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: A4HP15
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 | 199 | 203 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.387 |
CLV_MEL_PAP_1 | 741 | 747 | PF00089 | 0.621 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 813 | 815 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 840 | 842 | PF00675 | 0.817 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 832 | 834 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 840 | 842 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 832 | 834 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.743 |
DEG_APCC_DBOX_1 | 500 | 508 | PF00400 | 0.428 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 152 | 156 | PF00917 | 0.477 |
DEG_SPOP_SBC_1 | 679 | 683 | PF00917 | 0.551 |
DOC_ANK_TNKS_1 | 7 | 14 | PF00023 | 0.561 |
DOC_CYCLIN_RxL_1 | 641 | 649 | PF00134 | 0.569 |
DOC_CYCLIN_RxL_1 | 772 | 783 | PF00134 | 0.738 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.695 |
DOC_MAPK_gen_1 | 735 | 743 | PF00069 | 0.805 |
DOC_MAPK_gen_1 | 840 | 847 | PF00069 | 0.773 |
DOC_MAPK_MEF2A_6 | 840 | 849 | PF00069 | 0.756 |
DOC_PP1_RVXF_1 | 478 | 485 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.660 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.666 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 733 | 737 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 792 | 796 | PF00917 | 0.688 |
DOC_USP7_MATH_2 | 823 | 829 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 646 | 651 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 197 | 207 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 255 | 263 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 480 | 485 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 523 | 529 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 594 | 602 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 630 | 635 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 744 | 748 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 781 | 786 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 790 | 798 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 840 | 847 | PF00244 | 0.756 |
LIG_Actin_WH2_2 | 362 | 379 | PF00022 | 0.533 |
LIG_Actin_WH2_2 | 391 | 408 | PF00022 | 0.563 |
LIG_APCC_ABBA_1 | 290 | 295 | PF00400 | 0.437 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.800 |
LIG_BIR_III_4 | 345 | 349 | PF00653 | 0.458 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.679 |
LIG_DLG_GKlike_1 | 480 | 487 | PF00625 | 0.643 |
LIG_DLG_GKlike_1 | 630 | 638 | PF00625 | 0.615 |
LIG_EH1_1 | 409 | 417 | PF00400 | 0.463 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.539 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.611 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.626 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.700 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.794 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.719 |
LIG_FHA_1 | 840 | 846 | PF00498 | 0.758 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.519 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.403 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.424 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.633 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.553 |
LIG_FHA_2 | 756 | 762 | PF00498 | 0.569 |
LIG_FHA_2 | 807 | 813 | PF00498 | 0.641 |
LIG_LIR_Apic_2 | 552 | 558 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.671 |
LIG_LIR_Gen_1 | 483 | 492 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 483 | 487 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 657 | 662 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 696 | 701 | PF02991 | 0.792 |
LIG_MYND_1 | 69 | 73 | PF01753 | 0.637 |
LIG_PDZ_Class_2 | 844 | 849 | PF00595 | 0.754 |
LIG_PTAP_UEV_1 | 218 | 223 | PF05743 | 0.686 |
LIG_SH2_CRK | 500 | 504 | PF00017 | 0.613 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.542 |
LIG_SH2_CRK | 659 | 663 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 555 | 559 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 665 | 669 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.798 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.729 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.534 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.668 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.523 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.745 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.568 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.731 |
LIG_SUMO_SIM_anti_2 | 431 | 437 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 76 | 82 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 603 | 609 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.708 |
LIG_SxIP_EBH_1 | 594 | 608 | PF03271 | 0.532 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.490 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.361 |
LIG_WRC_WIRS_1 | 481 | 486 | PF05994 | 0.645 |
LIG_WW_3 | 544 | 548 | PF00397 | 0.564 |
LIG_WW_3 | 747 | 751 | PF00397 | 0.666 |
MOD_CDC14_SPxK_1 | 671 | 674 | PF00782 | 0.530 |
MOD_CDK_SPK_2 | 827 | 832 | PF00069 | 0.590 |
MOD_CDK_SPxK_1 | 668 | 674 | PF00069 | 0.532 |
MOD_CDK_SPxK_1 | 827 | 833 | PF00069 | 0.590 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.633 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.697 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.671 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.679 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.642 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.344 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.553 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.751 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.531 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.485 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.757 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.744 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.554 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.748 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.683 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.678 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.650 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.584 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.605 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.416 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.481 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.630 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.636 |
MOD_Cter_Amidation | 398 | 401 | PF01082 | 0.500 |
MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.626 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.663 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.570 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.626 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.681 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.575 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.600 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.501 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.413 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.547 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.665 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.593 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.551 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.710 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.692 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.574 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.611 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.649 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.631 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.667 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.709 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.623 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.581 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.469 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.681 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.599 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.485 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.550 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.371 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.534 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.569 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.642 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.626 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.558 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.648 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.731 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.547 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.512 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.747 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.694 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.805 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.696 |
MOD_N-GLC_1 | 781 | 786 | PF02516 | 0.704 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.533 |
MOD_N-GLC_2 | 198 | 200 | PF02516 | 0.512 |
MOD_N-GLC_2 | 477 | 479 | PF02516 | 0.660 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.746 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.504 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.336 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.422 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.515 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.607 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.561 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.554 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.604 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.650 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.685 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.718 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.541 |
MOD_NEK2_2 | 212 | 217 | PF00069 | 0.567 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.536 |
MOD_NEK2_2 | 685 | 690 | PF00069 | 0.549 |
MOD_NEK2_2 | 733 | 738 | PF00069 | 0.544 |
MOD_OFUCOSY | 233 | 240 | PF10250 | 0.340 |
MOD_OFUCOSY | 294 | 300 | PF10250 | 0.437 |
MOD_OFUCOSY | 417 | 422 | PF10250 | 0.343 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.697 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.631 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.642 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.410 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.518 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.352 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.716 |
MOD_PIKK_1 | 652 | 658 | PF00454 | 0.540 |
MOD_PIKK_1 | 835 | 841 | PF00454 | 0.764 |
MOD_PK_1 | 781 | 787 | PF00069 | 0.551 |
MOD_PKA_1 | 400 | 406 | PF00069 | 0.564 |
MOD_PKA_1 | 522 | 528 | PF00069 | 0.558 |
MOD_PKA_1 | 814 | 820 | PF00069 | 0.743 |
MOD_PKA_1 | 840 | 846 | PF00069 | 0.758 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.690 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.348 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.529 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.494 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.534 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.583 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.718 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.549 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.547 |
MOD_PKA_2 | 737 | 743 | PF00069 | 0.799 |
MOD_PKA_2 | 780 | 786 | PF00069 | 0.622 |
MOD_PKA_2 | 839 | 845 | PF00069 | 0.796 |
MOD_PKB_1 | 630 | 638 | PF00069 | 0.652 |
MOD_PKB_1 | 833 | 841 | PF00069 | 0.586 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.688 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.603 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.522 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.627 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.545 |
MOD_Plk_1 | 781 | 787 | PF00069 | 0.551 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.548 |
MOD_Plk_2-3 | 459 | 465 | PF00069 | 0.416 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.560 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.660 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.522 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.586 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.650 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.524 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.617 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.760 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.533 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.618 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.649 |
MOD_ProDKin_1 | 646 | 652 | PF00069 | 0.632 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.532 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.590 |
MOD_SUMO_rev_2 | 128 | 133 | PF00179 | 0.510 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 546 | 548 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 749 | 751 | PF00400 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 763 | 768 | PF00026 | 0.563 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAN9 | Leishmania donovani | 65% | 100% |
A4IDC4 | Leishmania infantum | 64% | 100% |
E9ASS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4Q1S1 | Leishmania major | 64% | 99% |