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prdE | Putative component of proline reductase. (156 aa) | ||||
tadA | Putative cytosine deaminase; Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2); Belongs to the cytidine and deoxycytidylate deaminase family. (145 aa) | ||||
arcA1 | Arginine deiminase; Similar to Enterococcus faecalis arginine deiminase ArcA or ef0104 SWALL:Q93K67 (EMBL:AJ312276) (408 aa) fasta scores: E(): 1.6e-80, 55.06 38d in 405 aa, and to Bacillus licheniformis arginine deiminase ArcA SWALL:ARCA_BACLI (SWALL:O86131) (413 aa) fasta scores: E(): 3.7e-77, 51.22 id in 408 aa; Also similar to CBO1587 (57.03 38d). (403 aa) | ||||
CBO0068 | Similar to Clostridium tetani putative polysaccharide deacetylase ctc00229 SWALL:Q899F2 (EMBL:AE015936) (293 aa) fasta scores: E(): 4.7e-50,52.05 38d in 292 aa, and to Clostridium acetobutylicum predicted xylanase/chitin deacetilase, similar to yxkh b.subtilis cac0436 SWALL:Q97LW8 (EMBL:AE007558) (295 aa) fasta scores: E(): 8.6e-38, 47.03 38d in 253 aa. (289 aa) | ||||
pyrG | CTP synthase; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates. (533 aa) | ||||
CBO0146 | Putative zinc-binding protein; Similar to Clostridium tetani comE operon protein 2 ctc00309 SWALL:Q898X8 (EMBL:AE015936) (162 aa) fasta scores: E(): 6.7e-56, 81.48 38d in 162 aa, and to Clostridium acetobutylicum deoxycytidylate deaminase cac2876 SWALL:Q97F76 (EMBL:AE007785) (162 aa) fasta scores: E(): 1.9e-44, 67.28 38d in 162 aa. (162 aa) | ||||
CBO0223 | Similar to Bacillus subtilis probable polysaccharide deacetylase PdaA precursor PdaA or bsu07980 SWALL:PDAA_BACSU (SWALL:O34928) (263 aa) fasta scores: E(): 1.1e-13, 34.95 38d in 206 aa, and to Clostridium perfringens probable endo-1,4-beta-xylanase cpe1477 SWALL:Q8XKC3 (EMBL:AP003190) (238 aa) fasta scores: E(): 8.6e-33, 44.58 38d in 240 aa. (241 aa) | ||||
CBO0253 | Cytidine deaminase; Similar to Bacillus caldolyticus cytidine deaminase Cdd SWALL:Q9R2S1 (EMBL:AJ237979) (132 aa) fasta scores: E(): 1.2e-05, 30.4 38d in 125 aa, and to Aspergillus terreus blasticidin-S deaminase Bsd SWALL:BSD_ASPTE (SWALL:P78986) (130 aa) fasta scores: E(): 3.9e-05, 31.49 id in 127 aa. (125 aa) | ||||
adeC | Adenine deaminase; Similar to Bacillus subtilis adenine deaminase AdeC or Ade or bsu14520 SWALL:ADEC_BACSU (SWALL:P39761) (577 aa) fasta scores: E(): 5e-63, 36.17 38d in 575 aa; Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family. (599 aa) | ||||
CBO0351 | Probable polysaccharide deacetylase; Similar to Clostridium acetobutylicum predicted xylanase/chitin deacetylase cac2396 SWALL:Q97GH1 (EMBL:AE007739) (280 aa) fasta scores: E(): 3.1e-34, 45.6 id in 250 aa. (270 aa) | ||||
CBO0410 | Conserved hypothetical protein; Similar to Clostridium acetobutylicum cobyric acid synthase CobQ cac0961 SWALL:Q97KF8 (EMBL:AE007611) (243 aa) fasta scores: E(): 8.8e-72, 77.08 38d in 240 aa. (242 aa) | ||||
nadE | Glutamine-dependent NAD(+) synthetase; Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source. (638 aa) | ||||
CBO0629 | N-carbamoyl-L-amino acid hydrolase. (407 aa) | ||||
CBO0716 | Putative transcriptional regulator (partial); Partial CDS. Similar to the C-terminal region of Clostridium tetani putative transcriptional regulatory protein ctc01439 SWALL:Q894U5 (EMBL:AE015941) (235 aa) fasta scores: E(): 2.1e-12, 41.81 38d in 110 aa; was marked partial. (86 aa) | ||||
CBO0747 | Putative phage related lysin (partial); Partial CDS. Similar to an internal region of Bacteriophage PL-1 N-acetylmuramoyl-L-alanine amidase lyS SWALL:Q9MCC6 (EMBL:AB035861) (350 aa) fasta scores: E(): 4.4e-05, 40 38d in 70 aa, and to Enterococcus faecalis enterolysin a enlA SWALL:Q9F8B0 (EMBL:AF249740) (343 aa) fasta scores: E(): 0.00024, 38.09 38d in 63 aa; was marked partial. (242 aa) | ||||
CBO0812 | Putative amidohydrolase. (389 aa) | ||||
defA | Peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. (166 aa) | ||||
CBO0894 | Putative porphyromonas-type peptidyl-arginine deiminase; Belongs to the agmatine deiminase family. (410 aa) | ||||
CBO0908 | Hypothetical protein; No significant database matches. (568 aa) | ||||
CBO0985 | Conserved hypothetical protein. (107 aa) | ||||
add | Adenosine deaminase; Belongs to the metallo-dependent hydrolases superfamily. Adenosine and AMP deaminases family. Adenosine deaminase subfamily. (335 aa) | ||||
CBO1013 | Putative cyclase. (181 aa) | ||||
CBO1015 | Putative cyclase. (192 aa) | ||||
folD | Putative methylenetetrahydrofolate dehydrogenase; Catalyzes the oxidation of 5,10-methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10- methenyltetrahydrofolate to 10-formyltetrahydrofolate. (282 aa) | ||||
guaD | Guanine deaminase. (157 aa) | ||||
CBO1432 | Putative N-acetylmuramoyl-L-alanine amidase. (283 aa) | ||||
folE | Putative GTP cyclohydrolase I. (196 aa) | ||||
hisH | Imidazole glycerol phosphate synthase subunit; IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the synthesis of IGP and AICAR. The resulting ammonia molecule is channeled to the active site of HisF. (201 aa) | ||||
hisI | phosphoribosyl-AMP cyclohydrolase; Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP. (110 aa) | ||||
arcA2 | Arginine deiminase; Also similar to CBO0065 (57.03 38d). (408 aa) | ||||
CBO1737 | Putative phage protein. (720 aa) | ||||
CBO1751 | Bacteriophage endolysin (N-acetylmuramoyl-L-alanine amidase); Also similar to CBO1653 (81.6 38d), CBO2325 (86.1 id.), CBO3016 (50.0 38d.). (253 aa) | ||||
CBO1783 | Putative mannosyl-glycoprotein endo-beta-N-acetylglucosamidase. (309 aa) | ||||
codA | Putative RNA methyltransferase (partial CDS); Partial CDS. Similar to C-terminal region of many RNA methyltransferases including Bacillus cereus tRNA (uracil-5-)-methyltransferase bc0364 SWALL:Q814A6 (EMBL:AE016999) (458 aa) fasta scores: E(): 1.6e-11,62.96 38d in 54 aa; was marked partial. (421 aa) | ||||
CBO2188 | Amidohydrolase family protein. (450 aa) | ||||
def-2 | Putative peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. (150 aa) | ||||
CBO2325 | Putative N-acetylmuramoyl-L-alanine amidase; Similar to the N-terminal region of Anabaena sp. hypothetical protein ALL1140 SWALL:Q8YXS1 (EMBL:AP003584) (313 aa) fasta scores: E(): 5.2e-30, 45.1 38d in 235 aa; Also similar to CBO1751 (81.16 38d), CBO1653 (77.4 id.), CBO3016 (47.6 38d.). (253 aa) | ||||
def-3 | Putative peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. (147 aa) | ||||
CBO2516 | Putative L-asparaginase. (333 aa) | ||||
CBO2528 | Conserved hypothetical protein; Belongs to the multicopper oxidase YfiH/RL5 family. (239 aa) | ||||
purL | Formylglycinamidine ribonucleotide synthetase. (1221 aa) | ||||
def | Peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. (156 aa) | ||||
CBO2708 | Hypothetical protein; Note the database similarities are weak and only to the C-terminal region. (479 aa) | ||||
cheB | Chemotaxis response regulator protein-glutamate methylesterase; Involved in chemotaxis. Part of a chemotaxis signal transduction system that modulates chemotaxis in response to various stimuli. Catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins or MCP) by CheR. Also mediates the irreversible deamidation of specific glutamine residues to glutamic acid. Belongs to the CheB family. (354 aa) | ||||
cheD | Chemotaxis protein CheD; Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis; Belongs to the CheD family. (162 aa) | ||||
CBO2775 | Probable polysaccharide deacetylase. (297 aa) | ||||
CBO2801 | Probable polysaccharide deacetylase. (243 aa) | ||||
glsA | Glutaminase; Belongs to the glutaminase family. (305 aa) | ||||
nagA | N-acetylglucosamine-6-phosphate deacetylase. (378 aa) | ||||
ribA | 3,4-dihydroxy-2-butanone 4-phosphate synthase; Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate; In the C-terminal section; belongs to the GTP cyclohydrolase II family. (401 aa) | ||||
ribD | Diaminohydroxyphosphoribosylaminopyrimidine deaminase; Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'- phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'- phosphate; In the C-terminal section; belongs to the HTP reductase family. (365 aa) | ||||
purH | Bifunctional purine biosynthesis protein [includes: phosphoribosylaminoimidazolecarboxamide formyltransferase and IMP cyclohydrolase. (499 aa) | ||||
purN | Phosphoribosylglycinamide formyltransferase; Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate. (205 aa) | ||||
ssnA | Putative amidohydrolase. (442 aa) | ||||
hydA | D-hydantoinase. (464 aa) | ||||
CBO2907 | Putative peptidase. (543 aa) | ||||
cdd | Cytidine deaminase; This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis; Belongs to the cytidine and deoxycytidylate deaminase family. (132 aa) | ||||
CBO3016 | N-acetylmuramoyl-L-alanine amidase; Also similar to the prophage encoded CDSs, CBO1751 (50 38d), CBO2325 (48.8 0d.), CBO1653 (55.5 0d.). (256 aa) | ||||
CBO3029 | Conserved hypothetical protein; Weakly similar to the upstream CDS CB03028. (449 aa) | ||||
pdaA | Probable polysaccharide deacetylase. (324 aa) | ||||
CBO3110 | Putative N-acetylmuramoyl-L-alanine amidase; No significant database matches; similar to CBO3111 (42.304 38d. in 955 aa overlap). (949 aa) | ||||
CBO3111 | Putative N-acetylmuramoyl-L-alanine amidase; No significant database matches; similar to CBO3110 (42.304 38d. in 955 aa overlap). (967 aa) | ||||
pdaB | Probable polysaccharide deacetylase. (250 aa) | ||||
pyrC | Dihydroorotase; Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate; Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily. (396 aa) | ||||
CBO3275 | Conserved hypothetical protein. (667 aa) | ||||
iadA | Isoaspartyl dipeptidase; Catalyzes the hydrolytic cleavage of a subset of L- isoaspartyl (L-beta-aspartyl) dipeptides. Used to degrade proteins damaged by L-isoaspartyl residues formation. Belongs to the peptidase M38 family. (391 aa) | ||||
cwlD | Germination-specific N-acetylmuramoyl-L-alanine amidase. (234 aa) |