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: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H6H8
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.271 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 641 | 647 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.663 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.589 |
DEG_MDM2_SWIB_1 | 182 | 189 | PF02201 | 0.437 |
DEG_SPOP_SBC_1 | 11 | 15 | PF00917 | 0.446 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.647 |
DOC_ANK_TNKS_1 | 306 | 313 | PF00023 | 0.481 |
DOC_ANK_TNKS_1 | 536 | 543 | PF00023 | 0.477 |
DOC_CKS1_1 | 636 | 641 | PF01111 | 0.334 |
DOC_MAPK_DCC_7 | 252 | 261 | PF00069 | 0.641 |
DOC_MAPK_FxFP_2 | 33 | 36 | PF00069 | 0.528 |
DOC_MAPK_FxFP_2 | 462 | 465 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 651 | 660 | PF00069 | 0.339 |
DOC_MAPK_JIP1_4 | 543 | 549 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 252 | 261 | PF00069 | 0.642 |
DOC_MAPK_MEF2A_6 | 531 | 538 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 690 | 697 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 702 | 710 | PF00069 | 0.276 |
DOC_PP1_RVXF_1 | 603 | 610 | PF00149 | 0.315 |
DOC_PP1_RVXF_1 | 644 | 651 | PF00149 | 0.312 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.630 |
DOC_PP4_FxxP_1 | 299 | 302 | PF00568 | 0.498 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 462 | 465 | PF00568 | 0.356 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.415 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 28 | 32 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 363 | 370 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 432 | 441 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 583 | 591 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 595 | 601 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 645 | 649 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.370 |
LIG_APCC_ABBA_1 | 259 | 264 | PF00400 | 0.605 |
LIG_APCC_ABBAyCdc20_2 | 681 | 687 | PF00400 | 0.327 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.666 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.333 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.434 |
LIG_Clathr_ClatBox_1 | 669 | 673 | PF01394 | 0.343 |
LIG_eIF4E_1 | 146 | 152 | PF01652 | 0.503 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.613 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.560 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.581 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.522 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.439 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.398 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.370 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.291 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.700 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.562 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.647 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.403 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.378 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.564 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.710 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 30 | 36 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 375 | 379 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 136 | 145 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 371 | 381 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 503 | 513 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.658 |
LIG_NRBOX | 694 | 700 | PF00104 | 0.336 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.452 |
LIG_Rb_LxCxE_1 | 558 | 580 | PF01857 | 0.278 |
LIG_Rb_pABgroove_1 | 27 | 35 | PF01858 | 0.405 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.304 |
LIG_SH2_CRK | 604 | 608 | PF00017 | 0.309 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.337 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.250 |
LIG_SH2_SRC | 262 | 265 | PF00017 | 0.489 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.524 |
LIG_SH3_1 | 659 | 665 | PF00018 | 0.258 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.802 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.358 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.420 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.669 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.386 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.364 |
LIG_SUMO_SIM_par_1 | 477 | 485 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 545 | 551 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 668 | 674 | PF11976 | 0.397 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.496 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.301 |
LIG_TRAF2_1 | 482 | 485 | PF00917 | 0.571 |
LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.253 |
LIG_TYR_ITIM | 368 | 373 | PF00017 | 0.308 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.447 |
LIG_WW_3 | 36 | 40 | PF00397 | 0.544 |
MOD_CDC14_SPxK_1 | 551 | 554 | PF00782 | 0.381 |
MOD_CDK_SPK_2 | 75 | 80 | PF00069 | 0.463 |
MOD_CDK_SPxK_1 | 548 | 554 | PF00069 | 0.360 |
MOD_CDK_SPxK_1 | 635 | 641 | PF00069 | 0.339 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.553 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.632 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.588 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.719 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.668 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.633 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.760 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.552 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.447 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.374 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.646 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.450 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.706 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.552 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.592 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.657 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.397 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.329 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.748 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.378 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.714 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.488 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.372 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.564 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.677 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.683 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.592 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.388 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.376 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.325 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.420 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.341 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.513 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.485 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.378 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.555 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.409 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.344 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.608 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.355 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.371 |
MOD_NEK2_2 | 587 | 592 | PF00069 | 0.415 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.339 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.416 |
MOD_PIKK_1 | 671 | 677 | PF00454 | 0.318 |
MOD_PK_1 | 504 | 510 | PF00069 | 0.508 |
MOD_PK_1 | 630 | 636 | PF00069 | 0.381 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.324 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.616 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.552 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.633 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.509 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.507 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.365 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.412 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.397 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.432 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.616 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.383 |
MOD_Plk_1 | 587 | 593 | PF00069 | 0.390 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.286 |
MOD_Plk_2-3 | 555 | 561 | PF00069 | 0.456 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.533 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.480 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.484 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.325 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.568 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.336 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.462 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.361 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.506 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.462 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.343 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.626 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.360 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.339 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.389 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.398 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.461 |
MOD_SUMO_for_1 | 210 | 213 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 483 | 489 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 597 | 601 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_2 | 540 | 546 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 650 | 655 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 650 | 653 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.545 |
TRG_NES_CRM1_1 | 212 | 224 | PF08389 | 0.509 |
TRG_NES_CRM1_1 | 704 | 719 | PF08389 | 0.359 |
TRG_NLS_Bipartite_1 | 278 | 293 | PF00514 | 0.481 |
TRG_NLS_MonoExtC_3 | 288 | 294 | PF00514 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 537 | 541 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW55 | Leptomonas seymouri | 66% | 96% |
A0A0S4IV39 | Bodo saltans | 37% | 90% |
A0A1X0NVE2 | Trypanosomatidae | 46% | 100% |
A0A3S5H6I6 | Leishmania donovani | 83% | 100% |
A0A422MV99 | Trypanosoma rangeli | 45% | 100% |
A4HUW4 | Leishmania infantum | 83% | 100% |
D0A7I9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ANJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QH27 | Leishmania major | 84% | 100% |
V5BW97 | Trypanosoma cruzi | 45% | 100% |