Species | Zymoseptoria tritici | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Ascomycota; Dothideomycetes; ; Mycosphaerellaceae; Zymoseptoria; Zymoseptoria tritici | |||||||||||
CAZyme ID | ZTRI_4.640.mRNA-p1 | |||||||||||
CAZy Family | GT8 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
397462 | PAF-AH_p_II | 1.18e-31 | 5 | 302 | 6 | 253 | Platelet-activating factor acetylhydrolase, isoform II. Platelet-activating factor acetylhydrolase (PAF-AH) is a subfamily of phospholipases A2, responsible for inactivation of platelet-activating factor through cleavage of an acetyl group. Three known PAF-AHs are the brain heterotrimeric PAF-AH Ib, whose catalytic beta and gamma subunits are aligned in pfam02266, the extracellular, plasma PAF-AH (pPAF-AH), and the intracellular PAF-AH isoform II (PAF-AH II). This family aligns pPAF-AH and PAF-AH II, whose similarity was previously noted. |
226651 | COG4188 | 1.44e-07 | 138 | 287 | 67 | 179 | Predicted dienelactone hydrolase [General function prediction only]. |
223999 | FrsA | 7.26e-05 | 133 | 308 | 40 | 202 | Fermentation-respiration switch protein FrsA, has esterase activity, DUF1100 family [Signal transduction mechanisms]. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
0.0 | 441 | 898 | 4 | 461 | |
0.0 | 441 | 898 | 4 | 461 | |
0.0 | 441 | 898 | 4 | 461 | |
0.0 | 441 | 898 | 4 | 461 | |
7.42e-149 | 490 | 898 | 82 | 488 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
1.96e-13 | 6 | 349 | 1 | 291 | Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor [Homo sapiens],6M07_B Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor [Homo sapiens] |
|
1.99e-13 | 6 | 349 | 1 | 291 | Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor [Homo sapiens],6M06_B Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor [Homo sapiens],6M08_A Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor. [Homo sapiens],6M08_B Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor. [Homo sapiens] |
|
2.17e-13 | 6 | 349 | 8 | 298 | Crystal structure of human plasma platelet activating factor acetylhydrolase [Homo sapiens],3D59_B Crystal structure of human plasma platelet activating factor acetylhydrolase [Homo sapiens],3D5E_A Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by paraoxon [Homo sapiens],3D5E_B Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by paraoxon [Homo sapiens],3F97_A Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by soman [Homo sapiens],3F97_B Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by soman [Homo sapiens],3F98_A Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by tabun [Homo sapiens],3F98_B Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by tabun [Homo sapiens],3F98_C Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by tabun [Homo sapiens],3F9C_A Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by diisopropylfluorophosphate [Homo sapiens],3F9C_B Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by diisopropylfluorophosphate [Homo sapiens] |
|
2.25e-13 | 6 | 349 | 13 | 303 | Crystal structure of LP_PLA2 in complex with novel inhibitor [Homo sapiens],5I8P_B Crystal structure of LP_PLA2 in complex with novel inhibitor [Homo sapiens],5I9I_A Crystal structure of LP_PLA2 in complex with Darapladib [Homo sapiens],5I9I_B Crystal structure of LP_PLA2 in complex with Darapladib [Homo sapiens],5YE7_A The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YE7_B The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YE8_A The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YE8_B The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YE9_A The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YE9_B The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YEA_A The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens],5YEA_B The crystal structure of Lp-PLA2 in complex with a novel inhibitor [Homo sapiens] |
|
2.25e-13 | 6 | 349 | 9 | 299 | Compound binding to Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2)discovered through fragment screening [Homo sapiens],5JAH_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAL_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAN_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAO_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAP_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAR_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAS_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAT_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5JAU_A Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered Through X-Ray Fragment Screening [Homo sapiens],5LP1_A CRYSTAL STRUCTURE OF HUMAN LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 IN COMPLEX WITH A [1.1.1]BICYCLOPENTANE-CONTAINING INHIBITOR AT 1.91A RESOLUTION. [Homo sapiens],5LYY_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens],5LZ2_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens],5LZ4_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens],5LZ5_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens],5LZ7_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens],5LZ8_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens],5LZ9_A Fragment-based inhibitors of Lipoprotein associated Phospholipase A2 [Homo sapiens] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
3.38e-19 | 46 | 381 | 29 | 327 | Platelet-activating factor acetylhydrolase 2, cytoplasmic OS=Mus musculus OX=10090 GN=Pafah2 PE=1 SV=2 |
|
6.20e-19 | 51 | 405 | 34 | 357 | Platelet-activating factor acetylhydrolase 2, cytoplasmic OS=Bos taurus OX=9913 GN=PAFAH2 PE=1 SV=1 |
|
8.39e-18 | 46 | 405 | 29 | 355 | Platelet-activating factor acetylhydrolase 2, cytoplasmic OS=Rattus norvegicus OX=10116 GN=Pafah2 PE=1 SV=2 |
|
6.57e-17 | 51 | 405 | 34 | 357 | Platelet-activating factor acetylhydrolase 2, cytoplasmic OS=Homo sapiens OX=9606 GN=PAFAH2 PE=1 SV=1 |
|
9.42e-16 | 8 | 352 | 56 | 345 | Platelet-activating factor acetylhydrolase OS=Cavia porcellus OX=10141 GN=PLA2G7 PE=2 SV=1 |
Other | SP_Sec_SPI | CS Position |
---|---|---|
1.000057 | 0.000000 |
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