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: 53 |
NetGPI | no | yes: 0, no: 53 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 54 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
GO:0000139 | Golgi membrane | 5 | 14 |
GO:0031090 | organelle membrane | 3 | 14 |
GO:0098588 | bounding membrane of organelle | 4 | 14 |
Related structures:
AlphaFold database: A4H3B9
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 54 |
GO:0006807 | nitrogen compound metabolic process | 2 | 54 |
GO:0008152 | metabolic process | 1 | 54 |
GO:0019538 | protein metabolic process | 3 | 54 |
GO:0036211 | protein modification process | 4 | 54 |
GO:0043170 | macromolecule metabolic process | 3 | 54 |
GO:0043412 | macromolecule modification | 4 | 54 |
GO:0043413 | macromolecule glycosylation | 3 | 54 |
GO:0044238 | primary metabolic process | 2 | 54 |
GO:0070085 | glycosylation | 2 | 54 |
GO:0071704 | organic substance metabolic process | 2 | 54 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 54 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 54 |
GO:0016740 | transferase activity | 2 | 54 |
GO:0016757 | glycosyltransferase activity | 3 | 54 |
GO:0016758 | hexosyltransferase activity | 4 | 54 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.379 |
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.326 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 666 | 668 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 443 | 447 | PF00082 | 0.528 |
CLV_PCSK_FUR_1 | 91 | 95 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 881 | 883 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 881 | 883 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 844 | 848 | PF00082 | 0.496 |
DEG_APCC_DBOX_1 | 109 | 117 | PF00400 | 0.435 |
DEG_APCC_DBOX_1 | 478 | 486 | PF00400 | 0.317 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.290 |
DEG_SPOP_SBC_1 | 466 | 470 | PF00917 | 0.344 |
DOC_ANK_TNKS_1 | 143 | 150 | PF00023 | 0.382 |
DOC_CKS1_1 | 767 | 772 | PF01111 | 0.240 |
DOC_CYCLIN_RxL_1 | 841 | 850 | PF00134 | 0.277 |
DOC_CYCLIN_yCln2_LP_2 | 489 | 495 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 108 | 116 | PF00069 | 0.668 |
DOC_MAPK_gen_1 | 667 | 674 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 80 | 87 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 117 | 124 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 328 | 335 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 80 | 89 | PF00069 | 0.566 |
DOC_MAPK_NFAT4_5 | 117 | 125 | PF00069 | 0.217 |
DOC_PP1_RVXF_1 | 172 | 178 | PF00149 | 0.376 |
DOC_PP1_RVXF_1 | 553 | 560 | PF00149 | 0.444 |
DOC_PP1_RVXF_1 | 842 | 848 | PF00149 | 0.279 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.316 |
DOC_PP2B_LxvP_1 | 489 | 492 | PF13499 | 0.518 |
DOC_PP2B_PxIxI_1 | 330 | 336 | PF00149 | 0.283 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.255 |
DOC_PP4_FxxP_1 | 408 | 411 | PF00568 | 0.361 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.623 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 766 | 771 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 789 | 794 | PF00397 | 0.364 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 354 | 358 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 445 | 450 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 454 | 462 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 613 | 621 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 633 | 643 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 691 | 695 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 707 | 717 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 736 | 740 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 755 | 761 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 80 | 89 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 171 | 188 | PF00022 | 0.364 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.610 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.259 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.468 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.531 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.412 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.492 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.650 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.331 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.269 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.309 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.464 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.310 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.374 |
LIG_FHA_1 | 884 | 890 | PF00498 | 0.403 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.510 |
LIG_FHA_2 | 709 | 715 | PF00498 | 0.307 |
LIG_FHA_2 | 736 | 742 | PF00498 | 0.291 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.302 |
LIG_FHA_2 | 790 | 796 | PF00498 | 0.371 |
LIG_LIR_Apic_2 | 407 | 411 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 265 | 276 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 487 | 496 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 561 | 572 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 578 | 588 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 589 | 595 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 757 | 767 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 820 | 830 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 83 | 92 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 696 | 700 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 757 | 763 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 778 | 782 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 820 | 826 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 885 | 890 | PF02991 | 0.417 |
LIG_LYPXL_yS_3 | 887 | 890 | PF13949 | 0.409 |
LIG_Pex14_2 | 697 | 701 | PF04695 | 0.315 |
LIG_PTB_Apo_2 | 695 | 702 | PF02174 | 0.325 |
LIG_REV1ctd_RIR_1 | 406 | 410 | PF16727 | 0.345 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.275 |
LIG_SH2_CRK | 767 | 771 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.275 |
LIG_SH2_PTP2 | 332 | 335 | PF00017 | 0.273 |
LIG_SH2_PTP2 | 581 | 584 | PF00017 | 0.315 |
LIG_SH2_SRC | 201 | 204 | PF00017 | 0.373 |
LIG_SH2_SRC | 562 | 565 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.275 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 705 | 709 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 644 | 647 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 739 | 742 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 775 | 778 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 780 | 783 | PF00017 | 0.402 |
LIG_SH3_1 | 472 | 478 | PF00018 | 0.339 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.425 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.332 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.387 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.375 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.483 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.402 |
LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.424 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.351 |
LIG_TRAF2_1 | 802 | 805 | PF00917 | 0.348 |
LIG_WW_1 | 329 | 332 | PF00397 | 0.297 |
LIG_WW_3 | 743 | 747 | PF00397 | 0.275 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.394 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.324 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.306 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.338 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.682 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.427 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.340 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.533 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.372 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.372 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.332 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.239 |
MOD_CK2_1 | 789 | 795 | PF00069 | 0.425 |
MOD_Cter_Amidation | 108 | 111 | PF01082 | 0.371 |
MOD_Cter_Amidation | 596 | 599 | PF01082 | 0.525 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.226 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.488 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.547 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.631 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.646 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.513 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.666 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.612 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.238 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.406 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.335 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.269 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.332 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.357 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.464 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.671 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.227 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.434 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.658 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.432 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.634 |
MOD_N-GLC_1 | 815 | 820 | PF02516 | 0.590 |
MOD_N-GLC_1 | 855 | 860 | PF02516 | 0.497 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.364 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.478 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.302 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.285 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.618 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.467 |
MOD_NEK2_1 | 830 | 835 | PF00069 | 0.344 |
MOD_NEK2_2 | 181 | 186 | PF00069 | 0.543 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.395 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.466 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.386 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.557 |
MOD_PKA_1 | 445 | 451 | PF00069 | 0.318 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.536 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.604 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.458 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.469 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.389 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.337 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.348 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.646 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.362 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.637 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.352 |
MOD_PKA_2 | 690 | 696 | PF00069 | 0.288 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.315 |
MOD_PKA_2 | 754 | 760 | PF00069 | 0.297 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.574 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.655 |
MOD_PKB_1 | 443 | 451 | PF00069 | 0.321 |
MOD_PKB_1 | 91 | 99 | PF00069 | 0.590 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.403 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.323 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.322 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.420 |
MOD_Plk_1 | 815 | 821 | PF00069 | 0.362 |
MOD_Plk_1 | 855 | 861 | PF00069 | 0.305 |
MOD_Plk_2-3 | 604 | 610 | PF00069 | 0.408 |
MOD_Plk_2-3 | 735 | 741 | PF00069 | 0.277 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.330 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.423 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.403 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.410 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.447 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.264 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.322 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.311 |
MOD_Plk_4 | 759 | 765 | PF00069 | 0.419 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.366 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.520 |
MOD_ProDKin_1 | 766 | 772 | PF00069 | 0.313 |
MOD_ProDKin_1 | 789 | 795 | PF00069 | 0.364 |
TRG_DiLeu_BaEn_2 | 711 | 717 | PF01217 | 0.291 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.268 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 779 | 782 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 887 | 890 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 598 | 601 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 631 | 634 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 70 | 73 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 844 | 849 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 34% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 41% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 65% | 90% |
A0A3S7WT86 | Leishmania donovani | 36% | 87% |
A0A3S7WWA6 | Leishmania donovani | 34% | 100% |
A0A451EJD9 | Leishmania donovani | 34% | 100% |
A0A451EJF4 | Leishmania donovani | 40% | 100% |
A0A451EJF6 | Leishmania donovani | 39% | 100% |
A0A451EJF8 | Leishmania donovani | 38% | 100% |
A0A451EJF9 | Leishmania donovani | 39% | 100% |
A4H3A9 | Leishmania braziliensis | 40% | 100% |
A4H3B4 | Leishmania braziliensis | 39% | 100% |
A4H3B6 | Leishmania braziliensis | 40% | 100% |
A4H3B7 | Leishmania braziliensis | 35% | 100% |
A4H3B8 | Leishmania braziliensis | 39% | 100% |
A4H4W8 | Leishmania braziliensis | 33% | 100% |
A4HJ20 | Leishmania braziliensis | 38% | 100% |
A4HNK3 | Leishmania braziliensis | 38% | 100% |
A4HNK6 | Leishmania braziliensis | 33% | 100% |
A4HRL9 | Leishmania infantum | 40% | 100% |
A4HRM0 | Leishmania infantum | 41% | 100% |
A4HRM1 | Leishmania infantum | 39% | 100% |
A4HRS1 | Leishmania infantum | 36% | 100% |
A4HRS3 | Leishmania infantum | 65% | 90% |
A4HRS5 | Leishmania infantum | 38% | 100% |
A4HZM0 | Leishmania infantum | 34% | 100% |
A4I7C7 | Leishmania infantum | 33% | 100% |
A4IAQ2 | Leishmania infantum | 33% | 100% |
E9AC91 | Leishmania major | 36% | 100% |
E9AC92 | Leishmania major | 40% | 100% |
E9AC94 | Leishmania major | 64% | 100% |
E9AC95 | Leishmania major | 38% | 100% |
E9AC96 | Leishmania major | 39% | 100% |
E9AC98 | Leishmania major | 64% | 100% |
E9AEH8 | Leishmania major | 34% | 100% |
E9AHA6 | Leishmania infantum | 33% | 100% |
E9AIP8 | Leishmania braziliensis | 36% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 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) | 62% | 90% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q4Q5T6 | Leishmania major | 34% | 100% |
Q4QCL8 | Leishmania major | 33% | 100% |
Q4QFJ3 | Leishmania major | 36% | 100% |
Q4QIG9 | Leishmania major | 33% | 100% |
Q7YXU9 | Leishmania major | 35% | 100% |
Q7YXV1 | Leishmania major | 33% | 100% |
Q7YXV2 | Leishmania major | 33% | 100% |