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pilN | Type IV pilus assembly protein PilN. (197 aa) | ||||
clpB | ATP-dependent Clp protease ATP-binding subunit ClpB; 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; Belongs to the ClpA/ClpB family. (858 aa) | ||||
secG | Preprotein translocase subunit SecG; Involved in protein export. Participates in an early event of protein translocation; Belongs to the SecG family. (109 aa) | ||||
RNAN_3194 | SEC-C motif domain protein. (158 aa) | ||||
ftsB | Cell division protein FtsB; 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. (99 aa) | ||||
exeC | General secretion pathway protein C. (317 aa) | ||||
epsD-2 | General secretion pathway protein D. (706 aa) | ||||
epsE-2 | General secretion pathway protein E; Involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins. (502 aa) | ||||
exeF | General secretion pathway protein F. (407 aa) | ||||
outG | General secretion pathway protein G. (150 aa) | ||||
xcpU | General secretion pathway protein H. (197 aa) | ||||
gspI | General secretion pathway protein I. (122 aa) | ||||
epsJ | General secretion pathway protein J. (207 aa) | ||||
exeK | General secretion pathway protein K. (331 aa) | ||||
exeL | General secretion pathway protein L; Involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins. (395 aa) | ||||
exeM | General secretion pathway protein M; Involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins. (156 aa) | ||||
RNAN_2895 | HlyD family secretion protein. (411 aa) | ||||
tatA | Sec-independent protein translocase protein tatA/E homolog; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system. (91 aa) | ||||
tatB | Sec-independent protein translocase protein tatB homolog. (111 aa) | ||||
tatC | Sec-independent protein translocase protein TatC; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides. (258 aa) | ||||
RNAN_2646 | Toxin secretion, membrane fusion protein. (416 aa) | ||||
traN | Conjugal transfer mating pair stabilization protein TraN. (929 aa) | ||||
oxaA | Inner membrane protein oxaA; Required for the insertion and/or proper folding and/or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins. Aids folding of multispanning membrane proteins. (545 aa) | ||||
slt | Soluble lytic murein transglycosylase. (631 aa) | ||||
RNAN_2489 | Rhs element Vgr protein. (595 aa) | ||||
RNAN_2034 | Type VI secretion system Vgr family protein. (604 aa) | ||||
RNAN_2033 | Hypothetical protein. (159 aa) | ||||
clpV1 | Protein ClpV1; Belongs to the ClpA/ClpB family. (866 aa) | ||||
RNAN_2023 | Protein phosphatase. (256 aa) | ||||
RNAN_2021 | Type VI secretion system protein ImpL. (1182 aa) | ||||
RNAN_2020 | Type VI secretion system protein ImpK. (436 aa) | ||||
RNAN_2018 | Type VI secretion system protein VasD. (160 aa) | ||||
RNAN_2017 | Type VI secretion system protein. (444 aa) | ||||
RNAN_2016 | Serine/threonine protein kinase, bacterial. (669 aa) | ||||
tolC | Outer membrane channel protein TolC. (451 aa) | ||||
lptC | Hypothetical protein; Involved in the assembly of lipopolysaccharide (LPS). Required for the translocation of LPS from the inner membrane to the outer membrane. Facilitates the transfer of LPS from the inner membrane to the periplasmic protein LptA. Could be a docking site for LptA. (184 aa) | ||||
hlyD | Hemolysin secretion protein D, chromosomal. (467 aa) | ||||
RNAN_1422 | Hypothetical protein. (482 aa) | ||||
RNAN_1417 | Hypothetical protein. (567 aa) | ||||
RNAN_1301 | Hypothetical protein. (303 aa) | ||||
RNAN_1300 | Hypothetical protein. (198 aa) | ||||
RNAN_1299 | Hypothetical protein. (216 aa) | ||||
RNAN_1297 | MSHA biogenesis protein MshL. (553 aa) | ||||
epsE | General secretion pathway protein E. (574 aa) | ||||
pilC | Type IV pilus assembly protein PilC. (409 aa) | ||||
RNAN_1292 | Hypothetical protein. (176 aa) | ||||
RNAN_1291 | Type II secretory pathway, pseudopilin. (170 aa) | ||||
RNAN_1290 | MSHA pilin protein MshC. (148 aa) | ||||
RNAN_1289 | Pilin protein. (182 aa) | ||||
RNAN_1288 | Tfp-like pilus assembly protein. (253 aa) | ||||
RNAN_1069 | Lytic transglycosylase. (229 aa) | ||||
secD-2 | Preprotein translocase subunit SecD; Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. (615 aa) | ||||
secF-2 | Preprotein translocase subunit SecF; Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. (312 aa) | ||||
RNAN_0938 | Protein serine/threonine phosphatase. (578 aa) | ||||
RNAN_0842 | Type IV pilus biogenesis protein, putative. (168 aa) | ||||
RNAN_0838 | Hypothetical protein. (316 aa) | ||||
RNAN_0837 | Hypothetical protein. (163 aa) | ||||
RNAN_0833 | Hypothetical protein. (328 aa) | ||||
RNAN_0832 | Pre-pilin leader sequence. (144 aa) | ||||
RNAN_0831 | Pre-pilin like leader sequence. (181 aa) | ||||
secA | Preprotein translocase subunit SecA; 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 both as a receptor for the preprotein-SecB complex and as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane. Belongs to the SecA family. (905 aa) | ||||
clpA | ATP-dependent Clp protease ATP-binding subunit ClpA; Belongs to the ClpA/ClpB family. (755 aa) | ||||
secB | Preprotein translocase subunit SecB; One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA. (162 aa) | ||||
pilQ | Type IV pilus assembly protein PilQ. (688 aa) | ||||
pilM | Type IV pilus assembly protein PilM. (359 aa) | ||||
ftsY | Fused signal recognition particle receptor; 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). Interaction with SRP-RNC leads to the transfer of the RNC complex to the Sec translocase for insertion into the membrane, the hydrolysis of GTP by both Ffh and FtsY, and the dissociation of the SRP-FtsY complex into the individual components. (396 aa) | ||||
tapB | Type IV pilus assembly protein tapB. (565 aa) | ||||
tapC | Type IV pilus assembly protein tapC. (410 aa) | ||||
tapD | Type 4 prepilin-like proteins leader peptide-processing enzyme; Cleaves type-4 fimbrial leader sequence and methylates the N- terminal (generally Phe) residue. (292 aa) | ||||
secF | Preprotein translocase subunit SecF; Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. (315 aa) | ||||
secD | Preprotein translocase subunit SecD; Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. (617 aa) | ||||
yajC | Preprotein translocase subunit YajC; The SecYEG-SecDF-YajC-YidC holo-translocon (HTL) protein secretase/insertase is a supercomplex required for protein secretion, insertion of proteins into membranes, and assembly of membrane protein complexes. While the SecYEG complex is essential for assembly of a number of proteins and complexes, the SecDF-YajC-YidC subcomplex facilitates these functions. (113 aa) | ||||
secE | Preprotein translocase subunit SecE; Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation; Belongs to the SecE/SEC61-gamma family. (124 aa) | ||||
secY | Preprotein translocase subunit SecY; 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. (442 aa) | ||||
ffh | Signal recognition particle subunit SRP54; 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. Interaction with FtsY leads to the transfer of the RNC complex to the Sec translocase for insertion into the membrane, the hydrolysis of GTP by both Ffh and FtsY, and the dissociation of the SRP-FtsY complex into the individual co [...] (455 aa) |