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: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 34 |
GO:0110165 | cellular anatomical entity | 1 | 34 |
GO:0005737 | cytoplasm | 2 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: A0A3S5H769
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016746 | acyltransferase activity | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 628 | 632 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.441 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.223 |
CLV_PCSK_PC7_1 | 573 | 579 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 484 | 492 | PF00400 | 0.538 |
DEG_APCC_DBOX_1 | 564 | 572 | PF00400 | 0.599 |
DEG_MDM2_SWIB_1 | 17 | 24 | PF02201 | 0.337 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.294 |
DEG_SCF_FBW7_1 | 643 | 648 | PF00400 | 0.357 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.543 |
DOC_CDC14_PxL_1 | 389 | 397 | PF14671 | 0.397 |
DOC_CYCLIN_RxL_1 | 68 | 78 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 337 | 343 | PF00134 | 0.379 |
DOC_MAPK_DCC_7 | 485 | 495 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 246 | 253 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 483 | 490 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 54 | 61 | PF00069 | 0.225 |
DOC_MAPK_MEF2A_6 | 483 | 490 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.372 |
DOC_MAPK_NFAT4_5 | 54 | 62 | PF00069 | 0.246 |
DOC_PP1_RVXF_1 | 257 | 264 | PF00149 | 0.301 |
DOC_PP1_SILK_1 | 374 | 379 | PF00149 | 0.350 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.379 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.817 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.625 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 254 | 259 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 378 | 387 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 485 | 491 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 564 | 568 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 573 | 581 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 670 | 676 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 71 | 77 | PF00244 | 0.605 |
LIG_Actin_WH2_2 | 244 | 261 | PF00022 | 0.327 |
LIG_Actin_WH2_2 | 410 | 426 | PF00022 | 0.307 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.294 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 524 | 528 | PF00533 | 0.400 |
LIG_CSL_BTD_1 | 110 | 113 | PF09270 | 0.625 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.489 |
LIG_deltaCOP1_diTrp_1 | 43 | 49 | PF00928 | 0.329 |
LIG_deltaCOP1_diTrp_1 | 463 | 471 | PF00928 | 0.494 |
LIG_EH_1 | 26 | 30 | PF12763 | 0.322 |
LIG_eIF4E_1 | 332 | 338 | PF01652 | 0.408 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.714 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.457 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.468 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.354 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.420 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.481 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.644 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.377 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.439 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.309 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.428 |
LIG_Integrin_isoDGR_2 | 555 | 557 | PF01839 | 0.446 |
LIG_LIR_Apic_2 | 144 | 148 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 326 | 335 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 348 | 357 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 674 | 682 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 674 | 678 | PF02991 | 0.574 |
LIG_NRBOX | 58 | 64 | PF00104 | 0.435 |
LIG_PAM2_1 | 577 | 589 | PF00658 | 0.536 |
LIG_Pex14_1 | 219 | 223 | PF04695 | 0.409 |
LIG_Pex14_1 | 249 | 253 | PF04695 | 0.323 |
LIG_Pex14_1 | 464 | 468 | PF04695 | 0.487 |
LIG_Pex14_1 | 471 | 475 | PF04695 | 0.487 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.338 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.344 |
LIG_Pex14_2 | 460 | 464 | PF04695 | 0.489 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.340 |
LIG_PTB_Apo_2 | 24 | 31 | PF02174 | 0.333 |
LIG_REV1ctd_RIR_1 | 27 | 36 | PF16727 | 0.337 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.316 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.291 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.455 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.330 |
LIG_SH2_CRK | 475 | 479 | PF00017 | 0.487 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 151 | 155 | PF00017 | 0.331 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.527 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.639 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.434 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.453 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.397 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.526 |
LIG_TRFH_1 | 335 | 339 | PF08558 | 0.460 |
LIG_TYR_ITIM | 418 | 423 | PF00017 | 0.434 |
LIG_TYR_ITIM | 473 | 478 | PF00017 | 0.327 |
LIG_UBA3_1 | 417 | 424 | PF00899 | 0.350 |
LIG_UBA3_1 | 678 | 683 | PF00899 | 0.512 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.348 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.369 |
LIG_WW_1 | 339 | 342 | PF00397 | 0.412 |
LIG_WW_3 | 112 | 116 | PF00397 | 0.488 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.674 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.523 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.550 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.600 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.425 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.354 |
MOD_CMANNOS | 461 | 464 | PF00535 | 0.332 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.686 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.484 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.408 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.343 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.554 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.693 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.376 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.466 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.738 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.541 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.554 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.597 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.399 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.499 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.521 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.523 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.538 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.562 |
MOD_LATS_1 | 356 | 362 | PF00433 | 0.304 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.482 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.366 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.366 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.305 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.340 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.505 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.384 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.562 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.427 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.469 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.420 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.350 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.548 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.643 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.516 |
MOD_PKB_1 | 121 | 129 | PF00069 | 0.513 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.415 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.505 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.456 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.378 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.413 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.377 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.430 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.566 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.327 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.373 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.558 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.323 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.598 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.570 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.571 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.522 |
TRG_DiLeu_BaEn_2 | 408 | 414 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.429 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 675 | 678 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 447 | 449 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 563 | 565 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRP6 | Bodo saltans | 36% | 100% |
A0A1X0P614 | Trypanosomatidae | 33% | 100% |
A0A1X0P616 | Trypanosomatidae | 40% | 100% |
A0A1X0P718 | Trypanosomatidae | 40% | 100% |
A0A3Q8IAC1 | Leishmania donovani | 99% | 100% |
A0A3Q8IBC3 | Leishmania donovani | 91% | 99% |
A0A3Q8IBE0 | Leishmania donovani | 74% | 100% |
A0A3Q8IDD7 | Leishmania donovani | 99% | 100% |
A0A3S5IRW9 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WVJ2 | Leishmania donovani | 74% | 81% |
A0A3S7WVK4 | Leishmania donovani | 97% | 88% |
A4HA75 | Leishmania braziliensis | 62% | 100% |
A4HA76 | Leishmania braziliensis | 62% | 100% |
A4HA77 | Leishmania braziliensis | 65% | 100% |
A4HA79 | Leishmania braziliensis | 70% | 100% |
A4HA80 | Leishmania braziliensis | 59% | 100% |
A4HA81 | Leishmania braziliensis | 66% | 100% |
A4HA82 | Leishmania braziliensis | 66% | 100% |
D0A0T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E8NHJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AGT0 | Leishmania infantum | 74% | 100% |
E9AGT1 | Leishmania infantum | 96% | 100% |
E9AGT2 | Leishmania infantum | 98% | 100% |
E9AGT3 | Leishmania infantum | 96% | 100% |
E9AGT4 | Leishmania infantum | 99% | 100% |
E9AS84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AS85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AS86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4QD78 | Leishmania major | 91% | 100% |
Q4QD79 | Leishmania major | 89% | 100% |
Q4QD80 | Leishmania major | 89% | 100% |
Q4QD81 | Leishmania major | 68% | 100% |