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. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HGL5
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004730 | pseudouridylate synthase activity | 5 | 2 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 2 |
GO:0016836 | hydro-lyase activity | 4 | 2 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.285 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 799 | 801 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.531 |
CLV_PCSK_FUR_1 | 306 | 310 | PF00082 | 0.406 |
CLV_PCSK_FUR_1 | 813 | 817 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 757 | 759 | PF00082 | 0.591 |
CLV_PCSK_PC7_1 | 426 | 432 | PF00082 | 0.265 |
CLV_PCSK_PC7_1 | 744 | 750 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 757 | 761 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 815 | 819 | PF00082 | 0.598 |
CLV_Separin_Metazoa | 607 | 611 | PF03568 | 0.265 |
DEG_APCC_DBOX_1 | 288 | 296 | PF00400 | 0.279 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.536 |
DOC_CYCLIN_RxL_1 | 610 | 622 | PF00134 | 0.358 |
DOC_CYCLIN_RxL_1 | 755 | 763 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 305 | 316 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 38 | 47 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 425 | 437 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 308 | 316 | PF00069 | 0.187 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.187 |
DOC_PP1_RVXF_1 | 755 | 762 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 664 | 667 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 722 | 725 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 605 | 608 | PF00568 | 0.265 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.567 |
DOC_PP4_FxxP_1 | 761 | 764 | PF00568 | 0.365 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.187 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 786 | 790 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 819 | 823 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.265 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 804 | 809 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 370 | 374 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 488 | 495 | PF00244 | 0.261 |
LIG_Actin_WH2_2 | 461 | 479 | PF00022 | 0.410 |
LIG_AP2alpha_2 | 729 | 731 | PF02296 | 0.623 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.619 |
LIG_BRCT_BRCA1_1 | 843 | 847 | PF00533 | 0.573 |
LIG_CaM_IQ_9 | 121 | 136 | PF13499 | 0.519 |
LIG_CtBP_PxDLS_1 | 616 | 620 | PF00389 | 0.279 |
LIG_deltaCOP1_diTrp_1 | 539 | 544 | PF00928 | 0.410 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.347 |
LIG_eIF4E_1 | 321 | 327 | PF01652 | 0.298 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.734 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.509 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.419 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.336 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.279 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.197 |
LIG_FHA_1 | 829 | 835 | PF00498 | 0.702 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.580 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.284 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.228 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.176 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.323 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.330 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.322 |
LIG_FHA_2 | 682 | 688 | PF00498 | 0.481 |
LIG_HCF-1_HBM_1 | 678 | 681 | PF13415 | 0.343 |
LIG_LIR_Apic_2 | 604 | 608 | PF02991 | 0.265 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 497 | 508 | PF02991 | 0.225 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.145 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 497 | 503 | PF02991 | 0.161 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 567 | 571 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 668 | 674 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 687 | 692 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 836 | 840 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.494 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.265 |
LIG_PCNA_PIPBox_1 | 575 | 584 | PF02747 | 0.298 |
LIG_PCNA_yPIPBox_3 | 575 | 588 | PF02747 | 0.420 |
LIG_PCNA_yPIPBox_3 | 638 | 650 | PF02747 | 0.265 |
LIG_Pex14_1 | 540 | 544 | PF04695 | 0.410 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.460 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.265 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.279 |
LIG_SH2_CRK | 641 | 645 | PF00017 | 0.265 |
LIG_SH2_CRK | 794 | 798 | PF00017 | 0.600 |
LIG_SH2_GRB2like | 641 | 644 | PF00017 | 0.265 |
LIG_SH2_NCK_1 | 623 | 627 | PF00017 | 0.333 |
LIG_SH2_NCK_1 | 641 | 645 | PF00017 | 0.211 |
LIG_SH2_SRC | 623 | 626 | PF00017 | 0.421 |
LIG_SH2_SRC | 641 | 644 | PF00017 | 0.202 |
LIG_SH2_SRC | 692 | 695 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 623 | 627 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 641 | 645 | PF00017 | 0.211 |
LIG_SH2_STAP1 | 794 | 798 | PF00017 | 0.600 |
LIG_SH2_STAT3 | 366 | 369 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 556 | 559 | PF00017 | 0.187 |
LIG_SH2_STAT3 | 581 | 584 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.199 |
LIG_SH2_STAT5 | 681 | 684 | PF00017 | 0.388 |
LIG_SH3_1 | 112 | 118 | PF00018 | 0.511 |
LIG_SH3_1 | 158 | 164 | PF00018 | 0.528 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.664 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.528 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.266 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.279 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.311 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.265 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.540 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 658 | 665 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 26 | 32 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 615 | 620 | PF11976 | 0.327 |
LIG_WRC_WIRS_1 | 495 | 500 | PF05994 | 0.410 |
LIG_WRC_WIRS_1 | 541 | 546 | PF05994 | 0.399 |
LIG_WRC_WIRS_1 | 834 | 839 | PF05994 | 0.653 |
LIG_WW_2 | 77 | 80 | PF00397 | 0.659 |
LIG_WW_3 | 607 | 611 | PF00397 | 0.265 |
MOD_CDK_SPK_2 | 804 | 809 | PF00069 | 0.618 |
MOD_CDK_SPxxK_3 | 760 | 767 | PF00069 | 0.358 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.483 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.276 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.778 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.388 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.671 |
MOD_CK1_1 | 830 | 836 | PF00069 | 0.596 |
MOD_CK1_1 | 841 | 847 | PF00069 | 0.352 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.619 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.288 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.323 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.291 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.392 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.566 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.556 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.553 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.557 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.642 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.598 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.339 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.358 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.624 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.567 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.560 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.627 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.782 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.578 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.350 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.298 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.392 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.416 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.727 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.724 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.642 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.346 |
MOD_LATS_1 | 270 | 276 | PF00433 | 0.410 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.358 |
MOD_N-GLC_1 | 786 | 791 | PF02516 | 0.580 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.438 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.589 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.469 |
MOD_NEK2_2 | 628 | 633 | PF00069 | 0.327 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.521 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.327 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.225 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.507 |
MOD_PIKK_1 | 736 | 742 | PF00454 | 0.658 |
MOD_PK_1 | 272 | 278 | PF00069 | 0.410 |
MOD_PK_1 | 291 | 297 | PF00069 | 0.410 |
MOD_PK_1 | 341 | 347 | PF00069 | 0.327 |
MOD_PKA_1 | 488 | 494 | PF00069 | 0.265 |
MOD_PKA_1 | 815 | 821 | PF00069 | 0.669 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.265 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.265 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.442 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.145 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.608 |
MOD_PKA_2 | 815 | 821 | PF00069 | 0.611 |
MOD_PKB_1 | 289 | 297 | PF00069 | 0.187 |
MOD_PKB_1 | 813 | 821 | PF00069 | 0.614 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.633 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.622 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.279 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.381 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.298 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.395 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.578 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.474 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.274 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.479 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.499 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.571 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.724 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.265 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.498 |
MOD_ProDKin_1 | 760 | 766 | PF00069 | 0.356 |
MOD_ProDKin_1 | 804 | 810 | PF00069 | 0.617 |
MOD_SUMO_rev_2 | 69 | 75 | PF00179 | 0.740 |
MOD_SUMO_rev_2 | 706 | 715 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 750 | 759 | PF00179 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 755 | 760 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 794 | 797 | PF00928 | 0.607 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 553 | 556 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 812 | 815 | PF00400 | 0.563 |
TRG_NES_CRM1_1 | 281 | 293 | PF08389 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 404 | 408 | PF00026 | 0.275 |
TRG_Pf-PMV_PEXEL_1 | 430 | 434 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 488 | 493 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 515 | 520 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 654 | 659 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 66 | 71 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 758 | 762 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 767 | 771 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P820 | Leptomonas seymouri | 66% | 86% |
A0A0S4K0L8 | Bodo saltans | 45% | 84% |
A0A1X0NQX7 | Trypanosomatidae | 56% | 92% |
A0A3Q8II50 | Leishmania donovani | 84% | 100% |
A0A3S5ISD4 | Trypanosoma rangeli | 53% | 97% |
A4I3P1 | Leishmania infantum | 89% | 100% |
D0A8C3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 92% |
E9AZY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q8A3 | Leishmania major | 84% | 100% |
V5BFB8 | Trypanosoma cruzi | 59% | 92% |