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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000127 | transcription factor TFIIIC complex | 4 | 10 |
GO:0005667 | transcription regulator complex | 2 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0090576 | RNA polymerase III transcription regulator complex | 3 | 10 |
Related structures:
AlphaFold database: A0A3S7WWK4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006352 | DNA-templated transcription initiation | 6 | 10 |
GO:0006384 | transcription initiation at RNA polymerase III promoter | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009059 | macromolecule biosynthetic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0018130 | heterocycle biosynthetic process | 4 | 10 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 10 |
GO:0032774 | RNA biosynthetic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 10 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.796 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.296 |
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.557 |
CLV_PCSK_FUR_1 | 213 | 217 | PF00082 | 0.685 |
CLV_PCSK_FUR_1 | 241 | 245 | PF00082 | 0.546 |
CLV_PCSK_FUR_1 | 538 | 542 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.718 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.597 |
CLV_PCSK_PC7_1 | 536 | 542 | PF00082 | 0.522 |
CLV_PCSK_PC7_1 | 602 | 608 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.492 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.684 |
DEG_APCC_DBOX_1 | 552 | 560 | PF00400 | 0.487 |
DEG_SCF_FBW7_1 | 33 | 38 | PF00400 | 0.662 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.665 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.676 |
DEG_SPOP_SBC_1 | 658 | 662 | PF00917 | 0.698 |
DOC_CDC14_PxL_1 | 318 | 326 | PF14671 | 0.638 |
DOC_CKS1_1 | 312 | 317 | PF01111 | 0.634 |
DOC_CYCLIN_RxL_1 | 525 | 537 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 302 | 308 | PF00134 | 0.561 |
DOC_CYCLIN_yCln2_LP_2 | 569 | 575 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 143 | 151 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 154 | 164 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 506 | 515 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 562 | 571 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 233 | 240 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 509 | 517 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 565 | 573 | PF00069 | 0.451 |
DOC_MAPK_NFAT4_5 | 233 | 241 | PF00069 | 0.585 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.501 |
DOC_PP2B_PxIxI_1 | 388 | 394 | PF00149 | 0.393 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.528 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.215 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 143 | 152 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 157 | 163 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 509 | 517 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 552 | 557 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 607 | 615 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 496 | 511 | PF00022 | 0.393 |
LIG_BIR_III_4 | 278 | 282 | PF00653 | 0.623 |
LIG_BIR_III_4 | 373 | 377 | PF00653 | 0.337 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.698 |
LIG_BRCT_BRCA1_1 | 678 | 682 | PF00533 | 0.652 |
LIG_CtBP_PxDLS_1 | 597 | 601 | PF00389 | 0.533 |
LIG_eIF4E_1 | 231 | 237 | PF01652 | 0.523 |
LIG_EVH1_2 | 331 | 335 | PF00568 | 0.321 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.570 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.562 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.677 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.739 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.662 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.379 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.306 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.370 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.417 |
LIG_FHA_2 | 650 | 656 | PF00498 | 0.755 |
LIG_GBD_Chelix_1 | 444 | 452 | PF00786 | 0.411 |
LIG_Integrin_RGD_1 | 86 | 88 | PF01839 | 0.685 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 23 | 32 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 497 | 508 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 497 | 503 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.428 |
LIG_NRBOX | 529 | 535 | PF00104 | 0.487 |
LIG_NRBOX | 625 | 631 | PF00104 | 0.492 |
LIG_PCNA_PIPBox_1 | 225 | 234 | PF02747 | 0.537 |
LIG_PCNA_yPIPBox_3 | 225 | 239 | PF02747 | 0.517 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.651 |
LIG_PTB_Apo_2 | 474 | 481 | PF02174 | 0.321 |
LIG_PTB_Phospho_1 | 226 | 232 | PF10480 | 0.655 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.639 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 492 | 496 | PF00017 | 0.375 |
LIG_SH2_NCK_1 | 500 | 504 | PF00017 | 0.331 |
LIG_SH2_PTP2 | 24 | 27 | PF00017 | 0.630 |
LIG_SH2_SRC | 346 | 349 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 615 | 619 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 622 | 626 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.435 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.698 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.569 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.393 |
LIG_SUMO_SIM_par_1 | 389 | 394 | PF11976 | 0.393 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.745 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.624 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.481 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.687 |
LIG_TRAF2_2 | 572 | 577 | PF00917 | 0.465 |
LIG_TYR_ITIM | 498 | 503 | PF00017 | 0.337 |
LIG_TYR_ITIM | 542 | 547 | PF00017 | 0.456 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.751 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.764 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.618 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.672 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.393 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.411 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.688 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.678 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.681 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.475 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.439 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.708 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.729 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.697 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.690 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.565 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.601 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.765 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.729 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.822 |
MOD_GlcNHglycan | 287 | 291 | PF01048 | 0.602 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.359 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.392 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.402 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.449 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.345 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.705 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.334 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.411 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.649 |
MOD_GlcNHglycan | 675 | 681 | PF01048 | 0.670 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.614 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.726 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.782 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.669 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.617 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.748 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.582 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.395 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.412 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.413 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.607 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.706 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.625 |
MOD_LATS_1 | 550 | 556 | PF00433 | 0.482 |
MOD_N-GLC_1 | 649 | 654 | PF02516 | 0.757 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.393 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.411 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.650 |
MOD_PKA_1 | 552 | 558 | PF00069 | 0.431 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.713 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.741 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.798 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.401 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.355 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.419 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.413 |
MOD_PKB_1 | 516 | 524 | PF00069 | 0.516 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.657 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.433 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.703 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.285 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.438 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.337 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.447 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.389 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.509 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.636 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.598 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.741 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.502 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.625 |
MOD_SUMO_rev_2 | 537 | 547 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.673 |
TRG_DiLeu_BaEn_2 | 60 | 66 | PF01217 | 0.645 |
TRG_DiLeu_BaEn_4 | 396 | 402 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 147 | 152 | PF01217 | 0.662 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 503 | 508 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 528 | 533 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 238 | 241 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 636 | 639 | PF00400 | 0.527 |
TRG_NLS_MonoCore_2 | 211 | 216 | PF00514 | 0.676 |
TRG_NLS_MonoExtC_3 | 211 | 216 | PF00514 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 435 | 439 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 531 | 535 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 639 | 644 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2I9 | Leptomonas seymouri | 52% | 94% |
A0A1X0NZE8 | Trypanosomatidae | 33% | 100% |
A0A422NAG1 | Trypanosoma rangeli | 34% | 100% |
A4HIW4 | Leishmania braziliensis | 83% | 99% |
D0A185 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AGX8 | Leishmania infantum | 100% | 100% |
E9AV94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
Q4QC86 | Leishmania major | 93% | 100% |