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. | yes | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: A0A3Q8IHT0
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 661 | 665 | PF00656 | 0.320 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.461 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 764 | 768 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.602 |
DEG_ODPH_VHL_1 | 376 | 389 | PF01847 | 0.366 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.473 |
DOC_AGCK_PIF_2 | 118 | 123 | PF00069 | 0.302 |
DOC_CYCLIN_RxL_1 | 387 | 397 | PF00134 | 0.263 |
DOC_MAPK_DCC_7 | 549 | 559 | PF00069 | 0.610 |
DOC_MAPK_FxFP_2 | 431 | 434 | PF00069 | 0.254 |
DOC_MAPK_gen_1 | 238 | 247 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 342 | 349 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 350 | 359 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 549 | 559 | PF00069 | 0.702 |
DOC_MAPK_HePTP_8 | 349 | 361 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 342 | 349 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 552 | 559 | PF00069 | 0.714 |
DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 65 | 72 | PF00069 | 0.206 |
DOC_PP1_RVXF_1 | 606 | 612 | PF00149 | 0.397 |
DOC_PP1_RVXF_1 | 640 | 647 | PF00149 | 0.311 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.224 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.405 |
DOC_PP4_FxxP_1 | 604 | 607 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.206 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.622 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 293 | 298 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 549 | 555 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 659 | 663 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 716 | 722 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 750 | 754 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 83 | 88 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 856 | 861 | PF00244 | 0.332 |
LIG_Actin_WH2_2 | 61 | 79 | PF00022 | 0.383 |
LIG_AP2alpha_2 | 98 | 100 | PF02296 | 0.288 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.380 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.218 |
LIG_Clathr_ClatBox_1 | 554 | 558 | PF01394 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 488 | 496 | PF00928 | 0.591 |
LIG_EH1_1 | 432 | 440 | PF00400 | 0.188 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.378 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.424 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.469 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.317 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.391 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.478 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.640 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.311 |
LIG_FHA_2 | 857 | 863 | PF00498 | 0.347 |
LIG_GBD_Chelix_1 | 579 | 587 | PF00786 | 0.380 |
LIG_LIR_Apic_2 | 379 | 384 | PF02991 | 0.314 |
LIG_LIR_Apic_2 | 603 | 607 | PF02991 | 0.392 |
LIG_LIR_Apic_2 | 741 | 745 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 813 | 817 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 229 | 237 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 488 | 495 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 628 | 638 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 696 | 702 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 720 | 730 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 771 | 781 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 454 | 458 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 628 | 633 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 696 | 700 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 720 | 725 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 771 | 776 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 778 | 784 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.289 |
LIG_LYPXL_yS_3 | 138 | 141 | PF13949 | 0.387 |
LIG_MLH1_MIPbox_1 | 114 | 118 | PF16413 | 0.380 |
LIG_NRBOX | 322 | 328 | PF00104 | 0.388 |
LIG_PCNA_PIPBox_1 | 620 | 629 | PF02747 | 0.289 |
LIG_PCNA_yPIPBox_3 | 616 | 627 | PF02747 | 0.307 |
LIG_Pex14_1 | 114 | 118 | PF04695 | 0.288 |
LIG_Pex14_1 | 429 | 433 | PF04695 | 0.269 |
LIG_Pex14_1 | 647 | 651 | PF04695 | 0.300 |
LIG_Pex14_2 | 117 | 121 | PF04695 | 0.215 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.418 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.477 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.585 |
LIG_Pex14_2 | 591 | 595 | PF04695 | 0.493 |
LIG_Pex14_2 | 97 | 101 | PF04695 | 0.267 |
LIG_PTB_Apo_2 | 716 | 723 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 716 | 722 | PF10480 | 0.324 |
LIG_SH2_CRK | 445 | 449 | PF00017 | 0.496 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.579 |
LIG_SH2_CRK | 742 | 746 | PF00017 | 0.372 |
LIG_SH2_CRK | 781 | 785 | PF00017 | 0.303 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.302 |
LIG_SH2_GRB2like | 418 | 421 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 742 | 746 | PF00017 | 0.330 |
LIG_SH2_PTP2 | 263 | 266 | PF00017 | 0.364 |
LIG_SH2_PTP2 | 697 | 700 | PF00017 | 0.287 |
LIG_SH2_SRC | 421 | 424 | PF00017 | 0.266 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.293 |
LIG_SH2_SRC | 92 | 95 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 777 | 781 | PF00017 | 0.361 |
LIG_SH2_STAT3 | 513 | 516 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 649 | 652 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.351 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.387 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.414 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.343 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.479 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.405 |
LIG_SH3_3 | 797 | 803 | PF00018 | 0.361 |
LIG_SH3_3 | 804 | 810 | PF00018 | 0.362 |
LIG_SUMO_SIM_anti_2 | 179 | 184 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 577 | 582 | PF11976 | 0.407 |
LIG_SxIP_EBH_1 | 197 | 210 | PF03271 | 0.349 |
LIG_TRAF2_1 | 545 | 548 | PF00917 | 0.594 |
LIG_TRAF2_2 | 512 | 517 | PF00917 | 0.580 |
LIG_TYR_ITIM | 419 | 424 | PF00017 | 0.202 |
LIG_TYR_ITSM | 227 | 234 | PF00017 | 0.329 |
LIG_UBA3_1 | 753 | 762 | PF00899 | 0.400 |
LIG_WRC_WIRS_1 | 227 | 232 | PF05994 | 0.329 |
LIG_WRC_WIRS_1 | 452 | 457 | PF05994 | 0.230 |
MOD_CDC14_SPxK_1 | 315 | 318 | PF00782 | 0.380 |
MOD_CDK_SPxK_1 | 312 | 318 | PF00069 | 0.288 |
MOD_CDK_SPxxK_3 | 743 | 750 | PF00069 | 0.376 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.364 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.661 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.630 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.349 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.336 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.341 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.602 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.249 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.404 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.617 |
MOD_CK2_1 | 856 | 862 | PF00069 | 0.355 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.569 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.518 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.499 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.572 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.589 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.394 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.349 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.732 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.529 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.306 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.673 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.734 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.642 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.342 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.328 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.570 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.514 |
MOD_N-GLC_1 | 790 | 795 | PF02516 | 0.530 |
MOD_N-GLC_2 | 163 | 165 | PF02516 | 0.443 |
MOD_N-GLC_2 | 218 | 220 | PF02516 | 0.288 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.345 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.374 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.367 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.222 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.258 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.347 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.312 |
MOD_NEK2_1 | 749 | 754 | PF00069 | 0.325 |
MOD_NEK2_1 | 854 | 859 | PF00069 | 0.335 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.329 |
MOD_PIKK_1 | 610 | 616 | PF00454 | 0.303 |
MOD_PK_1 | 360 | 366 | PF00069 | 0.426 |
MOD_PK_1 | 83 | 89 | PF00069 | 0.322 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.323 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.538 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.759 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.640 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.318 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.359 |
MOD_PKB_1 | 358 | 366 | PF00069 | 0.512 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.586 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.309 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.288 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.329 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.432 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.431 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.707 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.334 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.336 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.354 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.327 |
MOD_Plk_4 | 749 | 755 | PF00069 | 0.363 |
MOD_Plk_4 | 768 | 774 | PF00069 | 0.442 |
MOD_Plk_4 | 810 | 816 | PF00069 | 0.372 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.628 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.288 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.335 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.317 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.346 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.323 |
TRG_DiLeu_BaEn_1 | 686 | 691 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 463 | 468 | PF01217 | 0.295 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.719 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 781 | 784 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 349 | 352 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 387 | 390 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.628 |
TRG_NES_CRM1_1 | 321 | 336 | PF08389 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 390 | 395 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 83 | 88 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 858 | 862 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 52% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 55% | 100% |
A0A3Q8II34 | Leishmania donovani | 56% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 79% | 100% |
A0A3Q8IV37 | Leishmania donovani | 75% | 100% |
A0A422MX14 | Trypanosoma rangeli | 55% | 100% |
A4HFF9 | Leishmania braziliensis | 78% | 100% |
A4HMD5 | Leishmania braziliensis | 72% | 98% |
A4HMD6 | Leishmania braziliensis | 54% | 100% |
A4HMD7 | Leishmania braziliensis | 71% | 100% |
A4IB08 | Leishmania infantum | 100% | 100% |
A4IB09 | Leishmania infantum | 79% | 99% |
A4IB10 | Leishmania infantum | 56% | 99% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E2RG47 | Canis lupus familiaris | 30% | 100% |
E9AET6 | Leishmania major | 94% | 100% |
E9AET7 | Leishmania major | 77% | 99% |
E9AET8 | Leishmania major | 55% | 99% |
E9AET9 | Leishmania major | 73% | 100% |
E9AHU4 | Leishmania infantum | 76% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 97% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 99% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
F1PJP5 | Canis lupus familiaris | 30% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
P46975 | Caenorhabditis elegans | 31% | 100% |
P46977 | Homo sapiens | 30% | 100% |
P46978 | Mus musculus | 29% | 100% |
Q2KJI2 | Bos taurus | 30% | 100% |
Q3TDQ1 | Mus musculus | 30% | 100% |
Q5RCE2 | Pongo abelii | 30% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 30% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 30% | 100% |
Q93ZY3 | Arabidopsis thaliana | 32% | 100% |
Q9FX21 | Arabidopsis thaliana | 32% | 100% |
V5BDM6 | Trypanosoma cruzi | 56% | 100% |