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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AT37
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:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 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:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.696 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.703 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.640 |
DEG_SPOP_SBC_1 | 669 | 673 | PF00917 | 0.668 |
DOC_MAPK_gen_1 | 194 | 202 | PF00069 | 0.667 |
DOC_MAPK_MEF2A_6 | 194 | 202 | PF00069 | 0.727 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.299 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.669 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.648 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.696 |
DOC_PP2B_LxvP_1 | 554 | 557 | PF13499 | 0.702 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.825 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 611 | 615 | PF12436 | 0.694 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.423 |
LIG_14-3-3_CanoR_1 | 287 | 292 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 333 | 338 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 580 | 586 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 597 | 606 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 619 | 625 | PF00244 | 0.686 |
LIG_Actin_WH2_2 | 606 | 621 | PF00022 | 0.499 |
LIG_APCC_ABBA_1 | 31 | 36 | PF00400 | 0.647 |
LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.505 |
LIG_eIF4E_1 | 628 | 634 | PF01652 | 0.708 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.376 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.550 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.561 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.648 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.701 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.713 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.689 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.730 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.802 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.629 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.722 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.528 |
LIG_LIR_Gen_1 | 119 | 129 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 715 | 720 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.812 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 715 | 719 | PF02991 | 0.686 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.530 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.411 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.738 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.627 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.473 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 558 | 561 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 716 | 719 | PF00017 | 0.761 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 388 | 391 | PF00017 | 0.398 |
LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.715 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.715 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.761 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.731 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.445 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.713 |
LIG_SUMO_SIM_anti_2 | 67 | 75 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 252 | 257 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 661 | 666 | PF11976 | 0.702 |
LIG_SUMO_SIM_par_1 | 67 | 75 | PF11976 | 0.488 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.455 |
LIG_TYR_ITIM | 556 | 561 | PF00017 | 0.499 |
LIG_WRC_WIRS_1 | 633 | 638 | PF05994 | 0.495 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.587 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.717 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.525 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.555 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.642 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.803 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.759 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.741 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.569 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.538 |
MOD_CK2_1 | 683 | 689 | PF00069 | 0.574 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.541 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.475 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.616 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.660 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.730 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.478 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.385 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.689 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.546 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.822 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.626 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.772 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.587 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.700 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.627 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.716 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.531 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.536 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.635 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.707 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.675 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.376 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.542 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.541 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.398 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.599 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.678 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.607 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.443 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.633 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.719 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.713 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.711 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.754 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.742 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.740 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.610 |
MOD_LATS_1 | 331 | 337 | PF00433 | 0.545 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.623 |
MOD_N-GLC_1 | 703 | 708 | PF02516 | 0.700 |
MOD_N-GLC_2 | 322 | 324 | PF02516 | 0.376 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.618 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.376 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.313 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.531 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.548 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.707 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.362 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.497 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.703 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.462 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.707 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.682 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.430 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.465 |
MOD_PKA_1 | 333 | 339 | PF00069 | 0.483 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.547 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.690 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.733 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.801 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.675 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.562 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.557 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.592 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.686 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.452 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.357 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.420 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.592 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.730 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.588 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.663 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.389 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.776 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.647 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.783 |
MOD_Plk_4 | 696 | 702 | PF00069 | 0.728 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.687 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.501 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.721 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.734 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.637 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.626 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.702 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.809 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.425 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.689 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.347 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDB4 | Leptomonas seymouri | 42% | 100% |
A0A3S7XAY5 | Leishmania donovani | 89% | 100% |
A4HPC6 | Leishmania braziliensis | 71% | 100% |
A4ICG6 | Leishmania infantum | 89% | 100% |
Q4Q1G1 | Leishmania major | 90% | 100% |
V5BPT3 | Trypanosoma cruzi | 34% | 100% |