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: A4HDQ1
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 | 751 | 755 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.773 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.781 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.195 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 766 | 770 | PF00082 | 0.477 |
DEG_APCC_DBOX_1 | 758 | 766 | PF00400 | 0.481 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.696 |
DOC_CDC14_PxL_1 | 496 | 504 | PF14671 | 0.629 |
DOC_CKS1_1 | 121 | 126 | PF01111 | 0.320 |
DOC_CYCLIN_RxL_1 | 601 | 610 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 519 | 525 | PF00134 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 531 | 537 | PF00134 | 0.543 |
DOC_MAPK_gen_1 | 388 | 398 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 403 | 411 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 391 | 398 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 403 | 411 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 604 | 611 | PF00069 | 0.468 |
DOC_MAPK_RevD_3 | 362 | 377 | PF00069 | 0.615 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.416 |
DOC_PP2B_LxvP_1 | 519 | 522 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 768 | 771 | PF13499 | 0.331 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 429 | 433 | PF12436 | 0.424 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 752 | 757 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 770 | 775 | PF00397 | 0.400 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 596 | 606 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 649 | 655 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 703 | 710 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 711 | 716 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 763 | 769 | PF00244 | 0.484 |
LIG_Actin_WH2_1 | 780 | 798 | PF00022 | 0.506 |
LIG_Actin_WH2_2 | 781 | 798 | PF00022 | 0.511 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.606 |
LIG_Clathr_ClatBox_1 | 747 | 751 | PF01394 | 0.550 |
LIG_CtBP_PxDLS_1 | 729 | 733 | PF00389 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 143 | 151 | PF00928 | 0.408 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.411 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.483 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.479 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.475 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.475 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.408 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.534 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.548 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.583 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.492 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.541 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.583 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.544 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.499 |
LIG_FHA_1 | 685 | 691 | PF00498 | 0.554 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.571 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.559 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.468 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.540 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.571 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.554 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.457 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 436 | 445 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 586 | 593 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 436 | 440 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 586 | 591 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.562 |
LIG_NRBOX | 602 | 608 | PF00104 | 0.416 |
LIG_NRBOX | 764 | 770 | PF00104 | 0.487 |
LIG_PCNA_PIPBox_1 | 480 | 489 | PF02747 | 0.534 |
LIG_Pex14_1 | 320 | 324 | PF04695 | 0.498 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.475 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 565 | 569 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 432 | 435 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.571 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.544 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.611 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.484 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.571 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.540 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.521 |
LIG_SH3_3 | 768 | 774 | PF00018 | 0.587 |
LIG_SH3_3 | 814 | 820 | PF00018 | 0.525 |
LIG_SUMO_SIM_par_1 | 145 | 152 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 605 | 610 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 713 | 719 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 728 | 734 | PF11976 | 0.435 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.534 |
LIG_UBA3_1 | 787 | 796 | PF00899 | 0.409 |
LIG_WRC_WIRS_1 | 541 | 546 | PF05994 | 0.487 |
MOD_CAAXbox | 819 | 822 | PF01239 | 0.373 |
MOD_CDK_SPxxK_3 | 752 | 759 | PF00069 | 0.515 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.568 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.541 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.543 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.396 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.620 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.612 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.579 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.632 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.456 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.466 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.295 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.457 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.481 |
MOD_CK1_1 | 789 | 795 | PF00069 | 0.531 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.527 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.331 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.449 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.410 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.136 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.442 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.365 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.218 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.562 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.409 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.453 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.483 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.399 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.376 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.355 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.476 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.243 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.483 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.482 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.396 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.634 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.618 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.591 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.682 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.466 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.457 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.575 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.475 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.387 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.351 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.357 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.349 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.226 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.435 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.412 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.345 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.576 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.537 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.608 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.412 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.326 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.390 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.762 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.734 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.449 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.363 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.436 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.388 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.445 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.519 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.491 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.468 |
MOD_N-GLC_1 | 711 | 716 | PF02516 | 0.365 |
MOD_N-GLC_1 | 752 | 757 | PF02516 | 0.524 |
MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.413 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.488 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.523 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.331 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.712 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.588 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.466 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.466 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.345 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.514 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.341 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.428 |
MOD_PIKK_1 | 627 | 633 | PF00454 | 0.324 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.363 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.441 |
MOD_PKA_1 | 506 | 512 | PF00069 | 0.736 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.545 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.466 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.218 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.736 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.495 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.437 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.366 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.285 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.331 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.413 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.218 |
MOD_Plk_1 | 711 | 717 | PF00069 | 0.365 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.583 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.287 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.331 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.431 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.533 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.384 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.466 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.421 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.226 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.557 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.363 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.413 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.700 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.363 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.389 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.413 |
MOD_ProDKin_1 | 752 | 758 | PF00069 | 0.465 |
MOD_ProDKin_1 | 770 | 776 | PF00069 | 0.400 |
MOD_SUMO_rev_2 | 341 | 350 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 527 | 532 | PF01217 | 0.638 |
TRG_DiLeu_BaEn_3 | 481 | 487 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.466 |
TRG_DiLeu_LyEn_5 | 527 | 532 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.466 |
TRG_NES_CRM1_1 | 601 | 615 | PF08389 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.383 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAR3 | Leptomonas seymouri | 61% | 100% |
A0A0S4J046 | Bodo saltans | 36% | 100% |
A0A3Q8IC13 | Leishmania donovani | 86% | 99% |
A4I0Z7 | Leishmania infantum | 87% | 99% |
C9ZWB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 93% |
E9AX35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
O94289 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P27612 | Mus musculus | 27% | 100% |
P54319 | Rattus norvegicus | 28% | 100% |
Q4QAE1 | Leishmania major | 86% | 100% |
Q6GM65 | Xenopus laevis | 27% | 100% |