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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1S1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0005488 | binding | 1 | 6 |
GO:0008270 | zinc ion binding | 6 | 6 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0046914 | transition metal ion binding | 5 | 6 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 783 | 787 | PF00656 | 0.659 |
CLV_MEL_PAP_1 | 740 | 746 | PF00089 | 0.616 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.725 |
CLV_PCSK_FUR_1 | 419 | 423 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.706 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.701 |
DOC_CKS1_1 | 597 | 602 | PF01111 | 0.668 |
DOC_CYCLIN_RxL_1 | 771 | 782 | PF00134 | 0.695 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.520 |
DOC_MAPK_gen_1 | 3 | 11 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 734 | 742 | PF00069 | 0.697 |
DOC_MAPK_gen_1 | 839 | 846 | PF00069 | 0.721 |
DOC_MAPK_MEF2A_6 | 839 | 848 | PF00069 | 0.721 |
DOC_MAPK_RevD_3 | 383 | 398 | PF00069 | 0.473 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.628 |
DOC_PP2B_LxvP_1 | 827 | 830 | PF13499 | 0.645 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 278 | 285 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 448 | 454 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 477 | 482 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 627 | 632 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 658 | 663 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 743 | 747 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 762 | 771 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 789 | 796 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 797 | 807 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 839 | 846 | PF00244 | 0.721 |
LIG_Actin_WH2_2 | 359 | 376 | PF00022 | 0.503 |
LIG_Actin_WH2_2 | 388 | 405 | PF00022 | 0.518 |
LIG_Actin_WH2_2 | 657 | 673 | PF00022 | 0.548 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.405 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.688 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.542 |
LIG_deltaCOP1_diTrp_1 | 118 | 127 | PF00928 | 0.479 |
LIG_DLG_GKlike_1 | 477 | 484 | PF00625 | 0.595 |
LIG_DLG_GKlike_1 | 627 | 635 | PF00625 | 0.641 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.524 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.728 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.614 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.672 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.712 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.595 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.688 |
LIG_FHA_1 | 839 | 845 | PF00498 | 0.722 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.569 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.582 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.574 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.489 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.694 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.618 |
LIG_FHA_2 | 806 | 812 | PF00498 | 0.708 |
LIG_Integrin_RGD_1 | 568 | 570 | PF01839 | 0.553 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 697 | 702 | PF02991 | 0.692 |
LIG_MYND_1 | 643 | 647 | PF01753 | 0.562 |
LIG_MYND_1 | 69 | 73 | PF01753 | 0.478 |
LIG_PCNA_PIPBox_1 | 406 | 415 | PF02747 | 0.377 |
LIG_PDZ_Class_2 | 843 | 848 | PF00595 | 0.719 |
LIG_PTAP_UEV_1 | 215 | 220 | PF05743 | 0.666 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 806 | 809 | PF00017 | 0.692 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.798 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.650 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.715 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.693 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.585 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.713 |
LIG_SUMO_SIM_anti_2 | 76 | 82 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.541 |
LIG_WRC_WIRS_1 | 409 | 414 | PF05994 | 0.375 |
LIG_WRC_WIRS_1 | 478 | 483 | PF05994 | 0.583 |
MOD_CDK_SPK_2 | 686 | 691 | PF00069 | 0.571 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.613 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.649 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.646 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.631 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.376 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.555 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.556 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.713 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.786 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.558 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.709 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.686 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.567 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.620 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.491 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.488 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.620 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.506 |
MOD_CK2_1 | 760 | 766 | PF00069 | 0.759 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.473 |
MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.607 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.621 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.544 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.637 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.674 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.719 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.630 |
MOD_GlcNHglycan | 390 | 394 | PF01048 | 0.516 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.417 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.385 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.614 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.638 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.589 |
MOD_GlcNHglycan | 536 | 541 | PF01048 | 0.544 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.558 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.740 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.785 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.504 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.591 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.648 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.578 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.463 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.526 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.561 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.529 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.482 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.562 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.429 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.453 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.394 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.505 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.573 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.725 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.787 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.555 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.675 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.592 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.719 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.699 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.691 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.448 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.533 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.673 |
MOD_N-GLC_2 | 474 | 476 | PF02516 | 0.601 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.664 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.450 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.505 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.440 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.423 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.373 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.532 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.714 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.653 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.669 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.504 |
MOD_OFUCOSY | 163 | 170 | PF10250 | 0.436 |
MOD_OFUCOSY | 291 | 297 | PF10250 | 0.405 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.570 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.380 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.508 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.670 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.705 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.566 |
MOD_PIKK_1 | 834 | 840 | PF00454 | 0.729 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.520 |
MOD_PKA_1 | 813 | 819 | PF00069 | 0.700 |
MOD_PKA_1 | 839 | 845 | PF00069 | 0.722 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.528 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.530 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.461 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.380 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.521 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.486 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.738 |
MOD_PKA_2 | 690 | 696 | PF00069 | 0.561 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.706 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.624 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.723 |
MOD_PKB_1 | 621 | 629 | PF00069 | 0.682 |
MOD_PKB_1 | 656 | 664 | PF00069 | 0.552 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.564 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.482 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.428 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.380 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.465 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.664 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.660 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.668 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.543 |
MOD_Plk_1 | 823 | 829 | PF00069 | 0.650 |
MOD_Plk_2-3 | 760 | 766 | PF00069 | 0.668 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.471 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.398 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.428 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.471 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.448 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.422 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.698 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.706 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.631 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.640 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.520 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.639 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.668 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.568 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.665 |
MOD_SUMO_rev_2 | 228 | 236 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 350 | 359 | PF00179 | 0.462 |
TRG_DiLeu_BaEn_1 | 585 | 590 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 655 | 660 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.595 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 656 | 659 | PF00400 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 499 | 503 | PF00026 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 658 | 663 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAN9 | Leishmania donovani | 88% | 100% |
A4HP15 | Leishmania braziliensis | 64% | 100% |
A4IDC4 | Leishmania infantum | 88% | 100% |
E9ASS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |