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:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 8 |
GO:0005840 | ribosome | 5 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 8 |
Related structures:
AlphaFold database: Q4QAE1
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:0010992 | ubiquitin recycling | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0042592 | homeostatic process | 3 | 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:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0032182 | ubiquitin-like protein binding | 3 | 2 |
GO:0043130 | ubiquitin binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 756 | 760 | PF00656 | 0.534 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.380 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 506 | 508 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 716 | 720 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 771 | 775 | PF00082 | 0.334 |
DEG_APCC_DBOX_1 | 763 | 771 | PF00400 | 0.534 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.693 |
DEG_SPOP_SBC_1 | 350 | 354 | PF00917 | 0.627 |
DOC_CDC14_PxL_1 | 496 | 504 | PF14671 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 535 | 541 | PF00134 | 0.563 |
DOC_MAPK_gen_1 | 388 | 398 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 391 | 398 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 608 | 615 | PF00069 | 0.469 |
DOC_MAPK_RevD_3 | 362 | 377 | PF00069 | 0.612 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.505 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.585 |
DOC_USP7_MATH_2 | 529 | 535 | PF00917 | 0.660 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 757 | 762 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 600 | 610 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 654 | 660 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 708 | 715 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 716 | 721 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 768 | 774 | PF00244 | 0.534 |
LIG_Actin_WH2_1 | 785 | 803 | PF00022 | 0.651 |
LIG_Actin_WH2_2 | 786 | 803 | PF00022 | 0.654 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.609 |
LIG_Clathr_ClatBox_1 | 752 | 756 | PF01394 | 0.572 |
LIG_CtBP_PxDLS_1 | 493 | 497 | PF00389 | 0.571 |
LIG_deltaCOP1_diTrp_1 | 143 | 151 | PF00928 | 0.404 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.421 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.534 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.359 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.475 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.534 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.426 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.513 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.570 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.501 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.493 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.577 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.425 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.537 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.546 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.534 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.541 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.588 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.589 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.572 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.562 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.469 |
LIG_LIR_Gen_1 | 436 | 445 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 590 | 599 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 436 | 440 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 658 | 663 | PF02991 | 0.572 |
LIG_NRBOX | 769 | 775 | PF00104 | 0.534 |
LIG_PCNA_PIPBox_1 | 480 | 489 | PF02747 | 0.534 |
LIG_Pex14_1 | 320 | 324 | PF04695 | 0.495 |
LIG_Rb_pABgroove_1 | 539 | 547 | PF01858 | 0.458 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.500 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.500 |
LIG_SH2_STAT3 | 432 | 435 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.489 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.574 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.457 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.721 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.572 |
LIG_SH3_3 | 634 | 640 | PF00018 | 0.556 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.498 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.564 |
LIG_SH3_3 | 819 | 825 | PF00018 | 0.606 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 609 | 614 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 718 | 724 | PF11976 | 0.571 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.534 |
LIG_TRAF2_2 | 241 | 246 | PF00917 | 0.410 |
LIG_UBA3_1 | 147 | 154 | PF00899 | 0.364 |
LIG_WRC_WIRS_1 | 545 | 550 | PF05994 | 0.365 |
MOD_CDK_SPxxK_3 | 757 | 764 | PF00069 | 0.365 |
MOD_CDK_SPxxK_3 | 794 | 801 | PF00069 | 0.554 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.551 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.239 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.396 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.605 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.586 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.704 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.422 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.474 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.301 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.414 |
MOD_CK1_1 | 769 | 775 | PF00069 | 0.380 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.279 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.572 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.323 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.481 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.136 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.402 |
MOD_CK2_1 | 669 | 675 | PF00069 | 0.374 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.545 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.392 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.488 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.438 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.335 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.363 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.332 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.397 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.438 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.549 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.573 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.419 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.672 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.687 |
MOD_GlcNHglycan | 580 | 584 | PF01048 | 0.395 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.466 |
MOD_GlcNHglycan | 698 | 702 | PF01048 | 0.406 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.379 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.581 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.348 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.281 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.352 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.399 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.413 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.373 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.341 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.421 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.578 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.531 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.428 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.390 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.746 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.409 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.263 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.429 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.438 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.398 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.402 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.303 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.477 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.571 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.466 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.383 |
MOD_N-GLC_1 | 716 | 721 | PF02516 | 0.466 |
MOD_N-GLC_1 | 757 | 762 | PF02516 | 0.413 |
MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.413 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.394 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.545 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.375 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.750 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.537 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.466 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.425 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.311 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.341 |
MOD_NEK2_2 | 587 | 592 | PF00069 | 0.383 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.542 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.341 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.464 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.413 |
MOD_PKA_1 | 506 | 512 | PF00069 | 0.734 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.466 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.734 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.431 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.367 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.287 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.361 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.277 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.331 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.413 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.566 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.395 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.413 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.586 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.370 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.332 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.413 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.629 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.461 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.395 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.416 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.466 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.442 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.564 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.475 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.384 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.621 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.413 |
MOD_ProDKin_1 | 757 | 763 | PF00069 | 0.365 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.365 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.549 |
MOD_SUMO_rev_2 | 278 | 286 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 531 | 536 | PF01217 | 0.722 |
TRG_DiLeu_BaEn_3 | 481 | 487 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.489 |
TRG_NES_CRM1_1 | 605 | 619 | PF08389 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.239 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAR3 | Leptomonas seymouri | 62% | 100% |
A0A0S4J046 | Bodo saltans | 37% | 100% |
A0A1X0NVW7 | Trypanosomatidae | 37% | 92% |
A0A3Q8IC13 | Leishmania donovani | 94% | 100% |
A4HDQ1 | Leishmania braziliensis | 86% | 100% |
A4I0Z7 | Leishmania infantum | 94% | 100% |
E9AX35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O94289 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q6GM65 | Xenopus laevis | 27% | 100% |