| NZ_CP047916.1|WP_162322325.1|166981_169858_+|isoleucine--tRNA-ligase |
gnl|CDD|235681 |
PRK06039, ileS, isoleucyl-tRNA synthetase; Reviewed.
|
0 |
| NZ_CP047916.1|WP_162322324.1|166058_166898_+|glutamate-racemase |
gnl|CDD|234851 |
PRK00865, PRK00865, glutamate racemase; Provisional.
|
1.27239e-81 |
| NZ_CP047916.1|WP_162322329.1|174510_176178_+|LCP-family-protein |
gnl|CDD|224235 |
COG1316, LytR, Transcriptional regulator [Transcription].
|
1.27234e-29 |
| NZ_CP047916.1|WP_162322321.1|161928_163164_+|cell-division-protein-FtsA |
gnl|CDD|223918 |
COG0849, ftsA, Cell division ATPase FtsA [Cell division and chromosome partitioning].
|
7.74632e-106 |
| NZ_CP047916.1|WP_138059372.1|171759_172065_+|50S-ribosomal-protein-L21 |
gnl|CDD|376395 |
pfam00829, Ribosomal_L21p, Ribosomal prokaryotic L21 protein.
|
2.08365e-25 |
| NZ_CP047916.1|WP_162322320.1|161128_161893_+|type-I-methionyl-aminopeptidase |
gnl|CDD|238519 |
cd01086, MetAP1, Methionine Aminopeptidase 1. E.C. 3.4.11.18. Also known as methionyl aminopeptidase and Peptidase M. Catalyzes release of N-terminal amino acids, preferentially methionine, from peptides and arylamides.
|
7.88561e-94 |
| NZ_CP047916.1|WP_138059370.1|171131_171302_+|PspC-domain-containing-protein |
gnl|CDD|377200 |
pfam04024, PspC, PspC domain. This family includes Phage shock protein C (PspC) that is thought to be a transcriptional regulator. The presumed domain is 60 amino acid residues in length.
|
3.23473e-19 |
| NZ_CP047916.1|WP_138059360.1|160589_161141_+|nucleoside-monophosphate-kinase |
gnl|CDD|234711 |
PRK00279, adk, adenylate kinase; Reviewed.
|
2.16515e-37 |
| NZ_CP047916.1|WP_162322331.1|177013_178168_+|trypsin-like-peptidase-domain-containing-protein |
gnl|CDD|273938 |
TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].
|
3.11204e-90 |
| NZ_CP047916.1|WP_138059373.1|172154_172919_+|ParA-family-protein |
gnl|CDD|379293 |
pfam13614, AAA_31, AAA domain. This family includes a wide variety of AAA domains including some that have lost essential nucleotide binding residues in the P-loop.
|
4.66164e-82 |
| NZ_CP047916.1|WP_162322323.1|165175_165784_+|vitamin-K-epoxide-reductase-family-protein |
gnl|CDD|240605 |
cd12922, VKOR_5, Vitamin K epoxide reductase family in bacteria. This family includes vitamin K epoxide reductase (VKOR) mostly present in actinobacteria. VKOR (also named VKORC1) is an integral membrane protein that catalyzes the reduction of vitamin K 2,3-epoxide and vitamin K to vitamin K hydroquinone, an essential co-factor subsequently used in the gamma-carboxylation of glutamic acid residues in blood coagulation enzymes. All homologs of VKOR contain an active site CXXC motif, which is switched between reduced and disulfide-bonded states during the reaction cycle. In some bacterial homologs, the VKOR domain is fused with domains of the thioredoxin family of oxidoreductases which may function as redox partners in initiating the reduction cascade.
|
2.11511e-39 |
| NZ_CP047916.1|WP_162322319.1|160114_160570_+|GatB/YqeY-domain-containing-protein |
gnl|CDD|370480 |
pfam09424, YqeY, Yqey-like protein. The function of this domain found in the YqeY protein is uncertain.
|
1.81027e-41 |
| NZ_CP047916.1|WP_138059364.1|164460_164910_+|transcriptional-repressor-NrdR |
gnl|CDD|234774 |
PRK00464, nrdR, transcriptional repressor NrdR.
|
1.34004e-53 |
| NZ_CP047916.1|WP_162322322.1|163241_164435_+|cell-division-protein-FtsZ |
gnl|CDD|236468 |
PRK09330, PRK09330, cell division protein FtsZ; Validated.
|
0 |
| NZ_CP047916.1|WP_162322332.1|178160_178982_-|peptide-chain-release-factor-N(5)-glutamine-methyltransferase |
gnl|CDD|274634 |
TIGR03534, RF_mod_PrmC, protein-(glutamine-N5) methyltransferase, release factor-specific. Members of this protein family are HemK (PrmC), a protein once thought to be involved in heme biosynthesis but now recognized to be a protein-glutamine methyltransferase that modifies the peptide chain release factors. All members of the seed alignment are encoded next to the release factor 1 gene (prfA) and confirmed by phylogenetic analysis. SIMBAL analysis (manuscript in prep.) shows the motif [LIV]PRx[DE]TE (in Escherichia coli, IPRPDTE) confers specificity for the release factors rather than for ribosomal protein L3. [Protein fate, Protein modification and repair].
|
6.6027e-77 |
| NZ_CP047916.1|WP_138059375.1|173805_174414_-|signal-peptidase-I |
gnl|CDD|274044 |
TIGR02227, Inactive_signal_peptidase_IA., signal peptidase I, bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs, but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria, as well as a microsomal (endoplasmic reticulum) protein in eukaryotes. [Protein fate, Protein and peptide secretion and trafficking].
|
2.44234e-29 |
| NZ_CP047916.1|WP_162322328.1|172908_173796_+|ParB/RepB/Spo0J-family-partition-protein |
gnl|CDD|275105 |
TIGR04285, parB-like_partition_protein, nucleoid occlusion protein. This model describes nucleoid occlusion protein, a close homolog to ParB chromosome partitioning proteins including Spo0J in Bacillus subtilis. Its gene often is located near the gene for the Spo0J ortholog. This protein bind a specific DNA sequence and blocks cytokinesis from happening until chromosome segregation is complete.
|
7.31668e-66 |
