Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 93 |
NetGPI | no | yes: 0, no: 94 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0016020 | membrane | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: Q4Q9U3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 95 |
GO:0006807 | nitrogen compound metabolic process | 2 | 95 |
GO:0008152 | metabolic process | 1 | 95 |
GO:0019538 | protein metabolic process | 3 | 95 |
GO:0043170 | macromolecule metabolic process | 3 | 95 |
GO:0044238 | primary metabolic process | 2 | 95 |
GO:0071704 | organic substance metabolic process | 2 | 95 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 95 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 95 |
GO:0004175 | endopeptidase activity | 4 | 95 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 95 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 95 |
GO:0008233 | peptidase activity | 3 | 95 |
GO:0008234 | cysteine-type peptidase activity | 4 | 95 |
GO:0016787 | hydrolase activity | 2 | 95 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 95 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.438 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 74 | 78 | PF03568 | 0.152 |
DEG_MDM2_SWIB_1 | 474 | 481 | PF02201 | 0.443 |
DEG_SCF_TRCP1_1 | 80 | 85 | PF00400 | 0.156 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.454 |
DOC_CYCLIN_RxL_1 | 360 | 368 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 157 | 167 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 208 | 216 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 371 | 380 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 599 | 609 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 623 | 630 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 551 | 559 | PF00069 | 0.304 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.348 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.357 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 123 | 127 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 209 | 213 | PF12436 | 0.349 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.353 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 592 | 597 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 611 | 621 | PF00244 | 0.490 |
LIG_Actin_WH2_2 | 373 | 391 | PF00022 | 0.524 |
LIG_APCC_ABBAyCdc20_2 | 162 | 168 | PF00400 | 0.351 |
LIG_BIR_III_2 | 10 | 14 | PF00653 | 0.627 |
LIG_BRCT_BRCA1_1 | 481 | 485 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.452 |
LIG_CNOT1_NIM_1 | 498 | 507 | PF04054 | 0.208 |
LIG_deltaCOP1_diTrp_1 | 308 | 313 | PF00928 | 0.523 |
LIG_deltaCOP1_diTrp_1 | 42 | 46 | PF00928 | 0.224 |
LIG_deltaCOP1_diTrp_1 | 442 | 447 | PF00928 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 477 | 485 | PF00928 | 0.458 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.461 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.465 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.305 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.488 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.407 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.316 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.329 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.437 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.453 |
LIG_IRF3_LxIS_1 | 273 | 278 | PF10401 | 0.538 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 549 | 559 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 700 | 705 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 477 | 481 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 700 | 704 | PF02991 | 0.541 |
LIG_LYPXL_yS_3 | 457 | 460 | PF13949 | 0.411 |
LIG_MLH1_MIPbox_1 | 481 | 485 | PF16413 | 0.503 |
LIG_PCNA_yPIPBox_3 | 267 | 281 | PF02747 | 0.434 |
LIG_Pex14_1 | 372 | 376 | PF04695 | 0.339 |
LIG_Pex14_1 | 400 | 404 | PF04695 | 0.339 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.447 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.452 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.386 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.448 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.449 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.333 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.469 |
LIG_SH2_PTP2 | 532 | 535 | PF00017 | 0.371 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.310 |
LIG_SH2_STAT3 | 332 | 335 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.340 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.447 |
LIG_SH3_4 | 12 | 19 | PF00018 | 0.512 |
LIG_SUMO_SIM_anti_2 | 516 | 523 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 555 | 561 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 626 | 632 | PF11976 | 0.419 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.165 |
LIG_UBA3_1 | 216 | 223 | PF00899 | 0.353 |
LIG_UBA3_1 | 35 | 40 | PF00899 | 0.327 |
LIG_UBA3_1 | 365 | 374 | PF00899 | 0.467 |
LIG_UBA3_1 | 519 | 525 | PF00899 | 0.196 |
LIG_WRC_WIRS_1 | 507 | 512 | PF05994 | 0.494 |
LIG_WRC_WIRS_1 | 658 | 663 | PF05994 | 0.427 |
MOD_CDK_SPK_2 | 218 | 223 | PF00069 | 0.523 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.326 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.477 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.441 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.467 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.457 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.373 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.277 |
MOD_CMANNOS | 475 | 478 | PF00535 | 0.251 |
MOD_Cter_Amidation | 692 | 695 | PF01082 | 0.587 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.402 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.504 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.294 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.300 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.274 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.273 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.297 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.257 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.313 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.442 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.435 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.322 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.496 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.477 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.494 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.355 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.453 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.372 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.335 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.153 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.262 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.295 |
MOD_N-GLC_1 | 523 | 528 | PF02516 | 0.420 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.453 |
MOD_N-GLC_1 | 573 | 578 | PF02516 | 0.372 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.297 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.318 |
MOD_N-GLC_2 | 3 | 5 | PF02516 | 0.407 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.409 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.476 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.453 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.507 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.474 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.445 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.409 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.542 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.433 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.289 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.492 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.514 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.491 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.408 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.332 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.419 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.534 |
MOD_PIKK_1 | 629 | 635 | PF00454 | 0.490 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.453 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.457 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.491 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.465 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.381 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.503 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.322 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.442 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.320 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.466 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.474 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.362 |
MOD_SUMO_rev_2 | 10 | 17 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 546 | 553 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 89 | 98 | PF00179 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.256 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.451 |
TRG_NLS_Bipartite_1 | 611 | 627 | PF00514 | 0.544 |
TRG_NLS_MonoExtC_3 | 361 | 367 | PF00514 | 0.346 |
TRG_NLS_MonoExtC_3 | 690 | 695 | PF00514 | 0.531 |
TRG_NLS_MonoExtN_4 | 622 | 627 | PF00514 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 36% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 72% |
A0A0N1IGQ2 | Leptomonas seymouri | 70% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 33% | 90% |
A0A0N1P9P1 | Leptomonas seymouri | 30% | 83% |
A0A0N1PCA9 | Leptomonas seymouri | 28% | 96% |
A0A0N1PE91 | Leptomonas seymouri | 23% | 79% |
A0A0N1PFI4 | Leptomonas seymouri | 32% | 91% |
A0A0S4JLK6 | Bodo saltans | 33% | 87% |
A0A0S4JS70 | Bodo saltans | 24% | 92% |
A0A0S4KGT2 | Bodo saltans | 38% | 93% |
A0A1X0NJ61 | Trypanosomatidae | 45% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 33% | 93% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 91% |
A0A1X0NKT7 | Trypanosomatidae | 28% | 89% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 86% |
A0A1X0NMT3 | Trypanosomatidae | 33% | 83% |
A0A1X0NW84 | Trypanosomatidae | 34% | 100% |
A0A1X0NW85 | Trypanosomatidae | 31% | 100% |
A0A1X0NW89 | Trypanosomatidae | 34% | 82% |
A0A1X0NWA6 | Trypanosomatidae | 27% | 81% |
A0A1X0NWW1 | Trypanosomatidae | 34% | 98% |
A0A3Q8IBS3 | Leishmania donovani | 34% | 77% |
A0A3Q8IDD4 | Leishmania donovani | 97% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 94% |
A0A3S5H5A5 | Leishmania donovani | 31% | 82% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 91% |
A0A3S7WW18 | Leishmania donovani | 34% | 86% |
A0A3S7WW41 | Leishmania donovani | 29% | 95% |
A0A3S7WW71 | Leishmania donovani | 35% | 100% |
A0A3S7X430 | Leishmania donovani | 33% | 90% |
A0A3S7X438 | Leishmania donovani | 28% | 75% |
A0A3S7X460 | Leishmania donovani | 35% | 91% |
A0A3S7X463 | Leishmania donovani | 27% | 75% |
A0A3S7X470 | Leishmania donovani | 32% | 97% |
A0A422MYU1 | Trypanosoma rangeli | 33% | 77% |
A0A422MYX0 | Trypanosoma rangeli | 33% | 97% |
A4H3W4 | Leishmania braziliensis | 31% | 82% |
A4HE81 | Leishmania braziliensis | 83% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 90% |
A4HJ21 | Leishmania braziliensis | 24% | 79% |
A4HJ22 | Leishmania braziliensis | 31% | 74% |
A4HJ23 | Leishmania braziliensis | 32% | 100% |
A4HJ24 | Leishmania braziliensis | 36% | 99% |
A4HS39 | Leishmania infantum | 31% | 82% |
A4HYN0 | Leishmania infantum | 34% | 86% |
A4HYW1 | Leishmania infantum | 34% | 70% |
A4HYW2 | Leishmania infantum | 35% | 100% |
A4HYW3 | Leishmania infantum | 29% | 95% |
A4HYW4 | Leishmania infantum | 25% | 71% |
A4I1J4 | Leishmania infantum | 97% | 100% |
A4I6E4 | Leishmania infantum | 32% | 97% |
A4I6E6 | Leishmania infantum | 35% | 91% |
A4I6F0 | Leishmania infantum | 28% | 75% |
A4I6K4 | Leishmania infantum | 33% | 90% |
A4I6K5 | Leishmania infantum | 25% | 75% |
A4I6K6 | Leishmania infantum | 25% | 94% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 96% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 89% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 83% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 88% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 82% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 75% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 90% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AIH1 | Leishmania braziliensis | 34% | 86% |
E9AIH3 | Leishmania braziliensis | 33% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 95% |
E9AIH6 | Leishmania braziliensis | 24% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 88% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 75% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 95% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 90% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 75% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 94% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q22036 | Caenorhabditis elegans | 27% | 100% |
Q4Q6L7 | Leishmania major | 35% | 96% |
Q4Q6L9 | Leishmania major | 32% | 98% |
Q4Q6M0 | Leishmania major | 29% | 75% |
Q4Q6M2 | Leishmania major | 22% | 94% |
Q4Q6M3 | Leishmania major | 27% | 76% |
Q4Q6M4 | Leishmania major | 33% | 82% |
Q4QCS6 | Leishmania major | 29% | 95% |
Q4QCS7 | Leishmania major | 35% | 100% |
Q4QCS8 | Leishmania major | 34% | 86% |
Q4QCS9 | Leishmania major | 34% | 72% |
Q9U0T9 | Leishmania major | 30% | 83% |
V5AYJ1 | Trypanosoma cruzi | 35% | 99% |
V5B5I4 | Trypanosoma cruzi | 33% | 84% |
V5BA05 | Trypanosoma cruzi | 34% | 100% |
V5BEL3 | Trypanosoma cruzi | 34% | 100% |
V5BN20 | Trypanosoma cruzi | 33% | 91% |
V5D5V8 | Trypanosoma cruzi | 29% | 95% |
V5D9Y2 | Trypanosoma cruzi | 30% | 83% |
V5DES7 | Trypanosoma cruzi | 31% | 89% |