Your Input: | |||||
| h16_A2709 | Oligoribonuclease (3'->5' exoribonuclease); 3'-to-5' exoribonuclease specific for small oligoribonucleotides; Belongs to the oligoribonuclease family. (208 aa) | ||||
| h16_A2734 | Exonuclease VII small subunit; Bidirectionally degrades single-stranded DNA into large acid- insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides; Belongs to the XseB family. (102 aa) | ||||
| polA | DNA polymerase I; In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity; Belongs to the DNA polymerase type-A family. (938 aa) | ||||
| h16_A2915 | Predicted endonuclease involved in recombination; Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA; Belongs to the YqgF nuclease family. (141 aa) | ||||
| h16_A2929 | Predicted nucleic acid-binding protein,containsPIN domain; Toxic component of a toxin-antitoxin (TA) system. An RNase. Belongs to the PINc/VapC protein family. (138 aa) | ||||
| pilU | Type IV pilus twitching motility protein PilU. (379 aa) | ||||
| h16_A3152 | Guanyl-specific ribonuclease. (123 aa) | ||||
| h16_A3163 | Transcriptional regulator, Exoribonuclease II-family. (700 aa) | ||||
| h16_A3168 | Conserved hypothetical protein. (229 aa) | ||||
| h16_A3206 | GP29 like protein (of Bacteriophage phiE125). (174 aa) | ||||
| h16_A3214 | Hypothetical protein. (184 aa) | ||||
| h16_A3229 | Conserved hypothetical protein. (265 aa) | ||||
| stbB1 | Plasmid stability protein StbB. (140 aa) | ||||
| h16_A3546 | Uncharacterized conserved protein; Function unknown. (417 aa) | ||||
| h16_A3579 | Predicted endonuclease distantly to archaeal holliday junction resolvase; Belongs to the UPF0102 family. (131 aa) | ||||
| h16_A3583 | Conserved hypothetical protein. (213 aa) | ||||
| h16_A3746 | Ribonuclease P protein component; 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. (184 aa) | ||||
| h16_B0156 | Conserved hypothetical protein; Belongs to the UPF0213 family. (92 aa) | ||||
| sbcD | DNA repair exonuclease, SbcD; SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'->5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity; Belongs to the SbcD family. (395 aa) | ||||
| sbcC | DNA repair exonuclease, SbcC. (1020 aa) | ||||
| h16_B0576 | Nucleic acid-binding protein of Vap family; Toxic component of a toxin-antitoxin (TA) system. An RNase. Belongs to the PINc/VapC protein family. (132 aa) | ||||
| h16_B0631 | Conserved hypothetical protein. (321 aa) | ||||
| stbB2 | Plasmid stability protein StbB; Toxic component of a toxin-antitoxin (TA) system. An RNase. Belongs to the PINc/VapC protein family. (142 aa) | ||||
| h16_B0768 | Exconuclease. (528 aa) | ||||
| phnA | Phosphonoacetate hydrolase. (406 aa) | ||||
| h16_B0966 | Conserved hypothetical protein; Function unknown. (74 aa) | ||||
| h16_B0978 | Metal-dependent hydrolase of the beta-lactamase superfamily. (346 aa) | ||||
| ruvC | Crossover junction endodeoxyribonuclease RuvC; 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. (181 aa) | ||||
| h16_A0526 | Diacylglycerol kinase; Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA. (248 aa) | ||||
| xseA | Exodeoxyribonuclease VII, large subunit; Bidirectionally degrades single-stranded DNA into large acid- insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides; Belongs to the XseA family. (476 aa) | ||||
| h16_A0654 | Hemolysin-coregulated protein. (161 aa) | ||||
| h16_A0752 | Uncharacterized protein conserved in bacteria. (224 aa) | ||||
| dnaE1 | DNA polymerase III alpha subunit. (1173 aa) | ||||
| cafA1 | Ribonuclease G and E. (488 aa) | ||||
| h16_A0949 | Ribonuclease PH; Phosphorolytic 3'-5' exoribonuclease that plays an important role in tRNA 3'-end maturation. Removes nucleotide residues following the 3'-CCA terminus of tRNAs; can also add nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates, but this may not be physiologically important. Probably plays a role in initiation of 16S rRNA degradation (leading to ribosome degradation) during starvation. (239 aa) | ||||
| h16_A0952 | Stress-induced protein. (311 aa) | ||||
| h16_A1105 | Predicted nucleic acid-binding protein containing PIN domain. (153 aa) | ||||
| uvrB | Excinuclease ABC, helicase subunit (B); The UvrABC repair system catalyzes the recognition and processing of DNA lesions. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. Upon binding of the UvrA(2)B(2) complex to a putative 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 [...] (694 aa) | ||||
| dnaN | DNA polymerase III beta subunit; 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; Pol III exhibits 3'-5' exonuclease proofreading activity. The beta chain is required for initiation of [...] (371 aa) | ||||
| h16_A0006 | Type I restriction-modification system restriction subunit; Subunit R is required for both nuclease and ATPase activities, but not for modification. (1106 aa) | ||||
| h16_A0008 | 5-Methylcytosine-specific restriction enzyme B. (792 aa) | ||||
| h16_A0014 | Predicted restriction endonuclease. (371 aa) | ||||
| h16_A0023 | Conserved hypothetical protein. (186 aa) | ||||
| h16_A0057 | Conserved hypothetical protein. (399 aa) | ||||
| h16_A0223 | Exodeoxyribonuclease III. (258 aa) | ||||
| uvrA1 | Excinuclease ABC, ATPase subunit (A); 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. (953 aa) | ||||
| h16_A0456 | Metal-dependent hydrolase. (260 aa) | ||||
| cJ | Single-stranded-DNA-specific exonuclease RecJ. (565 aa) | ||||
| h16_A1175 | Mg-dependent DNase. (279 aa) | ||||
| h16_A1368 | Exonuclease III. (276 aa) | ||||
| h16_A1573 | Mg-dependent DNase. (264 aa) | ||||
| h16_A1593 | Lysophosphatidic acid acyltransferase LPAAT related acyltransferase. (300 aa) | ||||
| h16_A1654 | Hypothetical membrane spanning protein; 4 TMHs. (660 aa) | ||||
| h16_A1707 | Conserved hypothetical protein. (113 aa) | ||||
| h16_A2022 | Putative RNA Modifying Enzyme. (452 aa) | ||||
| rnhB | Ribonuclease HII; Endonuclease that specifically degrades the RNA of RNA-DNA hybrids; Belongs to the RNase HII family. (238 aa) | ||||
| h16_A2124 | Hypothetical protein. (61 aa) | ||||
| vacB | Exoribonuclease R; 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs. (909 aa) | ||||
| h16_A2371 | Metal-dependent hydrolase. (284 aa) | ||||
| h16_A2372 | Predicted 3'-5' exonuclease related to the exonuclease domain of PolB. (278 aa) | ||||
| h16_B2474 | Conserved hypothetical protein; Function unknown. (96 aa) | ||||
| h16_B2432 | Conserved hypothetical protein. (174 aa) | ||||
| h16_B2389 | Putative exonuclease. (220 aa) | ||||
| h16_B2374 | Conserved hypothetical protein. (60 aa) | ||||
| h16_B2352 | ATP-dependent DNA ligase. (910 aa) | ||||
| h16_B2261 | Hypothetical protein. (145 aa) | ||||
| h16_B2006 | Predicted nucleic acid-binding protein,containsPIN domain; Toxic component of a toxin-antitoxin (TA) system. An RNase. Belongs to the PINc/VapC protein family. (136 aa) | ||||
| h16_B1948 | Phosphonoacetate hydrolase. (420 aa) | ||||
| h16_B1861 | PemK-like protein DNA binding protein; Toxic component of a type II toxin-antitoxin (TA) system. (119 aa) | ||||
| uvrA2 | Excinuclease ABC, ATPase subunit (A2); 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. (1953 aa) | ||||
| elsH | Metal-dependent hydrolase. (243 aa) | ||||
| h16_B1204 | Conserved hypothetical protein. (126 aa) | ||||
| h16_B1168 | Conserved hypothetical protein. (667 aa) | ||||
| h16_B1120 | Extracellular nuclease. (600 aa) | ||||
| dnaE2 | DNA polymerase III alpha subunit; DNA polymerase involved in damage-induced mutagenesis and translesion synthesis (TLS). It is not the major replicative DNA polymerase. (1136 aa) | ||||
| cB | ATP-dependent exoDNAse (exonuclease V) beta subunit; Belongs to the helicase family. UvrD subfamily. (1200 aa) | ||||
| addB | Two domain protein: Inactivated superfamily I helicase and RecB family exonuclease. (955 aa) | ||||
| h16_A2430 | Hypothetical membrane associated protein,contains exonuclease domain. (247 aa) | ||||
| rnhA | Ribonuclease HI; Endonuclease that specifically degrades the RNA of RNA-DNA hybrids. (145 aa) | ||||
| dnaQ | DNA polymerase III epsilon subunit; DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. The epsilon subunit contain the editing function and is a proofreading 3'- 5' exonuclease. (246 aa) | ||||
| h16_A2475 | Hypothetical protein. (121 aa) | ||||
| h16_A2480 | MobA/MobL family protein. (457 aa) | ||||
| h16_A2491 | Conserved hypothetical protein. (403 aa) | ||||
| uvrC | Excinuclease ABC, nuclease subunit (C); 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. (681 aa) | ||||
| h16_A2555 | dsRNA-specific ribonuclease; 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. (256 aa) | ||||
| cafA2 | Ribonuclease G and E; Endoribonuclease that plays a central role in RNA processing and decay. Required for the maturation of 5S and 16S rRNAs and the majority of tRNAs. Also involved in the degradation of most mRNAs. Belongs to the RNase E/G family. RNase E subfamily. (1024 aa) | ||||
| h16_A2675 | Conserved hypothetical protein; Function unknown. (118 aa) | ||||