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: 1, no: 20 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 2 |
GO:0005929 | cilium | 4 | 22 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0042995 | cell projection | 2 | 22 |
GO:0043226 | organelle | 2 | 22 |
GO:0043227 | membrane-bounded organelle | 3 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 22 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: E9AEF0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006952 | defense response | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 491 | 495 | PF00656 | 0.448 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.732 |
CLV_PCSK_FUR_1 | 704 | 708 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.276 |
CLV_PCSK_PC7_1 | 734 | 740 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.363 |
DEG_MDM2_SWIB_1 | 729 | 736 | PF02201 | 0.412 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.440 |
DEG_ODPH_VHL_1 | 381 | 392 | PF01847 | 0.259 |
DEG_ODPH_VHL_1 | 516 | 527 | PF01847 | 0.285 |
DEG_ODPH_VHL_1 | 606 | 617 | PF01847 | 0.341 |
DOC_CDC14_PxL_1 | 270 | 278 | PF14671 | 0.387 |
DOC_CDC14_PxL_1 | 384 | 392 | PF14671 | 0.299 |
DOC_CDC14_PxL_1 | 519 | 527 | PF14671 | 0.303 |
DOC_CDC14_PxL_1 | 654 | 662 | PF14671 | 0.422 |
DOC_CDC14_PxL_1 | 699 | 707 | PF14671 | 0.444 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.398 |
DOC_CYCLIN_RxL_1 | 495 | 504 | PF00134 | 0.307 |
DOC_CYCLIN_RxL_1 | 54 | 65 | PF00134 | 0.365 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 448 | 457 | PF00134 | 0.271 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 180 | 186 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 588 | 597 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 678 | 687 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 207 | 215 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 320 | 327 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 678 | 687 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 679 | 685 | PF00149 | 0.407 |
DOC_PP1_RVXF_1 | 724 | 730 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.353 |
DOC_PP4_FxxP_1 | 9 | 12 | PF00568 | 0.394 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.461 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 118 | 124 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 253 | 258 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 302 | 306 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 341 | 348 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 371 | 378 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 391 | 400 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 469 | 478 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 601 | 607 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 62 | 69 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 691 | 697 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 165 | 182 | PF00022 | 0.364 |
LIG_Actin_WH2_2 | 467 | 483 | PF00022 | 0.290 |
LIG_Actin_WH2_2 | 555 | 573 | PF00022 | 0.422 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.256 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.423 |
LIG_BRCT_BRCA1_1 | 593 | 597 | PF00533 | 0.237 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.552 |
LIG_Clathr_ClatBox_1 | 682 | 686 | PF01394 | 0.387 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.602 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.396 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.398 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.492 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.514 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.288 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.313 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.335 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.426 |
LIG_FHA_2 | 772 | 778 | PF00498 | 0.659 |
LIG_IBAR_NPY_1 | 222 | 224 | PF08397 | 0.472 |
LIG_IRF3_LxIS_1 | 718 | 724 | PF10401 | 0.370 |
LIG_LIR_Gen_1 | 192 | 202 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 459 | 468 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 217 | 221 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 574 | 580 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 730 | 736 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.495 |
LIG_MAD2 | 526 | 534 | PF02301 | 0.271 |
LIG_NRBOX | 193 | 199 | PF00104 | 0.302 |
LIG_NRBOX | 56 | 62 | PF00104 | 0.359 |
LIG_PCNA_APIM_2 | 25 | 31 | PF02747 | 0.373 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.491 |
LIG_Pex14_2 | 729 | 733 | PF04695 | 0.397 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.398 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.403 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 224 | 227 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.660 |
LIG_SH3_3 | 761 | 767 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 324 | 329 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 146 | 151 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.330 |
LIG_TRFH_1 | 219 | 223 | PF08558 | 0.476 |
LIG_TRFH_1 | 224 | 228 | PF08558 | 0.461 |
LIG_TYR_ITIM | 159 | 164 | PF00017 | 0.365 |
LIG_TYR_ITIM | 345 | 350 | PF00017 | 0.410 |
LIG_WRC_WIRS_1 | 15 | 20 | PF05994 | 0.395 |
MOD_CDK_SPK_2 | 609 | 614 | PF00069 | 0.295 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 246 | 253 | PF00069 | 0.329 |
MOD_CDK_SPxxK_3 | 609 | 616 | PF00069 | 0.293 |
MOD_CDK_SPxxK_3 | 771 | 778 | PF00069 | 0.519 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.393 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.416 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.554 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.378 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.496 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.529 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.346 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.448 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.356 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.458 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.389 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.571 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.489 |
MOD_GlcNHglycan | 149 | 153 | PF01048 | 0.471 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.549 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.345 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.447 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.439 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.470 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.276 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.383 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.356 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.436 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.411 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.488 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.514 |
MOD_GlcNHglycan | 722 | 726 | PF01048 | 0.375 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.452 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.506 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.499 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.376 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.383 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.560 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.350 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.450 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.374 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.395 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.460 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.515 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.342 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.388 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.518 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.540 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.403 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.470 |
MOD_N-GLC_1 | 460 | 465 | PF02516 | 0.378 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.392 |
MOD_N-GLC_1 | 671 | 676 | PF02516 | 0.458 |
MOD_N-GLC_1 | 710 | 715 | PF02516 | 0.510 |
MOD_N-GLC_2 | 4 | 6 | PF02516 | 0.406 |
MOD_N-GLC_2 | 452 | 454 | PF02516 | 0.283 |
MOD_N-GLC_2 | 497 | 499 | PF02516 | 0.546 |
MOD_N-GLC_2 | 632 | 634 | PF02516 | 0.501 |
MOD_N-GLC_2 | 664 | 666 | PF02516 | 0.272 |
MOD_N-GLC_2 | 677 | 679 | PF02516 | 0.272 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.407 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.614 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.610 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.460 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.434 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.388 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.441 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.366 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.416 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.531 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.474 |
MOD_PK_1 | 591 | 597 | PF00069 | 0.236 |
MOD_PK_1 | 659 | 665 | PF00069 | 0.287 |
MOD_PKA_1 | 301 | 307 | PF00069 | 0.579 |
MOD_PKA_1 | 511 | 517 | PF00069 | 0.435 |
MOD_PKA_1 | 734 | 740 | PF00069 | 0.552 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.490 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.395 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.399 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.280 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.375 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.429 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.352 |
MOD_PKA_2 | 734 | 740 | PF00069 | 0.636 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.454 |
MOD_PKB_1 | 389 | 397 | PF00069 | 0.270 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.355 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.524 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.598 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.386 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.372 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.500 |
MOD_Plk_1 | 710 | 716 | PF00069 | 0.594 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.343 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.415 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.504 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.461 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.447 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.377 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.442 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.355 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.494 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.606 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.532 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.596 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.403 |
MOD_SUMO_rev_2 | 20 | 25 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 458 | 468 | PF00179 | 0.287 |
TRG_DiLeu_BaEn_1 | 3 | 8 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_1 | 557 | 562 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 533 | 538 | PF01217 | 0.250 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 658 | 661 | PF00400 | 0.269 |
TRG_ER_diArg_1 | 703 | 706 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 733 | 735 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 738 | 741 | PF00400 | 0.574 |
TRG_NES_CRM1_1 | 356 | 368 | PF08389 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 498 | 503 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F9 | Leptomonas seymouri | 34% | 100% |
A0A0N0P8N9 | Leptomonas seymouri | 33% | 100% |
A0A3Q8IAE2 | Leishmania donovani | 26% | 100% |
A0A3S5H5M6 | Leishmania donovani | 26% | 100% |
A0A3S7X2V4 | Leishmania donovani | 87% | 100% |
A0A451EJK8 | Leishmania donovani | 25% | 73% |
A4H3H4 | Leishmania braziliensis | 24% | 80% |
A4H3R1 | Leishmania braziliensis | 69% | 100% |
A4H4H0 | Leishmania braziliensis | 24% | 100% |
A4HSP5 | Leishmania infantum | 26% | 100% |
C9ZK22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 95% |
D0A4F4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 92% |
E9ACE9 | Leishmania major | 26% | 78% |
E9AG21 | Leishmania infantum | 25% | 77% |
E9AGT5 | Leishmania infantum | 28% | 100% |
E9AHJ6 | Leishmania infantum | 87% | 100% |
E9AIU4 | Leishmania braziliensis | 24% | 100% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4QJ77 | Leishmania major | 26% | 100% |
V5BXQ3 | Trypanosoma cruzi | 23% | 84% |