
AHMNLFMI_04348 | 5e-229 | 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 | |
AHMNLFMI_04349 | 2.8e-108 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
AHMNLFMI_04350 | 1e-29 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_04351 | 3.3e-126 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
AHMNLFMI_04352 | 1.1e-43 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_04353 | 1.1e-141 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
AHMNLFMI_04354 | 1.8e-47 | 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 | |
AHMNLFMI_04355 | 8.8e-129 | 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 | |
AHMNLFMI_04356 | 2.5e-35 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AHMNLFMI_04357 | 2.6e-64 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AHMNLFMI_04358 | 7.6e-73 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AHMNLFMI_04359 | 5.1e-148 | DegV | S | EDD domain protein, DegV family | ||
AHMNLFMI_04360 | 0.0 | oatA | I | Acyltransferase | ||
AHMNLFMI_04361 | 3.6e-117 | K | LytTr DNA-binding domain | |||
AHMNLFMI_04362 | 4.1e-50 | T | Universal stress protein family | |||
AHMNLFMI_04363 | 4.1e-289 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHMNLFMI_04364 | 2.4e-28 | 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 | |
AHMNLFMI_04365 | 1.1e-34 | 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 | |
AHMNLFMI_04366 | 4.8e-88 | 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 | |
AHMNLFMI_04367 | 2.7e-16 | 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 | |
AHMNLFMI_04368 | 2.4e-144 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_04371 | 1.5e-34 | lytE | M | LysM domain protein | ||
AHMNLFMI_04372 | 7.7e-17 | tagE6 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHMNLFMI_04373 | 1.1e-64 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
AHMNLFMI_04374 | 3.2e-53 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase family | |
AHMNLFMI_04375 | 3.8e-64 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase family | |
AHMNLFMI_04376 | 1.6e-77 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHMNLFMI_04377 | 7.3e-29 | S | Protein of unknown function (DUF2929) | |||
AHMNLFMI_04378 | 3.5e-42 | 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 | ||
AHMNLFMI_04379 | 2e-64 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AHMNLFMI_04380 | 2.2e-168 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
AHMNLFMI_04381 | 8.6e-59 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHMNLFMI_04382 | 3.7e-34 | |||||
AHMNLFMI_04383 | 5.7e-112 | S | Protein of unknown function (DUF1211) | |||
AHMNLFMI_04384 | 1.3e-162 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
AHMNLFMI_04385 | 7.8e-157 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_04386 | 5.6e-225 | 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 | ||
AHMNLFMI_04388 | 8.9e-42 | V | ABC transporter | |||
AHMNLFMI_04389 | 1.6e-65 | |||||
AHMNLFMI_04390 | 8.3e-41 | K | HxlR-like helix-turn-helix | |||
AHMNLFMI_04391 | 2.2e-24 | K | HxlR-like helix-turn-helix | |||
AHMNLFMI_04392 | 3.2e-60 | ydeA | S | intracellular protease amidase | ||
AHMNLFMI_04393 | 1.8e-68 | L | Putative transposase of IS4/5 family (DUF4096) | |||
AHMNLFMI_04394 | 5.4e-77 | L | Transposase DDE domain | |||
AHMNLFMI_04395 | 5.1e-39 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
AHMNLFMI_04396 | 3.8e-39 | mleR | K | LysR family transcriptional regulator | ||
AHMNLFMI_04397 | 3.6e-94 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
AHMNLFMI_04398 | 1.7e-139 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHMNLFMI_04399 | 4.2e-77 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AHMNLFMI_04400 | 2.8e-157 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
AHMNLFMI_04401 | 4.6e-143 | |||||
AHMNLFMI_04402 | 8.3e-54 | K | Transcriptional regulator PadR-like family | |||
AHMNLFMI_04403 | 1.6e-129 | K | UbiC transcription regulator-associated domain protein | |||
AHMNLFMI_04405 | 1.4e-34 | K | UbiC transcription regulator-associated domain protein | |||
AHMNLFMI_04406 | 5e-96 | puuR | K | Cupin domain | ||
AHMNLFMI_04407 | 4.5e-46 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
AHMNLFMI_04408 | 1e-37 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
AHMNLFMI_04409 | 1.3e-26 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
AHMNLFMI_04410 | 6e-146 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
AHMNLFMI_04411 | 3.3e-58 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_04412 | 6.5e-10 | mcbG | S | Pentapeptide repeats (8 copies) | ||
AHMNLFMI_04413 | 8.5e-145 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_04414 | 4.7e-91 | thrC | 4.2.3.1 | E | Threonine synthase | |
AHMNLFMI_04415 | 3.8e-17 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
AHMNLFMI_04416 | 4.4e-51 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
AHMNLFMI_04417 | 2.2e-51 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
AHMNLFMI_04418 | 6.6e-66 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
AHMNLFMI_04419 | 3e-116 | hly | S | protein, hemolysin III | ||
AHMNLFMI_04420 | 5.1e-54 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
AHMNLFMI_04421 | 2.1e-92 | czcD | P | cation diffusion facilitator family transporter | ||
AHMNLFMI_04422 | 7.7e-88 | |||||
AHMNLFMI_04423 | 1.6e-205 | ftsW | D | Belongs to the SEDS family | ||
AHMNLFMI_04424 | 1.9e-62 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04425 | 1.3e-123 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04426 | 3.6e-58 | mccF | V | LD-carboxypeptidase | ||
AHMNLFMI_04427 | 2.7e-61 | mccF | V | LD-carboxypeptidase | ||
AHMNLFMI_04428 | 1.1e-130 | |||||
AHMNLFMI_04429 | 7.1e-12 | 3.2.1.14 | GH18 | |||
AHMNLFMI_04430 | 1.3e-81 | zur | P | Belongs to the Fur family | ||
AHMNLFMI_04431 | 1.2e-48 | zur | P | Belongs to the Fur family | ||
AHMNLFMI_04432 | 4.3e-77 | L | Primase C terminal 1 (PriCT-1) | |||
AHMNLFMI_04433 | 1.2e-27 | |||||
AHMNLFMI_04434 | 3.1e-21 | |||||
AHMNLFMI_04437 | 3.2e-41 | |||||
AHMNLFMI_04438 | 3.3e-81 | S | Phage regulatory protein Rha (Phage_pRha) | |||
AHMNLFMI_04442 | 2.3e-32 | sip | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_04443 | 6.9e-40 | 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 | |
AHMNLFMI_04444 | 1.9e-53 | 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 | |
AHMNLFMI_04445 | 3.1e-74 | yabR | J | RNA binding | ||
AHMNLFMI_04446 | 1.1e-63 | divIC | D | Septum formation initiator | ||
AHMNLFMI_04448 | 2.2e-42 | yabO | J | S4 domain protein | ||
AHMNLFMI_04449 | 2.5e-75 | yabM | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04450 | 3e-151 | 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 | |
AHMNLFMI_04451 | 2.3e-210 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_04452 | 2.9e-14 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_04454 | 3.4e-132 | S | Protein of unknown function (DUF975) | |||
AHMNLFMI_04455 | 8.1e-40 | yjcF | 3.5.4.33, 4.4.1.8 | K | protein acetylation | |
AHMNLFMI_04456 | 2.8e-76 | yjbQ | P | TrkA C-terminal domain protein | ||
AHMNLFMI_04457 | 6.5e-63 | pgm3 | G | Phosphoglycerate mutase family | ||
AHMNLFMI_04458 | 1.2e-12 | NU | Mycoplasma protein of unknown function, DUF285 | |||
AHMNLFMI_04459 | 0.0 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_04460 | 1.7e-73 | |||||
AHMNLFMI_04461 | 4e-60 | |||||
AHMNLFMI_04462 | 1.6e-111 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
AHMNLFMI_04463 | 1.6e-32 | whiA | K | May be required for sporulation | ||
AHMNLFMI_04464 | 1.3e-156 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
AHMNLFMI_04465 | 3.8e-78 | ywiB | S | Domain of unknown function (DUF1934) | ||
AHMNLFMI_04466 | 4.4e-52 | patA | 1.1.1.28, 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHMNLFMI_04467 | 2e-39 | |||||
AHMNLFMI_04469 | 1.2e-118 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_04470 | 1.5e-241 | 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) | |
AHMNLFMI_04471 | 1.8e-84 | hmpT | S | Pfam:DUF3816 | ||
AHMNLFMI_04472 | 7.4e-297 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
AHMNLFMI_04473 | 6.3e-23 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
AHMNLFMI_04474 | 3.1e-26 | |||||
AHMNLFMI_04475 | 8.6e-142 | |||||
AHMNLFMI_04476 | 2e-247 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_04477 | 1.3e-68 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_04478 | 2.5e-71 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_04479 | 1.4e-49 | |||||
AHMNLFMI_04480 | 5.1e-262 | 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 | ||
AHMNLFMI_04481 | 8e-29 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AHMNLFMI_04482 | 1.9e-74 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AHMNLFMI_04483 | 2e-42 | plsC | 2.3.1.51 | I | Acyltransferase | |
AHMNLFMI_04484 | 5.4e-68 | plsC | 2.3.1.51 | I | Acyltransferase | |
AHMNLFMI_04485 | 2.2e-123 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
AHMNLFMI_04486 | 2e-49 | yazA | L | GIY-YIG catalytic domain protein | ||
AHMNLFMI_04487 | 1.2e-35 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
AHMNLFMI_04488 | 4.2e-29 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
AHMNLFMI_04489 | 4.2e-29 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
AHMNLFMI_04491 | 1.1e-82 | G | Glycogen debranching enzyme | |||
AHMNLFMI_04492 | 3.4e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
AHMNLFMI_04493 | 5.3e-92 | yjdB | S | Domain of unknown function (DUF4767) | ||
AHMNLFMI_04494 | 1.5e-63 | yjfP | S | Dienelactone hydrolase family | ||
AHMNLFMI_04495 | 1.8e-29 | yjfP | S | Dienelactone hydrolase family | ||
AHMNLFMI_04496 | 1.2e-67 | |||||
AHMNLFMI_04497 | 3e-226 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_04498 | 2e-143 | yvpB | S | Peptidase_C39 like family | ||
AHMNLFMI_04499 | 2.5e-300 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
AHMNLFMI_04500 | 1.2e-19 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
AHMNLFMI_04501 | 4.4e-40 | rplO | J | Binds to the 23S rRNA | ||
AHMNLFMI_04502 | 6.3e-70 | rplO | J | Binds to the 23S rRNA | ||
AHMNLFMI_04503 | 2.2e-24 | rpmD | J | Ribosomal protein L30 | ||
AHMNLFMI_04504 | 2.2e-18 | rpmD | J | Ribosomal protein L30 | ||
AHMNLFMI_04505 | 4e-51 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
AHMNLFMI_04506 | 3.4e-54 | |||||
AHMNLFMI_04507 | 9.1e-89 | |||||
AHMNLFMI_04508 | 1.9e-138 | flhF | N | Uncharacterized conserved protein (DUF2075) | ||
AHMNLFMI_04512 | 8.3e-210 | xylR | GK | ROK family | ||
AHMNLFMI_04513 | 1.7e-14 | K | AI-2E family transporter | |||
AHMNLFMI_04514 | 1.1e-22 | |||||
AHMNLFMI_04517 | 1.2e-56 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_04518 | 6e-16 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_04519 | 2.4e-29 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_04520 | 1e-114 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
AHMNLFMI_04521 | 8.7e-107 | larE | S | NAD synthase | ||
AHMNLFMI_04522 | 2.7e-80 | larE | S | NAD synthase | ||
AHMNLFMI_04523 | 1.5e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_04525 | 2.2e-131 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
AHMNLFMI_04526 | 1.1e-19 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
AHMNLFMI_04527 | 8.6e-37 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AHMNLFMI_04528 | 1.1e-75 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AHMNLFMI_04529 | 1.2e-216 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
AHMNLFMI_04530 | 2.7e-49 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
AHMNLFMI_04531 | 1.8e-151 | ypbG | 2.7.1.2 | GK | ROK family | |
AHMNLFMI_04532 | 1.4e-47 | 3.6.4.12 | K | HxlR-like helix-turn-helix | ||
AHMNLFMI_04533 | 2.1e-111 | K | Transcriptional regulator C-terminal region | |||
AHMNLFMI_04534 | 3.2e-133 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_04535 | 1.8e-52 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_04536 | 9.6e-56 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
AHMNLFMI_04537 | 4.9e-36 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
AHMNLFMI_04538 | 2.5e-103 | ropB | K | Helix-turn-helix XRE-family like proteins | ||
AHMNLFMI_04539 | 1.5e-233 | yxiO | S | Vacuole effluxer Atg22 like | ||
AHMNLFMI_04540 | 9.3e-42 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AHMNLFMI_04542 | 1.2e-25 | K | sequence-specific DNA binding | |||
AHMNLFMI_04544 | 1.3e-143 | L | PFAM Integrase, catalytic core | |||
AHMNLFMI_04545 | 2.1e-28 | L | PFAM Integrase, catalytic core | |||
AHMNLFMI_04546 | 1.9e-33 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AHMNLFMI_04547 | 9.3e-11 | S | Domain of unknown function (DUF4811) | |||
AHMNLFMI_04549 | 4.6e-45 | |||||
AHMNLFMI_04550 | 5.9e-132 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AHMNLFMI_04555 | 5.3e-44 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AHMNLFMI_04556 | 2.3e-43 | S | Protein of unknown function (DUF1093) | |||
AHMNLFMI_04557 | 2e-77 | S | Threonine/Serine exporter, ThrE | |||
AHMNLFMI_04558 | 5.9e-56 | thrE | S | Putative threonine/serine exporter | ||
AHMNLFMI_04559 | 3.9e-23 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
AHMNLFMI_04560 | 4.3e-59 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHMNLFMI_04561 | 5.8e-21 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_04562 | 4e-161 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_04563 | 1.6e-28 | 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 | ||
AHMNLFMI_04564 | 3.8e-229 | nadR | 2.7.1.22, 2.7.7.1 | H | This enzyme has three activities DNA binding, nicotinamide mononucleotide (NMN) adenylyltransferase and ribosylnicotinamide (RN) kinase. The DNA-binding domain binds to the nadB operator sequence in an NAD- and ATP-dependent manner. As NAD levels increase within the cell, the affinity of NadR for the nadB operator regions of nadA, nadB, and pncB increases, repressing the transcription of these genes. The RN kinase activity catalyzes the phosphorylation of RN to form nicotinamide ribonucleotide. The NMN adenylyltransferase activity catalyzes the transfer of the AMP moiety of ATP to nicotinamide ribonucleotide to form NAD( ). The NMN adenylyltransferase domain also functions as the NAD and ATP sensor | |
AHMNLFMI_04565 | 6.7e-69 | S | RelE toxin of RelE / RelB toxin-antitoxin system | |||
AHMNLFMI_04566 | 2e-43 | K | Helix-turn-helix domain | |||
AHMNLFMI_04567 | 7.5e-103 | yjjK | 3.6.3.25 | S | A translation factor that gates the progression of the 70S ribosomal initiation complex (IC, containing tRNA(fMet) in the P site) into the translation elongation cycle by using a mechanism sensitive to the ATP ADP ratio. Binds to the 70S ribosome E site where it modulates the state of the translating ribosome during subunit translocation | |
AHMNLFMI_04568 | 7.7e-227 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_04569 | 1.1e-34 | ykuJ | S | Protein of unknown function (DUF1797) | ||
AHMNLFMI_04570 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_04571 | 9.5e-38 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHMNLFMI_04572 | 3.8e-44 | |||||
AHMNLFMI_04573 | 1e-201 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
AHMNLFMI_04574 | 3.2e-138 | tagG | U | Transport permease protein | ||
AHMNLFMI_04575 | 2.1e-52 | ydgH | S | MMPL family | ||
AHMNLFMI_04576 | 1.2e-26 | ydgH | S | MMPL family | ||
AHMNLFMI_04577 | 1e-59 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
AHMNLFMI_04578 | 5.2e-09 | lysM | M | LysM domain | ||
AHMNLFMI_04579 | 2.8e-266 | yjeM | E | Amino Acid | ||
AHMNLFMI_04580 | 1.3e-33 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_04581 | 2e-13 | |||||
AHMNLFMI_04582 | 7.8e-112 | 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 | ||
AHMNLFMI_04583 | 3.3e-71 | 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 | ||
AHMNLFMI_04584 | 1.2e-36 | yggT | S | YGGT family | ||
AHMNLFMI_04585 | 1.7e-37 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AHMNLFMI_04586 | 7.1e-52 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AHMNLFMI_04587 | 1.1e-225 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AHMNLFMI_04588 | 1.3e-85 | |||||
AHMNLFMI_04589 | 2.4e-69 | |||||
AHMNLFMI_04590 | 2.1e-49 | |||||
AHMNLFMI_04591 | 6.5e-54 | |||||
AHMNLFMI_04592 | 4.3e-110 | |||||
AHMNLFMI_04593 | 1.6e-09 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_04594 | 3.6e-13 | EG | EamA-like transporter family | |||
AHMNLFMI_04595 | 7.3e-78 | EG | EamA-like transporter family | |||
AHMNLFMI_04596 | 8.9e-38 | gcvR | T | Belongs to the UPF0237 family | ||
AHMNLFMI_04597 | 3e-243 | XK27_08635 | S | UPF0210 protein | ||
AHMNLFMI_04598 | 1.6e-32 | copZ | P | Heavy-metal-associated domain | ||
AHMNLFMI_04599 | 3.3e-118 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | ||
AHMNLFMI_04600 | 4.9e-54 | gshR | 1.8.1.7 | C | Pyridine nucleotide-disulphide oxidoreductase | |
AHMNLFMI_04601 | 4.2e-132 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_04602 | 3e-133 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_04603 | 5.7e-144 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
AHMNLFMI_04604 | 9.5e-62 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
AHMNLFMI_04605 | 1.3e-143 | ttdA | 4.2.1.32 | C | Fumarate hydratase (Fumerase) | |
AHMNLFMI_04606 | 3.4e-42 | K | Helix-turn-helix domain | |||
AHMNLFMI_04607 | 1e-86 | 1.5.1.39 | C | nitroreductase | ||
AHMNLFMI_04608 | 6.7e-72 | |||||
AHMNLFMI_04609 | 1.5e-52 | |||||
AHMNLFMI_04610 | 5.9e-43 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_04611 | 3.2e-57 | ywjH | S | Protein of unknown function (DUF1634) | ||
AHMNLFMI_04612 | 5.5e-126 | yxaA | S | membrane transporter protein | ||
AHMNLFMI_04614 | 8.2e-39 | S | Protein of unknown function | |||
AHMNLFMI_04615 | 6.8e-224 | tetP | J | elongation factor G | ||
AHMNLFMI_04616 | 5.6e-33 | tetP | J | elongation factor G | ||
AHMNLFMI_04617 | 3.5e-23 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
AHMNLFMI_04618 | 7.1e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
AHMNLFMI_04619 | 2.4e-12 | XK27_04120 | S | Putative amino acid metabolism | ||
AHMNLFMI_04620 | 4.6e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
AHMNLFMI_04621 | 9.9e-56 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
AHMNLFMI_04622 | 8.7e-105 | L | Belongs to the 'phage' integrase family | |||
AHMNLFMI_04623 | 6.8e-47 | liaI | S | membrane | ||
AHMNLFMI_04624 | 4e-75 | XK27_02470 | K | LytTr DNA-binding domain | ||
AHMNLFMI_04625 | 1.5e-39 | liaI | S | membrane | ||
AHMNLFMI_04626 | 2.5e-71 | asp | S | Asp23 family, cell envelope-related function | ||
AHMNLFMI_04627 | 7.2e-23 | |||||
AHMNLFMI_04628 | 2.6e-84 | |||||
AHMNLFMI_04629 | 7.1e-37 | S | Transglycosylase associated protein | |||
AHMNLFMI_04630 | 7.4e-42 | XK27_09800 | I | Acyltransferase family | ||
AHMNLFMI_04631 | 2.2e-100 | L | Transposase | |||
AHMNLFMI_04632 | 5.1e-39 | L | Transposase | |||
AHMNLFMI_04635 | 9.3e-82 | |||||
AHMNLFMI_04636 | 4.7e-232 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_04637 | 1.7e-70 | |||||
AHMNLFMI_04638 | 2.7e-34 | |||||
AHMNLFMI_04639 | 8.2e-36 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
AHMNLFMI_04640 | 1.6e-09 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
AHMNLFMI_04641 | 2.8e-47 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
AHMNLFMI_04643 | 3.3e-31 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
AHMNLFMI_04644 | 3.1e-113 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
AHMNLFMI_04645 | 3.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
AHMNLFMI_04646 | 1.5e-100 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
AHMNLFMI_04647 | 6.6e-22 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
AHMNLFMI_04649 | 2.2e-301 | pccB | 2.1.3.1, 2.1.3.15, 6.4.1.3 | I | Carboxyl transferase domain | |
AHMNLFMI_04650 | 2.1e-34 | S | Acyl-CoA carboxylase epsilon subunit | |||
AHMNLFMI_04651 | 2.5e-121 | maf | 1.1.1.25, 2.1.1.190 | D | Maf-like protein | |
AHMNLFMI_04653 | 9.2e-58 | E | arginine | |||
AHMNLFMI_04654 | 6.9e-125 | S | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_04655 | 5.4e-164 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | Phosphomethylpyrimidine kinase | |
AHMNLFMI_04656 | 4.4e-123 | P | metal ion transport | |||
AHMNLFMI_04657 | 1.7e-55 | P | metal ion transport | |||
AHMNLFMI_04659 | 2.4e-22 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04660 | 6.6e-119 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04661 | 6.1e-104 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04663 | 1.7e-84 | yliE | T | EAL domain | ||
AHMNLFMI_04665 | 1.7e-97 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04666 | 1.9e-43 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04667 | 2.7e-30 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
AHMNLFMI_04668 | 5.1e-18 | |||||
AHMNLFMI_04669 | 1.7e-84 | dps | P | Belongs to the Dps family | ||
AHMNLFMI_04670 | 1.7e-84 | dps | P | Belongs to the Dps family | ||
AHMNLFMI_04671 | 3.7e-79 | pgaC | GT2 | M | Glycosyl transferase | |
AHMNLFMI_04672 | 5.8e-94 | |||||
AHMNLFMI_04673 | 4e-101 | T | EAL domain | |||
AHMNLFMI_04674 | 6.5e-19 | T | EAL domain | |||
AHMNLFMI_04675 | 1.5e-40 | |||||
AHMNLFMI_04676 | 2e-82 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
AHMNLFMI_04677 | 1.4e-20 | |||||
AHMNLFMI_04678 | 1.4e-33 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04679 | 1.9e-54 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04680 | 3.5e-282 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04681 | 3e-101 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_04682 | 4.4e-57 | 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 | |
AHMNLFMI_04683 | 1.4e-15 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
AHMNLFMI_04684 | 1.6e-58 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHMNLFMI_04685 | 1.4e-49 | |||||
AHMNLFMI_04686 | 1.3e-15 | |||||
AHMNLFMI_04687 | 9.7e-77 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHMNLFMI_04688 | 1.4e-50 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHMNLFMI_04689 | 8.2e-19 | L | Transposase | |||
AHMNLFMI_04690 | 7.9e-15 | L | Transposase | |||
AHMNLFMI_04691 | 2.3e-30 | arpU | S | Transcriptional regulator, ArpU family | ||
AHMNLFMI_04692 | 3.8e-22 | mraZ | K | Belongs to the MraZ family | ||
AHMNLFMI_04693 | 3.8e-22 | mraZ | K | Belongs to the MraZ family | ||
AHMNLFMI_04694 | 1.3e-18 | mraZ | K | Belongs to the MraZ family | ||
AHMNLFMI_04695 | 3.8e-22 | mraZ | K | Belongs to the MraZ family | ||
AHMNLFMI_04696 | 3.8e-22 | mraZ | K | Belongs to the MraZ family | ||
AHMNLFMI_04697 | 1.5e-44 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_04698 | 1.5e-44 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_04699 | 1.5e-44 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_04700 | 1.5e-44 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_04701 | 1e-55 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04702 | 1.3e-67 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04703 | 1.3e-67 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04704 | 1.3e-67 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04705 | 4e-42 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04706 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04707 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04708 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04709 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04710 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04711 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04712 | 8.4e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04713 | 2.3e-107 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
AHMNLFMI_04714 | 5.3e-59 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
AHMNLFMI_04715 | 5.3e-59 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
AHMNLFMI_04716 | 2.4e-40 | K | prlF antitoxin for toxin YhaV_toxin | |||
AHMNLFMI_04717 | 2.3e-107 | L | Integrase | |||
AHMNLFMI_04724 | 3.5e-20 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_04725 | 3.8e-23 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_04726 | 3.8e-23 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_04727 | 3.8e-23 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHMNLFMI_04728 | 7.3e-43 | S | Protein of unknown function (DUF2089) | |||
AHMNLFMI_04729 | 1.7e-42 | |||||
AHMNLFMI_04730 | 1.8e-54 | treR | K | UTRA | ||
AHMNLFMI_04731 | 3.4e-18 | treR | K | UTRA | ||
AHMNLFMI_04732 | 1.4e-22 | treR | K | UTRA | ||
AHMNLFMI_04733 | 3.4e-18 | treR | K | UTRA | ||
AHMNLFMI_04734 | 1e-81 | gntR | K | rpiR family | ||
AHMNLFMI_04735 | 5.8e-61 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04736 | 9.4e-51 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_04737 | 5e-100 | S | Phage Terminase | |||
AHMNLFMI_04738 | 3.4e-24 | K | Transcriptional regulator | |||
AHMNLFMI_04739 | 1.7e-42 | K | Transcriptional regulator | |||
AHMNLFMI_04740 | 4.2e-20 | gntR | K | rpiR family | ||
AHMNLFMI_04741 | 1.3e-38 | |||||
AHMNLFMI_04742 | 1.1e-84 | |||||
AHMNLFMI_04743 | 4.4e-07 | L | transposase and inactivated derivatives, IS30 family | |||
AHMNLFMI_04744 | 9.1e-46 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04745 | 8.3e-36 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04746 | 1.4e-21 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04747 | 1.7e-70 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_04748 | 6.5e-08 | |||||
AHMNLFMI_04749 | 3.9e-72 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_04750 | 1.3e-22 | gntR | K | rpiR family | ||
AHMNLFMI_04751 | 3.1e-37 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04752 | 5.8e-61 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04753 | 5.8e-61 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04754 | 2e-39 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
AHMNLFMI_04755 | 1.4e-39 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
AHMNLFMI_04756 | 1.1e-60 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
AHMNLFMI_04757 | 3.5e-24 | nikMN | P | PDGLE domain | ||
AHMNLFMI_04758 | 1.5e-33 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_04759 | 1.9e-71 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
AHMNLFMI_04760 | 1.5e-33 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_04761 | 1.9e-71 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
AHMNLFMI_04762 | 1.9e-24 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_04763 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
AHMNLFMI_04764 | 3.4e-40 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
AHMNLFMI_04765 | 1.4e-44 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
AHMNLFMI_04767 | 5.1e-33 | |||||
AHMNLFMI_04768 | 7.4e-13 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHMNLFMI_04769 | 1e-27 | 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) | |
AHMNLFMI_04770 | 3.5e-100 | 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) | |
AHMNLFMI_04771 | 6.7e-48 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AHMNLFMI_04772 | 6.7e-48 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AHMNLFMI_04773 | 1.7e-32 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04774 | 1.7e-32 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04775 | 1.7e-32 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_04776 | 2.7e-62 | L | HNH nucleases | |||
AHMNLFMI_04777 | 2e-59 | |||||
AHMNLFMI_04779 | 3e-40 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_04788 | 1.2e-24 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
AHMNLFMI_04789 | 2.5e-74 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
AHMNLFMI_04790 | 2e-21 | Q | Imidazolonepropionase and related amidohydrolases | |||
AHMNLFMI_04791 | 1.7e-19 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_04792 | 1.7e-68 | hipB | K | Helix-turn-helix | ||
AHMNLFMI_04794 | 2.5e-37 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_04795 | 9e-40 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_04796 | 6.4e-54 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AHMNLFMI_04797 | 3.4e-28 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AHMNLFMI_04798 | 5.4e-40 | yjjC | V | ABC transporter | ||
AHMNLFMI_04799 | 5.4e-40 | yjjC | V | ABC transporter | ||
AHMNLFMI_04815 | 6.4e-41 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04817 | 0.0 | mdlB | V | ABC transporter | ||
AHMNLFMI_04818 | 1.7e-224 | mdlA | V | ABC transporter | ||
AHMNLFMI_04819 | 7.4e-119 | mdlA | V | ABC transporter | ||
AHMNLFMI_04820 | 3.3e-15 | mdlA | V | ABC transporter | ||
AHMNLFMI_04821 | 1e-68 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_04822 | 1.4e-81 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_04823 | 1.2e-66 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_04824 | 2.5e-62 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
AHMNLFMI_04825 | 4.3e-61 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
AHMNLFMI_04826 | 1.3e-98 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_04827 | 4.6e-67 | metQ | P | NLPA lipoprotein | ||
AHMNLFMI_04830 | 2.7e-45 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_04831 | 4.5e-22 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHMNLFMI_04832 | 3.9e-36 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
AHMNLFMI_04833 | 3.9e-36 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
AHMNLFMI_04836 | 1.6e-44 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AHMNLFMI_04837 | 1.1e-22 | GM | NmrA-like family | |||
AHMNLFMI_04838 | 3.4e-48 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_04839 | 4.9e-31 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_04840 | 1e-33 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
AHMNLFMI_04841 | 1e-33 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
AHMNLFMI_04842 | 7.2e-50 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_04843 | 2.3e-31 | yslB | S | Protein of unknown function (DUF2507) | ||
AHMNLFMI_04844 | 2.9e-49 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_04845 | 3.1e-40 | yslB | S | Protein of unknown function (DUF2507) | ||
AHMNLFMI_04846 | 2.3e-66 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_04847 | 7.6e-126 | yslB | S | Protein of unknown function (DUF2507) | ||
AHMNLFMI_04848 | 3.3e-19 | rplD | J | Forms part of the polypeptide exit tunnel | ||
AHMNLFMI_04849 | 2.8e-83 | rplD | J | Forms part of the polypeptide exit tunnel | ||
AHMNLFMI_04850 | 2.5e-65 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
AHMNLFMI_04851 | 1.2e-30 | secG | U | Preprotein translocase | ||
AHMNLFMI_04852 | 1.9e-12 | dnaD | L | Replication initiation and membrane attachment | ||
AHMNLFMI_04855 | 1.1e-36 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_04856 | 6.3e-25 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_04857 | 6.3e-25 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_04858 | 3e-56 | dps | P | Belongs to the Dps family | ||
AHMNLFMI_04859 | 1.1e-84 | |||||
AHMNLFMI_04860 | 4.5e-50 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_04861 | 5.9e-30 | mutT | 3.6.1.55 | F | DNA mismatch repair protein MutT | |
AHMNLFMI_04862 | 6.9e-30 | mutT | 3.6.1.55 | F | DNA mismatch repair protein MutT | |
AHMNLFMI_04863 | 8.9e-21 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_04864 | 7e-18 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_04865 | 7e-18 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_04866 | 7e-18 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_04867 | 7e-18 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHMNLFMI_04868 | 1.3e-38 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHMNLFMI_04879 | 6.9e-48 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_04880 | 6.9e-48 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_04901 | 2.4e-87 | cobQ | S | glutamine amidotransferase | ||
AHMNLFMI_04902 | 2.2e-12 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AHMNLFMI_04904 | 7.1e-14 | |||||
AHMNLFMI_04905 | 7.1e-14 | |||||
AHMNLFMI_04906 | 7.1e-14 | |||||
AHMNLFMI_04907 | 3.8e-11 | uvrA3 | L | excinuclease ABC | ||
AHMNLFMI_04908 | 7.4e-40 | 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 | |
AHMNLFMI_04909 | 2e-85 | S | membrane | |||
AHMNLFMI_04910 | 9.5e-30 | 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 | |
AHMNLFMI_04911 | 9.5e-30 | 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 | |
AHMNLFMI_04912 | 3.5e-22 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_04913 | 5.8e-26 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_04914 | 3.5e-22 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_04915 | 3.5e-22 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_04916 | 3.5e-22 | copB | 3.6.3.4 | P | P-type ATPase | |
AHMNLFMI_04918 | 3.6e-20 | dps | P | Belongs to the Dps family | ||
AHMNLFMI_04919 | 8.6e-60 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
AHMNLFMI_04920 | 4.8e-10 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_04921 | 1.6e-13 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_04922 | 1.6e-13 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_04923 | 1.6e-13 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_04924 | 1.6e-13 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_04925 | 1.6e-13 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_04926 | 3.5e-36 | treR | K | UTRA | ||
AHMNLFMI_04927 | 8e-39 | treR | K | UTRA | ||
AHMNLFMI_04931 | 2.4e-27 | L | Transposase | |||
AHMNLFMI_04933 | 1.2e-31 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
AHMNLFMI_04934 | 1.6e-15 | pbuX | F | xanthine permease | ||
AHMNLFMI_04935 | 1.6e-15 | pbuX | F | xanthine permease | ||
AHMNLFMI_04938 | 2.1e-25 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04939 | 2.1e-25 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04940 | 2.1e-25 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_04941 | 7.1e-40 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04942 | 8e-38 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04943 | 2.9e-13 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_04944 | 1.1e-14 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_04945 | 9.7e-17 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_04946 | 2.8e-19 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_04947 | 5.5e-15 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
AHMNLFMI_04948 | 1.1e-140 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
AHMNLFMI_04949 | 8.3e-45 | ulaB | 2.7.1.194, 2.7.1.200 | G | Phosphotransferase system galactitol-specific IIB component | |
AHMNLFMI_04950 | 2e-77 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_04951 | 8.5e-204 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_04952 | 2.4e-35 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHMNLFMI_04953 | 2e-69 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04954 | 3e-49 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04955 | 1.8e-30 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04956 | 1.4e-45 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04957 | 2e-29 | M | Glycosyltransferase, group 2 family protein | |||
AHMNLFMI_04958 | 1.4e-22 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_04959 | 1.4e-22 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_04960 | 1.2e-14 | cps4J | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_04961 | 1e-176 | cps4I | M | Glycosyltransferase like family 2 | ||
AHMNLFMI_04962 | 1.9e-46 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_04963 | 6.4e-57 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
AHMNLFMI_04964 | 1.4e-13 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AHMNLFMI_04965 | 7.2e-49 | 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 | |
AHMNLFMI_04966 | 1.4e-84 | 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 | |
AHMNLFMI_04967 | 5.8e-77 | 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 | |
AHMNLFMI_04968 | 2.5e-40 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
AHMNLFMI_04969 | 0.0 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_04970 | 3.4e-22 | scrA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_04971 | 1e-24 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
AHMNLFMI_04972 | 1.5e-27 | G | Major Facilitator | |||
AHMNLFMI_04973 | 1.4e-38 | K | Transcriptional regulator, LacI family | |||
AHMNLFMI_04974 | 7.2e-92 | G | Major Facilitator | |||
AHMNLFMI_04975 | 1.4e-13 | E | IrrE N-terminal-like domain | |||
AHMNLFMI_04978 | 1.4e-47 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
AHMNLFMI_04979 | 5.7e-14 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_04980 | 4.1e-12 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHMNLFMI_04981 | 1.4e-22 | S | portal protein | |||
AHMNLFMI_04982 | 2.9e-113 | S | Phage terminase, large subunit, PBSX family | |||
AHMNLFMI_04983 | 7.1e-32 | S | CAAX protease self-immunity | |||
AHMNLFMI_04984 | 6.7e-23 | |||||
AHMNLFMI_04985 | 2.4e-22 | plnF | ||||
AHMNLFMI_04986 | 2.4e-87 | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | ||
AHMNLFMI_04990 | 4.8e-72 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AHMNLFMI_04991 | 4.5e-177 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AHMNLFMI_04992 | 2.9e-134 | 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 | |
AHMNLFMI_04993 | 9.2e-42 | 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 | |
AHMNLFMI_04994 | 7.1e-246 | 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 | |
AHMNLFMI_04995 | 4.8e-185 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHMNLFMI_04996 | 6e-76 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHMNLFMI_04997 | 1.1e-40 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHMNLFMI_04998 | 3.7e-38 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHMNLFMI_04999 | 6.7e-47 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHMNLFMI_05000 | 1.1e-40 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHMNLFMI_05001 | 1.3e-49 | gor | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_05002 | 1.9e-226 | gor | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_05003 | 7.2e-107 | helD | 3.6.4.12 | L | DNA helicase | |
AHMNLFMI_05004 | 5.4e-14 | zmp1 | O | Zinc-dependent metalloprotease | ||
AHMNLFMI_05005 | 5.9e-24 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05006 | 4.1e-98 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
AHMNLFMI_05007 | 2.4e-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 | |
AHMNLFMI_05008 | 6.9e-33 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
AHMNLFMI_05009 | 3.8e-96 | 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 | |
AHMNLFMI_05010 | 1.4e-190 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_05011 | 1e-85 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_05012 | 2.3e-31 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_05013 | 1.2e-45 | |||||
AHMNLFMI_05014 | 8.7e-30 | |||||
AHMNLFMI_05015 | 6.2e-99 | dut | S | Protein conserved in bacteria | ||
AHMNLFMI_05016 | 3.1e-29 | |||||
AHMNLFMI_05017 | 4.2e-47 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_05018 | 1e-51 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_05019 | 2.7e-50 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_05020 | 2e-132 | L | Transposase | |||
AHMNLFMI_05021 | 4.7e-144 | frlB | M | SIS domain | ||
AHMNLFMI_05022 | 8.2e-58 | XK27_07075 | V | CAAX protease self-immunity | ||
AHMNLFMI_05023 | 2.3e-182 | 2.7.7.7, 3.6.4.12 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. The epsilon subunit contain the editing function and is a proofreading 3'-5' exonuclease | ||
AHMNLFMI_05024 | 1.2e-114 | pipD | E | Dipeptidase | ||
AHMNLFMI_05025 | 2e-64 | pipD | E | Dipeptidase | ||
AHMNLFMI_05026 | 1.5e-227 | pipD | E | Dipeptidase | ||
AHMNLFMI_05027 | 9.9e-199 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
AHMNLFMI_05028 | 3.4e-24 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
AHMNLFMI_05029 | 5.2e-45 | S | Psort location CytoplasmicMembrane, score | |||
AHMNLFMI_05030 | 2.3e-34 | S | Psort location CytoplasmicMembrane, score | |||
AHMNLFMI_05031 | 7e-21 | S | Psort location CytoplasmicMembrane, score | |||
AHMNLFMI_05032 | 1.4e-46 | chbC | 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 | ||
AHMNLFMI_05039 | 1.1e-51 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
AHMNLFMI_05040 | 1.1e-21 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AHMNLFMI_05041 | 3.3e-35 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AHMNLFMI_05043 | 4.9e-08 | pbuG | S | permease | ||
AHMNLFMI_05044 | 7.9e-21 | pbuG | S | permease | ||
AHMNLFMI_05045 | 1.5e-19 | |||||
AHMNLFMI_05046 | 1.3e-82 | K | Transcriptional regulator | |||
AHMNLFMI_05047 | 5e-153 | licD | M | LicD family | ||
AHMNLFMI_05048 | 9.1e-289 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_05049 | 2.5e-56 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
AHMNLFMI_05050 | 4.3e-206 | XK27_05220 | S | AI-2E family transporter | ||
AHMNLFMI_05051 | 1.7e-41 | 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 | ||
AHMNLFMI_05052 | 1.1e-161 | rrmA | 2.1.1.187 | H | Methyltransferase | |
AHMNLFMI_05053 | 3.3e-102 | rrmA | 2.1.1.187 | H | Methyltransferase | |
AHMNLFMI_05054 | 7.1e-17 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_05055 | 4.3e-25 | |||||
AHMNLFMI_05056 | 4.1e-29 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_05057 | 8.4e-29 | |||||
AHMNLFMI_05058 | 2.2e-43 | cps4G | M | Glycosyltransferase Family 4 | ||
AHMNLFMI_05059 | 4.2e-11 | dnaB | L | replication initiation and membrane attachment | ||
AHMNLFMI_05060 | 6.6e-125 | dnaI | L | Primosomal protein DnaI | ||
AHMNLFMI_05061 | 8.9e-81 | dnaB | L | replication initiation and membrane attachment | ||
AHMNLFMI_05062 | 6.2e-20 | fdoG | 1.17.1.9 | C | Formate dehydrogenase allows E.coli to use formate as major electron donor during anaerobic respiration, when nitrate is used as electron acceptor. The alpha subunit FdnG contains the formate oxidation site. Electrons are transferred from formate to menaquinone in the gamma subunit (FdnI), through the 4Fe-4S clusters in the beta subunit (FdnH). Formate dehydrogenase-N is part of a system that generates proton motive force, together with the dissimilatory nitrate reductase (Nar) | |
AHMNLFMI_05063 | 8.5e-95 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
AHMNLFMI_05064 | 3.9e-111 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
AHMNLFMI_05065 | 1.8e-56 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_05066 | 1.1e-45 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_05067 | 1.6e-46 | EG | EamA-like transporter family | |||
AHMNLFMI_05068 | 2.5e-52 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
AHMNLFMI_05069 | 1.5e-26 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05070 | 1.1e-42 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05071 | 7.2e-57 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05072 | 1.5e-28 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05073 | 2.3e-93 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05074 | 7e-25 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05075 | 2.2e-31 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_05076 | 1.1e-110 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_05077 | 6.3e-10 | |||||
AHMNLFMI_05078 | 1.1e-48 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_05079 | 1.9e-71 | T | Calcineurin-like phosphoesterase superfamily domain | |||
AHMNLFMI_05080 | 2.5e-48 | drrB | U | ABC-2 type transporter | ||
AHMNLFMI_05081 | 1.1e-220 | M | O-Antigen ligase | |||
AHMNLFMI_05082 | 1.6e-126 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
AHMNLFMI_05083 | 3.6e-49 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
AHMNLFMI_05084 | 1.3e-22 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
AHMNLFMI_05085 | 5.1e-38 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_05086 | 4.4e-83 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_05087 | 4.6e-67 | S | Psort location Cytoplasmic, score | |||
AHMNLFMI_05088 | 5.5e-23 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_05089 | 6.3e-201 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
AHMNLFMI_05090 | 2.4e-56 | 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 | |
AHMNLFMI_05091 | 9.1e-26 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
AHMNLFMI_05092 | 1.3e-30 | 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 | |
AHMNLFMI_05093 | 1e-167 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHMNLFMI_05094 | 3.4e-39 | 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) | |
AHMNLFMI_05095 | 1.5e-171 | 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) | |
AHMNLFMI_05096 | 1.4e-59 | 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) | |
AHMNLFMI_05097 | 3.5e-110 | P | ATPases associated with a variety of cellular activities | |||
AHMNLFMI_05098 | 6.3e-159 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_05099 | 1.9e-18 | yjbQ | P | TrkA C-terminal domain protein | ||
AHMNLFMI_05100 | 1e-91 | yqkA | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
AHMNLFMI_05101 | 5.8e-71 | yqkA | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
AHMNLFMI_05102 | 7.9e-99 | yjbQ | P | TrkA C-terminal domain protein | ||
AHMNLFMI_05103 | 2e-59 | yjbQ | P | TrkA C-terminal domain protein | ||
AHMNLFMI_05104 | 1.3e-51 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
AHMNLFMI_05105 | 1.2e-132 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
AHMNLFMI_05106 | 1.4e-14 | GM | NAD(P)H-binding | |||
AHMNLFMI_05109 | 1.3e-87 | GM | NAD(P)H-binding | |||
AHMNLFMI_05110 | 6e-28 | akr5f | 1.1.1.346 | S | reductase | |
AHMNLFMI_05111 | 1.7e-17 | glcU | U | sugar transport | ||
AHMNLFMI_05112 | 1.6e-63 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
AHMNLFMI_05113 | 2.4e-122 | 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) | |
AHMNLFMI_05114 | 2.1e-145 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_05115 | 3.1e-82 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_05116 | 1.2e-106 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_05117 | 3.5e-41 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_05118 | 7.6e-49 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_05119 | 1.3e-28 | ylqC | S | Belongs to the UPF0109 family | ||
AHMNLFMI_05120 | 1.3e-28 | ylqC | S | Belongs to the UPF0109 family | ||
AHMNLFMI_05121 | 6.4e-73 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_05122 | 1.7e-45 | |||||
AHMNLFMI_05123 | 5.2e-19 | |||||
AHMNLFMI_05124 | 5.7e-28 | dut | S | Protein conserved in bacteria | ||
AHMNLFMI_05125 | 5.7e-28 | dut | S | Protein conserved in bacteria | ||
AHMNLFMI_05126 | 5.2e-19 | |||||
AHMNLFMI_05127 | 2e-91 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_05128 | 2e-78 | uspA | T | universal stress protein | ||
AHMNLFMI_05129 | 1.6e-30 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
AHMNLFMI_05130 | 2.2e-102 | tetP | J | elongation factor G | ||
AHMNLFMI_05131 | 2.2e-52 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_05132 | 6e-14 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_05133 | 1.5e-172 | pts29C | 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 | ||
AHMNLFMI_05134 | 1.8e-93 | K | UTRA domain | |||
AHMNLFMI_05135 | 1.1e-38 | K | UTRA domain | |||
AHMNLFMI_05136 | 3.2e-40 | K | UTRA domain | |||
AHMNLFMI_05137 | 2.5e-35 | E | lipolytic protein G-D-S-L family | |||
AHMNLFMI_05138 | 2.9e-61 | yicL | EG | EamA-like transporter family | ||
AHMNLFMI_05139 | 7.5e-43 | E | lipolytic protein G-D-S-L family | |||
AHMNLFMI_05140 | 1.6e-70 | E | lipolytic protein G-D-S-L family | |||
AHMNLFMI_05141 | 2e-66 | 4.1.1.52 | S | Amidohydrolase | ||
AHMNLFMI_05142 | 1.6e-149 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_05144 | 5.6e-253 | cycA | E | Amino acid permease | ||
AHMNLFMI_05145 | 1.6e-67 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_05146 | 1.3e-27 | 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 | |
AHMNLFMI_05147 | 1.4e-18 | |||||
AHMNLFMI_05148 | 4.7e-31 | ygzD | K | Transcriptional | ||
AHMNLFMI_05149 | 7.4e-132 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
AHMNLFMI_05150 | 5.4e-68 | P | Major Facilitator Superfamily | |||
AHMNLFMI_05153 | 5.8e-62 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
AHMNLFMI_05154 | 4.4e-71 | mutT | 3.6.1.55 | F | DNA mismatch repair protein MutT | |
AHMNLFMI_05155 | 1.3e-81 | yunF | F | Protein of unknown function DUF72 | ||
AHMNLFMI_05156 | 1.7e-22 | S | Domain of unknown function (DUF4811) | |||
AHMNLFMI_05157 | 1.7e-57 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05158 | 1.7e-22 | S | Domain of unknown function (DUF4811) | |||
AHMNLFMI_05159 | 6.3e-27 | lmrB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05160 | 6.8e-33 | S | Domain of unknown function (DUF4811) | |||
AHMNLFMI_05161 | 4.3e-64 | 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 | |
AHMNLFMI_05162 | 1.6e-68 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHMNLFMI_05163 | 8e-174 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
AHMNLFMI_05164 | 5.2e-51 | N | WxL domain surface cell wall-binding | |||
AHMNLFMI_05165 | 2e-106 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_05166 | 5.1e-120 | N | WxL domain surface cell wall-binding | |||
AHMNLFMI_05167 | 1.4e-104 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
AHMNLFMI_05168 | 6.2e-93 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
AHMNLFMI_05169 | 6.1e-76 | xylP1 | G | MFS/sugar transport protein | ||
AHMNLFMI_05170 | 6.7e-122 | qmcA | O | prohibitin homologues | ||
AHMNLFMI_05171 | 1.6e-37 | xylP1 | G | MFS/sugar transport protein | ||
AHMNLFMI_05172 | 1.5e-29 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
AHMNLFMI_05173 | 2.4e-38 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
AHMNLFMI_05174 | 5.4e-74 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
AHMNLFMI_05175 | 6.1e-19 | |||||
AHMNLFMI_05176 | 5.4e-74 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
AHMNLFMI_05177 | 1.4e-36 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_05180 | 9.9e-85 | F | NUDIX domain | |||
AHMNLFMI_05181 | 8.4e-154 | yifK | E | Amino acid permease | ||
AHMNLFMI_05182 | 9.5e-39 | K | Helix-turn-helix domain | |||
AHMNLFMI_05183 | 7.5e-22 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_05184 | 1.5e-24 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_05185 | 1.3e-77 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_05186 | 4.6e-46 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_05187 | 8.7e-91 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
AHMNLFMI_05188 | 3.2e-62 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
AHMNLFMI_05189 | 5.1e-51 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
AHMNLFMI_05190 | 1.3e-49 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
AHMNLFMI_05191 | 3.5e-26 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
AHMNLFMI_05192 | 4.7e-43 | znuB | U | ABC 3 transport family | ||
AHMNLFMI_05193 | 1.1e-107 | fhuC | 3.6.3.35 | P | ABC transporter | |
AHMNLFMI_05194 | 9.3e-27 | znuB | U | ABC 3 transport family | ||
AHMNLFMI_05195 | 1.2e-39 | fhuC | 3.6.3.35 | P | ABC transporter | |
AHMNLFMI_05196 | 7e-37 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_05197 | 1.4e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AHMNLFMI_05198 | 2.8e-102 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AHMNLFMI_05199 | 2.2e-176 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_05200 | 1.2e-17 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AHMNLFMI_05201 | 1.3e-48 | ymdB | S | Macro domain protein | ||
AHMNLFMI_05202 | 4.8e-13 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AHMNLFMI_05203 | 1.7e-41 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AHMNLFMI_05204 | 2.8e-129 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AHMNLFMI_05205 | 8.2e-91 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AHMNLFMI_05206 | 4e-38 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AHMNLFMI_05207 | 8e-21 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AHMNLFMI_05208 | 4.6e-28 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
AHMNLFMI_05209 | 1.2e-38 | rmaD | K | Transcriptional regulator | ||
AHMNLFMI_05212 | 4.3e-09 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_05213 | 1.1e-261 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_05214 | 1.5e-54 | pepF | E | oligoendopeptidase F | ||
AHMNLFMI_05215 | 2e-12 | pepF | E | oligoendopeptidase F | ||
AHMNLFMI_05216 | 9e-102 | yhdP | S | Transporter associated domain | ||
AHMNLFMI_05217 | 2.7e-20 | yhdP | S | Transporter associated domain | ||
AHMNLFMI_05218 | 3.1e-52 | M1-874 | K | Domain of unknown function (DUF1836) | ||
AHMNLFMI_05219 | 7.7e-61 | |||||
AHMNLFMI_05220 | 1.4e-36 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05221 | 5.7e-103 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05222 | 4.7e-42 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05223 | 3.9e-32 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05224 | 3.9e-32 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05225 | 6.8e-28 | N | domain, Protein | |||
AHMNLFMI_05226 | 6.8e-28 | N | domain, Protein | |||
AHMNLFMI_05227 | 2.8e-21 | M | domain protein | |||
AHMNLFMI_05228 | 1.7e-25 | M | self proteolysis | |||
AHMNLFMI_05229 | 2.8e-21 | M | domain protein | |||
AHMNLFMI_05230 | 2.6e-63 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
AHMNLFMI_05231 | 9.1e-184 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_05232 | 6e-31 | cspC | K | Cold shock protein | ||
AHMNLFMI_05233 | 1.8e-111 | thrE | S | Putative threonine/serine exporter | ||
AHMNLFMI_05234 | 3.2e-169 | pepC | 3.4.22.40 | E | aminopeptidase | |
AHMNLFMI_05235 | 5.5e-42 | 2.6.1.2, 2.6.1.66 | K | Bacteriophage CI repressor helix-turn-helix domain | ||
AHMNLFMI_05236 | 8e-88 | thrE | S | Putative threonine/serine exporter | ||
AHMNLFMI_05237 | 9.4e-40 | S | Threonine/Serine exporter, ThrE | |||
AHMNLFMI_05238 | 3.7e-38 | thrE | S | Putative threonine/serine exporter | ||
AHMNLFMI_05239 | 1.1e-77 | L | Phage terminase, small subunit | |||
AHMNLFMI_05240 | 7.4e-15 | S | Phage Terminase | |||
AHMNLFMI_05241 | 4.1e-51 | S | Phage Terminase | |||
AHMNLFMI_05242 | 5.5e-26 | S | Phage Terminase | |||
AHMNLFMI_05243 | 6.5e-49 | S | Phage Terminase | |||
AHMNLFMI_05244 | 1.7e-29 | S | CAAX protease self-immunity | |||
AHMNLFMI_05245 | 1.5e-66 | mesE | M | Transport protein ComB | ||
AHMNLFMI_05246 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
AHMNLFMI_05247 | 6.7e-23 | |||||
AHMNLFMI_05249 | 7.7e-92 | S | ECF-type riboflavin transporter, S component | |||
AHMNLFMI_05250 | 8.6e-48 | |||||
AHMNLFMI_05251 | 2.6e-127 | yceI | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05252 | 1.2e-52 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
AHMNLFMI_05253 | 1.2e-163 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
AHMNLFMI_05254 | 7.8e-102 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
AHMNLFMI_05255 | 8.6e-11 | K | Helix-turn-helix domain | |||
AHMNLFMI_05256 | 3.7e-71 | K | Helix-turn-helix domain | |||
AHMNLFMI_05257 | 1.3e-83 | rsmC | 2.1.1.172 | J | Methyltransferase | |
AHMNLFMI_05258 | 5.1e-99 | rsmC | 2.1.1.172 | J | Methyltransferase | |
AHMNLFMI_05259 | 1.4e-72 | rsmC | 2.1.1.172 | J | Methyltransferase | |
AHMNLFMI_05260 | 3e-57 | gntR | K | rpiR family | ||
AHMNLFMI_05261 | 9.8e-53 | gntR | K | rpiR family | ||
AHMNLFMI_05262 | 1.7e-54 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AHMNLFMI_05263 | 1.8e-65 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
AHMNLFMI_05264 | 1.7e-72 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AHMNLFMI_05265 | 2.3e-27 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
AHMNLFMI_05266 | 4e-90 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
AHMNLFMI_05270 | 2.6e-41 | xylP1 | G | MFS/sugar transport protein | ||
AHMNLFMI_05272 | 2.4e-80 | 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) | |
AHMNLFMI_05273 | 6.8e-84 | 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) | |
AHMNLFMI_05274 | 6.3e-49 | S | head-tail joining protein | |||
AHMNLFMI_05275 | 1.1e-34 | L | HNH endonuclease | |||
AHMNLFMI_05276 | 1.6e-120 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
AHMNLFMI_05277 | 7.5e-20 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
AHMNLFMI_05278 | 8.3e-40 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
AHMNLFMI_05279 | 7.7e-135 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_05280 | 3.5e-37 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_05281 | 6.6e-34 | pbuG | S | Permease family | ||
AHMNLFMI_05282 | 1.8e-12 | pbuG | S | Permease family | ||
AHMNLFMI_05283 | 5.3e-23 | 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 | |
AHMNLFMI_05284 | 1.9e-192 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
AHMNLFMI_05285 | 9.3e-37 | 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 | ||
AHMNLFMI_05286 | 6.4e-67 | 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 | ||
AHMNLFMI_05287 | 1.5e-68 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
AHMNLFMI_05288 | 3.3e-77 | 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 | ||
AHMNLFMI_05289 | 4.9e-10 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AHMNLFMI_05290 | 2.9e-23 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHMNLFMI_05291 | 2.4e-18 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHMNLFMI_05292 | 4.9e-10 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AHMNLFMI_05293 | 9.6e-37 | S | Domain of unknown function (DUF956) | |||
AHMNLFMI_05294 | 3.6e-56 | manN | G | system, mannose fructose sorbose family IID component | ||
AHMNLFMI_05295 | 1.4e-29 | S | Domain of unknown function (DUF956) | |||
AHMNLFMI_05296 | 1.4e-59 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_05297 | 3.3e-65 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_05298 | 9.6e-47 | levR | K | Sigma-54 interaction domain | ||
AHMNLFMI_05299 | 2.3e-49 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
AHMNLFMI_05300 | 2.5e-26 | uup | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_05301 | 6.1e-11 | uup | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_05302 | 1.1e-63 | accB | 2.3.1.12 | I | Biotin-requiring enzyme | |
AHMNLFMI_05303 | 2.2e-86 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
AHMNLFMI_05304 | 9.7e-65 | accB | 2.3.1.12 | I | Biotin-requiring enzyme | |
AHMNLFMI_05305 | 5.3e-133 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_05306 | 5.4e-33 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_05307 | 9.4e-18 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_05308 | 1.4e-26 | |||||
AHMNLFMI_05309 | 3.6e-17 | plnA | ||||
AHMNLFMI_05310 | 1e-235 | plnB | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_05311 | 9.1e-133 | plnC | K | LytTr DNA-binding domain | ||
AHMNLFMI_05312 | 3.7e-134 | plnD | K | LytTr DNA-binding domain | ||
AHMNLFMI_05313 | 1.7e-79 | S | CAAX protease self-immunity | |||
AHMNLFMI_05314 | 6.9e-27 | 2.7.7.65 | T | diguanylate cyclase activity | ||
AHMNLFMI_05315 | 3.5e-39 | 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 | |
AHMNLFMI_05316 | 1.6e-74 | pstA | P | Phosphate transport system permease protein PstA | ||
AHMNLFMI_05317 | 7.3e-30 | 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 | ||
AHMNLFMI_05318 | 4.1e-242 | 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 | ||
AHMNLFMI_05319 | 5.5e-33 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_05320 | 6.6e-116 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AHMNLFMI_05321 | 7.3e-21 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AHMNLFMI_05322 | 7e-26 | 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 | ||
AHMNLFMI_05323 | 7.7e-299 | 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 | ||
AHMNLFMI_05324 | 4.5e-53 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
AHMNLFMI_05325 | 1.5e-90 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
AHMNLFMI_05326 | 8.9e-56 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
AHMNLFMI_05327 | 3.2e-36 | lsgC | M | Glycosyl transferases group 1 | ||
AHMNLFMI_05328 | 1.4e-43 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_05329 | 1.5e-39 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_05330 | 4.3e-63 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_05331 | 8.9e-33 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_05332 | 2.9e-76 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_05333 | 1e-75 | mutY | L | A G-specific adenine glycosylase | ||
AHMNLFMI_05334 | 1.6e-38 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_05335 | 9.4e-36 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_05336 | 1.7e-156 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_05337 | 1.2e-176 | S | Bacterial protein of unknown function (DUF871) | |||
AHMNLFMI_05338 | 4e-10 | S | Cupin domain | |||
AHMNLFMI_05344 | 1.4e-99 | lysR5 | K | LysR substrate binding domain | ||
AHMNLFMI_05345 | 1.3e-19 | yxaA | S | membrane transporter protein | ||
AHMNLFMI_05346 | 5.7e-103 | lysR5 | K | LysR substrate binding domain | ||
AHMNLFMI_05347 | 1e-93 | 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 |
AHMNLFMI_05348 | 2e-38 | 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 |
AHMNLFMI_05350 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
AHMNLFMI_05351 | 2.6e-33 | 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 |
AHMNLFMI_05352 | 1.4e-156 | K | LysR substrate binding domain | |||
AHMNLFMI_05353 | 4.6e-88 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
AHMNLFMI_05354 | 5.6e-33 | luxT | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_05355 | 2.8e-144 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_05356 | 2.5e-14 | mreB | D | cell shape determining protein MreB | ||
AHMNLFMI_05357 | 2.9e-132 | mreB | D | cell shape determining protein MreB | ||
AHMNLFMI_05358 | 7.1e-29 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_05359 | 1.1e-32 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_05360 | 1.4e-86 | |||||
AHMNLFMI_05361 | 1.2e-123 | ecsA_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
AHMNLFMI_05362 | 6.6e-50 | ecsA_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
AHMNLFMI_05363 | 6.4e-37 | lacL | 3.2.1.23 | G | hydrolase activity, hydrolyzing O-glycosyl compounds | |
AHMNLFMI_05364 | 1.8e-44 | lacL | 3.2.1.23 | G | hydrolase activity, hydrolyzing O-glycosyl compounds | |
AHMNLFMI_05365 | 6.6e-69 | lacL | 3.2.1.23 | G | hydrolase activity, hydrolyzing O-glycosyl compounds | |
AHMNLFMI_05366 | 1.4e-34 | lacL | 3.2.1.23 | G | hydrolase activity, hydrolyzing O-glycosyl compounds | |
AHMNLFMI_05367 | 1.8e-63 | S | Virulence-associated protein E | |||
AHMNLFMI_05368 | 1.6e-68 | S | Virulence-associated protein E | |||
AHMNLFMI_05369 | 1e-64 | |||||
AHMNLFMI_05371 | 1.8e-18 | S | UPF0316 protein | |||
AHMNLFMI_05372 | 1.2e-32 | 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 | |
AHMNLFMI_05374 | 9.1e-104 | 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 | |
AHMNLFMI_05375 | 3.7e-26 | S | UPF0316 protein | |||
AHMNLFMI_05376 | 6.9e-39 | yjjH | S | Calcineurin-like phosphoesterase | ||
AHMNLFMI_05379 | 1e-29 | yjjH | S | Calcineurin-like phosphoesterase | ||
AHMNLFMI_05382 | 9e-77 | sip | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_05383 | 3.2e-78 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05384 | 7.9e-34 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05385 | 3.7e-118 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05386 | 5.3e-58 | S | Phage major capsid protein E | |||
AHMNLFMI_05388 | 2e-175 | S | Phage major capsid protein E | |||
AHMNLFMI_05389 | 1.1e-29 | |||||
AHMNLFMI_05390 | 4.7e-34 | znuB | U | ABC 3 transport family | ||
AHMNLFMI_05391 | 3.3e-128 | znuB | U | ABC 3 transport family | ||
AHMNLFMI_05398 | 8.8e-33 | yttB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05399 | 1.8e-212 | yttB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05400 | 2.9e-269 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_05401 | 4.9e-87 | nrdI | F | Belongs to the NrdI family | ||
AHMNLFMI_05402 | 2.9e-08 | nrdI | F | Belongs to the NrdI family | ||
AHMNLFMI_05403 | 1.4e-15 | 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 | ||
AHMNLFMI_05404 | 1.7e-25 | 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 | ||
AHMNLFMI_05405 | 1.5e-20 | 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 | ||
AHMNLFMI_05406 | 5.1e-42 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_05407 | 3.9e-40 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_05408 | 1.1e-35 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_05409 | 1.5e-09 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_05410 | 5.4e-77 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
AHMNLFMI_05411 | 5.4e-77 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
AHMNLFMI_05412 | 4.7e-33 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
AHMNLFMI_05413 | 9.7e-59 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
AHMNLFMI_05414 | 4.9e-78 | yneH | 1.20.4.1 | K | ArsC family | |
AHMNLFMI_05416 | 7.9e-41 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
AHMNLFMI_05417 | 5.4e-81 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05418 | 1.3e-88 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05419 | 5.3e-28 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
AHMNLFMI_05420 | 6.8e-57 | |||||
AHMNLFMI_05421 | 1.5e-26 | |||||
AHMNLFMI_05422 | 1.5e-26 | |||||
AHMNLFMI_05423 | 3.1e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_05424 | 1.2e-50 | |||||
AHMNLFMI_05425 | 4.5e-55 | |||||
AHMNLFMI_05426 | 1.6e-137 | pltR | K | LytTr DNA-binding domain | ||
AHMNLFMI_05427 | 6e-28 | pltK | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_05428 | 2.3e-44 | ypbD | S | CAAX protease self-immunity | ||
AHMNLFMI_05429 | 5.5e-95 | S | CAAX protease self-immunity | |||
AHMNLFMI_05430 | 1e-227 | mesE | M | Transport protein ComB | ||
AHMNLFMI_05431 | 1.9e-52 | S | Putative adhesin | |||
AHMNLFMI_05432 | 9.6e-58 | |||||
AHMNLFMI_05433 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
AHMNLFMI_05434 | 8.5e-78 | 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 | ||
AHMNLFMI_05435 | 1.9e-18 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_05436 | 3.7e-60 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
AHMNLFMI_05437 | 3.9e-162 | GM | NmrA-like family | |||
AHMNLFMI_05438 | 6.2e-15 | pbuG | S | Permease family | ||
AHMNLFMI_05440 | 2.3e-122 | phnE | 3.6.1.63 | U | Phosphonate ABC transporter permease | |
AHMNLFMI_05441 | 2.8e-10 | phnE1 | 3.6.1.63 | U | ABC transporter permease | |
AHMNLFMI_05442 | 1.1e-55 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05443 | 1.3e-52 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AHMNLFMI_05444 | 3e-25 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHMNLFMI_05445 | 8.1e-39 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHMNLFMI_05446 | 4.5e-41 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHMNLFMI_05447 | 1.1e-80 | S | Protein of unknown function (DUF3021) | |||
AHMNLFMI_05448 | 2.9e-57 | treR | K | UTRA | ||
AHMNLFMI_05449 | 6.3e-159 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_05450 | 1.8e-10 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AHMNLFMI_05451 | 1.2e-120 | scrR | K | Transcriptional regulator, LacI family | ||
AHMNLFMI_05452 | 5e-28 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHMNLFMI_05453 | 1.6e-78 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
AHMNLFMI_05455 | 1e-29 | 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) | |
AHMNLFMI_05456 | 1.8e-84 | 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 | ||
AHMNLFMI_05457 | 1.9e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
AHMNLFMI_05458 | 7.3e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
AHMNLFMI_05459 | 9.9e-57 | |||||
AHMNLFMI_05460 | 2.8e-230 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AHMNLFMI_05461 | 5.7e-177 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
AHMNLFMI_05462 | 9e-124 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AHMNLFMI_05463 | 1.9e-23 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AHMNLFMI_05464 | 2.9e-129 | M | hydrolase, family 25 | |||
AHMNLFMI_05465 | 7.1e-104 | mccF | V | LD-carboxypeptidase | ||
AHMNLFMI_05466 | 4.5e-44 | mccF | V | LD-carboxypeptidase | ||
AHMNLFMI_05467 | 2.5e-164 | mccF | V | LD-carboxypeptidase | ||
AHMNLFMI_05468 | 3.1e-104 | K | transcriptional regulator | |||
AHMNLFMI_05469 | 2.7e-123 | 2.7.6.5 | S | RelA SpoT domain protein | ||
AHMNLFMI_05470 | 1.3e-47 | |||||
AHMNLFMI_05471 | 1.6e-45 | |||||
AHMNLFMI_05472 | 1.4e-52 | 2.7.6.5 | S | RelA SpoT domain protein | ||
AHMNLFMI_05473 | 1.6e-24 | 2.7.6.5 | S | RelA SpoT domain protein | ||
AHMNLFMI_05474 | 7.6e-63 | 2.7.6.5 | S | RelA SpoT domain protein | ||
AHMNLFMI_05475 | 1.4e-31 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
AHMNLFMI_05476 | 4e-69 | S | Bacterial protein of unknown function (DUF871) | |||
AHMNLFMI_05477 | 6.9e-159 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
AHMNLFMI_05478 | 1.4e-31 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
AHMNLFMI_05479 | 2.7e-46 | S | Bacterial protein of unknown function (DUF871) | |||
AHMNLFMI_05481 | 1.8e-209 | S | Phage integrase family | |||
AHMNLFMI_05485 | 3.1e-25 | L | Belongs to the 'phage' integrase family | |||
AHMNLFMI_05486 | 1.1e-25 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
AHMNLFMI_05487 | 1.5e-17 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_05488 | 6.3e-67 | 1.14.99.53 | AA10 | S | Lytic polysaccharide mono-oxygenase, cellulose-degrading | |
AHMNLFMI_05489 | 3.8e-20 | 1.14.99.53 | AA10 | S | Lytic polysaccharide mono-oxygenase, cellulose-degrading | |
AHMNLFMI_05490 | 1.6e-82 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
AHMNLFMI_05491 | 1.2e-113 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_05492 | 8.7e-22 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_05493 | 7.7e-28 | nlhH_1 | I | alpha/beta hydrolase fold | ||
AHMNLFMI_05494 | 1.2e-77 | xylP2 | G | symporter | ||
AHMNLFMI_05495 | 1.5e-38 | xylP2 | G | symporter | ||
AHMNLFMI_05496 | 8.8e-94 | yvgN | C | Aldo keto reductase | ||
AHMNLFMI_05497 | 2.7e-45 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_05498 | 2.8e-184 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_05499 | 3.6e-51 | ylbB | V | ABC transporter permease | ||
AHMNLFMI_05500 | 2.9e-51 | 1.14.14.9 | Q | 4-hydroxyphenylacetate | ||
AHMNLFMI_05501 | 7.7e-103 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHMNLFMI_05502 | 9.6e-169 | 1.14.14.9 | Q | 4-hydroxyphenylacetate | ||
AHMNLFMI_05503 | 1.5e-25 | 1.14.14.9 | Q | 4-hydroxyphenylacetate | ||
AHMNLFMI_05504 | 1e-118 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AHMNLFMI_05505 | 7.1e-48 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_05506 | 3.3e-84 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_05507 | 1.7e-51 | proV | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
AHMNLFMI_05508 | 4.5e-25 | proWX | P | ABC-type proline glycine betaine transport systems, permease component | ||
AHMNLFMI_05509 | 2e-132 | proV | E | ABC transporter, ATP-binding protein | ||
AHMNLFMI_05510 | 3e-34 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_05511 | 9.6e-43 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_05512 | 5.9e-36 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_05513 | 4.6e-08 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_05514 | 6.2e-39 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_05515 | 1.4e-185 | D | NLP P60 protein | |||
AHMNLFMI_05516 | 2.2e-33 | |||||
AHMNLFMI_05517 | 6.3e-64 | |||||
AHMNLFMI_05518 | 6.9e-78 | S | Phage tail tube protein, TTP | |||
AHMNLFMI_05519 | 1.4e-54 | |||||
AHMNLFMI_05520 | 2.7e-89 | |||||
AHMNLFMI_05521 | 1.5e-25 | |||||
AHMNLFMI_05522 | 4.3e-21 | |||||
AHMNLFMI_05523 | 2.2e-187 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AHMNLFMI_05524 | 2.4e-87 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
AHMNLFMI_05525 | 6.5e-38 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
AHMNLFMI_05526 | 2.4e-77 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
AHMNLFMI_05527 | 3.8e-18 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_05528 | 2.4e-104 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_05529 | 1.3e-22 | mdlA | V | ABC transporter | ||
AHMNLFMI_05530 | 7.7e-25 | |||||
AHMNLFMI_05531 | 4.3e-65 | |||||
AHMNLFMI_05532 | 7e-43 | |||||
AHMNLFMI_05534 | 6.4e-41 | |||||
AHMNLFMI_05536 | 2.9e-42 | |||||
AHMNLFMI_05537 | 1.2e-25 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_05538 | 8e-111 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_05539 | 1.6e-08 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
AHMNLFMI_05540 | 2.1e-38 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_05541 | 6.4e-49 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_05542 | 5.1e-49 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_05543 | 1.3e-46 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_05544 | 1.3e-11 | S | Membrane | |||
AHMNLFMI_05545 | 1.5e-69 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_05546 | 1.3e-118 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_05547 | 4.3e-64 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_05548 | 2.9e-38 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_05549 | 5.1e-27 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
AHMNLFMI_05550 | 8.9e-126 | czcD | P | cation diffusion facilitator family transporter | ||
AHMNLFMI_05551 | 1.5e-70 | czcD | P | cation diffusion facilitator family transporter | ||
AHMNLFMI_05552 | 2e-82 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_05553 | 3.7e-76 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AHMNLFMI_05554 | 4.3e-26 | citP | P | Sodium:sulfate symporter transmembrane region | ||
AHMNLFMI_05555 | 1.2e-31 | mesE | M | Transport protein ComB | ||
AHMNLFMI_05556 | 7.5e-75 | mesE | M | Transport protein ComB | ||
AHMNLFMI_05557 | 5.8e-82 | 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 | ||
AHMNLFMI_05558 | 9.1e-56 | 1.6.5.5 | C | Alcohol dehydrogenase GroES-like domain | ||
AHMNLFMI_05559 | 1.2e-39 | uspA | T | Belongs to the universal stress protein A family | ||
AHMNLFMI_05560 | 2.7e-55 | uspA | T | Belongs to the universal stress protein A family | ||
AHMNLFMI_05561 | 1.2e-39 | uspA | T | Belongs to the universal stress protein A family | ||
AHMNLFMI_05562 | 1.8e-51 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05563 | 9.6e-63 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05564 | 2.6e-72 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05565 | 2.7e-80 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05566 | 7.4e-97 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
AHMNLFMI_05567 | 8e-68 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
AHMNLFMI_05568 | 7.4e-37 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
AHMNLFMI_05569 | 5.9e-21 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
AHMNLFMI_05570 | 5.8e-38 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHMNLFMI_05571 | 1.2e-08 | 1.14.99.53 | AA10 | S | Lytic polysaccharide mono-oxygenase, cellulose-degrading | |
AHMNLFMI_05572 | 1.4e-20 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AHMNLFMI_05573 | 1.7e-69 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AHMNLFMI_05574 | 9.7e-36 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AHMNLFMI_05575 | 4.4e-168 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AHMNLFMI_05576 | 6.2e-157 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHMNLFMI_05577 | 6.9e-44 | mdtG | EGP | Major Facilitator Superfamily | ||
AHMNLFMI_05578 | 6.3e-29 | yajC | U | Preprotein translocase | ||
AHMNLFMI_05579 | 1.1e-204 | 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) | |
AHMNLFMI_05582 | 7.5e-65 | S | DNA/RNA non-specific endonuclease | |||
AHMNLFMI_05583 | 1.6e-91 | cwlO | M | NlpC/P60 family | ||
AHMNLFMI_05584 | 4.1e-106 | ygaC | J | Belongs to the UPF0374 family | ||
AHMNLFMI_05585 | 6.7e-63 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
AHMNLFMI_05586 | 8.1e-13 | cwlO | M | NlpC/P60 family | ||
AHMNLFMI_05587 | 8.1e-13 | cwlO | M | NlpC/P60 family | ||
AHMNLFMI_05588 | 8.1e-13 | cwlO | M | NlpC/P60 family | ||
AHMNLFMI_05589 | 8.1e-13 | cwlO | M | NlpC/P60 family | ||
AHMNLFMI_05590 | 8.1e-13 | cwlO | M | NlpC/P60 family | ||
AHMNLFMI_05591 | 1.3e-208 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_05592 | 2.1e-32 | 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 | ||
AHMNLFMI_05593 | 1.3e-145 | 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 | ||
AHMNLFMI_05594 | 9e-12 | S | Phage tail protein | |||
AHMNLFMI_05595 | 5.8e-24 | S | Phage tail protein | |||
AHMNLFMI_05597 | 1.1e-71 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_05598 | 1.9e-26 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_05599 | 1.9e-297 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05600 | 2.4e-124 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_05601 | 8.9e-238 | M | MucBP domain | |||
AHMNLFMI_05602 | 6.5e-75 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_05603 | 8.3e-32 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_05604 | 9.5e-22 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHMNLFMI_05605 | 3.1e-59 | pnb | C | nitroreductase | ||
AHMNLFMI_05606 | 2.6e-64 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
AHMNLFMI_05607 | 2e-103 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHMNLFMI_05608 | 1e-102 | 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 | |
AHMNLFMI_05609 | 2.7e-39 | 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 | ||
AHMNLFMI_05610 | 6.7e-81 | |||||
AHMNLFMI_05611 | 5.5e-99 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_05612 | 9.6e-41 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_05613 | 1.2e-79 | 3.1.3.18 | J | HAD-hyrolase-like | ||
AHMNLFMI_05614 | 1.2e-61 | 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 | ||
AHMNLFMI_05615 | 2.3e-127 | yniA | G | Fructosamine kinase | ||
AHMNLFMI_05616 | 7.3e-95 | 3.1.3.18 | J | HAD-hyrolase-like | ||
AHMNLFMI_05617 | 1.1e-71 | 3.1.3.18 | J | HAD-hyrolase-like | ||
AHMNLFMI_05618 | 8.4e-52 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AHMNLFMI_05619 | 4.1e-91 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AHMNLFMI_05620 | 1.2e-71 | cps4J | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_05621 | 2.6e-55 | cpdA | S | Calcineurin-like phosphoesterase | ||
AHMNLFMI_05622 | 3.2e-173 | cpdA | S | Calcineurin-like phosphoesterase | ||
AHMNLFMI_05623 | 7.6e-169 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
AHMNLFMI_05624 | 1.1e-68 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHMNLFMI_05625 | 1.2e-43 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
AHMNLFMI_05626 | 1.8e-101 | tarL | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_05628 | 2.2e-07 | ybbL | S | ATPases associated with a variety of cellular activities | ||
AHMNLFMI_05629 | 6.8e-128 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
AHMNLFMI_05630 | 3.1e-39 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
AHMNLFMI_05631 | 8.5e-33 | rbsU | U | ribose uptake protein RbsU | ||
AHMNLFMI_05632 | 7.9e-67 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
AHMNLFMI_05633 | 3.6e-55 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
AHMNLFMI_05634 | 8e-163 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
AHMNLFMI_05635 | 5.9e-188 | rbsR | K | helix_turn _helix lactose operon repressor | ||
AHMNLFMI_05636 | 2.5e-109 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHMNLFMI_05637 | 1.7e-15 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
AHMNLFMI_05638 | 4.1e-37 | gabR | K | Bacterial regulatory proteins, gntR family | ||
AHMNLFMI_05639 | 7e-236 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
AHMNLFMI_05640 | 3.2e-44 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AHMNLFMI_05641 | 8e-49 | 2.7.7.65 | T | diguanylate cyclase activity | ||
AHMNLFMI_05642 | 3.3e-19 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AHMNLFMI_05643 | 3.2e-109 | tarL | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_05644 | 1.5e-39 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_05645 | 2.9e-188 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_05646 | 3.3e-40 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_05647 | 9.6e-68 | ktrA | P | domain protein | ||
AHMNLFMI_05648 | 3.3e-36 | ktrB | P | Potassium uptake protein | ||
AHMNLFMI_05649 | 2.4e-37 | D | NLP P60 protein | |||
AHMNLFMI_05650 | 2.1e-215 | D | NLP P60 protein | |||
AHMNLFMI_05651 | 5e-60 | |||||
AHMNLFMI_05652 | 3e-47 | sidC | GT2,GT4 | LM | DNA recombination | |
AHMNLFMI_05653 | 7.6e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
AHMNLFMI_05654 | 5e-24 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
AHMNLFMI_05655 | 1.5e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
AHMNLFMI_05656 | 6.8e-62 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
AHMNLFMI_05658 | 3.6e-45 | dnaD | L | Replication initiation and membrane attachment | ||
AHMNLFMI_05660 | 1.3e-114 | dnaD | L | Replication initiation and membrane attachment | ||
AHMNLFMI_05661 | 5.5e-56 | whiA | K | May be required for sporulation | ||
AHMNLFMI_05662 | 1.7e-55 | XK27_08835 | S | ABC transporter | ||
AHMNLFMI_05663 | 1.8e-24 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AHMNLFMI_05664 | 4.6e-20 | XK27_08835 | S | ABC transporter | ||
AHMNLFMI_05665 | 4.4e-56 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_05666 | 4.6e-140 | 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 | |
AHMNLFMI_05667 | 4.5e-73 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
AHMNLFMI_05669 | 2.4e-50 | L | Transposase | |||
AHMNLFMI_05670 | 2.4e-32 | L | Transposase | |||
AHMNLFMI_05671 | 1.7e-142 | S | membrane | |||
AHMNLFMI_05672 | 1.4e-96 | L | Transposase | |||
AHMNLFMI_05673 | 3.2e-54 | L | Transposase | |||
AHMNLFMI_05674 | 5e-34 | lemA | S | LemA family | ||
AHMNLFMI_05676 | 1.7e-41 | lemA | S | LemA family | ||
AHMNLFMI_05677 | 4.6e-139 | htpX | O | Belongs to the peptidase M48B family | ||
AHMNLFMI_05678 | 6.3e-30 | htpX | O | Belongs to the peptidase M48B family | ||
AHMNLFMI_05679 | 1.1e-33 | htpX | O | Belongs to the peptidase M48B family | ||
AHMNLFMI_05680 | 1.3e-19 | htpX | O | Belongs to the peptidase M48B family | ||
AHMNLFMI_05681 | 1.4e-90 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_05683 | 4.8e-91 | rfbX | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
AHMNLFMI_05684 | 9.6e-74 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_05685 | 1.8e-183 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
AHMNLFMI_05686 | 1.6e-90 | pbuX | F | xanthine permease | ||
AHMNLFMI_05687 | 1.3e-64 | pucR | QT | Purine catabolism regulatory protein-like family | ||
AHMNLFMI_05688 | 1.1e-92 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_05690 | 1.6e-13 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
AHMNLFMI_05691 | 8.4e-108 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
AHMNLFMI_05693 | 1.2e-85 | S | AAA domain | |||
AHMNLFMI_05694 | 2.9e-139 | K | sequence-specific DNA binding | |||
AHMNLFMI_05695 | 2.5e-20 | E | lipolytic protein G-D-S-L family | |||
AHMNLFMI_05696 | 3.9e-171 | fhuG | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHMNLFMI_05697 | 7.8e-38 | fhuG | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHMNLFMI_05698 | 4.4e-40 | fhuG | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHMNLFMI_05699 | 3.4e-07 | S | Protein conserved in bacteria | |||
AHMNLFMI_05700 | 6.7e-67 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_05701 | 3.7e-39 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_05702 | 5e-16 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_05703 | 2.6e-199 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHMNLFMI_05704 | 3.5e-102 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_05705 | 1.2e-20 | mtlR | K | Mga helix-turn-helix domain | ||
AHMNLFMI_05706 | 3.6e-41 | oppD | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_05707 | 1.4e-104 | oppD | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_05708 | 8.4e-114 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
AHMNLFMI_05709 | 5.3e-76 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
AHMNLFMI_05710 | 3.4e-60 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
AHMNLFMI_05711 | 1.1e-74 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHMNLFMI_05712 | 4.6e-128 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_05713 | 9.1e-37 | S | Phage portal protein, SPP1 Gp6-like | |||
AHMNLFMI_05714 | 6.2e-27 | S | Phage terminase, large subunit, PBSX family | |||
AHMNLFMI_05716 | 2.3e-47 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_05717 | 2.1e-67 | npr | 1.11.1.1 | C | NADH oxidase | |
AHMNLFMI_05718 | 9.7e-55 | ecsA_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
AHMNLFMI_05719 | 2.2e-42 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
AHMNLFMI_05720 | 1.8e-60 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
AHMNLFMI_05721 | 7.4e-58 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05722 | 1.4e-55 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05723 | 2.1e-44 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05724 | 1.9e-39 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_05725 | 1.2e-84 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
AHMNLFMI_05726 | 7.3e-124 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
AHMNLFMI_05727 | 4.9e-68 | epsB | M | biosynthesis protein | ||
AHMNLFMI_05728 | 5.1e-54 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
AHMNLFMI_05729 | 6.9e-51 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
AHMNLFMI_05730 | 3.8e-90 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
AHMNLFMI_05731 | 7.5e-110 | S | Protein of unknown function (DUF2785) | |||
AHMNLFMI_05732 | 2.9e-35 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_05733 | 3.6e-69 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AHMNLFMI_05734 | 4.9e-174 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_05735 | 9.8e-30 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_05736 | 1.5e-94 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_05737 | 1.6e-41 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_05738 | 1.4e-31 | L | Transposase | |||
AHMNLFMI_05739 | 2.9e-46 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_05740 | 1.8e-142 | 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) | |
AHMNLFMI_05741 | 1.9e-244 | chbC | 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 | ||
AHMNLFMI_05742 | 2.4e-31 | 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 | ||
AHMNLFMI_05743 | 1.7e-17 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHMNLFMI_05744 | 1.6e-56 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHMNLFMI_05745 | 2.7e-31 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_05746 | 4.8e-29 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_05747 | 2.9e-90 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_05748 | 3.2e-25 | ypcB | S | integral membrane protein | ||
AHMNLFMI_05749 | 1.7e-163 | yesM | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_05750 | 4.1e-107 | ypcB | S | integral membrane protein | ||
AHMNLFMI_05751 | 2e-100 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_05752 | 1.1e-44 | 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 | ||
AHMNLFMI_05753 | 3.2e-46 | |||||
AHMNLFMI_05754 | 3.5e-26 | arlS | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_05755 | 1.8e-97 | arlS | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_05756 | 4.3e-121 | K | response regulator | |||
AHMNLFMI_05757 | 8.9e-87 | rarA | L | recombination factor protein RarA | ||
AHMNLFMI_05758 | 2.6e-62 | rarA | L | recombination factor protein RarA | ||
AHMNLFMI_05759 | 5.7e-25 | gabR | K | Bacterial regulatory proteins, gntR family | ||
AHMNLFMI_05761 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
AHMNLFMI_05762 | 1.9e-38 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_05763 | 6.4e-160 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
AHMNLFMI_05764 | 4.9e-22 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AHMNLFMI_05765 | 1.5e-66 | yycH | S | YycH protein | ||
AHMNLFMI_05766 | 6.5e-207 | yycH | S | YycH protein | ||
AHMNLFMI_05767 | 3.1e-27 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AHMNLFMI_05768 | 6.3e-93 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AHMNLFMI_05769 | 4.1e-52 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AHMNLFMI_05770 | 1.8e-26 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_05771 | 1.3e-57 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_05772 | 4.1e-38 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AHMNLFMI_05773 | 2.8e-32 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_05774 | 1.8e-30 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_05775 | 9.5e-44 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
AHMNLFMI_05776 | 8.5e-40 | |||||
AHMNLFMI_05777 | 1.5e-70 | |||||
AHMNLFMI_05778 | 3.6e-54 | |||||
AHMNLFMI_05779 | 3.6e-54 | |||||
AHMNLFMI_05780 | 3.5e-22 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
AHMNLFMI_05781 | 6.3e-196 | XK27_00915 | C | Luciferase-like monooxygenase | ||
AHMNLFMI_05782 | 1.1e-16 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
AHMNLFMI_05783 | 4.3e-39 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_05784 | 5.2e-84 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_05785 | 6e-30 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
AHMNLFMI_05786 | 1.1e-65 | 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 | ||
AHMNLFMI_05787 | 2.8e-38 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHMNLFMI_05788 | 3e-18 | |||||
AHMNLFMI_05789 | 3e-18 | |||||
AHMNLFMI_05790 | 1.9e-89 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHMNLFMI_05791 | 3e-18 | |||||
AHMNLFMI_05792 | 5.4e-126 | S | membrane transporter protein | |||
AHMNLFMI_05793 | 5.7e-31 | S | membrane transporter protein | |||
AHMNLFMI_05794 | 4.4e-83 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
AHMNLFMI_05795 | 9.3e-31 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
AHMNLFMI_05796 | 2.9e-74 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
AHMNLFMI_05798 | 2.9e-128 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
AHMNLFMI_05799 | 4.5e-10 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
AHMNLFMI_05813 | 5.5e-08 | |||||
AHMNLFMI_05822 | 5.1e-34 | S | protein disulfide oxidoreductase activity | |||
AHMNLFMI_05823 | 1.3e-66 | S | protein disulfide oxidoreductase activity | |||
AHMNLFMI_05824 | 1.4e-123 | ugpE | G | ABC transporter permease | ||
AHMNLFMI_05825 | 6e-52 | ugpA | U | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_05826 | 6.9e-48 | ugpA | U | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_05827 | 4.1e-23 | terL | S | overlaps another CDS with the same product name | ||
AHMNLFMI_05828 | 1.6e-78 | terL | S | overlaps another CDS with the same product name | ||
AHMNLFMI_05829 | 4.6e-181 | terL | S | overlaps another CDS with the same product name | ||
AHMNLFMI_05830 | 2.7e-82 | terS | L | overlaps another CDS with the same product name | ||
AHMNLFMI_05831 | 8.5e-257 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
AHMNLFMI_05832 | 8.2e-70 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
AHMNLFMI_05833 | 6e-31 | cspA | K | Cold shock protein | ||
AHMNLFMI_05834 | 1.4e-39 | |||||
AHMNLFMI_05837 | 4.5e-88 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_05838 | 1.2e-37 | yceI | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05839 | 1.2e-91 | nox | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_05840 | 2.8e-14 | S | Alpha beta hydrolase | |||
AHMNLFMI_05841 | 1.3e-44 | C | nadph quinone reductase | |||
AHMNLFMI_05842 | 1.1e-29 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_05843 | 3e-145 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_05844 | 6.3e-32 | ypcB | S | integral membrane protein | ||
AHMNLFMI_05845 | 9.2e-193 | V | FtsX-like permease family | |||
AHMNLFMI_05846 | 1.1e-110 | potD | P | ABC transporter | ||
AHMNLFMI_05847 | 6.2e-26 | potD | P | ABC transporter | ||
AHMNLFMI_05848 | 1.1e-125 | potD | P | ABC transporter | ||
AHMNLFMI_05849 | 2.1e-22 | L | Replication initiation and membrane attachment | |||
AHMNLFMI_05850 | 1.8e-69 | pi346 | L | IstB-like ATP binding protein | ||
AHMNLFMI_05851 | 3.6e-71 | L | DnaD domain protein | |||
AHMNLFMI_05852 | 3.7e-14 | S | Putative HNHc nuclease | |||
AHMNLFMI_05855 | 2.6e-14 | |||||
AHMNLFMI_05856 | 5.5e-50 | yvlA | ||||
AHMNLFMI_05857 | 2.9e-54 | K | transcriptional regulator | |||
AHMNLFMI_05858 | 1.4e-211 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_05859 | 2.9e-61 | treR | K | UTRA | ||
AHMNLFMI_05860 | 1.2e-54 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_05861 | 1.4e-46 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_05862 | 9.1e-12 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05863 | 2.7e-54 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05864 | 1.5e-199 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05865 | 4.3e-40 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05866 | 1e-19 | |||||
AHMNLFMI_05867 | 3.6e-45 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHMNLFMI_05868 | 3.7e-48 | |||||
AHMNLFMI_05869 | 2.1e-30 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHMNLFMI_05870 | 5.7e-25 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_05871 | 2.5e-28 | 2.7.1.191 | G | PTS system fructose IIA component | ||
AHMNLFMI_05872 | 4.2e-209 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
AHMNLFMI_05873 | 6.9e-28 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_05874 | 3.1e-13 | sidC | GT2,GT4 | LM | DNA recombination | |
AHMNLFMI_05875 | 8.7e-67 | sidC | GT2,GT4 | LM | DNA recombination | |
AHMNLFMI_05876 | 1.5e-99 | 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 | ||
AHMNLFMI_05877 | 4.6e-58 | 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 | ||
AHMNLFMI_05878 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
AHMNLFMI_05879 | 2.2e-90 | 3.6.1.55 | F | NUDIX domain | ||
AHMNLFMI_05881 | 2.2e-18 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
AHMNLFMI_05883 | 3.6e-134 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
AHMNLFMI_05884 | 3.5e-69 | S | LuxR family transcriptional regulator | |||
AHMNLFMI_05885 | 4.6e-128 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
AHMNLFMI_05886 | 3.1e-73 | 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 | |
AHMNLFMI_05887 | 6.4e-136 | 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 | |
AHMNLFMI_05888 | 1.2e-93 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
AHMNLFMI_05889 | 1e-27 | 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 | |
AHMNLFMI_05890 | 3.2e-40 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
AHMNLFMI_05891 | 2e-62 | |||||
AHMNLFMI_05892 | 5e-81 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
AHMNLFMI_05893 | 2.8e-160 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
AHMNLFMI_05894 | 5.2e-13 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
AHMNLFMI_05895 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
AHMNLFMI_05896 | 7.3e-26 | 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 | ||
AHMNLFMI_05897 | 1.1e-30 | 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 | ||
AHMNLFMI_05898 | 2.2e-24 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AHMNLFMI_05899 | 8.5e-50 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AHMNLFMI_05900 | 1.9e-83 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
AHMNLFMI_05901 | 4.8e-92 | nox | C | NADH oxidase | ||
AHMNLFMI_05902 | 4.7e-241 | amtB | P | ammonium transporter | ||
AHMNLFMI_05903 | 2.5e-21 | lacS | G | Transporter | ||
AHMNLFMI_05904 | 5.3e-27 | lacS | G | Transporter | ||
AHMNLFMI_05905 | 3.6e-47 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_05906 | 3.7e-156 | sidC | GT2,GT4 | LM | DNA recombination | |
AHMNLFMI_05907 | 5.1e-70 | S | Protein of unknown function (DUF1617) | |||
AHMNLFMI_05909 | 1.2e-10 | S | Protein of unknown function (DUF1617) | |||
AHMNLFMI_05910 | 4.2e-127 | yttB | EGP | Major facilitator Superfamily | ||
AHMNLFMI_05911 | 1.1e-54 | ypaA | S | Protein of unknown function (DUF1304) | ||
AHMNLFMI_05912 | 7.2e-88 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05913 | 7.7e-103 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05914 | 1.2e-46 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_05915 | 7.9e-15 | S | Uncharacterized protein conserved in bacteria (DUF2247) | |||
AHMNLFMI_05916 | 1.4e-124 | CP_1020 | S | zinc ion binding | ||
AHMNLFMI_05917 | 1.6e-168 | cps3A | S | Glycosyltransferase like family 2 | ||
AHMNLFMI_05918 | 1e-31 | cps3B | S | Glycosyltransferase like family 2 | ||
AHMNLFMI_05919 | 6.5e-171 | |||||
AHMNLFMI_05920 | 5e-11 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AHMNLFMI_05921 | 6.6e-99 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AHMNLFMI_05922 | 1.3e-116 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AHMNLFMI_05923 | 1.4e-77 | mraZ | K | Belongs to the MraZ family | ||
AHMNLFMI_05924 | 1.9e-62 | S | Protein of unknown function (DUF3397) | |||
AHMNLFMI_05925 | 1.6e-33 | S | Protein of unknown function (DUF3397) | |||
AHMNLFMI_05926 | 8.7e-93 | K | Transcriptional regulator PadR-like family | |||
AHMNLFMI_05927 | 1.3e-35 | pgm7 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHMNLFMI_05928 | 9.6e-39 | pgm7 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHMNLFMI_05929 | 9.6e-39 | pgm7 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHMNLFMI_05930 | 3.2e-101 | pgm7 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHMNLFMI_05931 | 3.4e-65 | |||||
AHMNLFMI_05932 | 3.5e-10 | |||||
AHMNLFMI_05933 | 7e-74 | |||||
AHMNLFMI_05934 | 7.4e-89 | |||||
AHMNLFMI_05935 | 8e-136 | |||||
AHMNLFMI_05936 | 1.3e-36 | gtcA | S | Teichoic acid glycosylation protein | ||
AHMNLFMI_05938 | 5.6e-54 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHMNLFMI_05939 | 1.6e-39 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
AHMNLFMI_05941 | 2.4e-09 | ylbE | GM | NAD(P)H-binding | ||
AHMNLFMI_05943 | 4e-28 | ylbE | GM | NAD(P)H-binding | ||
AHMNLFMI_05944 | 8.2e-96 | wecD | K | Acetyltransferase (GNAT) family | ||
AHMNLFMI_05945 | 1.6e-227 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_05946 | 2.8e-67 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_05947 | 2.7e-14 | 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 | |
AHMNLFMI_05949 | 7.2e-72 | macB | V | ABC transporter, ATP-binding protein | ||
AHMNLFMI_05952 | 5.5e-88 | M | transferase activity, transferring glycosyl groups | |||
AHMNLFMI_05953 | 3.8e-102 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
AHMNLFMI_05954 | 1.5e-50 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
AHMNLFMI_05956 | 3.7e-59 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_05957 | 5.5e-41 | V | Beta-lactamase | |||
AHMNLFMI_05958 | 3.7e-22 | D | protein tyrosine kinase activity | |||
AHMNLFMI_05959 | 1.5e-19 | cps1D | M | Domain of unknown function (DUF4422) | ||
AHMNLFMI_05960 | 3e-17 | yfeX | P | Peroxidase | ||
AHMNLFMI_05961 | 2.6e-149 | 4.1.1.46 | S | Amidohydrolase | ||
AHMNLFMI_05962 | 2.5e-74 | mleR | K | LysR family transcriptional regulator | ||
AHMNLFMI_05963 | 7.1e-68 | mleR | K | LysR family | ||
AHMNLFMI_05964 | 1.8e-40 | |||||
AHMNLFMI_05965 | 6e-76 | |||||
AHMNLFMI_05966 | 3.3e-130 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
AHMNLFMI_05967 | 2.4e-59 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
AHMNLFMI_05968 | 8.5e-50 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHMNLFMI_05969 | 3.6e-66 | FbpA | K | Domain of unknown function (DUF814) | ||
AHMNLFMI_05970 | 8.3e-11 | S | Phage head-tail joining protein | |||
AHMNLFMI_05971 | 1.1e-23 | |||||
AHMNLFMI_05972 | 1.2e-17 | S | Phage head-tail joining protein | |||
AHMNLFMI_05973 | 1.3e-38 | |||||
AHMNLFMI_05974 | 2.2e-25 | 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 | ||
AHMNLFMI_05975 | 3.8e-20 | 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 | ||
AHMNLFMI_05976 | 5.2e-50 | 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 | ||
AHMNLFMI_05977 | 3.4e-35 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
AHMNLFMI_05978 | 1.9e-64 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
AHMNLFMI_05979 | 8.3e-50 | ynhH | S | NusG domain II | ||
AHMNLFMI_05980 | 6.2e-13 | scrR | K | Transcriptional regulator, LacI family | ||
AHMNLFMI_05981 | 8e-51 | scrR | K | Transcriptional regulator, LacI family | ||
AHMNLFMI_05982 | 1.1e-52 | celB | 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 | ||
AHMNLFMI_05983 | 3.9e-24 | |||||
AHMNLFMI_05984 | 9.9e-76 | S | Domain of unknown function (DUF3284) | |||
AHMNLFMI_05985 | 4.8e-52 | V | FtsX-like permease family | |||
AHMNLFMI_05986 | 8e-42 | |||||
AHMNLFMI_05987 | 1.3e-16 | gntR1 | K | Transcriptional regulator, GntR family | ||
AHMNLFMI_05988 | 3.8e-93 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
AHMNLFMI_05989 | 1.7e-224 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
AHMNLFMI_05990 | 1e-165 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
AHMNLFMI_05991 | 1.2e-28 | lacS | G | Transporter | ||
AHMNLFMI_05992 | 1.1e-34 | lacS | G | Transporter | ||
AHMNLFMI_05993 | 1.5e-41 | lacS | G | Transporter | ||
AHMNLFMI_05994 | 3.8e-185 | pva2 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
AHMNLFMI_05995 | 9.8e-39 | pva2 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
AHMNLFMI_05996 | 2.6e-20 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
AHMNLFMI_05997 | 3.7e-91 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
AHMNLFMI_05998 | 2.4e-44 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
AHMNLFMI_05999 | 1.3e-07 | 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 | ||
AHMNLFMI_06000 | 2e-13 | 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 | ||
AHMNLFMI_06001 | 9.1e-39 | 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 | ||
AHMNLFMI_06002 | 2.1e-79 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHMNLFMI_06003 | 7.1e-203 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHMNLFMI_06004 | 2.6e-08 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_06005 | 1.8e-12 | L | Helix-turn-helix domain | |||
AHMNLFMI_06006 | 2.1e-08 | L | Helix-turn-helix domain | |||
AHMNLFMI_06009 | 2.9e-37 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_06011 | 4e-09 | |||||
AHMNLFMI_06014 | 6.8e-141 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
AHMNLFMI_06015 | 1.8e-95 | E | ABC transporter, substratebinding protein | |||
AHMNLFMI_06017 | 8.3e-44 | mco | Q | Multicopper oxidase | ||
AHMNLFMI_06018 | 1.9e-96 | 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 | |
AHMNLFMI_06019 | 6.1e-43 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AHMNLFMI_06020 | 8.6e-40 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
AHMNLFMI_06021 | 4.6e-97 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_06022 | 2.5e-48 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AHMNLFMI_06023 | 4e-38 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AHMNLFMI_06024 | 4.1e-38 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AHMNLFMI_06025 | 1.3e-30 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
AHMNLFMI_06027 | 9.8e-123 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
AHMNLFMI_06028 | 5.7e-92 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
AHMNLFMI_06029 | 5.1e-63 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_06030 | 5.4e-175 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
AHMNLFMI_06031 | 5.3e-99 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AHMNLFMI_06032 | 1.6e-146 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AHMNLFMI_06033 | 2.1e-73 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_06034 | 2.4e-44 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_06035 | 3.2e-20 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_06036 | 1.7e-50 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
AHMNLFMI_06037 | 5.2e-170 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
AHMNLFMI_06038 | 6.4e-106 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
AHMNLFMI_06039 | 1.3e-249 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_06041 | 1.5e-61 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
AHMNLFMI_06042 | 1.6e-13 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
AHMNLFMI_06043 | 1.8e-43 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_06044 | 2.6e-45 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_06045 | 2e-36 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_06046 | 1.1e-48 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_06047 | 1.1e-21 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_06048 | 2.7e-247 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_06049 | 1.6e-62 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase like | ||
AHMNLFMI_06050 | 3.6e-165 | 1.1.1.65 | C | Aldo keto reductase | ||
AHMNLFMI_06051 | 5.3e-59 | S | reductase | |||
AHMNLFMI_06052 | 5.3e-75 | S | reductase | |||
AHMNLFMI_06053 | 2e-126 | hchA | S | DJ-1/PfpI family | ||
AHMNLFMI_06054 | 5.4e-181 | 1.1.1.1 | C | nadph quinone reductase | ||
AHMNLFMI_06055 | 1.9e-47 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHMNLFMI_06056 | 4.1e-34 | mepA | V | MATE efflux family protein | ||
AHMNLFMI_06057 | 3e-20 | 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 | |
AHMNLFMI_06058 | 2.8e-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 | |
AHMNLFMI_06059 | 4.8e-26 | yajC | U | Preprotein translocase | ||
AHMNLFMI_06061 | 2.5e-24 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06062 | 2.2e-137 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
AHMNLFMI_06063 | 1.3e-48 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
AHMNLFMI_06064 | 2.5e-35 | tnp2PF3 | L | manually curated | ||
AHMNLFMI_06065 | 4.2e-28 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_06066 | 7.2e-44 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_06067 | 3.7e-45 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_06068 | 7.9e-46 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
AHMNLFMI_06069 | 4.8e-17 | hol | S | Bacteriophage holin | ||
AHMNLFMI_06070 | 6.8e-171 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_06072 | 6.2e-31 | 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 | ||
AHMNLFMI_06073 | 3.6e-49 | 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 | ||
AHMNLFMI_06074 | 6.4e-29 | 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 | ||
AHMNLFMI_06075 | 1.7e-24 | yrkD | S | Metal-sensitive transcriptional repressor | ||
AHMNLFMI_06076 | 1.7e-24 | yrkD | S | Metal-sensitive transcriptional repressor | ||
AHMNLFMI_06077 | 4.3e-40 | yrkD | S | Metal-sensitive transcriptional repressor | ||
AHMNLFMI_06078 | 1.5e-55 | txlA | O | Thioredoxin-like domain | ||
AHMNLFMI_06079 | 9.8e-143 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHMNLFMI_06080 | 1.4e-276 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
AHMNLFMI_06081 | 4.7e-168 | K | Transcriptional regulator, LysR family | |||
AHMNLFMI_06082 | 7.4e-112 | EGP | Major Facilitator Superfamily | |||
AHMNLFMI_06083 | 1.3e-38 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
AHMNLFMI_06084 | 8.4e-44 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain | |
AHMNLFMI_06085 | 1.2e-163 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain | |
AHMNLFMI_06086 | 2.4e-143 | S | Phosphotransferase system, EIIC | |||
AHMNLFMI_06087 | 3.8e-74 | S | Phosphotransferase system, EIIC | |||
AHMNLFMI_06089 | 2.1e-48 | L | transposase activity | |||
AHMNLFMI_06093 | 1.8e-66 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_06094 | 3.6e-18 | arpU | S | Phage transcriptional regulator, ArpU family | ||
AHMNLFMI_06095 | 1.8e-38 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_06096 | 5.8e-62 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_06097 | 6.2e-38 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_06098 | 1.2e-67 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
AHMNLFMI_06099 | 1.9e-121 | comFA | L | Helicase C-terminal domain protein | ||
AHMNLFMI_06100 | 4.8e-125 | comFC | S | Competence protein | ||
AHMNLFMI_06101 | 3.5e-19 | 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 | ||
AHMNLFMI_06102 | 1.2e-115 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
AHMNLFMI_06103 | 1.6e-91 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
AHMNLFMI_06104 | 3.2e-14 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
AHMNLFMI_06105 | 7.6e-53 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
AHMNLFMI_06106 | 4.2e-52 | 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 | ||
AHMNLFMI_06107 | 1.2e-146 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
AHMNLFMI_06108 | 6.2e-155 | xylP2 | G | symporter | ||
AHMNLFMI_06109 | 1.1e-17 | ps308 | K | AntA/AntB antirepressor | ||
AHMNLFMI_06110 | 1.2e-48 | |||||
AHMNLFMI_06111 | 1.2e-147 | 3.1.3.16 | L | DnaD domain protein | ||
AHMNLFMI_06112 | 3.7e-47 | L | Domain of unknown function (DUF4373) | |||
AHMNLFMI_06113 | 1.2e-29 | sepS16B | ||||
AHMNLFMI_06114 | 1.6e-20 | sepS16B | ||||
AHMNLFMI_06115 | 3.2e-55 | sepS16B | ||||
AHMNLFMI_06116 | 1e-70 | sepS16B | ||||
AHMNLFMI_06117 | 1.4e-114 | |||||
AHMNLFMI_06118 | 2e-106 | 3.2.2.20 | K | acetyltransferase | ||
AHMNLFMI_06119 | 6.7e-62 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHMNLFMI_06120 | 5.7e-24 | |||||
AHMNLFMI_06121 | 2.1e-55 | S | Protein of unknown function (DUF1648) | |||
AHMNLFMI_06122 | 2.5e-80 | yueI | S | Protein of unknown function (DUF1694) | ||
AHMNLFMI_06123 | 5.2e-113 | yktB | S | Belongs to the UPF0637 family | ||
AHMNLFMI_06124 | 8.1e-73 | 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 | ||
AHMNLFMI_06125 | 3.2e-46 | 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 | ||
AHMNLFMI_06126 | 6.5e-97 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
AHMNLFMI_06127 | 1.8e-102 | S | membrane | |||
AHMNLFMI_06128 | 2e-250 | S | membrane | |||
AHMNLFMI_06129 | 5e-195 | blaA6 | V | Beta-lactamase | ||
AHMNLFMI_06130 | 2.8e-41 | blaA6 | V | Beta-lactamase | ||
AHMNLFMI_06131 | 6.4e-24 | |||||
AHMNLFMI_06132 | 8.3e-29 | |||||
AHMNLFMI_06133 | 1.3e-39 | |||||
AHMNLFMI_06134 | 7.6e-42 | |||||
AHMNLFMI_06135 | 1e-53 | |||||
AHMNLFMI_06136 | 1.1e-53 | |||||
AHMNLFMI_06137 | 1.9e-16 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
AHMNLFMI_06138 | 9.5e-57 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
AHMNLFMI_06139 | 2e-25 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
AHMNLFMI_06140 | 3.8e-20 | 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 | ||
AHMNLFMI_06141 | 2.6e-101 | 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 | ||
AHMNLFMI_06142 | 5.7e-57 | 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 | ||
AHMNLFMI_06143 | 6.3e-26 | cycA | E | Amino acid permease | ||
AHMNLFMI_06144 | 7.9e-169 | cycA | E | Amino acid permease | ||
AHMNLFMI_06145 | 6.6e-24 | nhaC | C | Na H antiporter NhaC | ||
AHMNLFMI_06146 | 2.5e-107 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
AHMNLFMI_06147 | 1.3e-12 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
AHMNLFMI_06148 | 2.4e-237 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHMNLFMI_06149 | 6.8e-34 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHMNLFMI_06150 | 5.1e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
AHMNLFMI_06151 | 1.3e-37 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
AHMNLFMI_06152 | 2.4e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
AHMNLFMI_06153 | 1.9e-92 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_06154 | 3.3e-38 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_06155 | 1.2e-247 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_06156 | 1.2e-74 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_06157 | 4.6e-67 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_06158 | 3.7e-48 | fruR | K | DeoR C terminal sensor domain | ||
AHMNLFMI_06159 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHMNLFMI_06160 | 8.4e-192 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
AHMNLFMI_06161 | 1.8e-76 | 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 | ||
AHMNLFMI_06162 | 2.1e-21 | msmK | P | Belongs to the ABC transporter superfamily | ||
AHMNLFMI_06163 | 9e-22 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06164 | 4.8e-25 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06165 | 5.8e-95 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06166 | 3.4e-34 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06167 | 1.7e-159 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AHMNLFMI_06168 | 5.9e-85 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
AHMNLFMI_06169 | 9.5e-09 | lytE | M | LysM domain | ||
AHMNLFMI_06170 | 9.5e-09 | lytE | M | LysM domain | ||
AHMNLFMI_06171 | 5e-240 | ydaO | E | amino acid | ||
AHMNLFMI_06172 | 4.8e-82 | 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 | ||
AHMNLFMI_06173 | 1.7e-257 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
AHMNLFMI_06174 | 3.9e-216 | nhaC | C | Na H antiporter NhaC | ||
AHMNLFMI_06175 | 6.5e-125 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_06176 | 1.4e-86 | ynhH | S | NusG domain II | ||
AHMNLFMI_06177 | 6.7e-19 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
AHMNLFMI_06178 | 1.1e-30 | cad | S | FMN_bind | ||
AHMNLFMI_06179 | 2.5e-41 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_06180 | 1.9e-58 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_06181 | 3e-44 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_06182 | 1.6e-46 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_06183 | 1.9e-40 | lytE | M | LysM domain | ||
AHMNLFMI_06184 | 2.4e-87 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_06186 | 4.8e-100 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_06187 | 2.3e-64 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_06188 | 6.8e-78 | ywfO | S | HD domain protein | ||
AHMNLFMI_06189 | 4.6e-35 | ywfO | S | HD domain protein | ||
AHMNLFMI_06190 | 4.8e-174 | ywfO | S | HD domain protein | ||
AHMNLFMI_06191 | 1e-117 | ywfO | S | HD domain protein | ||
AHMNLFMI_06192 | 3.8e-60 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
AHMNLFMI_06193 | 3.3e-39 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
AHMNLFMI_06194 | 3.2e-41 | |||||
AHMNLFMI_06195 | 6.2e-24 | uvrA2 | L | ABC transporter | ||
AHMNLFMI_06196 | 2.5e-46 | |||||
AHMNLFMI_06197 | 0.0 | uvrA2 | L | ABC transporter | ||
AHMNLFMI_06199 | 9.3e-47 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_06200 | 1.1e-124 | K | AraC-like ligand binding domain | |||
AHMNLFMI_06201 | 7.3e-72 | mdlA2 | V | ABC transporter | ||
AHMNLFMI_06202 | 8.9e-39 | K | AraC-like ligand binding domain | |||
AHMNLFMI_06203 | 1.9e-104 | S | Protein of unknown function (DUF1648) | |||
AHMNLFMI_06204 | 8.6e-44 | czrA | K | Helix-turn-helix domain | ||
AHMNLFMI_06205 | 2.8e-49 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
AHMNLFMI_06206 | 2.2e-26 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
AHMNLFMI_06207 | 2.1e-11 | 2.7.1.191 | G | PTS system fructose IIA component | ||
AHMNLFMI_06208 | 1.7e-34 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
AHMNLFMI_06210 | 1.3e-23 | G | PTS system sorbose-specific iic component | |||
AHMNLFMI_06211 | 1.3e-82 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_06212 | 6.9e-29 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_06213 | 6.7e-113 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_06214 | 2.1e-120 | S | Protein of unknown function (DUF1361) | |||
AHMNLFMI_06215 | 2.7e-149 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
AHMNLFMI_06216 | 4.5e-104 | ybeC | E | amino acid | ||
AHMNLFMI_06217 | 1.9e-07 | asnB | 6.3.5.4 | E | Protein of unknown function (DUF3923) | |
AHMNLFMI_06218 | 2.6e-149 | ybeC | E | amino acid | ||
AHMNLFMI_06219 | 1.9e-56 | ybeC | E | amino acid | ||
AHMNLFMI_06220 | 8.1e-65 | 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) | |
AHMNLFMI_06221 | 3.2e-30 | rmeB | K | transcriptional regulator, MerR family | ||
AHMNLFMI_06222 | 1.4e-17 | GM | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_06223 | 1.5e-56 | GM | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_06224 | 3.4e-90 | mleR | K | LysR family | ||
AHMNLFMI_06225 | 5.4e-77 | mleR | K | LysR family | ||
AHMNLFMI_06226 | 4.2e-19 | M | Membrane | |||
AHMNLFMI_06227 | 1.6e-55 | S | peptidoglycan catabolic process | |||
AHMNLFMI_06228 | 1.4e-131 | uvrA3 | L | excinuclease ABC | ||
AHMNLFMI_06229 | 5.5e-45 | yitW | S | Iron-sulfur cluster assembly protein | ||
AHMNLFMI_06230 | 5.2e-153 | sufB | O | assembly protein SufB | ||
AHMNLFMI_06231 | 2.7e-28 | sufB | O | assembly protein SufB | ||
AHMNLFMI_06232 | 1.7e-25 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
AHMNLFMI_06233 | 9.1e-150 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
AHMNLFMI_06234 | 7.9e-252 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
AHMNLFMI_06235 | 1.1e-60 | ybbR | S | YbbR-like protein | ||
AHMNLFMI_06236 | 5.1e-116 | cutC | P | Participates in the control of copper homeostasis | ||
AHMNLFMI_06237 | 1.3e-193 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
AHMNLFMI_06238 | 1.9e-29 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
AHMNLFMI_06239 | 3.6e-28 | ddpX | 3.4.13.22 | S | L,D-transpeptidase catalytic domain | |
AHMNLFMI_06240 | 2.6e-14 | ddpX | 3.4.13.22 | S | L,D-transpeptidase catalytic domain | |
AHMNLFMI_06241 | 3.1e-247 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_06242 | 3.9e-35 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_06243 | 1.2e-26 | |||||
AHMNLFMI_06244 | 1.3e-90 | pgm3 | G | Phosphoglycerate mutase family | ||
AHMNLFMI_06245 | 5e-47 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_06246 | 1.4e-49 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_06247 | 1.3e-17 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_06250 | 3.3e-47 | |||||
AHMNLFMI_06251 | 4.9e-38 | dedA | S | SNARE associated Golgi protein | ||
AHMNLFMI_06252 | 7.3e-43 | dedA | S | SNARE associated Golgi protein | ||
AHMNLFMI_06253 | 8.8e-109 | dedA | S | SNARE associated Golgi protein | ||
AHMNLFMI_06254 | 6.7e-99 | K | transcriptional regulator | |||
AHMNLFMI_06255 | 1.5e-33 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_06256 | 1.9e-71 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
AHMNLFMI_06257 | 8.9e-175 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_06258 | 2e-53 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_06259 | 1.8e-127 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
AHMNLFMI_06260 | 3.2e-15 | M | hydrolase, family 25 | |||
AHMNLFMI_06261 | 8.3e-31 | M | hydrolase, family 25 | |||
AHMNLFMI_06263 | 4.1e-28 | hol | S | Bacteriophage holin | ||
AHMNLFMI_06264 | 4.7e-48 | |||||
AHMNLFMI_06265 | 8e-50 | M | hydrolase, family 25 | |||
AHMNLFMI_06266 | 1.5e-74 | yeaL | S | Protein of unknown function (DUF441) | ||
AHMNLFMI_06267 | 1.5e-157 | cvfB | S | S1 domain | ||
AHMNLFMI_06268 | 1.3e-120 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_06269 | 2.8e-09 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHMNLFMI_06270 | 1.5e-55 | FG | HIT domain | |||
AHMNLFMI_06271 | 2.9e-30 | FG | HIT domain | |||
AHMNLFMI_06272 | 7.7e-174 | S | Aldo keto reductase | |||
AHMNLFMI_06273 | 3.3e-33 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHMNLFMI_06274 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHMNLFMI_06275 | 5.7e-144 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHMNLFMI_06276 | 3.5e-68 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AHMNLFMI_06277 | 8.5e-198 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
AHMNLFMI_06278 | 9.9e-08 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
AHMNLFMI_06279 | 5.5e-30 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
AHMNLFMI_06280 | 5.9e-138 | 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 | |
AHMNLFMI_06281 | 2e-40 | 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 | |
AHMNLFMI_06282 | 1.2e-55 | 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 | |
AHMNLFMI_06283 | 1.7e-11 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_06284 | 3.4e-43 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_06285 | 5.8e-126 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_06286 | 3.6e-41 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
AHMNLFMI_06287 | 2.9e-131 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
AHMNLFMI_06288 | 1.5e-51 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
AHMNLFMI_06289 | 5.5e-98 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
AHMNLFMI_06290 | 5.5e-60 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
AHMNLFMI_06291 | 2e-24 | S | DsrE/DsrF-like family | |||
AHMNLFMI_06292 | 3.1e-164 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
AHMNLFMI_06293 | 7.6e-39 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHMNLFMI_06294 | 5.6e-49 | |||||
AHMNLFMI_06295 | 9e-20 | nlhH_1 | I | alpha/beta hydrolase fold | ||
AHMNLFMI_06296 | 4.7e-31 | nlhH_1 | I | alpha/beta hydrolase fold | ||
AHMNLFMI_06297 | 1.6e-15 | nlhH_1 | I | alpha/beta hydrolase fold | ||
AHMNLFMI_06298 | 3e-217 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AHMNLFMI_06299 | 6.8e-37 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AHMNLFMI_06300 | 9e-39 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
AHMNLFMI_06301 | 1.4e-83 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
AHMNLFMI_06302 | 2.5e-153 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
AHMNLFMI_06303 | 9.3e-33 | S | Cupin domain | |||
AHMNLFMI_06304 | 1.8e-35 | yabM | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_06305 | 1.3e-76 | yabM | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_06306 | 3.8e-12 | 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 | ||
AHMNLFMI_06307 | 6.2e-85 | S | Protein conserved in bacteria | |||
AHMNLFMI_06308 | 3.2e-105 | ydaM | M | Glycosyl transferase family group 2 | ||
AHMNLFMI_06310 | 2.4e-45 | 2.7.7.65 | T | diguanylate cyclase activity | ||
AHMNLFMI_06311 | 8.7e-23 | 2.7.7.65 | T | diguanylate cyclase activity | ||
AHMNLFMI_06312 | 7.8e-219 | 2.7.7.65 | T | diguanylate cyclase | ||
AHMNLFMI_06313 | 3.1e-123 | scrA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_06314 | 1.8e-127 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_06315 | 3e-27 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_06316 | 3.6e-53 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
AHMNLFMI_06318 | 6e-29 | mleR | K | LysR substrate binding domain | ||
AHMNLFMI_06319 | 3.1e-80 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
AHMNLFMI_06320 | 7.1e-224 | scrA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
AHMNLFMI_06321 | 7.7e-56 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
AHMNLFMI_06322 | 5.3e-124 | 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 | |
AHMNLFMI_06323 | 3.6e-58 | 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 | |
AHMNLFMI_06324 | 1.8e-36 | 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) | |
AHMNLFMI_06325 | 1.4e-50 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AHMNLFMI_06326 | 4.4e-45 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AHMNLFMI_06327 | 2.3e-44 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06328 | 4.9e-48 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06329 | 2.4e-50 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06330 | 6.9e-27 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
AHMNLFMI_06331 | 3.1e-25 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
AHMNLFMI_06332 | 1e-45 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
AHMNLFMI_06333 | 2e-118 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
AHMNLFMI_06334 | 3.3e-41 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHMNLFMI_06335 | 2.6e-101 | 3.2.2.20 | K | FR47-like protein | ||
AHMNLFMI_06336 | 1.5e-43 | yibF | S | overlaps another CDS with the same product name | ||
AHMNLFMI_06337 | 4.5e-74 | C | Aldo keto reductase family protein | |||
AHMNLFMI_06338 | 9.3e-63 | C | Aldo keto reductase family protein | |||
AHMNLFMI_06339 | 4.3e-49 | D | Alpha beta | |||
AHMNLFMI_06340 | 5e-90 | D | Alpha beta | |||
AHMNLFMI_06341 | 1.2e-45 | S | Enterocin A Immunity | |||
AHMNLFMI_06342 | 2.9e-36 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
AHMNLFMI_06343 | 1.6e-42 | |||||
AHMNLFMI_06344 | 1.3e-38 | V | ABC transporter, ATP-binding protein | |||
AHMNLFMI_06345 | 2.9e-148 | |||||
AHMNLFMI_06346 | 7.6e-81 | uspA | T | universal stress protein | ||
AHMNLFMI_06347 | 2.4e-31 | |||||
AHMNLFMI_06348 | 9.9e-34 | |||||
AHMNLFMI_06349 | 2.6e-99 | L | Transposase and inactivated derivatives, IS30 family | |||
AHMNLFMI_06350 | 2.5e-67 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
AHMNLFMI_06351 | 8.6e-162 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
AHMNLFMI_06353 | 2.6e-86 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
AHMNLFMI_06354 | 1.2e-140 | aatB | ET | ABC transporter substrate-binding protein | ||
AHMNLFMI_06356 | 3.3e-43 | |||||
AHMNLFMI_06359 | 1.7e-78 | |||||
AHMNLFMI_06360 | 1.1e-34 | |||||
AHMNLFMI_06361 | 3.5e-29 | |||||
AHMNLFMI_06362 | 4.9e-08 | |||||
AHMNLFMI_06363 | 1.7e-70 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
AHMNLFMI_06364 | 2.7e-73 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_06365 | 1.2e-33 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_06366 | 1.4e-11 | M | hydrolase, family 25 | |||
AHMNLFMI_06367 | 1.1e-21 | hol | S | Bacteriophage holin | ||
AHMNLFMI_06368 | 4.6e-29 | hol | S | Bacteriophage holin | ||
AHMNLFMI_06369 | 9.8e-15 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
AHMNLFMI_06370 | 7.3e-14 | azoB | GM | NmrA-like family | ||
AHMNLFMI_06371 | 6.8e-27 | azoB | GM | NmrA-like family | ||
AHMNLFMI_06372 | 2.7e-16 | azoB | GM | NmrA-like family | ||
AHMNLFMI_06373 | 7.3e-86 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
AHMNLFMI_06374 | 1.8e-167 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_06375 | 1.6e-138 | cycA | E | Amino acid permease | ||
AHMNLFMI_06376 | 8e-117 | 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 | |
AHMNLFMI_06377 | 9.3e-99 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_06378 | 2e-34 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_06379 | 5.2e-181 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
AHMNLFMI_06380 | 4.1e-60 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
AHMNLFMI_06381 | 6.7e-51 | S | haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_06382 | 4.5e-13 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
AHMNLFMI_06384 | 4.5e-143 | S | haloacid dehalogenase-like hydrolase | |||
AHMNLFMI_06385 | 1e-119 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHMNLFMI_06386 | 3e-68 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
AHMNLFMI_06387 | 4.6e-11 | S | Oxidoreductase, aldo keto reductase family protein | |||
AHMNLFMI_06388 | 9.2e-29 | S | Oxidoreductase, aldo keto reductase family protein | |||
AHMNLFMI_06389 | 7.9e-79 | K | Winged helix DNA-binding domain | |||
AHMNLFMI_06390 | 7.9e-51 | ycaM | E | amino acid | ||
AHMNLFMI_06391 | 5.8e-166 | ycaM | E | amino acid | ||
AHMNLFMI_06392 | 2.7e-149 | ycaM | E | amino acid | ||
AHMNLFMI_06393 | 2.1e-121 | aroD | 1.1.1.25, 4.2.1.10 | E | Type I 3-dehydroquinase | |
AHMNLFMI_06394 | 1.8e-130 | akr5f | 1.1.1.346 | S | reductase | |
AHMNLFMI_06395 | 3.3e-166 | S | Oxidoreductase, aldo keto reductase family protein | |||
AHMNLFMI_06397 | 1.4e-15 | L | Domain of unknown function (DUF4373) | |||
AHMNLFMI_06398 | 4.5e-83 | mltD | CBM50 | M | PFAM NLP P60 protein | |
AHMNLFMI_06399 | 3.9e-45 | mltD | CBM50 | M | PFAM NLP P60 protein | |
AHMNLFMI_06400 | 1e-29 | mltD | CBM50 | M | PFAM NLP P60 protein | |
AHMNLFMI_06401 | 2e-80 | |||||
AHMNLFMI_06402 | 2.7e-64 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_06403 | 2.1e-69 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_06404 | 7.4e-95 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
AHMNLFMI_06405 | 4e-29 | 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 | ||
AHMNLFMI_06406 | 4.3e-184 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_06407 | 2.6e-65 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_06408 | 5.1e-70 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_06409 | 1.4e-55 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_06411 | 3e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
AHMNLFMI_06412 | 3.4e-129 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
AHMNLFMI_06413 | 9.2e-20 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
AHMNLFMI_06414 | 7.5e-24 | 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) | |
AHMNLFMI_06415 | 2.5e-28 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_06416 | 2.2e-30 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
AHMNLFMI_06417 | 1.9e-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 | ||
AHMNLFMI_06418 | 1.4e-50 | |||||
AHMNLFMI_06419 | 4.6e-73 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
AHMNLFMI_06420 | 1.9e-75 | papX3 | K | Transcriptional regulator | ||
AHMNLFMI_06421 | 1.7e-65 | S | NADPH-dependent FMN reductase | |||
AHMNLFMI_06422 | 8.8e-52 | XK27_05220 | S | AI-2E family transporter | ||
AHMNLFMI_06423 | 2e-25 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
AHMNLFMI_06424 | 1.7e-81 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
AHMNLFMI_06425 | 5.9e-67 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
AHMNLFMI_06426 | 1.5e-95 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
AHMNLFMI_06427 | 2.7e-16 | M | Lysin motif | |||
AHMNLFMI_06428 | 5.3e-266 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHMNLFMI_06429 | 4.1e-20 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
AHMNLFMI_06430 | 4.4e-113 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
AHMNLFMI_06431 | 4e-106 | 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 | |
AHMNLFMI_06432 | 2.9e-93 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_06433 | 2.6e-79 | I | alpha/beta hydrolase fold | |||
AHMNLFMI_06434 | 9.3e-51 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
AHMNLFMI_06435 | 5.8e-118 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
AHMNLFMI_06436 | 1e-24 | S | (CBS) domain | |||
AHMNLFMI_06437 | 8.6e-84 | S | (CBS) domain | |||
AHMNLFMI_06438 | 8.5e-35 | S | (CBS) domain | |||
AHMNLFMI_06439 | 1.4e-09 | |||||
AHMNLFMI_06440 | 2.8e-13 | potB | P | ABC transporter permease | ||
AHMNLFMI_06441 | 5.3e-103 | potB | P | ABC transporter permease | ||
AHMNLFMI_06442 | 4.7e-70 | potB | P | ABC transporter permease | ||
AHMNLFMI_06443 | 1.7e-140 | potC | P | ABC transporter permease | ||
AHMNLFMI_06444 | 2e-16 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_06445 | 8.6e-41 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHMNLFMI_06446 | 6.8e-22 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
AHMNLFMI_06448 | 2.7e-76 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
AHMNLFMI_06449 | 2.5e-130 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
AHMNLFMI_06450 | 3.5e-67 | |||||
AHMNLFMI_06451 | 1.1e-76 | |||||
AHMNLFMI_06452 | 7.1e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
AHMNLFMI_06454 | 1.2e-108 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHMNLFMI_06455 | 1.2e-168 | |||||
AHMNLFMI_06456 | 5.6e-58 | |||||
AHMNLFMI_06457 | 3.1e-19 | |||||
AHMNLFMI_06458 | 2.8e-43 | |||||
AHMNLFMI_06459 | 1.3e-32 | |||||
AHMNLFMI_06460 | 1.5e-26 | |||||
AHMNLFMI_06462 | 7.7e-45 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
AHMNLFMI_06463 | 1.5e-81 | |||||
AHMNLFMI_06464 | 1.1e-124 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
AHMNLFMI_06465 | 1.3e-45 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06466 | 1.3e-19 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
AHMNLFMI_06467 | 5.1e-11 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06468 | 1.4e-19 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
AHMNLFMI_06469 | 1.1e-31 | |||||
AHMNLFMI_06470 | 5.1e-66 | |||||
AHMNLFMI_06471 | 1.2e-33 | |||||
AHMNLFMI_06472 | 8.5e-31 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_06473 | 2.6e-17 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_06474 | 6e-25 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_06475 | 3.4e-71 | S | Bacterial protein of unknown function (DUF916) | |||
AHMNLFMI_06476 | 1.7e-129 | S | WxL domain surface cell wall-binding | |||
AHMNLFMI_06477 | 1.1e-22 | T | Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain | |||
AHMNLFMI_06478 | 1.3e-98 | 1.14.99.53 | AA10 | S | Lytic polysaccharide mono-oxygenase, cellulose-degrading | |
AHMNLFMI_06479 | 4e-49 | |||||
AHMNLFMI_06480 | 3.9e-25 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
AHMNLFMI_06481 | 1.6e-21 | rplI | J | Binds to the 23S rRNA | ||
AHMNLFMI_06482 | 1.2e-100 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHMNLFMI_06483 | 1.8e-43 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHMNLFMI_06484 | 2.5e-57 | yliE | T | Putative diguanylate phosphodiesterase | ||
AHMNLFMI_06485 | 1.7e-87 | yliE | T | Putative diguanylate phosphodiesterase | ||
AHMNLFMI_06486 | 3e-23 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_06487 | 1.9e-24 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
AHMNLFMI_06488 | 2.5e-53 | S | membrane | |||
AHMNLFMI_06489 | 1.3e-67 | S | membrane | |||
AHMNLFMI_06490 | 2.9e-123 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_06491 | 2.6e-08 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_06492 | 2.9e-27 | mdxE | G | Bacterial extracellular solute-binding protein | ||
AHMNLFMI_06493 | 6.9e-37 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHMNLFMI_06494 | 7.9e-34 | |||||
AHMNLFMI_06495 | 8.7e-17 | |||||
AHMNLFMI_06496 | 3.9e-43 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_06497 | 1.2e-35 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
AHMNLFMI_06498 | 1.5e-214 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AHMNLFMI_06499 | 2e-30 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_06500 | 2.5e-144 | T | diguanylate cyclase | |||
AHMNLFMI_06501 | 1.2e-73 | S | Psort location Cytoplasmic, score | |||
AHMNLFMI_06502 | 5.4e-31 | S | Psort location Cytoplasmic, score | |||
AHMNLFMI_06503 | 2.6e-43 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_06504 | 1.9e-41 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_06505 | 1.8e-30 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
AHMNLFMI_06506 | 2e-43 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
AHMNLFMI_06507 | 6.9e-119 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
AHMNLFMI_06508 | 2.5e-204 | ydiC1 | EGP | Major facilitator Superfamily | ||
AHMNLFMI_06509 | 3.3e-65 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_06510 | 1.2e-39 | T | PhoQ Sensor | |||
AHMNLFMI_06511 | 7.1e-110 | metQ | P | NLPA lipoprotein | ||
AHMNLFMI_06513 | 2.8e-60 | S | CHY zinc finger | |||
AHMNLFMI_06514 | 1.5e-59 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
AHMNLFMI_06515 | 4.8e-69 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AHMNLFMI_06516 | 2e-109 | xerD | D | recombinase XerD | ||
AHMNLFMI_06517 | 6.7e-26 | xerD | D | recombinase XerD | ||
AHMNLFMI_06518 | 5.5e-195 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHMNLFMI_06519 | 1e-31 | gabR | K | Bacterial regulatory proteins, gntR family | ||
AHMNLFMI_06520 | 2.3e-113 | gabR | K | Bacterial regulatory proteins, gntR family | ||
AHMNLFMI_06521 | 3.6e-35 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_06522 | 4.3e-90 | gabR | K | Bacterial regulatory proteins, gntR family | ||
AHMNLFMI_06523 | 2.6e-25 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
AHMNLFMI_06524 | 9.5e-200 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
AHMNLFMI_06525 | 2.1e-79 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_06526 | 2.5e-53 | yiaC | K | Acetyltransferase (GNAT) domain | ||
AHMNLFMI_06527 | 1.2e-102 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_06528 | 5.9e-33 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHMNLFMI_06529 | 1.3e-30 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_06531 | 6.9e-191 | yknV | V | ABC transporter | ||
AHMNLFMI_06532 | 1.9e-09 | yknV | V | ABC transporter | ||
AHMNLFMI_06533 | 1.5e-45 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_06534 | 7.3e-153 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_06535 | 1e-36 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_06536 | 9.6e-16 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_06537 | 5.7e-17 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHMNLFMI_06538 | 1e-24 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHMNLFMI_06539 | 1.1e-39 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHMNLFMI_06540 | 1.1e-39 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHMNLFMI_06541 | 6.6e-44 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_06543 | 1.9e-25 | uup | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_06544 | 2.2e-57 | uup | S | ABC transporter, ATP-binding protein | ||
AHMNLFMI_06545 | 1.4e-58 | C | Electron transfer flavoprotein FAD-binding domain | |||
AHMNLFMI_06546 | 1.4e-133 | C | Electron transfer flavoprotein FAD-binding domain | |||
AHMNLFMI_06547 | 3.8e-58 | C | Electron transfer flavoprotein FAD-binding domain | |||
AHMNLFMI_06548 | 8.9e-37 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
AHMNLFMI_06549 | 2.6e-43 | emrY | EGP | Major facilitator Superfamily | ||
AHMNLFMI_06550 | 2.2e-28 | XK27_00915 | C | Luciferase-like monooxygenase | ||
AHMNLFMI_06551 | 1.8e-55 | S | Sterol carrier protein domain | |||
AHMNLFMI_06552 | 1.3e-48 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
AHMNLFMI_06553 | 3.6e-78 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
AHMNLFMI_06554 | 7e-218 | lacS | G | Transporter | ||
AHMNLFMI_06555 | 9.4e-38 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
AHMNLFMI_06556 | 6.8e-53 | K | Transcriptional regulator | |||
AHMNLFMI_06557 | 5e-32 | KT | response to antibiotic | |||
AHMNLFMI_06558 | 3.9e-102 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
AHMNLFMI_06559 | 7.5e-222 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
AHMNLFMI_06560 | 5.2e-64 | M | Protein of unknown function (DUF3737) | |||
AHMNLFMI_06561 | 1.9e-08 | M | Protein of unknown function (DUF3737) | |||
AHMNLFMI_06562 | 2.1e-28 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_06563 | 2.1e-28 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_06564 | 2.8e-25 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_06565 | 2.1e-28 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_06566 | 1.5e-127 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
AHMNLFMI_06569 | 2.1e-226 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_06570 | 1.7e-35 | 1.1.1.219 | GM | Male sterility protein | ||
AHMNLFMI_06571 | 5.9e-50 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_06573 | 3e-89 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
AHMNLFMI_06574 | 4e-34 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHMNLFMI_06575 | 1.7e-54 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06576 | 3.7e-114 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06577 | 1.7e-54 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06578 | 1e-34 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AHMNLFMI_06579 | 1.1e-69 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_06580 | 1.8e-136 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AHMNLFMI_06581 | 1.5e-39 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AHMNLFMI_06582 | 3.1e-84 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_06583 | 1.4e-27 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHMNLFMI_06584 | 2e-24 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AHMNLFMI_06585 | 3.4e-38 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
AHMNLFMI_06586 | 4.2e-70 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
AHMNLFMI_06587 | 6.1e-31 | S | Phage terminase, large subunit, PBSX family | |||
AHMNLFMI_06588 | 1.5e-62 | mleR | K | LysR family transcriptional regulator | ||
AHMNLFMI_06589 | 2.2e-134 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHMNLFMI_06590 | 3.5e-23 | |||||
AHMNLFMI_06591 | 4.2e-55 | 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) | |
AHMNLFMI_06592 | 1.8e-16 | sidC | GT2,GT4 | LM | DNA recombination | |
AHMNLFMI_06593 | 3.3e-30 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
AHMNLFMI_06594 | 3.6e-114 | yjbH | Q | Thioredoxin | ||
AHMNLFMI_06595 | 5.5e-305 | pepF | E | oligoendopeptidase F | ||
AHMNLFMI_06596 | 1.4e-34 | 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 | |
AHMNLFMI_06597 | 5.6e-13 | thrE | S | Putative threonine/serine exporter | ||
AHMNLFMI_06598 | 5.2e-164 | yvgN | C | Aldo keto reductase | ||
AHMNLFMI_06599 | 1.4e-57 | esbA | S | Family of unknown function (DUF5322) | ||
AHMNLFMI_06600 | 1.3e-28 | esbA | S | Family of unknown function (DUF5322) | ||
AHMNLFMI_06601 | 2.7e-280 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
AHMNLFMI_06602 | 4.4e-74 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
AHMNLFMI_06603 | 1.7e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHMNLFMI_06604 | 1.3e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AHMNLFMI_06606 | 4.9e-162 | L | HIRAN domain | |||
AHMNLFMI_06607 | 1.5e-41 | L | HIRAN domain | |||
AHMNLFMI_06608 | 5.9e-171 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AHMNLFMI_06609 | 6.9e-162 | |||||
AHMNLFMI_06610 | 3.5e-158 | S | Caudovirus prohead serine protease | |||
AHMNLFMI_06611 | 4.3e-40 | S | Phage gp6-like head-tail connector protein | |||
AHMNLFMI_06612 | 9.9e-56 | |||||
AHMNLFMI_06614 | 5.1e-60 | C | FMN binding | |||
AHMNLFMI_06615 | 5.2e-96 | K | LysR family | |||
AHMNLFMI_06617 | 7.5e-19 | M | Bacterial Ig-like domain (group 3) | |||
AHMNLFMI_06618 | 4.3e-09 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_06621 | 4.1e-42 | araF | G | L-arabinose-binding periplasmic protein | ||
AHMNLFMI_06622 | 2.3e-20 | araF | G | L-arabinose-binding periplasmic protein | ||
AHMNLFMI_06623 | 1.5e-85 | araF | G | L-arabinose-binding periplasmic protein | ||
AHMNLFMI_06624 | 8.2e-137 | pi346 | L | IstB-like ATP binding protein | ||
AHMNLFMI_06625 | 4.1e-27 | L | DnaD domain protein | |||
AHMNLFMI_06626 | 3e-130 | S | Putative HNHc nuclease | |||
AHMNLFMI_06627 | 2.9e-14 | S | Protein of unknown function (DUF669) | |||
AHMNLFMI_06628 | 2e-112 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AHMNLFMI_06629 | 6.7e-47 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_06630 | 3.1e-44 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_06631 | 1.8e-39 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_06632 | 6.8e-42 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHMNLFMI_06633 | 9.4e-49 | S | Phosphatidylethanolamine-binding protein | |||
AHMNLFMI_06634 | 3e-116 | GM | NAD(P)H-binding | |||
AHMNLFMI_06635 | 1.3e-175 | C | C4-dicarboxylate transmembrane transporter activity | |||
AHMNLFMI_06636 | 3.8e-131 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_06637 | 5.9e-70 | |||||
AHMNLFMI_06638 | 2.4e-64 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
AHMNLFMI_06639 | 6.5e-34 | G | Xylose isomerase-like TIM barrel | |||
AHMNLFMI_06640 | 1e-156 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHMNLFMI_06641 | 4.6e-160 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AHMNLFMI_06642 | 1.6e-43 | V | CAAX protease self-immunity | |||
AHMNLFMI_06643 | 7.1e-121 | yclH | V | ABC transporter | ||
AHMNLFMI_06644 | 1.5e-126 | tuaA | M | Bacterial sugar transferase | ||
AHMNLFMI_06645 | 2e-64 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
AHMNLFMI_06646 | 4.5e-21 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
AHMNLFMI_06647 | 2.4e-67 | agrB | KOT | May be involved in the proteolytic processing of a quorum sensing system signal molecule precursor | ||
AHMNLFMI_06648 | 1.8e-12 | |||||
AHMNLFMI_06649 | 4.7e-74 | 2.7.13.3 | T | GHKL domain | ||
AHMNLFMI_06650 | 1.8e-71 | V | VanZ like family | |||
AHMNLFMI_06651 | 7.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
AHMNLFMI_06652 | 2.6e-37 | ysxB | J | Cysteine protease Prp | ||
AHMNLFMI_06653 | 3.2e-53 | ysxB | J | Cysteine protease Prp | ||
AHMNLFMI_06654 | 5.4e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
AHMNLFMI_06655 | 1.9e-44 | ysxB | J | Cysteine protease Prp | ||
AHMNLFMI_06656 | 3.8e-72 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
AHMNLFMI_06657 | 2.7e-12 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
AHMNLFMI_06658 | 1.9e-44 | 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 | ||
AHMNLFMI_06659 | 3e-15 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06660 | 5e-48 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06661 | 5.2e-61 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06662 | 1.2e-160 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06663 | 5.2e-120 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06664 | 3.6e-71 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_06665 | 1.2e-91 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_06666 | 1.3e-60 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AHMNLFMI_06667 | 7.1e-47 | treR | K | UTRA | ||
AHMNLFMI_06668 | 1.3e-57 | treR | K | UTRA | ||
AHMNLFMI_06669 | 7.1e-60 | treR | K | UTRA | ||
AHMNLFMI_06670 | 3.3e-38 | treR | K | UTRA | ||
AHMNLFMI_06671 | 1.5e-115 | |||||
AHMNLFMI_06672 | 1.2e-70 | |||||
AHMNLFMI_06673 | 2.9e-47 | |||||
AHMNLFMI_06674 | 2.2e-08 | |||||
AHMNLFMI_06675 | 1.8e-45 | |||||
AHMNLFMI_06676 | 5e-81 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
AHMNLFMI_06677 | 1.7e-26 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
AHMNLFMI_06678 | 1.7e-26 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
AHMNLFMI_06679 | 5e-209 | citP | P | Sodium:sulfate symporter transmembrane region | ||
AHMNLFMI_06680 | 5.4e-33 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHMNLFMI_06682 | 1.4e-150 | S | hydrolase | |||
AHMNLFMI_06683 | 8.7e-53 | K | Transcriptional regulator | |||
AHMNLFMI_06684 | 4.6e-33 | S | hydrolase | |||
AHMNLFMI_06685 | 8.9e-34 | S | hydrolase | |||
AHMNLFMI_06686 | 6.5e-28 | 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 | ||
AHMNLFMI_06687 | 7.8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
AHMNLFMI_06688 | 4.4e-118 | 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 | ||
AHMNLFMI_06689 | 1.7e-75 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
AHMNLFMI_06690 | 2.3e-93 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
AHMNLFMI_06691 | 2.7e-116 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
AHMNLFMI_06692 | 2e-15 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
AHMNLFMI_06693 | 4.2e-124 | nox | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_06694 | 2.9e-119 | nox | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
AHMNLFMI_06695 | 2.2e-49 | scrA | 2.7.1.193, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AHMNLFMI_06696 | 7.5e-231 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHMNLFMI_06698 | 5.9e-67 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_06699 | 1.8e-27 | |||||
AHMNLFMI_06700 | 3.9e-53 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHMNLFMI_06701 | 8.9e-228 | sip | L | Belongs to the 'phage' integrase family | ||
AHMNLFMI_06702 | 1.7e-09 | K | Transcriptional regulator | |||
AHMNLFMI_06704 | 1.1e-07 | |||||
AHMNLFMI_06706 | 2.7e-24 | |||||
AHMNLFMI_06707 | 4e-46 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
AHMNLFMI_06708 | 1.1e-40 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06709 | 6.9e-110 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06710 | 7.6e-104 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06711 | 3.1e-72 | holB | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_06712 | 2.7e-37 | holB | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_06713 | 1.9e-110 | holB | 2.7.7.7 | L | DNA polymerase III | |
AHMNLFMI_06714 | 1e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
AHMNLFMI_06715 | 5.5e-34 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
AHMNLFMI_06716 | 2.3e-38 | yabA | L | Involved in initiation control of chromosome replication | ||
AHMNLFMI_06717 | 2.6e-43 | lldP | C | L-lactate permease | ||
AHMNLFMI_06721 | 2.6e-12 | yjdF | S | Protein of unknown function (DUF2992) | ||
AHMNLFMI_06722 | 9.2e-38 | yjjC | V | ABC transporter | ||
AHMNLFMI_06723 | 2.6e-32 | yjjC | V | ABC transporter | ||
AHMNLFMI_06724 | 6.6e-68 | yjjC | V | ABC transporter | ||
AHMNLFMI_06725 | 5.4e-27 | M | Exporter of polyketide antibiotics | |||
AHMNLFMI_06726 | 2.4e-07 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHMNLFMI_06727 | 1.8e-47 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
AHMNLFMI_06728 | 1.4e-30 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
AHMNLFMI_06729 | 3.3e-120 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
AHMNLFMI_06730 | 2.8e-94 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_06731 | 8.8e-48 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_06732 | 3.6e-73 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_06733 | 5.6e-20 | gor | 1.8.1.7 | C | Glutathione reductase | |
AHMNLFMI_06734 | 6.4e-40 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AHMNLFMI_06735 | 1.7e-40 | ugpE | G | ABC transporter permease | ||
AHMNLFMI_06736 | 6e-260 | ugpB | G | Bacterial extracellular solute-binding protein | ||
AHMNLFMI_06737 | 3.4e-112 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AHMNLFMI_06738 | 6.5e-55 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AHMNLFMI_06739 | 6e-25 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
AHMNLFMI_06740 | 3.5e-42 | 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 | |
AHMNLFMI_06741 | 5.1e-58 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHMNLFMI_06742 | 4.8e-29 | 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 | |
AHMNLFMI_06743 | 1.2e-54 | drrB | U | ABC-2 type transporter | ||
AHMNLFMI_06744 | 5e-32 | drrA | V | ABC transporter | ||
AHMNLFMI_06745 | 3e-14 | drrB | U | ABC-2 type transporter | ||
AHMNLFMI_06746 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHMNLFMI_06747 | 3.8e-38 | ybhL | S | Belongs to the BI1 family | ||
AHMNLFMI_06748 | 4.5e-121 | ybhL | S | Belongs to the BI1 family | ||
AHMNLFMI_06749 | 1.2e-50 | hipB | K | Helix-turn-helix | ||
AHMNLFMI_06750 | 1.2e-109 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_06751 | 1.4e-52 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_06752 | 4.5e-112 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_06753 | 1.5e-84 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_06754 | 6.3e-89 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_06755 | 2.2e-42 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_06756 | 3.4e-33 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_06757 | 2.6e-42 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_06758 | 5.5e-30 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
AHMNLFMI_06759 | 7.5e-16 | |||||
AHMNLFMI_06760 | 2.5e-20 | |||||
AHMNLFMI_06761 | 1.2e-26 | |||||
AHMNLFMI_06762 | 1.2e-26 | |||||
AHMNLFMI_06763 | 1.2e-81 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHMNLFMI_06764 | 6e-12 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHMNLFMI_06765 | 3.6e-26 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHMNLFMI_06766 | 6.1e-24 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHMNLFMI_06767 | 6.9e-28 | flhF | N | Uncharacterized conserved protein (DUF2075) | ||
AHMNLFMI_06768 | 7e-46 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHMNLFMI_06769 | 3.1e-30 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHMNLFMI_06770 | 1.8e-12 | nox | C | NADH oxidase | ||
AHMNLFMI_06771 | 2.5e-118 | nox | C | NADH oxidase | ||
AHMNLFMI_06772 | 6.1e-79 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
AHMNLFMI_06773 | 6.9e-37 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHMNLFMI_06774 | 3.3e-106 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AHMNLFMI_06775 | 2.6e-49 | yycH | S | YycH protein | ||
AHMNLFMI_06776 | 2.5e-35 | vicK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_06777 | 6.7e-46 | K | response regulator | |||
AHMNLFMI_06778 | 1.4e-154 | vicK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_06779 | 3e-38 | vicK | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_06780 | 2.6e-36 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_06781 | 2.5e-24 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_06782 | 7.5e-24 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_06783 | 6.7e-185 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_06784 | 1.5e-86 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_06785 | 1.3e-75 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHMNLFMI_06786 | 3.8e-52 | K | transcriptional regulator | |||
AHMNLFMI_06787 | 3.9e-47 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
AHMNLFMI_06788 | 8e-79 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
AHMNLFMI_06789 | 7.3e-39 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHMNLFMI_06790 | 1.5e-12 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHMNLFMI_06791 | 2.2e-38 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHMNLFMI_06792 | 1.6e-85 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
AHMNLFMI_06793 | 1e-90 | |||||
AHMNLFMI_06794 | 2e-42 | |||||
AHMNLFMI_06795 | 4.9e-17 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_06796 | 1.3e-17 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_06797 | 4.7e-37 | M | Glycosyl hydrolases family 25 | |||
AHMNLFMI_06798 | 6.1e-82 | rliB | K | Transcriptional regulator | ||
AHMNLFMI_06799 | 0.0 | ypdD | G | Glycosyl hydrolase family 92 | ||
AHMNLFMI_06800 | 2.5e-83 | S | Membrane | |||
AHMNLFMI_06801 | 3.1e-203 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
AHMNLFMI_06803 | 7.9e-35 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_06804 | 5.2e-25 | uhpT | EGP | Major facilitator Superfamily | ||
AHMNLFMI_06805 | 9.7e-17 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_06806 | 9.7e-17 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_06807 | 9.7e-17 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_06808 | 9.7e-17 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AHMNLFMI_06809 | 4.5e-104 | ylbE | GM | NAD(P)H-binding | ||
AHMNLFMI_06810 | 1.6e-27 | yybC | S | Protein of unknown function (DUF2798) | ||
AHMNLFMI_06811 | 5e-82 | yybC | S | Protein of unknown function (DUF2798) | ||
AHMNLFMI_06812 | 4.8e-66 | yybC | S | Protein of unknown function (DUF2798) | ||
AHMNLFMI_06813 | 1e-28 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
AHMNLFMI_06814 | 4.5e-71 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
AHMNLFMI_06815 | 4.1e-144 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
AHMNLFMI_06816 | 9.5e-09 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
AHMNLFMI_06817 | 5.1e-122 | ymfH | S | Peptidase M16 | ||
AHMNLFMI_06818 | 3.7e-42 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AHMNLFMI_06819 | 3.7e-42 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AHMNLFMI_06820 | 6.9e-24 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
AHMNLFMI_06821 | 6.7e-76 | E | glutamate:sodium symporter activity | |||
AHMNLFMI_06822 | 5.9e-26 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHMNLFMI_06823 | 7.8e-42 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHMNLFMI_06824 | 3.9e-95 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHMNLFMI_06825 | 2.7e-44 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHMNLFMI_06826 | 1.1e-24 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHMNLFMI_06827 | 2.4e-36 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AHMNLFMI_06828 | 2.6e-43 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AHMNLFMI_06829 | 5.4e-51 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
AHMNLFMI_06830 | 2.3e-27 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AHMNLFMI_06831 | 1.7e-35 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
AHMNLFMI_06832 | 4.2e-61 | ydiN | 5.4.99.5 | G | Major Facilitator | |
AHMNLFMI_06833 | 6.1e-15 | D | NLP P60 protein | |||
AHMNLFMI_06834 | 5.3e-142 | D | NLP P60 protein | |||
AHMNLFMI_06835 | 1.2e-36 | rfbP | M | Bacterial sugar transferase | ||
AHMNLFMI_06836 | 3.4e-61 | rfbP | M | Bacterial sugar transferase | ||
AHMNLFMI_06837 | 5.9e-16 | rbsR | K | helix_turn _helix lactose operon repressor | ||
AHMNLFMI_06838 | 1.3e-23 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHMNLFMI_06839 | 4.1e-231 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHMNLFMI_06840 | 3.3e-68 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHMNLFMI_06842 | 1.1e-30 | D | NLP P60 protein | |||
AHMNLFMI_06843 | 1.4e-35 | ykuT | M | mechanosensitive ion channel | ||
AHMNLFMI_06844 | 6.1e-37 | ykuT | M | mechanosensitive ion channel | ||
AHMNLFMI_06845 | 1.1e-45 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_06846 | 1.5e-75 | pucR | QT | Purine catabolism regulatory protein-like family | ||
AHMNLFMI_06847 | 1.1e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AHMNLFMI_06848 | 2e-67 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
AHMNLFMI_06849 | 1.3e-122 | drgA | C | Nitroreductase family | ||
AHMNLFMI_06850 | 2.6e-16 | ptlF | S | KR domain | ||
AHMNLFMI_06851 | 6.3e-23 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
AHMNLFMI_06852 | 9.9e-31 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
AHMNLFMI_06853 | 1.8e-37 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_06854 | 5.2e-98 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_06855 | 2.1e-36 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_06856 | 3.4e-59 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
AHMNLFMI_06857 | 2.2e-18 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_06858 | 1e-35 | yobV1 | K | WYL domain | ||
AHMNLFMI_06859 | 2.6e-67 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
AHMNLFMI_06860 | 4.3e-43 | yobV1 | K | WYL domain | ||
AHMNLFMI_06861 | 6.1e-34 | M | Lysin motif | |||
AHMNLFMI_06862 | 4.7e-108 | S | SdpI/YhfL protein family | |||
AHMNLFMI_06863 | 1.9e-53 | nudA | S | ASCH | ||
AHMNLFMI_06864 | 9.1e-164 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHMNLFMI_06865 | 4.2e-92 | |||||
AHMNLFMI_06866 | 2e-120 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
AHMNLFMI_06867 | 4.7e-124 | T | diguanylate cyclase | |||
AHMNLFMI_06868 | 9.3e-81 | S | Protein of unknown function (DUF554) | |||
AHMNLFMI_06869 | 4.1e-99 | S | Protein of unknown function (DUF554) | |||
AHMNLFMI_06870 | 7.1e-55 | 3.1.3.1 | S | associated with various cellular activities | ||
AHMNLFMI_06871 | 1.1e-31 | 3.1.3.1 | S | associated with various cellular activities | ||
AHMNLFMI_06872 | 1.1e-87 | 3.1.3.1 | S | associated with various cellular activities | ||
AHMNLFMI_06873 | 5e-50 | S | Putative metallopeptidase domain | |||
AHMNLFMI_06874 | 1.2e-68 | S | Putative metallopeptidase domain | |||
AHMNLFMI_06875 | 1.8e-51 | S | Putative metallopeptidase domain | |||
AHMNLFMI_06876 | 3.6e-160 | S | Putative metallopeptidase domain | |||
AHMNLFMI_06877 | 8.2e-26 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHMNLFMI_06878 | 1.8e-27 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHMNLFMI_06879 | 1.1e-34 | patA | 2.6.1.1 | E | Aminotransferase | |
AHMNLFMI_06880 | 2e-97 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHMNLFMI_06881 | 4.3e-37 | S | protein disulfide oxidoreductase activity | |||
AHMNLFMI_06882 | 2.1e-39 | S | protein disulfide oxidoreductase activity | |||
AHMNLFMI_06884 | 3.4e-09 | |||||
AHMNLFMI_06886 | 1.3e-99 | mleR | K | LysR family | ||
AHMNLFMI_06887 | 2.2e-23 | |||||
AHMNLFMI_06888 | 9e-60 | |||||
AHMNLFMI_06889 | 2.5e-50 | |||||
AHMNLFMI_06890 | 1.5e-25 | |||||
AHMNLFMI_06891 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
AHMNLFMI_06892 | 2e-48 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_06893 | 1.7e-28 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AHMNLFMI_06894 | 8.5e-199 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
AHMNLFMI_06895 | 6.3e-113 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
AHMNLFMI_06896 | 2.7e-46 | pts29C | 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 | ||
AHMNLFMI_06897 | 1.9e-15 | glnPH2 | P | ABC transporter permease | ||
AHMNLFMI_06898 | 4.5e-31 | S | Iron-sulphur cluster biosynthesis | |||
AHMNLFMI_06899 | 1.2e-93 | pgm3 | G | Phosphoglycerate mutase family | ||
AHMNLFMI_06900 | 2.2e-28 | |||||
AHMNLFMI_06901 | 4.4e-78 | |||||
AHMNLFMI_06902 | 1.1e-09 | S | Domain of unknown function (DUF1508) | |||
AHMNLFMI_06904 | 3.2e-48 | S | Bacteriophage Mu Gam like protein | |||
AHMNLFMI_06906 | 5.4e-55 | S | Bacteriophage Mu Gam like protein | |||
AHMNLFMI_06907 | 3e-56 | |||||
AHMNLFMI_06908 | 1.2e-97 | |||||
AHMNLFMI_06909 | 7.3e-59 | |||||
AHMNLFMI_06910 | 9.3e-13 | |||||
AHMNLFMI_06911 | 1.5e-21 | |||||
AHMNLFMI_06912 | 5e-145 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
AHMNLFMI_06913 | 2.2e-165 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
AHMNLFMI_06914 | 3.4e-135 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
AHMNLFMI_06915 | 3.8e-17 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHMNLFMI_06916 | 1.1e-44 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
AHMNLFMI_06917 | 2.3e-116 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
AHMNLFMI_06918 | 1.4e-24 | bcr1 | EGP | Major facilitator Superfamily | ||
AHMNLFMI_06919 | 2e-118 | bcr1 | EGP | Major facilitator Superfamily | ||
AHMNLFMI_06920 | 5.7e-146 | tatD | L | hydrolase, TatD family | ||
AHMNLFMI_06921 | 1.9e-28 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
AHMNLFMI_06922 | 4.1e-26 | tatD | L | hydrolase, TatD family | ||
AHMNLFMI_06923 | 7.3e-81 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
AHMNLFMI_06924 | 4.8e-94 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
AHMNLFMI_06925 | 2.3e-54 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
AHMNLFMI_06926 | 6.8e-22 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_06927 | 2.9e-78 | S | Psort location Cytoplasmic, score | |||
AHMNLFMI_06928 | 6e-77 | proWX | P | ABC-type proline glycine betaine transport systems, permease component | ||
AHMNLFMI_06929 | 6.3e-114 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
AHMNLFMI_06930 | 5.9e-59 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_06931 | 1.3e-29 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_06932 | 7.1e-131 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_06933 | 3.8e-55 | EGP | Major facilitator Superfamily | |||
AHMNLFMI_06934 | 9.1e-110 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_06935 | 1.3e-132 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHMNLFMI_06936 | 1e-171 | arlS | 2.7.13.3 | T | Histidine kinase | |
AHMNLFMI_06937 | 1.3e-52 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06938 | 1.5e-77 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06939 | 1.2e-146 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06940 | 7.7e-12 | kup | P | Transport of potassium into the cell | ||
AHMNLFMI_06941 | 1.4e-13 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
AHMNLFMI_06942 | 2.3e-38 | QT | PucR C-terminal helix-turn-helix domain | |||
AHMNLFMI_06943 | 2.6e-129 | QT | PucR C-terminal helix-turn-helix domain | |||
AHMNLFMI_06944 | 9.4e-15 | xylP2 | G | symporter | ||
AHMNLFMI_06945 | 9e-192 | nlhH_1 | I | alpha/beta hydrolase fold | ||
AHMNLFMI_06946 | 4.9e-19 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHMNLFMI_06947 | 3.8e-47 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHMNLFMI_06948 | 3.6e-144 | ydiN | 5.4.99.5 | G | Major Facilitator | |
AHMNLFMI_06949 | 3.9e-36 | S | Protein of unknown function (DUF2785) | |||
AHMNLFMI_06950 | 2e-78 | S | Protein of unknown function (DUF2785) | |||
AHMNLFMI_06951 | 2.4e-52 | S | Protein of unknown function (DUF2785) | |||
AHMNLFMI_06952 | 6.8e-41 | S | Protein of unknown function (DUF2785) | |||
AHMNLFMI_06953 | 1.7e-54 | S | Protein of unknown function (DUF2785) | |||
AHMNLFMI_06954 | 6.9e-127 | mutS | L | MutS domain V | ||
AHMNLFMI_06955 | 1.3e-123 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_06956 | 5.9e-11 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_06957 | 7.9e-97 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHMNLFMI_06958 | 4.2e-175 | corA | P | CorA-like Mg2+ transporter protein | ||
AHMNLFMI_06959 | 2e-36 | corA | P | CorA-like Mg2+ transporter protein | ||
AHMNLFMI_06960 | 3.2e-37 | corA | P | CorA-like Mg2+ transporter protein | ||
AHMNLFMI_06961 | 1.7e-79 | natB | CP | ABC-2 family transporter protein | ||
AHMNLFMI_06962 | 1e-128 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AHMNLFMI_06963 | 1.7e-47 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
AHMNLFMI_06964 | 2.5e-65 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_06965 | 1.4e-167 | GM | NmrA-like family | |||
AHMNLFMI_06966 | 8.9e-20 | fadR | K | Bacterial regulatory proteins, tetR family | ||
AHMNLFMI_06967 | 1e-24 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_06969 | 3.6e-76 | smc | D | Required for chromosome condensation and partitioning | ||
AHMNLFMI_06970 | 7.9e-157 | smc | D | Required for chromosome condensation and partitioning | ||
AHMNLFMI_06971 | 3.1e-119 | smc | D | Required for chromosome condensation and partitioning | ||
AHMNLFMI_06972 | 9.2e-135 | S | Phage tail protein | |||
AHMNLFMI_06973 | 4.3e-43 | S | Phage tail protein | |||
AHMNLFMI_06974 | 6e-21 | S | AAA domain | |||
AHMNLFMI_06975 | 2.7e-52 | S | AAA domain | |||
AHMNLFMI_06976 | 5.5e-65 | S | Bacteriophage Mu Gam like protein | |||
AHMNLFMI_06977 | 1.5e-115 | S | AAA domain | |||
AHMNLFMI_06978 | 6.3e-38 | S | Protein of unknown function (DUF669) | |||
AHMNLFMI_06979 | 3.4e-37 | S | AAA domain | |||
AHMNLFMI_06981 | 1.4e-34 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
AHMNLFMI_06982 | 2.5e-101 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
AHMNLFMI_06983 | 6.2e-168 | murB | 1.3.1.98 | M | Cell wall formation | |
AHMNLFMI_06984 | 0.0 | yjcE | P | Sodium proton antiporter | ||
AHMNLFMI_06988 | 3.1e-95 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AHMNLFMI_06989 | 7.4e-180 | phnT | 3.6.3.30 | P | ATPases associated with a variety of cellular activities | |
AHMNLFMI_06991 | 1.6e-16 | Q | Imidazolonepropionase and related amidohydrolases | |||
AHMNLFMI_06992 | 1.7e-122 | E | ABC transporter, substratebinding protein | |||
AHMNLFMI_06993 | 3.8e-27 | Q | Imidazolonepropionase and related amidohydrolases | |||
AHMNLFMI_06994 | 1.2e-151 | azoB | GM | NmrA-like family | ||
AHMNLFMI_06995 | 3.9e-157 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
AHMNLFMI_06996 | 7.9e-50 | rliB | K | Transcriptional regulator | ||
AHMNLFMI_06997 | 4.9e-22 | |||||
AHMNLFMI_06998 | 1.1e-29 | |||||
AHMNLFMI_06999 | 8.6e-66 | |||||
AHMNLFMI_07000 | 9.5e-109 | C | Oxidoreductase | |||
AHMNLFMI_07001 | 1.9e-30 | |||||
AHMNLFMI_07002 | 5.8e-146 | C | Oxidoreductase | |||
AHMNLFMI_07003 | 3.7e-175 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_07004 | 1.1e-70 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_07005 | 1.4e-41 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHMNLFMI_07006 | 1.4e-102 | lacR | K | Transcriptional regulator | ||
AHMNLFMI_07007 | 4.5e-13 | lacR | K | Transcriptional regulator | ||
AHMNLFMI_07008 | 5.9e-31 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
AHMNLFMI_07009 | 5.6e-40 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
AHMNLFMI_07011 | 2.8e-97 | ccpA | K | catabolite control protein A | ||
AHMNLFMI_07013 | 5.6e-22 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHMNLFMI_07014 | 1.3e-25 | K | helix_turn_helix, mercury resistance | |||
AHMNLFMI_07015 | 4.3e-50 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_07016 | 2.3e-103 | K | LysR family | |||
AHMNLFMI_07017 | 2e-36 | K | LysR family | |||
AHMNLFMI_07018 | 1.8e-150 | ptlF | S | KR domain | ||
AHMNLFMI_07019 | 1.1e-74 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AHMNLFMI_07020 | 7.8e-29 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AHMNLFMI_07021 | 5.1e-57 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
AHMNLFMI_07022 | 2.3e-32 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
AHMNLFMI_07024 | 1.3e-17 | 6.3.2.2, 6.3.2.4 | M | Belongs to the D-alanine--D-alanine ligase family | ||
AHMNLFMI_07025 | 3e-18 | ytqB | 2.1.1.176 | J | Putative rRNA methylase | |
AHMNLFMI_07026 | 3e-18 | ytqB | 2.1.1.176 | J | Putative rRNA methylase | |
AHMNLFMI_07027 | 4.9e-19 | C | Aldo/keto reductase family | |||
AHMNLFMI_07028 | 2.8e-151 | C | Aldo/keto reductase family | |||
AHMNLFMI_07029 | 3.1e-72 | M | Protein of unknown function (DUF3737) | |||
AHMNLFMI_07030 | 2.1e-36 | C | Aldo/keto reductase family | |||
AHMNLFMI_07031 | 2.2e-58 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHMNLFMI_07033 | 1.3e-73 | |||||
AHMNLFMI_07034 | 2.4e-15 | yvaO | K | Helix-turn-helix domain | ||
AHMNLFMI_07035 | 9.2e-26 | K | Helix-turn-helix | |||
AHMNLFMI_07036 | 4.5e-61 | yvaO | K | Helix-turn-helix domain | ||
AHMNLFMI_07037 | 4.3e-76 | E | IrrE N-terminal-like domain | |||
AHMNLFMI_07038 | 6.8e-77 | |||||
AHMNLFMI_07040 | 5.8e-56 | |||||
AHMNLFMI_07043 | 5.9e-18 | S | DNA/RNA non-specific endonuclease | |||
AHMNLFMI_07044 | 8e-105 | S | DNA/RNA non-specific endonuclease | |||
AHMNLFMI_07046 | 3.8e-27 | nox | C | NADH oxidase | ||
AHMNLFMI_07047 | 1e-13 | K | LysR substrate binding domain | |||
AHMNLFMI_07048 | 1e-13 | K | LysR substrate binding domain | |||
AHMNLFMI_07049 | 9.1e-178 | K | LysR substrate binding domain | |||
AHMNLFMI_07050 | 6.4e-27 | K | LysR substrate binding domain | |||
AHMNLFMI_07051 | 5.2e-38 | livJ | E | Receptor family ligand binding region | ||
AHMNLFMI_07052 | 3.5e-50 | livJ | E | Receptor family ligand binding region | ||
AHMNLFMI_07053 | 3e-46 | livH | U | Branched-chain amino acid transport system / permease component | ||
AHMNLFMI_07054 | 7.5e-36 | livJ | E | Receptor family ligand binding region | ||
AHMNLFMI_07059 | 2.4e-12 | S | Domain of unknown function (DUF1508) | |||
AHMNLFMI_07062 | 5.8e-35 | sufC | O | FeS assembly ATPase SufC | ||
AHMNLFMI_07063 | 1.4e-105 | sufD | O | FeS assembly protein SufD | ||
AHMNLFMI_07064 | 2.5e-189 | sufD | O | FeS assembly protein SufD | ||
AHMNLFMI_07065 | 8.9e-234 | 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 | |
AHMNLFMI_07066 | 5.8e-52 | nifU | C | SUF system FeS assembly protein, NifU family | ||
AHMNLFMI_07067 | 2.3e-93 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
AHMNLFMI_07068 | 1.8e-59 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
AHMNLFMI_07069 | 1.8e-43 | K | Transcriptional regulator | |||
AHMNLFMI_07070 | 2e-49 | K | Transcriptional regulator | |||
AHMNLFMI_07071 | 7.2e-32 | K | Transcriptional regulator | |||
AHMNLFMI_07072 | 1.8e-43 | K | Transcriptional regulator | |||
AHMNLFMI_07073 | 9.9e-67 | K | Transcriptional regulator | |||
AHMNLFMI_07074 | 1.9e-77 | elaA | S | GNAT family | ||
AHMNLFMI_07075 | 5.6e-18 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_07077 | 1.9e-17 | S | Short C-terminal domain | |||
AHMNLFMI_07078 | 9.3e-124 | K | LysR substrate binding domain | |||
AHMNLFMI_07079 | 2.4e-243 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_07080 | 8.9e-64 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
AHMNLFMI_07081 | 1.2e-174 | |||||
AHMNLFMI_07082 | 1.4e-32 | mtnE | 2.6.1.83 | E | Aminotransferase | |
AHMNLFMI_07083 | 1.6e-204 | mtnE | 2.6.1.83 | E | Aminotransferase | |
AHMNLFMI_07084 | 7.7e-148 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AHMNLFMI_07085 | 1.3e-85 | metI | U | Binding-protein-dependent transport system inner membrane component | ||
AHMNLFMI_07086 | 6.3e-80 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHMNLFMI_07088 | 5e-43 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
AHMNLFMI_07089 | 3.6e-103 | G | PTS system sorbose-specific iic component | |||
AHMNLFMI_07090 | 2.5e-99 | G | PTS system mannose/fructose/sorbose family IID component | |||
AHMNLFMI_07091 | 1.3e-51 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
AHMNLFMI_07092 | 9e-84 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
AHMNLFMI_07093 | 1.7e-210 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
AHMNLFMI_07095 | 1.4e-94 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_07096 | 4.6e-44 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_07098 | 9.7e-15 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_07099 | 2.5e-37 | ychO | 3.2.1.14 | GH18 | M | entry into host |
AHMNLFMI_07100 | 6e-49 | narL | K | This protein activates the expression of the nitrate reductase (narGHJI) and formate dehydrogenase-N (fdnGHI) operons and represses the transcription of the fumarate reductase (frdABCD) operon in response to a nitrate nitrite induction signal transmitted by either the NarX or NarQ proteins | ||
AHMNLFMI_07101 | 1.7e-112 | ychO | 3.2.1.14 | GH18 | M | entry into host |
AHMNLFMI_07102 | 6e-49 | narL | K | This protein activates the expression of the nitrate reductase (narGHJI) and formate dehydrogenase-N (fdnGHI) operons and represses the transcription of the fumarate reductase (frdABCD) operon in response to a nitrate nitrite induction signal transmitted by either the NarX or NarQ proteins | ||
AHMNLFMI_07103 | 6.1e-10 | drrA | V | ABC transporter | ||
AHMNLFMI_07104 | 1.5e-105 | drrB | U | ABC-2 type transporter | ||
AHMNLFMI_07105 | 6.7e-32 | 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 | |
AHMNLFMI_07106 | 8e-61 | 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 | ||
AHMNLFMI_07107 | 8e-61 | 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 | ||
AHMNLFMI_07108 | 5.1e-137 | 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 | ||
AHMNLFMI_07109 | 1.4e-133 | K | Helix-turn-helix domain, rpiR family | |||
AHMNLFMI_07110 | 2e-163 | GK | ROK family | |||
AHMNLFMI_07111 | 9.5e-140 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHMNLFMI_07112 | 2.9e-100 | nhaC | C | Na H antiporter NhaC | ||
AHMNLFMI_07115 | 1.5e-25 | pbuG | S | Permease family | ||
AHMNLFMI_07116 | 6.1e-75 | pbuG | S | Permease family | ||
AHMNLFMI_07117 | 7.4e-63 | pbuG | S | Permease family | ||
AHMNLFMI_07118 | 4e-87 | mleR | K | LysR family | ||
AHMNLFMI_07119 | 6.9e-53 | mleR | K | LysR family | ||
AHMNLFMI_07120 | 1.8e-30 | mleR | K | LysR family | ||
AHMNLFMI_07121 | 2.5e-32 | wecD | K | Acetyltransferase (GNAT) family | ||
AHMNLFMI_07122 | 1e-49 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHMNLFMI_07123 | 2.9e-103 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
AHMNLFMI_07124 | 1.3e-128 | livM | E | Branched-chain amino acid transport system / permease component | ||
AHMNLFMI_07125 | 1.1e-139 | livH | U | Branched-chain amino acid transport system / permease component | ||
AHMNLFMI_07126 | 4.4e-58 | |||||
AHMNLFMI_07127 | 1.4e-35 | |||||
AHMNLFMI_07128 | 1.9e-44 | |||||
AHMNLFMI_07129 | 2.1e-07 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHMNLFMI_07131 | 1.8e-66 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHMNLFMI_07132 | 6.7e-32 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHMNLFMI_07133 | 3.1e-57 | ydaN | S | Bacterial cellulose synthase subunit | ||
AHMNLFMI_07134 | 8.2e-275 | ydaN | S | Bacterial cellulose synthase subunit | ||
AHMNLFMI_07135 | 1.4e-84 | ydaM | M | Glycosyl transferase family group 2 | ||
AHMNLFMI_07136 | 2e-24 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
AHMNLFMI_07137 | 7.6e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
AHMNLFMI_07138 | 3.2e-18 | 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 | ||
AHMNLFMI_07139 | 9.3e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
AHMNLFMI_07140 | 2.3e-77 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_07141 | 5.4e-51 | S | Calcineurin-like phosphoesterase | |||
AHMNLFMI_07142 | 1.7e-45 | C | C4-dicarboxylate transmembrane transporter activity | |||
AHMNLFMI_07144 | 1.4e-143 | hipB | K | Helix-turn-helix | ||
AHMNLFMI_07145 | 1.8e-68 | oppA | E | ABC transporter, substratebinding protein | ||
AHMNLFMI_07146 | 1.2e-29 | |||||
AHMNLFMI_07147 | 3.5e-35 | V | ABC transporter, ATP-binding protein | |||
AHMNLFMI_07148 | 3.9e-162 | V | ABC transporter, ATP-binding protein | |||
AHMNLFMI_07149 | 2.3e-128 | S | ABC-2 family transporter protein | |||
AHMNLFMI_07150 | 3.7e-151 | |||||
AHMNLFMI_07151 | 2e-29 | 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 |
AHMNLFMI_07152 | 1.3e-57 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AHMNLFMI_07153 | 3.3e-49 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AHMNLFMI_07154 | 7.4e-55 | czcD | P | cation diffusion facilitator family transporter | ||
AHMNLFMI_07155 | 8.4e-45 | K | Helix-turn-helix XRE-family like proteins | |||
AHMNLFMI_07156 | 1.2e-57 | scrA | 2.7.1.193, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AHMNLFMI_07157 | 9.2e-169 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHMNLFMI_07158 | 2e-45 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
AHMNLFMI_07159 | 1.8e-74 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_07160 | 4.3e-34 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_07161 | 4.4e-38 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_07162 | 1.9e-89 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHMNLFMI_07163 | 1.3e-08 | S | Predicted membrane protein (DUF2207) | |||
AHMNLFMI_07164 | 1.3e-197 | S | Predicted membrane protein (DUF2207) | |||
AHMNLFMI_07165 | 1.6e-92 | 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
AHMNLFMI_07166 | 5.1e-12 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHMNLFMI_07167 | 4.9e-148 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
AHMNLFMI_07168 | 3.1e-50 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
AHMNLFMI_07169 | 5.2e-41 | licD | M | LicD family | ||
AHMNLFMI_07170 | 2.7e-29 | K | Transcriptional regulator | |||
AHMNLFMI_07171 | 8.9e-12 | licD | M | LicD family | ||
AHMNLFMI_07172 | 1e-47 | K | Transcriptional regulator | |||
AHMNLFMI_07173 | 1.7e-44 | licD | M | LicD family | ||
AHMNLFMI_07174 | 9e-44 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
AHMNLFMI_07175 | 1.8e-105 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
AHMNLFMI_07176 | 5.6e-110 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
AHMNLFMI_07177 | 1.3e-109 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
AHMNLFMI_07178 | 8.4e-60 | pltK | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_07179 | 6.8e-22 | pltK | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_07180 | 1.3e-52 | L | Transposase | |||
AHMNLFMI_07181 | 1.6e-83 | L | Transposase | |||
AHMNLFMI_07182 | 2.2e-18 | L | Transposase | |||
AHMNLFMI_07183 | 3.8e-67 | L | Transposase | |||
AHMNLFMI_07184 | 6.1e-71 | L | Transposase | |||
AHMNLFMI_07185 | 2e-25 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_07186 | 4.4e-221 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHMNLFMI_07187 | 2.7e-24 | ftsL | D | Cell division protein FtsL | ||
AHMNLFMI_07188 | 4.4e-60 | IQ | KR domain | |||
AHMNLFMI_07189 | 8.1e-52 | IQ | KR domain | |||
AHMNLFMI_07190 | 6.5e-154 | IQ | KR domain | |||
AHMNLFMI_07192 | 3.2e-59 | |||||
AHMNLFMI_07193 | 4.7e-50 | |||||
AHMNLFMI_07194 | 1.7e-43 | |||||
AHMNLFMI_07196 | 6.9e-23 | ywfO | S | HD domain protein | ||
AHMNLFMI_07197 | 1.6e-27 | yxeH | S | hydrolase | ||
AHMNLFMI_07198 | 4.3e-08 | ywiB | S | Domain of unknown function (DUF1934) | ||
AHMNLFMI_07199 | 5.3e-167 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
AHMNLFMI_07200 | 4.2e-44 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
AHMNLFMI_07201 | 9.7e-68 | lssY | 3.6.1.27 | I | phosphatase | |
AHMNLFMI_07202 | 4.8e-39 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AHMNLFMI_07203 | 3e-94 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AHMNLFMI_07204 | 1e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
AHMNLFMI_07205 | 9.4e-89 | 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 | |
AHMNLFMI_07207 | 3.1e-26 | dicA | K | Helix-turn-helix domain | ||
AHMNLFMI_07208 | 6.8e-75 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
AHMNLFMI_07209 | 2e-149 | dicA | K | Helix-turn-helix domain | ||
AHMNLFMI_07210 | 3.6e-54 | |||||
AHMNLFMI_07211 | 9.5e-51 | lldP | C | L-lactate permease | ||
AHMNLFMI_07212 | 4.5e-47 | lldP | C | L-lactate permease | ||
AHMNLFMI_07213 | 3.5e-81 | K | Bacterial regulatory proteins, tetR family | |||
AHMNLFMI_07214 | 5.8e-129 | CP_1020 | S | Zinc finger, swim domain protein | ||
AHMNLFMI_07215 | 6.6e-62 | potD | P | ABC transporter | ||
AHMNLFMI_07216 | 1.9e-21 | U | Preprotein translocase subunit SecB | |||
AHMNLFMI_07217 | 1.7e-30 | |||||
AHMNLFMI_07218 | 1.1e-08 | S | Motility quorum-sensing regulator, toxin of MqsA | |||
AHMNLFMI_07219 | 3.1e-38 | |||||
AHMNLFMI_07220 | 3e-226 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHMNLFMI_07221 | 5.7e-22 | |||||
AHMNLFMI_07222 | 1e-21 | K | LysR family | |||
AHMNLFMI_07223 | 5.2e-44 | P | Sodium:sulfate symporter transmembrane region | |||
AHMNLFMI_07224 | 4.1e-82 | |||||
AHMNLFMI_07225 | 1.2e-62 | cps4I | M | Glycosyltransferase like family 2 | ||
AHMNLFMI_07226 | 1.1e-18 | cps4J | S | Polysaccharide biosynthesis protein | ||
AHMNLFMI_07227 | 2.2e-58 | 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 | ||
AHMNLFMI_07228 | 2.3e-101 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
AHMNLFMI_07229 | 1.8e-29 | K | Helix-turn-helix domain | |||
AHMNLFMI_07230 | 9.6e-40 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
AHMNLFMI_07231 | 2.4e-60 | yhcA | V | MacB-like periplasmic core domain | ||
AHMNLFMI_07232 | 1.9e-262 | yhcA | V | MacB-like periplasmic core domain | ||
AHMNLFMI_07233 | 4.1e-102 | |||||
AHMNLFMI_07234 | 3.2e-37 | |||||
AHMNLFMI_07235 | 6.5e-58 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_07236 | 2.7e-52 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_07237 | 2.4e-13 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHMNLFMI_07238 | 1.3e-45 | FbpA | K | Domain of unknown function (DUF814) | ||
AHMNLFMI_07239 | 7.7e-53 | S | Domain of unknown function (DU1801) | |||
AHMNLFMI_07240 | 3.8e-162 | FbpA | K | Domain of unknown function (DUF814) | ||
AHMNLFMI_07241 | 6.5e-35 | FbpA | K | Domain of unknown function (DUF814) | ||
AHMNLFMI_07242 | 1.3e-238 | T | PhoQ Sensor | |||
AHMNLFMI_07243 | 6.7e-34 | T | PhoQ Sensor | |||
AHMNLFMI_07244 | 3.4e-129 | K | Transcriptional regulatory protein, C terminal | |||
AHMNLFMI_07245 | 1.8e-49 | |||||
AHMNLFMI_07246 | 1.1e-32 | K | Transcriptional regulatory protein, C terminal | |||
AHMNLFMI_07247 | 1.8e-30 | K | Transcriptional regulatory protein, C terminal | |||
AHMNLFMI_07248 | 7.3e-15 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_07249 | 1.7e-24 | tcyB | E | ABC transporter | ||
AHMNLFMI_07250 | 8.1e-123 | tcyB | E | ABC transporter | ||
AHMNLFMI_07251 | 8.1e-76 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHMNLFMI_07252 | 1.7e-08 | L | Transposase and inactivated derivatives, IS30 family | |||
AHMNLFMI_07253 | 2.1e-47 | L | Transposase and inactivated derivatives, IS30 family | |||
AHMNLFMI_07254 | 6.2e-29 | L | Transposase and inactivated derivatives, IS30 family | |||
AHMNLFMI_07256 | 5.4e-27 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_07257 | 5.4e-27 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_07258 | 3.3e-09 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AHMNLFMI_07259 | 9.2e-26 | S | Short C-terminal domain | |||
AHMNLFMI_07261 | 4.4e-26 | L | HTH-like domain | |||
AHMNLFMI_07262 | 4.9e-43 | L | HTH-like domain | |||
AHMNLFMI_07264 | 1.1e-62 | 1.3.5.4 | C | FMN_bind | ||
AHMNLFMI_07265 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHMNLFMI_07266 | 2.9e-44 | M | ErfK YbiS YcfS YnhG | |||
AHMNLFMI_07267 | 2.1e-39 | |||||
AHMNLFMI_07268 | 4.3e-280 | pipD | E | Dipeptidase | ||
AHMNLFMI_07269 | 5.1e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
AHMNLFMI_07270 | 4.2e-124 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AHMNLFMI_07271 | 3.8e-54 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AHMNLFMI_07272 | 1.9e-30 | potB | P | ABC transporter permease | ||
AHMNLFMI_07273 | 8.7e-82 | potB | P | ABC transporter permease | ||
AHMNLFMI_07274 | 1.8e-84 | |||||
AHMNLFMI_07275 | 3.4e-117 | hpk9 | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_07276 | 8.5e-54 | hpk9 | 2.7.13.3 | T | GHKL domain | |
AHMNLFMI_07277 | 9e-130 | K | UbiC transcription regulator-associated domain protein | |||
AHMNLFMI_07278 | 2e-141 | celB | 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 | ||
AHMNLFMI_07279 | 5.5e-145 | celB | 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 | ||
AHMNLFMI_07280 | 4.3e-15 | K | UbiC transcription regulator-associated domain protein | |||
AHMNLFMI_07282 | 1.4e-86 | EGP | Transmembrane secretion effector | |||
AHMNLFMI_07283 | 5.5e-66 | EGP | Transmembrane secretion effector |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)