Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 12 |
GO:0005786 | signal recognition particle, endoplasmic reticulum targeting | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0048500 | signal recognition particle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HA36
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 12 |
GO:0006612 | protein targeting to membrane | 5 | 12 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 12 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0045047 | protein targeting to ER | 6 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0051668 | localization within membrane | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 12 |
GO:0072657 | protein localization to membrane | 4 | 12 |
GO:0090150 | establishment of protein localization to membrane | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008312 | 7S RNA binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 695 | 697 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 659 | 663 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 665 | 667 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 695 | 697 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 711 | 713 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 711 | 713 | PF00082 | 0.624 |
CLV_PCSK_PC7_1 | 661 | 667 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.451 |
CLV_Separin_Metazoa | 234 | 238 | PF03568 | 0.484 |
CLV_Separin_Metazoa | 433 | 437 | PF03568 | 0.417 |
DEG_APCC_DBOX_1 | 115 | 123 | PF00400 | 0.564 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.490 |
DOC_CKS1_1 | 69 | 74 | PF01111 | 0.427 |
DOC_CYCLIN_RxL_1 | 28 | 36 | PF00134 | 0.288 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.612 |
DOC_MAPK_gen_1 | 289 | 296 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 327 | 337 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 449 | 456 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 54 | 62 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 563 | 572 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 237 | 244 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.455 |
DOC_MAPK_RevD_3 | 386 | 399 | PF00069 | 0.595 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.585 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.670 |
DOC_USP7_MATH_2 | 735 | 741 | PF00917 | 0.579 |
DOC_USP7_UBL2_3 | 697 | 701 | PF12436 | 0.439 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.588 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 24 | 33 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 340 | 347 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 414 | 423 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 513 | 521 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 54 | 63 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 536 | 554 | PF00022 | 0.514 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.608 |
LIG_eIF4E_1 | 85 | 91 | PF01652 | 0.564 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.467 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.514 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.288 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.445 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.420 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.445 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.578 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.561 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.567 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.610 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.715 |
LIG_GBD_Chelix_1 | 308 | 316 | PF00786 | 0.511 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 678 | 683 | PF02991 | 0.524 |
LIG_NRBOX | 6 | 12 | PF00104 | 0.441 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.574 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.510 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.552 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.617 |
LIG_SH2_NCK_1 | 129 | 133 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 544 | 548 | PF00017 | 0.525 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.589 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 430 | 434 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.503 |
LIG_SH3_1 | 399 | 405 | PF00018 | 0.516 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.516 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.550 |
LIG_Sin3_3 | 202 | 209 | PF02671 | 0.302 |
LIG_Sin3_3 | 569 | 576 | PF02671 | 0.542 |
LIG_SUMO_SIM_anti_2 | 47 | 53 | PF11976 | 0.590 |
LIG_SUMO_SIM_anti_2 | 568 | 574 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 388 | 394 | PF11976 | 0.562 |
LIG_TYR_ITIM | 311 | 316 | PF00017 | 0.541 |
LIG_TYR_ITIM | 630 | 635 | PF00017 | 0.638 |
MOD_CDC14_SPxK_1 | 259 | 262 | PF00782 | 0.465 |
MOD_CDC14_SPxK_1 | 411 | 414 | PF00782 | 0.532 |
MOD_CDK_SPxK_1 | 256 | 262 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 408 | 414 | PF00069 | 0.532 |
MOD_CDK_SPxK_1 | 68 | 74 | PF00069 | 0.463 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.406 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.420 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.543 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.450 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.707 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.390 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.507 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.677 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.639 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.476 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.403 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.473 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.452 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.434 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.573 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.728 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.662 |
MOD_GlcNHglycan | 479 | 483 | PF01048 | 0.427 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.429 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.696 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.682 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.678 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.824 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.787 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.478 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.451 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.561 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.434 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.628 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.517 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.552 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.463 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.683 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.581 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.246 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.524 |
MOD_LATS_1 | 334 | 340 | PF00433 | 0.594 |
MOD_LATS_1 | 52 | 58 | PF00433 | 0.250 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.453 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.599 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.529 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.463 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.451 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.465 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.474 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.545 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.519 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.530 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.317 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.447 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.523 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.460 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.522 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.594 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.250 |
MOD_PKA_1 | 633 | 639 | PF00069 | 0.713 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.456 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.608 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.573 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.250 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.638 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.408 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.622 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.514 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.569 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.473 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.466 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.390 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.582 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.501 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.746 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.511 |
MOD_SUMO_for_1 | 5 | 8 | PF00179 | 0.525 |
MOD_SUMO_for_1 | 96 | 99 | PF00179 | 0.288 |
MOD_SUMO_rev_2 | 176 | 183 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 694 | 703 | PF00179 | 0.448 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_1 | 566 | 571 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.623 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.249 |
TRG_ER_diArg_1 | 632 | 634 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 659 | 662 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 664 | 666 | PF00400 | 0.355 |
TRG_NES_CRM1_1 | 381 | 394 | PF08389 | 0.466 |
TRG_NES_CRM1_1 | 499 | 512 | PF08389 | 0.587 |
TRG_NLS_Bipartite_1 | 436 | 453 | PF00514 | 0.436 |
TRG_NLS_Bipartite_1 | 695 | 715 | PF00514 | 0.632 |
TRG_NLS_MonoCore_2 | 395 | 400 | PF00514 | 0.553 |
TRG_NLS_MonoExtN_4 | 393 | 400 | PF00514 | 0.540 |
TRG_NLS_MonoExtN_4 | 698 | 705 | PF00514 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 116 | 121 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 690 | 694 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 704 | 708 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I027 | Leptomonas seymouri | 64% | 100% |
A0A0S4J0A8 | Bodo saltans | 33% | 100% |
A0A1X0P6G4 | Trypanosomatidae | 41% | 100% |
A0A3Q8IDA7 | Leishmania donovani | 83% | 100% |
A0A422NHC6 | Trypanosoma rangeli | 42% | 100% |
A4HY99 | Leishmania infantum | 82% | 100% |
D0A0N5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AS31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O76094 | Homo sapiens | 23% | 100% |
P33731 | Canis lupus familiaris | 23% | 100% |
Q4QDE2 | Leishmania major | 83% | 99% |
V5BJ44 | Trypanosoma cruzi | 43% | 100% |