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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 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: A4HKA1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.318 |
CLV_Separin_Metazoa | 307 | 311 | PF03568 | 0.270 |
CLV_Separin_Metazoa | 611 | 615 | PF03568 | 0.449 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.474 |
DEG_SCF_TRCP1_1 | 235 | 241 | PF00400 | 0.486 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.457 |
DOC_ANK_TNKS_1 | 391 | 398 | PF00023 | 0.580 |
DOC_CYCLIN_RxL_1 | 291 | 301 | PF00134 | 0.323 |
DOC_MAPK_gen_1 | 392 | 400 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 583 | 591 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.521 |
DOC_PP2B_PxIxI_1 | 353 | 359 | PF00149 | 0.401 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 704 | 708 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.520 |
DOC_USP7_UBL2_3 | 746 | 750 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.284 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 338 | 346 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 542 | 548 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 583 | 591 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 622 | 630 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 641 | 646 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.656 |
LIG_Actin_WH2_2 | 391 | 407 | PF00022 | 0.600 |
LIG_APCC_ABBA_1 | 718 | 723 | PF00400 | 0.386 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 712 | 716 | PF00533 | 0.388 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.459 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.485 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.391 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.391 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.349 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.380 |
LIG_FHA_1 | 735 | 741 | PF00498 | 0.417 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.717 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.397 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.745 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.431 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.517 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.741 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.775 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.530 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.452 |
LIG_LIR_Gen_1 | 18 | 25 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 183 | 191 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 479 | 487 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 573 | 582 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 586 | 595 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 650 | 658 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 72 | 81 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 479 | 483 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 545 | 550 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 573 | 578 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 586 | 591 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 606 | 612 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 650 | 654 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 665 | 671 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.583 |
LIG_MYND_1 | 636 | 640 | PF01753 | 0.329 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.382 |
LIG_NRBOX | 577 | 583 | PF00104 | 0.467 |
LIG_PTB_Apo_2 | 486 | 493 | PF02174 | 0.399 |
LIG_PTB_Phospho_1 | 486 | 492 | PF10480 | 0.399 |
LIG_REV1ctd_RIR_1 | 173 | 182 | PF16727 | 0.508 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.627 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.411 |
LIG_SH2_GRB2like | 21 | 24 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 21 | 25 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 492 | 495 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.627 |
LIG_SH2_STAP1 | 480 | 484 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 651 | 655 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 671 | 675 | PF00017 | 0.205 |
LIG_SH2_STAP1 | 686 | 690 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 660 | 663 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.448 |
LIG_SH3_1 | 121 | 127 | PF00018 | 0.517 |
LIG_SH3_2 | 636 | 641 | PF14604 | 0.334 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.666 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.607 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.644 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.532 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.564 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.615 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.564 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.640 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.464 |
LIG_SUMO_SIM_anti_2 | 687 | 692 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 126 | 133 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 687 | 692 | PF11976 | 0.441 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.584 |
LIG_TRAF2_2 | 262 | 267 | PF00917 | 0.561 |
LIG_TYR_ITIM | 478 | 483 | PF00017 | 0.425 |
LIG_UBA3_1 | 187 | 192 | PF00899 | 0.312 |
LIG_UBA3_1 | 467 | 475 | PF00899 | 0.491 |
LIG_UBA3_1 | 578 | 585 | PF00899 | 0.423 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.476 |
LIG_WW_3 | 260 | 264 | PF00397 | 0.544 |
LIG_WW_3 | 638 | 642 | PF00397 | 0.427 |
MOD_CDK_SPK_2 | 617 | 622 | PF00069 | 0.477 |
MOD_CDK_SPK_2 | 679 | 684 | PF00069 | 0.284 |
MOD_CDK_SPxxK_3 | 145 | 152 | PF00069 | 0.541 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.796 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.686 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.572 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.444 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.697 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.561 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.678 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.530 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.620 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.610 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.574 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.598 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.741 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.491 |
MOD_CMANNOS | 642 | 645 | PF00535 | 0.476 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.673 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.749 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.599 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.654 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.582 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.630 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.789 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.567 |
MOD_GlcNHglycan | 527 | 531 | PF01048 | 0.635 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.599 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.626 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.594 |
MOD_GlcNHglycan | 705 | 709 | PF01048 | 0.470 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.617 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.565 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.484 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.736 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.571 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.470 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.531 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.597 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.399 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.590 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.775 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.581 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.532 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.514 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.442 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.437 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.645 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.542 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.501 |
MOD_N-GLC_2 | 8 | 10 | PF02516 | 0.615 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.378 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.427 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.588 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.532 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.510 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.443 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.566 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.518 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.788 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.491 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.527 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.298 |
MOD_PIKK_1 | 593 | 599 | PF00454 | 0.276 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.531 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.683 |
MOD_PK_1 | 310 | 316 | PF00069 | 0.422 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.572 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.317 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.465 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.649 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.658 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.507 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.515 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.653 |
MOD_PKB_1 | 88 | 96 | PF00069 | 0.494 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.553 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.617 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.588 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.645 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.636 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.465 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.440 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.668 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.640 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.561 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.555 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.470 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.614 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.765 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.279 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.197 |
TRG_ENDOCYTIC_2 | 686 | 689 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 721 | 724 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 657 | 660 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 724 | 726 | PF00400 | 0.505 |
TRG_NLS_Bipartite_1 | 369 | 387 | PF00514 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGR3 | Leptomonas seymouri | 49% | 100% |
A0A1X0NVZ4 | Trypanosomatidae | 30% | 100% |
A0A3Q8IG45 | Leishmania donovani | 68% | 100% |
A0A3R7NTQ6 | Trypanosoma rangeli | 29% | 100% |
A4I7T1 | Leishmania infantum | 68% | 100% |
D0A9Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B2N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q5G8 | Leishmania major | 68% | 99% |
V5BQR4 | Trypanosoma cruzi | 28% | 100% |