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 | 5 |
GO:0005783 | endoplasmic reticulum | 5 | 5 |
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 |
Related structures:
AlphaFold database: E9AS86
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.325 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 697 | 701 | PF00656 | 0.277 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.376 |
CLV_PCSK_FUR_1 | 148 | 152 | PF00082 | 0.367 |
CLV_PCSK_FUR_1 | 629 | 633 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.299 |
CLV_PCSK_PC7_1 | 720 | 726 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.455 |
CLV_Separin_Metazoa | 721 | 725 | PF03568 | 0.623 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.602 |
DEG_APCC_KENBOX_2 | 99 | 103 | PF00400 | 0.290 |
DEG_MDM2_SWIB_1 | 588 | 595 | PF02201 | 0.235 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.612 |
DEG_ODPH_VHL_1 | 246 | 259 | PF01847 | 0.325 |
DEG_SCF_FBW7_1 | 445 | 452 | PF00400 | 0.227 |
DEG_SPOP_SBC_1 | 459 | 463 | PF00917 | 0.200 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.198 |
DEG_SPOP_SBC_1 | 7 | 11 | PF00917 | 0.622 |
DOC_CDC14_PxL_1 | 608 | 616 | PF14671 | 0.193 |
DOC_CKS1_1 | 292 | 297 | PF01111 | 0.252 |
DOC_CKS1_1 | 446 | 451 | PF01111 | 0.227 |
DOC_CKS1_1 | 746 | 751 | PF01111 | 0.604 |
DOC_CYCLIN_yCln2_LP_2 | 103 | 109 | PF00134 | 0.305 |
DOC_CYCLIN_yCln2_LP_2 | 732 | 738 | PF00134 | 0.538 |
DOC_MAPK_DCC_7 | 578 | 587 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 724 | 734 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 727 | 736 | PF00069 | 0.550 |
DOC_MAPK_RevD_3 | 134 | 148 | PF00069 | 0.244 |
DOC_PP1_RVXF_1 | 307 | 314 | PF00149 | 0.318 |
DOC_PP1_RVXF_1 | 596 | 603 | PF00149 | 0.259 |
DOC_PP2B_LxvP_1 | 103 | 106 | PF13499 | 0.381 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.315 |
DOC_PP2B_LxvP_1 | 732 | 735 | PF13499 | 0.547 |
DOC_PP2B_LxvP_1 | 736 | 739 | PF13499 | 0.531 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.289 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.626 |
DOC_USP7_MATH_2 | 357 | 363 | PF00917 | 0.270 |
DOC_USP7_UBL2_3 | 100 | 104 | PF12436 | 0.298 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.303 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.293 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.227 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.212 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 309 | 314 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.619 |
LIG_Actin_RPEL_3 | 414 | 433 | PF02755 | 0.411 |
LIG_Actin_WH2_2 | 582 | 600 | PF00022 | 0.345 |
LIG_BRCT_BRCA1_1 | 503 | 507 | PF00533 | 0.215 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.312 |
LIG_CSL_BTD_1 | 292 | 295 | PF09270 | 0.291 |
LIG_deltaCOP1_diTrp_1 | 290 | 299 | PF00928 | 0.364 |
LIG_deltaCOP1_diTrp_1 | 518 | 527 | PF00928 | 0.244 |
LIG_deltaCOP1_diTrp_1 | 555 | 563 | PF00928 | 0.504 |
LIG_EH1_1 | 233 | 241 | PF00400 | 0.325 |
LIG_eIF4E_1 | 138 | 144 | PF01652 | 0.244 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.292 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.408 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.742 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.222 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.427 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.395 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.383 |
LIG_FHA_1 | 727 | 733 | PF00498 | 0.566 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.633 |
LIG_LIR_Apic_2 | 531 | 536 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 504 | 515 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 577 | 587 | PF02991 | 0.220 |
LIG_LIR_Gen_1 | 683 | 694 | PF02991 | 0.226 |
LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.291 |
LIG_LIR_LC3C_4 | 613 | 616 | PF02991 | 0.193 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 380 | 385 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 405 | 409 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 683 | 689 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.280 |
LIG_MLH1_MIPbox_1 | 503 | 507 | PF16413 | 0.193 |
LIG_MYND_2 | 201 | 205 | PF01753 | 0.517 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.336 |
LIG_Pex14_1 | 420 | 424 | PF04695 | 0.411 |
LIG_Pex14_1 | 556 | 560 | PF04695 | 0.498 |
LIG_Pex14_1 | 563 | 567 | PF04695 | 0.498 |
LIG_Pex14_2 | 284 | 288 | PF04695 | 0.285 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.361 |
LIG_Pex14_2 | 523 | 527 | PF04695 | 0.520 |
LIG_Pex14_2 | 552 | 556 | PF04695 | 0.499 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.327 |
LIG_Pex14_2 | 588 | 592 | PF04695 | 0.355 |
LIG_REV1ctd_RIR_1 | 521 | 529 | PF16727 | 0.459 |
LIG_SH2_CRK | 567 | 571 | PF00017 | 0.498 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.248 |
LIG_SH2_NCK_1 | 533 | 537 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 439 | 442 | PF00017 | 0.283 |
LIG_SH2_SRC | 244 | 247 | PF00017 | 0.397 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.293 |
LIG_SH2_SRC | 533 | 536 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 706 | 710 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.279 |
LIG_SH2_STAT3 | 469 | 472 | PF00017 | 0.191 |
LIG_SH2_STAT3 | 706 | 709 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 715 | 718 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 690 | 693 | PF00017 | 0.315 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.313 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.579 |
LIG_SH3_3 | 736 | 742 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 208 | 213 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 490 | 495 | PF11976 | 0.227 |
LIG_SUMO_SIM_anti_2 | 645 | 651 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 681 | 686 | PF11976 | 0.214 |
LIG_SUMO_SIM_par_1 | 430 | 435 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 489 | 495 | PF11976 | 0.225 |
LIG_SUMO_SIM_par_1 | 648 | 653 | PF11976 | 0.217 |
LIG_SUMO_SIM_par_1 | 694 | 702 | PF11976 | 0.405 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.258 |
LIG_TYR_ITIM | 386 | 391 | PF00017 | 0.255 |
LIG_TYR_ITIM | 437 | 442 | PF00017 | 0.205 |
LIG_TYR_ITIM | 565 | 570 | PF00017 | 0.496 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.320 |
LIG_UBA3_1 | 245 | 251 | PF00899 | 0.325 |
LIG_UBA3_1 | 710 | 714 | PF00899 | 0.619 |
LIG_WRC_WIRS_1 | 310 | 315 | PF05994 | 0.277 |
LIG_WRC_WIRS_1 | 397 | 402 | PF05994 | 0.365 |
LIG_WRC_WIRS_1 | 549 | 554 | PF05994 | 0.470 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.303 |
LIG_WW_3 | 749 | 753 | PF00397 | 0.618 |
MOD_CDK_SPxxK_3 | 745 | 752 | PF00069 | 0.606 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.656 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.597 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.243 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.205 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.682 |
MOD_CK1_1 | 661 | 667 | PF00069 | 0.372 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.689 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.376 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.611 |
MOD_CMANNOS | 553 | 556 | PF00535 | 0.299 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.531 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.460 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.471 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.467 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.481 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.427 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.425 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.678 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.695 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.610 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.560 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.333 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.329 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.211 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.227 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.425 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.232 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.495 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.381 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.284 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.451 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.391 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.391 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.417 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.587 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.340 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.413 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.309 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.227 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.248 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.198 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.495 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.535 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.230 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.569 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.334 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.363 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.432 |
MOD_PK_1 | 207 | 213 | PF00069 | 0.435 |
MOD_PK_1 | 578 | 584 | PF00069 | 0.345 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.505 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.501 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.552 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.501 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.550 |
MOD_PKA_2 | 726 | 732 | PF00069 | 0.640 |
MOD_PKB_1 | 148 | 156 | PF00069 | 0.509 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.472 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.250 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.227 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.538 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.244 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.356 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.581 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.656 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.357 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.374 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.258 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.747 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.449 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.319 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.293 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.470 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.420 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.226 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.354 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.339 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.399 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.291 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.227 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.212 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.646 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.727 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.600 |
MOD_SUMO_rev_2 | 413 | 419 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 697 | 705 | PF00179 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 595 | 600 | PF01217 | 0.299 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 147 | 150 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 723 | 725 | PF00400 | 0.567 |
TRG_NES_CRM1_1 | 518 | 531 | PF08389 | 0.422 |
TRG_NES_CRM1_1 | 537 | 550 | PF08389 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 641 | 646 | PF00026 | 0.244 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRP6 | Bodo saltans | 33% | 100% |
A0A1X0P614 | Trypanosomatidae | 40% | 100% |
A0A1X0P616 | Trypanosomatidae | 36% | 100% |
A0A1X0P718 | Trypanosomatidae | 34% | 100% |
A0A3Q8IAC1 | Leishmania donovani | 31% | 97% |
A0A3Q8IBC3 | Leishmania donovani | 32% | 100% |
A0A3Q8IBE0 | Leishmania donovani | 32% | 90% |
A0A3Q8IDD7 | Leishmania donovani | 31% | 97% |
A0A3S5H769 | Leishmania donovani | 31% | 100% |
A0A3S5IRW9 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WVJ2 | Leishmania donovani | 32% | 90% |
A0A3S7WVK4 | Leishmania donovani | 31% | 97% |
A0A3S7WVM5 | Leishmania donovani | 83% | 100% |
A4HA75 | Leishmania braziliensis | 29% | 97% |
A4HA76 | Leishmania braziliensis | 31% | 100% |
A4HA77 | Leishmania braziliensis | 28% | 100% |
A4HA80 | Leishmania braziliensis | 28% | 100% |
A4HA81 | Leishmania braziliensis | 30% | 100% |
A4HA82 | Leishmania braziliensis | 28% | 100% |
A4HYG3 | Leishmania infantum | 83% | 100% |
E8NHJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AGT0 | Leishmania infantum | 32% | 90% |
E9AGT1 | Leishmania infantum | 32% | 100% |
E9AGT2 | Leishmania infantum | 32% | 100% |
E9AGT3 | Leishmania infantum | 31% | 97% |
E9AGT4 | Leishmania infantum | 31% | 97% |
E9AS85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4QD77 | Leishmania major | 81% | 100% |
Q4QD78 | Leishmania major | 30% | 100% |
Q4QD79 | Leishmania major | 30% | 100% |
Q4QD80 | Leishmania major | 30% | 100% |
Q4QD81 | Leishmania major | 30% | 100% |