Publication identifier(s): 31356625
GPI-anchored cell surface protease. Broad-spectrum ectoenzyme involved in pathogenesis. Heavily expanded family in all parazitic species.. Localization: Cell surface (experimental)
                
                    by homology
Contact email: albert.descoteaux@iaf.inrs.ca
Publication title: The host cell secretory pathway mediates the export of Leishmania virulence factors out of the parasitophorous vacuole
Publication 1st author(s): Amandine Isnard
Publication Identifier(s): 25826301
Host organism: -1
Interaction detection method(s): protease assay
Interaction type: physical association
Identification method participant A: monoclonal antibody western blot
Identification method participant B: monoclonal antibody western blot
ID(s) interactor A: P05627
ID(s) interactor B: P08148
Taxid interactor A: Mus musculus
Taxid interactor B: Leishmania major
Biological role(s) interactor A: enzyme
Biological role(s) interactor B: enzyme target
Experimental role(s) interactor A: neutral component
                
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Cuervo et al. | no | yes: 0 | 
| Hassani et al. | no | yes: 0 | 
| Forrest at al. (metacyclic) | no | yes: 2 | 
| Forrest at al. (procyclic) | no | yes: 4 | 
| Silverman et al. | no | yes: 0 | 
| Pissara et al. | yes | yes: 51 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Pires et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Silverman et al. | no | yes: 5 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Jamdhade et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | yes | yes: 41, no: 8 | 
| NetGPI | no | yes: 0, no: 49 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 50 | 
| GO:0110165 | cellular anatomical entity | 1 | 50 | 
| GO:0005737 | cytoplasm | 2 | 4 | 
| GO:0018995 | host cellular component | 2 | 4 | 
| GO:0033643 | host cell part | 3 | 4 | 
| GO:0033646 | host intracellular part | 4 | 4 | 
| GO:0033647 | host intracellular organelle | 5 | 4 | 
| GO:0033648 | host intracellular membrane-bounded organelle | 6 | 4 | 
| GO:0042025 | host cell nucleus | 7 | 4 | 
Related structures:
AlphaFold database: A4H639
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 50 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 50 | 
| GO:0007155 | cell adhesion | 2 | 50 | 
| GO:0008152 | metabolic process | 1 | 50 | 
| GO:0009987 | cellular process | 1 | 50 | 
| GO:0019538 | protein metabolic process | 3 | 50 | 
| GO:0043170 | macromolecule metabolic process | 3 | 50 | 
| GO:0044238 | primary metabolic process | 2 | 50 | 
| GO:0071704 | organic substance metabolic process | 2 | 50 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 50 | 
| GO:0009966 | regulation of signal transduction | 4 | 4 | 
| GO:0010646 | regulation of cell communication | 4 | 4 | 
| GO:0010749 | regulation of nitric oxide mediated signal transduction | 6 | 4 | 
| GO:0023051 | regulation of signaling | 3 | 4 | 
| GO:0035821 | modulation of process of another organism | 2 | 4 | 
| GO:0044003 | modulation by symbiont of host process | 3 | 4 | 
| GO:0044068 | modulation by symbiont of host cellular process | 4 | 4 | 
| GO:0044081 | modulation by symbiont of host nitric oxide-mediated signal transduction | 5 | 4 | 
| GO:0044403 | biological process involved in symbiotic interaction | 2 | 4 | 
| GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 4 | 
| GO:0044501 | modulation of signal transduction in another organism | 3 | 4 | 
| GO:0048583 | regulation of response to stimulus | 3 | 4 | 
| GO:0050789 | regulation of biological process | 2 | 4 | 
| GO:0050794 | regulation of cellular process | 3 | 4 | 
| GO:0051701 | biological process involved in interaction with host | 3 | 4 | 
| GO:0052027 | modulation by symbiont of host signal transduction pathway | 4 | 4 | 
| GO:0065007 | biological regulation | 1 | 4 | 
| GO:0075130 | modulation by symbiont of host protein kinase-mediated signal transduction | 5 | 4 | 
| GO:1902531 | regulation of intracellular signal transduction | 5 | 4 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 50 | 
| GO:0004175 | endopeptidase activity | 4 | 50 | 
| GO:0004222 | metalloendopeptidase activity | 5 | 50 | 
| GO:0005488 | binding | 1 | 50 | 
| GO:0008233 | peptidase activity | 3 | 50 | 
| GO:0008237 | metallopeptidase activity | 4 | 50 | 
| GO:0016787 | hydrolase activity | 2 | 50 | 
| GO:0043167 | ion binding | 2 | 50 | 
| GO:0043169 | cation binding | 3 | 50 | 
| GO:0046872 | metal ion binding | 4 | 50 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 50 | 
| GO:0008047 | enzyme activator activity | 3 | 4 | 
| GO:0008160 | protein tyrosine phosphatase activator activity | 6 | 4 | 
| GO:0019208 | phosphatase regulator activity | 3 | 4 | 
| GO:0019211 | phosphatase activator activity | 4 | 4 | 
| GO:0019888 | protein phosphatase regulator activity | 4 | 4 | 
| GO:0030234 | enzyme regulator activity | 2 | 4 | 
| GO:0072542 | protein phosphatase activator activity | 5 | 4 | 
| GO:0098772 | molecular function regulator activity | 1 | 4 | 
| GO:0140677 | molecular function activator activity | 2 | 4 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 115 | 121 | PF00089 | 0.463 | 
| CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.700 | 
| CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.473 | 
| CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.584 | 
| CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.459 | 
| CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.713 | 
| CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.624 | 
| CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.472 | 
| CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.584 | 
| CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.459 | 
| CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.613 | 
| CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.601 | 
| CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.605 | 
| CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.466 | 
| CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.541 | 
| DEG_APCC_DBOX_1 | 527 | 535 | PF00400 | 0.373 | 
| DOC_CKS1_1 | 417 | 422 | PF01111 | 0.264 | 
| DOC_CYCLIN_yCln2_LP_2 | 331 | 337 | PF00134 | 0.346 | 
| DOC_MAPK_gen_1 | 182 | 192 | PF00069 | 0.251 | 
| DOC_MAPK_MEF2A_6 | 185 | 192 | PF00069 | 0.251 | 
| DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.428 | 
| DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.449 | 
| DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.337 | 
| DOC_PP4_MxPP_1 | 545 | 548 | PF00568 | 0.241 | 
| DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.574 | 
| DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.343 | 
| DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.420 | 
| DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.271 | 
| DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.274 | 
| DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.453 | 
| LIG_14-3-3_CanoR_1 | 10 | 15 | PF00244 | 0.642 | 
| LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.274 | 
| LIG_14-3-3_CanoR_1 | 415 | 420 | PF00244 | 0.310 | 
| LIG_14-3-3_CanoR_1 | 485 | 490 | PF00244 | 0.329 | 
| LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.417 | 
| LIG_14-3-3_CanoR_1 | 579 | 586 | PF00244 | 0.300 | 
| LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.434 | 
| LIG_AP2alpha_1 | 428 | 432 | PF02296 | 0.257 | 
| LIG_APCC_ABBA_1 | 152 | 157 | PF00400 | 0.453 | 
| LIG_APCC_ABBA_1 | 346 | 351 | PF00400 | 0.426 | 
| LIG_APCC_ABBA_1 | 468 | 473 | PF00400 | 0.453 | 
| LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.377 | 
| LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.316 | 
| LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.453 | 
| LIG_FHA_1 | 100 | 106 | PF00498 | 0.373 | 
| LIG_FHA_1 | 172 | 178 | PF00498 | 0.317 | 
| LIG_FHA_1 | 187 | 193 | PF00498 | 0.336 | 
| LIG_FHA_1 | 214 | 220 | PF00498 | 0.347 | 
| LIG_FHA_1 | 244 | 250 | PF00498 | 0.400 | 
| LIG_FHA_1 | 265 | 271 | PF00498 | 0.270 | 
| LIG_FHA_1 | 343 | 349 | PF00498 | 0.444 | 
| LIG_FHA_1 | 402 | 408 | PF00498 | 0.425 | 
| LIG_FHA_1 | 409 | 415 | PF00498 | 0.361 | 
| LIG_FHA_1 | 507 | 513 | PF00498 | 0.434 | 
| LIG_FHA_1 | 534 | 540 | PF00498 | 0.326 | 
| LIG_FHA_1 | 585 | 591 | PF00498 | 0.343 | 
| LIG_FHA_1 | 93 | 99 | PF00498 | 0.370 | 
| LIG_FHA_2 | 104 | 110 | PF00498 | 0.284 | 
| LIG_FHA_2 | 128 | 134 | PF00498 | 0.377 | 
| LIG_FHA_2 | 358 | 364 | PF00498 | 0.281 | 
| LIG_FHA_2 | 522 | 528 | PF00498 | 0.304 | 
| LIG_LIR_Apic_2 | 145 | 149 | PF02991 | 0.278 | 
| LIG_LIR_Apic_2 | 180 | 184 | PF02991 | 0.435 | 
| LIG_LIR_Apic_2 | 297 | 302 | PF02991 | 0.271 | 
| LIG_LIR_Apic_2 | 397 | 403 | PF02991 | 0.282 | 
| LIG_LIR_Apic_2 | 416 | 420 | PF02991 | 0.251 | 
| LIG_LIR_Gen_1 | 303 | 311 | PF02991 | 0.448 | 
| LIG_LIR_Gen_1 | 423 | 433 | PF02991 | 0.336 | 
| LIG_LIR_Gen_1 | 467 | 475 | PF02991 | 0.326 | 
| LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.420 | 
| LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.411 | 
| LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.372 | 
| LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.339 | 
| LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.334 | 
| LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.340 | 
| LIG_MLH1_MIPbox_1 | 260 | 264 | PF16413 | 0.262 | 
| LIG_Pex14_1 | 388 | 392 | PF04695 | 0.442 | 
| LIG_Pex14_2 | 259 | 263 | PF04695 | 0.390 | 
| LIG_Pex14_2 | 428 | 432 | PF04695 | 0.275 | 
| LIG_PTB_Apo_2 | 191 | 198 | PF02174 | 0.438 | 
| LIG_PTB_Apo_2 | 426 | 433 | PF02174 | 0.236 | 
| LIG_SH2_CRK | 299 | 303 | PF00017 | 0.268 | 
| LIG_SH2_CRK | 341 | 345 | PF00017 | 0.453 | 
| LIG_SH2_CRK | 400 | 404 | PF00017 | 0.286 | 
| LIG_SH2_CRK | 417 | 421 | PF00017 | 0.283 | 
| LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.260 | 
| LIG_SH2_GRB2like | 427 | 430 | PF00017 | 0.249 | 
| LIG_SH2_PTP2 | 549 | 552 | PF00017 | 0.449 | 
| LIG_SH2_PTP2 | 78 | 81 | PF00017 | 0.341 | 
| LIG_SH2_SRC | 146 | 149 | PF00017 | 0.295 | 
| LIG_SH2_SRC | 306 | 309 | PF00017 | 0.339 | 
| LIG_SH2_SRC | 549 | 552 | PF00017 | 0.449 | 
| LIG_SH2_STAP1 | 436 | 440 | PF00017 | 0.247 | 
| LIG_SH2_STAP1 | 510 | 514 | PF00017 | 0.453 | 
| LIG_SH2_STAT3 | 510 | 513 | PF00017 | 0.438 | 
| LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.320 | 
| LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.430 | 
| LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.413 | 
| LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.375 | 
| LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.437 | 
| LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.267 | 
| LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.384 | 
| LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.449 | 
| LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.383 | 
| LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.423 | 
| LIG_SH3_3 | 202 | 208 | PF00018 | 0.301 | 
| LIG_SH3_3 | 478 | 484 | PF00018 | 0.301 | 
| LIG_SH3_3 | 71 | 77 | PF00018 | 0.337 | 
| LIG_SUMO_SIM_par_1 | 604 | 609 | PF11976 | 0.289 | 
| LIG_TYR_ITIM | 304 | 309 | PF00017 | 0.436 | 
| LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.386 | 
| MOD_CDK_SPK_2 | 488 | 493 | PF00069 | 0.286 | 
| MOD_CDK_SPxK_1 | 41 | 47 | PF00069 | 0.416 | 
| MOD_CDK_SPxxK_3 | 486 | 493 | PF00069 | 0.255 | 
| MOD_CDK_SPxxK_3 | 521 | 528 | PF00069 | 0.463 | 
| MOD_CK1_1 | 203 | 209 | PF00069 | 0.530 | 
| MOD_CK1_1 | 317 | 323 | PF00069 | 0.473 | 
| MOD_CK1_1 | 469 | 475 | PF00069 | 0.328 | 
| MOD_CK1_1 | 5 | 11 | PF00069 | 0.666 | 
| MOD_CK1_1 | 69 | 75 | PF00069 | 0.297 | 
| MOD_CK2_1 | 357 | 363 | PF00069 | 0.543 | 
| MOD_CK2_1 | 521 | 527 | PF00069 | 0.345 | 
| MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.460 | 
| MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.323 | 
| MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.402 | 
| MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.475 | 
| MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.354 | 
| MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.474 | 
| MOD_GSK3_1 | 164 | 171 | PF00069 | 0.386 | 
| MOD_GSK3_1 | 186 | 193 | PF00069 | 0.533 | 
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.430 | 
| MOD_GSK3_1 | 416 | 423 | PF00069 | 0.324 | 
| MOD_GSK3_1 | 484 | 491 | PF00069 | 0.327 | 
| MOD_GSK3_1 | 578 | 585 | PF00069 | 0.249 | 
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.373 | 
| MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.369 | 
| MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.273 | 
| MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.336 | 
| MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.457 | 
| MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.382 | 
| MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.282 | 
| MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.271 | 
| MOD_N-GLC_2 | 378 | 380 | PF02516 | 0.345 | 
| MOD_NEK2_1 | 257 | 262 | PF00069 | 0.472 | 
| MOD_NEK2_1 | 264 | 269 | PF00069 | 0.368 | 
| MOD_NEK2_1 | 3 | 8 | PF00069 | 0.540 | 
| MOD_NEK2_1 | 428 | 433 | PF00069 | 0.356 | 
| MOD_NEK2_1 | 606 | 611 | PF00069 | 0.432 | 
| MOD_NEK2_2 | 258 | 263 | PF00069 | 0.276 | 
| MOD_PIKK_1 | 383 | 389 | PF00454 | 0.426 | 
| MOD_PK_1 | 10 | 16 | PF00069 | 0.633 | 
| MOD_PK_1 | 466 | 472 | PF00069 | 0.271 | 
| MOD_PKA_1 | 10 | 16 | PF00069 | 0.560 | 
| MOD_PKA_2 | 10 | 16 | PF00069 | 0.532 | 
| MOD_PKA_2 | 117 | 123 | PF00069 | 0.311 | 
| MOD_PKA_2 | 484 | 490 | PF00069 | 0.278 | 
| MOD_PKA_2 | 514 | 520 | PF00069 | 0.359 | 
| MOD_PKA_2 | 57 | 63 | PF00069 | 0.380 | 
| MOD_PKA_2 | 578 | 584 | PF00069 | 0.262 | 
| MOD_PKB_1 | 399 | 407 | PF00069 | 0.307 | 
| MOD_Plk_1 | 342 | 348 | PF00069 | 0.288 | 
| MOD_Plk_1 | 383 | 389 | PF00069 | 0.453 | 
| MOD_Plk_1 | 428 | 434 | PF00069 | 0.295 | 
| MOD_Plk_1 | 466 | 472 | PF00069 | 0.286 | 
| MOD_Plk_2-3 | 133 | 139 | PF00069 | 0.445 | 
| MOD_Plk_4 | 142 | 148 | PF00069 | 0.346 | 
| MOD_Plk_4 | 258 | 264 | PF00069 | 0.376 | 
| MOD_Plk_4 | 420 | 426 | PF00069 | 0.376 | 
| MOD_Plk_4 | 428 | 434 | PF00069 | 0.315 | 
| MOD_Plk_4 | 539 | 545 | PF00069 | 0.378 | 
| MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.416 | 
| MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.288 | 
| MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.293 | 
| MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.543 | 
| MOD_SUMO_for_1 | 327 | 330 | PF00179 | 0.386 | 
| MOD_SUMO_rev_2 | 176 | 184 | PF00179 | 0.395 | 
| TRG_DiLeu_BaEn_3 | 137 | 143 | PF01217 | 0.319 | 
| TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.486 | 
| TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.543 | 
| TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.377 | 
| TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.425 | 
| TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.518 | 
| TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.538 | 
| TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.386 | 
| TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.627 | 
| TRG_ER_diArg_1 | 158 | 161 | PF00400 | 0.284 | 
| TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.310 | 
| TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.305 | 
| TRG_ER_diArg_1 | 573 | 575 | PF00400 | 0.402 | 
| TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.273 | 
| TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.356 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1IL11 | Leptomonas seymouri | 36% | 93% | 
| A0A0S4IN60 | Bodo saltans | 32% | 68% | 
| A0A0S4IUT6 | Bodo saltans | 30% | 74% | 
| A0A0S4IUU1 | Bodo saltans | 31% | 93% | 
| A0A0S4IYM3 | Bodo saltans | 30% | 84% | 
| A0A1X0NDG7 | Trypanosomatidae | 29% | 94% | 
| A0A1X0NDJ3 | Trypanosomatidae | 27% | 85% | 
| A0A1X0NDK2 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NDK7 | Trypanosomatidae | 30% | 86% | 
| A0A1X0NDK9 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NDM7 | Trypanosomatidae | 30% | 95% | 
| A0A1X0NDU8 | Trypanosomatidae | 28% | 92% | 
| A0A1X0NE71 | Trypanosomatidae | 29% | 100% | 
| A0A1X0NER9 | Trypanosomatidae | 33% | 95% | 
| A0A1X0NET7 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NEX7 | Trypanosomatidae | 34% | 93% | 
| A0A1X0NEZ6 | Trypanosomatidae | 30% | 93% | 
| A0A1X0NF32 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NF41 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NFJ0 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NFK3 | Trypanosomatidae | 30% | 91% | 
| A0A1X0NFS0 | Trypanosomatidae | 32% | 70% | 
| A0A1X0NFT1 | Trypanosomatidae | 31% | 67% | 
| A0A1X0NFU4 | Trypanosomatidae | 27% | 75% | 
| A0A1X0NG20 | Trypanosomatidae | 30% | 99% | 
| A0A1X0NGP3 | Trypanosomatidae | 28% | 71% | 
| A0A1X0NGY3 | Trypanosomatidae | 30% | 80% | 
| A0A1X0NGZ3 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NH86 | Trypanosomatidae | 31% | 69% | 
| A0A1X0NHP6 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NHQ6 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NI38 | Trypanosomatidae | 29% | 70% | 
| A0A1X0NI74 | Trypanosomatidae | 30% | 82% | 
| A0A1X0NII4 | Trypanosomatidae | 30% | 73% | 
| A0A1X0NIZ3 | Trypanosomatidae | 32% | 100% | 
| A0A1X0NJS3 | Trypanosomatidae | 28% | 93% | 
| A0A1X0NJU4 | Trypanosomatidae | 29% | 71% | 
| A0A1X0NK29 | Trypanosomatidae | 31% | 66% | 
| A0A1X0NK66 | Trypanosomatidae | 33% | 92% | 
| A0A1X0NKJ8 | Trypanosomatidae | 29% | 82% | 
| A0A1X0NKW9 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NME2 | Trypanosomatidae | 31% | 97% | 
| A0A1X0NMK3 | Trypanosomatidae | 28% | 100% | 
| A0A1X0NMK7 | Trypanosomatidae | 36% | 100% | 
| A0A1X0NMV0 | Trypanosomatidae | 32% | 83% | 
| A0A1X0NN43 | Trypanosomatidae | 30% | 85% | 
| A0A1X0NNK8 | Trypanosomatidae | 32% | 93% | 
| A0A1X0NP64 | Trypanosomatidae | 30% | 69% | 
| A0A1X0NPW0 | Trypanosomatidae | 31% | 95% | 
| A0A1X0NQM4 | Trypanosomatidae | 35% | 100% | 
| A0A1X0NQN3 | Trypanosomatidae | 34% | 100% | 
| A0A1X0NQU4 | Trypanosomatidae | 35% | 95% | 
| A0A1X0NQW6 | Trypanosomatidae | 32% | 100% | 
| A0A1X0NRF3 | Trypanosomatidae | 33% | 91% | 
| A0A1X0NRY8 | Trypanosomatidae | 35% | 100% | 
| A0A1X0NU16 | Trypanosomatidae | 35% | 100% | 
| A0A1X0NUR2 | Trypanosomatidae | 31% | 83% | 
| A0A1X0NV28 | Trypanosomatidae | 36% | 100% | 
| A0A1X0NVE0 | Trypanosomatidae | 29% | 78% | 
| A0A1X0NW07 | Trypanosomatidae | 27% | 98% | 
| A0A1X0NX94 | Trypanosomatidae | 32% | 94% | 
| A0A1X0NX98 | Trypanosomatidae | 31% | 76% | 
| A0A1X0NXB6 | Trypanosomatidae | 30% | 87% | 
| A0A1X0NXH6 | Trypanosomatidae | 33% | 84% | 
| A0A1X0NXQ4 | Trypanosomatidae | 28% | 90% | 
| A0A1X0NXR7 | Trypanosomatidae | 34% | 81% | 
| A0A1X0NYE3 | Trypanosomatidae | 30% | 98% | 
| A0A1X0NYE7 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NYN2 | Trypanosomatidae | 34% | 100% | 
| A0A1X0NYN4 | Trypanosomatidae | 26% | 86% | 
| A0A1X0NYS5 | Trypanosomatidae | 32% | 100% | 
| A0A1X0NYZ2 | Trypanosomatidae | 36% | 100% | 
| A0A1X0NZ46 | Trypanosomatidae | 26% | 100% | 
| A0A1X0NZ63 | Trypanosomatidae | 30% | 96% | 
| A0A1X0NZN6 | Trypanosomatidae | 28% | 94% | 
| A0A1X0P055 | Trypanosomatidae | 36% | 100% | 
| A0A1X0P154 | Trypanosomatidae | 28% | 100% | 
| A0A1X0P331 | Trypanosomatidae | 33% | 100% | 
| A0A1X0P3K0 | Trypanosomatidae | 27% | 84% | 
| A0A1X0P3S2 | Trypanosomatidae | 28% | 100% | 
| A0A1X0P4L8 | Trypanosomatidae | 32% | 100% | 
| A0A1X0P4Y5 | Trypanosomatidae | 28% | 95% | 
| A0A1X0P544 | Trypanosomatidae | 31% | 95% | 
| A0A1X0P5J0 | Trypanosomatidae | 32% | 89% | 
| A0A1X0P7K5 | Trypanosomatidae | 29% | 69% | 
| A0A1X0P7R3 | Trypanosomatidae | 35% | 100% | 
| A0A1X0P8B4 | Trypanosomatidae | 32% | 100% | 
| A0A1X0P9Z4 | Trypanosomatidae | 33% | 100% | 
| A0A1X0PB04 | Trypanosomatidae | 33% | 100% | 
| A0A3Q8I8N3 | Leishmania donovani | 65% | 100% | 
| A0A3Q8I8P8 | Leishmania donovani | 67% | 100% | 
| A0A3Q8I8S6 | Leishmania donovani | 68% | 95% | 
| A0A3Q8I8S9 | Leishmania donovani | 67% | 100% | 
| A0A3Q8IAZ8 | Leishmania donovani | 65% | 100% | 
| A0A3Q8IC35 | Leishmania donovani | 65% | 100% | 
| A0A3Q8IC44 | Leishmania donovani | 67% | 100% | 
| A0A3Q8IH61 | Leishmania donovani | 68% | 100% | 
| A0A3Q8IIN4 | Leishmania donovani | 38% | 96% | 
| A0A3R7JT49 | Trypanosoma rangeli | 35% | 72% | 
| A0A3R7JTB6 | Trypanosoma rangeli | 33% | 87% | 
| A0A3R7JV87 | Trypanosoma rangeli | 34% | 100% | 
| A0A3R7K7T9 | Trypanosoma rangeli | 33% | 100% | 
| A0A3R7K9S1 | Trypanosoma rangeli | 34% | 100% | 
| A0A3R7KB14 | Trypanosoma rangeli | 35% | 70% | 
| A0A3R7KLR6 | Trypanosoma rangeli | 33% | 95% | 
| A0A3R7KMY2 | Trypanosoma rangeli | 34% | 91% | 
| A0A3R7LFC4 | Trypanosoma rangeli | 34% | 91% | 
| A0A3R7LFZ4 | Trypanosoma rangeli | 35% | 100% | 
| A0A3R7LWG1 | Trypanosoma rangeli | 34% | 100% | 
| A0A3R7LX11 | Trypanosoma rangeli | 36% | 100% | 
| A0A3R7M1R8 | Trypanosoma rangeli | 35% | 100% | 
| A0A3R7M574 | Trypanosoma rangeli | 34% | 95% | 
| A0A3R7M7N6 | Trypanosoma rangeli | 35% | 89% | 
| A0A3R7MTS2 | Trypanosoma rangeli | 37% | 100% | 
| A0A3R7MW36 | Trypanosoma rangeli | 34% | 100% | 
| A0A3R7MXF4 | Trypanosoma rangeli | 35% | 100% | 
| A0A3R7N1W7 | Trypanosoma rangeli | 35% | 100% | 
| A0A3R7N289 | Trypanosoma rangeli | 34% | 84% | 
| A0A3R7NTI8 | Trypanosoma rangeli | 35% | 100% | 
| A0A3R7R2J4 | Trypanosoma rangeli | 33% | 95% | 
| A0A3R7R5R1 | Trypanosoma rangeli | 34% | 100% | 
| A0A3R7R818 | Trypanosoma rangeli | 31% | 100% | 
| A0A3S5H6G0 | Leishmania donovani | 67% | 100% | 
| A0A3S5IQY2 | Trypanosoma rangeli | 37% | 100% | 
| A0A3S7WR43 | Leishmania donovani | 65% | 100% | 
| A0A3S7WR46 | Leishmania donovani | 67% | 100% | 
| A0A3S7WR60 | Leishmania donovani | 68% | 100% | 
| A0A3S7X192 | Leishmania donovani | 37% | 100% | 
| A0A422MRQ6 | Trypanosoma rangeli | 35% | 82% | 
| A0A422MU95 | Trypanosoma rangeli | 36% | 100% | 
| A0A422MVF5 | Trypanosoma rangeli | 32% | 100% | 
| A0A422MVS3 | Trypanosoma rangeli | 34% | 100% | 
| A0A422MW99 | Trypanosoma rangeli | 32% | 82% | 
| A0A422MZ47 | Trypanosoma rangeli | 36% | 100% | 
| A0A422MZG4 | Trypanosoma rangeli | 36% | 100% | 
| A0A422N361 | Trypanosoma rangeli | 33% | 100% | 
| A0A422N7Q6 | Trypanosoma rangeli | 33% | 94% | 
| A0A422NDS2 | Trypanosoma rangeli | 34% | 100% | 
| A0A422NDT3 | Trypanosoma rangeli | 31% | 100% | 
| A0A422NP82 | Trypanosoma rangeli | 36% | 100% | 
| A4H626 | Leishmania braziliensis | 69% | 100% | 
| A4H627 | Leishmania braziliensis | 64% | 99% | 
| A4H630 | Leishmania braziliensis | 87% | 100% | 
| A4H631 | Leishmania braziliensis | 70% | 99% | 
| A4H632 | Leishmania braziliensis | 82% | 100% | 
| A4H633 | Leishmania braziliensis | 69% | 100% | 
| A4H634 | Leishmania braziliensis | 82% | 100% | 
| A4H635 | Leishmania braziliensis | 81% | 100% | 
| A4H636 | Leishmania braziliensis | 69% | 100% | 
| A4H637 | Leishmania braziliensis | 80% | 99% | 
| A4H638 | Leishmania braziliensis | 84% | 99% | 
| A4H640 | Leishmania braziliensis | 80% | 98% | 
| A4H6D3 | Leishmania braziliensis | 67% | 100% | 
| A4H6D5 | Leishmania braziliensis | 68% | 86% | 
| A4H6D7 | Leishmania braziliensis | 64% | 100% | 
| A4H6D8 | Leishmania braziliensis | 68% | 100% | 
| A4H6D9 | Leishmania braziliensis | 68% | 100% | 
| A4H6E0 | Leishmania braziliensis | 69% | 86% | 
| A4H6E1 | Leishmania braziliensis | 66% | 100% | 
| A4H6E2 | Leishmania braziliensis | 66% | 100% | 
| A4H6E3 | Leishmania braziliensis | 67% | 100% | 
| A4H6E5 | Leishmania braziliensis | 84% | 100% | 
| A4HJI2 | Leishmania braziliensis | 37% | 94% | 
| A4HUF6 | Leishmania infantum | 65% | 100% | 
| A4HUF8 | Leishmania infantum | 67% | 100% | 
| A4HUF9 | Leishmania infantum | 68% | 95% | 
| A4HUG0 | Leishmania infantum | 66% | 80% | 
| A4I6X5 | Leishmania infantum | 38% | 96% | 
| C9ZUT5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% | 
| D0A1R8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% | 
| D0A7S8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 91% | 
| D0A855 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 99% | 
| E9AHH5 | Leishmania infantum | 37% | 100% | 
| E9AN53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 93% | 
| E9AN54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% | 
| E9AN55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 95% | 
| E9AN56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 95% | 
| E9AN57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% | 
| E9AZL8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% | 
| E9B1Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 96% | 
| O62446 | Caenorhabditis elegans | 26% | 92% | 
| P08148 | Leishmania major | 66% | 100% | 
| P15706 | Leishmania chagasi | 67% | 100% | 
| P23223 | Leishmania donovani | 67% | 100% | 
| P43150 | Leishmania mexicana | 65% | 95% | 
| Q00689 | Leishmania guyanensis | 82% | 98% | 
| Q06031 | Crithidia fasciculata | 52% | 94% | 
| Q27673 | Leishmania amazonensis | 66% | 100% | 
| Q29AK2 | Drosophila pseudoobscura pseudoobscura | 25% | 89% | 
| Q4Q662 | Leishmania major | 36% | 100% | 
| Q4Q8L3 | Leishmania major | 37% | 100% | 
| Q4QHG9 | Leishmania major | 65% | 99% | 
| Q4QHH0 | Leishmania major | 67% | 100% | 
| Q4QHH1 | Leishmania major | 66% | 99% | 
| Q4QHH2 | Leishmania major | 66% | 99% | 
| Q61YG1 | Caenorhabditis briggsae | 26% | 92% | 
| Q6LA77 | Leishmania infantum | 67% | 100% | 
| Q8BMN4 | Mus musculus | 25% | 90% | 
| Q8MNZ1 | Leishmania tropica | 67% | 93% | 
| Q96KR4 | Homo sapiens | 21% | 93% | 
| Q9VH19 | Drosophila melanogaster | 24% | 89% | 
| V5A359 | Trypanosoma cruzi | 38% | 100% | 
| V5A488 | Trypanosoma cruzi | 34% | 76% | 
| V5AII7 | Trypanosoma cruzi | 39% | 100% | 
| V5APQ4 | Trypanosoma cruzi | 35% | 77% | 
| V5AX72 | Trypanosoma cruzi | 36% | 83% | 
| V5B5M0 | Trypanosoma cruzi | 35% | 83% | 
| V5B9W5 | Trypanosoma cruzi | 29% | 90% | 
| V5BAL3 | Trypanosoma cruzi | 38% | 100% | 
| V5BAN1 | Trypanosoma cruzi | 35% | 78% | 
| V5BD39 | Trypanosoma cruzi | 41% | 100% | 
| V5BLT3 | Trypanosoma cruzi | 32% | 97% | 
| V5CI97 | Trypanosoma cruzi | 32% | 96% | 
| V5D358 | Trypanosoma cruzi | 34% | 72% |