Disulfide Bond Formation
Oxidoreductases
Acting on hydrogen as donors
Hydrogenase-2 operon protein HybA (hybA )
| function | periplasmic electron-transferring activity of hydrogenase 2
|
| interaction | HybCO
|
| cofactors | Binds 4 4Fe-4S clusters
|
| regulation |
|
| MW | 36003 Da; 328 aa |
Hydrogenase-2 large chain (hybC )
| function | NiFe hydrogenase, H2 + A = AH 2
|
| interaction | HybAO |
| cofactors | Binds 1 nickel ion per subunit |
| regulation | |
| MW | 62360 Da; 566 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 |
Acting on the CH-NH2 Group of Donors With Oxygen as Acceptor
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 | |
| structure | dimer
PDB |
| MW | 84378 Da; 757 aa |
Oxidoreductase Acting on NADH or NADPH with a Nitrogenous Group as Acceptor
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 | molybdopterin |
| regulation | |
| structure | |
| MW | 94456 Da; 848 aa |
Oxidoreductase Acting on Other Nitrogenous Compounds
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 |
Oxidoreductase Acting on acting on various sulfoxide and N-oxide compounds
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 |
Oxidoreductase Acting on a Peroxide as Acceptor
Thiol peroxidase precursor (tpx )
| function | antioxidant, removing peroxides or H2O2 |
| interaction | |
| cofactors | |
| regulation | |
| MW | 17704 Da; 167 aa |
Oxidoreductase Acting on Superoxide Radicals as Acceptor
Superoxide dismutase precursor (sodC )
| function | destroys radicals
Catalytic activity: 2 Peroxide radical + 2 H+ = O2 + H2O2 |
| interaction | |
| cofactors | |
| regulation | |
| structure | monomer
PDB |
| MW | 17681 Da; 173 aa |
Multicopper Oxidase
Probable 53.4 kD blue copper oxidase precursor CueO (yacK )
| function | Multicopper oxidase |
| interaction | |
| cofactors | 3 Cu |
| regulation | via CueR at elevated leveles of Cu |
| structure | dimer
PDB |
| MW | 56556 Da; 516 aa |
Transferases
Aminoacyltransferase
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 |
Hydrolases
Acting on Ester Bonds:
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 |
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 | |
| structure | monomer
PDB |
| MW | 70832 Da; 647 aa |
Endonuclease I (endA )
| function | Endonucleolytic cleavage to 5'-phosphodinucleotide and 5'-phosphooligonucleotides
|
| interaction |
|
| regulation |
|
| | 3d-structure |
| MW | 26709 Da; 2351 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 | GlpT, glycerol-3-phosphate inducible |
| MW | 40843 Da; 358 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 |
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 |
| structure | monomer
PDB |
| MW | 60824 Da; 550 aa
|
Phosphatases
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
PDB |
| MW | 47056 Da; 432 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, |
| | dimer
PDB |
| MW | 45683 Da; 413 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 |
Alkaline phosphatase precursor (phoA )
| function | Broad spectrum dephosphorylating enzyme
Extensively used as a reporter enzyme and in gene fusion experiments |
| interaction | |
| cofactors | metalloenzyme containing two zinc atoms and a magnesium ion |
| regulation | induced by low phosphate |
| structure | three isoforms dimer
PDB |
| MW | 49438 Da; 471 aa
|
Sulfatases
Putative sulfatase YdeN (ydeN )
| function | belongs to the sulfatase family |
| interaction | |
| cofactors | |
| regulation | |
| MW | 62802 Da; 560 aa
|
Glucosidases
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 |
Beta-glucosidase precursor (bglX )
| function | hydrolysis of terminal non-reducing beta-D glucose residues |
| interaction | |
| cofactors | |
| regulation | |
| MW | 83460 Da; 765 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 |
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 | |
| |
PDB |
| MW | 73369 Da; 645 aa |
Trehalase precursor (treA )
| function | alpha- 1,1 glycosidic bond, to use trehalose as osmoprotectant |
| interaction | |
| cofactors | |
| regulation | slightly induced by high osmolarity and stationary phase |
| MW | 63636 Da; 565 aa
|
Hydrolases Aminohydrolases
Putative L-asparaginase AsgX (ybiK
)
| function | L-asparagine + H 2O = L-aspartate + NH 3
|
| interaction |
|
| regulation |
|
| structure |
PDB |
| MW | 33394 Da; 321 aa
|
Hydrolases Acting on Peptide Bonds
Murein Endopeptidases (Cell Wall Synthesis):
Penicillin-Binding Protein 4 precursor (dacB )
| function | final stages in peptidoglycan synthesis |
| interaction | penicillin sensitive |
| cofactors | |
| regulation | |
| MW | 51798 Da; 477 aa
|
Penicillin-binding protein 5 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
|
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 protein 7 precursor (pbpG )
| function | cell wall formation |
| interaction | penicillin sensitieve |
| cofactors | |
| regulation | |
| MW | 34245 Da; 313 aa
|
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
|
Proteases
Metalloproteases
Alkaline phosphatase isozyme conversion protein IAP
(iap or b2753
)
| Peptidase family | M28C
|
| Function |
|
| Structure |
|
| MW | 37920 Da 345 aa (1-24 signal
pept.)
|
ProteaseIII precursor (ptr )
| function | May prefer small substrates |
| interaction | |
| cofactors | requires divalent cations, binds Zn2+ |
| regulation | |
| | monomer |
| MW | 107708 Da; 962 aa |
Hypothetical protein YebA
(yebA
)
| Peptidase family | M37 InterPro
|
| Function |
|
| Structure |
|
| MW | 49057 Da 440 aa (1-34 signal
pept.)
|
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 |
Serine Proteases
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 |
| structure | hexamer
PDB |
| MW | 49439 Da; 474 aa |
Protease DegQ precursor (hhoA )
| function | shared specificity with HtrA/DegP |
| interaction | |
| cofactors | |
| regulation | | |
| MW | 47205 Da; 455 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
|
UmuD
(umuD
)
| Peptidase family | S24 InterPro
|
| Function |
|
| Structure |
|
| MW | 15063 Da 139 aa (1-24 signal
pept.)
|
Hydrolase Acting on Carbon-Nitrogen Bonds, Others Than Above
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 | |
| structure | monomer
PDB |
| 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 |
L-asparaginase II precursor (ansB )
| function | aspartate synthesis
Catalytic activity: L-asparagine + H2O = L-aspartate + NH3 |
| interaction | |
| cofactors | |
| regulation | induction by cAMP and anaerobiosis |
| structure | tetramer
PDB |
| MW | 36850 Da, 348 aa |
Penicillin acylase precursor (pac )
| function | penicillin resistance Catalytic activity:
penicillin + H2O = a fatty acid anion + 6-aminopenicillanate |
| interaction | |
| cofactors | |
| regulation | |
| | dimer
PDB |
| MW | 94642 Da; 846 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 |
Carboxy Lyase
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 |
Isomerases
Proline Cis-Trans-Isomerases (Folding Catalysts)
Peptidyl-prolyl cis-trans isomerase A precursor (ppiA )
| function | accelerate the folding of proteins |
| interaction | |
| cofactors | |
| regulation | inhibition by cyclosporin A |
| structure | monomer
PDB |
| MW | 20431 Da; 190 aa |
FkbP-type peptidyl-prolyl cis-trans isomerase FkpA precursor (fkpA )
| function | folding of extracytoplasmic proteins |
| interaction | |
| cofactors | |
| regulation | |
| MW | 28882 Da; 270 aa
|
Survival protein SurA precursor (surA )
| function | folding of extracytoplasmic proteins, essential in stationary phase |
| interaction | |
| cofactors | |
| regulation | |
| structure | PDB |
| MW | 47283 Da; 428 aa
|
Mutarotases
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
|
Disulfide Bond Formation(Folding Catalysts)
Thiol:disulfide interchange protein DsbA precursor (dsbA )
| function | disulfide bond formation in e.g. PhoA, OmpA, pilus biogenesis |
| interaction | reoxidised by DsbB |
| cofactors | |
| regulation | |
| structure |
PDB |
| MW | 23104 Da; 208 aa |
Thiol:disulfide interchange Protein DsbC precursor (dsbC )
| function | disulfide bond formation, also acts as disulfide isomerase |
| interaction | reoxidised by DsbD |
| cofactors | |
| regulation | |
| structure | dimer
PDB |
| MW | 25622 Da; 236 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
|
Thiol:disulfide interchange protein DsbG precursor (dsbG )
| function | involved in disulfide bond formation |
| interaction | |
| cofactors | |
| regulation | |
| MW | 27495 Da; 248 aa
|