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. | no | yes: 0 |
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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QCP1
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0051301 | cell division | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 143 | 147 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 697 | 701 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 806 | 810 | PF00656 | 0.732 |
CLV_C14_Caspase3-7 | 841 | 845 | PF00656 | 0.564 |
CLV_MEL_PAP_1 | 430 | 436 | PF00089 | 0.529 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 764 | 766 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 528 | 530 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 764 | 766 | PF00082 | 0.557 |
CLV_PCSK_PC7_1 | 761 | 767 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.265 |
DEG_APCC_DBOX_1 | 303 | 311 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 331 | 339 | PF00400 | 0.513 |
DEG_SPOP_SBC_1 | 363 | 367 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.408 |
DOC_CKS1_1 | 424 | 429 | PF01111 | 0.308 |
DOC_CYCLIN_RxL_1 | 615 | 624 | PF00134 | 0.412 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 331 | 339 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 527 | 533 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 626 | 633 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 729 | 739 | PF00069 | 0.279 |
DOC_MAPK_JIP1_4 | 729 | 735 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 729 | 737 | PF00069 | 0.279 |
DOC_PP2B_LxvP_1 | 354 | 357 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 591 | 594 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 673 | 676 | PF13499 | 0.279 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.531 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 816 | 820 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 860 | 864 | PF00917 | 0.539 |
DOC_USP7_UBL2_3 | 803 | 807 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 842 | 847 | PF00397 | 0.695 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 209 | 217 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 440 | 450 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 690 | 696 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 765 | 772 | PF00244 | 0.607 |
LIG_Actin_WH2_2 | 29 | 47 | PF00022 | 0.358 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.361 |
LIG_Clathr_ClatBox_1 | 341 | 345 | PF01394 | 0.502 |
LIG_Clathr_ClatBox_1 | 376 | 380 | PF01394 | 0.303 |
LIG_CSL_BTD_1 | 82 | 85 | PF09270 | 0.467 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.620 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.651 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.615 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.520 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.497 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.419 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.370 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.516 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.468 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.402 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.649 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.419 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.373 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.245 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.478 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.495 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.528 |
LIG_FHA_1 | 824 | 830 | PF00498 | 0.532 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.694 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.488 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.351 |
LIG_FHA_2 | 695 | 701 | PF00498 | 0.187 |
LIG_Integrin_isoDGR_2 | 189 | 191 | PF01839 | 0.581 |
LIG_Integrin_RGD_1 | 842 | 844 | PF01839 | 0.565 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 559 | 567 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.410 |
LIG_LYPXL_S_1 | 371 | 375 | PF13949 | 0.314 |
LIG_LYPXL_yS_3 | 372 | 375 | PF13949 | 0.299 |
LIG_MYND_1 | 818 | 822 | PF01753 | 0.575 |
LIG_NRBOX | 290 | 296 | PF00104 | 0.411 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.468 |
LIG_NRBOX | 691 | 697 | PF00104 | 0.279 |
LIG_PTAP_UEV_1 | 502 | 507 | PF05743 | 0.514 |
LIG_Rb_pABgroove_1 | 648 | 656 | PF01858 | 0.306 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.478 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.596 |
LIG_SH2_CRK | 561 | 565 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 561 | 565 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 796 | 799 | PF00017 | 0.567 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.467 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.446 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.641 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.649 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.521 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.410 |
LIG_SH3_3 | 812 | 818 | PF00018 | 0.645 |
LIG_SH3_3 | 843 | 849 | PF00018 | 0.579 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 337 | 343 | PF11976 | 0.483 |
LIG_SUMO_SIM_anti_2 | 345 | 351 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 583 | 590 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 634 | 640 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 708 | 714 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 782 | 788 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 337 | 343 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 374 | 381 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 489 | 495 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 583 | 590 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 710 | 716 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 780 | 788 | PF11976 | 0.553 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.407 |
LIG_TYR_ITIM | 370 | 375 | PF00017 | 0.325 |
LIG_WRC_WIRS_1 | 416 | 421 | PF05994 | 0.457 |
LIG_WW_3 | 674 | 678 | PF00397 | 0.279 |
MOD_CDK_SPxxK_3 | 297 | 304 | PF00069 | 0.474 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.703 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.696 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.631 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.561 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.279 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.306 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.386 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.582 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.715 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.613 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.456 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.421 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.410 |
MOD_CK2_1 | 818 | 824 | PF00069 | 0.525 |
MOD_Cter_Amidation | 616 | 619 | PF01082 | 0.306 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.642 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.612 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.620 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.555 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.666 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.542 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.738 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.282 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.317 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.578 |
MOD_GlcNHglycan | 861 | 865 | PF01048 | 0.469 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.669 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.490 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.390 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.776 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.544 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.619 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.565 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.601 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.483 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.540 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.446 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.554 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.680 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.674 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.312 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.407 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.294 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.248 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.504 |
MOD_N-GLC_1 | 684 | 689 | PF02516 | 0.402 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.547 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.458 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.511 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.226 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.560 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.588 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.378 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.417 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.533 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.527 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.330 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.357 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.447 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.462 |
MOD_PIKK_1 | 694 | 700 | PF00454 | 0.410 |
MOD_PKA_1 | 765 | 771 | PF00069 | 0.603 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.655 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.619 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.607 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.322 |
MOD_PKA_2 | 765 | 771 | PF00069 | 0.603 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.557 |
MOD_Plk_1 | 688 | 694 | PF00069 | 0.279 |
MOD_Plk_1 | 810 | 816 | PF00069 | 0.736 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.655 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.458 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.336 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.494 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.402 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.500 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.404 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.532 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.297 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.279 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.497 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.576 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.597 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.628 |
MOD_ProDKin_1 | 842 | 848 | PF00069 | 0.699 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.473 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.380 |
TRG_DiLeu_BaEn_1 | 380 | 385 | PF01217 | 0.360 |
TRG_DiLeu_BaEn_1 | 788 | 793 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_2 | 96 | 102 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 243 | 249 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 626 | 628 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 676 | 679 | PF00400 | 0.297 |
TRG_NES_CRM1_1 | 576 | 590 | PF08389 | 0.520 |
TRG_NLS_MonoExtC_3 | 763 | 769 | PF00514 | 0.555 |
TRG_NLS_MonoExtN_4 | 761 | 768 | PF00514 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 202 | 207 | PF00026 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E7 | Leptomonas seymouri | 49% | 100% |
A0A1X0NXH5 | Trypanosomatidae | 35% | 100% |
A0A3Q8IBN9 | Leishmania donovani | 93% | 100% |
A0A3R7NWG6 | Trypanosoma rangeli | 35% | 100% |
A4HZ08 | Leishmania infantum | 92% | 100% |
C9ZIP1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AIL0 | Leishmania braziliensis | 76% | 100% |
E9AUU2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BCV9 | Trypanosoma cruzi | 34% | 100% |