Species | Aeromonas hydrophila | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Proteobacteria; Gammaproteobacteria; Enterobacterales; Aeromonadaceae; Aeromonas; Aeromonas hydrophila | |||||||||||
CAZyme ID | MGYG000002526_01592 | |||||||||||
CAZy Family | GH73 | |||||||||||
CAZyme Description | Peptidoglycan hydrolase FlgJ | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 1702470; End: 1703561 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GH73 | 210 | 347 | 1.3e-35 | 0.9609375 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
PRK05684 | flgJ | 1.38e-113 | 17 | 354 | 13 | 309 | flagellar assembly peptidoglycan hydrolase FlgJ. |
TIGR02541 | flagell_FlgJ | 6.97e-84 | 17 | 349 | 4 | 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. |
PRK12712 | flgJ | 1.20e-55 | 27 | 346 | 26 | 340 | flagellar rod assembly protein/muramidase FlgJ; Provisional |
PRK12709 | flgJ | 5.90e-52 | 17 | 346 | 17 | 317 | flagellar rod assembly protein/muramidase FlgJ; Provisional |
COG1705 | FlgJ | 1.72e-50 | 203 | 360 | 44 | 200 | Flagellum-specific peptidoglycan hydrolase FlgJ [Cell wall/membrane/envelope biogenesis, Cell motility]. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
ANT67365.1 | 6.19e-263 | 1 | 363 | 1 | 363 |
QSR77752.1 | 2.52e-262 | 1 | 363 | 1 | 363 |
APJ16063.1 | 2.52e-262 | 1 | 363 | 1 | 363 |
AXV33738.1 | 2.52e-262 | 1 | 363 | 1 | 363 |
QSR81944.1 | 2.52e-262 | 1 | 363 | 1 | 363 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
3VWO_A | 2.73e-35 | 203 | 350 | 2 | 148 | Crystalstructure of peptidoglycan hydrolase mutant from Sphingomonas sp. A1 [Sphingomonas sp. A1] |
2ZYC_A | 3.54e-35 | 203 | 350 | 3 | 149 | ChainA, Peptidoglycan hydrolase FlgJ [Sphingomonas sp. A1] |
5DN5_A | 5.20e-35 | 203 | 346 | 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 | 8.01e-35 | 203 | 346 | 4 | 146 | Structureof the glycoside hydrolase domain from Salmonella typhimurium FlgJ [Salmonella enterica subsp. enterica serovar Typhimurium str. LT2] |
3K3T_A | 2.67e-34 | 203 | 350 | 3 | 149 | E185Amutant of peptidoglycan hydrolase from Sphingomonas sp. A1 [Sphingomonas sp. A1] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q9X9J3 | 2.40e-65 | 11 | 344 | 7 | 301 | Peptidoglycan hydrolase FlgJ OS=Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) OX=223926 GN=flgJ PE=3 SV=1 |
Q9KQ15 | 4.43e-63 | 7 | 344 | 3 | 302 | Peptidoglycan hydrolase FlgJ OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) OX=243277 GN=flgJ PE=3 SV=2 |
Q9I4P4 | 4.05e-61 | 8 | 346 | 11 | 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 | 1.43e-46 | 17 | 346 | 14 | 292 | Peptidoglycan hydrolase FlgJ OS=Escherichia coli O157:H7 OX=83334 GN=flgJ PE=3 SV=1 |
P75942 | 2.82e-46 | 17 | 346 | 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 |
---|---|---|---|---|---|
1.000060 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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