| 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. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 10 |
| NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QCN1
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
| GO:0006396 | RNA processing | 6 | 11 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016070 | RNA metabolic process | 5 | 11 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
| GO:0043170 | macromolecule metabolic process | 3 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044238 | primary metabolic process | 2 | 11 |
| GO:0046483 | heterocycle metabolic process | 3 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:0090304 | nucleic acid metabolic process | 4 | 11 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0008168 | methyltransferase activity | 4 | 11 |
| GO:0008173 | RNA methyltransferase activity | 4 | 11 |
| GO:0016740 | transferase activity | 2 | 11 |
| GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
| GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 592 | 596 | PF00656 | 0.670 |
| CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.662 |
| CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.410 |
| CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.350 |
| CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.413 |
| CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.311 |
| CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.492 |
| CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.646 |
| CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.490 |
| CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.460 |
| CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.344 |
| CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.231 |
| CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.311 |
| CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.506 |
| CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.646 |
| CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.490 |
| CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.327 |
| CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.289 |
| CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.407 |
| CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.357 |
| CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.288 |
| DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.455 |
| DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.510 |
| DEG_SCF_FBW7_2 | 382 | 388 | PF00400 | 0.384 |
| DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.531 |
| DOC_CDC14_PxL_1 | 357 | 365 | PF14671 | 0.466 |
| DOC_CKS1_1 | 382 | 387 | PF01111 | 0.384 |
| DOC_CKS1_1 | 81 | 86 | PF01111 | 0.449 |
| DOC_MAPK_gen_1 | 152 | 159 | PF00069 | 0.383 |
| DOC_MAPK_gen_1 | 422 | 432 | PF00069 | 0.311 |
| DOC_MAPK_MEF2A_6 | 191 | 198 | PF00069 | 0.385 |
| DOC_MAPK_MEF2A_6 | 284 | 293 | PF00069 | 0.382 |
| DOC_MAPK_MEF2A_6 | 425 | 432 | PF00069 | 0.311 |
| DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.423 |
| DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.508 |
| DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.311 |
| DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.690 |
| DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.454 |
| DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.522 |
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.462 |
| DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.504 |
| DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.678 |
| DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.222 |
| DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.481 |
| DOC_USP7_UBL2_3 | 525 | 529 | PF12436 | 0.309 |
| DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.529 |
| DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.396 |
| DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.456 |
| DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.308 |
| DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.311 |
| DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.381 |
| DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.451 |
| LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.516 |
| LIG_14-3-3_CanoR_1 | 561 | 569 | PF00244 | 0.432 |
| LIG_14-3-3_CanoR_1 | 87 | 97 | PF00244 | 0.509 |
| LIG_AP2alpha_1 | 174 | 178 | PF02296 | 0.520 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.711 |
| LIG_BIR_III_4 | 595 | 599 | PF00653 | 0.672 |
| LIG_BRCT_BRCA1_1 | 196 | 200 | PF00533 | 0.469 |
| LIG_Clathr_ClatBox_1 | 26 | 30 | PF01394 | 0.421 |
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.431 |
| LIG_FHA_1 | 218 | 224 | PF00498 | 0.357 |
| LIG_FHA_1 | 297 | 303 | PF00498 | 0.444 |
| LIG_FHA_1 | 329 | 335 | PF00498 | 0.370 |
| LIG_FHA_1 | 362 | 368 | PF00498 | 0.356 |
| LIG_FHA_1 | 402 | 408 | PF00498 | 0.338 |
| LIG_FHA_1 | 411 | 417 | PF00498 | 0.393 |
| LIG_FHA_1 | 548 | 554 | PF00498 | 0.311 |
| LIG_FHA_2 | 136 | 142 | PF00498 | 0.548 |
| LIG_FHA_2 | 225 | 231 | PF00498 | 0.526 |
| LIG_FHA_2 | 296 | 302 | PF00498 | 0.513 |
| LIG_FHA_2 | 313 | 319 | PF00498 | 0.333 |
| LIG_FHA_2 | 360 | 366 | PF00498 | 0.361 |
| LIG_FHA_2 | 403 | 409 | PF00498 | 0.311 |
| LIG_FHA_2 | 448 | 454 | PF00498 | 0.418 |
| LIG_FHA_2 | 532 | 538 | PF00498 | 0.378 |
| LIG_FHA_2 | 590 | 596 | PF00498 | 0.723 |
| LIG_FHA_2 | 81 | 87 | PF00498 | 0.471 |
| LIG_Integrin_RGD_1 | 475 | 477 | PF01839 | 0.456 |
| LIG_LIR_Apic_2 | 355 | 361 | PF02991 | 0.522 |
| LIG_LIR_Gen_1 | 138 | 145 | PF02991 | 0.487 |
| LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.479 |
| LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.450 |
| LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.478 |
| LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.453 |
| LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.395 |
| LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.386 |
| LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.434 |
| LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.404 |
| LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.450 |
| LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.466 |
| LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.301 |
| LIG_PCNA_yPIPBox_3 | 486 | 497 | PF02747 | 0.456 |
| LIG_PCNA_yPIPBox_3 | 54 | 66 | PF02747 | 0.625 |
| LIG_Pex14_2 | 174 | 178 | PF04695 | 0.520 |
| LIG_PTB_Apo_2 | 448 | 455 | PF02174 | 0.295 |
| LIG_SH2_CRK | 35 | 39 | PF00017 | 0.496 |
| LIG_SH2_CRK | 358 | 362 | PF00017 | 0.485 |
| LIG_SH2_NCK_1 | 35 | 39 | PF00017 | 0.496 |
| LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.520 |
| LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.305 |
| LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.508 |
| LIG_SH3_1 | 54 | 60 | PF00018 | 0.652 |
| LIG_SH3_3 | 379 | 385 | PF00018 | 0.384 |
| LIG_SH3_3 | 54 | 60 | PF00018 | 0.556 |
| LIG_SH3_4 | 525 | 532 | PF00018 | 0.330 |
| LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.313 |
| LIG_SUMO_SIM_anti_2 | 554 | 560 | PF11976 | 0.311 |
| LIG_SUMO_SIM_par_1 | 309 | 318 | PF11976 | 0.362 |
| LIG_SUMO_SIM_par_1 | 404 | 411 | PF11976 | 0.389 |
| LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.313 |
| LIG_SUMO_SIM_par_1 | 554 | 560 | PF11976 | 0.384 |
| LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.458 |
| LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.415 |
| LIG_TRAF2_1 | 588 | 591 | PF00917 | 0.769 |
| LIG_TRFH_1 | 372 | 376 | PF08558 | 0.311 |
| LIG_UBA3_1 | 61 | 70 | PF00899 | 0.537 |
| LIG_WW_3 | 483 | 487 | PF00397 | 0.311 |
| MOD_CDK_SPK_2 | 107 | 112 | PF00069 | 0.569 |
| MOD_CDK_SPxxK_3 | 80 | 87 | PF00069 | 0.498 |
| MOD_CK1_1 | 135 | 141 | PF00069 | 0.448 |
| MOD_CK1_1 | 184 | 190 | PF00069 | 0.448 |
| MOD_CK1_1 | 401 | 407 | PF00069 | 0.423 |
| MOD_CK1_1 | 465 | 471 | PF00069 | 0.368 |
| MOD_CK1_1 | 527 | 533 | PF00069 | 0.222 |
| MOD_CK2_1 | 135 | 141 | PF00069 | 0.489 |
| MOD_CK2_1 | 212 | 218 | PF00069 | 0.607 |
| MOD_CK2_1 | 312 | 318 | PF00069 | 0.359 |
| MOD_CK2_1 | 359 | 365 | PF00069 | 0.379 |
| MOD_CK2_1 | 447 | 453 | PF00069 | 0.404 |
| MOD_CK2_1 | 531 | 537 | PF00069 | 0.378 |
| MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.481 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.515 |
| MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.408 |
| MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.311 |
| MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.576 |
| MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.651 |
| MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.463 |
| MOD_GSK3_1 | 131 | 138 | PF00069 | 0.686 |
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.385 |
| MOD_GSK3_1 | 324 | 331 | PF00069 | 0.407 |
| MOD_GSK3_1 | 340 | 347 | PF00069 | 0.441 |
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.342 |
| MOD_GSK3_1 | 408 | 415 | PF00069 | 0.295 |
| MOD_GSK3_1 | 462 | 469 | PF00069 | 0.222 |
| MOD_GSK3_1 | 521 | 528 | PF00069 | 0.313 |
| MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.473 |
| MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.510 |
| MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.456 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.701 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.555 |
| MOD_NEK2_1 | 418 | 423 | PF00069 | 0.410 |
| MOD_NEK2_1 | 432 | 437 | PF00069 | 0.214 |
| MOD_NEK2_1 | 536 | 541 | PF00069 | 0.372 |
| MOD_NEK2_2 | 499 | 504 | PF00069 | 0.354 |
| MOD_PIKK_1 | 135 | 141 | PF00454 | 0.472 |
| MOD_PKB_1 | 100 | 108 | PF00069 | 0.526 |
| MOD_Plk_1 | 194 | 200 | PF00069 | 0.510 |
| MOD_Plk_1 | 489 | 495 | PF00069 | 0.456 |
| MOD_Plk_1 | 589 | 595 | PF00069 | 0.566 |
| MOD_Plk_2-3 | 589 | 595 | PF00069 | 0.566 |
| MOD_Plk_4 | 212 | 218 | PF00069 | 0.574 |
| MOD_Plk_4 | 402 | 408 | PF00069 | 0.233 |
| MOD_Plk_4 | 462 | 468 | PF00069 | 0.384 |
| MOD_Plk_4 | 489 | 495 | PF00069 | 0.311 |
| MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.524 |
| MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.396 |
| MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.449 |
| MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.308 |
| MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.311 |
| MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.381 |
| MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.445 |
| MOD_SUMO_for_1 | 283 | 286 | PF00179 | 0.466 |
| MOD_SUMO_rev_2 | 510 | 516 | PF00179 | 0.300 |
| TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.603 |
| TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.508 |
| TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.453 |
| TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.492 |
| TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.508 |
| TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.525 |
| TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.695 |
| TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.503 |
| TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.489 |
| TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.311 |
| TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.510 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1V8 | Leptomonas seymouri | 75% | 100% |
| A0A1X0NXG3 | Trypanosomatidae | 58% | 100% |
| A0A3Q8IAY6 | Leishmania donovani | 93% | 100% |
| A0A3R7L6W3 | Trypanosoma rangeli | 62% | 100% |
| A4HZ00 | Leishmania infantum | 93% | 100% |
| A4QP75 | Danio rerio | 31% | 100% |
| A5IBU7 | Legionella pneumophila (strain Corby) | 25% | 100% |
| C9ZIM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
| E9AIL9 | Leishmania braziliensis | 85% | 100% |
| E9AUV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
| O31503 | Bacillus subtilis (strain 168) | 26% | 100% |
| P0DG16 | Streptococcus pyogenes serotype M3 (strain ATCC BAA-595 / MGAS315) | 25% | 100% |
| P0DG17 | Streptococcus pyogenes serotype M3 (strain SSI-1) | 25% | 100% |
| P33753 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 94% |
| P73374 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 26% | 100% |
| Q02I93 | Pseudomonas aeruginosa (strain UCBPP-PA14) | 26% | 100% |
| Q5HEM5 | Staphylococcus aureus (strain COL) | 26% | 100% |
| Q5HN37 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 24% | 100% |
| Q5WW81 | Legionella pneumophila (strain Lens) | 24% | 100% |
| Q5X5A8 | Legionella pneumophila (strain Paris) | 25% | 100% |
| Q5XAU1 | Streptococcus pyogenes serotype M6 (strain ATCC BAA-946 / MGAS10394) | 25% | 100% |
| Q5ZVI4 | Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) | 25% | 100% |
| Q6G836 | Staphylococcus aureus (strain MSSA476) | 26% | 100% |
| Q6GFG0 | Staphylococcus aureus (strain MRSA252) | 26% | 100% |
| Q73E18 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 26% | 100% |
| Q73EJ5 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 26% | 100% |
| Q74I68 | Lactobacillus johnsonii (strain CNCM I-12250 / La1 / NCC 533) | 26% | 100% |
| Q74N58 | Nanoarchaeum equitans (strain Kin4-M) | 25% | 100% |
| Q7A4Q9 | Staphylococcus aureus (strain N315) | 26% | 100% |
| Q7MVG9 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 28% | 100% |
| Q7NGN4 | Gloeobacter violaceus (strain ATCC 29082 / PCC 7421) | 28% | 100% |
| Q814A6 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 27% | 100% |
| Q81Z48 | Bacillus anthracis | 26% | 100% |
| Q81ZD6 | Bacillus anthracis | 27% | 100% |
| Q830R6 | Enterococcus faecalis (strain ATCC 700802 / V583) | 28% | 100% |
| Q891A0 | Clostridium tetani (strain Massachusetts / E88) | 24% | 100% |
| Q892Z2 | Clostridium tetani (strain Massachusetts / E88) | 27% | 100% |
| Q8AA22 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 27% | 100% |
| Q8BNV1 | Mus musculus | 32% | 98% |
| Q8CRU6 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 24% | 100% |
| Q8IZ69 | Homo sapiens | 31% | 96% |
| Q8L7S3 | Arabidopsis thaliana | 30% | 74% |
| Q8NVT4 | Staphylococcus aureus (strain MW2) | 26% | 100% |
| Q8P017 | Streptococcus pyogenes serotype M18 (strain MGAS8232) | 24% | 100% |
| Q8R5Z8 | Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / DSM 15643 / BCRC 10681 / CIP 101130 / JCM 8532 / KCTC 2640 / LMG 13131 / VPI 4355) | 25% | 100% |
| Q8R933 | Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) | 31% | 100% |
| Q8XIK5 | Clostridium perfringens (strain 13 / Type A) | 29% | 100% |
| Q8YR05 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 28% | 100% |
| Q97J51 | Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) | 28% | 100% |
| Q97LN4 | Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) | 28% | 100% |
| Q99SY9 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 26% | 100% |
| Q99YP3 | Streptococcus pyogenes serotype M1 | 25% | 100% |
| Q9CDP0 | Lactococcus lactis subsp. lactis (strain IL1403) | 26% | 100% |
| Q9CGB9 | Lactococcus lactis subsp. lactis (strain IL1403) | 27% | 100% |
| Q9I525 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 26% | 100% |
| V5ASX3 | Trypanosoma cruzi | 61% | 100% |