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. | yes | 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: A0A3S5H4Y6
| 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_NRD_NRD_1 | 129 | 131 | PF00675 | 0.610 |
| CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.561 |
| CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.544 |
| CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.610 |
| CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.674 |
| CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.630 |
| CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.562 |
| CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.689 |
| CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.583 |
| CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.488 |
| CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.565 |
| CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.531 |
| CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.465 |
| CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.456 |
| CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.634 |
| CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.561 |
| CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.561 |
| CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.548 |
| CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.626 |
| CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.674 |
| CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.629 |
| CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.562 |
| CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.617 |
| CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.575 |
| CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.502 |
| CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.597 |
| CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.622 |
| CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.536 |
| CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.585 |
| CLV_PCSK_KEX2_1 | 795 | 797 | PF00082 | 0.547 |
| CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.479 |
| CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.455 |
| CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.598 |
| CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.539 |
| CLV_PCSK_PC1ET2_1 | 659 | 661 | PF00082 | 0.518 |
| CLV_PCSK_PC1ET2_1 | 725 | 727 | PF00082 | 0.622 |
| CLV_PCSK_PC1ET2_1 | 745 | 747 | PF00082 | 0.509 |
| CLV_PCSK_PC1ET2_1 | 769 | 771 | PF00082 | 0.567 |
| CLV_PCSK_PC1ET2_1 | 795 | 797 | PF00082 | 0.508 |
| CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.415 |
| CLV_PCSK_PC7_1 | 302 | 308 | PF00082 | 0.519 |
| CLV_PCSK_PC7_1 | 404 | 410 | PF00082 | 0.550 |
| CLV_PCSK_PC7_1 | 655 | 661 | PF00082 | 0.510 |
| CLV_PCSK_PC7_1 | 80 | 86 | PF00082 | 0.403 |
| CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.575 |
| CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.572 |
| CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.575 |
| CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.557 |
| CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.591 |
| CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.475 |
| CLV_PCSK_SKI1_1 | 788 | 792 | PF00082 | 0.512 |
| DEG_APCC_DBOX_1 | 361 | 369 | PF00400 | 0.396 |
| DEG_SCF_FBW7_1 | 447 | 454 | PF00400 | 0.493 |
| DEG_SCF_FBW7_2 | 416 | 423 | PF00400 | 0.321 |
| DOC_CKS1_1 | 280 | 285 | PF01111 | 0.345 |
| DOC_CKS1_1 | 448 | 453 | PF01111 | 0.423 |
| DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.386 |
| DOC_CYCLIN_yCln2_LP_2 | 445 | 451 | PF00134 | 0.539 |
| DOC_MAPK_gen_1 | 586 | 594 | PF00069 | 0.282 |
| DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.656 |
| DOC_MAPK_JIP1_4 | 91 | 97 | PF00069 | 0.458 |
| DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.372 |
| DOC_MAPK_MEF2A_6 | 232 | 240 | PF00069 | 0.366 |
| DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.355 |
| DOC_MAPK_MEF2A_6 | 499 | 508 | PF00069 | 0.336 |
| DOC_MAPK_MEF2A_6 | 89 | 97 | PF00069 | 0.694 |
| DOC_PP1_RVXF_1 | 30 | 37 | PF00149 | 0.607 |
| DOC_PP1_RVXF_1 | 473 | 480 | PF00149 | 0.333 |
| DOC_PP1_RVXF_1 | 509 | 516 | PF00149 | 0.435 |
| DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.537 |
| DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.378 |
| DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.590 |
| DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.377 |
| DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.522 |
| DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.377 |
| DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.481 |
| DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.481 |
| DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.629 |
| DOC_USP7_UBL2_3 | 791 | 795 | PF12436 | 0.298 |
| DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.394 |
| DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.388 |
| DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.653 |
| DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.504 |
| DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.416 |
| DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.303 |
| DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.347 |
| LIG_14-3-3_CanoR_1 | 204 | 211 | PF00244 | 0.454 |
| LIG_14-3-3_CanoR_1 | 306 | 310 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.625 |
| LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.453 |
| LIG_14-3-3_CanoR_1 | 362 | 370 | PF00244 | 0.389 |
| LIG_14-3-3_CanoR_1 | 427 | 432 | PF00244 | 0.441 |
| LIG_14-3-3_CanoR_1 | 49 | 53 | PF00244 | 0.647 |
| LIG_14-3-3_CanoR_1 | 586 | 590 | PF00244 | 0.279 |
| LIG_14-3-3_CanoR_1 | 641 | 650 | PF00244 | 0.285 |
| LIG_14-3-3_CanoR_1 | 746 | 754 | PF00244 | 0.351 |
| LIG_Actin_WH2_2 | 246 | 262 | PF00022 | 0.383 |
| LIG_APCC_ABBA_1 | 93 | 98 | PF00400 | 0.409 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.589 |
| LIG_EH1_1 | 599 | 607 | PF00400 | 0.248 |
| LIG_eIF4E_1 | 102 | 108 | PF01652 | 0.243 |
| LIG_eIF4E_1 | 28 | 34 | PF01652 | 0.590 |
| LIG_FHA_1 | 107 | 113 | PF00498 | 0.310 |
| LIG_FHA_1 | 151 | 157 | PF00498 | 0.380 |
| LIG_FHA_1 | 188 | 194 | PF00498 | 0.557 |
| LIG_FHA_1 | 242 | 248 | PF00498 | 0.508 |
| LIG_FHA_1 | 280 | 286 | PF00498 | 0.344 |
| LIG_FHA_1 | 377 | 383 | PF00498 | 0.367 |
| LIG_FHA_1 | 433 | 439 | PF00498 | 0.431 |
| LIG_FHA_1 | 597 | 603 | PF00498 | 0.284 |
| LIG_FHA_2 | 309 | 315 | PF00498 | 0.415 |
| LIG_FHA_2 | 369 | 375 | PF00498 | 0.502 |
| LIG_FHA_2 | 642 | 648 | PF00498 | 0.275 |
| LIG_FHA_2 | 700 | 706 | PF00498 | 0.288 |
| LIG_FHA_2 | 747 | 753 | PF00498 | 0.335 |
| LIG_FHA_2 | 756 | 762 | PF00498 | 0.293 |
| LIG_IRF3_LxIS_1 | 97 | 104 | PF10401 | 0.216 |
| LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.382 |
| LIG_LIR_Apic_2 | 497 | 503 | PF02991 | 0.464 |
| LIG_LIR_Gen_1 | 135 | 142 | PF02991 | 0.479 |
| LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.336 |
| LIG_LIR_Gen_1 | 311 | 316 | PF02991 | 0.326 |
| LIG_LIR_Gen_1 | 517 | 528 | PF02991 | 0.345 |
| LIG_LIR_Gen_1 | 534 | 544 | PF02991 | 0.311 |
| LIG_LIR_Gen_1 | 675 | 683 | PF02991 | 0.349 |
| LIG_LIR_Gen_1 | 692 | 698 | PF02991 | 0.362 |
| LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.247 |
| LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.477 |
| LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.327 |
| LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.476 |
| LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.367 |
| LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.293 |
| LIG_LIR_Nem_3 | 675 | 680 | PF02991 | 0.351 |
| LIG_LIR_Nem_3 | 692 | 696 | PF02991 | 0.367 |
| LIG_LIR_Nem_3 | 705 | 709 | PF02991 | 0.274 |
| LIG_NRBOX | 649 | 655 | PF00104 | 0.283 |
| LIG_REV1ctd_RIR_1 | 710 | 719 | PF16727 | 0.281 |
| LIG_SH2_GRB2like | 785 | 788 | PF00017 | 0.305 |
| LIG_SH2_PTP2 | 537 | 540 | PF00017 | 0.310 |
| LIG_SH2_SRC | 312 | 315 | PF00017 | 0.339 |
| LIG_SH2_SRC | 518 | 521 | PF00017 | 0.371 |
| LIG_SH2_SRC | 708 | 711 | PF00017 | 0.266 |
| LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.462 |
| LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.352 |
| LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.264 |
| LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.389 |
| LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.420 |
| LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.380 |
| LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.339 |
| LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.336 |
| LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.366 |
| LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.353 |
| LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.443 |
| LIG_SH2_STAT5 | 789 | 792 | PF00017 | 0.320 |
| LIG_SH3_3 | 277 | 283 | PF00018 | 0.459 |
| LIG_SH3_3 | 445 | 451 | PF00018 | 0.510 |
| LIG_SH3_3 | 535 | 541 | PF00018 | 0.314 |
| LIG_SH3_3 | 555 | 561 | PF00018 | 0.347 |
| LIG_SH3_3 | 607 | 613 | PF00018 | 0.327 |
| LIG_SH3_3 | 801 | 807 | PF00018 | 0.285 |
| LIG_SUMO_SIM_anti_2 | 588 | 593 | PF11976 | 0.253 |
| LIG_SUMO_SIM_anti_2 | 621 | 626 | PF11976 | 0.316 |
| LIG_SUMO_SIM_par_1 | 621 | 626 | PF11976 | 0.337 |
| LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.350 |
| LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.549 |
| LIG_TYR_ITSM | 280 | 287 | PF00017 | 0.394 |
| LIG_UBA3_1 | 112 | 117 | PF00899 | 0.407 |
| LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.487 |
| MOD_CK1_1 | 19 | 25 | PF00069 | 0.557 |
| MOD_CK1_1 | 344 | 350 | PF00069 | 0.631 |
| MOD_CK1_1 | 35 | 41 | PF00069 | 0.610 |
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.471 |
| MOD_CK1_1 | 436 | 442 | PF00069 | 0.581 |
| MOD_CK1_1 | 48 | 54 | PF00069 | 0.587 |
| MOD_CK1_1 | 585 | 591 | PF00069 | 0.322 |
| MOD_CK2_1 | 206 | 212 | PF00069 | 0.538 |
| MOD_CK2_1 | 308 | 314 | PF00069 | 0.497 |
| MOD_CK2_1 | 353 | 359 | PF00069 | 0.580 |
| MOD_CK2_1 | 368 | 374 | PF00069 | 0.655 |
| MOD_CK2_1 | 452 | 458 | PF00069 | 0.450 |
| MOD_CK2_1 | 725 | 731 | PF00069 | 0.511 |
| MOD_CK2_1 | 746 | 752 | PF00069 | 0.357 |
| MOD_CK2_1 | 755 | 761 | PF00069 | 0.339 |
| MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.470 |
| MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.584 |
| MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.656 |
| MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.639 |
| MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.614 |
| MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.561 |
| MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.474 |
| MOD_GlcNHglycan | 434 | 438 | PF01048 | 0.592 |
| MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.537 |
| MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.561 |
| MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.375 |
| MOD_GSK3_1 | 116 | 123 | PF00069 | 0.483 |
| MOD_GSK3_1 | 12 | 19 | PF00069 | 0.487 |
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.509 |
| MOD_GSK3_1 | 199 | 206 | PF00069 | 0.576 |
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.590 |
| MOD_GSK3_1 | 341 | 348 | PF00069 | 0.695 |
| MOD_GSK3_1 | 423 | 430 | PF00069 | 0.554 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.641 |
| MOD_GSK3_1 | 432 | 439 | PF00069 | 0.530 |
| MOD_GSK3_1 | 443 | 450 | PF00069 | 0.462 |
| MOD_GSK3_1 | 637 | 644 | PF00069 | 0.316 |
| MOD_GSK3_1 | 717 | 724 | PF00069 | 0.395 |
| MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.448 |
| MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.525 |
| MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.555 |
| MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.529 |
| MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.317 |
| MOD_N-GLC_1 | 615 | 620 | PF02516 | 0.389 |
| MOD_N-GLC_1 | 689 | 694 | PF02516 | 0.342 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.471 |
| MOD_NEK2_1 | 101 | 106 | PF00069 | 0.368 |
| MOD_NEK2_1 | 116 | 121 | PF00069 | 0.449 |
| MOD_NEK2_1 | 16 | 21 | PF00069 | 0.532 |
| MOD_NEK2_1 | 238 | 243 | PF00069 | 0.435 |
| MOD_NEK2_1 | 36 | 41 | PF00069 | 0.556 |
| MOD_NEK2_1 | 383 | 388 | PF00069 | 0.444 |
| MOD_NEK2_1 | 615 | 620 | PF00069 | 0.478 |
| MOD_NEK2_1 | 717 | 722 | PF00069 | 0.355 |
| MOD_NEK2_1 | 76 | 81 | PF00069 | 0.422 |
| MOD_NEK2_2 | 12 | 17 | PF00069 | 0.469 |
| MOD_NEK2_2 | 187 | 192 | PF00069 | 0.707 |
| MOD_OFUCOSY | 18 | 25 | PF10250 | 0.473 |
| MOD_PIKK_1 | 506 | 512 | PF00454 | 0.548 |
| MOD_PIKK_1 | 615 | 621 | PF00454 | 0.378 |
| MOD_PIKK_1 | 733 | 739 | PF00454 | 0.429 |
| MOD_PKA_1 | 427 | 433 | PF00069 | 0.418 |
| MOD_PKA_1 | 486 | 492 | PF00069 | 0.632 |
| MOD_PKA_1 | 725 | 731 | PF00069 | 0.388 |
| MOD_PKA_1 | 745 | 751 | PF00069 | 0.375 |
| MOD_PKA_2 | 16 | 22 | PF00069 | 0.489 |
| MOD_PKA_2 | 203 | 209 | PF00069 | 0.580 |
| MOD_PKA_2 | 305 | 311 | PF00069 | 0.588 |
| MOD_PKA_2 | 363 | 369 | PF00069 | 0.489 |
| MOD_PKA_2 | 427 | 433 | PF00069 | 0.548 |
| MOD_PKA_2 | 48 | 54 | PF00069 | 0.582 |
| MOD_PKA_2 | 486 | 492 | PF00069 | 0.581 |
| MOD_PKA_2 | 585 | 591 | PF00069 | 0.292 |
| MOD_PKA_2 | 725 | 731 | PF00069 | 0.415 |
| MOD_PKA_2 | 745 | 751 | PF00069 | 0.390 |
| MOD_PKB_1 | 161 | 169 | PF00069 | 0.440 |
| MOD_PKB_1 | 639 | 647 | PF00069 | 0.265 |
| MOD_Plk_1 | 175 | 181 | PF00069 | 0.449 |
| MOD_Plk_1 | 433 | 439 | PF00069 | 0.434 |
| MOD_Plk_1 | 689 | 695 | PF00069 | 0.404 |
| MOD_Plk_4 | 106 | 112 | PF00069 | 0.327 |
| MOD_Plk_4 | 175 | 181 | PF00069 | 0.501 |
| MOD_Plk_4 | 436 | 442 | PF00069 | 0.418 |
| MOD_Plk_4 | 596 | 602 | PF00069 | 0.337 |
| MOD_Plk_4 | 692 | 698 | PF00069 | 0.508 |
| MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.464 |
| MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.555 |
| MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.625 |
| MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.496 |
| MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.341 |
| MOD_ProDKin_1 | 768 | 774 | PF00069 | 0.402 |
| TRG_DiLeu_BaLyEn_6 | 601 | 606 | PF01217 | 0.398 |
| TRG_DiLeu_BaLyEn_6 | 649 | 654 | PF01217 | 0.246 |
| TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.465 |
| TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.588 |
| TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.451 |
| TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.265 |
| TRG_ENDOCYTIC_2 | 706 | 709 | PF00928 | 0.279 |
| TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.468 |
| TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.440 |
| TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.512 |
| TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.586 |
| TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.559 |
| TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.427 |
| TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.477 |
| TRG_ER_diArg_1 | 554 | 557 | PF00400 | 0.435 |
| TRG_ER_diArg_1 | 638 | 641 | PF00400 | 0.315 |
| TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.555 |
| TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.556 |
| TRG_NLS_MonoExtC_3 | 554 | 559 | PF00514 | 0.347 |
| TRG_NLS_MonoExtC_3 | 724 | 729 | PF00514 | 0.414 |
| TRG_NLS_MonoExtN_4 | 725 | 730 | PF00514 | 0.399 |
| TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.428 |
| TRG_Pf-PMV_PEXEL_1 | 604 | 608 | PF00026 | 0.448 |
| TRG_Pf-PMV_PEXEL_1 | 641 | 646 | PF00026 | 0.287 |
| TRG_Pf-PMV_PEXEL_1 | 652 | 657 | PF00026 | 0.294 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IGN9 | Leishmania donovani | 38% | 100% |
| A0A3S5H4Y9 | Leishmania donovani | 35% | 81% |
| A0A3S7WT86 | Leishmania donovani | 44% | 79% |
| A0A3S7WWA6 | Leishmania donovani | 41% | 99% |
| A0A451EJD9 | Leishmania donovani | 40% | 99% |
| A0A451EJF4 | Leishmania donovani | 74% | 99% |
| A0A451EJF6 | Leishmania donovani | 75% | 100% |
| A0A451EJF8 | Leishmania donovani | 66% | 100% |
| A0A451EJF9 | Leishmania donovani | 62% | 94% |
| A4H3A9 | Leishmania braziliensis | 62% | 100% |
| A4H3B4 | Leishmania braziliensis | 59% | 100% |
| A4H3B6 | Leishmania braziliensis | 63% | 100% |
| A4H3B8 | Leishmania braziliensis | 59% | 100% |
| A4H3B9 | Leishmania braziliensis | 41% | 100% |
| A4H4W8 | Leishmania braziliensis | 37% | 100% |
| A4HJ20 | Leishmania braziliensis | 60% | 100% |
| A4HNK3 | Leishmania braziliensis | 41% | 99% |
| A4HNK6 | Leishmania braziliensis | 37% | 100% |
| A4HRL9 | Leishmania infantum | 84% | 100% |
| A4HRM0 | Leishmania infantum | 88% | 99% |
| A4HRM1 | Leishmania infantum | 76% | 100% |
| A4HRS1 | Leishmania infantum | 63% | 100% |
| A4HRS3 | Leishmania infantum | 35% | 100% |
| A4HRS5 | Leishmania infantum | 66% | 99% |
| A4HZM0 | Leishmania infantum | 37% | 100% |
| A4I7C7 | Leishmania infantum | 40% | 100% |
| A4IAQ2 | Leishmania infantum | 39% | 100% |
| E9AC91 | Leishmania major | 79% | 100% |
| E9AC92 | Leishmania major | 77% | 100% |
| E9AC94 | Leishmania major | 35% | 100% |
| E9AC95 | Leishmania major | 64% | 98% |
| E9AC96 | Leishmania major | 65% | 100% |
| E9AC98 | Leishmania major | 35% | 100% |
| E9AEH8 | Leishmania major | 39% | 100% |
| E9AHA6 | Leishmania infantum | 37% | 100% |
| E9AIP8 | Leishmania braziliensis | 38% | 100% |
| E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
| E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
| E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 99% |
| E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
| E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
| E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
| E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
| Q4Q5T6 | Leishmania major | 40% | 100% |
| Q4QCL8 | Leishmania major | 40% | 100% |
| Q4QFJ3 | Leishmania major | 44% | 100% |
| Q4QIG9 | Leishmania major | 40% | 100% |
| Q7YXU9 | Leishmania major | 39% | 100% |
| Q7YXV1 | Leishmania major | 40% | 100% |
| Q7YXV2 | Leishmania major | 38% | 98% |