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:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QCE5
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016311 | dephosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 11 |
GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016791 | phosphatase activity | 5 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.678 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 544 | 546 | PF00082 | 0.752 |
CLV_PCSK_PC7_1 | 149 | 155 | PF00082 | 0.276 |
CLV_PCSK_PC7_1 | 528 | 534 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.793 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.693 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.612 |
DEG_SCF_FBW7_1 | 458 | 465 | PF00400 | 0.755 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.761 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.617 |
DOC_CKS1_1 | 404 | 409 | PF01111 | 0.633 |
DOC_CKS1_1 | 506 | 511 | PF01111 | 0.595 |
DOC_MAPK_gen_1 | 215 | 223 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 298 | 305 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 532 | 541 | PF00069 | 0.619 |
DOC_PP1_RVXF_1 | 80 | 87 | PF00149 | 0.294 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.633 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.355 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.294 |
DOC_USP7_UBL2_3 | 411 | 415 | PF12436 | 0.680 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 329 | 333 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 428 | 438 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 463 | 467 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 493 | 497 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 499 | 504 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 507 | 516 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 532 | 537 | PF00244 | 0.662 |
LIG_Actin_WH2_2 | 253 | 271 | PF00022 | 0.580 |
LIG_Actin_WH2_2 | 315 | 331 | PF00022 | 0.592 |
LIG_BIR_III_4 | 62 | 66 | PF00653 | 0.408 |
LIG_CaM_IQ_9 | 339 | 354 | PF13499 | 0.507 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.308 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.705 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.244 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.681 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.706 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.710 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.610 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.760 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.322 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.631 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.595 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.656 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.627 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.661 |
LIG_GBD_Chelix_1 | 83 | 91 | PF00786 | 0.196 |
LIG_LIR_Apic_2 | 503 | 509 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 340 | 344 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.372 |
LIG_NRBOX | 184 | 190 | PF00104 | 0.509 |
LIG_PCNA_yPIPBox_3 | 181 | 189 | PF02747 | 0.497 |
LIG_PTB_Apo_2 | 193 | 200 | PF02174 | 0.517 |
LIG_PTB_Phospho_1 | 193 | 199 | PF10480 | 0.515 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.692 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.607 |
LIG_SH2_CRK | 506 | 510 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.687 |
LIG_SH2_STAT3 | 190 | 193 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.276 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.536 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.649 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.670 |
LIG_SH3_4 | 141 | 148 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 25 | 30 | PF11976 | 0.348 |
LIG_TYR_ITIM | 374 | 379 | PF00017 | 0.689 |
LIG_UBA3_1 | 128 | 132 | PF00899 | 0.348 |
LIG_UBA3_1 | 184 | 191 | PF00899 | 0.407 |
LIG_UBA3_1 | 26 | 31 | PF00899 | 0.348 |
MOD_CDC14_SPxK_1 | 515 | 518 | PF00782 | 0.677 |
MOD_CDK_SPK_2 | 403 | 408 | PF00069 | 0.627 |
MOD_CDK_SPK_2 | 458 | 463 | PF00069 | 0.766 |
MOD_CDK_SPK_2 | 563 | 568 | PF00069 | 0.673 |
MOD_CDK_SPxK_1 | 512 | 518 | PF00069 | 0.676 |
MOD_CDK_SPxxK_3 | 280 | 287 | PF00069 | 0.528 |
MOD_CDK_SPxxK_3 | 403 | 410 | PF00069 | 0.624 |
MOD_CDK_SPxxK_3 | 512 | 519 | PF00069 | 0.776 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.646 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.639 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.642 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.659 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.704 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.684 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.694 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.634 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.651 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.619 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.627 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.395 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.699 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.642 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.550 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.245 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.729 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.677 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.662 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.749 |
MOD_Cter_Amidation | 270 | 273 | PF01082 | 0.678 |
MOD_DYRK1A_RPxSP_1 | 280 | 284 | PF00069 | 0.567 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.319 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.582 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.597 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.677 |
MOD_GlcNHglycan | 345 | 350 | PF01048 | 0.495 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.770 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.709 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.686 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.680 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.621 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.641 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.817 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.543 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.679 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.580 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.521 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.566 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.538 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.588 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.643 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.617 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.702 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.655 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.609 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.663 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.624 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.628 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.631 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.624 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.537 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.665 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.661 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.519 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.628 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.646 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.510 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.625 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.487 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.409 |
MOD_LATS_1 | 418 | 424 | PF00433 | 0.778 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.699 |
MOD_N-GLC_1 | 580 | 585 | PF02516 | 0.727 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.693 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.382 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.533 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.563 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.764 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.784 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.593 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.695 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.305 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.494 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.533 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.697 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.815 |
MOD_PK_1 | 273 | 279 | PF00069 | 0.614 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.669 |
MOD_PKA_1 | 410 | 416 | PF00069 | 0.691 |
MOD_PKA_1 | 532 | 538 | PF00069 | 0.784 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.348 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.668 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.664 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.776 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.710 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.636 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.627 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.517 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.561 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.631 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.457 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.408 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.737 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.479 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.377 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.408 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.741 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.453 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.632 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.355 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.355 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.276 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.566 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.538 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.598 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.640 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.631 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.647 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.582 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.624 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.587 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.492 |
MOD_SUMO_rev_2 | 137 | 142 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 340 | 349 | PF00179 | 0.631 |
MOD_SUMO_rev_2 | 554 | 560 | PF00179 | 0.664 |
TRG_DiLeu_BaEn_2 | 254 | 260 | PF01217 | 0.658 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.698 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.276 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.660 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8I8 | Leptomonas seymouri | 58% | 93% |
A0A0S4JFG5 | Bodo saltans | 43% | 81% |
A0A1X0NXL0 | Trypanosomatidae | 47% | 100% |
A0A3Q8IAA7 | Leishmania donovani | 95% | 100% |
A0A3R7MFE4 | Trypanosoma rangeli | 45% | 100% |
A4HBR6 | Leishmania braziliensis | 80% | 100% |
A4HZ69 | Leishmania infantum | 95% | 100% |
D0A1G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AV36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |