Proteases, calpain-like cysteine peptidase
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. | yes | 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: 2, no: 102 |
NetGPI | no | yes: 0, no: 104 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
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 |
GO:0005930 | axoneme | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HYN0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 105 |
GO:0006807 | nitrogen compound metabolic process | 2 | 105 |
GO:0008152 | metabolic process | 1 | 105 |
GO:0019538 | protein metabolic process | 3 | 105 |
GO:0043170 | macromolecule metabolic process | 3 | 105 |
GO:0044238 | primary metabolic process | 2 | 105 |
GO:0071704 | organic substance metabolic process | 2 | 105 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 105 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 105 |
GO:0004175 | endopeptidase activity | 4 | 105 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 105 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 105 |
GO:0008233 | peptidase activity | 3 | 105 |
GO:0008234 | cysteine-type peptidase activity | 4 | 105 |
GO:0016787 | hydrolase activity | 2 | 105 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 105 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 617 | 621 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.372 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 804 | 806 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 774 | 776 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 804 | 806 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.161 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 716 | 720 | PF00082 | 0.438 |
DEG_SCF_FBW7_2 | 156 | 161 | PF00400 | 0.496 |
DEG_SIAH_1 | 117 | 125 | PF03145 | 0.347 |
DOC_PP1_RVXF_1 | 419 | 425 | PF00149 | 0.457 |
DOC_PP1_RVXF_1 | 577 | 584 | PF00149 | 0.515 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.275 |
DOC_PP4_FxxP_1 | 322 | 325 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 402 | 405 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.621 |
DOC_USP7_MATH_2 | 355 | 361 | PF00917 | 0.512 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.456 |
DOC_USP7_UBL2_3 | 619 | 623 | PF12436 | 0.482 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 421 | 425 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 711 | 720 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 257 | 274 | PF00022 | 0.309 |
LIG_Actin_WH2_2 | 432 | 449 | PF00022 | 0.540 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.477 |
LIG_BIR_III_2 | 595 | 599 | PF00653 | 0.362 |
LIG_BRCT_BRCA1_1 | 769 | 773 | PF00533 | 0.452 |
LIG_Clathr_ClatBox_1 | 793 | 797 | PF01394 | 0.541 |
LIG_CtBP_PxDLS_1 | 355 | 359 | PF00389 | 0.364 |
LIG_deltaCOP1_diTrp_1 | 582 | 587 | PF00928 | 0.453 |
LIG_deltaCOP1_diTrp_1 | 715 | 719 | PF00928 | 0.408 |
LIG_eIF4E_1 | 544 | 550 | PF01652 | 0.471 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.589 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.313 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.448 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.415 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.430 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.392 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.491 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.491 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.467 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.553 |
LIG_LIR_Apic_2 | 187 | 192 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 464 | 475 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 490 | 497 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 508 | 519 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 542 | 550 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 663 | 669 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 714 | 725 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 436 | 441 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 663 | 668 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 697 | 702 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 714 | 720 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 770 | 776 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 784 | 789 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 9 | 13 | PF02991 | 0.500 |
LIG_PDZ_Class_3 | 816 | 821 | PF00595 | 0.476 |
LIG_Pex14_2 | 614 | 618 | PF04695 | 0.454 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.451 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.451 |
LIG_SH2_CRK | 522 | 526 | PF00017 | 0.473 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.446 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.381 |
LIG_SH2_CRK | 699 | 703 | PF00017 | 0.460 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.489 |
LIG_SH2_GRB2like | 280 | 283 | PF00017 | 0.497 |
LIG_SH2_GRB2like | 624 | 627 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 544 | 548 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 86 | 90 | PF00017 | 0.489 |
LIG_SH2_NCK_1 | 93 | 97 | PF00017 | 0.473 |
LIG_SH2_PTP2 | 736 | 739 | PF00017 | 0.371 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 638 | 642 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.736 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.779 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.750 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 754 | 757 | PF00017 | 0.334 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.297 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.505 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.539 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.359 |
LIG_SH3_3 | 745 | 751 | PF00018 | 0.575 |
LIG_SH3_3 | 793 | 799 | PF00018 | 0.437 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.677 |
LIG_SH3_5 | 636 | 640 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 724 | 729 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 652 | 658 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 684 | 689 | PF11976 | 0.360 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.788 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.786 |
LIG_TYR_ITIM | 194 | 199 | PF00017 | 0.321 |
LIG_UBA3_1 | 194 | 202 | PF00899 | 0.327 |
LIG_UBA3_1 | 613 | 619 | PF00899 | 0.362 |
LIG_UBA3_1 | 727 | 735 | PF00899 | 0.430 |
LIG_WRPW_2 | 342 | 345 | PF00400 | 0.362 |
MOD_CDK_SPxK_1 | 525 | 531 | PF00069 | 0.468 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.475 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.427 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.480 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.728 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.443 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.537 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.354 |
MOD_CMANNOS | 615 | 618 | PF00535 | 0.255 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.515 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.530 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.287 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.291 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.246 |
MOD_GlcNHglycan | 582 | 586 | PF01048 | 0.310 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.468 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.413 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.442 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.454 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.476 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.421 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.299 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.322 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.704 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.585 |
MOD_N-GLC_1 | 703 | 708 | PF02516 | 0.375 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.488 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.262 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.371 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.467 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.494 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.464 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.514 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.455 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.416 |
MOD_NEK2_2 | 491 | 496 | PF00069 | 0.541 |
MOD_NEK2_2 | 767 | 772 | PF00069 | 0.521 |
MOD_OFUCOSY | 181 | 188 | PF10250 | 0.171 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.522 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.338 |
MOD_PIKK_1 | 811 | 817 | PF00454 | 0.549 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.436 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.551 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.563 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.308 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.276 |
MOD_Plk_1 | 497 | 503 | PF00069 | 0.497 |
MOD_Plk_1 | 723 | 729 | PF00069 | 0.355 |
MOD_Plk_1 | 767 | 773 | PF00069 | 0.440 |
MOD_Plk_2-3 | 499 | 505 | PF00069 | 0.496 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.574 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.460 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.488 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.493 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.473 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.407 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.621 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.417 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.722 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.463 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.406 |
MOD_SUMO_for_1 | 787 | 790 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 498 | 507 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 559 | 568 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 681 | 686 | PF00179 | 0.448 |
TRG_DiLeu_BaEn_2 | 254 | 260 | PF01217 | 0.235 |
TRG_DiLeu_BaEn_4 | 15 | 21 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 699 | 702 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 33% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 83% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 40% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 40% | 96% |
A0A0N1PCA9 | Leptomonas seymouri | 35% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 28% | 92% |
A0A0N1PFI4 | Leptomonas seymouri | 36% | 100% |
A0A0S4JLK6 | Bodo saltans | 30% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A0S4KKP7 | Bodo saltans | 24% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 67% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 32% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 41% | 96% |
A0A1X0NW84 | Trypanosomatidae | 39% | 100% |
A0A1X0NW85 | Trypanosomatidae | 38% | 100% |
A0A1X0NW89 | Trypanosomatidae | 55% | 95% |
A0A1X0NWA6 | Trypanosomatidae | 30% | 94% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 99% | 90% |
A0A3Q8IDD4 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 96% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 74% |
A0A3S7WW18 | Leishmania donovani | 100% | 100% |
A0A3S7WW41 | Leishmania donovani | 35% | 100% |
A0A3S7WW71 | Leishmania donovani | 40% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 30% | 87% |
A0A3S7X460 | Leishmania donovani | 35% | 100% |
A0A3S7X463 | Leishmania donovani | 26% | 88% |
A0A3S7X470 | Leishmania donovani | 35% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 52% | 89% |
A0A422MYX0 | Trypanosoma rangeli | 38% | 100% |
A4H3W4 | Leishmania braziliensis | 40% | 100% |
A4HE81 | Leishmania braziliensis | 34% | 100% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ22 | Leishmania braziliensis | 32% | 100% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 41% | 100% |
A4HYW1 | Leishmania infantum | 99% | 81% |
A4HYW2 | Leishmania infantum | 40% | 100% |
A4HYW3 | Leishmania infantum | 36% | 100% |
A4HYW4 | Leishmania infantum | 28% | 82% |
A4I1J4 | Leishmania infantum | 34% | 100% |
A4I6E4 | Leishmania infantum | 35% | 100% |
A4I6E6 | Leishmania infantum | 35% | 100% |
A4I6F0 | Leishmania infantum | 30% | 87% |
A4I6K4 | Leishmania infantum | 34% | 100% |
A4I6K5 | Leishmania infantum | 26% | 88% |
A4I6K6 | Leishmania infantum | 25% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 76% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 96% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 96% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AIH1 | Leishmania braziliensis | 84% | 99% |
E9AIH3 | Leishmania braziliensis | 40% | 100% |
E9AIH4 | Leishmania braziliensis | 36% | 100% |
E9AIH6 | Leishmania braziliensis | 28% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q4Q6L7 | Leishmania major | 35% | 100% |
Q4Q6L9 | Leishmania major | 35% | 100% |
Q4Q6M0 | Leishmania major | 31% | 100% |
Q4Q6M2 | Leishmania major | 26% | 100% |
Q4Q6M3 | Leishmania major | 27% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 34% | 100% |
Q4QCS6 | Leishmania major | 36% | 100% |
Q4QCS7 | Leishmania major | 40% | 100% |
Q4QCS8 | Leishmania major | 95% | 100% |
Q4QCS9 | Leishmania major | 95% | 100% |
Q9U0T9 | Leishmania major | 41% | 100% |
V5AYJ1 | Trypanosoma cruzi | 31% | 100% |
V5B5I4 | Trypanosoma cruzi | 54% | 98% |
V5BA05 | Trypanosoma cruzi | 41% | 100% |
V5BEL3 | Trypanosoma cruzi | 37% | 100% |
V5BII7 | Trypanosoma cruzi | 29% | 67% |
V5BN20 | Trypanosoma cruzi | 33% | 100% |
V5D9Y2 | Trypanosoma cruzi | 41% | 97% |
V5DES7 | Trypanosoma cruzi | 32% | 100% |