|
|
|
 |
| ecce/ outer membrane proteins/ listed by size |
---Up to 20 kDa
---20 - 30 kDa
---30 - 40kDa
---40 - 50 kDa
---50 - 60 kDa
---60 - 80 kDa
---80 - 90 kDa
---90 - 100 kDa
---Above 100 kDa
Up to 20 kDa
(b1369) ENTREZ AAC74451
| function | hypothetical outer membrane protein
| | interaction |
| | regulation |
| | MW | 5888 Da; 51 aa
|
Major outer membrane lipoprotein precursor (lpp
)
| function |
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor 3d-structure
| | MW | 8323 Da;
78 aa
|
Hypothetical 9.5 kD lipoprotein in metC-sufI intergenic region (yqhH )
| function |
| | interaction |
| | regulation |
| | | attached to the outer membrane by a lipid anchor
| | MW | 9513 Da; 85 aa
|
(b1966) ENTREZ AAC75032
| function | putative outer membrane protein
| | interaction |
| | regulation |
| | MW | 15099 Da; 134 aa
|
Outer membrane lipoprotein SlyB precursor (slyB
)>
| function |
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor
| | MW | 15602 Da; 155 aa
|
ENTREZ AAC75056 (b1995)
| function | hypothetical outer membrane protein
| | interaction |
| | regulation |
| | MW | 15653 Da; 139 aa
|
GspH
| function | PUTATIVE GENERAL SECRETION PATHWAY PROTEIN H
| | interaction |
| | regulation |
| | MW | 18565 Da; 169 aa
|
Outer membrane protein X precursor (ompX
)
| function |
| | interaction |
| | regulation |
| | | transmembrane domains: 8 (potential)
| | MW | 18603 Da; 171 aa
|
Peptidoglycan-associated lipoprotein precursor (pal
)
| function | strongly associated with the peptidoglycan
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor
| | MW | 18824 Da; 173 aa
|
Outer membrane lipoprotein Blc precursor (blc
)
| function | may serve a starvation response
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor
| | MW | 19851 Da; 177 aa
|
20 - 30 kDa
outer membrane protein Slp precursor (slp
)
| function | may help to stabilize the outer membrane during carbon starvation and stationary phase
| | interaction |
| | regulation | induced upon starvation and slowed growth, cAMP/CRP-independent
| | | attached to the membrane by a lipid anchor
| | MW | 20964 Da; 188 aa
|
yiaD
| function | putative lipoprotein IN BISC-CSPA INTERGENIC REGION
| | interaction |
| | regulation |
| | MW | 22169 Da; 219 aa
|
Hypothetical 22.9 kD Protein in tonB-trpA intergenic region precursor (yciD )
| function |
| | interaction |
| | regulation |
| | MW | 22928 Da; 212 aa
|
Flagellar L-ring protein precursor (flgH
)
| function | part of the basal body of the flagellar organelle
| | interaction |
| | regulation |
| | | attached to the outer membrane by a lipid anchor
| | MW | 24615 Da; 232 aa
|
Copper homeostasis protein CutF precursor; (LIPOPROTEIN NlpE) (cutF
)
| function | involved in copper homeostasis, could be involved in both copper efflux and the delivery of copper to copper-dependent enzymes
| | interaction |
| | cofactors |
| | regulation |
| | | attached to the outer membrane by a lipid anchor
| | MW | 25844 Da; 236 aa
|
Membrane-bound lytic murein Transglycosylase E precursor (mltE )
| function | murein-degrading enzyme, may play a role in recycling of muropeptides during cell elongation and/or cell division
| | interaction |
| | cofactors |
| | regulation |
| | MW | 26574 Da; 241 aa
|
Hypothetical 27.4 kD Protein in avtA-selB intergenic region precursor (yiaT )
| function |
| | interaction |
| | cofactors |
| | regulation |
| | MW | 27413 Da; 246 aa
|
Hypothetical 27.8 kD Protein in gapA-rnd intergenic region precursor (yeaF )
| function |
| | interaction |
| | regulation |
| | MW | 27831 Da; 248 aa
|
VacJ lipoprotein precursor (vacJ )>
| function |
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor
| | MW | attached to the membrane by a lipid anchor 28041 Da; 251 aa
|
Phosphatidylglycerophosphatase B
(pgpB
)
| function | hydrolyzes phosphatidylglycerophosphate, phosphatidic acid and lysophosphatic acid, the pattern of activities varies according to subcellular location
| | interaction |
| | cofactors |
| | regulation |
| | | integral membrane protein of the inner and the outer membrane
|
| MW | 29021 Da; 254 aa
|
nlpA
| function | putative lipoprotein
| | interaction |
| | regulation |
| | MW | 29423 Da; 272 aa
|
yaeC
| function | putative lipoprotein
| | interaction |
| | regulation |
| | MW | 29431 Da; 271 aa
|
30 - 40 kDa
ENTREZ AAC75397 (b2337)
| function | putative outer membrane protein, homologous to PapC/E. coli
| | interaction |
| | regulation |
| | MW | 31643 Da; 298 aa
|
Phospholipase A1 precursor
(pldA
)
| function | hydrolysis of phosphatidylcholine with phospholipase A2 and phospholipase A1 activities. Required for efficient secretion of bacteriocins, seems to be dormant in normal growing cells
| | interaction |
| | cofactors | requires calcium ions for activity
| | regulation | induction: by membrane damaging, e.g. phage-induced lysis or temperature shock
| | MW | 33163 Da; 289 aa
|
Nucleoside-specific channel-forming protein Tsx precursor (tsx
)
| function | substrate-specific channel for nucleosides and deoxynucleosides
| | receptor | for colicin K and bacteriophage T6
| | interaction |
| | regulation |
| | MW | 33589 Da; 294 aa
|
Outer membrane protein G precursor (ompG
)
| function |
| | receptor |
| | interaction |
| | regulation |
| | | monomer large channel
| | MW | 34913 Da;
301 aa
|
Outer membrane protease OmpP precursor
(ompP
)
| function | protease, also acts as receptor for bacteriophage Ox2
| | interaction |
| | cofactors |
| | regulation |
| | | homopentamer
| | MW | 35499 Da; 315 aa
|
Protease VII Precursor
(ompT
)
| function | cleaves T7 RNA polymerase, ferric enterobactin receptor protein and other proteins, specificity for paired basic residues
| | interaction |
| | cofactors |
| | regulation | inhibited by zinc ions
| | | homopentamer
| | MW | 35562 Da; 317 aa
|
Lipoprotein-34 precursor (nlpB
)
| function | non-essential lipoprotein
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor
| | &MW | 36842 Da; 344 aa
|
Outer membrane protein A precursor (ompA
)
| function | required for the actions of colicins K and L and for the stabilization of mating aggregates in conjugation
| | receptor | for a number of T-even like phages
| | interaction |
| | regulation |
| | | monomer 3d-structure spans the membrane 8 times
| | MW | 37201 Da; 346 aa
|
Outer membrane pore protein E precursor (phoE
)
| function | pore for efficient uptake of inorganic phosphate, phosphorylated compounds and some negatively charged solutes
| | receptor |
| | interaction |
| | regulation | induced when cells are grown under phosphate limitation
| | | homotrimer 3d-structure
spans the membrane 16 times
| | MW | 38922 Da; 351 aa
|
Outer membrane protein F precursor (ompF
)
| function | passive diffusion pore for small molecular weight hydrophilic materials
| | receptor | for bacteriophage T2
| | interaction |
| | regulation |
| | | homotrimer 3d-structure spans the membrane 16 times
| | MW | 39333 Da; 362 aa
|
40 - 50 kDa
Membrane-bound lytic murein Transglycosylase C precursor (mltC )
| function | murein-degrading enzyme, may play a role in recycling of muropeptides during cell elongation and/or cell division
| | interaction |
| | cofactors |
| | regulation |
| | | attached to the outer membrane by a lipid anchor (probable)
| | MW | 40112 Da; 359 aa
|
Membrane-bound lytic murein Transglycosylase B precursor (mltB )
| function | murein-degrading enzyme, may play a role in recycling of muropeptides during cell elongation and/or cell division
| | interaction |
| | cofactors |
| | regulation |
| | | attached to the outer membrane by a lipid anchor and exposed to the periplasmic side (probable)
| | MW | 40256 Da; 361 aa
|
Outer membrane porin protein NmpC precursor (nmpC
)
| function |
| | interaction |
| | receptor |
| | regulation |
| | | in wild-type strains of e.coli K12 the nmpC open reading frame is interrupted by an IS5 insertion and generates a hybrid open reading frame that is not expressed
however in mutant strain CS348 the IS6 element has been deleted ane nmpC is expressed
| | MW | 40316 Da; 344 aa
|
Outer membrane protein C precursor (ompC
)
| function | passive diffusion pore for small molecular weight hydrophilic materials
| | receptor | for bacteriophage ???
| | interaction |
| | regulation |
| | | homotrimer
| | MW | 40368 Da; 367 aa
|
Membrane-bound lytic murein Transglycosylase A precursor (mltA )
| function | murein-degrading enzyme, may play a role in recycling of muropeptides during cell elongation and/or cell division
| | interaction |
| | cofactors |
| | regulation | optimal activity is between pH 4.0 and 4.5, loses its activity rapidly above 30°C
| | | attached to the outer membrane by a lipid anchor (probable)
| | MW | 40410 Da; 365 aa
|
ENTREZ AAC76082 (b1377)
| function | putative outer membrane protein
| | interaction |
| | regulation |
| | MW | 41220 Da; 377 aa
|
b1505ENTREZ AAC74578
| function | putative outer membrane protein
| | interaction |
| | regulation |
| | MW | 41616 Da; 382 aa
|
Putative polysaccharide export protein YccZ precursor (yccZ
)
| function | may be involved in polysaccharide transport
| | interaction |
| | regulation |
| | MW | 41740 Da; 379 aa
|
Putative polysaccharide export protein Wza precursor (wza
)
| function | may be involved in polysaccharide transport
| | receptor |
| | interaction |
| | regulation |
| | MW | 41910 Da; 379 aa
|
Protein transport protein HofQ precursor
(hofQ
)
| function |
| | interaction |
| | cofactors |
| | regulation |
| | MW | 44716 Da; 412 aa
|
Hypothetical 46.1 kD Protein in modC-bioA intergenic region precursor (ybhC )
| function |
| | interaction |
| | regulation |
| | | attached to the membrane by a lipid anchor
| | MW | 46082 Da; 427 aa
|
Long-chain fatty acid transport protein precursor (fadL
)
| function | involved in translocation of long-chain fatty acids across the outer membrane
| | receptor | for bacteriophage T2
| | interaction |
| | regulation | induction by long-chain fatty acids, expression of fadL is under control of FadR repressor
| | MW | 48857 Da; 448 aa
|
Membrane-bound lytic murein Transglycosylase D precursor (mltD )
| function | murein-degrading enzyme, may play a role in recycling of muropeptides during cell elongation and/or cell division
| | interaction |
| | cofactors |
| | regulation | optimal activity is between pH 4.0 and 4.5, loses its activity rapidly above 30°C
| | | attached to the outer membrane by a lipid anchor (probable)
| | MW | 49417 Da; 452 aa
|
Maltoporin precursor (lamB
)
| function | involved in the transport of maltose, maltodextrines and trehalose
| | interaction |
| | receptor | for several bacteriophages including lambda and Tp1
| | regulation | MalT dependent, inducer is maltotriose
| | structure | homotrimer 3d-structure spans the membrane 18 times
| | MW | 49912 Da; 446 aa
|
50 - 60 kDa
ylcB (o457)ENTREZ AAC73673
| function | putative resistance protein
| | interaction |
| | regulation |
| | MW | 50270 Da; 457 aa
|
YjcP
| function | HYPOTHETICAL 53.4 KDA PROTEIN IN FDHF-ALSK INTERGENIC REGION; similar toPseudomonas cepacia fusaric acid resistance protein FusA
| | interaction |
| | regulation |
| | MW | 77261 Da; 700 aa
|
Outer membrane protein TolC precursor (tolC
)
| function | outer membrane component of several efflux pumps (Acr, Emr, Col, Hly). Involved in multiple drug, detergent and dye resistance. Also involved in extracellular secretion of virulence factors, toxins and colicins.
| | receptor | Phage U3
| | interaction | with efflux pumps
| | regulation |
| | structure | 3d-structure homotrimer each monomer spans the membrane 4 times has large helical periplasmic domains
| | MW | 54014 Da; 495 aa
|
60 - 80 kDa
ytfM
| function | HYPOTHETICAL 64.8 KDA PROTEIN IN MSRA-CHPBI INTERGENIC REGION
| | interaction |
| | regulation |
| | MW | 64796 Da; 577 aa
|
Vitamin B12 receptor precursor (btuB
)
| function | receptor for cobalmin and bacteriophage Bf23, necesarry for the uptake of E colicins
| | interaction |
| | receptor | for cobalmin and bacteriophage Bf23
| | regulation |
| | MW | 68407 Da; 614 aa
|
Probable general secretion pathway protein D precursor (gspD
)
| function | involved in a general secretion pathway for the export of proteins
| | interaction |
| | cofactors |
| | regulation |
| | MW | 71146 Da; 654 aa
|
Colicin I receptor precursor (cirA
)
| function | not yet known, postulated to participate in iron transport
| | interaction |
| | receptor | for colicins IA and IB
| | regulation | induction: by iron and by cAMP/cAMP-receptor protein complex
| | MW | 73895 Da; 663 aa
|
b1451ENTREZ AAC74533
| function | putative outer membrane receptor for iron transport
| | interaction |
| | regulation |
| | MW | 77261 Da; 700 aa
|
80 - 90 kDa
Outer membrane receptor for FeIII-coprogen, FeIII-ferrioxamine B and FeIII-rhodotorulic acid (fhuE
)
| function | required for the uptake of ironIII via coprogen, ferrioxamine B and rhodotorulic acid
| | interaction |
| | receptor | for ferric-rhodotorulic acid
| | regulation | for induction, the TonB and the ExbB protein have to be active
| | MW | 81232 Da; 729 aa
|
f955ENTREZ AAC73892
| function | putative outer membrane receptor for iron transport
| | interaction |
| | regulation |
| | MW | 81960 Da; 760 aa
|
Ferrienterobactin receptor precursor (fepA
)
| function | involved in the initial step in iron uptake by binding ferrienterobactin
| | interaction |
| | receptors | for colicins B and D
| | regulation |
| | | monomer 3d-structure
spans the membrane 22 times
| | MW | 82107 Da; 746 aa
|
Ferrichrome-iron receptor precursor (fhuA
)
| function | binds the ferrichrome-iron ligand
| | interaction | with TonB
binding of bacteriophage T5 triggers the opening of a high conductance ion channel
| | receptor | for bacteriophages T5, T1, PHI80 and for colicin M
| | regulation |
| | | monomer 3d-structure
spans the membrane 22 times
| | MW | 82182 Da; 747 aa
|
IronIII dicitrate transport protein FecA precursor (fecA
)
| function |
| | receptor | for ironIII dicitrate
| | interaction | for induction TonB and ExbB have to be active
| | regulation | by the iron level mediated by the Fur protein
| | MW | 85321 Da; 774 aa
|
Hypothetical outer membrane usher protein in gltF-nanT intergenic region precursor (yhcD )
| function | could be involved in the export and assembly of a fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | MW | 86289 Da; 793 aa
|
Organic Solvents Tolerance Protein precursor (ostA )
| function | determines n-hexane tolerance, involved in OM permeability
| | interaction |
| | regulation |
| | MW | 89671 Da; 784 aa |
90 - 100 kDa
Outer membrane usher protein CssD precursor (Csd2) (cssD
)
| function | involved in the export and assembly of C6 fimbrial subunits across the outer membrane
| | interaction |
| | regulation |
| | MW | 90393 Da; 802 aa
|
Unknown protein/Surface antigen D15 family (yaeT )
| function |
| | interaction |
| | regulation |
| | | | | MW | 90552; 810 aa
|
yqiG ENTREZ AAC76082
| function | putative outer membrane protein
| | interaction |
| | regulation |
| | MW | 90553 Da; 821 aa
|
Hypothetical outer membrane usher protein in nei-gltA intergenic region precursor (ybgQ )
| function | could be involved in the export and assembly of the putative YbgD fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | MW | 90443 Da; 818 aa
|
Outer membrane usher protein PapC (papC
)
| function | involved in the export and assembly of PapA fimbrial subunits across the outer membrane
appears to form a channel in the outer membrane through wich pilin subunits are transported to the surface
| | interaction |
| | regulation |
| | MW | 91076 Da; 836 aa
|
Hypothetical 91.2 kD Protein in rplY-narP intergenic region precursor (yejO )
| function |
| | interaction |
| | regulation |
| | MW | 91202 Da; 863 aa
|
Hypothetical outer membrane usher protein in ribB-glgS intergenic region precursor (yqiG )
| function | could be involved in the export and assembly of a fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | MW | 91886 Da; 821 aa
|
Hypothetical 92.2 kD Protein in phoH-csgG intergenic region precursor (ycdS
)
| function |
| | interaction |
| | regulation |
| | MW | 92207 Da; 807 aa
|
Hypothetical outer membrane usher protein in gatY-mrp intergenic region precursor (yehB )
| function | could be involved in the export and assembly of a fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | MW | 92282 Da; 826 aa
|
Outer membrane usher protein CssD precursor (Csd1) (cssD
)
| function | involved in the export and assembly of C6 fimbrial subunits across the outer membrane
| | interaction |
| | regulation |
| | MW | 92378 Da; 819 aa
|
Outer membrane usher protein FasD precursor (fasD
)
| function | involved in the export and assembly of 987P fimbrial subunits across the outer membrane
| | interaction |
| | regulation |
| | MW | 92354 Da; 835 aa
|
Hypothetical outer membrane usher protein in agaL-mtr intergenic region precursor (yraJ )
| function | could be involved in the export and assembly of the putative YraH fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | MW | 93616 Da; 838 aa
|
Hypothetical outer membrane usher protein in pepN-pyrD intergenic region precursor (ycbS )
| function | could be involved in the export and assembly of the putative YcbQ fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | MW | 95241 Da; 866 aa
|
Outer membrane usher protein HtrE precursor (htrE
)
| function | probable porin-like protein necessary for the assembly of a pilin-like protein
| | interaction |
| | regulation | induced by heat shock
| | MW | 95499 Da; 865 aa
|
Outer membrane usher protein SfmD precursor (sfmD
)
| function | involved in the export and assembly of SfmA fimbrial subunits across the outer membrane
| | interaction |
| | regulation |
| | MW | 95677 Da; 867 aa
|
Outer membrane usher protein FocD (focD
)
| function | involved in the export and assembly of F1C fimbrial subunits across the outer membrane
| | interaction |
| | regulation |
| | MW | 96210 Da; 875 aa
|
Outer membrane usher protein FimD precursor (fimD
)
| function | involved in the export and assembly of FimA fimbrial subunits across the outer membrane
| | interaction |
| | regulation |
| | MW | 96482 Da; 878 aa
|
Hypothetical outer membrane usher protein in aroC-fadL intergenic region precursor (yfcU )
| function | could be involved in the export and assembly of a fimbrial subunit across the outer membrane
| | interaction |
| | regulation |
| | | 97437 Da; 881 aa
|
f955ENTREZ AAC74286
| function | putative adhesion and penetration protein
| | interaction |
| | regulation |
| | MW | 99685 Da; 955 aa
|
Above 100 kDa
Intimin (Eae2) (eaeA
)
| function | necessary for the production of attaching and effacing lesions on tissue culture cells, believed to mediate adherence
| | interaction |
| | regulation |
| | MW | 102014 Da; 934 aa
|
Intimin (Eae1) (eaeA
)
| function | necessary for the production of attaching and effacing lesions on tissue culture cells, believed to mediate adherence
| | interaction |
| | regulation |
| | MW | 102410 Da; 939 aa
|
Antigen 43 precursor (flu )
| function | controls colony form variation and autoaggregation
| | interaction |
| | regulation |
| | | outer membrane associated BR>consists of two subunits (alpha and beta)
| | MW | 106841 Da; 1039 aa
|
Bacteriophage N4 adsorption protein A precursor (nrfA
)
| function | required for bacteriophage N4 adsorption, serves as phage receptor
| | interaction |
| | regulation |
| | MW | 111307 Da; 990 aa
|
fluENTREZ AAC75061
| function | outer membrane fluffing protein, similar to adhesin
| | interaction |
| | regulation |
| | MW | 112778 Da; 1091 aa
|
Hypothetical 98.4 kD Protein in alpA-gabD intergenic region precursor (ypjA
)
| function |
| | interaction |
| | regulation |
| | MW | 162774 Da; 1569 aa
|
|
|
|