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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 8 |
GO:0005840 | ribosome | 5 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043228 | non-membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AX35
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0010992 | ubiquitin recycling | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
GO:0043130 | ubiquitin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 755 | 759 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.396 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.244 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 770 | 774 | PF00082 | 0.273 |
DEG_APCC_DBOX_1 | 762 | 770 | PF00400 | 0.494 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.552 |
DEG_SPOP_SBC_1 | 350 | 354 | PF00917 | 0.549 |
DOC_CDC14_PxL_1 | 496 | 504 | PF14671 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 535 | 541 | PF00134 | 0.482 |
DOC_MAPK_FxFP_2 | 599 | 602 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 388 | 398 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 391 | 398 | PF00069 | 0.457 |
DOC_MAPK_RevD_3 | 362 | 377 | PF00069 | 0.487 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.494 |
DOC_PP4_FxxP_1 | 599 | 602 | PF00568 | 0.354 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.516 |
DOC_USP7_MATH_2 | 529 | 535 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 429 | 433 | PF12436 | 0.412 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 756 | 761 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 793 | 798 | PF00397 | 0.397 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 600 | 610 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 707 | 714 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 715 | 720 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 746 | 754 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 767 | 773 | PF00244 | 0.494 |
LIG_Actin_WH2_1 | 784 | 802 | PF00022 | 0.494 |
LIG_Actin_WH2_2 | 785 | 802 | PF00022 | 0.583 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.305 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 751 | 755 | PF01394 | 0.479 |
LIG_CtBP_PxDLS_1 | 493 | 497 | PF00389 | 0.523 |
LIG_deltaCOP1_diTrp_1 | 143 | 151 | PF00928 | 0.340 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.494 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.276 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.427 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.500 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.378 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.494 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.465 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.479 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.438 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.605 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.479 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.456 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.496 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.487 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.415 |
LIG_FHA_1 | 716 | 722 | PF00498 | 0.514 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.560 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.447 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.479 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.341 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.441 |
LIG_LIR_Gen_1 | 436 | 445 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 590 | 599 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 436 | 440 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 657 | 662 | PF02991 | 0.510 |
LIG_NRBOX | 768 | 774 | PF00104 | 0.494 |
LIG_PCNA_PIPBox_1 | 480 | 489 | PF02747 | 0.494 |
LIG_Pex14_1 | 320 | 324 | PF04695 | 0.442 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.456 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 432 | 435 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.479 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.445 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.412 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.479 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.507 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.435 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.470 |
LIG_SH3_3 | 818 | 824 | PF00018 | 0.494 |
LIG_SUMO_SIM_anti_2 | 74 | 79 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 717 | 723 | PF11976 | 0.479 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.494 |
LIG_TRAF2_2 | 158 | 163 | PF00917 | 0.444 |
LIG_WRC_WIRS_1 | 545 | 550 | PF05994 | 0.298 |
MOD_CDK_SPxxK_3 | 756 | 763 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 793 | 800 | PF00069 | 0.400 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.499 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.529 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.365 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.562 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.556 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.635 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.381 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.469 |
MOD_CK1_1 | 727 | 733 | PF00069 | 0.352 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.373 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.284 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.517 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.442 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.264 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.358 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.137 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.318 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.308 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.460 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.398 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.413 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.322 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.268 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.227 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.201 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.445 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.431 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.398 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.537 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.547 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.607 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.613 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.655 |
MOD_GlcNHglycan | 580 | 584 | PF01048 | 0.381 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.385 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.383 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.441 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.365 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.555 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.317 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.240 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.300 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.332 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.279 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.163 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.439 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.312 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.444 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.594 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.553 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.343 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.683 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.304 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.392 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.400 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.371 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.440 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.400 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.253 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.393 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.440 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.337 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.450 |
MOD_N-GLC_1 | 715 | 720 | PF02516 | 0.360 |
MOD_N-GLC_1 | 756 | 761 | PF02516 | 0.358 |
MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.358 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.358 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.416 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.329 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.633 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.509 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.223 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.380 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.399 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.287 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.274 |
MOD_NEK2_2 | 587 | 592 | PF00069 | 0.287 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.477 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.274 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.442 |
MOD_PIKK_1 | 623 | 629 | PF00454 | 0.253 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.274 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.390 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.413 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.452 |
MOD_PKA_2 | 745 | 751 | PF00069 | 0.179 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.314 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.300 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.226 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.300 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.225 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.298 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.264 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.358 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.604 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.333 |
MOD_Plk_1 | 715 | 721 | PF00069 | 0.358 |
MOD_Plk_1 | 724 | 730 | PF00069 | 0.358 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.460 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.259 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.298 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.435 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.598 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.343 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.333 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.339 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.393 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.337 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.499 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.387 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.447 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.358 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.594 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.273 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.326 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.386 |
MOD_ProDKin_1 | 756 | 762 | PF00069 | 0.384 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.358 |
MOD_ProDKin_1 | 793 | 799 | PF00069 | 0.393 |
MOD_SUMO_rev_2 | 278 | 286 | PF00179 | 0.423 |
MOD_SUMO_rev_2 | 341 | 350 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 531 | 536 | PF01217 | 0.606 |
TRG_DiLeu_BaEn_3 | 481 | 487 | PF01217 | 0.298 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAR3 | Leptomonas seymouri | 61% | 100% |
A0A0S4J046 | Bodo saltans | 37% | 100% |
A0A3Q8IC13 | Leishmania donovani | 93% | 100% |
A0A3R7L9T6 | Trypanosoma rangeli | 37% | 94% |
A4HDQ1 | Leishmania braziliensis | 87% | 99% |
A4I0Z7 | Leishmania infantum | 93% | 100% |
O94289 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P27612 | Mus musculus | 27% | 100% |
P54319 | Rattus norvegicus | 27% | 100% |
Q4QAE1 | Leishmania major | 93% | 100% |
Q6GM65 | Xenopus laevis | 27% | 100% |
Q9Y263 | Homo sapiens | 26% | 100% |