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: A4HPC6
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 | 139 | 143 | PF00656 | 0.719 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 592 | 596 | PF00656 | 0.728 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.697 |
DEG_COP1_1 | 595 | 605 | PF00400 | 0.535 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.640 |
DEG_SPOP_SBC_1 | 566 | 570 | PF00917 | 0.534 |
DOC_CDC14_PxL_1 | 286 | 294 | PF14671 | 0.315 |
DOC_CYCLIN_yCln2_LP_2 | 686 | 692 | PF00134 | 0.546 |
DOC_MAPK_DCC_7 | 197 | 207 | PF00069 | 0.714 |
DOC_MAPK_gen_1 | 333 | 343 | PF00069 | 0.389 |
DOC_MAPK_HePTP_8 | 700 | 712 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 703 | 712 | PF00069 | 0.511 |
DOC_PP1_SILK_1 | 614 | 619 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.690 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.718 |
DOC_PP2B_LxvP_1 | 554 | 557 | PF13499 | 0.693 |
DOC_PP4_FxxP_1 | 524 | 527 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.603 |
DOC_USP7_UBL2_3 | 610 | 614 | PF12436 | 0.680 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.773 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 597 | 603 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 618 | 624 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 703 | 711 | PF00244 | 0.583 |
LIG_APCC_ABBA_1 | 31 | 36 | PF00400 | 0.640 |
LIG_APCC_ABBA_1 | 513 | 518 | PF00400 | 0.522 |
LIG_BIR_III_4 | 170 | 174 | PF00653 | 0.488 |
LIG_CtBP_PxDLS_1 | 206 | 210 | PF00389 | 0.494 |
LIG_eIF4E_1 | 627 | 633 | PF01652 | 0.666 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.376 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.560 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.673 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.525 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.543 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.531 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.647 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.693 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.796 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.701 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.528 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.693 |
LIG_LIR_Apic_2 | 521 | 527 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 423 | 434 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 59 | 65 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 714 | 719 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.744 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 668 | 674 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 714 | 718 | PF02991 | 0.682 |
LIG_NRBOX | 631 | 637 | PF00104 | 0.468 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.354 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.740 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.622 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.489 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.376 |
LIG_SH2_PTP2 | 715 | 718 | PF00017 | 0.755 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.489 |
LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.755 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.580 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.668 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.469 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.646 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.595 |
LIG_SH3_3 | 705 | 711 | PF00018 | 0.508 |
LIG_SUMO_SIM_anti_2 | 67 | 75 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 252 | 257 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 67 | 75 | PF11976 | 0.504 |
LIG_TRAF2_1 | 545 | 548 | PF00917 | 0.539 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.451 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.608 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.654 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.666 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.609 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.504 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.668 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.457 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.735 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.731 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.536 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.673 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.599 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.550 |
MOD_Cter_Amidation | 363 | 366 | PF01082 | 0.558 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.430 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.618 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.669 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.686 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.478 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.632 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.441 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.757 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.701 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.713 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.611 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.709 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.656 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.537 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.557 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.678 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.613 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.376 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.686 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.643 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.440 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.738 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.693 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.744 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.732 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.665 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.575 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.722 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.618 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.629 |
MOD_N-GLC_1 | 573 | 578 | PF02516 | 0.618 |
MOD_N-GLC_1 | 669 | 674 | PF02516 | 0.529 |
MOD_N-GLC_2 | 179 | 181 | PF02516 | 0.546 |
MOD_N-GLC_2 | 322 | 324 | PF02516 | 0.376 |
MOD_N-GLC_2 | 562 | 564 | PF02516 | 0.768 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.567 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.553 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.376 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.634 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.357 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.694 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.694 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.482 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.683 |
MOD_NEK2_2 | 432 | 437 | PF00069 | 0.436 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.531 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.465 |
MOD_PK_1 | 337 | 343 | PF00069 | 0.390 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.682 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.572 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.778 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.614 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.559 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.578 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.421 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.435 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.591 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.646 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.472 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.502 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.357 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.420 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.646 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.426 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.768 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.606 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.747 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.723 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.684 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.510 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.722 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.638 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.442 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.746 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.705 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.770 |
MOD_SUMO_rev_2 | 182 | 188 | PF00179 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 487 | 492 | PF01217 | 0.659 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.698 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.683 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 402 | 407 | PF00026 | 0.669 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDB4 | Leptomonas seymouri | 43% | 100% |
A0A3S7XAY5 | Leishmania donovani | 71% | 100% |
A4ICG6 | Leishmania infantum | 71% | 100% |
E9AT37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q1G1 | Leishmania major | 72% | 100% |
V5BPT3 | Trypanosoma cruzi | 34% | 100% |