Structural Proteins, cytoskeleton-associated CAP5.5
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | yes | yes: 3 |
Forrest at al. (procyclic) | yes | 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: 99 |
NetGPI | no | yes: 0, no: 101 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
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 |
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: A4I6E4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 102 |
GO:0006807 | nitrogen compound metabolic process | 2 | 102 |
GO:0008152 | metabolic process | 1 | 102 |
GO:0019538 | protein metabolic process | 3 | 102 |
GO:0043170 | macromolecule metabolic process | 3 | 102 |
GO:0044238 | primary metabolic process | 2 | 102 |
GO:0071704 | organic substance metabolic process | 2 | 102 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 102 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 102 |
GO:0004175 | endopeptidase activity | 4 | 102 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 102 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 102 |
GO:0008233 | peptidase activity | 3 | 102 |
GO:0008234 | cysteine-type peptidase activity | 4 | 102 |
GO:0016787 | hydrolase activity | 2 | 102 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 102 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.397 |
CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.240 |
CLV_MEL_PAP_1 | 111 | 117 | PF00089 | 0.281 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 577 | 579 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 679 | 681 | PF00082 | 0.495 |
CLV_PCSK_PC7_1 | 675 | 681 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.399 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.456 |
DEG_APCC_DBOX_1 | 645 | 653 | PF00400 | 0.248 |
DOC_CKS1_1 | 420 | 425 | PF01111 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 588 | 594 | PF00134 | 0.450 |
DOC_MAPK_gen_1 | 443 | 451 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 7 | 17 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 36 | 43 | PF00149 | 0.320 |
DOC_PP1_RVXF_1 | 565 | 571 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 588 | 591 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 535 | 538 | PF00568 | 0.396 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.420 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.618 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.468 |
LIG_14-3-3_CanoR_1 | 254 | 258 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 43 | 51 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 433 | 442 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 567 | 573 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 680 | 688 | PF00244 | 0.430 |
LIG_BRCT_BRCA1_1 | 617 | 621 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 684 | 688 | PF00533 | 0.463 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.343 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.441 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.317 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.499 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.447 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.567 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.467 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.489 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.469 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.380 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.361 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.487 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.404 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.419 |
LIG_LIR_Apic_2 | 341 | 345 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 654 | 659 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.209 |
LIG_LIR_Gen_1 | 331 | 339 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 363 | 372 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 618 | 629 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 638 | 649 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 363 | 367 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 618 | 624 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 638 | 644 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.283 |
LIG_MAD2 | 567 | 575 | PF02301 | 0.405 |
LIG_PDZ_Class_1 | 719 | 724 | PF00595 | 0.424 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.448 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.453 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.428 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.363 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.457 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.454 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.459 |
LIG_SH2_CRK | 641 | 645 | PF00017 | 0.401 |
LIG_SH2_CRK | 656 | 660 | PF00017 | 0.475 |
LIG_SH2_GRB2like | 342 | 345 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 342 | 346 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 364 | 368 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 656 | 660 | PF00017 | 0.475 |
LIG_SH2_PTP2 | 215 | 218 | PF00017 | 0.457 |
LIG_SH2_SRC | 342 | 345 | PF00017 | 0.504 |
LIG_SH2_SRC | 660 | 663 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.352 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.561 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.295 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.434 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.450 |
LIG_SH3_3 | 705 | 711 | PF00018 | 0.362 |
LIG_SUMO_SIM_par_1 | 263 | 268 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 321 | 327 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 460 | 467 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 555 | 561 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 590 | 595 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 660 | 666 | PF11976 | 0.407 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.479 |
LIG_TRAF2_1 | 617 | 620 | PF00917 | 0.405 |
LIG_TRAF2_1 | 695 | 698 | PF00917 | 0.505 |
LIG_TRFH_1 | 641 | 645 | PF08558 | 0.340 |
LIG_UBA3_1 | 569 | 577 | PF00899 | 0.400 |
LIG_UBA3_1 | 88 | 94 | PF00899 | 0.331 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.449 |
MOD_CDK_SPxxK_3 | 379 | 386 | PF00069 | 0.486 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.465 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.593 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.484 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.513 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.441 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.446 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.621 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.459 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.468 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.416 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.560 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.405 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.387 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.374 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.447 |
MOD_CMANNOS | 518 | 521 | PF00535 | 0.256 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.267 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.523 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.266 |
MOD_GlcNHglycan | 378 | 382 | PF01048 | 0.268 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.238 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.576 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.469 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.435 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.475 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.688 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.420 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.456 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.427 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.384 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.339 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.388 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.363 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.304 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.526 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.396 |
MOD_N-GLC_2 | 71 | 73 | PF02516 | 0.388 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.475 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.457 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.457 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.473 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.518 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.466 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.414 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.369 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.360 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.316 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.366 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.275 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.470 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.521 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.559 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.540 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.365 |
MOD_PIKK_1 | 703 | 709 | PF00454 | 0.476 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.444 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.471 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.410 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.417 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.451 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.315 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.482 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.384 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.392 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.359 |
MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.464 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.652 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.471 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.489 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.429 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.491 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.481 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.462 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.403 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.400 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.405 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.314 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.311 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.464 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.468 |
MOD_SPalmitoyl_4 | 1 | 7 | PF01529 | 0.507 |
MOD_SUMO_rev_2 | 6 | 12 | PF00179 | 0.569 |
MOD_SUMO_rev_2 | 671 | 681 | PF00179 | 0.301 |
TRG_DiLeu_BaEn_1 | 147 | 152 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_1 | 467 | 472 | PF01217 | 0.584 |
TRG_DiLeu_BaEn_1 | 639 | 644 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 618 | 624 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.314 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.501 |
TRG_NES_CRM1_1 | 259 | 270 | PF08389 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 192 | 197 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 31% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 74% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 31% | 92% |
A0A0N1P9P1 | Leptomonas seymouri | 36% | 85% |
A0A0N1PCA9 | Leptomonas seymouri | 30% | 98% |
A0A0N1PE91 | Leptomonas seymouri | 25% | 81% |
A0A0N1PFI4 | Leptomonas seymouri | 57% | 93% |
A0A0S4JLK6 | Bodo saltans | 30% | 89% |
A0A0S4JS70 | Bodo saltans | 25% | 94% |
A0A0S4KGT2 | Bodo saltans | 38% | 96% |
A0A1X0NJ61 | Trypanosomatidae | 32% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 30% | 95% |
A0A1X0NJX8 | Trypanosomatidae | 32% | 93% |
A0A1X0NKT7 | Trypanosomatidae | 29% | 91% |
A0A1X0NKX8 | Trypanosomatidae | 38% | 89% |
A0A1X0NMT3 | Trypanosomatidae | 32% | 85% |
A0A1X0NW84 | Trypanosomatidae | 34% | 100% |
A0A1X0NW85 | Trypanosomatidae | 34% | 100% |
A0A1X0NW89 | Trypanosomatidae | 33% | 84% |
A0A1X0NWA6 | Trypanosomatidae | 28% | 83% |
A0A1X0NWW1 | Trypanosomatidae | 35% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 35% | 80% |
A0A3Q8IDD4 | Leishmania donovani | 32% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 27% | 96% |
A0A3S5H5A5 | Leishmania donovani | 34% | 85% |
A0A3S5ISG2 | Trypanosoma rangeli | 39% | 94% |
A0A3S7WW18 | Leishmania donovani | 36% | 88% |
A0A3S7WW41 | Leishmania donovani | 29% | 97% |
A0A3S7WW71 | Leishmania donovani | 33% | 100% |
A0A3S7X430 | Leishmania donovani | 30% | 92% |
A0A3S7X438 | Leishmania donovani | 32% | 77% |
A0A3S7X460 | Leishmania donovani | 32% | 93% |
A0A3S7X463 | Leishmania donovani | 28% | 77% |
A0A3S7X470 | Leishmania donovani | 98% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 34% | 79% |
A0A422MYX0 | Trypanosoma rangeli | 34% | 100% |
A4H3W4 | Leishmania braziliensis | 33% | 100% |
A4HE81 | Leishmania braziliensis | 32% | 100% |
A4HJ14 | Leishmania braziliensis | 29% | 100% |
A4HJ21 | Leishmania braziliensis | 26% | 81% |
A4HJ22 | Leishmania braziliensis | 31% | 100% |
A4HJ23 | Leishmania braziliensis | 68% | 100% |
A4HJ24 | Leishmania braziliensis | 33% | 100% |
A4HS39 | Leishmania infantum | 34% | 100% |
A4HYN0 | Leishmania infantum | 35% | 100% |
A4HYW1 | Leishmania infantum | 35% | 71% |
A4HYW2 | Leishmania infantum | 33% | 100% |
A4HYW3 | Leishmania infantum | 29% | 100% |
A4HYW4 | Leishmania infantum | 28% | 100% |
A4I1J4 | Leishmania infantum | 33% | 100% |
A4I6E6 | Leishmania infantum | 32% | 93% |
A4I6F0 | Leishmania infantum | 32% | 77% |
A4I6K4 | Leishmania infantum | 30% | 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) | 34% | 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) | 37% | 85% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 90% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AIH1 | Leishmania braziliensis | 34% | 100% |
E9AIH3 | Leishmania braziliensis | 32% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 100% |
E9AIH6 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 77% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
P16259 | Rattus norvegicus | 26% | 88% |
P20807 | Homo sapiens | 25% | 88% |
P43368 | Sus scrofa | 25% | 88% |
P51186 | Bos taurus | 25% | 88% |
Q22036 | Caenorhabditis elegans | 25% | 100% |
Q4Q6L7 | Leishmania major | 33% | 100% |
Q4Q6L9 | Leishmania major | 91% | 100% |
Q4Q6M0 | Leishmania major | 31% | 100% |
Q4Q6M2 | Leishmania major | 25% | 100% |
Q4Q6M3 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 31% | 100% |
Q4Q9U3 | Leishmania major | 32% | 100% |
Q4QCS6 | Leishmania major | 30% | 100% |
Q4QCS7 | Leishmania major | 33% | 100% |
Q4QCS8 | Leishmania major | 35% | 100% |
Q4QCS9 | Leishmania major | 35% | 100% |
Q64691 | Mus musculus | 26% | 88% |
Q9GLG7 | Macaca fascicularis | 26% | 89% |
Q9TTH8 | Ovis aries | 26% | 88% |
Q9U0T9 | Leishmania major | 33% | 100% |
V5AYJ1 | Trypanosoma cruzi | 32% | 100% |
V5B5I4 | Trypanosoma cruzi | 33% | 86% |
V5BA05 | Trypanosoma cruzi | 35% | 100% |
V5BEL3 | Trypanosoma cruzi | 34% | 100% |
V5BN20 | Trypanosoma cruzi | 34% | 94% |
V5D5V8 | Trypanosoma cruzi | 30% | 98% |
V5D9Y2 | Trypanosoma cruzi | 31% | 85% |
V5DES7 | Trypanosoma cruzi | 39% | 91% |