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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASS5
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 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:0043170 | macromolecule metabolic process | 3 | 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:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0008270 | zinc ion binding | 6 | 6 |
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: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 | 20 | 24 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 679 | 683 | PF00656 | 0.652 |
CLV_C14_Caspase3-7 | 783 | 787 | PF00656 | 0.744 |
CLV_C14_Caspase3-7 | 821 | 825 | PF00656 | 0.655 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.826 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.837 |
CLV_PCSK_FUR_1 | 419 | 423 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.806 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.805 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.818 |
DEG_APCC_DBOX_1 | 641 | 649 | PF00400 | 0.540 |
DEG_SPOP_SBC_1 | 26 | 30 | PF00917 | 0.525 |
DOC_CKS1_1 | 597 | 602 | PF01111 | 0.761 |
DOC_CYCLIN_RxL_1 | 771 | 782 | PF00134 | 0.812 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.675 |
DOC_MAPK_gen_1 | 3 | 11 | PF00069 | 0.733 |
DOC_MAPK_gen_1 | 734 | 742 | PF00069 | 0.821 |
DOC_MAPK_gen_1 | 839 | 846 | PF00069 | 0.838 |
DOC_MAPK_MEF2A_6 | 4 | 13 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 839 | 848 | PF00069 | 0.836 |
DOC_MAPK_RevD_3 | 383 | 398 | PF00069 | 0.581 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.691 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.754 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 401 | 409 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 448 | 454 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 477 | 482 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 627 | 633 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 743 | 747 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 789 | 796 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 797 | 807 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 839 | 846 | PF00244 | 0.837 |
LIG_Actin_WH2_2 | 359 | 376 | PF00022 | 0.646 |
LIG_Actin_WH2_2 | 388 | 405 | PF00022 | 0.654 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.530 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.808 |
LIG_BIR_III_4 | 342 | 346 | PF00653 | 0.537 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.747 |
LIG_BRCT_BRCA1_1 | 824 | 828 | PF00533 | 0.541 |
LIG_deltaCOP1_diTrp_1 | 118 | 127 | PF00928 | 0.604 |
LIG_DLG_GKlike_1 | 477 | 484 | PF00625 | 0.765 |
LIG_EH1_1 | 406 | 414 | PF00400 | 0.560 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.526 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.808 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.674 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.681 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.816 |
LIG_FHA_1 | 839 | 845 | PF00498 | 0.839 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.691 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.490 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.642 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.631 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.580 |
LIG_FHA_2 | 806 | 812 | PF00498 | 0.703 |
LIG_LIR_Apic_2 | 550 | 555 | PF02991 | 0.605 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.715 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 67 | 74 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.737 |
LIG_LIR_Nem_3 | 697 | 702 | PF02991 | 0.643 |
LIG_PDZ_Class_2 | 843 | 848 | PF00595 | 0.834 |
LIG_PTAP_UEV_1 | 215 | 220 | PF05743 | 0.770 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.722 |
LIG_SH2_NCK_1 | 552 | 556 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.822 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 806 | 809 | PF00017 | 0.825 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.441 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.777 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.524 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.833 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.657 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.835 |
LIG_SUMO_SIM_anti_2 | 76 | 82 | PF11976 | 0.582 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.688 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.481 |
LIG_WRC_WIRS_1 | 478 | 483 | PF05994 | 0.766 |
LIG_WW_3 | 746 | 750 | PF00397 | 0.742 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.679 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.753 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.756 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.720 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.678 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.414 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.848 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.639 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.516 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.833 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.795 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.624 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.571 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.579 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.504 |
MOD_CK2_1 | 760 | 766 | PF00069 | 0.648 |
MOD_Cter_Amidation | 395 | 398 | PF01082 | 0.556 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.500 |
MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.672 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.649 |
MOD_GlcNHglycan | 189 | 193 | PF01048 | 0.576 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.604 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.613 |
MOD_GlcNHglycan | 390 | 394 | PF01048 | 0.510 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.523 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.373 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.714 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.614 |
MOD_GlcNHglycan | 536 | 541 | PF01048 | 0.643 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.563 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.631 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.773 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.520 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.623 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.664 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.654 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.700 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.749 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.615 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.553 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.544 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.645 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.455 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.460 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.626 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.675 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.718 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.708 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.613 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.719 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.841 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.789 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.802 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.491 |
MOD_N-GLC_2 | 474 | 476 | PF02516 | 0.736 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.512 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.418 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.592 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.469 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.379 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.645 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.530 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.593 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.664 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.519 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.717 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.500 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.654 |
MOD_OFUCOSY | 205 | 212 | PF10250 | 0.484 |
MOD_OFUCOSY | 291 | 297 | PF10250 | 0.530 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.767 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.786 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.592 |
MOD_PIKK_1 | 834 | 840 | PF00454 | 0.836 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.651 |
MOD_PKA_1 | 813 | 819 | PF00069 | 0.825 |
MOD_PKA_1 | 839 | 845 | PF00069 | 0.839 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.762 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.625 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.592 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.583 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.843 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.580 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.673 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.657 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.839 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.454 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.597 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.787 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.624 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.382 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.579 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.565 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.761 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.752 |
MOD_Plk_1 | 666 | 672 | PF00069 | 0.681 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.757 |
MOD_Plk_2-3 | 760 | 766 | PF00069 | 0.750 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.471 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.607 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.538 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.464 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.724 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.800 |
MOD_Plk_4 | 694 | 700 | PF00069 | 0.515 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.503 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.744 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.480 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.526 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.532 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.630 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.762 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.754 |
MOD_SUMO_rev_2 | 228 | 236 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 350 | 359 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 585 | 590 | PF01217 | 0.762 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 597 | 602 | PF01217 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 655 | 660 | PF01217 | 0.724 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 748 | 750 | PF00400 | 0.628 |
TRG_NES_CRM1_1 | 69 | 82 | PF08389 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.660 |
TRG_Pf-PMV_PEXEL_1 | 499 | 503 | PF00026 | 0.723 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAN9 | Leishmania donovani | 84% | 100% |
A4HP15 | Leishmania braziliensis | 63% | 100% |
A4IDC4 | Leishmania infantum | 84% | 100% |
Q4Q1S1 | Leishmania major | 83% | 100% |