|
|
|
 |
| ecce/ periplasmic proteins/ listed by size |
---Up to 20 kDa
---20 - 30 kDa
---30 - 40kDa
---40 - 50 kDa
---50 - 60 kDa
---60 - 70 kDa
---70 - 80 kDa
---80 - 90 kDa
---90 - 100 kDa
---Above 100 kDa
Up to 20 kDa
HokC (hokC )
| function | Toxin |
| interaction | |
| regulation | |
| MW | 55021 Da; 50 aa
|
HokD (hokD )
| function | Toxin |
| interaction | |
| regulation | |
| MW | 57371 Da; 51 aa
|
Protein YpdH precursor (ypdH )
| function | has short stretch of homology to PTS EIIB domain
| | interaction |
| | regulation |
| | MW | 11735 Da; 108 aa |
Protein HdeA precursor (hdeA )
| function |
| | interaction |
| | regulation | H-NS-dpendent
| | MW | 11858 Da; 110 aa |
c-type cytochrome biogenesis protein CycY precursor (cycY )
| function | Divalent cation tolerance |
| interaction | |
| regulation | |
| MW | 12331 Da; 112 aa
|
Protein FrwD precursor (frwD )
| function | has short stretch of homology to PTS EIIB domain
| | interaction |
| | regulation |
| | MW | 12637 Da; 113 aa |
Chaperone protein PrsD fragment precursor
(prsD
)
| function | mediates assembly of pili
| | interaction | forms soluble multimeric complexes with pili subunits
| | regulation |
| | MW | 13080 Da; 115 aa |
YobA proteinr
(yobA
)
| function | potentially mediates copper resistance by sequestration of copper
| | interaction |
| | regulation |
| | MW | 13410 Da; 124 aa |
11.9 kD protein in parC-mdaB intergenic region precursor (ygiW
)
| function |
| | interaction |
| | regulation |
| | MW | 14011 Da; 130 aa |
Soluble cytochrome b562 precursor
(cybC
)
| function | Electron-transport protein of unknown function. Its midpoint redox potential is about +180 mV.
| | interaction |
| | regulation |
| | | 3d-structure | | MW | 14061 Da; 128 aa |
Cytochrome c-type biogenesis protein NrfF precursor (nrfF )
| function | may be required for biogenesis of c-type cytochrome, possible subunit of a heme lyase | | interaction | |
| regulation | |
| MW | 14523 Da; 127 aa
|
Cytochrome c-type protein NapB precursor
(napB
)
| function | small subunit of the periplasmic nitrate reductase (NAP), may have role in anaerobic metabolism and essential for nitrate assimilation
interactions heterodimer with NapA, NapAB receives electrons from membrane anchored tetrahem NapC-protein
| | interaction | binds two heme groups per molecule
| | cofactors |
| | regulation | expressed at high levels only during aerobic growth
| | | heterodimer of catalytic subunit and a cytochrome c<
| | MW | 16296 Da; 156 aa
|
Inhibitor of vertebrate lysozyme IVY (ykfE
)
| function | inhibitor of lysozyme C
| | interaction |
| | regulation |
| | | dimer | | MW | 16872 Da; 157 aa |
Superoxide dismutase precursor (sodC )
| function | destroys radicals
Catalytic activity: 2 Peroxide radical + 2 H+ = O2 + H2O2 |
| interaction | |
| cofactors | |
| regulation | |
| | monomer
3D structure |
| MW | 17681 Da; 173 aa |
Skp
| function | chaperone for OM proteins
| | interaction |
| | regulation |
| | | homotetramer | | MW | 17688 Da; 161 aa |
Thiol peroxidase precursor (tpx )
| function | antioxidant, removing peroxides or H2O2 |
| interaction | |
| cofactors | |
| regulation | |
| MW | 17704 Da; 167 aa |
Ecotin precursor (eco
)
| function | inhibitor of a variety of proteases, strength of inhibition does not correlate with particular protease
| | interaction |
| | regulation |
| | | homodimer 3d-structure | | MW | 18192 Da; 162 aa |
Spheroplast Protein Y precursor
(spy
)
| function |
| | interaction |
| | regulation | produced in spheroplast
| | MW | 18199 Da; 161 aa
|
CpxP precursor (b3913
)
| function | inhibitor of CpxA, involved in unfolded stress response in the cell envelope
| | interaction | with CpxA
| | regulation | via CpxR
| | | homologous to spy | | MW | 18965 Da; 166 aa |
YbcL protein (ybcL )
| function | Belongs to the UPF0098 family, bacterial homologue ofo a Raf kinase inhibitor protein
| | interaction |
| | regulation |
| | MW | 19476 Da; 183 aa |
Hypothetical ABC transporter binding protein YrbD precursor (yrbD )
| function | probably part of a binding-protein-dependent transport system involved in toluene tolerance
| | interaction |
| | regulation |
| | MW | 19576 Da; 183 aa
|
20 - 30 kDa
Hypothetical 20.0 kD protein in agaI-mtr intergenic region precursor (yraP
)
| function |
| | interaction |
| | regulation |
| | MW | 20028 Da; 191 aa
|
17.3 kD protein in murA-rpoN intergenic region precursor (yhbN
)
| function |
| | interaction |
| | regulation |
| | MW | 20127 Da; 185 aa |
18.2 kD protein in cysQ-msrA intergenic region precursor (ytfJ )
| function |
| | interaction |
| | regulation |
| | MW | 20420 Da; 184 aa |
Peptidyl-prolyl cis-trans isomerase A precursor (ppiA )
| function | accelerate the folding of proteins |
| interaction | |
| cofactors | |
| regulation | inhibition by cyclosporin A |
| | 3d-structure | | MW | 20431 Da; 190 aa |
Vitamin B12 transport protein precursor
(btuE )
| function | not essential for B12 transport, but auxiliary component of the transport system
| | interaction |
| | regulation |
| | MW | 20469 Da; 183 aa |
Cytochrome c-type protein NrfB precursor
(nrfB
)
| function | terminal reductase of the formate-dependent pathway for nitrite reduction to ammonia
| | interaction | binds five heme groups per molecule
| | regulation |
| | MW | 20714 Da; 188 aa
|
PapJ protein precursor
(papJ
)
| function | maintains pilus integrity, may function as chaperone in the correct assembly of PapA subunits
| | interaction |
| | regulation |
| | MW | 20729 Da; 193 aa |
Thiol:disulfide interchange protein DsbE precursor (ccmG )
| function | disulfide bond formation, also acts as disulfide oxidoreductase in cytochrome c biogenensis |
| interaction | |
| cofactors | |
| regulation | |
| MW | 20809 Da; 185 aa
|
PrsJ protein precursor (prsJ )
| function | maintains pilus integrity, may function as chaperone in the correct assembly of PapA
| | interaction |
| | regulation |
| | MW | 20836 Da; 193 aa |
18,7 kD protein in htrB-dinI intergenic region precursor (yceI
)
| function |
| | interaction |
| | regulation |
| | MW | 20912 Da; 191 aa |
Osmotically inducable protein Y precursor
(osmY
)
| function |
| | interaction |
| | regulation | induced at high osmolariry
| | MW | 21074 Da; 201 aa |
Outer membrane lipoproteins carrier precursor
(lolA )
| function | translocates lipoproteins from IM to OM
| | interaction | forms complex with lipoprotein
| | regulation |
| | MW | 22628 Da; 204 aa |
Thiol:disulfide interchange protein DsbA precursor (dsbA )
| function | disulfide bond formation in e.g. PhoA, OmpA, pilus biogenesis |
| interaction | reoxidised by DsbB |
| cofactors | |
| regulation | |
| | 3d-structure | | MW | 23104 Da; 208 aa |
Flagella Basal Body P-Ring Formation Protein FlgA precursor
(flgA
)
| function | involved in assembly process of p-ring formation
| | interaction | probably with FlgF
| | regulation |
| | MW | 23519 Da; 219 aa
|
Acyl-CoA thioesterase I precursor (tesA )
| function | hydrolyzes only long chain (C12-C18) acyl thioesters
Catalytic activity: 2-lysophosphatidiylcholine + H2O = glycerophosphocholine + a fatty acid anion |
| interaction | |
| cofactors | |
| regulation | |
| |
monomer |
| MW |
23622 Da; 516 aa |
Hypothetical ABC transporter binding protein Yrbc precursor (yrbC )
| function | probably part of a binding-protein-dependent transport system involved in toluene tolerance
| | interaction |
| | regulation |
| | MW | 23962 Da; 211 aa
|
Chaperone protein FocC precursor
(focC
)
| function | involved in biogenesis of F1C fimbriae
| | interaction |
| | regulation |
| | MW | 25199 Da; 227 aa |
Hypothetical 25.3 kD fimbrial chaperone in gltF-nanT intergenic region precursor (yhcA
)
| function |
| | interaction |
| | regulation |
| | MW | 25339 Da; 224 aa
|
Hypothetical 25.4 kD fimbrial chaperone in pepN-pyrD intergenic region precursor (ycbR
)
| function | could be required for the biogenesis of the putative YcbQ fimbria
| | interaction |
| | regulation |
| | MW | 25388 Da; 233 aa
|
Chaperone protein SfmC precursor
(sfmC
)
| function | required for the biogenesis of SfmA Fimbriae
| | interaction | binds and interacts with SfmH
| | regulation |
| | MW | 25457 Da; 230 aa |
Thiol:disulfide interchange Protein DsbC precursor (dsbC )
| function | disulfide bond formation, also acts as disulfide isomerase |
| interaction | reoxidised by DsbD |
| cofactors | |
| regulation | |
| | homodimer | | MW | 25622 Da; 236 aa |
Hypothetical 25.7 kD fimbrial chaperone in agaI-mtr intergenic region precursor (yraI
)
| function | could be required for the biogenesis of the putative YraH fimbria
| | interaction |
| | regulation |
| | MW | 25676 Da; 231 aa
|
Class B acid phosphatase precursor (aphA )
| function | Broad spectrum dephosphorylating enzyme |
| interaction | |
| cofactors | |
| regulation | Activated by Mg2+ and ethanol; inhibited by EDTA, nucleosides, inorganic phosphate and Ca2+ |
| | homotetramer | | MW | 26103 Da; 237 aa |
Hypothetical 26.6 kD fimbrial chaperone in gatY-mrp intergenic region precursor (yehC
)
| function |
| | interaction |
| | regulation |
| | MW | 26589 Da; 239 aa
|
Hypothetical protein YggE (yggE
)
| function |
| | interaction |
| | regulation |
| | MW | 26635 Da; 246 aa
|
Chaperone protein FimC precursor (fimC )
| function | required for the biogenesis of type 1 fimbriae
| | interaction | binds and interacts with FimH
| | regulation |
| | | 3d-structure |
| MW | 26689 Da; 241 aa |
Endonuclease I (endA )
| function | Endonucleolytic cleavage to 5'-phosphodinucleotide and 5'-phosphooligonucleotides
| | interaction |
| | regulation |
| | | 3d-structure |
| MW | 26709 Da; 2351 aa |
Chaperone protein PapD precursor
(papD
)
| function | mediates assembly of P pili
| | interaction | forms soluble multimeric complexes with pili subunits
| | regulation |
| | | 3d-structure |
| MW | 26803 Da; 239 aa |
Chaperone protein CssC precursor (CSC1) (cssC )
| function | involved in the biogenesis of the CS6 fimbria
| | interaction |
| | regulation |
| | MW | 26832 Da; 232 aa |
Chaperone protein CssC precursor (CSC2)
(cssC
)
| function | involved in the biogenesis of the CS6 fimbria
| | interaction |
| | regulation |
| | MW | 26716 Da; 232 aa |
Arginine-binding protein 2 precursor
(artJ )
| function | binds arginine
| | interaction |
| | regulation |
| | MW | 26829 Da; 243 aa |
Chaperone protein Cs31 precursor (CS31)
| function | essential for biogenesis of mature cs3 pili
| | interaction |
| | regulation |
| | MW | 26908 Da; 241 aa |
Arginine-binding protein 1 precursor
(artI )
| function | binds arginine
| | interaction |
| | regulation |
| | MW | 26929 Da; 243 aa |
Hypothetical fimbrial chaperone in nei-gltA intergenic region precursor (ybgP
)
| function | could be required for the biogenesis of the putative YbgD fimbria
| | interaction |
| | regulation |
| | MW | 26954 Da; 242 aa
|
Hypothetical fimbrial chaperone in pepN-pyrD intergenic region precursor (ycbF
)
| function |
| | interaction |
| | regulation |
| | MW | 26982 Da; 245 aa
|
Chaperone protein NfaE precursor
(nfaE
)
| function | involved in the biogenensis of Nfa-I adhesin
| | interaction |
| | regulation |
| | MW | 27048 Da; 247 aa |
Chaperone protein EcpD precursor (ecpD )
| function | probably mediates assembly of a pilin
| | interaction |
| | regulation | induction by heat shock
| | MW | 27054 Da; 246 aa |
Glutamine-binding protein precursor
(glnH )
| function | involved in Gln -transport
| | interaction |
| | regulation | induction: lack of glutamin
| | | 3d-structure | | MW | 27190 Da; 248 aa |
Molybdate-binding protein precursor
(modA )
| function | binds molybdate with high specificity and affinity
| | interaction |
| | regulation |
| | MW | 27364 Da; 257 aa |
Thiol:disulfide interchange protein DsbG precursor (dsbG )
| function | involved in disulfide bond formation |
| interaction | |
| cofactors | |
| regulation | |
| MW | 27495 Da; 248 aa
|
Hypothetical fimbrial chaperone in aroC-fadL intergenic region precursor (yfcS
)
| function |
| | interaction |
| | regulation |
| | MW | 27728 Da; 250 aa
|
Lysine-arginine-ornithine-binding protein precursor
(argT)
| function |
| | interaction | ArgT and HisJ interact with HisP
| | regulation |
| | MW | 27991 Da; 260 aa |
Histidine-binding protein HBP precursor
(hisJ )
| function | component of high-affinity histidine permease
| | interaction |
| | regulation |
| | | 3d-structure | | MW | 28483 Da; 260 aa |
Hypothetical fimbrial chaperone in ribB-glgS intergenic region precursor (yqiH
)
| function |
| | interaction |
| | regulation |
| | MW | 28864 Da; 252 aa
|
FkbP-type peptidyl-prolyl cis-trans isomerase FkpA precursor (fkpA )
| function | folding of extracytoplasmic proteins |
| interaction | |
| cofactors | |
| regulation | |
| MW | 28882 Da; 270 aa
|
FliY protein precursor (fliY
)
| function | Cystin binding protein
| | interaction |
| | regulation | sulfate starvation induced
| | MW | 29039 Da; 266 aa |
Chaperone Protein ClpE precursor (clpE )
| function | involved in the biogenesis of cs31 capsule-like antigen
| | interaction |
| | regulation |
| | | immunglobulin fold | | MW | 29041 Da; 263 aa |
BtuF protein precursor (btuF
)
| function | Vitamin B12 binding protein
| | interaction |
| | regulation |
| | MW | 29367 Da; 266 aa |
Ribonuclease Iprecursor (rna )
| function | Cleaves the phosphodiester bond between any two nucleotides. Preference for cytidylic or guanylic acid. |
| interaction | two isoforms encoded by same gene |
| cofactors | |
| regulation | |
| |
four disulfide bonds | | MW | 29617 Da; 268 aa |
30 - 40 kDa
Penicillin-insensitive murein endopeptidase precursor (mepA )
| function | murein removal from the sacculus, may faciliate integration of nascent murein strands into sacculus |
| interaction | penicillin insensitive |
| cofactors | |
| regulation | |
| MW | 30136 Da; 274 aa
|
D-ribose-binding protein precursor
(rbsB )
| function | high affinity D-ribose transport, primary chemoreceptor for chemotaxis
| | interaction |
| | regulation |
| | | 3d-structure | | MW | 30950 Da; 296 aa |
Probable N-acetylmuramoyl-L-alanine amidase YbjR
(ybjR )
| function | Hydrolyzes the link between N-acetylmuramoyl residues and L-amino acid residues in certain cell-wall glycopeptides
| | interaction |
| | regulation |
| | MW | 31072 Da; 276 aa |
Maltose operon protein precursor
(malM )
| function | not yet known
| | interaction |
| | regulation | MalT-dependent
| | MW | 31943 Da; 306 aa |
Potential choline binding protein (yehz
)
| function |
| | interaction |
| | regulation |
| | MW | 32609 Da; 305 aa |
Potential YeiE protein (yeiE
)
| function | unclear, has homology to DNA binding proteins and an unusual signal sequence
| | interaction |
| | regulation |
| | MW | 32724 Da; 293 aa |
D-allose-binding protein precursor (alsB
)
| function | Part of the binding-protein-dependent transport system alsbac for D-allose
| | interaction |
| | regulation |
| | MW | 32910 Da; 311 aa
|
Ferrichrome-binding protein precursor
(fhuD )
| function | involved in high-affinity transport of ironIII -ferrichrome into the cell
| | interaction |
| | regulation |
| | MW | 32998 Da; 296 aa |
IronIII Dicitrate-binding protein precursor
(fecB )
| function | binds citrate dependent IronIII
| | interaction |
| | regulation |
| | MW | 33120 Da; 300 aa |
Hypothetical 33.3 kD Protein in ompX-moeB intergenic region precursor (ybiS
)
| function |
| | interaction |
| | regulation |
| | MW | 33325 Da; 306 aa
|
Putative L-asparaginase AsgX (ybiK
)
| function | L-asparagine + H 2O = L-aspartate + NH 3
| | interaction |
| | regulation |
| | MW | 33394 Da; 321 aa
|
Glutamate/aspartate periplasmic binding protein (gltI
)
| function | Part of the binding-protein-dependent transport system for glutamate and aspartate. Binds to both aspartate and glutamate
| | interaction |
| | regulation |
| | MW | 33420 Da; 302 aa |
Amino-acid ABC transporter binding protein in acrF-rrnD intergenic region precursor (yhdW
)
| function | probably part of a binding-protein-dependent aa transport system
| | interaction |
| | regulation |
| | MW | 33425 Da; 305 aa
|
High-affinity zinc binding protein ZnuA (znuA )
| function |
| | interaction |
| | regulation |
| | MW | 33777 Da; 310 aa |
Penicillin-binding protein7 precursor (pbpG )
| function | cell wall formation |
| interaction | penicillin sensitieve |
| cofactors | |
| regulation | |
| MW | 34245 Da; 313 aa
|
Taurine-binding protein precursor
(tauA )
| function |
| | interaction |
| | regulation | sulfate starvation induced
| | MW | 34266 Da; 320 aa |
Ferrienterobactin-binding protein precursor
(fepB )
| function | binds ferrienterobactin
| | interaction |
| | regulation | induction in part controlled by the amount of available iron | | MW | 34283 Da; 318 aa |
32.1 kD protein in ppa-fbp intergenic region precursor (ytfQ )
| function | potential monosaccharide transporter
| | interaction |
| | regulation |
| | MW | 34344 Da; 318 aa |
Protein ErfK precursor
(erfK
)
| function |
| | interaction |
| | regulation |
| | MW | 34411 Da; 310 aa |
Sulfonate-binding protein precursor SsuA
(ssuA )
| function | specifically binds aliphatic sulfonates, involved in transport
| | interaction |
| | regulation | sulfate starvation induced
| | MW | 34557 Da; 319 aa |
Hypothetical 34.6 kD protein in nhd-mfd intergenic region precursor (ycfS
)
| function |
| | interaction |
| | regulation |
| | MW | 34636 Da; 320 aa
|
Hypothetical periplasmic protein YahB (yahB
)
| function | unclear, has homology to DNA binding proteins
| | interaction |
| | regulation |
| | MW | 34866 Da; 310 aa
|
Hypothetical ABC transporter binding protein YphF precursor (yphF )
| function | probably part of a binding-protein-dependent transport system YphDEF potentially transporting a monosaccharide
| | interaction |
| | regulation |
| | MW | 35058 Da; 327 aa
|
FecR protein precursor (fecR )
| function | regulates iron dicitrat transport via FecI, sensory transduction
| | interaction | inactivates FecI in absence of citrate
| | regulation |
| | MW | 35532 Da; 317 aa |
L-Arabinose-binding protein precursor
(araF )
| function | high affinity to arabinose, can also bind D-galactose and D-fucose
| | interaction |
| | regulation |
| | | 3d-structure | | MW | 35541 Da; 329 aa |
D-galactose-binding protein precursor
(mglB )
| function | involved in the active transport of D-galactose and D-glucose role in chemotaxis
| | interaction | with Trg chemoreceptor
| | regulation |
| | | calcium-binding site 3d-structure | | MW | 35712 Da; 332 aa |
D-xylose-binding protein precursor
(xylF )
| function | binds xylose with high affinity
| | interaction | energized by high-energy phosphate compounds
| | regulation | sensitiv to cold osmotic shock
| | MW | 35734 Da; 330 aa |
Sigma E factor regulatory protein RseB precursor
(rseB
)
| function | seems to modulate the activity of RpoE
| | interaction |
| | regulation |
| | MW | 35749 Da; 318 aa |
Hypothetical 36.0 kD protein in avtA-selB intergenic region precursor (yiaO
)
| function |
| | interaction |
| | regulation |
| | MW | 35970 Da; 328 aa
|
Hydrogenase-2 operon protein HybA (hybA )
| function | periplasmic electron-transferring activity of hydrogenase 2
| | interaction | HybBO
| | cofactors | Binds 4 4Fe-4S clusters
| | regulation |
| | MW | 36003 Da; 328 aa |
Glycine betaine-binding protein precursor
(proX )
| function | member of multicomponent binding-protein-dependent transport system
| | interaction |
| | regulation |
| | MW | 36022 Da; 330 aa |
Hypothetical 36.1 kD protein in llp-aroD intergenic region precursor (ynhG
)
| function |
| | interaction |
| | regulation |
| | MW | 36082 Da; 334 aa
|
Thiamine-binding protein precursor
(sfuA )
| function |
| | interaction |
| | regulation |
| | MW | 36163 Da; 327 aa |
Hypothetical protein YneA
(yneA )
| function |
| | interaction |
| | regulation |
| | MW | 36685 Da; 340 aa |
Sulfate-binding protein precursor
(sbp )
| function | specifically binds sulfate, involved in transport
| | interaction |
| | regulation | sulfate starvation induced
| | MW | 36689 Da; 329 aa |
L-asparaginase II precursor (ansB )
| function | aspartate synthesis
Catalytic activity: L-asparagine + H2O = L-aspartate + NH3 |
| interaction | |
| cofactors | |
| regulation | induction by cAMP and anaerobiosis |
| | homotetramer 3d-structure | | MW | 36850 Da, 348 aa |
Potential binding protein for amino acids (yhdW
)
| function | Putative amino-acid binding protein
| | interaction |
| | regulation |
| | MW | 37020 Da; 341 aa |
Phosphate-binding protein precursor
(pstS )
| function | BP mediated phosphate transport
| | interaction |
| | regulation | induction by phosphate deprivation, subject to positive control by PhoB and negative control by PhoR
| | | 3d-structure | | MW | 37024 Da; 346 aa |
Phosphonates-binding protein precursor
(phnD )
| function | alkylophosphonates binding protein
| | interaction |
| | regulation |
| | MW | 37370 Da; 338 aa |
Thiosulfate-binding protein precursor
(cysP )
| function | binding and transmembrane transport
| | interaction |
| | regulation |
| | MW | 37614 Da; 338 aa |
Protein TorT (torT
)
| function | role in torCAD operon induction
| | interaction | binds putative inducer, interacts with TorS
| | regulation |
| | MW | 37864 Da; 342 aa |
Flagella P-Ring Protein precursor
(flgI
)
| function | part of basal body
| | interaction |
| | regulation |
| | MW | 38169 Da; 365 aa
|
Mutarotase
(galM
)
| function | Aldose 1-epimerase, converts alpha-aldose to the beta-anomer. Acts on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose.
| | interaction |
| | regulation |
| | MW | 38190 Da; 346 aa
|
Spermidine/putrescine-binding protein precursor SPBP
(potD )
| function | polyamine-binding protein | | interaction |
| | regulation |
| | | 3d-structure | | MW | 38867 Da; 348 aa |
Leu/Ile/Val-binding protein LIV-BP precursor
(livJ )
| function | component of leucine, isoleucine, valine (threonine) transport
| | interaction |
| | regulation |
| | | 3d-structure |
| MW | 39076 Da; 367 aa |
Cytochrome c-type biogenesis protein CcmH precursor (ccmH )
| function | may be required in biogenesis of c-type cytochrome, possible subunit of heme lyase |
| interaction | |
| regulation | |
| | 39089 Da; 350 aa
|
Leucine-specific binding protein precursor
(livK )
| function | component of the leucine-specific transport system
| | interaction |
| | regulation |
| | | 3d-structure |
| MW | 39306 Da; 369 aa |
Hydrogenase-2 small chain HybO (hybO )
| function | NiFe hydrogenase Membrane-bound hydrogenase 2 small subunit
| | interaction | HybAC
| | cofactors | Binds two 4Fe-4S clusters and one 3Fe-4S cluster
| | regulation |
| | MW | 39652 Da; 372 aa |
40 - 50 kDa
Putrescine-binding protein precursor
(potF )
| function | polyamine-binding protein | | interaction |
| | regulation |
| | MW | 40839 Da; 370 aa |
Glycerophosphoryl diester posphodiesterase precursor (glpQ )
| function | multigene fam., hydrolyzes deacylated phospholiopids
Catalytic activity: a glycerophosphodiester + H2O = an alcohol + sn-glycerol 3-phosphate | | interaction | |
| cofactors | |
| regulation | |
| MW | 40843 Da; 358 aa
|
Penicillin acylase precursor (ampC )
| function | penicillin resistance Catalytic activity:
beta-lactam + H2O = a substituted beta-amino acid the N4-C7 bond of the lactam ring is cleaved |
| interaction | |
| cofactors | |
| regulation | |
| | monomer 3d-structure |
| MW | 41555 Da; 377 aa |
Penicillin-binding protein AmpH (ampH )
| function | Binds penicillin & belongs to the beta-lactamase family |
| interaction | |
| cofactors | |
| regulation | |
MW | 41849 Da; 385 aa |
Potential polyamine binding protein (ydcS
)
| function |
| | interaction |
| | regulation |
| | MW | 42295 Da; 381 aa |
Potential binding protein (ynjB
)
| function |
| | interaction |
| | regulation |
| | MW | 42844 Da; 388 aa |
Maltose-binding protein MBP precursor
(malE )
| function | binds maltoligosaccharides, involved inhigh affinity maltose-transport system, chemotaxis
| | interaction | with MalF and MalG
| | regulation |
| | | 3d-structure | | MW | 43387 Da; 396 aa |
Penicillin-binding protein 6 precursor (dacC )
| function | D-alanine carboxypeptidase Removes C-terminal d-ala residues from sugar-peptide cell wall precursors
Belongs to Ser protease family S11
|
| interaction | |
| cofactors | |
| regulation | |
| MW | 43609 Da; 400 aa
|
Penicillin-binding protein5 precursor (dacA )
| function | D-alanine carboxypeptidase Removes C-terminal d-ala residues from sugar-peptide cell wall precursors
Belongs to Ser protease family S11
|
| interaction | |
| cofactors | |
| regulation | |
| MW | 44444 Da; 403 aa
|
Glucose-1-phosphatase precursor (agp )
| function | required for growth in high phosphate with G-1-P as sole carbon source
Catalytic activity: D-glucose 1-phosphate + H2O = D-GLUCOSE + orthophosphate |
| interaction | |
| cofactors | |
| regulation | independent from inorganic phosphate availability, catabolite repression, positively by cAMP/CRP, |
| | homodimer |
| MW | 45683 Da; 413 aa |
TolB protein precursor (tolB )
| function | involved in the TonB-independent uptake of a group of colicins
| | interaction |
| | regulation |
| | | 3d-structure | | MW | 45955 Da; 430 aa |
Potential binding protein (ycjN
)
| function |
| | interaction |
| | regulation |
| | MW | 46808 Da; 430 aa |
pH 2.5 acid phosphatase precursor (appA )
| function | Catalytic activity: an orthophosphoric monoester + H2O = an alcohol + orthophosphate |
| interaction | |
| cofactors | |
| regulation | cAMP regulated, induced when reaching stationary phase, synthesis triggered by phosphate starvation or shift from aerobic to anaerobic condit. |
| | monomer | | MW | 47056 Da; 432 aa |
Protease DegQ precursor (hhoA )
| function | shared specificity with HtrA/DegP |
| interaction | |
| cofactors | |
| regulation | | |
| MW | 47205 Da; 455 aa
|
Survival protein SurA precursor (surA )
| function | folding of extracytoplasmic proteins, essential in stationary phase |
| interaction | |
| cofactors | |
| regulation | |
| MW | 47283 Da; 428 aa
|
Putative beta-lactamase YfeW (yfeW )
| function | |
| interaction | |
| cofactors | |
| regulation | |
| MW | 47752 Da; 434 aa
|
Glycerol-3-phosphate-binding protein precursor (ugpB )
| function | sn-glycerol-3-phosphate and glycerophosphoryl diester-binding
| | interaction | UgpACE
| | regulation |
| | MW | 48452 Da; 438 aa |
Alkaline phosphatase precursor (phoA )
| function | Broad spectrum dephosphorylating enzyme |
| interaction | |
| cofactors | metalloenzyme containing two zinc atoms and a magnesium ion |
| regulation | |
| | three isoforms 3d-structure Extensively used as a reporter enzyme and in gene fusion experiments | | MW | 49438 Da; 471 aa
|
Protease DegP (Do) precursor (htrA )
| function | required at high temp., degradation of damaged prot., chaperone activity at low temperature, shared specificity with DegQ |
| interaction | |
| cofactors | |
| regulation | induction by heat shock |
| | multimeric; 2 PDZ domains | | MW | 49439 Da; 474 aa |
50 - 60 kDa
Penicillin-Binding Protein 4 precursor (dacB )
| function | final stages in peptidoglycan synthesis |
| interaction | penicillin sensitive |
| cofactors | |
| regulation | |
| MW | 51798 Da; 477 aa
|
SufI Protein precursor
(sufI
)
| function | involved in cell division, supresses a ftsI mutation
| | interaction |
| | regulation |
| | MW | 51858 Da; 470 aa
|
Cytochrome c552precursor
(nrfA
)
| function | terminal reductase of the formate-dependent pathway for nitrite reduction to ammonia
interactions
| | interaction | binds five heme groups per molecule
| | regulation | induction in presence of nitrite, subject to glucose and nitrate repression
| | MW | 53703 Da; 478 aa
|
55.5 kD protein in kdgK-dctA intergenic region precursor (yhjJ )
| function | metalloprotease |
| interaction | |
| cofactors | binds zinc? |
| regulation | |
| | has lost the active site residues |
| MW | 55527 Da; 498 aa |
Putative binding protein YliB (yliB )
| function | Probably part of the binding-protein-dependent transport system yliABCD | | interaction | |
| cofactors | |
| regulation | |
| MW | 56470 Da; 512 aa |
Probable 53.4 kD blue copper protein precursor YacQ (yacK )
| function | Multicopper oxidase | | interaction | |
| cofactors | |
| regulation | |
| | homodimer |
| MW | 56556 Da; 516 aa |
Potential binding protein (yddS
)
| function |
| | interaction |
| | regulation |
| | MW | 57641 Da; 516 aa |
Glucans Biosynthesis Protein MdoG precursor
(mdoG
)
| function | involved in MDO synthesis
| | interaction |
| | regulation |
| | MW | 57912 Da; 511 aa
|
Nickel-binding protein precursor
(nikA )
| function | probably binds nickel
| | interaction |
| | regulation |
| | MW | 58719 Da; 524 aa |
Murein peptide-binding protein precursor
(mppA )
| function | binds L-alanyl-gamma-d-glutamyl-meso-diaminopimelate with high affinity
| | interaction |
| | regulation |
| | MW | 59900 Da; 537 aa |
60 - 70 kDa
Dipeptide transport protein precursor
(dppA)
| function | dipeptide-binding, required for chemotaxis
| | interaction |
| | regulation | osmotic shockable transport system
| | | 3d-structure | | MW | 60293 Da; 535 aa |
Polysialic acid transport protein KpsD precursor (KSD5)
(kpsD )
| function | involved in translocation of PSA across OM, binds polysaccharide
| | interaction |
| | regulation |
| | MW | 60484 Da; 558 aa |
Potential binding protein (ygiS
)
| function |
| | interaction |
| | regulation |
| | MW | 60694 Da; 535 aa |
UDP-sugar hydrolase precursor (ushA )
| function | multifunctional: hydrolase, 5'-Nucleotidase
Catalytic activity 1: UDP-sugar + H(2)O = UMP + sugar 1-phosphate.
Catalytic activity 2: A 5'-ribonucleotide + H(2)O = A ribonucleoside + orthophosphate
|
| interaction | |
| cofactors | Binds two Zn2+; Co2+ for Nucleotidase |
| regulation | inhibition by an intracellular protein inhibitor |
| MW | 60824 Da; 550 aa
|
Oligopeptide-binding protein precursor
(oppA )
| function | component of the oligopeptide permease, binds oligopeptides up to five amino acids with high affinity
| | interaction |
| | regulation |
| | MW | 60899 Da; 543 aa |
Glucans biosynthesis protein D (mdoD
)
| function | Probably involved in the control of the structural glucose backbone of MDOs, MdoG homologue
| | interaction |
| | regulation |
| | MW | 62758 Da; 551 aa |
Peptide transport protein SapA precursor
(sapA )
| function | involved in peptide intake transport system that plays a role in resistance to antimicrobial peptides
| | interaction |
| | regulation |
| | MW | 61564 Da; 547 aa |
Aminoacyltransferase precursor (ggt )
| function | role in glutathion degradation & synthesis,(g-Glutamyl cycle)
Catalytic activity: (5-L-glutamyl)-peptide + an amino acid = peptide + 5-L-glutamyl-amino acid |
| interaction | |
| cofactors | |
| regulation | |
| | consists of two polypeptide chains, which are synthesised from a single polypeptide |
| MW | 61768 Da, 580 aa |
Hydrogenase-2 large chain (hybC )
| function | NiFe hydrogenase, H2 + A = AH 2
|
| interaction | Heterodimer of a large and a small subunit |
| cofactors | Binds 1 nickel ion per subunit |
| regulation | |
| MW | 62360 Da; 566 aa
|
Putative sulfatase YdeN (ydeN )
| function | belongs to the sulfatase family |
| interaction | |
| cofactors | |
| regulation | |
| MW | 62802 Da; 560 aa
|
Trehalase precursor (treA )
| function | hydrolyses alpha- 1,1 glycosidic bond in trehalose |
| interaction | |
| cofactors | |
| regulation | slightly induced by high osmolarity and stationary phase |
| MW | 63636 Da; 565 aa
|
NiFe hydrogenase subunit (hyaB )
| function | Membrane-bound hydrogenase 1 large subunit, catalytic activity: H 2+ A = AH 2
|
| interaction | |
| cofactors | |
| | might be cotranslocated with HyaA which has a proper TAT signal sequence |
| MW | 66253 Da; 579 aa
|
AsmA Protein precursor
(asmA
)
| function | involved in inhibitionof assembly of mutant OmpF proteins, could be involved in OM protein assembly
| | interaction |
| | regulation |
| | MW | 68962 Da; 617 aa
|
Potential binding protein (yejA
)
| function |
| | interaction |
| | regulation |
| | MW | 69669 Da; 604 aa |
60 - 70 kDa
2',3'-Cyclic-nucleotide 2'-phosphodiesterase precursor (cpdB )
| function | bifunctional, catalyzes two consecutive reactions converting 2',3'-cyclic-nucleotide to 3'-nucleotide and then 3'-nucleotide to nucleic acid and phosphate |
| interaction | |
| cofactors | |
| regulation | |
| |
two distinguishable active sites |
| MW | 70832 Da; 647 aa |
Lytic murein transglycosylase precursor (slt )
| function | Murein-degrading, may play role in recaycling muropeptides during cell elongation and/or cell division | | interaction | energy conserving reaction |
| cofactors | |
| regulation | |
| | tightly associated with murein sacculus 3d-structure | | MW | 73369 Da; 645 aa |
Biosynthetic arginine decarboxylase precursor (ADC) (speA )
| function | biosynthetic and biodegradative form, first step in the spermidine synthesis from arginine, the biodegradive form may ply a role in regulating pH by consuming proteins |
| interaction | |
| cofactors | pyridoxal phosphate and Mg2+ |
| regulation | induction: growth in acidic enriched medium containing arginine (biodegr.), growth in MMA at neitral pH (biosynth.), repression of speA and feedback inhibition of ADC by putrescine and spermidine, |
| | homotetramer | | MW | 73983 Da; 658 aa |
Alpha-amylase precursor (malS )
| function | Alpha-amylase; degradation of maltooligosaccharides with a preference for chain length longer than 6 glucose units |
| interaction | |
| cofactors | |
| regulation | MalT (maltose regulon) |
| | monomer 2 disulfide bonds | | MW | 75712 Da; 676 aa |
Tail specific protease precursor (prc )
| function | selectively degrades proteins with nonpolar C- terminus (that arises for example from the action of 10sRNA), PBP3 maturation |
| interaction | |
| cofactors | |
| regulation | |
| MW | 76663 Da; 682 aa
|
80 - 90 kDa
Beta-glucosidase precursor (bglX )
| function | hydrolysis of terminal non-reducing beta-D glucose residues |
| interaction | |
| cofactors | |
| regulation | |
| MW | 83460 Da; 765 aa |
Copper amine oxidase precursor (maoA )
| function | initial steps of 2-phenylethylamine catabolism
Catalytic activity: 2-Phenylethylamine + H2O + O2 =
Phenylacetaldehyde + NH3 + H2O2
|
| interaction | |
| cofactors | copper and topaquinon |
| regulation | |
| | homodimer 3D-structure |
| MW | 84378 Da; 757 aa |
Hypothetical protein YgjK (ygjK )
| function | |
| interaction | |
| cofactors | |
| regulation | |
| MW | 88321 Da; 783 aa |
Putative dimethyl sulfoxide reductase chain YnfE (ynfE )
| function | DMSO reductase |
| interaction | with YfnF and YfnG |
| cofactors | Molybdenum (molybdopterin); may bind a 4Fe-4S cluster |
| regulation | |
| MW | 89780 Da; 808 aa |
Putative dimethyl sulfoxide reductase chain YnfF (ynfF )
| function | DMSO reductase |
| interaction | with YfnE and YfnG |
| cofactors | Molybdenum (molybdopterin); may bind a 4Fe-4S cluster |
| regulation | |
| MW | 89987 Da; 807 aa |
90 - 100 kDa
Nitrate reductase precursor (napA )
| function | a role in anaerobic growth with limiting concentrations of nitrate, large subunit of the periplasmic nitrate reductase (NAP)
Catalytic activity:
nitrite + acceptor = nitrate + reduced acceptor |
| interaction | |
| cofactors | molybdopterin guanine dinucleotide (MGD) |
| regulation | expressed during anaerobic growth (via FNR), further induction by low concentrations of nitrate (via NarP) |
| MW | 93042 Da; 828 aa |
Trimethylamine-N-oxide reductase precursor (torA )
| function | reduces trimethylamine-n-oxide into trimethylamine, an anaerobic reaction coupled to energy yielding reaction
Catalytic activity: NADH + Trimethylamine-N-Oxide = NAD+ +
Trimethylamine + H2O |
| interaction | |
| cofactors | |
| regulation | |
| | contains molybdopterin |
| MW | 94456 Da; 848 aa |
Penicillin acylase precursor (pac )
| function | penicillin resistance Catalytic activity:
penicillin + H2O = a fatty acid anion + 6-aminopenicillanate |
| interaction | |
| cofactors | |
| regulation | |
| | heterodimer 3d-structure |
| MW | 94642 Da; 846 aa |
Probable bifunctional chitinase/lysozyme precursor (chiA )
| function | hydrolysis of [[beta]]-1,4 glucosidic linkages between N-acetylmuramic acid and
N-acetylglucosamine and/or chitin degradation | | interaction | | | cofactors | |
| regulation | | | MW | 97057 Da; 897 aa |
Above 100 kDa
ProteaseIII precursor (ptr )
| function | May prefer small substrates |
| interaction | |
| cofactors | requires divalent cations, binds Zn2+ |
| regulation | |
| | monomer | | MW | 107708 Da; 962 aa |
Formate dehydrogenase alpha subunit FdnG (fdnG )
| function | |
| interaction | |
| cofactors | 1 molybdenum ion, 2 molybdopterin guanine dinucleotide (MGD) groups, 1 4Fe-4S cluster, and 1 selenocysteine per subunit |
| regulation | |
| MW | 112916 Da; 1015 aa |
|
|
|