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: 6 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HMG1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016579 | protein deubiquitination | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070646 | protein modification by small protein removal | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 2 |
GO:0008234 | cysteine-type peptidase activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 1 |
GO:0101005 | deubiquitinase activity | 5 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 604 | 608 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.432 |
CLV_PCSK_FUR_1 | 373 | 377 | PF00082 | 0.388 |
CLV_PCSK_FUR_1 | 577 | 581 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.618 |
CLV_PCSK_PC7_1 | 371 | 377 | PF00082 | 0.391 |
CLV_PCSK_PC7_1 | 609 | 615 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.572 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.581 |
DEG_SCF_FBW7_1 | 620 | 627 | PF00400 | 0.531 |
DEG_SPOP_SBC_1 | 147 | 151 | PF00917 | 0.652 |
DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.468 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.431 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.761 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.466 |
DOC_MAPK_gen_1 | 213 | 220 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 472 | 480 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 70 | 79 | PF00069 | 0.435 |
DOC_MAPK_HePTP_8 | 69 | 81 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 472 | 480 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.502 |
DOC_MIT_MIM_1 | 381 | 391 | PF04212 | 0.546 |
DOC_PP1_RVXF_1 | 56 | 62 | PF00149 | 0.561 |
DOC_PP2B_LxvP_1 | 647 | 650 | PF13499 | 0.546 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.579 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.755 |
DOC_USP7_MATH_2 | 225 | 231 | PF00917 | 0.477 |
DOC_USP7_UBL2_3 | 579 | 583 | PF12436 | 0.394 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 650 | 655 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 119 | 124 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 590 | 599 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 640 | 649 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 668 | 675 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 85 | 89 | PF00244 | 0.512 |
LIG_Actin_RPEL_3 | 112 | 131 | PF02755 | 0.398 |
LIG_BRCT_BRCA1_1 | 702 | 706 | PF00533 | 0.560 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.444 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.694 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.538 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.543 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.462 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.522 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.561 |
LIG_GSK3_LRP6_1 | 694 | 699 | PF00069 | 0.679 |
LIG_LIR_Apic_2 | 178 | 183 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 311 | 322 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 435 | 446 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 87 | 96 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.449 |
LIG_MYND_1 | 665 | 669 | PF01753 | 0.680 |
LIG_NRBOX | 3 | 9 | PF00104 | 0.509 |
LIG_NRBOX | 565 | 571 | PF00104 | 0.560 |
LIG_PCNA_yPIPBox_3 | 563 | 577 | PF02747 | 0.340 |
LIG_Pex14_1 | 488 | 492 | PF04695 | 0.482 |
LIG_PTB_Apo_2 | 186 | 193 | PF02174 | 0.559 |
LIG_PTB_Apo_2 | 408 | 415 | PF02174 | 0.513 |
LIG_SH2_CRK | 438 | 442 | PF00017 | 0.475 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.389 |
LIG_SH2_GRB2like | 314 | 317 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 295 | 299 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 506 | 510 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 553 | 557 | PF00017 | 0.430 |
LIG_SH2_SRC | 553 | 556 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.455 |
LIG_SH3_1 | 600 | 606 | PF00018 | 0.529 |
LIG_SH3_1 | 685 | 691 | PF00018 | 0.757 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.552 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.624 |
LIG_SH3_3 | 622 | 628 | PF00018 | 0.759 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.729 |
LIG_SH3_3 | 680 | 686 | PF00018 | 0.739 |
LIG_SH3_3 | 688 | 694 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 87 | 93 | PF11976 | 0.481 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.583 |
LIG_TYR_ITIM | 551 | 556 | PF00017 | 0.411 |
LIG_WRC_WIRS_1 | 184 | 189 | PF05994 | 0.524 |
MOD_CDC14_SPxK_1 | 67 | 70 | PF00782 | 0.593 |
MOD_CDK_SPK_2 | 624 | 629 | PF00069 | 0.522 |
MOD_CDK_SPxK_1 | 620 | 626 | PF00069 | 0.532 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.592 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.547 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.587 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.545 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.650 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.445 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.643 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.480 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.364 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.661 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.726 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.785 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.639 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.685 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.445 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.650 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.626 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.488 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.651 |
MOD_Cter_Amidation | 611 | 614 | PF01082 | 0.542 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.613 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.559 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.731 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.685 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.607 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.598 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.663 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.515 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.557 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.669 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.315 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.435 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.629 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.627 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.675 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.480 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.609 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.656 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.451 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.784 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.562 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.637 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.745 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.665 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.710 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.465 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.560 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.513 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.510 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.759 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.490 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.664 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.696 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.636 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.693 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.658 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.520 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.422 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.580 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.396 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.660 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.476 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.531 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.454 |
MOD_PKA_1 | 156 | 162 | PF00069 | 0.495 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.454 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.534 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.545 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.470 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.558 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.794 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.529 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.813 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.705 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.477 |
MOD_PKB_1 | 638 | 646 | PF00069 | 0.545 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.471 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.472 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.552 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.767 |
MOD_Plk_1 | 615 | 621 | PF00069 | 0.752 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.570 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.511 |
MOD_Plk_2-3 | 457 | 463 | PF00069 | 0.447 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.602 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.610 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.566 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.505 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.495 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.537 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.504 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.694 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.461 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.658 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.510 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.453 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.749 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.592 |
MOD_ProDKin_1 | 650 | 656 | PF00069 | 0.721 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.725 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.719 |
MOD_SUMO_rev_2 | 309 | 315 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 99 | 109 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_2 | 196 | 202 | PF01217 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.552 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 637 | 640 | PF00400 | 0.645 |
TRG_NLS_MonoExtC_3 | 575 | 580 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 576 | 583 | PF00514 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.365 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V7 | Leptomonas seymouri | 57% | 100% |
A0A1X0NIV4 | Trypanosomatidae | 33% | 90% |
A0A3Q8IJ90 | Leishmania donovani | 69% | 100% |
A0A3R7MGK1 | Trypanosoma rangeli | 37% | 100% |
A4IB32 | Leishmania infantum | 69% | 100% |
C9ZNN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 77% |
E9AEW2 | Leishmania major | 68% | 100% |
E9B618 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
V5BC93 | Trypanosoma cruzi | 38% | 100% |