Species | Aeromonas caviae | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Proteobacteria; Gammaproteobacteria; Enterobacterales; Aeromonadaceae; Aeromonas; Aeromonas caviae | |||||||||||
CAZyme ID | MGYG000002527_02238 | |||||||||||
CAZy Family | GH73 | |||||||||||
CAZyme Description | Peptidoglycan hydrolase FlgJ | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 307034; End: 308134 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GH73 | 208 | 345 | 3.8e-35 | 0.9609375 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
PRK05684 | flgJ | 2.31e-114 | 8 | 353 | 4 | 310 | flagellar assembly peptidoglycan hydrolase FlgJ. |
TIGR02541 | flagell_FlgJ | 2.90e-84 | 15 | 347 | 2 | 294 | flagellar rod assembly protein/muramidase FlgJ. The N-terminal region of this protein acts directly in flagellar rod assembly. The C-terminal region is a flagellum-specific muramidase (peptidoglycan hydrolase) required for formation of the outer membrane L ring. |
PRK12709 | flgJ | 8.75e-53 | 17 | 344 | 17 | 317 | flagellar rod assembly protein/muramidase FlgJ; Provisional |
COG1705 | FlgJ | 1.42e-52 | 180 | 357 | 22 | 199 | Flagellum-specific peptidoglycan hydrolase FlgJ [Cell wall/membrane/envelope biogenesis, Cell motility]. |
PRK12712 | flgJ | 2.41e-52 | 17 | 344 | 19 | 340 | flagellar rod assembly protein/muramidase FlgJ; Provisional |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
ATP91068.1 | 8.16e-265 | 1 | 366 | 1 | 366 |
AUT44156.1 | 3.32e-264 | 1 | 366 | 1 | 366 |
AUU21545.1 | 9.52e-264 | 1 | 366 | 1 | 366 |
AUV13203.1 | 9.52e-264 | 1 | 366 | 1 | 366 |
QLL85234.1 | 9.52e-264 | 1 | 366 | 1 | 366 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
3VWO_A | 1.94e-36 | 201 | 348 | 2 | 148 | Crystalstructure of peptidoglycan hydrolase mutant from Sphingomonas sp. A1 [Sphingomonas sp. A1] |
2ZYC_A | 2.53e-36 | 201 | 348 | 3 | 149 | ChainA, Peptidoglycan hydrolase FlgJ [Sphingomonas sp. A1] |
3K3T_A | 1.92e-35 | 201 | 348 | 3 | 149 | E185Amutant of peptidoglycan hydrolase from Sphingomonas sp. A1 [Sphingomonas sp. A1] |
5DN5_A | 5.86e-34 | 201 | 344 | 4 | 146 | Structureof a C-terminally truncated glycoside hydrolase domain from Salmonella typhimurium FlgJ [Salmonella enterica subsp. enterica serovar Typhimurium str. LT2],5DN5_B Structure of a C-terminally truncated glycoside hydrolase domain from Salmonella typhimurium FlgJ [Salmonella enterica subsp. enterica serovar Typhimurium str. LT2],5DN5_C Structure of a C-terminally truncated glycoside hydrolase domain from Salmonella typhimurium FlgJ [Salmonella enterica subsp. enterica serovar Typhimurium str. LT2] |
5DN4_A | 8.99e-34 | 201 | 344 | 4 | 146 | Structureof the glycoside hydrolase domain from Salmonella typhimurium FlgJ [Salmonella enterica subsp. enterica serovar Typhimurium str. LT2] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q9KQ15 | 4.62e-70 | 11 | 342 | 7 | 302 | Peptidoglycan hydrolase FlgJ OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) OX=243277 GN=flgJ PE=3 SV=2 |
Q9X9J3 | 1.69e-69 | 11 | 342 | 7 | 301 | Peptidoglycan hydrolase FlgJ OS=Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) OX=223926 GN=flgJ PE=3 SV=1 |
Q9I4P4 | 2.01e-66 | 20 | 344 | 20 | 383 | Peptidoglycan hydrolase FlgJ OS=Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) OX=208964 GN=flgJ PE=3 SV=1 |
P58231 | 3.05e-46 | 17 | 344 | 14 | 292 | Peptidoglycan hydrolase FlgJ OS=Escherichia coli O157:H7 OX=83334 GN=flgJ PE=3 SV=1 |
P75942 | 4.27e-46 | 17 | 344 | 14 | 292 | Peptidoglycan hydrolase FlgJ OS=Escherichia coli (strain K12) OX=83333 GN=flgJ PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000042 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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