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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4HLH5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 19 |
GO:0003824 | catalytic activity | 1 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0005524 | ATP binding | 5 | 19 |
GO:0016462 | pyrophosphatase activity | 5 | 19 |
GO:0016787 | hydrolase activity | 2 | 19 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 19 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 19 |
GO:0016887 | ATP hydrolysis activity | 7 | 19 |
GO:0017076 | purine nucleotide binding | 4 | 19 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 19 |
GO:0030554 | adenyl nucleotide binding | 5 | 19 |
GO:0032553 | ribonucleotide binding | 3 | 19 |
GO:0032555 | purine ribonucleotide binding | 4 | 19 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 19 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 19 |
GO:0036094 | small molecule binding | 2 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043168 | anion binding | 3 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:0097367 | carbohydrate derivative binding | 2 | 19 |
GO:1901265 | nucleoside phosphate binding | 3 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.769 |
CLV_C14_Caspase3-7 | 581 | 585 | PF00656 | 0.516 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.574 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 341 | 343 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.474 |
CLV_PCSK_PC7_1 | 425 | 431 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.446 |
CLV_Separin_Metazoa | 624 | 628 | PF03568 | 0.519 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.393 |
DEG_SCF_FBW7_1 | 436 | 442 | PF00400 | 0.668 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 594 | 598 | PF00917 | 0.569 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.548 |
DOC_ANK_TNKS_1 | 160 | 167 | PF00023 | 0.603 |
DOC_CKS1_1 | 436 | 441 | PF01111 | 0.668 |
DOC_CYCLIN_RxL_1 | 193 | 201 | PF00134 | 0.727 |
DOC_CYCLIN_yCln2_LP_2 | 286 | 292 | PF00134 | 0.491 |
DOC_MAPK_gen_1 | 278 | 288 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 341 | 349 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 486 | 496 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 262 | 268 | PF00149 | 0.556 |
DOC_SPAK_OSR1_1 | 366 | 370 | PF12202 | 0.439 |
DOC_SPAK_OSR1_1 | 97 | 101 | PF12202 | 0.708 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.762 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.589 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 368 | 372 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.790 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.758 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 140 | 147 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.626 |
LIG_Actin_WH2_2 | 1 | 19 | PF00022 | 0.460 |
LIG_Actin_WH2_2 | 134 | 150 | PF00022 | 0.715 |
LIG_Actin_WH2_2 | 517 | 532 | PF00022 | 0.631 |
LIG_Actin_WH2_2 | 99 | 116 | PF00022 | 0.589 |
LIG_BIR_III_2 | 130 | 134 | PF00653 | 0.654 |
LIG_BRCT_BRCA1_1 | 284 | 288 | PF00533 | 0.500 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.657 |
LIG_CSL_BTD_1 | 44 | 47 | PF09270 | 0.645 |
LIG_eIF4E_1 | 254 | 260 | PF01652 | 0.603 |
LIG_eIF4E_1 | 339 | 345 | PF01652 | 0.525 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.700 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.676 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.399 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.492 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.661 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.538 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.476 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.579 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.593 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.625 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.660 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.691 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.704 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.720 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.573 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.737 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.736 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.727 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.516 |
LIG_LIR_Apic_2 | 305 | 311 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 102 | 113 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 280 | 290 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.724 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.686 |
LIG_MLH1_MIPbox_1 | 284 | 288 | PF16413 | 0.499 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.433 |
LIG_NRBOX | 568 | 574 | PF00104 | 0.516 |
LIG_Pex14_2 | 283 | 287 | PF04695 | 0.459 |
LIG_Pex14_2 | 363 | 367 | PF04695 | 0.512 |
LIG_PTB_Apo_2 | 6 | 13 | PF02174 | 0.402 |
LIG_Rb_LxCxE_1 | 608 | 624 | PF01857 | 0.429 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.521 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.586 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.621 |
LIG_SH2_PTP2 | 105 | 108 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.284 |
LIG_SH2_SRC | 308 | 311 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.683 |
LIG_SH2_STAT3 | 240 | 243 | PF00017 | 0.509 |
LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.591 |
LIG_SH3_1 | 308 | 314 | PF00018 | 0.618 |
LIG_SH3_2 | 311 | 316 | PF14604 | 0.545 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.601 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.535 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.358 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.690 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.684 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 620 | 627 | PF11976 | 0.541 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.618 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.574 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.673 |
LIG_UBA3_1 | 181 | 188 | PF00899 | 0.544 |
LIG_UBA3_1 | 294 | 303 | PF00899 | 0.559 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.526 |
LIG_WRC_WIRS_1 | 587 | 592 | PF05994 | 0.562 |
MOD_CDK_SPxxK_3 | 595 | 602 | PF00069 | 0.577 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.385 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.743 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.655 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.689 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.589 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.500 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.527 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.750 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.650 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.593 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.622 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.527 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.585 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.792 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.583 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.668 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.777 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.709 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.705 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.706 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.604 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.523 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.485 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.445 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.428 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.292 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.580 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.327 |
MOD_GlcNHglycan | 591 | 595 | PF01048 | 0.533 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.473 |
MOD_GlcNHglycan | 71 | 75 | PF01048 | 0.492 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.696 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.436 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.744 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.675 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.723 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.653 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.627 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.688 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.636 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.768 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.617 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.647 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.392 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.340 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.158 |
MOD_N-GLC_1 | 594 | 599 | PF02516 | 0.455 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.414 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.715 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.697 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.573 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.549 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.343 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.473 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.425 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.625 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.637 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.638 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.734 |
MOD_NEK2_2 | 177 | 182 | PF00069 | 0.614 |
MOD_NEK2_2 | 532 | 537 | PF00069 | 0.521 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.675 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.703 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.613 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.601 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.723 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.463 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.596 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.701 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.452 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.547 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.535 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.588 |
MOD_Plk_2-3 | 568 | 574 | PF00069 | 0.582 |
MOD_Plk_2-3 | 615 | 621 | PF00069 | 0.565 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.636 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.652 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.719 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.484 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.652 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.598 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.538 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.626 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.626 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.663 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.550 |
MOD_SUMO_for_1 | 411 | 414 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 299 | 305 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 442 | 448 | PF00179 | 0.731 |
MOD_SUMO_rev_2 | 99 | 106 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_1 | 568 | 573 | PF01217 | 0.623 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 290 | 295 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.613 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.350 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.624 |
TRG_NES_CRM1_1 | 136 | 149 | PF08389 | 0.611 |
TRG_NES_CRM1_1 | 357 | 371 | PF08389 | 0.542 |
TRG_NLS_MonoCore_2 | 428 | 433 | PF00514 | 0.744 |
TRG_NLS_MonoExtC_3 | 428 | 434 | PF00514 | 0.750 |
TRG_NLS_MonoExtN_4 | 426 | 433 | PF00514 | 0.677 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 570 | 574 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V2 | Leptomonas seymouri | 60% | 94% |
A0A0S4JAD3 | Bodo saltans | 32% | 100% |
A0A0S4JHU3 | Bodo saltans | 33% | 100% |
A0A1X0NTT2 | Trypanosomatidae | 28% | 94% |
A0A1X0P9I4 | Trypanosomatidae | 28% | 79% |
A0A3S7X6K2 | Leishmania donovani | 73% | 97% |
A0A422NUH1 | Trypanosoma rangeli | 27% | 94% |
A0A422P3P3 | Trypanosoma rangeli | 31% | 100% |
A4I8Y5 | Leishmania infantum | 73% | 97% |
C9ZQW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 95% |
D0A1W6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 88% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 88% |
E9B3V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 97% |
Q4Q470 | Leishmania major | 71% | 99% |
V5DMJ8 | Trypanosoma cruzi | 25% | 88% |
V5DQN5 | Trypanosoma cruzi | 32% | 100% |