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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HI75
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0072344 | rescue of stalled ribosome | 6 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 12 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 12 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0005488 | binding | 1 | 4 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.417 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.350 |
DEG_APCC_KENBOX_2 | 350 | 354 | PF00400 | 0.646 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.273 |
DOC_ANK_TNKS_1 | 6 | 13 | PF00023 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.434 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.368 |
DOC_PP1_RVXF_1 | 296 | 302 | PF00149 | 0.509 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.599 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 669 | 674 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 199 | 203 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 60 | 65 | PF00244 | 0.417 |
LIG_Actin_WH2_2 | 97 | 114 | PF00022 | 0.448 |
LIG_AP2alpha_2 | 144 | 146 | PF02296 | 0.499 |
LIG_AP2alpha_2 | 626 | 628 | PF02296 | 0.503 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.734 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.376 |
LIG_EVH1_2 | 206 | 210 | PF00568 | 0.424 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.474 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.404 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.547 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.748 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.417 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.398 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.658 |
LIG_LIR_Apic_2 | 129 | 133 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 144 | 152 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 161 | 169 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 335 | 342 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 422 | 431 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 486 | 497 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 694 | 700 | PF02991 | 0.578 |
LIG_LRP6_Inhibitor_1 | 700 | 706 | PF00058 | 0.598 |
LIG_NRP_CendR_1 | 723 | 724 | PF00754 | 0.664 |
LIG_Pex14_1 | 138 | 142 | PF04695 | 0.420 |
LIG_Pex14_2 | 242 | 246 | PF04695 | 0.523 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.650 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.415 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.354 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.400 |
LIG_SH2_SRC | 142 | 145 | PF00017 | 0.413 |
LIG_SH2_SRC | 385 | 388 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.338 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.519 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 271 | 276 | PF11976 | 0.570 |
LIG_SUMO_SIM_anti_2 | 282 | 287 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.356 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.520 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.530 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.344 |
LIG_TRAF2_1 | 558 | 561 | PF00917 | 0.379 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.550 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.515 |
LIG_TRAF2_2 | 621 | 626 | PF00917 | 0.724 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.318 |
MOD_CDK_SPxxK_3 | 585 | 592 | PF00069 | 0.728 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.516 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.695 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.384 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.692 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.650 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.609 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.602 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.680 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.480 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.575 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.562 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.545 |
MOD_Cter_Amidation | 590 | 593 | PF01082 | 0.573 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.610 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.654 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.670 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.718 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.627 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.427 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.580 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.607 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.776 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.633 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.582 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.613 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.622 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.486 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.480 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.683 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.469 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.500 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.487 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.669 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.621 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.522 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.641 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.633 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.439 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.722 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.690 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.413 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.482 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.777 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.423 |
MOD_NEK2_2 | 643 | 648 | PF00069 | 0.738 |
MOD_OFUCOSY | 132 | 137 | PF10250 | 0.410 |
MOD_OFUCOSY | 49 | 54 | PF10250 | 0.406 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.460 |
MOD_PK_1 | 60 | 66 | PF00069 | 0.193 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.558 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.507 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.646 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.383 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.458 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.477 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.572 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.553 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.684 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.671 |
MOD_ProDKin_1 | 669 | 675 | PF00069 | 0.738 |
MOD_SUMO_for_1 | 595 | 598 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 24 | 30 | PF00179 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 505 | 510 | PF01217 | 0.345 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 705 | 707 | PF00400 | 0.647 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA72 | Leptomonas seymouri | 62% | 100% |
A0A0S4KKN7 | Bodo saltans | 38% | 100% |
A0A1X0P1Y0 | Trypanosomatidae | 43% | 100% |
A0A3S7X380 | Leishmania donovani | 81% | 100% |
A0A422P542 | Trypanosoma rangeli | 43% | 100% |
A4I5F4 | Leishmania infantum | 81% | 100% |
C9ZQU0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B0Q2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q7I1 | Leishmania major | 80% | 100% |
V5BYZ6 | Trypanosoma cruzi | 37% | 100% |