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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ARP8
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009451 | RNA modification | 5 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016070 | RNA metabolic process | 5 | 13 |
GO:0032259 | methylation | 2 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0043414 | macromolecule methylation | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 14 |
GO:0003723 | RNA binding | 4 | 14 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0008168 | methyltransferase activity | 4 | 14 |
GO:0016740 | transferase activity | 2 | 14 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
GO:0000049 | tRNA binding | 5 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0016428 | tRNA (cytosine-5-)-methyltransferase activity | 7 | 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 | 194 | 198 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.366 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.572 |
CLV_MEL_PAP_1 | 689 | 695 | PF00089 | 0.484 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 357 | 361 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 687 | 689 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 271 | 273 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 359 | 361 | PF00082 | 0.285 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.676 |
CLV_PCSK_PC7_1 | 683 | 689 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 716 | 720 | PF00082 | 0.569 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.712 |
DEG_ODPH_VHL_1 | 680 | 693 | PF01847 | 0.503 |
DEG_SIAH_1 | 731 | 739 | PF03145 | 0.631 |
DEG_SPOP_SBC_1 | 598 | 602 | PF00917 | 0.573 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.494 |
DOC_CKS1_1 | 238 | 243 | PF01111 | 0.567 |
DOC_CKS1_1 | 625 | 630 | PF01111 | 0.489 |
DOC_CYCLIN_RxL_1 | 434 | 446 | PF00134 | 0.508 |
DOC_CYCLIN_RxL_1 | 683 | 694 | PF00134 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 507 | 513 | PF00134 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 565 | 571 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 625 | 631 | PF00134 | 0.487 |
DOC_MAPK_gen_1 | 562 | 571 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 638 | 647 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 798 | 805 | PF00069 | 0.332 |
DOC_MAPK_HePTP_8 | 635 | 647 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 638 | 647 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 798 | 805 | PF00069 | 0.321 |
DOC_MAPK_NFAT4_5 | 798 | 806 | PF00069 | 0.352 |
DOC_PP1_RVXF_1 | 685 | 692 | PF00149 | 0.542 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 679 | 682 | PF00568 | 0.541 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.620 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.484 |
DOC_USP7_UBL2_3 | 733 | 737 | PF12436 | 0.684 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 278 | 288 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 347 | 355 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 415 | 425 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 622 | 628 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 683 | 691 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 825 | 829 | PF00244 | 0.630 |
LIG_APCC_ABBA_1 | 524 | 529 | PF00400 | 0.484 |
LIG_BRCT_BRCA1_1 | 675 | 679 | PF00533 | 0.514 |
LIG_CSL_BTD_1 | 420 | 423 | PF09270 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 203 | 209 | PF00928 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 572 | 582 | PF00928 | 0.413 |
LIG_Dynein_DLC8_1 | 347 | 353 | PF01221 | 0.523 |
LIG_eIF4E_1 | 438 | 444 | PF01652 | 0.366 |
LIG_FAT_LD_1 | 75 | 83 | PF03623 | 0.546 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.533 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.392 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.427 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.484 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.548 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.444 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.601 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.560 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.540 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.484 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.463 |
LIG_FHA_2 | 752 | 758 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 546 | 550 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 637 | 643 | PF02991 | 0.465 |
LIG_LIR_Apic_2 | 676 | 682 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 156 | 162 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 393 | 404 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 573 | 583 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 89 | 97 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 580 | 585 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 590 | 596 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 713 | 718 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.591 |
LIG_MYND_1 | 510 | 514 | PF01753 | 0.574 |
LIG_NRBOX | 699 | 705 | PF00104 | 0.565 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.544 |
LIG_NRBOX | 741 | 747 | PF00104 | 0.619 |
LIG_NRBOX | 759 | 765 | PF00104 | 0.453 |
LIG_Pex14_1 | 376 | 380 | PF04695 | 0.508 |
LIG_Pex14_1 | 421 | 425 | PF04695 | 0.484 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.479 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.508 |
LIG_SH2_CRK | 640 | 644 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 596 | 600 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 791 | 794 | PF00017 | 0.391 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.645 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.471 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.505 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.512 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.538 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 475 | 481 | PF11976 | 0.484 |
LIG_SUMO_SIM_anti_2 | 756 | 764 | PF11976 | 0.581 |
LIG_TRAF2_1 | 287 | 290 | PF00917 | 0.370 |
LIG_TRAF2_1 | 756 | 759 | PF00917 | 0.622 |
LIG_TRAF2_1 | 841 | 844 | PF00917 | 0.799 |
LIG_TRFH_1 | 611 | 615 | PF08558 | 0.462 |
LIG_TYR_ITIM | 436 | 441 | PF00017 | 0.177 |
LIG_WRC_WIRS_1 | 470 | 475 | PF05994 | 0.313 |
LIG_WRC_WIRS_1 | 579 | 584 | PF05994 | 0.507 |
LIG_WW_1 | 513 | 516 | PF00397 | 0.468 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.681 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.469 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.553 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.467 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.398 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.379 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.318 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.589 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.644 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.743 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.374 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.560 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.666 |
MOD_CK2_1 | 753 | 759 | PF00069 | 0.481 |
MOD_CK2_1 | 763 | 769 | PF00069 | 0.460 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.662 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.507 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.527 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.403 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.431 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.375 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.418 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.388 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.318 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.399 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.690 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.570 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.382 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.395 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.416 |
MOD_GlcNHglycan | 834 | 837 | PF01048 | 0.742 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.512 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.537 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.520 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.414 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.428 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.318 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.318 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.318 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.177 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.617 |
MOD_GSK3_1 | 776 | 783 | PF00069 | 0.518 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.392 |
MOD_LATS_1 | 130 | 136 | PF00433 | 0.727 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.700 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.540 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.432 |
MOD_N-GLC_1 | 830 | 835 | PF02516 | 0.735 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.592 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.570 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.491 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.385 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.306 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.549 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.516 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.318 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.521 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.525 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.343 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.635 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.343 |
MOD_PIKK_1 | 744 | 750 | PF00454 | 0.645 |
MOD_PIKK_1 | 763 | 769 | PF00454 | 0.560 |
MOD_PK_1 | 413 | 419 | PF00069 | 0.421 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.535 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.726 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.705 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.575 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.516 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.475 |
MOD_PKA_2 | 824 | 830 | PF00069 | 0.724 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.581 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.570 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.421 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.447 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.490 |
MOD_Plk_1 | 751 | 757 | PF00069 | 0.574 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.346 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.376 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.358 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.583 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.473 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.505 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.413 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.527 |
MOD_Plk_4 | 824 | 830 | PF00069 | 0.684 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.644 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.422 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.542 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.208 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.339 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.490 |
MOD_SUMO_rev_2 | 656 | 663 | PF00179 | 0.466 |
TRG_DiLeu_BaEn_1 | 759 | 764 | PF01217 | 0.605 |
TRG_DiLeu_BaEn_1 | 824 | 829 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_2 | 204 | 210 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_2 | 674 | 680 | PF01217 | 0.510 |
TRG_DiLeu_LyEn_5 | 145 | 150 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.177 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 620 | 622 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 635 | 638 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 687 | 689 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 697 | 701 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H1 | Leptomonas seymouri | 71% | 99% |
A0A0S4KJ12 | Bodo saltans | 42% | 100% |
A0A1X0P6Y3 | Trypanosomatidae | 53% | 100% |
A0A3R7M922 | Trypanosoma rangeli | 52% | 100% |
A0A3R7NNX1 | Trypanosoma rangeli | 25% | 100% |
A0A3S7WV22 | Leishmania donovani | 92% | 100% |
A4H9M1 | Leishmania braziliensis | 84% | 99% |
A4HXY5 | Leishmania infantum | 93% | 100% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A5C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
Q4QDT1 | Leishmania major | 91% | 100% |
V5DFH6 | Trypanosoma cruzi | 52% | 100% |