Membrane-bound O-acyltransferase involved in the remodeling of glycosylphosphatidylinositol (GPI) anchors. Related to fungal GUP1 proteins.
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: 32 |
NetGPI | no | yes: 0, no: 32 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 5 |
GO:0005783 | endoplasmic reticulum | 5 | 5 |
GO:0016020 | membrane | 2 | 33 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 33 |
Related structures:
AlphaFold database: Q4QD81
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016746 | acyltransferase activity | 3 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.373 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.373 |
CLV_PCSK_PC7_1 | 568 | 574 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.406 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.453 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.562 |
DEG_APCC_DBOX_1 | 559 | 567 | PF00400 | 0.609 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.308 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.568 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.604 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.601 |
DOC_CKS1_1 | 26 | 31 | PF01111 | 0.284 |
DOC_CKS1_1 | 637 | 642 | PF01111 | 0.283 |
DOC_CYCLIN_yCln2_LP_2 | 332 | 338 | PF00134 | 0.411 |
DOC_MAPK_DCC_7 | 23 | 32 | PF00069 | 0.291 |
DOC_MAPK_DCC_7 | 480 | 490 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 239 | 248 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 362 | 371 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 478 | 485 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 72 | 82 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 478 | 485 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 221 | 228 | PF00149 | 0.460 |
DOC_PP1_RVXF_1 | 252 | 259 | PF00149 | 0.305 |
DOC_PP1_SILK_1 | 369 | 374 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.411 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.357 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.815 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.291 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 353 | 361 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 373 | 382 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 399 | 403 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 633 | 642 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 75 | 79 | PF00244 | 0.656 |
LIG_Actin_WH2_2 | 239 | 256 | PF00022 | 0.338 |
LIG_Actin_WH2_2 | 383 | 401 | PF00022 | 0.197 |
LIG_Actin_WH2_2 | 405 | 421 | PF00022 | 0.332 |
LIG_Actin_WH2_2 | 664 | 680 | PF00022 | 0.478 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_1 | 519 | 523 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 592 | 596 | PF00533 | 0.257 |
LIG_CtBP_PxDLS_1 | 439 | 443 | PF00389 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 44 | 50 | PF00928 | 0.347 |
LIG_deltaCOP1_diTrp_1 | 458 | 466 | PF00928 | 0.504 |
LIG_eIF4E_1 | 19 | 25 | PF01652 | 0.300 |
LIG_eIF4E_1 | 327 | 333 | PF01652 | 0.442 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.736 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.379 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.369 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.343 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.491 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.444 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.321 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.446 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.627 |
LIG_GBD_Chelix_1 | 600 | 608 | PF00786 | 0.223 |
LIG_Integrin_isoDGR_2 | 550 | 552 | PF01839 | 0.469 |
LIG_LIR_Gen_1 | 28 | 39 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 343 | 352 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 377 | 387 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 427 | 438 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.382 |
LIG_OCRL_FandH_1 | 11 | 23 | PF00620 | 0.274 |
LIG_Pex14_1 | 141 | 145 | PF04695 | 0.197 |
LIG_Pex14_1 | 214 | 218 | PF04695 | 0.441 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.331 |
LIG_Pex14_1 | 459 | 463 | PF04695 | 0.498 |
LIG_Pex14_1 | 466 | 470 | PF04695 | 0.498 |
LIG_Pex14_1 | 638 | 642 | PF04695 | 0.264 |
LIG_Pex14_2 | 420 | 424 | PF04695 | 0.353 |
LIG_Pex14_2 | 455 | 459 | PF04695 | 0.500 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.353 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.337 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.304 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.550 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.498 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.223 |
LIG_SH2_GRB2like | 39 | 42 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.354 |
LIG_SH2_PTP2 | 379 | 382 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.224 |
LIG_SH2_STAT3 | 213 | 216 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.310 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.618 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.450 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.542 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.453 |
LIG_Sin3_3 | 59 | 66 | PF02671 | 0.206 |
LIG_SUMO_SIM_anti_2 | 194 | 201 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 654 | 660 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 646 | 652 | PF11976 | 0.375 |
LIG_SxIP_EBH_1 | 138 | 148 | PF03271 | 0.406 |
LIG_TRFH_1 | 330 | 334 | PF08558 | 0.459 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.482 |
LIG_TYR_ITIM | 413 | 418 | PF00017 | 0.432 |
LIG_TYR_ITIM | 468 | 473 | PF00017 | 0.341 |
LIG_UBA3_1 | 412 | 419 | PF00899 | 0.376 |
LIG_UBA3_1 | 667 | 676 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.365 |
LIG_WW_1 | 334 | 337 | PF00397 | 0.411 |
MOD_CDK_SPK_2 | 572 | 577 | PF00069 | 0.379 |
MOD_CDK_SPxxK_3 | 572 | 579 | PF00069 | 0.352 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.373 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.504 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.405 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.273 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.657 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.546 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.585 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.556 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.489 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.454 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.458 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.438 |
MOD_CMANNOS | 456 | 459 | PF00535 | 0.346 |
MOD_CMANNOS | 638 | 641 | PF00535 | 0.308 |
MOD_DYRK1A_RPxSP_1 | 75 | 79 | PF00069 | 0.398 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.512 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.442 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.368 |
MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.530 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.447 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.549 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.471 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.531 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.690 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.329 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.498 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.537 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.518 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.623 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.537 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.352 |
MOD_N-GLC_1 | 609 | 614 | PF02516 | 0.369 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.474 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.466 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.528 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.345 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.394 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.377 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.364 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.249 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.357 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.472 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.377 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.409 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.696 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.775 |
MOD_NEK2_2 | 591 | 596 | PF00069 | 0.305 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.335 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.493 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.538 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.382 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.442 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.470 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.376 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.552 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.411 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.477 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.587 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.445 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.377 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.298 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.399 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.407 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.420 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.333 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.293 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.406 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.559 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.326 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.558 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.550 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.613 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.528 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.589 |
TRG_DiLeu_BaEn_2 | 403 | 409 | PF01217 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 251 | 256 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.373 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.804 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRP6 | Bodo saltans | 35% | 100% |
A0A1X0P614 | Trypanosomatidae | 33% | 100% |
A0A1X0P616 | Trypanosomatidae | 42% | 100% |
A0A3Q8IAC1 | Leishmania donovani | 68% | 89% |
A0A3Q8IBC3 | Leishmania donovani | 66% | 100% |
A0A3Q8IBE0 | Leishmania donovani | 89% | 83% |
A0A3Q8IDD7 | Leishmania donovani | 68% | 89% |
A0A3S5H769 | Leishmania donovani | 68% | 100% |
A0A3S5IRW9 | Trypanosoma rangeli | 38% | 100% |
A0A3S7WVJ2 | Leishmania donovani | 89% | 82% |
A0A3S7WVK4 | Leishmania donovani | 71% | 89% |
A4HA75 | Leishmania braziliensis | 61% | 95% |
A4HA76 | Leishmania braziliensis | 64% | 100% |
A4HA77 | Leishmania braziliensis | 61% | 100% |
A4HA79 | Leishmania braziliensis | 68% | 100% |
A4HA80 | Leishmania braziliensis | 61% | 75% |
A4HA81 | Leishmania braziliensis | 63% | 100% |
A4HA82 | Leishmania braziliensis | 61% | 92% |
D0A0T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E8NHJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9AGT0 | Leishmania infantum | 89% | 82% |
E9AGT1 | Leishmania infantum | 75% | 100% |
E9AGT2 | Leishmania infantum | 71% | 100% |
E9AGT3 | Leishmania infantum | 71% | 89% |
E9AGT4 | Leishmania infantum | 68% | 89% |
E9AS84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
E9AS85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 89% |
E9AS86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 92% |
Q4QD78 | Leishmania major | 72% | 100% |
Q4QD79 | Leishmania major | 75% | 100% |
Q4QD80 | Leishmania major | 75% | 100% |