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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 19 |
GO:0042995 | cell projection | 2 | 19 |
GO:0043226 | organelle | 2 | 19 |
GO:0043227 | membrane-bounded organelle | 3 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 19 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AHJ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 1 |
GO:0006952 | defense response | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 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: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: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:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.398 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.313 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.259 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 739 | 741 | PF00675 | 0.681 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 739 | 741 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 27 | 35 | PF00400 | 0.373 |
DEG_APCC_DBOX_1 | 397 | 405 | PF00400 | 0.422 |
DEG_MDM2_SWIB_1 | 730 | 737 | PF02201 | 0.385 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.539 |
DEG_ODPH_VHL_1 | 517 | 528 | PF01847 | 0.288 |
DEG_ODPH_VHL_1 | 607 | 618 | PF01847 | 0.317 |
DOC_CDC14_PxL_1 | 271 | 279 | PF14671 | 0.454 |
DOC_CDC14_PxL_1 | 385 | 393 | PF14671 | 0.478 |
DOC_CDC14_PxL_1 | 520 | 528 | PF14671 | 0.457 |
DOC_CDC14_PxL_1 | 655 | 663 | PF14671 | 0.306 |
DOC_CYCLIN_RxL_1 | 496 | 505 | PF00134 | 0.426 |
DOC_CYCLIN_yCln2_LP_2 | 199 | 205 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 33 | 39 | PF00134 | 0.374 |
DOC_MAPK_gen_1 | 181 | 187 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 589 | 598 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 679 | 688 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 321 | 328 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 679 | 688 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 680 | 686 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 725 | 731 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.392 |
DOC_PP2B_LxvP_1 | 199 | 202 | PF13499 | 0.325 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.335 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 700 | 705 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 119 | 123 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 155 | 161 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 347 | 352 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 390 | 395 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 46 | 56 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 470 | 479 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 512 | 518 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 602 | 608 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 648 | 653 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 692 | 698 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.458 |
LIG_Actin_WH2_2 | 165 | 183 | PF00022 | 0.433 |
LIG_Actin_WH2_2 | 387 | 404 | PF00022 | 0.460 |
LIG_Actin_WH2_2 | 468 | 484 | PF00022 | 0.430 |
LIG_Actin_WH2_2 | 556 | 574 | PF00022 | 0.457 |
LIG_BRCT_BRCA1_1 | 15 | 19 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.283 |
LIG_Clathr_ClatBox_1 | 683 | 687 | PF01394 | 0.427 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.355 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.357 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.502 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.382 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.415 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.465 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.436 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.317 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 26 | 34 | PF00786 | 0.356 |
LIG_IBAR_NPY_1 | 223 | 225 | PF08397 | 0.370 |
LIG_LIR_Gen_1 | 10 | 19 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 460 | 469 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 731 | 737 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 10 | 15 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 731 | 737 | PF02991 | 0.542 |
LIG_MAD2 | 527 | 535 | PF02301 | 0.281 |
LIG_NRBOX | 29 | 35 | PF00104 | 0.364 |
LIG_PCNA_APIM_2 | 26 | 32 | PF02747 | 0.373 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.490 |
LIG_Pex14_2 | 730 | 734 | PF04695 | 0.387 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.317 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.401 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 12 | 15 | PF00017 | 0.401 |
LIG_SH2_PTP2 | 732 | 735 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 732 | 735 | PF00017 | 0.426 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.374 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.407 |
LIG_SH3_3 | 762 | 768 | PF00018 | 0.533 |
LIG_SUMO_SIM_anti_2 | 303 | 308 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 534 | 540 | PF11976 | 0.285 |
LIG_TRFH_1 | 220 | 224 | PF08558 | 0.357 |
LIG_TRFH_1 | 225 | 229 | PF08558 | 0.344 |
LIG_TYR_ITIM | 104 | 109 | PF00017 | 0.272 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.359 |
LIG_TYR_ITIM | 346 | 351 | PF00017 | 0.275 |
LIG_UBA3_1 | 30 | 35 | PF00899 | 0.371 |
MOD_CDK_SPK_2 | 430 | 435 | PF00069 | 0.251 |
MOD_CDK_SPK_2 | 610 | 615 | PF00069 | 0.301 |
MOD_CDK_SPxxK_3 | 125 | 132 | PF00069 | 0.477 |
MOD_CDK_SPxxK_3 | 430 | 437 | PF00069 | 0.335 |
MOD_CDK_SPxxK_3 | 610 | 617 | PF00069 | 0.300 |
MOD_CDK_SPxxK_3 | 700 | 707 | PF00069 | 0.294 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.551 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.400 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.244 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.409 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.506 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.557 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.304 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.513 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.300 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.495 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.378 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.420 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.576 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.354 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.480 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.516 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.524 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.524 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.429 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.439 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.520 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.404 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.327 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.364 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.320 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.425 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.384 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.513 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.418 |
MOD_GlcNHglycan | 723 | 727 | PF01048 | 0.387 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.488 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.441 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.555 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.686 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.482 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.443 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.402 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.327 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.419 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.481 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.419 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.358 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.344 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.442 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.320 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.467 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.541 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.481 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.495 |
MOD_N-GLC_1 | 506 | 511 | PF02516 | 0.455 |
MOD_N-GLC_1 | 672 | 677 | PF02516 | 0.428 |
MOD_N-GLC_1 | 711 | 716 | PF02516 | 0.560 |
MOD_N-GLC_2 | 4 | 6 | PF02516 | 0.396 |
MOD_N-GLC_2 | 49 | 51 | PF02516 | 0.419 |
MOD_N-GLC_2 | 498 | 500 | PF02516 | 0.330 |
MOD_N-GLC_2 | 633 | 635 | PF02516 | 0.360 |
MOD_N-GLC_2 | 644 | 646 | PF02516 | 0.334 |
MOD_N-GLC_2 | 665 | 667 | PF02516 | 0.274 |
MOD_N-GLC_2 | 678 | 680 | PF02516 | 0.317 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.556 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.532 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.461 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.364 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.417 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.357 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.404 |
MOD_OFUCOSY | 57 | 63 | PF10250 | 0.400 |
MOD_PK_1 | 22 | 28 | PF00069 | 0.358 |
MOD_PK_1 | 660 | 666 | PF00069 | 0.297 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.358 |
MOD_PKA_1 | 512 | 518 | PF00069 | 0.331 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.499 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.551 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.520 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.493 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.485 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.298 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.587 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.364 |
MOD_PKB_1 | 390 | 398 | PF00069 | 0.301 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.430 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.369 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.479 |
MOD_Plk_1 | 711 | 717 | PF00069 | 0.518 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.337 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.322 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.337 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.430 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.306 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.411 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.331 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.477 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.337 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.388 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.484 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.464 |
MOD_ProDKin_1 | 700 | 706 | PF00069 | 0.303 |
MOD_SUMO_rev_2 | 459 | 469 | PF00179 | 0.493 |
TRG_DiLeu_BaEn_1 | 3 | 8 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_2 | 368 | 374 | PF01217 | 0.217 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.358 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 732 | 735 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 389 | 392 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 614 | 617 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 706 | 708 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 739 | 742 | PF00400 | 0.644 |
TRG_NES_CRM1_1 | 357 | 369 | PF08389 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 321 | 325 | PF00026 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 499 | 504 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N9 | Leptomonas seymouri | 33% | 100% |
A0A0N1P921 | Leptomonas seymouri | 27% | 95% |
A0A0S4J2Y5 | Bodo saltans | 24% | 92% |
A0A3S5H5M6 | Leishmania donovani | 28% | 100% |
A0A3S5ISR4 | Trypanosoma rangeli | 24% | 92% |
A0A3S7X2V4 | Leishmania donovani | 100% | 100% |
A4H3R1 | Leishmania braziliensis | 69% | 100% |
A4H4H0 | Leishmania braziliensis | 25% | 100% |
A4HSP5 | Leishmania infantum | 28% | 100% |
C9ZK22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 95% |
D0A4F4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 91% |
E9AEF0 | Leishmania major | 87% | 100% |
E9AGT5 | Leishmania infantum | 28% | 100% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4QJ77 | Leishmania major | 28% | 100% |
Q4QJ80 | Leishmania major | 28% | 100% |
V5BKI3 | Trypanosoma cruzi | 26% | 93% |