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:0000139 | Golgi membrane | 5 | 15 | 
| GO:0016020 | membrane | 2 | 53 | 
| GO:0031090 | organelle membrane | 3 | 15 | 
| GO:0098588 | bounding membrane of organelle | 4 | 15 | 
| GO:0110165 | cellular anatomical entity | 1 | 53 | 
Related structures:
AlphaFold database: Q4QIG9
| 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:0008194 | UDP-glycosyltransferase activity | 4 | 15 | 
| GO:0016740 | transferase activity | 2 | 53 | 
| GO:0016757 | glycosyltransferase activity | 3 | 53 | 
| GO:0016758 | hexosyltransferase activity | 4 | 53 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.432 | 
| CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.608 | 
| CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.574 | 
| CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.575 | 
| CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.625 | 
| CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.514 | 
| CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.555 | 
| CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.469 | 
| CLV_PCSK_FUR_1 | 105 | 109 | PF00082 | 0.387 | 
| CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.405 | 
| CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.599 | 
| CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.673 | 
| CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.577 | 
| CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.476 | 
| CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.587 | 
| CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.521 | 
| CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.547 | 
| CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.552 | 
| CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.469 | 
| CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.472 | 
| CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.534 | 
| CLV_PCSK_PC1ET2_1 | 730 | 732 | PF00082 | 0.547 | 
| CLV_PCSK_PC7_1 | 796 | 802 | PF00082 | 0.501 | 
| CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.540 | 
| CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.566 | 
| CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.554 | 
| CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.522 | 
| CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.495 | 
| CLV_Separin_Metazoa | 269 | 273 | PF03568 | 0.340 | 
| DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.620 | 
| DEG_Kelch_Keap1_1 | 292 | 297 | PF01344 | 0.412 | 
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.655 | 
| DEG_SCF_FBW7_1 | 452 | 459 | PF00400 | 0.480 | 
| DEG_SPOP_SBC_1 | 438 | 442 | PF00917 | 0.344 | 
| DOC_CKS1_1 | 453 | 458 | PF01111 | 0.481 | 
| DOC_CYCLIN_yCln2_LP_2 | 24 | 27 | PF00134 | 0.632 | 
| DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.342 | 
| DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.531 | 
| DOC_CYCLIN_yCln2_LP_2 | 632 | 638 | PF00134 | 0.335 | 
| DOC_MAPK_DCC_7 | 572 | 581 | PF00069 | 0.350 | 
| DOC_MAPK_gen_1 | 105 | 114 | PF00069 | 0.513 | 
| DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.400 | 
| DOC_MAPK_gen_1 | 496 | 503 | PF00069 | 0.348 | 
| DOC_MAPK_gen_1 | 561 | 569 | PF00069 | 0.296 | 
| DOC_MAPK_gen_1 | 639 | 647 | PF00069 | 0.286 | 
| DOC_MAPK_gen_1 | 693 | 702 | PF00069 | 0.271 | 
| DOC_MAPK_HePTP_8 | 102 | 114 | PF00069 | 0.557 | 
| DOC_MAPK_JIP1_4 | 298 | 304 | PF00069 | 0.358 | 
| DOC_MAPK_JIP1_4 | 561 | 567 | PF00069 | 0.304 | 
| DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.571 | 
| DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.325 | 
| DOC_MAPK_MEF2A_6 | 480 | 487 | PF00069 | 0.438 | 
| DOC_MAPK_MEF2A_6 | 536 | 545 | PF00069 | 0.285 | 
| DOC_MAPK_MEF2A_6 | 561 | 569 | PF00069 | 0.313 | 
| DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.338 | 
| DOC_MAPK_MEF2A_6 | 642 | 649 | PF00069 | 0.290 | 
| DOC_MAPK_NFAT4_5 | 300 | 308 | PF00069 | 0.274 | 
| DOC_MAPK_NFAT4_5 | 480 | 488 | PF00069 | 0.340 | 
| DOC_MAPK_NFAT4_5 | 642 | 650 | PF00069 | 0.290 | 
| DOC_PP1_RVXF_1 | 514 | 521 | PF00149 | 0.419 | 
| DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.302 | 
| DOC_PP1_RVXF_1 | 694 | 700 | PF00149 | 0.311 | 
| DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.632 | 
| DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.270 | 
| DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.536 | 
| DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.297 | 
| DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.479 | 
| DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.448 | 
| DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.387 | 
| DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.714 | 
| DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.394 | 
| DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.393 | 
| DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.648 | 
| DOC_USP7_UBL2_3 | 492 | 496 | PF12436 | 0.353 | 
| DOC_USP7_UBL2_3 | 654 | 658 | PF12436 | 0.264 | 
| DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.343 | 
| DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.462 | 
| DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.490 | 
| DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.455 | 
| DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.665 | 
| LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.431 | 
| LIG_14-3-3_CanoR_1 | 323 | 327 | PF00244 | 0.402 | 
| LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.404 | 
| LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.313 | 
| LIG_14-3-3_CanoR_1 | 563 | 568 | PF00244 | 0.377 | 
| LIG_14-3-3_CanoR_1 | 779 | 785 | PF00244 | 0.349 | 
| LIG_14-3-3_CanoR_1 | 93 | 100 | PF00244 | 0.669 | 
| LIG_Actin_WH2_2 | 538 | 555 | PF00022 | 0.257 | 
| LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.423 | 
| LIG_EH_1 | 618 | 622 | PF12763 | 0.355 | 
| LIG_FHA_1 | 128 | 134 | PF00498 | 0.432 | 
| LIG_FHA_1 | 14 | 20 | PF00498 | 0.698 | 
| LIG_FHA_1 | 195 | 201 | PF00498 | 0.557 | 
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.470 | 
| LIG_FHA_1 | 259 | 265 | PF00498 | 0.444 | 
| LIG_FHA_1 | 338 | 344 | PF00498 | 0.356 | 
| LIG_FHA_1 | 426 | 432 | PF00498 | 0.370 | 
| LIG_FHA_1 | 438 | 444 | PF00498 | 0.468 | 
| LIG_FHA_1 | 564 | 570 | PF00498 | 0.348 | 
| LIG_FHA_1 | 576 | 582 | PF00498 | 0.382 | 
| LIG_FHA_1 | 65 | 71 | PF00498 | 0.673 | 
| LIG_FHA_2 | 326 | 332 | PF00498 | 0.408 | 
| LIG_FHA_2 | 370 | 376 | PF00498 | 0.492 | 
| LIG_FHA_2 | 739 | 745 | PF00498 | 0.306 | 
| LIG_FHA_2 | 781 | 787 | PF00498 | 0.340 | 
| LIG_IBAR_NPY_1 | 634 | 636 | PF08397 | 0.310 | 
| LIG_Integrin_RGD_1 | 775 | 777 | PF01839 | 0.560 | 
| LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.348 | 
| LIG_LIR_Apic_2 | 504 | 508 | PF02991 | 0.426 | 
| LIG_LIR_Gen_1 | 154 | 161 | PF02991 | 0.509 | 
| LIG_LIR_Gen_1 | 482 | 488 | PF02991 | 0.378 | 
| LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.431 | 
| LIG_LIR_Gen_1 | 641 | 649 | PF02991 | 0.379 | 
| LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.354 | 
| LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.510 | 
| LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.467 | 
| LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.372 | 
| LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.339 | 
| LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.328 | 
| LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.349 | 
| LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.368 | 
| LIG_LIR_Nem_3 | 641 | 647 | PF02991 | 0.349 | 
| LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.357 | 
| LIG_NRBOX | 111 | 117 | PF00104 | 0.308 | 
| LIG_NRBOX | 627 | 633 | PF00104 | 0.345 | 
| LIG_NRP_CendR_1 | 813 | 814 | PF00754 | 0.591 | 
| LIG_PCNA_yPIPBox_3 | 625 | 639 | PF02747 | 0.292 | 
| LIG_Pex14_2 | 769 | 773 | PF04695 | 0.271 | 
| LIG_PTB_Apo_2 | 208 | 215 | PF02174 | 0.426 | 
| LIG_PTB_Phospho_1 | 208 | 214 | PF10480 | 0.424 | 
| LIG_RPA_C_Fungi | 678 | 690 | PF08784 | 0.301 | 
| LIG_SH2_GRB2like | 595 | 598 | PF00017 | 0.365 | 
| LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.498 | 
| LIG_SH2_NCK_1 | 782 | 786 | PF00017 | 0.408 | 
| LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.693 | 
| LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.513 | 
| LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.344 | 
| LIG_SH2_STAP1 | 636 | 640 | PF00017 | 0.424 | 
| LIG_SH2_STAP1 | 793 | 797 | PF00017 | 0.449 | 
| LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.438 | 
| LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.559 | 
| LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.432 | 
| LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.383 | 
| LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.344 | 
| LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.292 | 
| LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.363 | 
| LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.427 | 
| LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.297 | 
| LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.425 | 
| LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.394 | 
| LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.458 | 
| LIG_SH3_3 | 450 | 456 | PF00018 | 0.624 | 
| LIG_SH3_3 | 526 | 532 | PF00018 | 0.389 | 
| LIG_SH3_3 | 564 | 570 | PF00018 | 0.450 | 
| LIG_SH3_3 | 571 | 577 | PF00018 | 0.460 | 
| LIG_SH3_4 | 492 | 499 | PF00018 | 0.411 | 
| LIG_SUMO_SIM_anti_2 | 139 | 146 | PF11976 | 0.551 | 
| LIG_SUMO_SIM_anti_2 | 698 | 704 | PF11976 | 0.283 | 
| LIG_SUMO_SIM_par_1 | 577 | 583 | PF11976 | 0.367 | 
| LIG_TRAF2_1 | 741 | 744 | PF00917 | 0.381 | 
| LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.543 | 
| MOD_CK1_1 | 127 | 133 | PF00069 | 0.516 | 
| MOD_CK1_1 | 155 | 161 | PF00069 | 0.562 | 
| MOD_CK1_1 | 292 | 298 | PF00069 | 0.554 | 
| MOD_CK1_1 | 356 | 362 | PF00069 | 0.639 | 
| MOD_CK1_1 | 514 | 520 | PF00069 | 0.241 | 
| MOD_CK1_1 | 66 | 72 | PF00069 | 0.652 | 
| MOD_CK2_1 | 136 | 142 | PF00069 | 0.571 | 
| MOD_CK2_1 | 162 | 168 | PF00069 | 0.553 | 
| MOD_CK2_1 | 291 | 297 | PF00069 | 0.521 | 
| MOD_CK2_1 | 325 | 331 | PF00069 | 0.490 | 
| MOD_CK2_1 | 33 | 39 | PF00069 | 0.584 | 
| MOD_CK2_1 | 369 | 375 | PF00069 | 0.635 | 
| MOD_CK2_1 | 738 | 744 | PF00069 | 0.409 | 
| MOD_CK2_1 | 780 | 786 | PF00069 | 0.354 | 
| MOD_CMANNOS | 275 | 278 | PF00535 | 0.313 | 
| MOD_Cter_Amidation | 62 | 65 | PF01082 | 0.574 | 
| MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.530 | 
| MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.527 | 
| MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.621 | 
| MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.621 | 
| MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.640 | 
| MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.540 | 
| MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.622 | 
| MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.544 | 
| MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.398 | 
| MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.650 | 
| MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.260 | 
| MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.558 | 
| MOD_GSK3_1 | 124 | 131 | PF00069 | 0.476 | 
| MOD_GSK3_1 | 132 | 139 | PF00069 | 0.630 | 
| MOD_GSK3_1 | 151 | 158 | PF00069 | 0.751 | 
| MOD_GSK3_1 | 177 | 184 | PF00069 | 0.555 | 
| MOD_GSK3_1 | 222 | 229 | PF00069 | 0.627 | 
| MOD_GSK3_1 | 235 | 242 | PF00069 | 0.520 | 
| MOD_GSK3_1 | 287 | 294 | PF00069 | 0.749 | 
| MOD_GSK3_1 | 33 | 40 | PF00069 | 0.646 | 
| MOD_GSK3_1 | 353 | 360 | PF00069 | 0.559 | 
| MOD_GSK3_1 | 425 | 432 | PF00069 | 0.515 | 
| MOD_GSK3_1 | 444 | 451 | PF00069 | 0.524 | 
| MOD_GSK3_1 | 452 | 459 | PF00069 | 0.439 | 
| MOD_GSK3_1 | 53 | 60 | PF00069 | 0.647 | 
| MOD_GSK3_1 | 64 | 71 | PF00069 | 0.611 | 
| MOD_GSK3_1 | 753 | 760 | PF00069 | 0.406 | 
| MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.527 | 
| MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.511 | 
| MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.394 | 
| MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.419 | 
| MOD_N-GLC_1 | 744 | 749 | PF02516 | 0.440 | 
| MOD_N-GLC_2 | 87 | 89 | PF02516 | 0.521 | 
| MOD_NEK2_1 | 170 | 175 | PF00069 | 0.604 | 
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.588 | 
| MOD_NEK2_1 | 240 | 245 | PF00069 | 0.562 | 
| MOD_NEK2_1 | 286 | 291 | PF00069 | 0.467 | 
| MOD_NEK2_1 | 501 | 506 | PF00069 | 0.449 | 
| MOD_NEK2_1 | 565 | 570 | PF00069 | 0.452 | 
| MOD_NEK2_1 | 621 | 626 | PF00069 | 0.497 | 
| MOD_NEK2_1 | 706 | 711 | PF00069 | 0.269 | 
| MOD_NEK2_1 | 85 | 90 | PF00069 | 0.584 | 
| MOD_NEK2_2 | 194 | 199 | PF00069 | 0.720 | 
| MOD_PIKK_1 | 124 | 130 | PF00454 | 0.453 | 
| MOD_PIKK_1 | 132 | 138 | PF00454 | 0.551 | 
| MOD_PIKK_1 | 170 | 176 | PF00454 | 0.500 | 
| MOD_PIKK_1 | 25 | 31 | PF00454 | 0.565 | 
| MOD_PIKK_1 | 287 | 293 | PF00454 | 0.562 | 
| MOD_PIKK_1 | 511 | 517 | PF00454 | 0.523 | 
| MOD_PIKK_1 | 744 | 750 | PF00454 | 0.418 | 
| MOD_PIKK_1 | 753 | 759 | PF00454 | 0.382 | 
| MOD_PK_1 | 235 | 241 | PF00069 | 0.490 | 
| MOD_PKA_1 | 491 | 497 | PF00069 | 0.590 | 
| MOD_PKA_1 | 64 | 70 | PF00069 | 0.560 | 
| MOD_PKA_2 | 13 | 19 | PF00069 | 0.615 | 
| MOD_PKA_2 | 168 | 174 | PF00069 | 0.514 | 
| MOD_PKA_2 | 223 | 229 | PF00069 | 0.700 | 
| MOD_PKA_2 | 292 | 298 | PF00069 | 0.565 | 
| MOD_PKA_2 | 322 | 328 | PF00069 | 0.485 | 
| MOD_PKA_2 | 426 | 432 | PF00069 | 0.502 | 
| MOD_PKA_2 | 479 | 485 | PF00069 | 0.442 | 
| MOD_PKA_2 | 57 | 63 | PF00069 | 0.600 | 
| MOD_PKA_2 | 64 | 70 | PF00069 | 0.572 | 
| MOD_PKA_2 | 92 | 98 | PF00069 | 0.530 | 
| MOD_Plk_1 | 203 | 209 | PF00069 | 0.569 | 
| MOD_Plk_1 | 210 | 216 | PF00069 | 0.488 | 
| MOD_Plk_1 | 563 | 569 | PF00069 | 0.344 | 
| MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.609 | 
| MOD_Plk_2-3 | 738 | 744 | PF00069 | 0.341 | 
| MOD_Plk_4 | 235 | 241 | PF00069 | 0.519 | 
| MOD_Plk_4 | 322 | 328 | PF00069 | 0.489 | 
| MOD_Plk_4 | 426 | 432 | PF00069 | 0.449 | 
| MOD_Plk_4 | 479 | 485 | PF00069 | 0.376 | 
| MOD_Plk_4 | 514 | 520 | PF00069 | 0.255 | 
| MOD_Plk_4 | 695 | 701 | PF00069 | 0.404 | 
| MOD_Plk_4 | 758 | 764 | PF00069 | 0.377 | 
| MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.570 | 
| MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.611 | 
| MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.551 | 
| MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.574 | 
| MOD_SUMO_rev_2 | 486 | 494 | PF00179 | 0.412 | 
| MOD_SUMO_rev_2 | 646 | 656 | PF00179 | 0.307 | 
| MOD_SUMO_rev_2 | 722 | 732 | PF00179 | 0.342 | 
| TRG_DiLeu_BaEn_1 | 728 | 733 | PF01217 | 0.361 | 
| TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.403 | 
| TRG_DiLeu_LyEn_5 | 728 | 733 | PF01217 | 0.358 | 
| TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.587 | 
| TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.525 | 
| TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.425 | 
| TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.402 | 
| TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.541 | 
| TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.480 | 
| TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.575 | 
| TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.438 | 
| TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.383 | 
| TRG_ER_diArg_1 | 799 | 802 | PF00400 | 0.412 | 
| TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.638 | 
| TRG_NLS_MonoExtN_4 | 493 | 500 | PF00514 | 0.432 | 
| TRG_NLS_MonoExtN_4 | 672 | 677 | PF00514 | 0.327 | 
| TRG_Pf-PMV_PEXEL_1 | 199 | 203 | PF00026 | 0.519 | 
| TRG_Pf-PMV_PEXEL_1 | 611 | 615 | PF00026 | 0.448 | 
| TRG_Pf-PMV_PEXEL_1 | 731 | 735 | PF00026 | 0.376 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A3Q8IGN9 | Leishmania donovani | 83% | 100% | 
| A0A3S5H4Y6 | Leishmania donovani | 40% | 100% | 
| A0A3S5H4Y9 | Leishmania donovani | 32% | 82% | 
| A0A3S7WT86 | Leishmania donovani | 36% | 79% | 
| A0A3S7WWA6 | Leishmania donovani | 83% | 100% | 
| A0A451EJD9 | Leishmania donovani | 74% | 100% | 
| A0A451EJF4 | Leishmania donovani | 41% | 100% | 
| A0A451EJF6 | Leishmania donovani | 41% | 100% | 
| A0A451EJF8 | Leishmania donovani | 37% | 100% | 
| A0A451EJF9 | Leishmania donovani | 41% | 94% | 
| A4H3A9 | Leishmania braziliensis | 42% | 100% | 
| A4H3B4 | Leishmania braziliensis | 39% | 100% | 
| A4H3B6 | Leishmania braziliensis | 39% | 100% | 
| A4H3B8 | Leishmania braziliensis | 41% | 98% | 
| A4H3B9 | Leishmania braziliensis | 33% | 91% | 
| A4H4W8 | Leishmania braziliensis | 62% | 100% | 
| A4HJ20 | Leishmania braziliensis | 39% | 100% | 
| A4HNK3 | Leishmania braziliensis | 71% | 100% | 
| A4HNK6 | Leishmania braziliensis | 62% | 100% | 
| A4HRL9 | Leishmania infantum | 41% | 100% | 
| A4HRM0 | Leishmania infantum | 39% | 100% | 
| A4HRM1 | Leishmania infantum | 41% | 100% | 
| A4HRS1 | Leishmania infantum | 41% | 94% | 
| A4HRS3 | Leishmania infantum | 32% | 82% | 
| A4HRS5 | Leishmania infantum | 37% | 100% | 
| A4HZM0 | Leishmania infantum | 74% | 100% | 
| A4I7C7 | Leishmania infantum | 75% | 100% | 
| A4IAQ2 | Leishmania infantum | 71% | 100% | 
| E9AC91 | Leishmania major | 43% | 100% | 
| E9AC92 | Leishmania major | 43% | 100% | 
| E9AC94 | Leishmania major | 32% | 69% | 
| E9AC95 | Leishmania major | 38% | 100% | 
| E9AC96 | Leishmania major | 41% | 100% | 
| E9AC98 | Leishmania major | 32% | 100% | 
| E9AEH8 | Leishmania major | 80% | 100% | 
| E9AHA6 | Leishmania infantum | 73% | 100% | 
| E9AIP8 | Leishmania braziliensis | 64% | 100% | 
| E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 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) | 31% | 82% | 
| E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% | 
| E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% | 
| E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% | 
| E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% | 
| Q4Q5T6 | Leishmania major | 83% | 100% | 
| Q4QCL8 | Leishmania major | 96% | 100% | 
| Q4QFJ3 | Leishmania major | 36% | 100% | 
| Q7YXU9 | Leishmania major | 94% | 100% | 
| Q7YXV1 | Leishmania major | 96% | 96% | 
| Q7YXV2 | Leishmania major | 94% | 100% |