ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HELEIBLM_00001 | 1.1e-287 | mphA | S | Aminoglycoside phosphotransferase | ||
HELEIBLM_00002 | 1.2e-32 | S | Protein of unknown function (DUF3107) | |||
HELEIBLM_00003 | 2.5e-169 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
HELEIBLM_00004 | 1.6e-126 | S | Vitamin K epoxide reductase | |||
HELEIBLM_00005 | 1.2e-163 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine | |
HELEIBLM_00006 | 7.9e-143 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HELEIBLM_00007 | 1.3e-156 | S | Patatin-like phospholipase | |||
HELEIBLM_00008 | 3.7e-115 | XK27_08050 | O | prohibitin homologues | ||
HELEIBLM_00009 | 1.6e-109 | E | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00010 | 8.1e-143 | tcyA | ET | Bacterial periplasmic substrate-binding proteins | ||
HELEIBLM_00011 | 1.9e-138 | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00012 | 2.4e-242 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
HELEIBLM_00013 | 2.2e-229 | S | Peptidase dimerisation domain | |||
HELEIBLM_00014 | 0.0 | E | ATPases associated with a variety of cellular activities | |||
HELEIBLM_00015 | 0.0 | E | Branched-chain amino acid transport system / permease component | |||
HELEIBLM_00016 | 4.5e-219 | E | Receptor family ligand binding region | |||
HELEIBLM_00017 | 5.4e-200 | 4.1.1.37 | H | Uroporphyrinogen decarboxylase (URO-D) | ||
HELEIBLM_00018 | 3.2e-144 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HELEIBLM_00019 | 3.8e-153 | E | Glyoxalase-like domain | |||
HELEIBLM_00020 | 9.5e-42 | XAC3035 | O | Glutaredoxin | ||
HELEIBLM_00021 | 1.4e-223 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
HELEIBLM_00022 | 3.1e-127 | cjaA | ET | Bacterial periplasmic substrate-binding proteins | ||
HELEIBLM_00023 | 4.1e-115 | glnQ | 3.6.3.21 | E | ATP binding protein of ABC transporter for glutamate aspartate K02028 | |
HELEIBLM_00024 | 6.8e-111 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00025 | 6.4e-98 | papP | E | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00026 | 5.9e-120 | ypfH | S | Phospholipase/Carboxylesterase | ||
HELEIBLM_00027 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
HELEIBLM_00028 | 8.1e-131 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
HELEIBLM_00030 | 7.8e-103 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
HELEIBLM_00031 | 6.3e-168 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
HELEIBLM_00032 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
HELEIBLM_00033 | 1.2e-239 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
HELEIBLM_00034 | 5.4e-77 | 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 | ||
HELEIBLM_00035 | 4e-104 | 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 | ||
HELEIBLM_00036 | 6.3e-113 | ybbL | V | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00037 | 8.6e-129 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
HELEIBLM_00038 | 7.3e-270 | T | Diguanylate cyclase, GGDEF domain | |||
HELEIBLM_00039 | 6.7e-99 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_00041 | 3.1e-83 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
HELEIBLM_00044 | 5.8e-99 | L | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_00045 | 1.6e-80 | S | N-methyltransferase activity | |||
HELEIBLM_00046 | 1.4e-79 | int | L | Phage integrase, N-terminal SAM-like domain | ||
HELEIBLM_00047 | 1.4e-36 | |||||
HELEIBLM_00048 | 2.6e-129 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
HELEIBLM_00049 | 1.1e-61 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
HELEIBLM_00050 | 0.0 | helY | L | DEAD DEAH box helicase | ||
HELEIBLM_00051 | 2.3e-48 | |||||
HELEIBLM_00052 | 0.0 | pafB | K | WYL domain | ||
HELEIBLM_00053 | 5e-295 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
HELEIBLM_00055 | 0.0 | der | 1.1.1.399, 1.1.1.95, 2.7.4.25 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HELEIBLM_00056 | 6.5e-142 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HELEIBLM_00057 | 2.3e-160 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HELEIBLM_00058 | 2e-30 | |||||
HELEIBLM_00060 | 1e-153 | cbiO | V | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00061 | 1e-187 | lanT | 3.6.3.27 | V | ABC transporter | |
HELEIBLM_00062 | 1e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HELEIBLM_00063 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
HELEIBLM_00064 | 1.3e-246 | pbuO | S | Permease family | ||
HELEIBLM_00065 | 3.6e-138 | 3.2.1.8 | S | alpha beta | ||
HELEIBLM_00066 | 3.1e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HELEIBLM_00067 | 1.1e-33 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HELEIBLM_00068 | 2.4e-187 | T | Forkhead associated domain | |||
HELEIBLM_00069 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
HELEIBLM_00070 | 1.7e-30 | |||||
HELEIBLM_00071 | 1.6e-93 | flgA | NO | SAF | ||
HELEIBLM_00072 | 2.5e-31 | fmdB | S | Putative regulatory protein | ||
HELEIBLM_00073 | 4.8e-118 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
HELEIBLM_00074 | 1.1e-126 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
HELEIBLM_00075 | 6.1e-186 | |||||
HELEIBLM_00076 | 6.7e-47 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HELEIBLM_00077 | 2.6e-40 | megL | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
HELEIBLM_00081 | 4.1e-25 | rpmG | J | Ribosomal protein L33 | ||
HELEIBLM_00082 | 2.1e-219 | murB | 1.3.1.98 | M | Cell wall formation | |
HELEIBLM_00083 | 4.4e-267 | E | aromatic amino acid transport protein AroP K03293 | |||
HELEIBLM_00084 | 1.7e-59 | fdxA | C | 4Fe-4S binding domain | ||
HELEIBLM_00085 | 2.7e-214 | dapC | E | Aminotransferase class I and II | ||
HELEIBLM_00086 | 2.1e-231 | 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 | |
HELEIBLM_00089 | 8.7e-187 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HELEIBLM_00090 | 5.5e-110 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
HELEIBLM_00091 | 4.9e-107 | |||||
HELEIBLM_00092 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
HELEIBLM_00093 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HELEIBLM_00094 | 3.7e-82 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HELEIBLM_00095 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HELEIBLM_00096 | 5.2e-223 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
HELEIBLM_00097 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HELEIBLM_00098 | 1.6e-38 | ywiC | S | YwiC-like protein | ||
HELEIBLM_00099 | 4.5e-143 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
HELEIBLM_00100 | 8e-51 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HELEIBLM_00101 | 1.1e-115 | 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 | ||
HELEIBLM_00102 | 1.2e-115 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HELEIBLM_00103 | 3.4e-46 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HELEIBLM_00104 | 8e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
HELEIBLM_00105 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HELEIBLM_00106 | 4.3e-56 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
HELEIBLM_00107 | 2.4e-102 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HELEIBLM_00108 | 1.7e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HELEIBLM_00109 | 4.1e-37 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HELEIBLM_00110 | 6.4e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HELEIBLM_00111 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HELEIBLM_00112 | 1.8e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HELEIBLM_00113 | 4.4e-103 | 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 | ||
HELEIBLM_00114 | 9.2e-18 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HELEIBLM_00115 | 5.5e-68 | 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 | ||
HELEIBLM_00116 | 1.6e-94 | 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 | ||
HELEIBLM_00117 | 2.1e-57 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
HELEIBLM_00118 | 1.5e-95 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HELEIBLM_00119 | 9.2e-26 | rpmD | J | Ribosomal protein L30p/L7e | ||
HELEIBLM_00120 | 1.1e-75 | rplO | J | binds to the 23S rRNA | ||
HELEIBLM_00121 | 7.6e-247 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
HELEIBLM_00122 | 6.5e-99 | 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 | |
HELEIBLM_00123 | 1.6e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
HELEIBLM_00124 | 8.4e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HELEIBLM_00125 | 4.7e-61 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
HELEIBLM_00126 | 1.5e-65 | 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 | ||
HELEIBLM_00127 | 2e-183 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HELEIBLM_00128 | 1.7e-61 | rplQ | J | Ribosomal protein L17 | ||
HELEIBLM_00129 | 2.6e-166 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HELEIBLM_00130 | 0.0 | gcs2 | S | A circularly permuted ATPgrasp | ||
HELEIBLM_00131 | 8.8e-150 | E | Transglutaminase/protease-like homologues | |||
HELEIBLM_00132 | 6.1e-217 | S | Psort location Cytoplasmic, score | |||
HELEIBLM_00134 | 2.6e-12 | L | Integrase core domain | |||
HELEIBLM_00135 | 2.4e-159 | P | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00136 | 6.3e-174 | P | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00137 | 8.1e-244 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_00138 | 9.9e-124 | |||||
HELEIBLM_00139 | 9.5e-184 | nusA | K | Participates in both transcription termination and antitermination | ||
HELEIBLM_00140 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
HELEIBLM_00141 | 8.1e-69 | 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 | ||
HELEIBLM_00142 | 1.1e-209 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HELEIBLM_00143 | 2.8e-218 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
HELEIBLM_00144 | 4.7e-277 | 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 | ||
HELEIBLM_00145 | 3.9e-92 | |||||
HELEIBLM_00147 | 1.5e-124 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HELEIBLM_00148 | 8.7e-124 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HELEIBLM_00150 | 1.4e-274 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HELEIBLM_00151 | 2.9e-67 | K | Transcriptional regulator | |||
HELEIBLM_00152 | 8.4e-185 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
HELEIBLM_00153 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
HELEIBLM_00154 | 0.0 | crr | 2.7.1.193 | G | pts system, glucose-specific IIABC component | |
HELEIBLM_00155 | 6.1e-160 | arbG | K | CAT RNA binding domain | ||
HELEIBLM_00156 | 1.7e-202 | I | Diacylglycerol kinase catalytic domain | |||
HELEIBLM_00157 | 1.7e-240 | 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) | |
HELEIBLM_00159 | 0.0 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
HELEIBLM_00160 | 9.3e-187 | mdsC | 2.7.1.162, 2.7.1.39 | S | Phosphotransferase enzyme family | |
HELEIBLM_00161 | 2.3e-300 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
HELEIBLM_00162 | 4.8e-185 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HELEIBLM_00163 | 2.7e-110 | degU | K | helix_turn_helix, Lux Regulon | ||
HELEIBLM_00164 | 5.8e-225 | tcsS3 | KT | PspC domain | ||
HELEIBLM_00165 | 1.1e-165 | pspC | KT | PspC domain | ||
HELEIBLM_00166 | 3.9e-53 | |||||
HELEIBLM_00167 | 2.1e-280 | S | alpha beta | |||
HELEIBLM_00168 | 1.2e-112 | S | Protein of unknown function (DUF4125) | |||
HELEIBLM_00169 | 8e-280 | S | Domain of unknown function (DUF4037) | |||
HELEIBLM_00170 | 0.0 | phoC | 3.1.3.5 | I | PAP2 superfamily | |
HELEIBLM_00171 | 3.7e-205 | araJ | EGP | Major facilitator Superfamily | ||
HELEIBLM_00173 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HELEIBLM_00174 | 2.1e-174 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
HELEIBLM_00175 | 1.4e-138 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HELEIBLM_00176 | 1.7e-114 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HELEIBLM_00177 | 1.5e-193 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
HELEIBLM_00178 | 4.3e-37 | |||||
HELEIBLM_00179 | 8.8e-212 | 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 | |
HELEIBLM_00181 | 1.5e-167 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
HELEIBLM_00182 | 1.1e-78 | M | NlpC/P60 family | |||
HELEIBLM_00183 | 4.4e-103 | M | NlpC/P60 family | |||
HELEIBLM_00184 | 2.6e-186 | T | Universal stress protein family | |||
HELEIBLM_00185 | 2e-73 | attW | O | OsmC-like protein | ||
HELEIBLM_00186 | 1.1e-172 | 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 | |
HELEIBLM_00187 | 4e-124 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
HELEIBLM_00188 | 1.1e-97 | ptpA | 3.1.3.48 | T | low molecular weight | |
HELEIBLM_00189 | 2.4e-110 | vex2 | V | ABC transporter, ATP-binding protein | ||
HELEIBLM_00190 | 3e-210 | vex1 | V | Efflux ABC transporter, permease protein | ||
HELEIBLM_00191 | 3.4e-218 | vex3 | V | ABC transporter permease | ||
HELEIBLM_00192 | 5.5e-228 | 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 | |
HELEIBLM_00193 | 5.5e-46 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
HELEIBLM_00194 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
HELEIBLM_00195 | 2.4e-181 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
HELEIBLM_00196 | 3.3e-132 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HELEIBLM_00197 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
HELEIBLM_00198 | 6.8e-125 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
HELEIBLM_00199 | 1.5e-124 | apl | 3.1.3.1 | S | SNARE associated Golgi protein | |
HELEIBLM_00200 | 3.9e-287 | arc | O | AAA ATPase forming ring-shaped complexes | ||
HELEIBLM_00201 | 0.0 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
HELEIBLM_00202 | 9.5e-169 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
HELEIBLM_00204 | 1.2e-269 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
HELEIBLM_00205 | 0.0 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_00206 | 5.9e-10 | yvnB | 3.1.4.53 | S | Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes | |
HELEIBLM_00207 | 3.5e-121 | S | AAA ATPase domain | |||
HELEIBLM_00208 | 1.7e-281 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
HELEIBLM_00209 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
HELEIBLM_00210 | 6.2e-42 | hup | L | Belongs to the bacterial histone-like protein family | ||
HELEIBLM_00211 | 5.7e-32 | L | HTH-like domain | |||
HELEIBLM_00213 | 3.9e-152 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00214 | 1.6e-150 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00215 | 3.3e-161 | P | Cation efflux family | |||
HELEIBLM_00216 | 9.5e-300 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HELEIBLM_00217 | 1.1e-137 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
HELEIBLM_00218 | 0.0 | yjjK | S | ABC transporter | ||
HELEIBLM_00219 | 2.1e-62 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
HELEIBLM_00220 | 8.6e-44 | stbC | S | Plasmid stability protein | ||
HELEIBLM_00221 | 3.8e-91 | ilvN | 2.2.1.6 | E | ACT domain | |
HELEIBLM_00222 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
HELEIBLM_00223 | 2e-132 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
HELEIBLM_00224 | 7.6e-31 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HELEIBLM_00225 | 6.3e-119 | yceD | S | Uncharacterized ACR, COG1399 | ||
HELEIBLM_00226 | 1.2e-120 | |||||
HELEIBLM_00227 | 2.1e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HELEIBLM_00228 | 2e-51 | S | Protein of unknown function (DUF3039) | |||
HELEIBLM_00229 | 9.6e-194 | yghZ | C | Aldo/keto reductase family | ||
HELEIBLM_00230 | 6.3e-70 | soxR | K | MerR, DNA binding | ||
HELEIBLM_00231 | 7.2e-115 | |||||
HELEIBLM_00232 | 3.7e-246 | 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 | |
HELEIBLM_00233 | 4.6e-81 | V | ABC-2 family transporter protein | |||
HELEIBLM_00234 | 1.1e-108 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_00235 | 4.1e-21 | tnp7109-21 | L | Integrase core domain | ||
HELEIBLM_00236 | 5.9e-27 | tnp7109-21 | L | Integrase core domain | ||
HELEIBLM_00237 | 9.3e-152 | M | Glycosyltransferase like family 2 | |||
HELEIBLM_00239 | 1.4e-223 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
HELEIBLM_00240 | 9.5e-114 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HELEIBLM_00241 | 2.8e-10 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HELEIBLM_00242 | 4.7e-41 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HELEIBLM_00243 | 4.8e-19 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HELEIBLM_00244 | 4.1e-86 | K | Periplasmic binding protein domain | |||
HELEIBLM_00245 | 3e-77 | F | Inosine-uridine preferring nucleoside hydrolase | |||
HELEIBLM_00246 | 1e-118 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_00247 | 7.1e-103 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00248 | 1.4e-84 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00249 | 5.6e-52 | rbsK | 2.7.1.15 | G | 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 | |
HELEIBLM_00250 | 7.8e-39 | F | Permease family | |||
HELEIBLM_00251 | 7.3e-121 | F | Permease family | |||
HELEIBLM_00252 | 4.3e-161 | L | HTH-like domain | |||
HELEIBLM_00253 | 7.2e-155 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
HELEIBLM_00254 | 5e-268 | 2.7.1.17 | GH19 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
HELEIBLM_00255 | 2.7e-255 | 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 | |
HELEIBLM_00256 | 5.2e-220 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
HELEIBLM_00257 | 1.8e-110 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
HELEIBLM_00258 | 5e-97 | |||||
HELEIBLM_00259 | 2e-120 | 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 | ||
HELEIBLM_00260 | 6.3e-131 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
HELEIBLM_00261 | 1.7e-19 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
HELEIBLM_00262 | 2.6e-263 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
HELEIBLM_00263 | 6.8e-186 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00264 | 2.8e-131 | appC | EP | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00265 | 4.7e-177 | EP | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00266 | 0.0 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
HELEIBLM_00267 | 5.1e-309 | P | Belongs to the ABC transporter superfamily | |||
HELEIBLM_00268 | 3.5e-172 | M | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses | |||
HELEIBLM_00269 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
HELEIBLM_00270 | 5.8e-123 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
HELEIBLM_00271 | 8.2e-274 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HELEIBLM_00272 | 3e-176 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
HELEIBLM_00273 | 6.7e-157 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
HELEIBLM_00274 | 6.6e-128 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
HELEIBLM_00275 | 1.3e-35 | M | Lysin motif | |||
HELEIBLM_00276 | 5.3e-78 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HELEIBLM_00277 | 4.9e-229 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
HELEIBLM_00278 | 0.0 | L | DNA helicase | |||
HELEIBLM_00279 | 5.5e-92 | mraZ | K | Belongs to the MraZ family | ||
HELEIBLM_00280 | 2.7e-194 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HELEIBLM_00281 | 3.2e-72 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
HELEIBLM_00282 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
HELEIBLM_00283 | 7.1e-153 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HELEIBLM_00284 | 1.2e-245 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HELEIBLM_00285 | 1.7e-204 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HELEIBLM_00286 | 7.1e-275 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HELEIBLM_00287 | 1.3e-224 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
HELEIBLM_00288 | 5.9e-219 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
HELEIBLM_00289 | 9.5e-286 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
HELEIBLM_00290 | 2.8e-183 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
HELEIBLM_00291 | 4.1e-15 | |||||
HELEIBLM_00292 | 3.9e-248 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
HELEIBLM_00293 | 0.0 | M | probably involved in cell wall | |||
HELEIBLM_00294 | 5e-121 | S | Membrane transport protein | |||
HELEIBLM_00295 | 1.3e-32 | ybbL | V | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00296 | 2.3e-82 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
HELEIBLM_00297 | 0.0 | G | Glycosyl hydrolase family 20, domain 2 | |||
HELEIBLM_00298 | 6.2e-202 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
HELEIBLM_00299 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
HELEIBLM_00300 | 0.0 | S | Tetratricopeptide repeat | |||
HELEIBLM_00301 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HELEIBLM_00302 | 9.4e-139 | bioM | P | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00303 | 2.5e-231 | E | Aminotransferase class I and II | |||
HELEIBLM_00304 | 4.6e-140 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
HELEIBLM_00305 | 1.8e-200 | S | Glycosyltransferase, group 2 family protein | |||
HELEIBLM_00306 | 1.9e-102 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
HELEIBLM_00307 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
HELEIBLM_00308 | 9.1e-47 | yhbY | J | CRS1_YhbY | ||
HELEIBLM_00309 | 5.4e-54 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
HELEIBLM_00310 | 6.5e-53 | J | TM2 domain | |||
HELEIBLM_00311 | 1.2e-185 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
HELEIBLM_00312 | 3.4e-248 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00313 | 3e-246 | rarA | L | Recombination factor protein RarA | ||
HELEIBLM_00314 | 0.0 | L | DEAD DEAH box helicase | |||
HELEIBLM_00315 | 5.1e-177 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
HELEIBLM_00316 | 4e-284 | phoN | I | PAP2 superfamily | ||
HELEIBLM_00317 | 1.2e-184 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00318 | 3.9e-106 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00319 | 4.4e-152 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HELEIBLM_00320 | 1e-140 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
HELEIBLM_00321 | 7.9e-182 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein of unknown function (DUF559) | |
HELEIBLM_00323 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
HELEIBLM_00324 | 5.7e-261 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
HELEIBLM_00325 | 2.1e-210 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
HELEIBLM_00326 | 5.6e-306 | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
HELEIBLM_00327 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
HELEIBLM_00328 | 1.6e-177 | uspA | T | Belongs to the universal stress protein A family | ||
HELEIBLM_00329 | 6e-163 | S | Protein of unknown function (DUF3027) | |||
HELEIBLM_00330 | 6.5e-66 | cspB | K | 'Cold-shock' DNA-binding domain | ||
HELEIBLM_00331 | 0.0 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
HELEIBLM_00332 | 5.6e-133 | KT | Response regulator receiver domain protein | |||
HELEIBLM_00333 | 8.6e-66 | |||||
HELEIBLM_00334 | 1.7e-34 | S | Proteins of 100 residues with WXG | |||
HELEIBLM_00335 | 4.7e-291 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HELEIBLM_00336 | 1.4e-37 | K | 'Cold-shock' DNA-binding domain | |||
HELEIBLM_00337 | 3.1e-71 | S | LytR cell envelope-related transcriptional attenuator | |||
HELEIBLM_00338 | 6e-131 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
HELEIBLM_00339 | 3.3e-192 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
HELEIBLM_00340 | 3.1e-170 | S | Protein of unknown function DUF58 | |||
HELEIBLM_00341 | 1.1e-90 | |||||
HELEIBLM_00342 | 6.1e-183 | S | von Willebrand factor (vWF) type A domain | |||
HELEIBLM_00343 | 1.8e-163 | S | von Willebrand factor (vWF) type A domain | |||
HELEIBLM_00344 | 3.5e-45 | |||||
HELEIBLM_00345 | 5.5e-48 | |||||
HELEIBLM_00346 | 5.6e-305 | S | PGAP1-like protein | |||
HELEIBLM_00347 | 6.2e-13 | |||||
HELEIBLM_00348 | 1e-108 | ykoE | S | ABC-type cobalt transport system, permease component | ||
HELEIBLM_00349 | 3.4e-208 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_00350 | 1.5e-147 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HELEIBLM_00351 | 1.5e-139 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HELEIBLM_00352 | 1.1e-59 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
HELEIBLM_00353 | 0.0 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00354 | 4.3e-256 | abcT3 | P | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00355 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HELEIBLM_00358 | 5.8e-167 | S | Auxin Efflux Carrier | |||
HELEIBLM_00359 | 2e-113 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_00360 | 9.1e-95 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_00361 | 2.2e-235 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_00363 | 1.9e-130 | 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 | |
HELEIBLM_00364 | 4.1e-144 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
HELEIBLM_00365 | 3.4e-160 | |||||
HELEIBLM_00366 | 7.1e-50 | thiF | 2.7.7.80 | H | Involved in molybdopterin and thiamine biosynthesis, family 2 | |
HELEIBLM_00367 | 3.9e-240 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00368 | 2.9e-34 | D | Filamentation induced by cAMP protein fic | |||
HELEIBLM_00369 | 1.3e-202 | L | Transposase, Mutator family | |||
HELEIBLM_00370 | 8.6e-11 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
HELEIBLM_00372 | 3.3e-26 | |||||
HELEIBLM_00373 | 2.1e-140 | fic | D | Fic/DOC family | ||
HELEIBLM_00374 | 1.5e-52 | L | Phage integrase family | |||
HELEIBLM_00375 | 3e-150 | L | Phage integrase family | |||
HELEIBLM_00376 | 1.7e-184 | V | Abi-like protein | |||
HELEIBLM_00377 | 1.3e-14 | V | Abi-like protein | |||
HELEIBLM_00380 | 3.9e-43 | yxaM | EGP | Major Facilitator Superfamily | ||
HELEIBLM_00381 | 2.6e-12 | S | YcaO cyclodehydratase, ATP-ad Mg2+-binding | |||
HELEIBLM_00382 | 4.7e-09 | L | Transposase | |||
HELEIBLM_00383 | 2.1e-206 | K | Transposase IS116 IS110 IS902 | |||
HELEIBLM_00384 | 4.4e-113 | L | IstB-like ATP binding protein | |||
HELEIBLM_00385 | 2.2e-123 | L | PFAM Integrase catalytic | |||
HELEIBLM_00386 | 2.2e-11 | S | EamA-like transporter family | |||
HELEIBLM_00387 | 6.8e-43 | |||||
HELEIBLM_00388 | 0.0 | E | Sodium:solute symporter family | |||
HELEIBLM_00389 | 2.5e-47 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HELEIBLM_00390 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_00391 | 0.0 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
HELEIBLM_00392 | 1.3e-255 | fucA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
HELEIBLM_00393 | 4.2e-69 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
HELEIBLM_00394 | 4.7e-152 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
HELEIBLM_00395 | 1.5e-141 | IQ | KR domain | |||
HELEIBLM_00396 | 1.8e-242 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
HELEIBLM_00397 | 1.3e-95 | S | Protein of unknown function, DUF624 | |||
HELEIBLM_00398 | 1.7e-81 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
HELEIBLM_00399 | 6.5e-22 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
HELEIBLM_00400 | 7.3e-74 | uhpT | EGP | Major facilitator Superfamily | ||
HELEIBLM_00401 | 5e-94 | L | HTH-like domain | |||
HELEIBLM_00402 | 2.3e-31 | L | HTH-like domain | |||
HELEIBLM_00403 | 1.5e-59 | K | Virulence activator alpha C-term | |||
HELEIBLM_00404 | 5.9e-263 | V | FtsX-like permease family | |||
HELEIBLM_00405 | 1.5e-94 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_00406 | 1.2e-29 | |||||
HELEIBLM_00407 | 2.6e-17 | L | Transposase, Mutator family | |||
HELEIBLM_00408 | 2.3e-85 | |||||
HELEIBLM_00409 | 6.6e-21 | |||||
HELEIBLM_00410 | 6.8e-60 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_00411 | 3.5e-114 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HELEIBLM_00412 | 1.3e-108 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
HELEIBLM_00413 | 2.5e-234 | rfbP | 2.7.8.6 | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | |
HELEIBLM_00416 | 4.9e-45 | ytrE_1 | 3.6.3.21 | V | ABC transporter | |
HELEIBLM_00417 | 6.1e-22 | V | efflux transmembrane transporter activity | |||
HELEIBLM_00418 | 2.1e-55 | |||||
HELEIBLM_00419 | 5.8e-112 | K | helix_turn_helix, mercury resistance | |||
HELEIBLM_00420 | 1.1e-74 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
HELEIBLM_00421 | 2.1e-138 | S | Bacterial protein of unknown function (DUF881) | |||
HELEIBLM_00422 | 1.2e-28 | sbp | S | Protein of unknown function (DUF1290) | ||
HELEIBLM_00423 | 1.6e-124 | S | Bacterial protein of unknown function (DUF881) | |||
HELEIBLM_00424 | 6e-106 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HELEIBLM_00425 | 2.1e-157 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
HELEIBLM_00426 | 9.9e-42 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
HELEIBLM_00427 | 2.3e-103 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
HELEIBLM_00428 | 1.2e-185 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HELEIBLM_00429 | 3.9e-159 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
HELEIBLM_00430 | 0.0 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
HELEIBLM_00431 | 5.5e-132 | S | SOS response associated peptidase (SRAP) | |||
HELEIBLM_00432 | 4.3e-155 | 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 | |
HELEIBLM_00433 | 9.7e-253 | mmuP | E | amino acid | ||
HELEIBLM_00434 | 4.2e-80 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00435 | 1.1e-189 | V | VanZ like family | |||
HELEIBLM_00436 | 4e-14 | cefD | 5.1.1.17 | E | Aminotransferase, class V | |
HELEIBLM_00437 | 6.5e-19 | cefD | 5.1.1.17 | E | Aminotransferase, class V | |
HELEIBLM_00438 | 4.2e-56 | S | EamA-like transporter family | |||
HELEIBLM_00439 | 1.6e-206 | L | Transposase | |||
HELEIBLM_00440 | 4.6e-88 | |||||
HELEIBLM_00441 | 3.8e-170 | V | MacB-like periplasmic core domain | |||
HELEIBLM_00442 | 5e-128 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_00443 | 1.3e-119 | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | |||
HELEIBLM_00444 | 2e-30 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_00445 | 4.9e-22 | K | trisaccharide binding | |||
HELEIBLM_00446 | 4.9e-109 | K | COG COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HELEIBLM_00447 | 3.5e-117 | T | PhoQ Sensor | |||
HELEIBLM_00448 | 1.2e-110 | V | ABC transporter | |||
HELEIBLM_00449 | 2.8e-276 | V | FtsX-like permease family | |||
HELEIBLM_00450 | 9.3e-27 | K | Psort location Cytoplasmic, score | |||
HELEIBLM_00453 | 7.2e-190 | 3.6.4.12 | K | Divergent AAA domain protein | ||
HELEIBLM_00454 | 2e-120 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_00455 | 2.2e-99 | |||||
HELEIBLM_00456 | 4.4e-80 | |||||
HELEIBLM_00458 | 5.9e-17 | spaB | S | Lantibiotic biosynthesis dehydratase C-term | ||
HELEIBLM_00459 | 3.2e-18 | V | Lanthionine synthetase C-like protein | |||
HELEIBLM_00460 | 9.6e-41 | V | ATPase activity | |||
HELEIBLM_00461 | 1.6e-43 | V | ABC-2 type transporter | |||
HELEIBLM_00462 | 0.0 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
HELEIBLM_00463 | 1.3e-271 | S | Psort location Cytoplasmic, score | |||
HELEIBLM_00464 | 5.5e-125 | |||||
HELEIBLM_00466 | 4.8e-25 | |||||
HELEIBLM_00467 | 3e-69 | |||||
HELEIBLM_00468 | 1.7e-35 | |||||
HELEIBLM_00469 | 2.3e-102 | parA | D | AAA domain | ||
HELEIBLM_00470 | 8e-83 | S | Transcription factor WhiB | |||
HELEIBLM_00471 | 4.3e-233 | S | Helix-turn-helix domain | |||
HELEIBLM_00472 | 2.2e-21 | |||||
HELEIBLM_00473 | 2.6e-11 | |||||
HELEIBLM_00475 | 1.1e-158 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
HELEIBLM_00476 | 2.6e-199 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HELEIBLM_00478 | 7.9e-257 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
HELEIBLM_00479 | 4.9e-202 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
HELEIBLM_00480 | 1.5e-177 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
HELEIBLM_00481 | 4.8e-267 | S | AI-2E family transporter | |||
HELEIBLM_00482 | 8.2e-232 | epsG | M | Glycosyl transferase family 21 | ||
HELEIBLM_00483 | 6.1e-147 | natA | V | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00484 | 1.1e-300 | |||||
HELEIBLM_00485 | 4.5e-256 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
HELEIBLM_00486 | 1.1e-212 | 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 | |
HELEIBLM_00487 | 1.4e-96 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HELEIBLM_00488 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
HELEIBLM_00490 | 5.8e-106 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
HELEIBLM_00491 | 2.5e-158 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
HELEIBLM_00492 | 2.1e-263 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
HELEIBLM_00493 | 7.2e-92 | S | Protein of unknown function (DUF3180) | |||
HELEIBLM_00494 | 4.3e-169 | tesB | I | Thioesterase-like superfamily | ||
HELEIBLM_00495 | 0.0 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
HELEIBLM_00496 | 1.1e-09 | L | Transposase, Mutator family | |||
HELEIBLM_00497 | 4.4e-206 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00498 | 6.9e-72 | C | Domain of unknown function (DUF4365) | |||
HELEIBLM_00499 | 5.8e-165 | res | 3.1.21.5 | V | Type III restriction enzyme, res subunit | |
HELEIBLM_00501 | 5.8e-97 | K | Helix-turn-helix domain protein | |||
HELEIBLM_00503 | 1.6e-99 | S | Acetyltransferase (GNAT) domain | |||
HELEIBLM_00504 | 5.4e-36 | S | Uncharacterized protein conserved in bacteria (DUF2316) | |||
HELEIBLM_00505 | 1.3e-90 | MA20_25245 | K | FR47-like protein | ||
HELEIBLM_00506 | 6.2e-46 | L | Transposase | |||
HELEIBLM_00507 | 3.6e-194 | |||||
HELEIBLM_00508 | 1e-133 | ytrE | V | ABC transporter | ||
HELEIBLM_00509 | 2.2e-188 | V | Putative peptidoglycan binding domain | |||
HELEIBLM_00510 | 1.1e-119 | |||||
HELEIBLM_00511 | 2.9e-48 | |||||
HELEIBLM_00512 | 4.6e-120 | K | Transcriptional regulatory protein, C terminal | |||
HELEIBLM_00513 | 3.9e-232 | qseC | 2.7.13.3 | T | GHKL domain | |
HELEIBLM_00514 | 3.5e-97 | K | transcriptional regulator | |||
HELEIBLM_00515 | 6.4e-37 | |||||
HELEIBLM_00516 | 4.4e-29 | |||||
HELEIBLM_00517 | 7.6e-144 | |||||
HELEIBLM_00518 | 1.1e-65 | S | PrgI family protein | |||
HELEIBLM_00519 | 2.1e-131 | trsE | U | type IV secretory pathway VirB4 | ||
HELEIBLM_00520 | 4.3e-24 | |||||
HELEIBLM_00522 | 7.5e-124 | V | ABC transporter | |||
HELEIBLM_00525 | 2e-26 | U | Type IV secretory system Conjugative DNA transfer | |||
HELEIBLM_00526 | 1.7e-230 | T | Histidine kinase | |||
HELEIBLM_00527 | 1.1e-122 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_00528 | 7.3e-121 | V | ABC transporter | |||
HELEIBLM_00529 | 1.4e-17 | |||||
HELEIBLM_00530 | 8.9e-93 | E | Asparagine synthase | |||
HELEIBLM_00531 | 1.6e-138 | V | ABC transporter | |||
HELEIBLM_00532 | 1.8e-222 | V | Efflux ABC transporter, permease protein | |||
HELEIBLM_00533 | 2.3e-66 | |||||
HELEIBLM_00534 | 5.2e-41 | |||||
HELEIBLM_00535 | 1.4e-194 | T | Histidine kinase | |||
HELEIBLM_00536 | 1.9e-116 | K | Bacterial regulatory proteins, luxR family | |||
HELEIBLM_00537 | 1.2e-116 | V | VanZ like family | |||
HELEIBLM_00538 | 5.3e-96 | rpoE4 | K | Sigma-70 region 2 | ||
HELEIBLM_00539 | 1.1e-22 | S | Psort location CytoplasmicMembrane, score | |||
HELEIBLM_00540 | 2.1e-106 | |||||
HELEIBLM_00541 | 1.4e-136 | |||||
HELEIBLM_00542 | 2.4e-169 | yfiL | V | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00543 | 1.1e-65 | |||||
HELEIBLM_00544 | 1.1e-140 | G | Glycosyl hydrolase family 20, domain 2 | |||
HELEIBLM_00545 | 5.3e-68 | G | Glycosyl hydrolase family 20, domain 2 | |||
HELEIBLM_00546 | 1e-33 | G | Glycosyl hydrolase family 20, domain 2 | |||
HELEIBLM_00547 | 4.4e-244 | L | Phage integrase family | |||
HELEIBLM_00549 | 3.6e-20 | S | Protein of unknown function (DUF2599) | |||
HELEIBLM_00550 | 2.5e-127 | |||||
HELEIBLM_00551 | 5.6e-78 | |||||
HELEIBLM_00552 | 1.7e-211 | L | Phage integrase family | |||
HELEIBLM_00553 | 2.6e-139 | M | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_00554 | 3e-52 | GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
HELEIBLM_00555 | 2e-07 | |||||
HELEIBLM_00556 | 8.9e-63 | C | Polysaccharide pyruvyl transferase | |||
HELEIBLM_00557 | 2.9e-119 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HELEIBLM_00558 | 1.3e-46 | M | Glycosyltransferase like family 2 | |||
HELEIBLM_00559 | 1.3e-177 | menD | 2.2.1.9 | H | Thiamine pyrophosphate enzyme, N-terminal TPP binding domain | |
HELEIBLM_00560 | 6e-20 | L | Phage integrase family | |||
HELEIBLM_00561 | 1e-167 | L | Phage integrase, N-terminal SAM-like domain | |||
HELEIBLM_00562 | 4.9e-47 | insK | L | Integrase core domain | ||
HELEIBLM_00563 | 2e-62 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
HELEIBLM_00564 | 1.2e-296 | S | domain protein | |||
HELEIBLM_00565 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
HELEIBLM_00566 | 1.2e-283 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
HELEIBLM_00567 | 1.5e-129 | 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 | |
HELEIBLM_00568 | 3.7e-132 | KT | Transcriptional regulatory protein, C terminal | |||
HELEIBLM_00569 | 1.2e-78 | |||||
HELEIBLM_00570 | 4.8e-97 | mntP | P | Probably functions as a manganese efflux pump | ||
HELEIBLM_00571 | 2.8e-90 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
HELEIBLM_00572 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
HELEIBLM_00573 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
HELEIBLM_00574 | 8e-75 | S | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_00575 | 2.8e-08 | phyR | K | Psort location Cytoplasmic, score | ||
HELEIBLM_00576 | 3e-95 | G | Hypothetical glycosyl hydrolase 6 | |||
HELEIBLM_00579 | 8.9e-12 | |||||
HELEIBLM_00580 | 3.2e-22 | S | Ribonuclease toxin, BrnT, of type II toxin-antitoxin system | |||
HELEIBLM_00581 | 1.2e-204 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
HELEIBLM_00582 | 5.1e-145 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HELEIBLM_00583 | 1.5e-30 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
HELEIBLM_00584 | 2.9e-61 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HELEIBLM_00585 | 2.3e-146 | 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 | ||
HELEIBLM_00586 | 7.4e-305 | 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 | |
HELEIBLM_00587 | 4.1e-159 | 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 | ||
HELEIBLM_00588 | 4.4e-280 | 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 | |
HELEIBLM_00589 | 1.6e-48 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HELEIBLM_00590 | 5e-134 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
HELEIBLM_00591 | 9.2e-157 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
HELEIBLM_00592 | 3.9e-185 | |||||
HELEIBLM_00593 | 1.9e-181 | |||||
HELEIBLM_00594 | 3.7e-166 | trxA2 | O | Tetratricopeptide repeat | ||
HELEIBLM_00595 | 2.4e-118 | cyaA | 4.6.1.1 | S | CYTH | |
HELEIBLM_00597 | 4e-63 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
HELEIBLM_00598 | 9.3e-183 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
HELEIBLM_00599 | 4.1e-181 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
HELEIBLM_00600 | 3.8e-226 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HELEIBLM_00601 | 2.8e-205 | P | Bacterial extracellular solute-binding protein | |||
HELEIBLM_00602 | 2.6e-156 | U | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00603 | 1.4e-129 | U | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00604 | 9.9e-228 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
HELEIBLM_00605 | 1.1e-176 | S | CAAX protease self-immunity | |||
HELEIBLM_00606 | 5.5e-128 | M | Mechanosensitive ion channel | |||
HELEIBLM_00607 | 2.2e-268 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
HELEIBLM_00608 | 7.3e-135 | K | Bacterial regulatory proteins, tetR family | |||
HELEIBLM_00609 | 3.3e-237 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
HELEIBLM_00610 | 6.5e-87 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
HELEIBLM_00615 | 2.8e-23 | yxiO | G | Major facilitator Superfamily | ||
HELEIBLM_00616 | 1.6e-11 | S | Alpha/beta hydrolase family | |||
HELEIBLM_00617 | 5.2e-21 | |||||
HELEIBLM_00618 | 9.8e-189 | K | Helix-turn-helix XRE-family like proteins | |||
HELEIBLM_00619 | 5e-19 | yxiO | G | Major facilitator Superfamily | ||
HELEIBLM_00620 | 9e-53 | relB | L | RelB antitoxin | ||
HELEIBLM_00621 | 2.7e-20 | T | Toxic component of a toxin-antitoxin (TA) module | |||
HELEIBLM_00622 | 1.1e-130 | K | helix_turn_helix, mercury resistance | |||
HELEIBLM_00623 | 2.1e-230 | yxiO | S | Vacuole effluxer Atg22 like | ||
HELEIBLM_00624 | 4.6e-196 | yegV | G | pfkB family carbohydrate kinase | ||
HELEIBLM_00625 | 5.5e-29 | rpmB | J | Ribosomal L28 family | ||
HELEIBLM_00626 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
HELEIBLM_00627 | 3.1e-09 | steT | E | amino acid | ||
HELEIBLM_00628 | 2.3e-152 | L | Helix-turn-helix domain | |||
HELEIBLM_00629 | 5.5e-96 | L | Resolvase, N terminal domain | |||
HELEIBLM_00630 | 7.3e-38 | O | Bacterial Ig-like domain (group 3) | |||
HELEIBLM_00631 | 4.1e-176 | U | Sodium:dicarboxylate symporter family | |||
HELEIBLM_00632 | 2.5e-104 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
HELEIBLM_00633 | 1.3e-153 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HELEIBLM_00634 | 0.0 | yegQ | O | Peptidase family U32 C-terminal domain | ||
HELEIBLM_00635 | 3.1e-181 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
HELEIBLM_00636 | 1.3e-157 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
HELEIBLM_00637 | 3.5e-123 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
HELEIBLM_00638 | 1.3e-59 | D | nuclear chromosome segregation | |||
HELEIBLM_00639 | 2.6e-263 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HELEIBLM_00640 | 6.7e-212 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HELEIBLM_00641 | 1.4e-234 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HELEIBLM_00642 | 3.1e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
HELEIBLM_00643 | 1.7e-230 | EGP | Sugar (and other) transporter | |||
HELEIBLM_00644 | 1.3e-204 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
HELEIBLM_00645 | 1.8e-139 | KT | Transcriptional regulatory protein, C terminal | |||
HELEIBLM_00646 | 8.8e-180 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
HELEIBLM_00647 | 3.5e-153 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HELEIBLM_00648 | 1.1e-168 | pstA | P | Phosphate transport system permease | ||
HELEIBLM_00649 | 1.2e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
HELEIBLM_00650 | 4.3e-90 | lemA | S | LemA family | ||
HELEIBLM_00651 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
HELEIBLM_00652 | 4.5e-168 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
HELEIBLM_00653 | 2.6e-194 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HELEIBLM_00654 | 5.6e-122 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_00655 | 1.5e-140 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_00656 | 1.6e-118 | U | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00657 | 7.6e-112 | U | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00658 | 2.4e-226 | |||||
HELEIBLM_00659 | 0.0 | tetP | J | elongation factor G | ||
HELEIBLM_00660 | 2.4e-28 | Q | Psort location Cytoplasmic, score | |||
HELEIBLM_00661 | 5e-28 | 2.7.11.1 | S | Pfam:HipA_N | ||
HELEIBLM_00662 | 7.5e-117 | 2.7.11.1 | S | Pfam:HipA_N | ||
HELEIBLM_00663 | 1.5e-109 | 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 | ||
HELEIBLM_00664 | 6.1e-35 | CP_0960 | S | Belongs to the UPF0109 family | ||
HELEIBLM_00665 | 8.3e-60 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HELEIBLM_00666 | 3.7e-140 | pabC | 2.6.1.42, 2.6.1.85, 4.1.3.38 | E | branched-chain-amino-acid transaminase activity | |
HELEIBLM_00667 | 4e-267 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | chorismate binding enzyme | |
HELEIBLM_00668 | 5e-212 | 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 | |
HELEIBLM_00669 | 2.8e-111 | ribE | 2.5.1.9 | H | Lumazine binding domain | |
HELEIBLM_00670 | 7.1e-236 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
HELEIBLM_00671 | 2.5e-80 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
HELEIBLM_00672 | 4e-161 | S | Endonuclease/Exonuclease/phosphatase family | |||
HELEIBLM_00673 | 1.2e-260 | 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 | |
HELEIBLM_00674 | 8.4e-30 | L | Phage integrase family | |||
HELEIBLM_00675 | 2.7e-227 | xerC_1 | L | Belongs to the 'phage' integrase family | ||
HELEIBLM_00676 | 1.4e-80 | L | Phage integrase, N-terminal SAM-like domain | |||
HELEIBLM_00677 | 2.8e-31 | L | Phage integrase, N-terminal SAM-like domain | |||
HELEIBLM_00678 | 8e-288 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
HELEIBLM_00679 | 0.0 | S | Zincin-like metallopeptidase | |||
HELEIBLM_00680 | 7.4e-158 | lon | T | Belongs to the peptidase S16 family | ||
HELEIBLM_00681 | 2e-44 | S | Protein of unknown function (DUF3052) | |||
HELEIBLM_00683 | 8e-233 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
HELEIBLM_00684 | 4e-215 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
HELEIBLM_00685 | 8.2e-232 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
HELEIBLM_00686 | 7.6e-284 | I | acetylesterase activity | |||
HELEIBLM_00687 | 2.2e-112 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HELEIBLM_00688 | 5.8e-154 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HELEIBLM_00689 | 4.8e-208 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
HELEIBLM_00690 | 7e-203 | P | NMT1/THI5 like | |||
HELEIBLM_00691 | 5.8e-138 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
HELEIBLM_00692 | 9.6e-302 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
HELEIBLM_00693 | 3.1e-240 | lacY | P | LacY proton/sugar symporter | ||
HELEIBLM_00694 | 7.1e-192 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_00695 | 1.6e-242 | O | SERine Proteinase INhibitors | |||
HELEIBLM_00696 | 9.2e-39 | |||||
HELEIBLM_00697 | 1.2e-61 | S | Thiamine-binding protein | |||
HELEIBLM_00698 | 1.1e-144 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HELEIBLM_00699 | 4.9e-229 | O | AAA domain (Cdc48 subfamily) | |||
HELEIBLM_00700 | 0.0 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
HELEIBLM_00701 | 5.7e-164 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
HELEIBLM_00702 | 8.2e-295 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
HELEIBLM_00703 | 1e-237 | 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 | ||
HELEIBLM_00704 | 6.3e-192 | 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 | ||
HELEIBLM_00705 | 7.5e-80 | 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 | ||
HELEIBLM_00706 | 3.9e-42 | yggT | S | YGGT family | ||
HELEIBLM_00707 | 7.8e-37 | tccB2 | V | DivIVA protein | ||
HELEIBLM_00708 | 1.2e-89 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HELEIBLM_00709 | 2.9e-179 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HELEIBLM_00710 | 7.1e-129 | S | Virulence factor BrkB | |||
HELEIBLM_00711 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
HELEIBLM_00712 | 3.1e-75 | yneG | S | Domain of unknown function (DUF4186) | ||
HELEIBLM_00713 | 0.0 | 4.2.1.53 | S | MCRA family | ||
HELEIBLM_00714 | 1.5e-48 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_00716 | 1.7e-09 | K | Helix-turn-helix domain | |||
HELEIBLM_00718 | 9.5e-275 | L | PFAM Integrase catalytic | |||
HELEIBLM_00719 | 7.3e-133 | L | IstB-like ATP binding protein | |||
HELEIBLM_00720 | 1.4e-47 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_00721 | 2.5e-113 | |||||
HELEIBLM_00722 | 1.2e-49 | |||||
HELEIBLM_00723 | 7.3e-112 | S | AIPR protein | |||
HELEIBLM_00724 | 9e-106 | M | domain protein | |||
HELEIBLM_00725 | 0.0 | Q | von Willebrand factor (vWF) type A domain | |||
HELEIBLM_00726 | 1e-109 | |||||
HELEIBLM_00728 | 8.9e-26 | dexB | 2.4.1.7, 3.2.1.20, 3.2.1.51, 3.2.1.70, 3.2.1.93, 3.2.1.97 | GH101,GH13,GH29,GH31 | G | hydrolase activity, hydrolyzing O-glycosyl compounds |
HELEIBLM_00729 | 2.7e-97 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
HELEIBLM_00731 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HELEIBLM_00732 | 5.5e-292 | pccB | I | Carboxyl transferase domain | ||
HELEIBLM_00733 | 0.0 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
HELEIBLM_00734 | 1e-13 | bioY | S | BioY family | ||
HELEIBLM_00735 | 1.5e-142 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
HELEIBLM_00736 | 0.0 | |||||
HELEIBLM_00737 | 5.4e-137 | QT | PucR C-terminal helix-turn-helix domain | |||
HELEIBLM_00738 | 2.5e-24 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_00739 | 7e-117 | 2.2.1.1 | G | Transketolase, pyrimidine binding domain | ||
HELEIBLM_00740 | 3.2e-108 | tktN | 2.2.1.1 | G | Dehydrogenase E1 component | |
HELEIBLM_00741 | 0.0 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
HELEIBLM_00742 | 6.2e-130 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00743 | 2.1e-08 | ycnE | S | Antibiotic biosynthesis monooxygenase | ||
HELEIBLM_00744 | 2.5e-115 | iolT | EGP | Major facilitator Superfamily | ||
HELEIBLM_00745 | 1.2e-128 | iolE | 4.2.1.44 | G | dehydratase | |
HELEIBLM_00746 | 4e-139 | iolG | 1.1.1.18, 1.1.1.369 | C | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
HELEIBLM_00747 | 1.8e-104 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
HELEIBLM_00748 | 2.5e-48 | K | helix_turn_helix, arabinose operon control protein | |||
HELEIBLM_00749 | 1.5e-157 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
HELEIBLM_00750 | 1.3e-83 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HELEIBLM_00751 | 5.2e-75 | K | Sugar-specific transcriptional regulator TrmB | |||
HELEIBLM_00752 | 9.5e-69 | K | Bacterial transcriptional regulator | |||
HELEIBLM_00753 | 7.1e-206 | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Aldehyde dehydrogenase family | ||
HELEIBLM_00754 | 2.4e-161 | 1.1.1.1 | C | Alcohol dehydrogenase GroES-like domain | ||
HELEIBLM_00755 | 1.9e-129 | iolB | 5.3.1.30 | G | PFAM Myo-inositol catabolism IolB domain protein | |
HELEIBLM_00756 | 1.4e-275 | iolD | 3.7.1.22 | E | Thiamine pyrophosphate enzyme, central domain | |
HELEIBLM_00757 | 7.7e-29 | insK | L | Integrase core domain | ||
HELEIBLM_00758 | 3.5e-52 | FG | bis(5'-adenosyl)-triphosphatase activity | |||
HELEIBLM_00759 | 6.8e-177 | uxaC | 5.3.1.12 | G | Glucuronate isomerase | |
HELEIBLM_00760 | 2e-194 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
HELEIBLM_00761 | 2e-233 | rspA | 4.2.1.8 | M | mandelate racemase muconate lactonizing | |
HELEIBLM_00762 | 3.6e-232 | 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 | |
HELEIBLM_00763 | 2.4e-67 | K | Periplasmic binding proteins and sugar binding domain of LacI family | |||
HELEIBLM_00764 | 3.3e-61 | K | Periplasmic binding proteins and sugar binding domain of LacI family | |||
HELEIBLM_00765 | 8.9e-48 | G | MFS/sugar transport protein | |||
HELEIBLM_00766 | 1.3e-43 | G | MFS/sugar transport protein | |||
HELEIBLM_00767 | 3e-19 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
HELEIBLM_00768 | 9e-169 | uxuT | G | MFS/sugar transport protein | ||
HELEIBLM_00769 | 7.6e-91 | L | Transposase | |||
HELEIBLM_00770 | 1.4e-31 | L | Transposase | |||
HELEIBLM_00771 | 1.4e-50 | L | Phage integrase family | |||
HELEIBLM_00773 | 1.9e-49 | |||||
HELEIBLM_00774 | 1.1e-100 | L | PFAM Integrase catalytic | |||
HELEIBLM_00775 | 1.2e-25 | L | PFAM Integrase catalytic | |||
HELEIBLM_00776 | 8.2e-09 | D | nuclear chromosome segregation | |||
HELEIBLM_00779 | 0.0 | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | ||
HELEIBLM_00780 | 0.0 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
HELEIBLM_00781 | 4.7e-120 | K | Bacterial regulatory proteins, tetR family | |||
HELEIBLM_00782 | 2.2e-117 | S | Protein of unknown function, DUF624 | |||
HELEIBLM_00783 | 3.3e-250 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
HELEIBLM_00784 | 0.0 | G | transport | |||
HELEIBLM_00785 | 1.4e-167 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00786 | 1.7e-179 | P | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00787 | 3.2e-77 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_00788 | 4.4e-166 | dcm | 2.1.1.37 | L | Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family | |
HELEIBLM_00789 | 1.1e-50 | ybjQ | S | Putative heavy-metal-binding | ||
HELEIBLM_00790 | 3.8e-127 | yplQ | S | Haemolysin-III related | ||
HELEIBLM_00791 | 3.9e-64 | hsp20 | O | Hsp20/alpha crystallin family | ||
HELEIBLM_00792 | 1.7e-60 | yoaZ | S | PfpI family | ||
HELEIBLM_00794 | 4.4e-32 | T | Toxic component of a toxin-antitoxin (TA) module | |||
HELEIBLM_00797 | 1e-25 | L | Transposase DDE domain | |||
HELEIBLM_00799 | 3.7e-254 | 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) | |
HELEIBLM_00800 | 8.3e-245 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
HELEIBLM_00801 | 0.0 | cadA | P | E1-E2 ATPase | ||
HELEIBLM_00802 | 6.5e-195 | urtA | E | Receptor family ligand binding region | ||
HELEIBLM_00803 | 2.5e-129 | urtB | U | Branched-chain amino acid transport system / permease component | ||
HELEIBLM_00804 | 2.6e-160 | urtC | U | Branched-chain amino acid transport system / permease component | ||
HELEIBLM_00805 | 3.4e-113 | urtD | S | Branched-chain amino acid ATP-binding cassette transporter | ||
HELEIBLM_00806 | 1.1e-98 | urtE | E | ABC transporter | ||
HELEIBLM_00807 | 1.7e-110 | hoxN | S | rRNA processing | ||
HELEIBLM_00808 | 3.2e-95 | ureB | 3.5.1.5 | E | Urease, gamma subunit | |
HELEIBLM_00809 | 1.6e-305 | ureC | 3.5.1.5 | E | Urease alpha-subunit, N-terminal domain | |
HELEIBLM_00810 | 2.5e-86 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
HELEIBLM_00811 | 2.8e-82 | ureF | J | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
HELEIBLM_00812 | 3.2e-99 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
HELEIBLM_00813 | 1.4e-92 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
HELEIBLM_00815 | 2.3e-265 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
HELEIBLM_00816 | 8.4e-160 | htpX | O | Belongs to the peptidase M48B family | ||
HELEIBLM_00817 | 6.9e-116 | 3.2.1.4 | GH5,GH9 | S | acid phosphatase activity | |
HELEIBLM_00819 | 1.8e-204 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_00820 | 2.9e-119 | mug | 3.2.2.28, 6.3.3.2 | L | Uracil DNA glycosylase superfamily | |
HELEIBLM_00821 | 1.4e-206 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
HELEIBLM_00822 | 2.9e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
HELEIBLM_00823 | 2.4e-281 | clcA | P | Voltage gated chloride channel | ||
HELEIBLM_00824 | 1.7e-121 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HELEIBLM_00825 | 8.7e-58 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HELEIBLM_00826 | 7.1e-203 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_00827 | 8.2e-298 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
HELEIBLM_00828 | 6e-270 | scrT | G | Transporter major facilitator family protein | ||
HELEIBLM_00829 | 1e-251 | yhjE | EGP | Sugar (and other) transporter | ||
HELEIBLM_00830 | 1.2e-202 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
HELEIBLM_00831 | 1.8e-51 | bioN | P | Cobalt transport protein | ||
HELEIBLM_00832 | 1.8e-72 | cbiO | P | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00833 | 1.5e-58 | bioY | S | BioY family | ||
HELEIBLM_00834 | 1.5e-78 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
HELEIBLM_00835 | 1.9e-112 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
HELEIBLM_00836 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
HELEIBLM_00837 | 1.5e-186 | K | Psort location Cytoplasmic, score | |||
HELEIBLM_00838 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
HELEIBLM_00839 | 5.8e-311 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
HELEIBLM_00840 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
HELEIBLM_00841 | 7e-55 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
HELEIBLM_00842 | 5.7e-170 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
HELEIBLM_00843 | 1.5e-98 | hspR | K | transcriptional regulator, MerR family | ||
HELEIBLM_00844 | 6.5e-214 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
HELEIBLM_00845 | 3.2e-206 | luxE | 6.2.1.19 | H | long-chain-fatty-acid--luciferin-component ligase, acyl-protein synthase | |
HELEIBLM_00846 | 9.4e-230 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
HELEIBLM_00847 | 5.6e-141 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
HELEIBLM_00848 | 9.1e-124 | S | HAD hydrolase, family IA, variant 3 | |||
HELEIBLM_00849 | 6.1e-134 | dedA | S | SNARE associated Golgi protein | ||
HELEIBLM_00850 | 2.9e-93 | cpaE | D | bacterial-type flagellum organization | ||
HELEIBLM_00851 | 1.5e-192 | cpaF | U | Type II IV secretion system protein | ||
HELEIBLM_00852 | 2.1e-104 | U | Type ii secretion system | |||
HELEIBLM_00853 | 3.1e-99 | gspF | NU | Type II secretion system (T2SS), protein F | ||
HELEIBLM_00854 | 4.6e-40 | S | Protein of unknown function (DUF4244) | |||
HELEIBLM_00855 | 1.5e-53 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
HELEIBLM_00856 | 4.2e-214 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
HELEIBLM_00857 | 3.7e-100 | K | Bacterial regulatory proteins, tetR family | |||
HELEIBLM_00858 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
HELEIBLM_00859 | 1.9e-109 | 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 | ||
HELEIBLM_00860 | 3.6e-205 | 3.4.22.70 | M | Sortase family | ||
HELEIBLM_00861 | 1.3e-38 | S | Psort location Cytoplasmic, score | |||
HELEIBLM_00862 | 2.3e-131 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
HELEIBLM_00863 | 8e-97 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
HELEIBLM_00864 | 3e-209 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
HELEIBLM_00865 | 1.3e-113 | |||||
HELEIBLM_00866 | 1.1e-308 | S | Calcineurin-like phosphoesterase | |||
HELEIBLM_00867 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
HELEIBLM_00868 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HELEIBLM_00869 | 1.2e-166 | 3.6.1.27 | I | PAP2 superfamily | ||
HELEIBLM_00870 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
HELEIBLM_00871 | 6.8e-122 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HELEIBLM_00872 | 4e-204 | holB | 2.7.7.7 | L | DNA polymerase III | |
HELEIBLM_00873 | 8.6e-100 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_00874 | 3.3e-37 | ptsH | G | PTS HPr component phosphorylation site | ||
HELEIBLM_00876 | 9.5e-292 | 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) | |
HELEIBLM_00877 | 5.6e-106 | S | Phosphatidylethanolamine-binding protein | |||
HELEIBLM_00878 | 0.0 | pepD | E | Peptidase family C69 | ||
HELEIBLM_00879 | 2.4e-289 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
HELEIBLM_00880 | 5.1e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
HELEIBLM_00881 | 2.4e-95 | S | GtrA-like protein | |||
HELEIBLM_00882 | 5.5e-259 | EGP | Major facilitator Superfamily | |||
HELEIBLM_00883 | 1.7e-122 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
HELEIBLM_00884 | 4.9e-157 | |||||
HELEIBLM_00885 | 8.4e-170 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
HELEIBLM_00886 | 1.1e-139 | S | Protein of unknown function (DUF805) | |||
HELEIBLM_00887 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
HELEIBLM_00888 | 4.5e-169 | V | Abi-like protein | |||
HELEIBLM_00889 | 1.4e-29 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
HELEIBLM_00890 | 4.1e-110 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
HELEIBLM_00892 | 3.7e-293 | hsdM | 2.1.1.72 | V | modification (methylase) protein of type I restriction-modification system K03427 | |
HELEIBLM_00893 | 2.7e-293 | gltX | 6.1.1.17 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
HELEIBLM_00896 | 1.3e-66 | |||||
HELEIBLM_00897 | 9.4e-134 | yoaK | S | Protein of unknown function (DUF1275) | ||
HELEIBLM_00898 | 5e-96 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HELEIBLM_00900 | 5.6e-177 | 2.7.7.7 | L | Transposase, Mutator family | ||
HELEIBLM_00902 | 4.6e-311 | |||||
HELEIBLM_00903 | 0.0 | efeU_1 | P | Iron permease FTR1 family | ||
HELEIBLM_00904 | 5.5e-108 | tpd | P | Fe2+ transport protein | ||
HELEIBLM_00905 | 1.7e-232 | S | Predicted membrane protein (DUF2318) | |||
HELEIBLM_00906 | 9.1e-213 | macB_2 | V | ABC transporter permease | ||
HELEIBLM_00907 | 1.6e-214 | Z012_06715 | V | FtsX-like permease family | ||
HELEIBLM_00908 | 5.9e-146 | macB | V | ABC transporter, ATP-binding protein | ||
HELEIBLM_00909 | 2.8e-65 | S | FMN_bind | |||
HELEIBLM_00910 | 8.3e-105 | K | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_00911 | 2e-305 | pip | S | YhgE Pip domain protein | ||
HELEIBLM_00912 | 0.0 | pip | S | YhgE Pip domain protein | ||
HELEIBLM_00913 | 8.6e-232 | S | Putative ABC-transporter type IV | |||
HELEIBLM_00914 | 2.3e-273 | 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 | |
HELEIBLM_00915 | 8.7e-140 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
HELEIBLM_00916 | 2e-183 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
HELEIBLM_00917 | 1.8e-300 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HELEIBLM_00919 | 1.5e-39 | |||||
HELEIBLM_00920 | 7.1e-09 | |||||
HELEIBLM_00921 | 1.1e-257 | pepD | E | Peptidase family C69 | ||
HELEIBLM_00922 | 3.4e-186 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
HELEIBLM_00923 | 1.6e-123 | icaR | K | Bacterial regulatory proteins, tetR family | ||
HELEIBLM_00924 | 1.1e-44 | S | Protein of unknown function (DUF2089) | |||
HELEIBLM_00925 | 4.6e-17 | |||||
HELEIBLM_00926 | 2.7e-169 | 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) | ||
HELEIBLM_00927 | 4.5e-228 | amt | U | Ammonium Transporter Family | ||
HELEIBLM_00928 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
HELEIBLM_00929 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
HELEIBLM_00930 | 1.3e-249 | dinF | V | MatE | ||
HELEIBLM_00931 | 4.4e-275 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HELEIBLM_00932 | 3.1e-254 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
HELEIBLM_00933 | 1.2e-140 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
HELEIBLM_00934 | 1e-31 | S | granule-associated protein | |||
HELEIBLM_00935 | 0.0 | ubiB | S | ABC1 family | ||
HELEIBLM_00936 | 3.5e-133 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
HELEIBLM_00937 | 2.6e-191 | 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) | |
HELEIBLM_00938 | 4.6e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HELEIBLM_00939 | 6.2e-66 | ssb1 | L | Single-stranded DNA-binding protein | ||
HELEIBLM_00940 | 2.6e-36 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
HELEIBLM_00941 | 1.9e-69 | rplI | J | Binds to the 23S rRNA | ||
HELEIBLM_00943 | 1.7e-37 | L | Transposase | |||
HELEIBLM_00944 | 3.8e-117 | |||||
HELEIBLM_00945 | 4e-130 | V | ABC transporter | |||
HELEIBLM_00946 | 6.2e-107 | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | |||
HELEIBLM_00947 | 3.2e-201 | 2.7.13.3 | T | Histidine kinase | ||
HELEIBLM_00948 | 9.7e-201 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_00949 | 1.8e-16 | ybiR | P | Citrate transporter | ||
HELEIBLM_00950 | 9.1e-273 | EK | Alanine-glyoxylate amino-transferase | |||
HELEIBLM_00951 | 1.2e-114 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
HELEIBLM_00952 | 2e-155 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
HELEIBLM_00953 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HELEIBLM_00954 | 7.9e-249 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
HELEIBLM_00955 | 2.6e-250 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HELEIBLM_00956 | 2.2e-271 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
HELEIBLM_00957 | 2.7e-102 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
HELEIBLM_00958 | 4.7e-93 | 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) | |
HELEIBLM_00959 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HELEIBLM_00960 | 4.2e-295 | enhA_2 | S | L,D-transpeptidase catalytic domain | ||
HELEIBLM_00961 | 3.4e-222 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
HELEIBLM_00962 | 4.1e-91 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
HELEIBLM_00964 | 7.1e-171 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_00965 | 1.2e-148 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HELEIBLM_00966 | 9.3e-09 | sapF | E | ATPases associated with a variety of cellular activities | ||
HELEIBLM_00967 | 9e-121 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
HELEIBLM_00968 | 8.8e-125 | EP | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00969 | 1.7e-160 | P | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_00970 | 2.4e-282 | E | ABC transporter, substrate-binding protein, family 5 | |||
HELEIBLM_00971 | 8.5e-243 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
HELEIBLM_00972 | 9.3e-141 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
HELEIBLM_00973 | 3.2e-264 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_00974 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_00975 | 1.5e-111 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
HELEIBLM_00976 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
HELEIBLM_00977 | 1.3e-148 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
HELEIBLM_00978 | 4.8e-150 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00979 | 2.8e-163 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HELEIBLM_00980 | 8.6e-144 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HELEIBLM_00981 | 1.8e-78 | 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 | ||
HELEIBLM_00982 | 2.6e-157 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
HELEIBLM_00983 | 5.4e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
HELEIBLM_00984 | 4.7e-176 | ftsE | D | Cell division ATP-binding protein FtsE | ||
HELEIBLM_00985 | 2.4e-206 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HELEIBLM_00986 | 1.1e-253 | S | Domain of unknown function (DUF4143) | |||
HELEIBLM_00987 | 1e-273 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
HELEIBLM_00988 | 5.2e-124 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
HELEIBLM_00989 | 4.9e-257 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HELEIBLM_00990 | 6.8e-98 | ugpA | P | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_00991 | 3.6e-153 | ugpB | G | Bacterial extracellular solute-binding protein | ||
HELEIBLM_00992 | 1.2e-99 | ugpQ | 3.1.4.46 | C | Domain of unknown function | |
HELEIBLM_00993 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
HELEIBLM_00994 | 0.0 | rnj | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HELEIBLM_00995 | 1e-165 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HELEIBLM_00996 | 1e-131 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HELEIBLM_00997 | 2.3e-224 | G | Major Facilitator Superfamily | |||
HELEIBLM_00998 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HELEIBLM_00999 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HELEIBLM_01000 | 2.2e-260 | KLT | Protein tyrosine kinase | |||
HELEIBLM_01001 | 0.0 | S | Fibronectin type 3 domain | |||
HELEIBLM_01002 | 2e-175 | S | ATPase family associated with various cellular activities (AAA) | |||
HELEIBLM_01003 | 1.8e-223 | S | Protein of unknown function DUF58 | |||
HELEIBLM_01004 | 0.0 | E | Transglutaminase-like superfamily | |||
HELEIBLM_01005 | 9.3e-26 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
HELEIBLM_01006 | 4e-68 | B | Belongs to the OprB family | |||
HELEIBLM_01007 | 1.9e-83 | T | Forkhead associated domain | |||
HELEIBLM_01008 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HELEIBLM_01009 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HELEIBLM_01010 | 7.5e-108 | |||||
HELEIBLM_01011 | 2.5e-183 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
HELEIBLM_01012 | 7.6e-115 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HELEIBLM_01013 | 3e-251 | S | UPF0210 protein | |||
HELEIBLM_01014 | 1.9e-43 | gcvR | T | Belongs to the UPF0237 family | ||
HELEIBLM_01016 | 1.7e-232 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
HELEIBLM_01017 | 1.4e-250 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
HELEIBLM_01018 | 6.9e-122 | glpR | K | DeoR C terminal sensor domain | ||
HELEIBLM_01019 | 1.3e-226 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
HELEIBLM_01020 | 1e-222 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
HELEIBLM_01021 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HELEIBLM_01022 | 2.8e-132 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
HELEIBLM_01023 | 1.5e-197 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
HELEIBLM_01024 | 1.6e-191 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
HELEIBLM_01025 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
HELEIBLM_01026 | 3.3e-250 | S | Uncharacterized conserved protein (DUF2183) | |||
HELEIBLM_01027 | 3.6e-70 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
HELEIBLM_01028 | 3.4e-228 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
HELEIBLM_01029 | 7.7e-160 | mhpC | I | Alpha/beta hydrolase family | ||
HELEIBLM_01030 | 4e-124 | F | Domain of unknown function (DUF4916) | |||
HELEIBLM_01031 | 1.9e-59 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
HELEIBLM_01032 | 1.7e-171 | S | G5 | |||
HELEIBLM_01033 | 1.1e-18 | hipB | K | Helix-turn-helix XRE-family like proteins | ||
HELEIBLM_01034 | 4.4e-133 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
HELEIBLM_01035 | 4.4e-112 | |||||
HELEIBLM_01036 | 1.6e-231 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
HELEIBLM_01037 | 3e-262 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HELEIBLM_01038 | 1.5e-20 | S | enterobacterial common antigen metabolic process | |||
HELEIBLM_01039 | 1.6e-185 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
HELEIBLM_01040 | 3.9e-79 | S | RloB-like protein | |||
HELEIBLM_01042 | 3e-19 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HELEIBLM_01044 | 1.6e-24 | |||||
HELEIBLM_01045 | 4.9e-59 | L | Helix-turn-helix domain | |||
HELEIBLM_01046 | 2.9e-125 | S | AAA-like domain | |||
HELEIBLM_01047 | 3.5e-211 | S | AAA-like domain | |||
HELEIBLM_01048 | 8.3e-50 | S | SIR2-like domain | |||
HELEIBLM_01049 | 6.9e-146 | tnp7109-21 | L | Integrase core domain | ||
HELEIBLM_01050 | 3.7e-27 | L | Transposase | |||
HELEIBLM_01052 | 4e-125 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HELEIBLM_01053 | 0.0 | pacS | 1.9.3.1, 3.6.3.54 | P | E1-E2 ATPase | |
HELEIBLM_01054 | 1.1e-41 | csoR | S | Metal-sensitive transcriptional repressor | ||
HELEIBLM_01055 | 5e-188 | rmuC | S | RmuC family | ||
HELEIBLM_01056 | 4.7e-98 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
HELEIBLM_01057 | 1.4e-158 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
HELEIBLM_01058 | 4.6e-185 | K | Psort location Cytoplasmic, score | |||
HELEIBLM_01059 | 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) | |
HELEIBLM_01060 | 5.1e-287 | gatA | 6.3.5.6, 6.3.5.7 | F | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
HELEIBLM_01061 | 7.9e-285 | gatB | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HELEIBLM_01062 | 5.2e-198 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
HELEIBLM_01063 | 3.3e-52 | S | Protein of unknown function (DUF2469) | |||
HELEIBLM_01064 | 4.6e-282 | S | Histidine phosphatase superfamily (branch 2) | |||
HELEIBLM_01065 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
HELEIBLM_01066 | 7.7e-243 | 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 | ||
HELEIBLM_01067 | 1.8e-201 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_01068 | 3e-291 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_01070 | 1.4e-173 | glkA | 2.7.1.2 | G | ROK family | |
HELEIBLM_01071 | 6.4e-62 | EGP | Major facilitator superfamily | |||
HELEIBLM_01072 | 1.1e-163 | dkgB | S | Oxidoreductase, aldo keto reductase family protein | ||
HELEIBLM_01073 | 1.1e-69 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HELEIBLM_01074 | 1.3e-145 | |||||
HELEIBLM_01075 | 1.2e-22 | EGP | Major facilitator Superfamily | |||
HELEIBLM_01076 | 1.7e-69 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
HELEIBLM_01077 | 7.2e-228 | xylR | GK | ROK family | ||
HELEIBLM_01079 | 1.3e-36 | rpmE | J | Binds the 23S rRNA | ||
HELEIBLM_01080 | 5.3e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HELEIBLM_01081 | 1.1e-153 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
HELEIBLM_01082 | 9.5e-201 | livK | E | Receptor family ligand binding region | ||
HELEIBLM_01083 | 1.2e-105 | U | Belongs to the binding-protein-dependent transport system permease family | |||
HELEIBLM_01084 | 1.1e-171 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
HELEIBLM_01085 | 3.1e-153 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
HELEIBLM_01086 | 1.5e-121 | livF | E | ATPases associated with a variety of cellular activities | ||
HELEIBLM_01087 | 1.2e-35 | yncA | 2.3.1.18, 2.3.1.79 | S | O-acyltransferase activity | |
HELEIBLM_01088 | 2.3e-119 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
HELEIBLM_01089 | 1.3e-203 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
HELEIBLM_01090 | 7.6e-291 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
HELEIBLM_01091 | 1e-116 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
HELEIBLM_01092 | 2.6e-269 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
HELEIBLM_01093 | 7.2e-63 | S | AMMECR1 | |||
HELEIBLM_01094 | 4e-183 | L | PFAM Integrase catalytic | |||
HELEIBLM_01095 | 6.6e-27 | gutA | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HELEIBLM_01097 | 1.8e-37 | gutA | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HELEIBLM_01098 | 0.0 | uidA | G | Belongs to the glycosyl hydrolase 2 family | ||
HELEIBLM_01099 | 2.1e-61 | L | Transposase | |||
HELEIBLM_01100 | 2.4e-11 | L | PFAM Relaxase mobilization nuclease family protein | |||
HELEIBLM_01101 | 5.1e-18 | bglK | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
HELEIBLM_01102 | 4.8e-219 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
HELEIBLM_01103 | 7.7e-70 | S | Nucleotidyltransferase substrate binding protein like | |||
HELEIBLM_01104 | 1.2e-45 | S | Nucleotidyltransferase domain | |||
HELEIBLM_01106 | 2.1e-254 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
HELEIBLM_01107 | 5.1e-54 | L | Helix-turn-helix domain | |||
HELEIBLM_01108 | 4.3e-15 | G | Glycosyl hydrolase family 85 | |||
HELEIBLM_01109 | 1e-176 | endOF2 | 3.2.1.14, 3.2.1.52, 3.2.1.96 | GH18,GH20 | G | Glycosyl hydrolase, family 20, catalytic domain |
HELEIBLM_01110 | 0.0 | bglX-2 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 C-terminal domain |
HELEIBLM_01111 | 1.6e-257 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | |||
HELEIBLM_01112 | 3e-156 | lacG | G | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01113 | 2.6e-164 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_01114 | 1.1e-245 | srrA1 | G | Bacterial extracellular solute-binding protein | ||
HELEIBLM_01115 | 6.3e-13 | L | Helix-turn-helix domain | |||
HELEIBLM_01116 | 3.4e-46 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase N-terminal region | |
HELEIBLM_01118 | 1.1e-09 | nagH | 2.7.13.3, 3.2.1.52 | GH20 | M | Domain of unknown function (DUF5011) |
HELEIBLM_01119 | 7.4e-186 | S | Domain of unknown function (DUF4143) | |||
HELEIBLM_01120 | 1.7e-12 | L | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_01121 | 7.2e-27 | L | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_01122 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
HELEIBLM_01123 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
HELEIBLM_01124 | 1.6e-85 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
HELEIBLM_01125 | 9.8e-46 | |||||
HELEIBLM_01126 | 6.4e-24 | S | Phage derived protein Gp49-like (DUF891) | |||
HELEIBLM_01127 | 3.9e-44 | K | Addiction module | |||
HELEIBLM_01128 | 9.5e-54 | S | enterobacterial common antigen metabolic process | |||
HELEIBLM_01129 | 9.7e-24 | pslL | G | Acyltransferase family | ||
HELEIBLM_01130 | 3.6e-36 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HELEIBLM_01131 | 1.3e-132 | L | Transposase, Mutator family | |||
HELEIBLM_01134 | 2.5e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
HELEIBLM_01135 | 4.4e-197 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HELEIBLM_01136 | 4.2e-135 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
HELEIBLM_01137 | 2e-80 | 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 | ||
HELEIBLM_01138 | 4.3e-26 | rpmI | J | Ribosomal protein L35 | ||
HELEIBLM_01139 | 1.3e-61 | 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 | ||
HELEIBLM_01140 | 1.2e-169 | xerD | D | recombinase XerD | ||
HELEIBLM_01141 | 8.1e-150 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HELEIBLM_01142 | 1.6e-155 | 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 | ||
HELEIBLM_01143 | 5.3e-114 | 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 | ||
HELEIBLM_01144 | 1.8e-153 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
HELEIBLM_01145 | 8.3e-251 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
HELEIBLM_01146 | 2.4e-303 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
HELEIBLM_01147 | 7.2e-161 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, N-terminal domain | |
HELEIBLM_01148 | 1.1e-215 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
HELEIBLM_01149 | 0.0 | typA | T | Elongation factor G C-terminus | ||
HELEIBLM_01150 | 1.3e-12 | EGP | Major facilitator Superfamily | |||
HELEIBLM_01151 | 1.4e-37 | L | PFAM Integrase catalytic | |||
HELEIBLM_01152 | 2.4e-72 | |||||
HELEIBLM_01153 | 4.3e-191 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
HELEIBLM_01154 | 1.1e-192 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
HELEIBLM_01155 | 2e-42 | |||||
HELEIBLM_01156 | 9.2e-179 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
HELEIBLM_01157 | 2.3e-311 | E | ABC transporter, substrate-binding protein, family 5 | |||
HELEIBLM_01158 | 1.1e-151 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01159 | 8.7e-171 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
HELEIBLM_01160 | 0.0 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
HELEIBLM_01161 | 6.3e-170 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
HELEIBLM_01162 | 1.1e-147 | S | Protein of unknown function (DUF3710) | |||
HELEIBLM_01163 | 9.6e-130 | S | Protein of unknown function (DUF3159) | |||
HELEIBLM_01164 | 2e-241 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HELEIBLM_01165 | 3.7e-104 | |||||
HELEIBLM_01166 | 0.0 | ctpE | P | E1-E2 ATPase | ||
HELEIBLM_01167 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
HELEIBLM_01168 | 3.6e-58 | relB | L | RelB antitoxin | ||
HELEIBLM_01169 | 2.1e-85 | S | PIN domain | |||
HELEIBLM_01170 | 0.0 | S | Protein of unknown function DUF262 | |||
HELEIBLM_01171 | 5.5e-118 | E | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_01172 | 1.5e-126 | ybhL | S | Belongs to the BI1 family | ||
HELEIBLM_01173 | 4.1e-176 | ydeD | EG | EamA-like transporter family | ||
HELEIBLM_01174 | 1.7e-135 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
HELEIBLM_01175 | 3.7e-279 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
HELEIBLM_01176 | 5.7e-183 | 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) | |
HELEIBLM_01177 | 2.3e-136 | fic | D | Fic/DOC family | ||
HELEIBLM_01178 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
HELEIBLM_01179 | 1.6e-49 | K | MarR family | |||
HELEIBLM_01180 | 8.7e-91 | V | ABC transporter, ATP-binding protein | |||
HELEIBLM_01181 | 4.4e-165 | V | ABC transporter, ATP-binding protein | |||
HELEIBLM_01182 | 0.0 | V | ABC transporter transmembrane region | |||
HELEIBLM_01183 | 1.3e-111 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HELEIBLM_01184 | 1.1e-90 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
HELEIBLM_01185 | 4.7e-80 | K | Helix-turn-helix XRE-family like proteins | |||
HELEIBLM_01186 | 5.3e-39 | S | Protein of unknown function (DUF3046) | |||
HELEIBLM_01187 | 2.6e-198 | 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 | ||
HELEIBLM_01188 | 5.2e-99 | recX | S | Modulates RecA activity | ||
HELEIBLM_01189 | 3.7e-109 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HELEIBLM_01190 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
HELEIBLM_01191 | 3.1e-65 | E | GDSL-like Lipase/Acylhydrolase family | |||
HELEIBLM_01192 | 7.4e-173 | 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) | |
HELEIBLM_01193 | 2.6e-75 | |||||
HELEIBLM_01194 | 1.7e-128 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
HELEIBLM_01195 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
HELEIBLM_01196 | 2.4e-190 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
HELEIBLM_01197 | 7.6e-123 | |||||
HELEIBLM_01198 | 5.8e-189 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
HELEIBLM_01199 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
HELEIBLM_01200 | 7e-199 | G | Major Facilitator Superfamily | |||
HELEIBLM_01201 | 1e-173 | 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 | |
HELEIBLM_01202 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
HELEIBLM_01203 | 2.4e-123 | KT | RESPONSE REGULATOR receiver | |||
HELEIBLM_01204 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
HELEIBLM_01205 | 2.4e-234 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
HELEIBLM_01206 | 6.1e-178 | S | Protein of unknown function (DUF3071) | |||
HELEIBLM_01207 | 3.9e-47 | S | Domain of unknown function (DUF4193) | |||
HELEIBLM_01208 | 6.1e-82 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
HELEIBLM_01209 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
HELEIBLM_01210 | 2.3e-74 | |||||
HELEIBLM_01212 | 1.5e-242 | S | HipA-like C-terminal domain | |||
HELEIBLM_01213 | 6e-157 | S | Fic/DOC family | |||
HELEIBLM_01214 | 1e-111 | pptA | 6.3.2.14 | Q | 4'-phosphopantetheinyl transferase superfamily | |
HELEIBLM_01215 | 5e-116 | K | WHG domain | |||
HELEIBLM_01216 | 2.9e-22 | 1.3.3.6, 2.3.1.39 | IQ | [acyl-carrier-protein] S-malonyltransferase activity | ||
HELEIBLM_01217 | 5.5e-265 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_01218 | 2.3e-24 | S | AAA ATPase domain | |||
HELEIBLM_01221 | 2.3e-241 | mloB | K | Putative DNA-binding domain | ||
HELEIBLM_01222 | 8.4e-29 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_01223 | 4.3e-17 | S | ATP diphosphatase activity | |||
HELEIBLM_01224 | 5.6e-196 | |||||
HELEIBLM_01225 | 6.9e-110 | 3.4.13.21 | E | Peptidase family S51 | ||
HELEIBLM_01226 | 2.2e-108 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
HELEIBLM_01227 | 1.2e-65 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
HELEIBLM_01228 | 5.1e-165 | M | pfam nlp p60 | |||
HELEIBLM_01229 | 4.8e-159 | I | Serine aminopeptidase, S33 | |||
HELEIBLM_01230 | 2.4e-40 | S | Protein of unknown function (DUF2975) | |||
HELEIBLM_01231 | 2.8e-31 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
HELEIBLM_01232 | 5.4e-240 | pbuX | F | Permease family | ||
HELEIBLM_01233 | 8.2e-105 | 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 | |
HELEIBLM_01234 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
HELEIBLM_01235 | 4.5e-62 | S | Domain of unknown function (DUF4418) | |||
HELEIBLM_01236 | 4.4e-217 | V | FtsX-like permease family | |||
HELEIBLM_01237 | 2.6e-135 | lolD | V | ABC transporter | ||
HELEIBLM_01238 | 4.5e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
HELEIBLM_01239 | 2.3e-150 | S | Peptidase C26 | |||
HELEIBLM_01240 | 3e-65 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
HELEIBLM_01241 | 1.2e-48 | relB | L | RelB antitoxin | ||
HELEIBLM_01242 | 1.2e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
HELEIBLM_01243 | 2e-62 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
HELEIBLM_01244 | 1.4e-34 | |||||
HELEIBLM_01245 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
HELEIBLM_01246 | 5.1e-78 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HELEIBLM_01247 | 2.5e-201 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
HELEIBLM_01248 | 2.6e-77 | 3.4.23.43 | S | Type IV leader peptidase family | ||
HELEIBLM_01249 | 1.1e-217 | 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 | |
HELEIBLM_01250 | 7.6e-310 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
HELEIBLM_01251 | 2e-79 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
HELEIBLM_01252 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
HELEIBLM_01253 | 1.1e-291 | sufB | O | FeS assembly protein SufB | ||
HELEIBLM_01254 | 2.5e-236 | sufD | O | FeS assembly protein SufD | ||
HELEIBLM_01255 | 1.6e-143 | sufC | O | FeS assembly ATPase SufC | ||
HELEIBLM_01256 | 9.4e-239 | 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 | |
HELEIBLM_01257 | 3.1e-101 | iscU | C | SUF system FeS assembly protein, NifU family | ||
HELEIBLM_01258 | 1.6e-111 | yitW | S | Iron-sulfur cluster assembly protein | ||
HELEIBLM_01259 | 2.9e-240 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
HELEIBLM_01260 | 7.6e-163 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
HELEIBLM_01262 | 1.6e-143 | 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 | |
HELEIBLM_01263 | 7.5e-58 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
HELEIBLM_01264 | 1.2e-211 | phoH | T | PhoH-like protein | ||
HELEIBLM_01265 | 1.4e-101 | 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 | |
HELEIBLM_01266 | 4.6e-250 | corC | S | CBS domain | ||
HELEIBLM_01267 | 2.3e-182 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HELEIBLM_01268 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
HELEIBLM_01269 | 1.4e-201 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
HELEIBLM_01270 | 2.7e-43 | pntAA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
HELEIBLM_01271 | 8.4e-236 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
HELEIBLM_01272 | 2.2e-193 | S | alpha beta | |||
HELEIBLM_01273 | 1.2e-82 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
HELEIBLM_01274 | 3.1e-225 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
HELEIBLM_01275 | 5.7e-74 | mazG | 3.6.1.66 | S | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_01276 | 1.9e-125 | S | UPF0126 domain | |||
HELEIBLM_01277 | 7.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HELEIBLM_01278 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
HELEIBLM_01279 | 5.4e-180 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
HELEIBLM_01280 | 3.3e-134 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HELEIBLM_01283 | 1e-177 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_01284 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
HELEIBLM_01285 | 1.7e-303 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
HELEIBLM_01286 | 3.8e-309 | E | ABC transporter, substrate-binding protein, family 5 | |||
HELEIBLM_01287 | 0.0 | S | Glycosyl hydrolases related to GH101 family, GH129 | |||
HELEIBLM_01288 | 1e-81 | |||||
HELEIBLM_01289 | 1.4e-239 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
HELEIBLM_01290 | 7.1e-158 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
HELEIBLM_01291 | 1.2e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HELEIBLM_01292 | 9.2e-113 | ybeM | S | Carbon-nitrogen hydrolase | ||
HELEIBLM_01293 | 4.9e-73 | bcp | 1.11.1.15 | O | Redoxin | |
HELEIBLM_01294 | 8e-130 | |||||
HELEIBLM_01296 | 5.9e-120 | 2.5.1.19 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
HELEIBLM_01297 | 5.2e-228 | K | SIR2-like domain | |||
HELEIBLM_01299 | 4.1e-108 | S | Putative inner membrane protein (DUF1819) | |||
HELEIBLM_01300 | 3e-125 | S | Domain of unknown function (DUF1788) | |||
HELEIBLM_01301 | 0.0 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
HELEIBLM_01302 | 0.0 | LV | DNA restriction-modification system | |||
HELEIBLM_01303 | 0.0 | K | SIR2-like domain | |||
HELEIBLM_01304 | 5.9e-256 | lexA | 3.6.4.12 | K | Putative DNA-binding domain | |
HELEIBLM_01305 | 0.0 | thiN | 2.7.6.2 | H | PglZ domain | |
HELEIBLM_01306 | 0.0 | 3.4.21.53 | O | Putative ATP-dependent Lon protease | ||
HELEIBLM_01307 | 4.8e-178 | CP_1020 | S | zinc ion binding | ||
HELEIBLM_01308 | 2.6e-169 | I | alpha/beta hydrolase fold | |||
HELEIBLM_01309 | 7.6e-12 | ydhF | S | Aldo/keto reductase family | ||
HELEIBLM_01310 | 2.5e-23 | ydhF | S | Aldo/keto reductase family | ||
HELEIBLM_01311 | 2e-44 | S | phosphoesterase or phosphohydrolase | |||
HELEIBLM_01312 | 7.1e-130 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
HELEIBLM_01314 | 7.9e-93 | S | Phospholipase/Carboxylesterase | |||
HELEIBLM_01315 | 2.3e-193 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
HELEIBLM_01316 | 3e-96 | sixA | 3.6.1.55 | T | Phosphoglycerate mutase family | |
HELEIBLM_01317 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HELEIBLM_01318 | 3.3e-155 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
HELEIBLM_01319 | 1.1e-186 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HELEIBLM_01320 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
HELEIBLM_01321 | 2.7e-177 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HELEIBLM_01322 | 1e-72 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
HELEIBLM_01323 | 5.1e-284 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HELEIBLM_01324 | 2.1e-174 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
HELEIBLM_01325 | 4.5e-157 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
HELEIBLM_01326 | 1.2e-180 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HELEIBLM_01327 | 1.5e-124 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
HELEIBLM_01328 | 9e-29 | |||||
HELEIBLM_01329 | 6.4e-207 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
HELEIBLM_01330 | 8e-171 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
HELEIBLM_01331 | 3.3e-120 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HELEIBLM_01332 | 0.0 | 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 | |
HELEIBLM_01333 | 1.8e-231 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_01334 | 9.7e-119 | XK27_08510 | KL | DEAD-like helicases superfamily | ||
HELEIBLM_01335 | 5e-61 | yeaO | K | Protein of unknown function, DUF488 | ||
HELEIBLM_01336 | 3e-21 | S | Virulence protein RhuM family | |||
HELEIBLM_01337 | 2e-07 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_01338 | 1.2e-15 | yijF | S | Domain of unknown function (DUF1287) | ||
HELEIBLM_01339 | 6.5e-156 | 3.6.4.12 | ||||
HELEIBLM_01340 | 3.8e-75 | |||||
HELEIBLM_01341 | 1.1e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
HELEIBLM_01343 | 1.2e-288 | mmuP | E | amino acid | ||
HELEIBLM_01344 | 6e-74 | 2.6.1.76 | EGP | Major Facilitator Superfamily | ||
HELEIBLM_01346 | 3.7e-93 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
HELEIBLM_01347 | 8.4e-116 | XK27_07525 | 3.6.1.55 | F | Hydrolase of X-linked nucleoside diphosphate N terminal | |
HELEIBLM_01348 | 1.3e-31 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
HELEIBLM_01349 | 1.2e-53 | hipA | 2.7.11.1 | S | kinase activity | |
HELEIBLM_01350 | 6.3e-45 | K | sequence-specific DNA binding | |||
HELEIBLM_01351 | 1.8e-26 | S | Polyketide cyclase / dehydrase and lipid transport | |||
HELEIBLM_01352 | 1.9e-107 | |||||
HELEIBLM_01355 | 5.2e-121 | |||||
HELEIBLM_01356 | 3.3e-50 | |||||
HELEIBLM_01358 | 2.4e-36 | |||||
HELEIBLM_01360 | 9e-29 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HELEIBLM_01361 | 1.7e-78 | GT2,GT4 | M | Glycosyl transferase family 2 | ||
HELEIBLM_01362 | 2.3e-112 | wbbX | GT2,GT4 | M | transferase activity, transferring glycosyl groups | |
HELEIBLM_01363 | 4.3e-92 | M | Polysaccharide pyruvyl transferase | |||
HELEIBLM_01364 | 2.4e-106 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
HELEIBLM_01365 | 3e-73 | rgpC | GM | Transport permease protein | ||
HELEIBLM_01366 | 1.1e-32 | L | Helix-turn-helix domain | |||
HELEIBLM_01367 | 8.2e-152 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HELEIBLM_01368 | 2.5e-264 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
HELEIBLM_01369 | 6.6e-24 | |||||
HELEIBLM_01370 | 6.5e-198 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HELEIBLM_01371 | 1.6e-72 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_01372 | 2.3e-20 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_01373 | 4.5e-09 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_01374 | 1.8e-153 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
HELEIBLM_01375 | 1.3e-171 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HELEIBLM_01376 | 3.3e-157 | ykoT | 2.4.1.83 | GT2 | M | Glycosyl transferase family 2 |
HELEIBLM_01377 | 3.3e-58 | rfbJ | M | Glycosyl transferase family 2 | ||
HELEIBLM_01378 | 2e-42 | rfbJ | M | Glycosyl transferase family 2 | ||
HELEIBLM_01379 | 0.0 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
HELEIBLM_01380 | 2.2e-160 | |||||
HELEIBLM_01381 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
HELEIBLM_01382 | 4.7e-279 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
HELEIBLM_01383 | 2.6e-267 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
HELEIBLM_01384 | 1.5e-309 | cotH | M | CotH kinase protein | ||
HELEIBLM_01385 | 3.2e-155 | P | VTC domain | |||
HELEIBLM_01386 | 6.1e-109 | S | Domain of unknown function (DUF4956) | |||
HELEIBLM_01387 | 0.0 | yliE | T | Putative diguanylate phosphodiesterase | ||
HELEIBLM_01388 | 6.7e-92 | V | ABC transporter, ATP-binding protein | |||
HELEIBLM_01389 | 5.4e-248 | V | ABC transporter transmembrane region | |||
HELEIBLM_01390 | 3e-134 | rbsR | K | helix_turn _helix lactose operon repressor | ||
HELEIBLM_01391 | 3.3e-164 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HELEIBLM_01392 | 6.7e-185 | EGP | Major facilitator Superfamily | |||
HELEIBLM_01393 | 5.2e-21 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HELEIBLM_01394 | 1.4e-162 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
HELEIBLM_01395 | 2.9e-174 | lacR | K | Transcriptional regulator, LacI family | ||
HELEIBLM_01396 | 1.7e-107 | K | FCD | |||
HELEIBLM_01397 | 1.8e-143 | L | Domain of unknown function (DUF4862) | |||
HELEIBLM_01398 | 1e-120 | 2.7.1.2 | GK | ROK family | ||
HELEIBLM_01399 | 1.6e-115 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
HELEIBLM_01400 | 0.0 | nanI | 3.2.1.18 | GH33 | G | BNR repeat-like domain |
HELEIBLM_01401 | 1.2e-270 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
HELEIBLM_01402 | 7.2e-167 | oppB6 | EP | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01403 | 0.0 | oppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
HELEIBLM_01404 | 8.5e-143 | oppF | E | ATPases associated with a variety of cellular activities | ||
HELEIBLM_01405 | 8.7e-160 | nanL | 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
HELEIBLM_01406 | 2.3e-242 | malY | 4.4.1.8 | E | Aminotransferase, class I II | |
HELEIBLM_01407 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
HELEIBLM_01408 | 3.4e-251 | L | DEAD-like helicases superfamily | |||
HELEIBLM_01409 | 6.6e-149 | cas7c | L | CRISPR-associated protein Cas7 | ||
HELEIBLM_01410 | 4.1e-111 | cas4 | 3.1.12.1 | L | Domain of unknown function DUF83 | |
HELEIBLM_01411 | 5.8e-178 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HELEIBLM_01412 | 1.3e-39 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HELEIBLM_01413 | 2.7e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HELEIBLM_01414 | 1e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HELEIBLM_01415 | 4.5e-110 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HELEIBLM_01416 | 1.2e-32 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
HELEIBLM_01418 | 9.9e-230 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
HELEIBLM_01419 | 8.3e-199 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HELEIBLM_01420 | 2.9e-304 | 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 | ||
HELEIBLM_01421 | 8.8e-40 | rpmA | J | Ribosomal L27 protein | ||
HELEIBLM_01422 | 2.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HELEIBLM_01423 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
HELEIBLM_01424 | 8e-230 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
HELEIBLM_01425 | 6.1e-166 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
HELEIBLM_01426 | 9.4e-77 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
HELEIBLM_01427 | 5.1e-147 | S | Amidohydrolase | |||
HELEIBLM_01428 | 1.4e-202 | fucP | G | Major Facilitator Superfamily | ||
HELEIBLM_01429 | 4.3e-141 | IQ | KR domain | |||
HELEIBLM_01430 | 1.4e-245 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
HELEIBLM_01431 | 1.5e-181 | K | Bacterial regulatory proteins, lacI family | |||
HELEIBLM_01432 | 1.2e-253 | V | Efflux ABC transporter, permease protein | |||
HELEIBLM_01433 | 1.5e-132 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_01435 | 3e-08 | K | Acetyltransferase (GNAT) family | |||
HELEIBLM_01436 | 2e-277 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
HELEIBLM_01437 | 2.9e-182 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HELEIBLM_01438 | 1.4e-232 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
HELEIBLM_01439 | 1.6e-291 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HELEIBLM_01440 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
HELEIBLM_01441 | 4.3e-172 | K | LysR substrate binding domain protein | |||
HELEIBLM_01442 | 2.3e-245 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
HELEIBLM_01443 | 4.1e-253 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HELEIBLM_01444 | 8.4e-254 | nox | 1.6.3.4 | C | Pyridine nucleotide-disulphide oxidoreductase | |
HELEIBLM_01445 | 1.9e-206 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
HELEIBLM_01446 | 3.5e-131 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
HELEIBLM_01447 | 5.7e-269 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
HELEIBLM_01448 | 1.6e-138 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
HELEIBLM_01449 | 1.4e-259 | S | Calcineurin-like phosphoesterase | |||
HELEIBLM_01450 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
HELEIBLM_01451 | 1.4e-212 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
HELEIBLM_01452 | 6.7e-129 | |||||
HELEIBLM_01453 | 2e-47 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HELEIBLM_01454 | 1e-282 | G | Glycosyl hydrolase family 85 | |||
HELEIBLM_01455 | 2e-54 | G | Glycosyl hydrolase family 85 | |||
HELEIBLM_01456 | 9.2e-74 | G | Glycosyl hydrolase family 85 | |||
HELEIBLM_01457 | 8.6e-204 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_01458 | 3e-234 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
HELEIBLM_01459 | 3.8e-259 | S | Metal-independent alpha-mannosidase (GH125) | |||
HELEIBLM_01460 | 1.2e-168 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
HELEIBLM_01461 | 3e-218 | GK | ROK family | |||
HELEIBLM_01462 | 3.3e-161 | 2.7.1.2 | GK | ROK family | ||
HELEIBLM_01463 | 1.6e-202 | GK | ROK family | |||
HELEIBLM_01464 | 1.7e-148 | 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 | |
HELEIBLM_01465 | 1.1e-234 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
HELEIBLM_01466 | 2.4e-192 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_01467 | 9.8e-105 | U | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_01468 | 7.9e-126 | G | Binding-protein-dependent transport systems inner membrane component | |||
HELEIBLM_01471 | 3.2e-189 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
HELEIBLM_01472 | 1e-74 | 3.6.1.55 | F | NUDIX domain | ||
HELEIBLM_01473 | 1.7e-301 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
HELEIBLM_01474 | 8.8e-160 | K | Psort location Cytoplasmic, score | |||
HELEIBLM_01475 | 3.5e-286 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
HELEIBLM_01476 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
HELEIBLM_01477 | 1.3e-190 | V | Acetyltransferase (GNAT) domain | |||
HELEIBLM_01478 | 4.6e-296 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HELEIBLM_01479 | 2.6e-138 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
HELEIBLM_01480 | 1.6e-54 | |||||
HELEIBLM_01481 | 8.1e-187 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
HELEIBLM_01482 | 2e-188 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
HELEIBLM_01483 | 2.3e-179 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
HELEIBLM_01484 | 3.6e-174 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
HELEIBLM_01485 | 4.5e-10 | tnp3503b | 2.7.7.7 | L | transposition, DNA-mediated | |
HELEIBLM_01486 | 2.7e-198 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_01487 | 1.4e-60 | L | Transposase, Mutator family | |||
HELEIBLM_01488 | 3.1e-34 | L | IstB-like ATP binding protein | |||
HELEIBLM_01489 | 3e-63 | E | GDSL-like Lipase/Acylhydrolase family | |||
HELEIBLM_01490 | 1e-284 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HELEIBLM_01491 | 1.4e-251 | V | ABC-2 family transporter protein | |||
HELEIBLM_01492 | 1.5e-225 | V | ABC-2 family transporter protein | |||
HELEIBLM_01493 | 2.9e-187 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_01494 | 1.8e-10 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
HELEIBLM_01495 | 4e-227 | T | Histidine kinase | |||
HELEIBLM_01496 | 2.3e-103 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_01497 | 2.1e-114 | MA20_27875 | P | Protein of unknown function DUF47 | ||
HELEIBLM_01498 | 3.1e-187 | pit | P | Phosphate transporter family | ||
HELEIBLM_01499 | 7.8e-249 | nplT | G | Alpha amylase, catalytic domain | ||
HELEIBLM_01500 | 1.2e-31 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_01502 | 0.0 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
HELEIBLM_01503 | 8.7e-232 | rutG | F | Permease family | ||
HELEIBLM_01504 | 3e-161 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
HELEIBLM_01505 | 1.3e-105 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
HELEIBLM_01506 | 3.7e-233 | EGP | Major facilitator Superfamily | |||
HELEIBLM_01509 | 1.5e-131 | S | Sulfite exporter TauE/SafE | |||
HELEIBLM_01510 | 6.6e-11 | |||||
HELEIBLM_01512 | 1e-35 | feoA | P | FeoA | ||
HELEIBLM_01513 | 4.3e-79 | S | Helix-turn-helix | |||
HELEIBLM_01514 | 4.6e-200 | S | Short C-terminal domain | |||
HELEIBLM_01515 | 9.2e-39 | |||||
HELEIBLM_01516 | 2.7e-216 | |||||
HELEIBLM_01517 | 4.2e-77 | K | Psort location Cytoplasmic, score | |||
HELEIBLM_01518 | 3.2e-282 | KLT | Protein tyrosine kinase | |||
HELEIBLM_01519 | 1e-260 | EGP | Transmembrane secretion effector | |||
HELEIBLM_01520 | 0.0 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
HELEIBLM_01521 | 2.2e-11 | |||||
HELEIBLM_01522 | 2.7e-118 | K | Bacterial regulatory proteins, tetR family | |||
HELEIBLM_01523 | 1.7e-216 | G | Transmembrane secretion effector | |||
HELEIBLM_01524 | 2.4e-17 | K | addiction module antidote protein HigA | |||
HELEIBLM_01525 | 3.7e-243 | S | HipA-like C-terminal domain | |||
HELEIBLM_01526 | 1.1e-37 | L | RelB antitoxin | |||
HELEIBLM_01527 | 2.9e-51 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
HELEIBLM_01528 | 8.7e-65 | S | Cupin 2, conserved barrel domain protein | |||
HELEIBLM_01529 | 2.1e-33 | ksgA | 2.1.1.182 | J | Methyltransferase domain | |
HELEIBLM_01530 | 7e-60 | yccF | S | Inner membrane component domain | ||
HELEIBLM_01531 | 3.2e-231 | XK27_00240 | K | Fic/DOC family | ||
HELEIBLM_01532 | 1.4e-26 | 2.7.7.7 | L | Transposase, Mutator family | ||
HELEIBLM_01533 | 0.0 | drrC | L | ABC transporter | ||
HELEIBLM_01534 | 2.5e-245 | V | MatE | |||
HELEIBLM_01535 | 3.4e-26 | S | rRNA binding | |||
HELEIBLM_01536 | 4e-164 | K | Arac family | |||
HELEIBLM_01537 | 1.2e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HELEIBLM_01538 | 2e-141 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HELEIBLM_01539 | 7.2e-283 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
HELEIBLM_01540 | 0.0 | tcsS2 | T | Histidine kinase | ||
HELEIBLM_01541 | 9e-132 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_01542 | 0.0 | MV | MacB-like periplasmic core domain | |||
HELEIBLM_01543 | 3.7e-144 | V | ABC transporter, ATP-binding protein | |||
HELEIBLM_01544 | 1.8e-248 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
HELEIBLM_01545 | 1.4e-164 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
HELEIBLM_01546 | 4.8e-93 | yraN | L | Belongs to the UPF0102 family | ||
HELEIBLM_01547 | 1.2e-293 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
HELEIBLM_01548 | 5.4e-306 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
HELEIBLM_01549 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
HELEIBLM_01550 | 6.8e-173 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
HELEIBLM_01551 | 4.3e-110 | safC | S | O-methyltransferase | ||
HELEIBLM_01552 | 2.8e-147 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
HELEIBLM_01553 | 1.2e-229 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
HELEIBLM_01556 | 1.8e-235 | 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 | ||
HELEIBLM_01557 | 2.1e-123 | 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 | |
HELEIBLM_01558 | 3.8e-116 | 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 | |
HELEIBLM_01559 | 2.1e-53 | |||||
HELEIBLM_01560 | 8.9e-233 | clcA_2 | P | Voltage gated chloride channel | ||
HELEIBLM_01561 | 5.8e-234 | 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 | ||
HELEIBLM_01562 | 1.3e-248 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
HELEIBLM_01563 | 1.3e-119 | S | Protein of unknown function (DUF3000) | |||
HELEIBLM_01564 | 1.9e-174 | 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 | |
HELEIBLM_01565 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
HELEIBLM_01566 | 8.5e-34 | |||||
HELEIBLM_01567 | 0.0 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
HELEIBLM_01568 | 1.6e-224 | S | Peptidase dimerisation domain | |||
HELEIBLM_01569 | 2.8e-112 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01570 | 3.9e-218 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HELEIBLM_01571 | 2.1e-169 | metQ | P | NLPA lipoprotein | ||
HELEIBLM_01572 | 2.2e-311 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
HELEIBLM_01573 | 3.4e-171 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
HELEIBLM_01574 | 7.4e-302 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HELEIBLM_01575 | 1.5e-243 | |||||
HELEIBLM_01576 | 1.9e-64 | |||||
HELEIBLM_01577 | 2.4e-37 | uvrA3 | L | excinuclease ABC | ||
HELEIBLM_01578 | 1.6e-57 | uvrA3 | L | Psort location Cytoplasmic, score | ||
HELEIBLM_01579 | 5.8e-125 | uvrA3 | L | Psort location Cytoplasmic, score | ||
HELEIBLM_01580 | 7.1e-267 | XK27_09800 | I | Psort location CytoplasmicMembrane, score 9.99 | ||
HELEIBLM_01581 | 1.1e-192 | 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) | |
HELEIBLM_01583 | 9.9e-258 | 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 | |
HELEIBLM_01584 | 3.7e-67 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
HELEIBLM_01585 | 1.5e-132 | 3.1.3.85 | G | Phosphoglycerate mutase family | ||
HELEIBLM_01587 | 0.0 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HELEIBLM_01588 | 4.2e-228 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HELEIBLM_01589 | 1.3e-246 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
HELEIBLM_01590 | 1.2e-195 | ykiI | ||||
HELEIBLM_01591 | 3.4e-135 | V | MatE | |||
HELEIBLM_01592 | 2.7e-18 | K | Transcriptional regulator | |||
HELEIBLM_01593 | 4.2e-32 | K | Transcriptional regulator | |||
HELEIBLM_01594 | 8.8e-52 | |||||
HELEIBLM_01596 | 5.6e-193 | |||||
HELEIBLM_01597 | 9.8e-269 | S | MvaI/BcnI restriction endonuclease family | |||
HELEIBLM_01598 | 7.7e-239 | dcm | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
HELEIBLM_01599 | 8.5e-37 | KL | Type III restriction enzyme res subunit | |||
HELEIBLM_01601 | 1.4e-39 | |||||
HELEIBLM_01603 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HELEIBLM_01604 | 7.5e-126 | 3.6.1.13 | L | NUDIX domain | ||
HELEIBLM_01605 | 2.3e-178 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
HELEIBLM_01606 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HELEIBLM_01607 | 2.9e-121 | pdtaR | T | Response regulator receiver domain protein | ||
HELEIBLM_01609 | 2.7e-274 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
HELEIBLM_01610 | 3.1e-165 | terC | P | Integral membrane protein, TerC family | ||
HELEIBLM_01611 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
HELEIBLM_01612 | 3.3e-55 | 2.1.1.80, 3.1.1.61 | T | Histidine kinase | ||
HELEIBLM_01613 | 4e-63 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_01615 | 1e-143 | XK27_10205 | ||||
HELEIBLM_01616 | 1.4e-73 | V | ABC transporter | |||
HELEIBLM_01617 | 2.3e-73 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HELEIBLM_01618 | 2.3e-252 | rpsA | J | Ribosomal protein S1 | ||
HELEIBLM_01619 | 4.8e-157 | 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 | |
HELEIBLM_01620 | 8.4e-173 | P | Zinc-uptake complex component A periplasmic | |||
HELEIBLM_01621 | 1.6e-163 | znuC | P | ATPases associated with a variety of cellular activities | ||
HELEIBLM_01622 | 3.1e-137 | znuB | U | ABC 3 transport family | ||
HELEIBLM_01623 | 1e-90 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
HELEIBLM_01624 | 1.6e-100 | carD | K | CarD-like/TRCF domain | ||
HELEIBLM_01625 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
HELEIBLM_01626 | 5e-128 | T | Response regulator receiver domain protein | |||
HELEIBLM_01627 | 6.2e-191 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
HELEIBLM_01628 | 1.8e-60 | KT | Peptidase S24-like | |||
HELEIBLM_01629 | 3.5e-57 | ctsW | S | Phosphoribosyl transferase domain | ||
HELEIBLM_01630 | 7.5e-149 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
HELEIBLM_01631 | 3.3e-64 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
HELEIBLM_01632 | 2.9e-266 | |||||
HELEIBLM_01633 | 0.0 | S | Glycosyl transferase, family 2 | |||
HELEIBLM_01634 | 4.7e-56 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
HELEIBLM_01635 | 1e-164 | K | Cell envelope-related transcriptional attenuator domain | |||
HELEIBLM_01636 | 0.0 | D | FtsK/SpoIIIE family | |||
HELEIBLM_01637 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
HELEIBLM_01638 | 6.7e-279 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
HELEIBLM_01639 | 1.1e-148 | yplQ | S | Haemolysin-III related | ||
HELEIBLM_01640 | 5.7e-80 | 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 | ||
HELEIBLM_01641 | 8.9e-74 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
HELEIBLM_01642 | 3.2e-275 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
HELEIBLM_01643 | 1.2e-92 | |||||
HELEIBLM_01644 | 1.3e-165 | int8 | L | Phage integrase family | ||
HELEIBLM_01645 | 8.1e-11 | |||||
HELEIBLM_01646 | 7.2e-65 | |||||
HELEIBLM_01647 | 1.7e-61 | L | Belongs to the 'phage' integrase family | |||
HELEIBLM_01650 | 9.5e-19 | S | Putative phage holin Dp-1 | |||
HELEIBLM_01651 | 9.3e-194 | M | Glycosyl hydrolases family 25 | |||
HELEIBLM_01657 | 1.3e-35 | |||||
HELEIBLM_01659 | 1.1e-22 | ebh | 2.1.1.80, 3.1.1.61 | S | cellulase activity | |
HELEIBLM_01660 | 0.0 | ebh | 2.1.1.80, 3.1.1.61 | S | cellulase activity | |
HELEIBLM_01662 | 3.5e-217 | NT | phage tail tape measure protein | |||
HELEIBLM_01664 | 8.9e-61 | |||||
HELEIBLM_01665 | 7.5e-107 | |||||
HELEIBLM_01666 | 7.1e-66 | |||||
HELEIBLM_01667 | 5.3e-41 | |||||
HELEIBLM_01668 | 1.8e-50 | |||||
HELEIBLM_01669 | 5.5e-20 | |||||
HELEIBLM_01671 | 2.3e-77 | xkdG | S | Phage capsid family | ||
HELEIBLM_01672 | 4.2e-32 | S | peptidase activity | |||
HELEIBLM_01673 | 2.4e-80 | S | Phage portal protein | |||
HELEIBLM_01674 | 3.3e-305 | S | Terminase | |||
HELEIBLM_01675 | 4e-41 | |||||
HELEIBLM_01677 | 3.3e-122 | |||||
HELEIBLM_01678 | 1.6e-14 | |||||
HELEIBLM_01682 | 2.2e-108 | |||||
HELEIBLM_01685 | 2.3e-08 | E | Transcription factor WhiB | |||
HELEIBLM_01688 | 4e-63 | |||||
HELEIBLM_01690 | 1.3e-48 | ssb1 | L | Single-strand binding protein family | ||
HELEIBLM_01692 | 4.1e-73 | recT | L | RecT family | ||
HELEIBLM_01693 | 3.3e-82 | yqaJ | L | YqaJ-like viral recombinase domain | ||
HELEIBLM_01698 | 1.6e-116 | K | BRO family, N-terminal domain | |||
HELEIBLM_01700 | 3.4e-47 | Q | methyltransferase | |||
HELEIBLM_01701 | 3.2e-19 | |||||
HELEIBLM_01704 | 6.6e-11 | |||||
HELEIBLM_01705 | 2.5e-08 | |||||
HELEIBLM_01706 | 5.1e-46 | |||||
HELEIBLM_01708 | 1e-41 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
HELEIBLM_01709 | 4.3e-83 | |||||
HELEIBLM_01711 | 1.7e-179 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HELEIBLM_01712 | 2.4e-101 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
HELEIBLM_01713 | 1.4e-75 | divIC | D | Septum formation initiator | ||
HELEIBLM_01714 | 1.3e-243 | 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 | |
HELEIBLM_01715 | 4.9e-173 | 1.1.1.65 | C | Aldo/keto reductase family | ||
HELEIBLM_01716 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
HELEIBLM_01717 | 2e-114 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HELEIBLM_01718 | 1.5e-71 | S | PIN domain | |||
HELEIBLM_01719 | 2.5e-47 | S | RelB antitoxin | |||
HELEIBLM_01720 | 4.6e-88 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
HELEIBLM_01721 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
HELEIBLM_01722 | 1.4e-207 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
HELEIBLM_01723 | 3.8e-137 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HELEIBLM_01724 | 7.9e-100 | |||||
HELEIBLM_01725 | 6.7e-232 | 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 | |
HELEIBLM_01726 | 1.9e-250 | 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 | |
HELEIBLM_01727 | 2.4e-281 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
HELEIBLM_01728 | 1.6e-205 | S | Protein of unknown function (DUF1648) | |||
HELEIBLM_01729 | 1.8e-75 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
HELEIBLM_01730 | 1.9e-237 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HELEIBLM_01731 | 2.5e-40 | pacL2 | 3.6.3.8 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
HELEIBLM_01732 | 1e-73 | S | ABC-2 family transporter protein | |||
HELEIBLM_01733 | 1.9e-119 | S | ABC-2 family transporter protein | |||
HELEIBLM_01734 | 7.2e-172 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_01735 | 1.4e-57 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
HELEIBLM_01736 | 1.4e-36 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_01737 | 1.2e-31 | 2.7.13.3 | T | Histidine kinase | ||
HELEIBLM_01738 | 2e-52 | EGP | Major facilitator Superfamily | |||
HELEIBLM_01739 | 3.1e-07 | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | ||
HELEIBLM_01740 | 9.1e-113 | S | Haloacid dehalogenase-like hydrolase | |||
HELEIBLM_01741 | 3e-307 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HELEIBLM_01742 | 5.3e-184 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
HELEIBLM_01743 | 1.1e-97 | |||||
HELEIBLM_01744 | 2e-138 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HELEIBLM_01746 | 3.1e-195 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
HELEIBLM_01747 | 7.4e-133 | L | Tetratricopeptide repeat | |||
HELEIBLM_01748 | 7.5e-255 | 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) | |
HELEIBLM_01749 | 2.9e-134 | S | Putative ABC-transporter type IV | |||
HELEIBLM_01750 | 8.9e-98 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HELEIBLM_01751 | 1.3e-55 | M1-798 | P | Rhodanese Homology Domain | ||
HELEIBLM_01752 | 7.8e-146 | moeB | 2.7.7.80 | H | ThiF family | |
HELEIBLM_01753 | 1.1e-156 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
HELEIBLM_01754 | 2.1e-28 | thiS | 2.8.1.10 | H | ThiS family | |
HELEIBLM_01755 | 4e-281 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
HELEIBLM_01756 | 4.6e-238 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HELEIBLM_01757 | 1.7e-82 | argR | K | Regulates arginine biosynthesis genes | ||
HELEIBLM_01758 | 8.6e-184 | 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 | |
HELEIBLM_01759 | 6.6e-248 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
HELEIBLM_01760 | 4.2e-161 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
HELEIBLM_01761 | 7.8e-214 | 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 | |
HELEIBLM_01762 | 7.9e-202 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
HELEIBLM_01763 | 2.6e-94 | |||||
HELEIBLM_01764 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
HELEIBLM_01765 | 3.8e-201 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HELEIBLM_01766 | 3e-159 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HELEIBLM_01767 | 4.2e-147 | cbiQ | P | Cobalt transport protein | ||
HELEIBLM_01768 | 4.7e-274 | ykoD | P | ATPases associated with a variety of cellular activities | ||
HELEIBLM_01769 | 9e-107 | ykoE | S | ABC-type cobalt transport system, permease component | ||
HELEIBLM_01770 | 2.4e-256 | argE | E | Peptidase dimerisation domain | ||
HELEIBLM_01771 | 4.2e-107 | S | Protein of unknown function (DUF3043) | |||
HELEIBLM_01772 | 1.2e-277 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HELEIBLM_01773 | 4.7e-140 | S | Domain of unknown function (DUF4191) | |||
HELEIBLM_01774 | 5e-281 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HELEIBLM_01775 | 4.3e-97 | uidA | 3.2.1.31 | G | Glycosyl hydrolases family 2, TIM barrel domain | |
HELEIBLM_01776 | 1.3e-67 | S | Membrane transport protein | |||
HELEIBLM_01777 | 1.3e-88 | S | Membrane transport protein | |||
HELEIBLM_01778 | 7e-79 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HELEIBLM_01779 | 2.5e-84 | laaE | K | Transcriptional regulator PadR-like family | ||
HELEIBLM_01780 | 4.3e-116 | magIII | L | endonuclease III | ||
HELEIBLM_01781 | 7.5e-242 | vbsD | V | MatE | ||
HELEIBLM_01782 | 0.0 | uvrA3 | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
HELEIBLM_01783 | 1.6e-305 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
HELEIBLM_01784 | 1.1e-94 | S | AAA domain | |||
HELEIBLM_01785 | 3.4e-132 | C | FMN binding | |||
HELEIBLM_01786 | 5.4e-97 | effR | K | helix_turn_helix multiple antibiotic resistance protein | ||
HELEIBLM_01787 | 3.4e-11 | S | AAA domain | |||
HELEIBLM_01788 | 1.5e-189 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_01789 | 4.5e-161 | P | Phosphate transporter family | |||
HELEIBLM_01790 | 7.8e-164 | ugpA | P | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01791 | 1.2e-141 | ugpE | G | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01792 | 1.5e-239 | ugpB | G | Bacterial extracellular solute-binding protein | ||
HELEIBLM_01793 | 7.1e-169 | ugpQ | 3.1.4.46 | C | Domain of unknown function | |
HELEIBLM_01794 | 7.6e-109 | P | Protein of unknown function DUF47 | |||
HELEIBLM_01795 | 1.4e-256 | S | Domain of unknown function (DUF4143) | |||
HELEIBLM_01796 | 0.0 | V | FtsX-like permease family | |||
HELEIBLM_01797 | 3.3e-124 | V | ABC transporter | |||
HELEIBLM_01798 | 7.7e-109 | K | Bacterial regulatory proteins, tetR family | |||
HELEIBLM_01799 | 9.3e-192 | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | ||
HELEIBLM_01800 | 3e-16 | K | MerR family regulatory protein | |||
HELEIBLM_01801 | 3.8e-10 | K | MerR family regulatory protein | |||
HELEIBLM_01802 | 3.8e-88 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HELEIBLM_01803 | 2.8e-58 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HELEIBLM_01804 | 1e-31 | S | Psort location CytoplasmicMembrane, score | |||
HELEIBLM_01805 | 8.6e-185 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
HELEIBLM_01806 | 6.6e-145 | rlrG | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
HELEIBLM_01807 | 3e-94 | tmp1 | S | Domain of unknown function (DUF4391) | ||
HELEIBLM_01808 | 1.8e-231 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HELEIBLM_01809 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
HELEIBLM_01810 | 1.6e-79 | 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 | ||
HELEIBLM_01811 | 9.3e-62 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
HELEIBLM_01812 | 4.1e-187 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
HELEIBLM_01814 | 1.1e-189 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
HELEIBLM_01815 | 3.2e-209 | M | Glycosyl transferase 4-like domain | |||
HELEIBLM_01816 | 1.3e-189 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
HELEIBLM_01817 | 8.7e-225 | purT | 2.1.2.2 | 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 | |
HELEIBLM_01818 | 2.7e-61 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
HELEIBLM_01819 | 2.1e-137 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HELEIBLM_01820 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
HELEIBLM_01821 | 7.5e-215 | I | alpha/beta hydrolase fold | |||
HELEIBLM_01822 | 1.7e-254 | Q | D-alanine [D-alanyl carrier protein] ligase activity | |||
HELEIBLM_01823 | 5.3e-108 | Q | D-alanine [D-alanyl carrier protein] ligase activity | |||
HELEIBLM_01824 | 5e-99 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
HELEIBLM_01825 | 5e-170 | hipA | 2.7.11.1 | S | HipA N-terminal domain | |
HELEIBLM_01826 | 1e-120 | C | Aldo/keto reductase family | |||
HELEIBLM_01827 | 1.6e-32 | |||||
HELEIBLM_01828 | 5.6e-276 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
HELEIBLM_01829 | 3.9e-191 | 3.3.1.1 | H | S-adenosyl-L-homocysteine hydrolase, NAD binding domain | ||
HELEIBLM_01830 | 2.1e-239 | ssnA | 3.5.4.40 | F | Amidohydrolase family | |
HELEIBLM_01831 | 1.8e-65 | MA20_39615 | S | Cupin superfamily (DUF985) | ||
HELEIBLM_01832 | 1.1e-126 | ET | Bacterial periplasmic substrate-binding proteins | |||
HELEIBLM_01833 | 1.9e-122 | E | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_01834 | 1.9e-120 | glnQ | 3.6.3.21 | E | AAA domain, putative AbiEii toxin, Type IV TA system | |
HELEIBLM_01835 | 7.2e-286 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HELEIBLM_01836 | 5.4e-184 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HELEIBLM_01837 | 2.7e-233 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HELEIBLM_01838 | 2.8e-275 | aldH | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | |
HELEIBLM_01839 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HELEIBLM_01840 | 1.5e-148 | P | Zinc-uptake complex component A periplasmic | |||
HELEIBLM_01841 | 4.7e-100 | S | cobalamin synthesis protein | |||
HELEIBLM_01842 | 1.9e-28 | rpmB | J | Ribosomal L28 family | ||
HELEIBLM_01843 | 1.4e-20 | rpmG | J | Ribosomal protein L33 | ||
HELEIBLM_01844 | 2.5e-44 | 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 | ||
HELEIBLM_01845 | 4.4e-34 | rpmE2 | J | Ribosomal protein L31 | ||
HELEIBLM_01846 | 1.1e-14 | rpmJ | J | Ribosomal protein L36 | ||
HELEIBLM_01847 | 2.6e-19 | J | Ribosomal L32p protein family | |||
HELEIBLM_01848 | 3.2e-27 | adcA | P | ZinT (YodA) periplasmic lipocalin-like zinc-recruitment | ||
HELEIBLM_01849 | 2.7e-165 | ycgR | S | Predicted permease | ||
HELEIBLM_01850 | 3.3e-138 | S | TIGRFAM TIGR03943 family protein | |||
HELEIBLM_01851 | 3.7e-21 | zur | P | Ferric uptake regulator family | ||
HELEIBLM_01852 | 1.7e-54 | zur | P | Ferric uptake regulator family | ||
HELEIBLM_01853 | 1.1e-58 | |||||
HELEIBLM_01854 | 2e-46 | tetR | K | Transcriptional regulator C-terminal region | ||
HELEIBLM_01855 | 1.4e-17 | XK27_06785 | V | ABC transporter | ||
HELEIBLM_01856 | 3.9e-85 | ylbB | V | FtsX-like permease family | ||
HELEIBLM_01857 | 1.2e-68 | zur | P | Belongs to the Fur family | ||
HELEIBLM_01858 | 1.8e-223 | 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) | |
HELEIBLM_01859 | 7.3e-86 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HELEIBLM_01860 | 1e-176 | adh3 | C | Zinc-binding dehydrogenase | ||
HELEIBLM_01861 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
HELEIBLM_01862 | 1.4e-252 | macB_8 | V | MacB-like periplasmic core domain | ||
HELEIBLM_01863 | 1.2e-131 | M | Conserved repeat domain | |||
HELEIBLM_01864 | 6.4e-121 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_01866 | 1.6e-216 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HELEIBLM_01867 | 6.8e-156 | K | Helix-turn-helix domain, rpiR family | |||
HELEIBLM_01868 | 0.0 | G | Alpha-L-arabinofuranosidase C-terminal domain | |||
HELEIBLM_01869 | 4.7e-28 | |||||
HELEIBLM_01870 | 5e-270 | pip | S | YhgE Pip domain protein | ||
HELEIBLM_01871 | 0.0 | pip | S | YhgE Pip domain protein | ||
HELEIBLM_01872 | 1.2e-140 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
HELEIBLM_01873 | 7.5e-59 | S | Protein of unknown function (DUF4235) | |||
HELEIBLM_01874 | 3.5e-134 | G | Phosphoglycerate mutase family | |||
HELEIBLM_01875 | 3.6e-246 | amyE | G | Bacterial extracellular solute-binding protein | ||
HELEIBLM_01876 | 5e-182 | K | Psort location Cytoplasmic, score | |||
HELEIBLM_01877 | 7.4e-147 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01878 | 1.5e-152 | rafG | G | ABC transporter permease | ||
HELEIBLM_01879 | 1.6e-101 | S | Protein of unknown function, DUF624 | |||
HELEIBLM_01880 | 2.3e-255 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
HELEIBLM_01881 | 6.1e-123 | V | ABC transporter | |||
HELEIBLM_01882 | 0.0 | V | FtsX-like permease family | |||
HELEIBLM_01883 | 1.3e-266 | cycA | E | Amino acid permease | ||
HELEIBLM_01884 | 7.8e-78 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
HELEIBLM_01885 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
HELEIBLM_01886 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
HELEIBLM_01887 | 2.6e-152 | 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 | |
HELEIBLM_01889 | 1.5e-181 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HELEIBLM_01890 | 8.3e-26 | |||||
HELEIBLM_01891 | 4.7e-114 | |||||
HELEIBLM_01892 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HELEIBLM_01893 | 4.4e-46 | |||||
HELEIBLM_01894 | 1.5e-169 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
HELEIBLM_01895 | 7e-262 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HELEIBLM_01896 | 2e-175 | appB | EP | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01897 | 9.2e-173 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
HELEIBLM_01898 | 0.0 | oppD | P | Belongs to the ABC transporter superfamily | ||
HELEIBLM_01899 | 0.0 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
HELEIBLM_01901 | 2.4e-251 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_01902 | 4.4e-266 | S | AAA domain | |||
HELEIBLM_01903 | 1.5e-58 | G | domain, Protein | |||
HELEIBLM_01904 | 2.5e-250 | S | Domain of unknown function (DUF4143) | |||
HELEIBLM_01905 | 3.9e-270 | S | ATPase domain predominantly from Archaea | |||
HELEIBLM_01906 | 0.0 | mdlA2 | V | ABC transporter | ||
HELEIBLM_01907 | 2.5e-311 | yknV | V | ABC transporter | ||
HELEIBLM_01908 | 7.5e-197 | S | Fic/DOC family | |||
HELEIBLM_01909 | 5.9e-185 | tatD | L | TatD related DNase | ||
HELEIBLM_01910 | 0.0 | kup | P | Transport of potassium into the cell | ||
HELEIBLM_01911 | 1.3e-159 | S | Glutamine amidotransferase domain | |||
HELEIBLM_01912 | 1.3e-133 | T | HD domain | |||
HELEIBLM_01914 | 2.6e-171 | V | ABC transporter | |||
HELEIBLM_01915 | 2.6e-216 | V | ABC transporter permease | |||
HELEIBLM_01916 | 0.0 | pflA | S | Protein of unknown function (DUF4012) | ||
HELEIBLM_01917 | 2.3e-194 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
HELEIBLM_01918 | 2.5e-52 | S | Predicted membrane protein (DUF2142) | |||
HELEIBLM_01919 | 6.2e-145 | cobB2 | K | Sir2 family | ||
HELEIBLM_01920 | 1e-232 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
HELEIBLM_01921 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
HELEIBLM_01922 | 6.6e-09 | L | Transposase | |||
HELEIBLM_01923 | 2.9e-154 | G | Binding-protein-dependent transport system inner membrane component | |||
HELEIBLM_01924 | 1.1e-143 | malC | G | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01925 | 4.9e-243 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
HELEIBLM_01926 | 2.1e-227 | nagC | GK | ROK family | ||
HELEIBLM_01927 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
HELEIBLM_01928 | 3.2e-78 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HELEIBLM_01929 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
HELEIBLM_01930 | 3e-147 | ypfH | S | Phospholipase/Carboxylesterase | ||
HELEIBLM_01931 | 2.6e-131 | |||||
HELEIBLM_01932 | 3.4e-111 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
HELEIBLM_01933 | 4.9e-80 | |||||
HELEIBLM_01934 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
HELEIBLM_01935 | 2e-16 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_01936 | 1.8e-84 | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
HELEIBLM_01937 | 5e-287 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
HELEIBLM_01938 | 1.1e-204 | EGP | Major facilitator Superfamily | |||
HELEIBLM_01939 | 7.5e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HELEIBLM_01940 | 6.3e-268 | KLT | Domain of unknown function (DUF4032) | |||
HELEIBLM_01941 | 1.8e-209 | ugpC | E | Belongs to the ABC transporter superfamily | ||
HELEIBLM_01942 | 5.9e-219 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
HELEIBLM_01943 | 3.7e-190 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HELEIBLM_01945 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HELEIBLM_01946 | 4.2e-80 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
HELEIBLM_01947 | 4.1e-43 | nrdH | O | Glutaredoxin | ||
HELEIBLM_01948 | 2.7e-109 | K | Helix-turn-helix XRE-family like proteins | |||
HELEIBLM_01949 | 1.2e-120 | S | Protein of unknown function (DUF3990) | |||
HELEIBLM_01950 | 9.2e-107 | kcsA | U | Ion channel | ||
HELEIBLM_01951 | 1.9e-203 | S | AAA ATPase domain | |||
HELEIBLM_01952 | 2.4e-46 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
HELEIBLM_01953 | 0.0 | KLT | Protein tyrosine kinase | |||
HELEIBLM_01954 | 1.2e-129 | O | Thioredoxin | |||
HELEIBLM_01956 | 7.7e-211 | S | G5 | |||
HELEIBLM_01957 | 4.5e-166 | ksgA | 2.1.1.182, 2.1.1.184 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
HELEIBLM_01958 | 1.2e-174 | 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 | |
HELEIBLM_01959 | 2.1e-106 | S | LytR cell envelope-related transcriptional attenuator | |||
HELEIBLM_01960 | 1.4e-275 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
HELEIBLM_01961 | 4.6e-116 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
HELEIBLM_01962 | 0.0 | |||||
HELEIBLM_01963 | 0.0 | murJ | KLT | MviN-like protein | ||
HELEIBLM_01964 | 6.3e-185 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HELEIBLM_01965 | 1.9e-216 | parB | K | Belongs to the ParB family | ||
HELEIBLM_01966 | 7.8e-177 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HELEIBLM_01967 | 5.5e-121 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HELEIBLM_01968 | 1.1e-92 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
HELEIBLM_01969 | 5.8e-175 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
HELEIBLM_01970 | 4e-33 | 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 | |
HELEIBLM_01971 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HELEIBLM_01972 | 4.6e-285 | 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 | ||
HELEIBLM_01974 | 7.6e-208 | 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 | |
HELEIBLM_01975 | 6.4e-224 | 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 | ||
HELEIBLM_01976 | 8.7e-81 | S | Protein of unknown function (DUF721) | |||
HELEIBLM_01977 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
HELEIBLM_01978 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
HELEIBLM_01979 | 2.1e-81 | S | Transmembrane domain of unknown function (DUF3566) | |||
HELEIBLM_01980 | 2.2e-273 | S | ATPase domain predominantly from Archaea | |||
HELEIBLM_01981 | 1e-14 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_01982 | 5.1e-251 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
HELEIBLM_01983 | 3.4e-27 | S | addiction module toxin, RelE StbE family | |||
HELEIBLM_01984 | 1.3e-28 | relB | L | RelB antitoxin | ||
HELEIBLM_01985 | 2.9e-34 | |||||
HELEIBLM_01987 | 1.1e-30 | L | Phage integrase family | |||
HELEIBLM_01990 | 4.9e-70 | cpdB | 3.1.3.6, 3.1.4.16 | F | Calcineurin-like phosphoesterase | |
HELEIBLM_01991 | 3.8e-81 | 3.6.1.63 | U | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_01992 | 3.4e-77 | phnE | 3.6.1.63 | U | Binding-protein-dependent transport system inner membrane component | |
HELEIBLM_01993 | 2e-82 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
HELEIBLM_01994 | 1.8e-114 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
HELEIBLM_01995 | 2.7e-35 | K | Helix-turn-helix domain, rpiR family | |||
HELEIBLM_01996 | 3.7e-30 | S | phosphoglycolate phosphatase activity | |||
HELEIBLM_01997 | 2.9e-203 | S | Domain of unknown function (DUF4143) | |||
HELEIBLM_01998 | 3e-146 | S | Protein of unknown function DUF45 | |||
HELEIBLM_01999 | 5e-92 | K | FCD | |||
HELEIBLM_02000 | 3.7e-215 | EG | GntP family permease | |||
HELEIBLM_02001 | 4.3e-87 | gntK | 1.1.1.343, 1.1.1.44, 2.7.1.12, 2.7.1.71 | F | Shikimate kinase | |
HELEIBLM_02002 | 4e-151 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase, C-terminal domain | |
HELEIBLM_02003 | 7.3e-83 | dps | P | Belongs to the Dps family | ||
HELEIBLM_02004 | 1e-235 | ytfL | P | Transporter associated domain | ||
HELEIBLM_02005 | 2.8e-202 | S | AAA ATPase domain | |||
HELEIBLM_02006 | 7.9e-72 | V | Forkhead associated domain | |||
HELEIBLM_02007 | 1.6e-120 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HELEIBLM_02008 | 1.1e-106 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
HELEIBLM_02009 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
HELEIBLM_02010 | 8.1e-238 | yhjX | EGP | Major facilitator Superfamily | ||
HELEIBLM_02011 | 4.5e-148 | S | Domain of unknown function (DUF4143) | |||
HELEIBLM_02012 | 9e-128 | S | Metallo-beta-lactamase domain protein | |||
HELEIBLM_02013 | 4.7e-26 | L | Transposase | |||
HELEIBLM_02014 | 2.2e-60 | L | Transposase | |||
HELEIBLM_02015 | 4.8e-84 | V | ABC-2 type transporter | |||
HELEIBLM_02016 | 7.2e-85 | V | ABC transporter, ATP-binding protein | |||
HELEIBLM_02017 | 6.8e-41 | L | PFAM Integrase catalytic | |||
HELEIBLM_02018 | 4.9e-59 | L | Transposase | |||
HELEIBLM_02019 | 1.7e-232 | S | AAA domain | |||
HELEIBLM_02020 | 2.9e-309 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HELEIBLM_02021 | 2e-25 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
HELEIBLM_02022 | 4.4e-191 | oppA5 | E | family 5 | ||
HELEIBLM_02023 | 1.9e-122 | appB | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
HELEIBLM_02024 | 2.5e-89 | appC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HELEIBLM_02025 | 5.4e-153 | P | Belongs to the ABC transporter superfamily | |||
HELEIBLM_02026 | 9.9e-37 | ybfG | M | Domain of unknown function (DUF1906) | ||
HELEIBLM_02028 | 7.2e-33 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HELEIBLM_02029 | 4.2e-171 | L | ATPase involved in DNA repair | |||
HELEIBLM_02031 | 1.2e-113 | |||||
HELEIBLM_02032 | 1.3e-36 | S | Sigma-70, region 4 | |||
HELEIBLM_02034 | 0.0 | M | Domain of unknown function (DUF1906) | |||
HELEIBLM_02035 | 2.7e-12 | |||||
HELEIBLM_02036 | 2.5e-155 | ybfG | M | Domain of unknown function (DUF1906) | ||
HELEIBLM_02038 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HELEIBLM_02039 | 0.0 | yjjP | S | Threonine/Serine exporter, ThrE | ||
HELEIBLM_02040 | 1.8e-298 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
HELEIBLM_02041 | 5.7e-181 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
HELEIBLM_02042 | 1e-123 | S | Amidohydrolase family | |||
HELEIBLM_02043 | 2.1e-166 | S | Amidohydrolase family | |||
HELEIBLM_02044 | 6.3e-199 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HELEIBLM_02045 | 3.9e-21 | S | Protein of unknown function (DUF3073) | |||
HELEIBLM_02046 | 2.3e-105 | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | |||
HELEIBLM_02047 | 5.6e-206 | 2.7.13.3 | T | Histidine kinase | ||
HELEIBLM_02048 | 4.5e-234 | EGP | Major Facilitator Superfamily | |||
HELEIBLM_02049 | 7.5e-76 | I | Sterol carrier protein | |||
HELEIBLM_02050 | 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 |
HELEIBLM_02051 | 1.7e-31 | |||||
HELEIBLM_02052 | 2.9e-125 | gluP | 3.4.21.105 | S | Rhomboid family | |
HELEIBLM_02053 | 1.3e-79 | crgA | D | Involved in cell division | ||
HELEIBLM_02054 | 1.7e-108 | S | Bacterial protein of unknown function (DUF881) | |||
HELEIBLM_02055 | 5.2e-234 | srtA | 3.4.22.70 | M | Sortase family | |
HELEIBLM_02056 | 1.1e-118 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
HELEIBLM_02057 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
HELEIBLM_02058 | 1.3e-171 | T | Protein tyrosine kinase | |||
HELEIBLM_02059 | 1e-260 | pbpA | M | penicillin-binding protein | ||
HELEIBLM_02060 | 1.2e-251 | rodA | D | Belongs to the SEDS family | ||
HELEIBLM_02061 | 1.9e-239 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
HELEIBLM_02062 | 8e-59 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
HELEIBLM_02063 | 2.6e-129 | fhaA | T | Protein of unknown function (DUF2662) | ||
HELEIBLM_02064 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
HELEIBLM_02065 | 3.1e-206 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
HELEIBLM_02066 | 9.8e-148 | yddG | EG | EamA-like transporter family | ||
HELEIBLM_02067 | 3.5e-231 | S | Putative esterase | |||
HELEIBLM_02068 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
HELEIBLM_02069 | 2.8e-190 | 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 | |
HELEIBLM_02070 | 2e-129 | S | Pyridoxamine 5'-phosphate oxidase | |||
HELEIBLM_02071 | 4.8e-79 | S | Fic/DOC family | |||
HELEIBLM_02072 | 5.7e-172 | L | Psort location Cytoplasmic, score | |||
HELEIBLM_02073 | 1.2e-106 | S | KR domain | |||
HELEIBLM_02074 | 8.2e-16 | tnp7109-2 | L | Transposase, Mutator family | ||
HELEIBLM_02075 | 1.5e-36 | |||||
HELEIBLM_02076 | 8.1e-21 | |||||
HELEIBLM_02077 | 2.2e-20 | L | Phage integrase family | |||
HELEIBLM_02078 | 9.2e-47 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_02079 | 2.9e-12 | |||||
HELEIBLM_02080 | 2.6e-44 | V | efflux transmembrane transporter activity | |||
HELEIBLM_02081 | 1.6e-199 | S | Psort location Cytoplasmic, score 7.50 | |||
HELEIBLM_02082 | 2.4e-117 | S | AAA ATPase domain | |||
HELEIBLM_02083 | 1.3e-259 | EGP | Major facilitator Superfamily | |||
HELEIBLM_02084 | 5.4e-216 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HELEIBLM_02085 | 5.7e-135 | L | Protein of unknown function (DUF1524) | |||
HELEIBLM_02086 | 1.8e-125 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
HELEIBLM_02087 | 6e-81 | ganB | 3.2.1.89 | G | Glycosyl hydrolase family 53 | |
HELEIBLM_02088 | 3.7e-170 | K | helix_turn _helix lactose operon repressor | |||
HELEIBLM_02090 | 1.4e-26 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_02091 | 2e-25 | |||||
HELEIBLM_02092 | 4.7e-101 | V | ABC transporter | |||
HELEIBLM_02093 | 1.1e-241 | XK27_10205 | ||||
HELEIBLM_02094 | 2.2e-19 | S | Bacteriocin (Lactococcin_972) | |||
HELEIBLM_02095 | 4.3e-41 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_02096 | 9.1e-101 | 2.7.13.3 | T | Histidine kinase | ||
HELEIBLM_02097 | 1.5e-247 | araE | EGP | Major facilitator Superfamily | ||
HELEIBLM_02098 | 1.3e-124 | cydD | V | ABC transporter transmembrane region | ||
HELEIBLM_02099 | 1.2e-58 | cydD | V | ABC transporter transmembrane region | ||
HELEIBLM_02100 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
HELEIBLM_02101 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
HELEIBLM_02102 | 1.1e-143 | 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 | |
HELEIBLM_02103 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
HELEIBLM_02104 | 7.7e-255 | 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 | |
HELEIBLM_02105 | 1.2e-43 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
HELEIBLM_02106 | 5.5e-233 | S | peptidyl-serine autophosphorylation | |||
HELEIBLM_02107 | 9.4e-92 | ywrO | 1.6.5.2 | S | Flavodoxin-like fold | |
HELEIBLM_02108 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
HELEIBLM_02109 | 4.5e-76 | F | Nucleoside 2-deoxyribosyltransferase | |||
HELEIBLM_02110 | 4.1e-10 | K | Acetyltransferase (GNAT) domain | |||
HELEIBLM_02112 | 2.1e-186 | S | Endonuclease/Exonuclease/phosphatase family | |||
HELEIBLM_02113 | 3.1e-11 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HELEIBLM_02114 | 6.4e-08 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HELEIBLM_02115 | 2.3e-223 | aspB | E | Aminotransferase class-V | ||
HELEIBLM_02116 | 7.2e-200 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
HELEIBLM_02117 | 6.4e-85 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
HELEIBLM_02118 | 2e-35 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
HELEIBLM_02119 | 1.1e-33 | |||||
HELEIBLM_02120 | 2.4e-78 | S | PFAM Uncharacterised protein family UPF0150 | |||
HELEIBLM_02121 | 0.0 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
HELEIBLM_02122 | 1.1e-211 | K | WYL domain | |||
HELEIBLM_02123 | 1.1e-144 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
HELEIBLM_02124 | 1.7e-248 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
HELEIBLM_02125 | 9.2e-152 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
HELEIBLM_02126 | 1.5e-98 | S | Short repeat of unknown function (DUF308) | |||
HELEIBLM_02127 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HELEIBLM_02128 | 3.9e-51 | L | Single-strand binding protein family | |||
HELEIBLM_02129 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
HELEIBLM_02130 | 1.6e-302 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HELEIBLM_02131 | 3.6e-236 | |||||
HELEIBLM_02132 | 5.3e-159 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
HELEIBLM_02133 | 3.8e-213 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
HELEIBLM_02134 | 6.3e-89 | 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 | |
HELEIBLM_02135 | 3.3e-37 | yajC | U | Preprotein translocase subunit | ||
HELEIBLM_02136 | 6.8e-190 | 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 | |
HELEIBLM_02137 | 5.2e-89 | 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 | |
HELEIBLM_02138 | 1.1e-96 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
HELEIBLM_02139 | 3.4e-127 | yebC | K | transcriptional regulatory protein | ||
HELEIBLM_02140 | 7.7e-111 | hit | 2.7.7.53 | FG | HIT domain | |
HELEIBLM_02141 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
HELEIBLM_02145 | 2.2e-162 | S | PAC2 family | |||
HELEIBLM_02146 | 6.5e-154 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
HELEIBLM_02147 | 7.3e-157 | G | Fructosamine kinase | |||
HELEIBLM_02148 | 2.8e-210 | 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 | ||
HELEIBLM_02149 | 6.7e-180 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HELEIBLM_02150 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
HELEIBLM_02151 | 5.7e-200 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
HELEIBLM_02152 | 6.4e-217 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HELEIBLM_02153 | 1.4e-216 | mepA_6 | V | MatE | ||
HELEIBLM_02154 | 8.5e-250 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
HELEIBLM_02155 | 8.2e-162 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HELEIBLM_02156 | 1.1e-175 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HELEIBLM_02157 | 2.5e-34 | secG | U | Preprotein translocase SecG subunit | ||
HELEIBLM_02158 | 9.5e-144 | 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) | |
HELEIBLM_02159 | 1.1e-220 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
HELEIBLM_02160 | 1.2e-169 | whiA | K | May be required for sporulation | ||
HELEIBLM_02161 | 3e-184 | rapZ | S | Displays ATPase and GTPase activities | ||
HELEIBLM_02162 | 1.9e-186 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
HELEIBLM_02163 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
HELEIBLM_02164 | 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 | ||
HELEIBLM_02165 | 7.3e-30 | S | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_02166 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_02167 | 5.6e-105 | S | Domain of unknown function (DUF4194) | |||
HELEIBLM_02168 | 2.5e-292 | S | Psort location Cytoplasmic, score 8.87 | |||
HELEIBLM_02169 | 3.9e-87 | macB | V | ATPases associated with a variety of cellular activities | ||
HELEIBLM_02170 | 4.3e-17 | XK27_08585 | S | Hypothetical bacterial integral membrane protein (Trep_Strep) | ||
HELEIBLM_02171 | 2.1e-38 | G | ATPases associated with a variety of cellular activities | |||
HELEIBLM_02172 | 4e-32 | S | Zincin-like metallopeptidase | |||
HELEIBLM_02173 | 8.2e-162 | 2.1.1.72 | S | Protein conserved in bacteria | ||
HELEIBLM_02174 | 4.9e-128 | yueD | S | Enoyl-(Acyl carrier protein) reductase | ||
HELEIBLM_02175 | 1.9e-300 | ybiT | S | ABC transporter | ||
HELEIBLM_02176 | 2.1e-118 | S | Protein of unknown function (DUF969) | |||
HELEIBLM_02177 | 7.5e-164 | S | Protein of unknown function (DUF979) | |||
HELEIBLM_02178 | 6.3e-114 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
HELEIBLM_02179 | 1.6e-293 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
HELEIBLM_02180 | 2.2e-69 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
HELEIBLM_02181 | 6.1e-140 | hisF | 4.1.3.27 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
HELEIBLM_02182 | 3.9e-75 | 3.5.1.124 | S | DJ-1/PfpI family | ||
HELEIBLM_02183 | 1.6e-221 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
HELEIBLM_02184 | 2.1e-169 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
HELEIBLM_02185 | 5.4e-90 | 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 | ||
HELEIBLM_02186 | 1.9e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HELEIBLM_02187 | 7.4e-139 | 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 | ||
HELEIBLM_02188 | 6e-141 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HELEIBLM_02189 | 1.3e-87 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
HELEIBLM_02190 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
HELEIBLM_02191 | 1.5e-70 | |||||
HELEIBLM_02192 | 2.6e-208 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
HELEIBLM_02193 | 1.9e-241 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
HELEIBLM_02194 | 9.2e-255 | G | ABC transporter substrate-binding protein | |||
HELEIBLM_02195 | 1.3e-104 | M | Peptidase family M23 | |||
HELEIBLM_02197 | 1.2e-120 | K | helix_turn_helix, Lux Regulon | |||
HELEIBLM_02198 | 3.6e-238 | T | Histidine kinase | |||
HELEIBLM_02200 | 4.4e-59 | |||||
HELEIBLM_02201 | 2e-139 | |||||
HELEIBLM_02202 | 1.9e-142 | S | ABC-2 family transporter protein | |||
HELEIBLM_02203 | 6.3e-199 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
HELEIBLM_02204 | 1.9e-46 | L | PFAM Relaxase mobilization nuclease family protein | |||
HELEIBLM_02205 | 6.9e-24 | L | transposase and inactivated derivatives, IS30 family | |||
HELEIBLM_02206 | 6.5e-110 | L | Transposase and inactivated derivatives IS30 family | |||
HELEIBLM_02207 | 1.4e-20 | |||||
HELEIBLM_02209 | 5.5e-56 | S | Fic/DOC family | |||
HELEIBLM_02212 | 6.2e-11 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
HELEIBLM_02213 | 1.9e-51 | xerH | L | Phage integrase family | ||
HELEIBLM_02215 | 1.2e-194 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
HELEIBLM_02216 | 7.8e-97 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
HELEIBLM_02217 | 1.4e-150 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
HELEIBLM_02218 | 4.8e-102 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
HELEIBLM_02219 | 6e-177 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HELEIBLM_02220 | 2.4e-248 | comE | S | Competence protein | ||
HELEIBLM_02221 | 7e-58 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
HELEIBLM_02222 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HELEIBLM_02223 | 4.6e-150 | ET | Bacterial periplasmic substrate-binding proteins | |||
HELEIBLM_02224 | 6.3e-171 | corA | P | CorA-like Mg2+ transporter protein | ||
HELEIBLM_02225 | 5.2e-161 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
HELEIBLM_02226 | 4.9e-235 | L | ribosomal rna small subunit methyltransferase | |||
HELEIBLM_02227 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
HELEIBLM_02228 | 5.4e-159 | EG | EamA-like transporter family | |||
HELEIBLM_02229 | 5.2e-88 | |||||
HELEIBLM_02230 | 2.7e-122 | T | PhoQ Sensor | |||
HELEIBLM_02231 | 1e-98 | T | Transcriptional regulatory protein, C terminal | |||
HELEIBLM_02232 | 1.8e-89 | |||||
HELEIBLM_02233 | 6.9e-56 | spaG | S | Lantibiotic protection ABC transporter permease subunit, MutG family | ||
HELEIBLM_02234 | 4.4e-63 | S | ABC-2 family transporter protein | |||
HELEIBLM_02235 | 1.5e-91 | mutF | V | ABC transporter ATP-binding | ||
HELEIBLM_02236 | 3.6e-38 | V | ABC-2 family transporter protein | |||
HELEIBLM_02237 | 2.1e-19 | L | Helix-turn-helix domain | |||
HELEIBLM_02238 | 3.5e-54 | |||||
HELEIBLM_02239 | 1.2e-55 | |||||
HELEIBLM_02240 | 1.3e-15 | L | Phage integrase family | |||
HELEIBLM_02241 | 3.6e-101 | V | ATPases associated with a variety of cellular activities | |||
HELEIBLM_02242 | 9.9e-171 | |||||
HELEIBLM_02243 | 5e-32 | |||||
HELEIBLM_02244 | 2.1e-19 | L | Helix-turn-helix domain | |||
HELEIBLM_02245 | 2.7e-123 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR repeat-like domain | |
HELEIBLM_02246 | 3.5e-137 | nanL | 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
HELEIBLM_02247 | 1.8e-57 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02248 | 4.4e-39 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02249 | 2.5e-124 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02250 | 2.2e-20 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02251 | 4.3e-40 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02252 | 7.9e-37 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02253 | 2.3e-226 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02254 | 3.6e-205 | G | Glycosyl hydrolase family 20, domain 2 | |||
HELEIBLM_02255 | 2e-94 | M1-431 | S | Protein of unknown function (DUF1706) | ||
HELEIBLM_02256 | 6.1e-128 | L | Helix-turn-helix domain | |||
HELEIBLM_02257 | 9.9e-41 | L | Resolvase, N terminal domain | |||
HELEIBLM_02258 | 1.1e-210 | phoN | I | PAP2 superfamily | ||
HELEIBLM_02259 | 3.3e-115 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HELEIBLM_02260 | 1.1e-75 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HELEIBLM_02261 | 6.1e-102 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
HELEIBLM_02262 | 1.8e-09 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HELEIBLM_02263 | 2e-202 | G | Bacterial extracellular solute-binding protein | |||
HELEIBLM_02264 | 3.6e-128 | ugpE | G | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_02265 | 9.9e-132 | ugpA | P | Binding-protein-dependent transport system inner membrane component | ||
HELEIBLM_02266 | 8e-159 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
HELEIBLM_02267 | 4.3e-157 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HELEIBLM_02268 | 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 | ||
HELEIBLM_02269 | 2.6e-74 | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | ||
HELEIBLM_02270 | 2.6e-157 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
HELEIBLM_02271 | 3.4e-23 | S | Domain of unknown function (DUF4190) | |||
HELEIBLM_02272 | 1.3e-72 | tnp3512a | L | Transposase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)