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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000127 | transcription factor TFIIIC complex | 4 | 11 |
GO:0005667 | transcription regulator complex | 2 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0090576 | RNA polymerase III transcription regulator complex | 3 | 11 |
Related structures:
AlphaFold database: A4HIW4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006352 | DNA-templated transcription initiation | 6 | 11 |
GO:0006384 | transcription initiation at RNA polymerase III promoter | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0032774 | RNA biosynthetic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 257 | 261 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.406 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.273 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.466 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.673 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 549 | 551 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.622 |
CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.399 |
CLV_PCSK_PC7_1 | 533 | 539 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 599 | 605 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.261 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.610 |
DEG_APCC_DBOX_1 | 549 | 557 | PF00400 | 0.464 |
DEG_SCF_FBW7_1 | 35 | 40 | PF00400 | 0.621 |
DEG_SCF_FBW7_1 | 80 | 85 | PF00400 | 0.497 |
DEG_SPOP_SBC_1 | 280 | 284 | PF00917 | 0.662 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.668 |
DOC_CDC14_PxL_1 | 315 | 323 | PF14671 | 0.576 |
DOC_CKS1_1 | 309 | 314 | PF01111 | 0.627 |
DOC_CYCLIN_RxL_1 | 146 | 155 | PF00134 | 0.466 |
DOC_CYCLIN_RxL_1 | 522 | 534 | PF00134 | 0.487 |
DOC_CYCLIN_RxL_1 | 546 | 555 | PF00134 | 0.274 |
DOC_CYCLIN_yCln2_LP_2 | 299 | 305 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 566 | 572 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 156 | 166 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 503 | 512 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 549 | 556 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 229 | 236 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 24 | 33 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 506 | 514 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 563 | 570 | PF00069 | 0.407 |
DOC_MAPK_NFAT4_5 | 229 | 237 | PF00069 | 0.649 |
DOC_PP2B_LxvP_1 | 18 | 21 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.495 |
DOC_PP2B_PxIxI_1 | 385 | 391 | PF00149 | 0.341 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 506 | 514 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 549 | 554 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 493 | 508 | PF00022 | 0.341 |
LIG_AP2alpha_2 | 247 | 249 | PF02296 | 0.478 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 682 | 686 | PF00533 | 0.557 |
LIG_CtBP_PxDLS_1 | 594 | 598 | PF00389 | 0.488 |
LIG_eIF4E_1 | 227 | 233 | PF01652 | 0.473 |
LIG_EVH1_2 | 328 | 332 | PF00568 | 0.292 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.555 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.544 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.670 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.595 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.621 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.316 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.273 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.531 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.399 |
LIG_GBD_Chelix_1 | 441 | 449 | PF00786 | 0.406 |
LIG_LIR_Apic_2 | 71 | 75 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 25 | 33 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 494 | 505 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 683 | 693 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 683 | 689 | PF02991 | 0.518 |
LIG_NRBOX | 526 | 532 | PF00104 | 0.452 |
LIG_NRBOX | 622 | 628 | PF00104 | 0.489 |
LIG_PCNA_PIPBox_1 | 221 | 230 | PF02747 | 0.500 |
LIG_PCNA_yPIPBox_3 | 221 | 229 | PF02747 | 0.503 |
LIG_PTB_Apo_2 | 222 | 229 | PF02174 | 0.629 |
LIG_PTB_Apo_2 | 471 | 478 | PF02174 | 0.292 |
LIG_PTB_Phospho_1 | 222 | 228 | PF10480 | 0.638 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.492 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.575 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 380 | 384 | PF00017 | 0.195 |
LIG_SH2_NCK_1 | 489 | 493 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 497 | 501 | PF00017 | 0.378 |
LIG_SH2_PTP2 | 26 | 29 | PF00017 | 0.640 |
LIG_SH2_SRC | 343 | 346 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.250 |
LIG_SH2_STAP1 | 619 | 623 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.395 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.492 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.575 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.348 |
LIG_SUMO_SIM_par_1 | 386 | 391 | PF11976 | 0.341 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.465 |
LIG_TRAF2_1 | 644 | 647 | PF00917 | 0.572 |
LIG_TRAF2_1 | 688 | 691 | PF00917 | 0.469 |
LIG_TRAF2_2 | 569 | 574 | PF00917 | 0.460 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.736 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.738 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.654 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.667 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.300 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.341 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.352 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.471 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.629 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.501 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.658 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.526 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.460 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.414 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.711 |
MOD_CK2_1 | 679 | 685 | PF00069 | 0.563 |
MOD_GlcNHglycan | 104 | 109 | PF01048 | 0.587 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.699 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.593 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.557 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.588 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.749 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.790 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.543 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.398 |
MOD_GlcNHglycan | 373 | 378 | PF01048 | 0.409 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.427 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.688 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.292 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.365 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.625 |
MOD_GlcNHglycan | 672 | 678 | PF01048 | 0.625 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.577 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.479 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.747 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.747 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.672 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.728 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.550 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.427 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.436 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.405 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.701 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.394 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.615 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.681 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.588 |
MOD_LATS_1 | 547 | 553 | PF00433 | 0.460 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.714 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.421 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.371 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.406 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.695 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.581 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.423 |
MOD_PKA_1 | 549 | 555 | PF00069 | 0.406 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.525 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.692 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.782 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.341 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.359 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.390 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.445 |
MOD_PKB_1 | 513 | 521 | PF00069 | 0.507 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.660 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.409 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.734 |
MOD_Plk_1 | 684 | 690 | PF00069 | 0.747 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.491 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.386 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.341 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.421 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.344 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.525 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.609 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.638 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.776 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.494 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.611 |
MOD_SUMO_rev_2 | 269 | 276 | PF00179 | 0.575 |
TRG_DiLeu_BaEn_1 | 219 | 224 | PF01217 | 0.669 |
TRG_DiLeu_BaEn_2 | 62 | 68 | PF01217 | 0.679 |
TRG_DiLeu_BaEn_4 | 393 | 399 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.635 |
TRG_DiLeu_BaLyEn_6 | 429 | 434 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 500 | 505 | PF01217 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 525 | 530 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 512 | 515 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 549 | 551 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 633 | 636 | PF00400 | 0.540 |
TRG_NLS_MonoCore_2 | 207 | 212 | PF00514 | 0.668 |
TRG_NLS_MonoExtC_3 | 207 | 212 | PF00514 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 528 | 532 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 636 | 641 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2I9 | Leptomonas seymouri | 50% | 93% |
A0A1X0NZE8 | Trypanosomatidae | 32% | 100% |
A0A3S7WWK4 | Leishmania donovani | 83% | 99% |
A0A422NAG1 | Trypanosoma rangeli | 35% | 100% |
D0A185 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AGX8 | Leishmania infantum | 84% | 99% |
E9AV94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QC86 | Leishmania major | 80% | 100% |
V5B9M4 | Trypanosoma cruzi | 38% | 100% |