A very conserved eukaryotic enzyme involved in sphingolipid biosynthesis. Localization: ER (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7X8D9
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006643 | membrane lipid metabolic process | 4 | 1 |
GO:0006665 | sphingolipid metabolic process | 4 | 1 |
GO:0006670 | sphingosine metabolic process | 6 | 1 |
GO:0006672 | ceramide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0030148 | sphingolipid biosynthetic process | 5 | 1 |
GO:0034311 | diol metabolic process | 5 | 1 |
GO:0034312 | diol biosynthetic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046165 | alcohol biosynthetic process | 4 | 1 |
GO:0046173 | polyol biosynthetic process | 5 | 1 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 1 |
GO:0046512 | sphingosine biosynthetic process | 5 | 1 |
GO:0046513 | ceramide biosynthetic process | 5 | 1 |
GO:0046519 | sphingoid metabolic process | 5 | 1 |
GO:0046520 | sphingoid biosynthetic process | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004758 | serine C-palmitoyltransferase activity | 7 | 8 |
GO:0005488 | binding | 1 | 12 |
GO:0016408 | C-acyltransferase activity | 5 | 8 |
GO:0016409 | palmitoyltransferase activity | 5 | 8 |
GO:0016454 | C-palmitoyltransferase activity | 6 | 8 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
GO:0019842 | vitamin binding | 3 | 12 |
GO:0030170 | pyridoxal phosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0070279 | vitamin B6 binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.343 |
CLV_PCSK_FUR_1 | 379 | 383 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.235 |
CLV_PCSK_PC7_1 | 374 | 380 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.234 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.435 |
DEG_COP1_1 | 74 | 84 | PF00400 | 0.635 |
DOC_CYCLIN_RxL_1 | 272 | 283 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 273 | 280 | PF00069 | 0.441 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.440 |
DOC_SPAK_OSR1_1 | 247 | 251 | PF12202 | 0.408 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.594 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 102 | 112 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 247 | 257 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 336 | 344 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 444 | 453 | PF00244 | 0.475 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.422 |
LIG_BIR_III_2 | 402 | 406 | PF00653 | 0.435 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.541 |
LIG_eIF4E_1 | 274 | 280 | PF01652 | 0.435 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.415 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.415 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.468 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.448 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.375 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.413 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.500 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.625 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.535 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.432 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.431 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.480 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.323 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.342 |
LIG_Integrin_RGD_1 | 192 | 194 | PF01839 | 0.258 |
LIG_LIR_Apic_2 | 239 | 244 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 298 | 303 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.601 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.415 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.518 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.470 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.614 |
LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.518 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.426 |
LIG_SH3_1 | 42 | 48 | PF00018 | 0.600 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.620 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.588 |
LIG_SUMO_SIM_anti_2 | 359 | 364 | PF11976 | 0.518 |
LIG_SUMO_SIM_anti_2 | 404 | 410 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 96 | 102 | PF11976 | 0.605 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.518 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.536 |
LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.395 |
LIG_UBA3_1 | 267 | 275 | PF00899 | 0.426 |
LIG_WRC_WIRS_1 | 119 | 124 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 174 | 179 | PF05994 | 0.440 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.465 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.457 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.417 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.485 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.417 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.470 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.671 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.647 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.541 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.565 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.358 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.506 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.440 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.350 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.426 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.323 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.574 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.317 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.270 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.235 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.255 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.524 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.375 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.417 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.426 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.415 |
MOD_LATS_1 | 334 | 340 | PF00433 | 0.418 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.305 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.439 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.426 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.437 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.426 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.415 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.399 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.374 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.504 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.418 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.441 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.483 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.419 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.426 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.686 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.415 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.420 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.500 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.484 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.482 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.415 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.533 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.563 |
TRG_DiLeu_BaEn_1 | 392 | 397 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_4 | 109 | 115 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.616 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.543 |
TRG_NLS_MonoExtC_3 | 377 | 382 | PF00514 | 0.435 |
TRG_NLS_MonoExtN_4 | 375 | 382 | PF00514 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.206 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.344 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYL3 | Leptomonas seymouri | 75% | 99% |
A0A0S4KPJ9 | Bodo saltans | 46% | 96% |
A0A1X0PAD7 | Trypanosomatidae | 48% | 99% |
A0A3R7KRA6 | Trypanosoma rangeli | 49% | 99% |
A1ITK1 | Neisseria meningitidis serogroup A / serotype 4A (strain DSM 15465 / Z2491) | 22% | 100% |
A1KVF6 | Neisseria meningitidis serogroup C / serotype 2a (strain ATCC 700532 / DSM 15464 / FAM18) | 22% | 100% |
A1V819 | Burkholderia mallei (strain SAVP1) | 28% | 100% |
A2S7R1 | Burkholderia mallei (strain NCTC 10229) | 28% | 100% |
A3MNG3 | Burkholderia mallei (strain NCTC 10247) | 28% | 100% |
A3N522 | Burkholderia pseudomallei (strain 668) | 28% | 100% |
A3NQS3 | Burkholderia pseudomallei (strain 1106a) | 28% | 100% |
A4HB93 | Leishmania braziliensis | 84% | 100% |
A4IAE1 | Leishmania infantum | 100% | 100% |
A4VR87 | Pseudomonas stutzeri (strain A1501) | 25% | 100% |
A6UYW1 | Pseudomonas aeruginosa (strain PA7) | 26% | 100% |
A9HJ57 | Gluconacetobacter diazotrophicus (strain ATCC 49037 / DSM 5601 / CCUG 37298 / CIP 103539 / LMG 7603 / PAl5) | 27% | 100% |
A9M251 | Neisseria meningitidis serogroup C (strain 053442) | 22% | 100% |
B0U6J0 | Xylella fastidiosa (strain M12) | 22% | 100% |
B1I4F9 | Desulforudis audaxviator (strain MP104C) | 28% | 100% |
B2AG98 | Cupriavidus taiwanensis (strain DSM 17343 / BCRC 17206 / CCUG 44338 / CIP 107171 / LMG 19424 / R1) | 26% | 100% |
B2I9H7 | Xylella fastidiosa (strain M23) | 22% | 100% |
B3PI88 | Cellvibrio japonicus (strain Ueda107) | 26% | 100% |
B4RP93 | Neisseria gonorrhoeae (strain NCCP11945) | 22% | 100% |
B5XZ74 | Klebsiella pneumoniae (strain 342) | 25% | 100% |
B7K0L9 | Rippkaea orientalis (strain PCC 8801) | 26% | 100% |
B7V486 | Pseudomonas aeruginosa (strain LESB58) | 27% | 100% |
C4LK80 | Corynebacterium kroppenstedtii (strain DSM 44385 / JCM 11950 / CIP 105744 / CCUG 35717) | 26% | 68% |
C8V1D1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 22% | 100% |
C9ZLV5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D4A2H2 | Rattus norvegicus | 34% | 100% |
E9B5G5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O15269 | Homo sapiens | 35% | 100% |
O35704 | Mus musculus | 34% | 100% |
O54695 | Cricetulus griseus | 34% | 100% |
O59682 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 96% |
P09950 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 89% |
P25045 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 87% |
P91079 | Caenorhabditis elegans | 34% | 100% |
Q02TR5 | Pseudomonas aeruginosa (strain UCBPP-PA14) | 27% | 100% |
Q12F38 | Polaromonas sp. (strain JS666 / ATCC BAA-500) | 25% | 100% |
Q2W3L2 | Magnetospirillum magneticum (strain AMB-1 / ATCC 700264) | 23% | 100% |
Q3JWR6 | Burkholderia pseudomallei (strain 1710b) | 28% | 100% |
Q3SLX9 | Thiobacillus denitrificans (strain ATCC 25259) | 27% | 100% |
Q48CS2 | Pseudomonas savastanoi pv. phaseolicola (strain 1448A / Race 6) | 26% | 100% |
Q55FL5 | Dictyostelium discoideum | 33% | 100% |
Q5F6R6 | Neisseria gonorrhoeae (strain ATCC 700825 / FA 1090) | 22% | 100% |
Q5R9T5 | Pongo abelii | 34% | 100% |
Q60HD1 | Macaca fascicularis | 34% | 100% |
Q62MX1 | Burkholderia mallei (strain ATCC 23344) | 28% | 100% |
Q63Y23 | Burkholderia pseudomallei (strain K96243) | 28% | 100% |
Q6FXE3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 92% |
Q6LPR3 | Photobacterium profundum (strain SS9) | 23% | 100% |
Q6XFB3 | Leishmania major | 96% | 100% |
Q7RVY5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 78% |
Q7VWP1 | Bordetella pertussis (strain Tohama I / ATCC BAA-589 / NCTC 13251) | 26% | 100% |
Q7W9I4 | Bordetella parapertussis (strain 12822 / ATCC BAA-587 / NCTC 13253) | 26% | 100% |
Q7WH76 | Bordetella bronchiseptica (strain ATCC BAA-588 / NCTC 13252 / RB50) | 26% | 100% |
Q87DT2 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 22% | 100% |
Q88A97 | Pseudomonas syringae pv. tomato (strain ATCC BAA-871 / DC3000) | 25% | 100% |
Q9I617 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 27% | 100% |
Q9K0U0 | Neisseria meningitidis serogroup B (strain MC58) | 22% | 100% |
Q9PDM2 | Xylella fastidiosa (strain 9a5c) | 23% | 100% |
V5BLV3 | Trypanosoma cruzi | 51% | 99% |