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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016604 | nuclear body | 2 | 1 |
GO:0016605 | PML body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3M3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 1 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 1 |
GO:0070260 | 5'-tyrosyl-DNA phosphodiesterase activity | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 485 | 489 | PF00656 | 0.736 |
CLV_C14_Caspase3-7 | 530 | 534 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 653 | 657 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.417 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 553 | 555 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.385 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.487 |
DEG_APCC_DBOX_1 | 358 | 366 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.484 |
DEG_Kelch_Keap1_1 | 657 | 662 | PF01344 | 0.547 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.657 |
DEG_SPOP_SBC_1 | 651 | 655 | PF00917 | 0.521 |
DOC_ANK_TNKS_1 | 612 | 619 | PF00023 | 0.542 |
DOC_CKS1_1 | 154 | 159 | PF01111 | 0.530 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.384 |
DOC_CKS1_1 | 197 | 202 | PF01111 | 0.595 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.458 |
DOC_CYCLIN_RxL_1 | 95 | 108 | PF00134 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 197 | 203 | PF00134 | 0.346 |
DOC_MAPK_gen_1 | 100 | 107 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 444 | 454 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 100 | 107 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 355 | 362 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.487 |
DOC_MAPK_NFAT4_5 | 100 | 108 | PF00069 | 0.400 |
DOC_PP1_RVXF_1 | 337 | 344 | PF00149 | 0.551 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.301 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 100 | 104 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 130 | 140 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 388 | 397 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 447 | 454 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 527 | 532 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 677 | 682 | PF00244 | 0.788 |
LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 243 | 259 | PF00022 | 0.558 |
LIG_APCC_ABBAyCdc20_2 | 339 | 345 | PF00400 | 0.531 |
LIG_BIR_III_4 | 587 | 591 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 602 | 606 | PF00533 | 0.473 |
LIG_CSL_BTD_1 | 416 | 419 | PF09270 | 0.589 |
LIG_eIF4E_1 | 67 | 73 | PF01652 | 0.573 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.518 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.437 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.348 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.411 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.696 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.503 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.601 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.528 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.496 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.483 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.472 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.489 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.485 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.565 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.482 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.538 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.401 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.424 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.513 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.663 |
LIG_LIR_Apic_2 | 488 | 494 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 246 | 256 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 603 | 612 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 443 | 448 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.386 |
LIG_MAD2 | 371 | 379 | PF02301 | 0.306 |
LIG_NRBOX | 102 | 108 | PF00104 | 0.468 |
LIG_NRBOX | 251 | 257 | PF00104 | 0.575 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.481 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.483 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.671 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.519 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.461 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.579 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.486 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.620 |
LIG_SUMO_SIM_anti_2 | 102 | 108 | PF11976 | 0.329 |
LIG_SUMO_SIM_anti_2 | 284 | 290 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 179 | 185 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 438 | 443 | PF11976 | 0.613 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 54 | 59 | PF11976 | 0.491 |
LIG_TRAF2_1 | 563 | 566 | PF00917 | 0.596 |
LIG_Vh1_VBS_1 | 545 | 563 | PF01044 | 0.552 |
LIG_WRC_WIRS_1 | 601 | 606 | PF05994 | 0.315 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.380 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.720 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.726 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.531 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.465 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.566 |
MOD_CK1_1 | 652 | 658 | PF00069 | 0.703 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.590 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.427 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.568 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.665 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.420 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.723 |
MOD_Cter_Amidation | 123 | 126 | PF01082 | 0.494 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.435 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.328 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.725 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.385 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.728 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.501 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.715 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.699 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.564 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.691 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.752 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.694 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.507 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.511 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.428 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.509 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.507 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.530 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.538 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.609 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.509 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.460 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.558 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.513 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.435 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.678 |
MOD_LATS_1 | 29 | 35 | PF00433 | 0.346 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.306 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.390 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.477 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.677 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.529 |
MOD_N-GLC_1 | 639 | 644 | PF02516 | 0.661 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.651 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.543 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.549 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.390 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.641 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.437 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.382 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.555 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.493 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.739 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.343 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.576 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.451 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.609 |
MOD_PK_1 | 337 | 343 | PF00069 | 0.582 |
MOD_PKA_1 | 277 | 283 | PF00069 | 0.268 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.557 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.268 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.469 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.554 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.558 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.580 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.500 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.397 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.486 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.403 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.390 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.343 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.475 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.523 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.523 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.683 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.465 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.427 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.463 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.318 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.477 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.371 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.425 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.348 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.475 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.412 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.681 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.490 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.610 |
MOD_SUMO_for_1 | 628 | 631 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 462 | 467 | PF00179 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.449 |
TRG_NLS_MonoExtC_3 | 549 | 554 | PF00514 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 543 | 547 | PF00026 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 558 | 562 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUJ3 | Leptomonas seymouri | 56% | 100% |
A0A0S4J9X6 | Bodo saltans | 31% | 84% |
A0A1X0P940 | Trypanosomatidae | 42% | 76% |
A0A3S5H550 | Leishmania donovani | 78% | 100% |
A0A422NMS5 | Trypanosoma rangeli | 40% | 75% |
C9ZRZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 76% |
D0A265 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 73% |
E9AG51 | Leishmania infantum | 78% | 100% |
E9AJU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q6T444 | Leishmania major | 77% | 98% |