Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | yes | 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. | yes | 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: 95 |
NetGPI | no | yes: 0, no: 97 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0020016 | ciliary pocket | 2 | 2 |
GO:0020038 | subpellicular network | 2 | 2 |
GO:0030863 | cortical cytoskeleton | 6 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0016020 | membrane | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
Related structures:
AlphaFold database: Q4Q6L9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 98 |
GO:0006807 | nitrogen compound metabolic process | 2 | 98 |
GO:0008152 | metabolic process | 1 | 98 |
GO:0019538 | protein metabolic process | 3 | 98 |
GO:0043170 | macromolecule metabolic process | 3 | 98 |
GO:0044238 | primary metabolic process | 2 | 98 |
GO:0071704 | organic substance metabolic process | 2 | 98 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 98 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 98 |
GO:0004175 | endopeptidase activity | 4 | 98 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 98 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 98 |
GO:0008233 | peptidase activity | 3 | 98 |
GO:0008234 | cysteine-type peptidase activity | 4 | 98 |
GO:0016787 | hydrolase activity | 2 | 98 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 98 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 497 | 501 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.340 |
CLV_MEL_PAP_1 | 110 | 116 | PF00089 | 0.377 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.580 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 124 | 132 | PF00400 | 0.550 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.338 |
DOC_CKS1_1 | 419 | 424 | PF01111 | 0.552 |
DOC_CYCLIN_yCln2_LP_2 | 587 | 593 | PF00134 | 0.578 |
DOC_MAPK_DCC_7 | 231 | 241 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 442 | 450 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 234 | 241 | PF00069 | 0.643 |
DOC_MAPK_MEF2A_6 | 444 | 452 | PF00069 | 0.523 |
DOC_PP2B_LxvP_1 | 587 | 590 | PF13499 | 0.631 |
DOC_PP2B_LxvP_1 | 641 | 644 | PF13499 | 0.434 |
DOC_PP4_FxxP_1 | 534 | 537 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.520 |
DOC_USP7_UBL2_3 | 354 | 358 | PF12436 | 0.553 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.707 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 432 | 441 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.593 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.560 |
LIG_BRCT_BRCA1_1 | 616 | 620 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 628 | 632 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 683 | 687 | PF00533 | 0.562 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.428 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.539 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.411 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.596 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.544 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.858 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.633 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.560 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.485 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.475 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.613 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.500 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.553 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.515 |
LIG_LIR_Apic_2 | 340 | 344 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 481 | 487 | PF02991 | 0.573 |
LIG_LIR_Apic_2 | 653 | 658 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 132 | 143 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 330 | 338 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 346 | 356 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 362 | 370 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 617 | 628 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 637 | 646 | PF02991 | 0.432 |
LIG_LIR_LC3C_4 | 638 | 643 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 684 | 690 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.375 |
LIG_MLH1_MIPbox_1 | 523 | 527 | PF16413 | 0.603 |
LIG_PDZ_Class_1 | 718 | 723 | PF00595 | 0.516 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.542 |
LIG_Pex14_2 | 516 | 520 | PF04695 | 0.550 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.754 |
LIG_SH2_CRK | 309 | 313 | PF00017 | 0.524 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.576 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.549 |
LIG_SH2_CRK | 363 | 367 | PF00017 | 0.549 |
LIG_SH2_CRK | 445 | 449 | PF00017 | 0.554 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.579 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 341 | 345 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 363 | 367 | PF00017 | 0.569 |
LIG_SH2_NCK_1 | 655 | 659 | PF00017 | 0.579 |
LIG_SH2_PTP2 | 214 | 217 | PF00017 | 0.518 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.600 |
LIG_SH2_SRC | 659 | 662 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 690 | 693 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 717 | 720 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.438 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.527 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.542 |
LIG_SH3_3 | 704 | 710 | PF00018 | 0.461 |
LIG_SUMO_SIM_par_1 | 262 | 267 | PF11976 | 0.668 |
LIG_SUMO_SIM_par_1 | 459 | 466 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 554 | 560 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 589 | 594 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 659 | 667 | PF11976 | 0.534 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.774 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.711 |
LIG_TRAF2_1 | 596 | 599 | PF00917 | 0.490 |
LIG_TRAF2_1 | 616 | 619 | PF00917 | 0.534 |
LIG_UBA3_1 | 87 | 93 | PF00899 | 0.426 |
LIG_WRC_WIRS_1 | 328 | 333 | PF05994 | 0.564 |
MOD_CDK_SPxxK_3 | 297 | 304 | PF00069 | 0.516 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.542 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.798 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.581 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.592 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.547 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.542 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.657 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.543 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.613 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.869 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.530 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.567 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.482 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.473 |
MOD_CMANNOS | 517 | 520 | PF00535 | 0.351 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.368 |
MOD_GlcNHglycan | 377 | 381 | PF01048 | 0.365 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.338 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.568 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.496 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.758 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.541 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.550 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.522 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.469 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.417 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.493 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.486 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.394 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.623 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.497 |
MOD_N-GLC_2 | 251 | 253 | PF02516 | 0.445 |
MOD_N-GLC_2 | 70 | 72 | PF02516 | 0.535 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.564 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.565 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.567 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.582 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.525 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.448 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.444 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.461 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.451 |
MOD_NEK2_2 | 144 | 149 | PF00069 | 0.379 |
MOD_NEK2_2 | 291 | 296 | PF00069 | 0.443 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.578 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.617 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.641 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.516 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.453 |
MOD_PK_1 | 42 | 48 | PF00069 | 0.671 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.567 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.507 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.546 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.399 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.553 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.563 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.470 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.480 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.455 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.613 |
MOD_Plk_2-3 | 29 | 35 | PF00069 | 0.544 |
MOD_Plk_2-3 | 392 | 398 | PF00069 | 0.603 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.567 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.585 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.526 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.632 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.587 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.588 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.558 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.498 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.504 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.500 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.411 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.405 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.487 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.564 |
MOD_SPalmitoyl_4 | 1 | 7 | PF01529 | 0.600 |
MOD_SUMO_for_1 | 12 | 15 | PF00179 | 0.611 |
MOD_SUMO_for_1 | 701 | 704 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 6 | 12 | PF00179 | 0.637 |
MOD_SUMO_rev_2 | 670 | 680 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 682 | 687 | PF00179 | 0.340 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.472 |
TRG_DiLeu_BaEn_1 | 466 | 471 | PF01217 | 0.591 |
TRG_DiLeu_BaEn_1 | 637 | 642 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 441 | 444 | PF00400 | 0.600 |
TRG_NES_CRM1_1 | 258 | 269 | PF08389 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 191 | 196 | PF00026 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 32% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 73% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 31% | 92% |
A0A0N1P9P1 | Leptomonas seymouri | 36% | 85% |
A0A0N1PCA9 | Leptomonas seymouri | 31% | 98% |
A0A0N1PE91 | Leptomonas seymouri | 24% | 81% |
A0A0N1PFI4 | Leptomonas seymouri | 56% | 93% |
A0A0S4JLK6 | Bodo saltans | 31% | 89% |
A0A0S4JS70 | Bodo saltans | 25% | 94% |
A0A0S4KGT2 | Bodo saltans | 38% | 96% |
A0A1X0NJ61 | Trypanosomatidae | 33% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 30% | 95% |
A0A1X0NJX8 | Trypanosomatidae | 31% | 93% |
A0A1X0NKT7 | Trypanosomatidae | 29% | 91% |
A0A1X0NKX8 | Trypanosomatidae | 40% | 88% |
A0A1X0NMT3 | Trypanosomatidae | 31% | 85% |
A0A1X0NW84 | Trypanosomatidae | 33% | 100% |
A0A1X0NW85 | Trypanosomatidae | 34% | 100% |
A0A1X0NW89 | Trypanosomatidae | 34% | 84% |
A0A1X0NWA6 | Trypanosomatidae | 28% | 83% |
A0A1X0NWW1 | Trypanosomatidae | 36% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 35% | 79% |
A0A3Q8IDD4 | Leishmania donovani | 32% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 27% | 96% |
A0A3S5H5A5 | Leishmania donovani | 34% | 85% |
A0A3S5ISG2 | Trypanosoma rangeli | 39% | 93% |
A0A3S7WW18 | Leishmania donovani | 35% | 88% |
A0A3S7WW41 | Leishmania donovani | 30% | 97% |
A0A3S7WW71 | Leishmania donovani | 33% | 100% |
A0A3S7X430 | Leishmania donovani | 29% | 92% |
A0A3S7X438 | Leishmania donovani | 31% | 77% |
A0A3S7X460 | Leishmania donovani | 32% | 93% |
A0A3S7X463 | Leishmania donovani | 28% | 77% |
A0A3S7X470 | Leishmania donovani | 90% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 34% | 79% |
A0A422MYX0 | Trypanosoma rangeli | 34% | 99% |
A4H3W4 | Leishmania braziliensis | 33% | 84% |
A4HE81 | Leishmania braziliensis | 32% | 100% |
A4HJ14 | Leishmania braziliensis | 29% | 92% |
A4HJ21 | Leishmania braziliensis | 26% | 81% |
A4HJ22 | Leishmania braziliensis | 30% | 76% |
A4HJ23 | Leishmania braziliensis | 67% | 100% |
A4HJ24 | Leishmania braziliensis | 32% | 100% |
A4HS39 | Leishmania infantum | 34% | 85% |
A4HYN0 | Leishmania infantum | 35% | 88% |
A4HYW1 | Leishmania infantum | 35% | 71% |
A4HYW2 | Leishmania infantum | 33% | 100% |
A4HYW3 | Leishmania infantum | 30% | 97% |
A4HYW4 | Leishmania infantum | 28% | 72% |
A4I1J4 | Leishmania infantum | 32% | 100% |
A4I6E4 | Leishmania infantum | 91% | 100% |
A4I6E6 | Leishmania infantum | 32% | 93% |
A4I6F0 | Leishmania infantum | 31% | 77% |
A4I6K4 | Leishmania infantum | 29% | 92% |
A4I6K5 | Leishmania infantum | 28% | 77% |
A4I6K6 | Leishmania infantum | 27% | 96% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 67% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 99% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 91% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 85% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 90% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 84% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 77% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 92% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AIH1 | Leishmania braziliensis | 33% | 89% |
E9AIH3 | Leishmania braziliensis | 31% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 97% |
E9AIH6 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 91% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 77% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 97% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 92% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 77% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 96% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
O14815 | Homo sapiens | 25% | 100% |
P16259 | Rattus norvegicus | 27% | 88% |
P20807 | Homo sapiens | 26% | 88% |
P43368 | Sus scrofa | 27% | 88% |
P51186 | Bos taurus | 26% | 88% |
Q22036 | Caenorhabditis elegans | 25% | 100% |
Q4Q6L7 | Leishmania major | 33% | 100% |
Q4Q6M0 | Leishmania major | 30% | 77% |
Q4Q6M2 | Leishmania major | 26% | 96% |
Q4Q6M3 | Leishmania major | 27% | 78% |
Q4Q6M4 | Leishmania major | 29% | 85% |
Q4Q9U3 | Leishmania major | 32% | 100% |
Q4QCS6 | Leishmania major | 30% | 97% |
Q4QCS7 | Leishmania major | 33% | 100% |
Q4QCS8 | Leishmania major | 35% | 88% |
Q4QCS9 | Leishmania major | 35% | 100% |
Q64691 | Mus musculus | 27% | 88% |
Q9GLG7 | Macaca fascicularis | 26% | 89% |
Q9TTH8 | Ovis aries | 26% | 88% |
Q9U0T9 | Leishmania major | 34% | 85% |
Q9VXH6 | Drosophila melanogaster | 23% | 100% |
V5AYJ1 | Trypanosoma cruzi | 32% | 100% |
V5B5I4 | Trypanosoma cruzi | 33% | 86% |
V5BA05 | Trypanosoma cruzi | 35% | 100% |
V5BEL3 | Trypanosoma cruzi | 34% | 100% |
V5BN20 | Trypanosoma cruzi | 33% | 93% |
V5D5V8 | Trypanosoma cruzi | 29% | 97% |
V5D9Y2 | Trypanosoma cruzi | 31% | 85% |
V5DES7 | Trypanosoma cruzi | 38% | 91% |