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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q7I1
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 11 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0072344 | rescue of stalled ribosome | 6 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 11 |
GO:0005488 | binding | 1 | 5 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 11 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 2 |
GO:0043022 | ribosome binding | 4 | 2 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 11 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 477 | 481 | PF00656 | 0.293 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.335 |
DEG_APCC_KENBOX_2 | 351 | 355 | PF00400 | 0.659 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.674 |
DOC_CKS1_1 | 669 | 674 | PF01111 | 0.575 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.349 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 103 | 112 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 419 | 428 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 463 | 469 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.404 |
LIG_Actin_WH2_2 | 98 | 115 | PF00022 | 0.434 |
LIG_AP2alpha_2 | 145 | 147 | PF02296 | 0.486 |
LIG_APCC_ABBA_1 | 24 | 29 | PF00400 | 0.498 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.733 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 664 | 668 | PF00533 | 0.563 |
LIG_eIF4E_1 | 219 | 225 | PF01652 | 0.364 |
LIG_EVH1_2 | 207 | 211 | PF00568 | 0.438 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.391 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.427 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.558 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.385 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.590 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.405 |
LIG_LIR_Apic_2 | 130 | 134 | PF02991 | 0.327 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 145 | 153 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 162 | 170 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 336 | 343 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 467 | 474 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 486 | 497 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.584 |
LIG_NRP_CendR_1 | 722 | 723 | PF00754 | 0.732 |
LIG_PCNA_yPIPBox_3 | 519 | 527 | PF02747 | 0.387 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.403 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.514 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.637 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.371 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.347 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.395 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.339 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.500 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.630 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.533 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.675 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.633 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.507 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.558 |
LIG_SUMO_SIM_anti_2 | 283 | 288 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.353 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.497 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.500 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.412 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.523 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.488 |
LIG_TRAF2_2 | 620 | 625 | PF00917 | 0.724 |
LIG_TYR_ITIM | 163 | 168 | PF00017 | 0.314 |
MOD_CDK_SPxxK_3 | 584 | 591 | PF00069 | 0.709 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.498 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.590 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.603 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.640 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.664 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.420 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.719 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.654 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.641 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.571 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.580 |
MOD_Cter_Amidation | 358 | 361 | PF01082 | 0.640 |
MOD_Cter_Amidation | 589 | 592 | PF01082 | 0.560 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.597 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.531 |
MOD_GlcNHglycan | 309 | 313 | PF01048 | 0.634 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.626 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.579 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.742 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.453 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.402 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.736 |
MOD_GlcNHglycan | 625 | 629 | PF01048 | 0.510 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.573 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.617 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.512 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.439 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.508 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.676 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.709 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.493 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.685 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.660 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.577 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.433 |
MOD_LATS_1 | 470 | 476 | PF00433 | 0.385 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.723 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.617 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.425 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.577 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.461 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.700 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.404 |
MOD_NEK2_2 | 642 | 647 | PF00069 | 0.741 |
MOD_OFUCOSY | 133 | 138 | PF10250 | 0.394 |
MOD_OFUCOSY | 50 | 55 | PF10250 | 0.390 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.581 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.345 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.518 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.658 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.477 |
MOD_Plk_1 | 692 | 698 | PF00069 | 0.644 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.361 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.372 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.577 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.575 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.461 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.524 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.622 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.606 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.544 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.757 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.711 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.692 |
MOD_SUMO_rev_2 | 545 | 555 | PF00179 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 505 | 510 | PF01217 | 0.347 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA72 | Leptomonas seymouri | 65% | 100% |
A0A0S4KKN7 | Bodo saltans | 39% | 100% |
A0A1X0P1Y0 | Trypanosomatidae | 43% | 100% |
A0A3S7X380 | Leishmania donovani | 94% | 100% |
A0A422P542 | Trypanosoma rangeli | 41% | 100% |
A4HI75 | Leishmania braziliensis | 80% | 100% |
A4I5F4 | Leishmania infantum | 94% | 100% |
E9B0Q2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BYZ6 | Trypanosoma cruzi | 36% | 100% |