Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. Localization: Golgi (by homology)
| 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: 60 |
| 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: 16 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 52 |
| NetGPI | no | yes: 0, no: 52 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 53 |
| GO:0110165 | cellular anatomical entity | 1 | 53 |
| GO:0000139 | Golgi membrane | 5 | 14 |
| GO:0031090 | organelle membrane | 3 | 14 |
| GO:0098588 | bounding membrane of organelle | 4 | 14 |
Related structures:
AlphaFold database: A0A3S7WWA6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006486 | protein glycosylation | 4 | 53 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 53 |
| GO:0008152 | metabolic process | 1 | 53 |
| GO:0019538 | protein metabolic process | 3 | 53 |
| GO:0036211 | protein modification process | 4 | 53 |
| GO:0043170 | macromolecule metabolic process | 3 | 53 |
| GO:0043412 | macromolecule modification | 4 | 53 |
| GO:0043413 | macromolecule glycosylation | 3 | 53 |
| GO:0044238 | primary metabolic process | 2 | 53 |
| GO:0070085 | glycosylation | 2 | 53 |
| GO:0071704 | organic substance metabolic process | 2 | 53 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 53 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 53 |
| GO:0016740 | transferase activity | 2 | 53 |
| GO:0016757 | glycosyltransferase activity | 3 | 53 |
| GO:0016758 | hexosyltransferase activity | 4 | 53 |
| GO:0008194 | UDP-glycosyltransferase activity | 4 | 14 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.359 |
| CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.355 |
| CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.283 |
| CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.634 |
| CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.659 |
| CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.667 |
| CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.574 |
| CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.555 |
| CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.517 |
| CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.454 |
| CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.408 |
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.777 |
| CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.594 |
| CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.655 |
| CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.542 |
| CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.665 |
| CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.504 |
| CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.601 |
| CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.532 |
| CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.548 |
| CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.454 |
| CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.409 |
| CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.654 |
| CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.516 |
| CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.545 |
| CLV_PCSK_PC1ET2_1 | 730 | 732 | PF00082 | 0.548 |
| CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.252 |
| CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.589 |
| CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.546 |
| CLV_Separin_Metazoa | 269 | 273 | PF03568 | 0.345 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.681 |
| DEG_SCF_FBW7_1 | 452 | 459 | PF00400 | 0.458 |
| DOC_CKS1_1 | 453 | 458 | PF01111 | 0.461 |
| DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.335 |
| DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.506 |
| DOC_MAPK_DCC_7 | 572 | 581 | PF00069 | 0.349 |
| DOC_MAPK_gen_1 | 106 | 114 | PF00069 | 0.537 |
| DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.387 |
| DOC_MAPK_gen_1 | 496 | 503 | PF00069 | 0.355 |
| DOC_MAPK_gen_1 | 693 | 702 | PF00069 | 0.273 |
| DOC_MAPK_HePTP_8 | 104 | 116 | PF00069 | 0.439 |
| DOC_MAPK_JIP1_4 | 298 | 304 | PF00069 | 0.364 |
| DOC_MAPK_MEF2A_6 | 106 | 114 | PF00069 | 0.575 |
| DOC_MAPK_MEF2A_6 | 480 | 487 | PF00069 | 0.432 |
| DOC_MAPK_MEF2A_6 | 536 | 545 | PF00069 | 0.302 |
| DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.338 |
| DOC_MAPK_MEF2A_6 | 642 | 649 | PF00069 | 0.297 |
| DOC_MAPK_NFAT4_5 | 480 | 488 | PF00069 | 0.333 |
| DOC_PP1_RVXF_1 | 500 | 506 | PF00149 | 0.379 |
| DOC_PP1_RVXF_1 | 514 | 521 | PF00149 | 0.352 |
| DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.307 |
| DOC_PP1_RVXF_1 | 694 | 700 | PF00149 | 0.312 |
| DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.506 |
| DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.310 |
| DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.416 |
| DOC_PP4_FxxP_1 | 706 | 709 | PF00568 | 0.269 |
| DOC_SPAK_OSR1_1 | 107 | 111 | PF12202 | 0.413 |
| DOC_SPAK_OSR1_1 | 128 | 132 | PF12202 | 0.371 |
| DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.413 |
| DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.462 |
| DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.496 |
| DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.348 |
| DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.468 |
| DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.716 |
| DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.349 |
| DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.367 |
| DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.648 |
| DOC_USP7_UBL2_3 | 492 | 496 | PF12436 | 0.353 |
| DOC_USP7_UBL2_3 | 669 | 673 | PF12436 | 0.278 |
| DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.322 |
| DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.450 |
| DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.648 |
| DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.488 |
| DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.425 |
| DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.433 |
| LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.438 |
| LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.381 |
| LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.408 |
| LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.410 |
| LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.355 |
| LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.311 |
| LIG_14-3-3_CanoR_1 | 563 | 570 | PF00244 | 0.427 |
| LIG_14-3-3_CanoR_1 | 779 | 785 | PF00244 | 0.348 |
| LIG_14-3-3_CanoR_1 | 93 | 100 | PF00244 | 0.657 |
| LIG_Actin_WH2_2 | 538 | 555 | PF00022 | 0.276 |
| LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.346 |
| LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.623 |
| LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.334 |
| LIG_EH_1 | 618 | 622 | PF12763 | 0.336 |
| LIG_FHA_1 | 128 | 134 | PF00498 | 0.463 |
| LIG_FHA_1 | 180 | 186 | PF00498 | 0.360 |
| LIG_FHA_1 | 195 | 201 | PF00498 | 0.488 |
| LIG_FHA_1 | 259 | 265 | PF00498 | 0.395 |
| LIG_FHA_1 | 338 | 344 | PF00498 | 0.330 |
| LIG_FHA_1 | 361 | 367 | PF00498 | 0.357 |
| LIG_FHA_1 | 426 | 432 | PF00498 | 0.374 |
| LIG_FHA_1 | 438 | 444 | PF00498 | 0.424 |
| LIG_FHA_1 | 564 | 570 | PF00498 | 0.324 |
| LIG_FHA_1 | 576 | 582 | PF00498 | 0.459 |
| LIG_FHA_2 | 163 | 169 | PF00498 | 0.346 |
| LIG_FHA_2 | 326 | 332 | PF00498 | 0.409 |
| LIG_FHA_2 | 370 | 376 | PF00498 | 0.449 |
| LIG_FHA_2 | 781 | 787 | PF00498 | 0.339 |
| LIG_IBAR_NPY_1 | 634 | 636 | PF08397 | 0.303 |
| LIG_LIR_Apic_2 | 151 | 156 | PF02991 | 0.415 |
| LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.345 |
| LIG_LIR_Apic_2 | 504 | 508 | PF02991 | 0.426 |
| LIG_LIR_Gen_1 | 155 | 161 | PF02991 | 0.462 |
| LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.372 |
| LIG_LIR_Gen_1 | 482 | 488 | PF02991 | 0.368 |
| LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.396 |
| LIG_LIR_Gen_1 | 622 | 632 | PF02991 | 0.282 |
| LIG_LIR_Gen_1 | 643 | 651 | PF02991 | 0.373 |
| LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.357 |
| LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.430 |
| LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.371 |
| LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.371 |
| LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.331 |
| LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.386 |
| LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.368 |
| LIG_LIR_Nem_3 | 622 | 627 | PF02991 | 0.294 |
| LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.393 |
| LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.359 |
| LIG_NRBOX | 111 | 117 | PF00104 | 0.300 |
| LIG_NRBOX | 627 | 633 | PF00104 | 0.335 |
| LIG_NRP_CendR_1 | 813 | 814 | PF00754 | 0.586 |
| LIG_Pex14_2 | 153 | 157 | PF04695 | 0.419 |
| LIG_PTB_Apo_2 | 208 | 215 | PF02174 | 0.378 |
| LIG_PTB_Apo_2 | 791 | 798 | PF02174 | 0.275 |
| LIG_PTB_Phospho_1 | 208 | 214 | PF10480 | 0.374 |
| LIG_PTB_Phospho_1 | 791 | 797 | PF10480 | 0.271 |
| LIG_RPA_C_Fungi | 678 | 690 | PF08784 | 0.314 |
| LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.470 |
| LIG_SH2_NCK_1 | 782 | 786 | PF00017 | 0.407 |
| LIG_SH2_PTP2 | 644 | 647 | PF00017 | 0.287 |
| LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.509 |
| LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.550 |
| LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.357 |
| LIG_SH2_STAP1 | 651 | 655 | PF00017 | 0.351 |
| LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.431 |
| LIG_SH2_STAT3 | 595 | 598 | PF00017 | 0.348 |
| LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.478 |
| LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.419 |
| LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.368 |
| LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.379 |
| LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.341 |
| LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.427 |
| LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.289 |
| LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.429 |
| LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.547 |
| LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.456 |
| LIG_SH3_3 | 450 | 456 | PF00018 | 0.589 |
| LIG_SH3_3 | 526 | 532 | PF00018 | 0.430 |
| LIG_SH3_3 | 571 | 577 | PF00018 | 0.466 |
| LIG_SH3_3 | 614 | 620 | PF00018 | 0.342 |
| LIG_SH3_3 | 706 | 712 | PF00018 | 0.348 |
| LIG_SH3_4 | 492 | 499 | PF00018 | 0.414 |
| LIG_SUMO_SIM_anti_2 | 698 | 704 | PF11976 | 0.286 |
| LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.443 |
| MOD_CDC14_SPxK_1 | 27 | 30 | PF00782 | 0.505 |
| MOD_CDK_SPxK_1 | 24 | 30 | PF00069 | 0.513 |
| MOD_CK1_1 | 127 | 133 | PF00069 | 0.520 |
| MOD_CK1_1 | 155 | 161 | PF00069 | 0.478 |
| MOD_CK1_1 | 292 | 298 | PF00069 | 0.553 |
| MOD_CK1_1 | 356 | 362 | PF00069 | 0.642 |
| MOD_CK1_1 | 393 | 399 | PF00069 | 0.349 |
| MOD_CK1_1 | 429 | 435 | PF00069 | 0.471 |
| MOD_CK1_1 | 65 | 71 | PF00069 | 0.607 |
| MOD_CK2_1 | 162 | 168 | PF00069 | 0.445 |
| MOD_CK2_1 | 325 | 331 | PF00069 | 0.489 |
| MOD_CK2_1 | 33 | 39 | PF00069 | 0.579 |
| MOD_CK2_1 | 369 | 375 | PF00069 | 0.578 |
| MOD_CK2_1 | 53 | 59 | PF00069 | 0.537 |
| MOD_CK2_1 | 780 | 786 | PF00069 | 0.367 |
| MOD_Cter_Amidation | 811 | 814 | PF01082 | 0.363 |
| MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.574 |
| MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.618 |
| MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.627 |
| MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.612 |
| MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.387 |
| MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.521 |
| MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.527 |
| MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.599 |
| MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.407 |
| MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.543 |
| MOD_GSK3_1 | 137 | 144 | PF00069 | 0.574 |
| MOD_GSK3_1 | 148 | 155 | PF00069 | 0.579 |
| MOD_GSK3_1 | 177 | 184 | PF00069 | 0.479 |
| MOD_GSK3_1 | 222 | 229 | PF00069 | 0.610 |
| MOD_GSK3_1 | 33 | 40 | PF00069 | 0.630 |
| MOD_GSK3_1 | 353 | 360 | PF00069 | 0.595 |
| MOD_GSK3_1 | 425 | 432 | PF00069 | 0.520 |
| MOD_GSK3_1 | 444 | 451 | PF00069 | 0.511 |
| MOD_GSK3_1 | 452 | 459 | PF00069 | 0.412 |
| MOD_GSK3_1 | 62 | 69 | PF00069 | 0.568 |
| MOD_GSK3_1 | 753 | 760 | PF00069 | 0.420 |
| MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.468 |
| MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.473 |
| MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.393 |
| MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.411 |
| MOD_N-GLC_1 | 636 | 641 | PF02516 | 0.335 |
| MOD_N-GLC_1 | 744 | 749 | PF02516 | 0.442 |
| MOD_NEK2_1 | 170 | 175 | PF00069 | 0.485 |
| MOD_NEK2_1 | 240 | 245 | PF00069 | 0.544 |
| MOD_NEK2_1 | 501 | 506 | PF00069 | 0.422 |
| MOD_NEK2_1 | 565 | 570 | PF00069 | 0.589 |
| MOD_NEK2_2 | 194 | 199 | PF00069 | 0.623 |
| MOD_PIKK_1 | 132 | 138 | PF00454 | 0.539 |
| MOD_PIKK_1 | 170 | 176 | PF00454 | 0.434 |
| MOD_PIKK_1 | 287 | 293 | PF00454 | 0.532 |
| MOD_PIKK_1 | 511 | 517 | PF00454 | 0.423 |
| MOD_PIKK_1 | 594 | 600 | PF00454 | 0.338 |
| MOD_PIKK_1 | 744 | 750 | PF00454 | 0.419 |
| MOD_PIKK_1 | 753 | 759 | PF00454 | 0.393 |
| MOD_PIKK_1 | 99 | 105 | PF00454 | 0.459 |
| MOD_PKA_1 | 491 | 497 | PF00069 | 0.591 |
| MOD_PKA_2 | 127 | 133 | PF00069 | 0.469 |
| MOD_PKA_2 | 13 | 19 | PF00069 | 0.617 |
| MOD_PKA_2 | 141 | 147 | PF00069 | 0.536 |
| MOD_PKA_2 | 148 | 154 | PF00069 | 0.524 |
| MOD_PKA_2 | 168 | 174 | PF00069 | 0.445 |
| MOD_PKA_2 | 223 | 229 | PF00069 | 0.599 |
| MOD_PKA_2 | 292 | 298 | PF00069 | 0.571 |
| MOD_PKA_2 | 353 | 359 | PF00069 | 0.492 |
| MOD_PKA_2 | 426 | 432 | PF00069 | 0.603 |
| MOD_PKA_2 | 479 | 485 | PF00069 | 0.436 |
| MOD_PKA_2 | 501 | 507 | PF00069 | 0.358 |
| MOD_PKA_2 | 681 | 687 | PF00069 | 0.328 |
| MOD_PKA_2 | 92 | 98 | PF00069 | 0.532 |
| MOD_Plk_1 | 203 | 209 | PF00069 | 0.468 |
| MOD_Plk_1 | 210 | 216 | PF00069 | 0.442 |
| MOD_Plk_1 | 230 | 236 | PF00069 | 0.470 |
| MOD_Plk_1 | 636 | 642 | PF00069 | 0.343 |
| MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.496 |
| MOD_Plk_4 | 181 | 187 | PF00069 | 0.631 |
| MOD_Plk_4 | 322 | 328 | PF00069 | 0.548 |
| MOD_Plk_4 | 393 | 399 | PF00069 | 0.397 |
| MOD_Plk_4 | 426 | 432 | PF00069 | 0.455 |
| MOD_Plk_4 | 479 | 485 | PF00069 | 0.416 |
| MOD_Plk_4 | 695 | 701 | PF00069 | 0.479 |
| MOD_Plk_4 | 758 | 764 | PF00069 | 0.424 |
| MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.537 |
| MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.546 |
| MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.609 |
| MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.508 |
| MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.520 |
| MOD_SUMO_rev_2 | 486 | 494 | PF00179 | 0.404 |
| MOD_SUMO_rev_2 | 646 | 656 | PF00179 | 0.297 |
| MOD_SUMO_rev_2 | 722 | 732 | PF00179 | 0.343 |
| TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.411 |
| TRG_DiLeu_BaEn_1 | 728 | 733 | PF01217 | 0.363 |
| TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.339 |
| TRG_DiLeu_LyEn_5 | 728 | 733 | PF01217 | 0.360 |
| TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.453 |
| TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.564 |
| TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.452 |
| TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.490 |
| TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.577 |
| TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.565 |
| TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.387 |
| TRG_ER_diArg_1 | 682 | 685 | PF00400 | 0.398 |
| TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.567 |
| TRG_NLS_MonoExtN_4 | 493 | 500 | PF00514 | 0.439 |
| TRG_NLS_MonoExtN_4 | 672 | 677 | PF00514 | 0.343 |
| TRG_Pf-PMV_PEXEL_1 | 199 | 203 | PF00026 | 0.439 |
| TRG_Pf-PMV_PEXEL_1 | 611 | 615 | PF00026 | 0.473 |
| TRG_Pf-PMV_PEXEL_1 | 658 | 662 | PF00026 | 0.298 |
| TRG_Pf-PMV_PEXEL_1 | 731 | 735 | PF00026 | 0.377 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IGN9 | Leishmania donovani | 100% | 100% |
| A0A3S5H4Y6 | Leishmania donovani | 41% | 100% |
| A0A3S5H4Y9 | Leishmania donovani | 31% | 100% |
| A0A3S7WT86 | Leishmania donovani | 37% | 100% |
| A0A451EJD9 | Leishmania donovani | 81% | 100% |
| A0A451EJF4 | Leishmania donovani | 39% | 100% |
| A0A451EJF6 | Leishmania donovani | 39% | 100% |
| A0A451EJF8 | Leishmania donovani | 38% | 100% |
| A0A451EJF9 | Leishmania donovani | 40% | 94% |
| A4H3A9 | Leishmania braziliensis | 42% | 100% |
| A4H3B4 | Leishmania braziliensis | 42% | 100% |
| A4H3B6 | Leishmania braziliensis | 41% | 100% |
| A4H3B8 | Leishmania braziliensis | 42% | 100% |
| A4H3B9 | Leishmania braziliensis | 34% | 100% |
| A4H4W8 | Leishmania braziliensis | 64% | 100% |
| A4HJ20 | Leishmania braziliensis | 41% | 100% |
| A4HNK3 | Leishmania braziliensis | 73% | 100% |
| A4HNK6 | Leishmania braziliensis | 64% | 100% |
| A4HRL9 | Leishmania infantum | 42% | 100% |
| A4HRM0 | Leishmania infantum | 40% | 100% |
| A4HRM1 | Leishmania infantum | 41% | 98% |
| A4HRS1 | Leishmania infantum | 41% | 100% |
| A4HRS3 | Leishmania infantum | 31% | 100% |
| A4HRS5 | Leishmania infantum | 38% | 100% |
| A4HZM0 | Leishmania infantum | 86% | 100% |
| A4I7C7 | Leishmania infantum | 85% | 100% |
| A4IAQ2 | Leishmania infantum | 77% | 100% |
| E9AC91 | Leishmania major | 41% | 100% |
| E9AC92 | Leishmania major | 42% | 100% |
| E9AC94 | Leishmania major | 33% | 69% |
| E9AC95 | Leishmania major | 37% | 100% |
| E9AC96 | Leishmania major | 40% | 100% |
| E9AC98 | Leishmania major | 33% | 100% |
| E9AEH8 | Leishmania major | 74% | 100% |
| E9AHA6 | Leishmania infantum | 81% | 100% |
| E9AIP8 | Leishmania braziliensis | 64% | 100% |
| E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
| E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
| E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
| E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
| E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
| E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
| E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
| E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
| Q4Q5T6 | Leishmania major | 74% | 100% |
| Q4QCL8 | Leishmania major | 82% | 100% |
| Q4QFJ3 | Leishmania major | 37% | 100% |
| Q4QIG9 | Leishmania major | 83% | 100% |
| Q7YXU9 | Leishmania major | 81% | 100% |
| Q7YXV1 | Leishmania major | 83% | 100% |
| Q7YXV2 | Leishmania major | 82% | 100% |