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: 5 |
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: Q4Q4C8
Term | Name | Level | Count |
---|---|---|---|
GO:0000079 | regulation of cyclin-dependent protein serine/threonine kinase activity | 6 | 6 |
GO:0001932 | regulation of protein phosphorylation | 7 | 6 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 6 |
GO:0019222 | regulation of metabolic process | 3 | 6 |
GO:0031323 | regulation of cellular metabolic process | 4 | 6 |
GO:0031399 | regulation of protein modification process | 6 | 6 |
GO:0042325 | regulation of phosphorylation | 7 | 6 |
GO:0043549 | regulation of kinase activity | 5 | 6 |
GO:0045859 | regulation of protein kinase activity | 6 | 6 |
GO:0050789 | regulation of biological process | 2 | 6 |
GO:0050790 | regulation of catalytic activity | 3 | 6 |
GO:0050794 | regulation of cellular process | 3 | 6 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 6 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 6 |
GO:0051246 | regulation of protein metabolic process | 5 | 6 |
GO:0051338 | regulation of transferase activity | 4 | 6 |
GO:0051726 | regulation of cell cycle | 4 | 6 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 6 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0065009 | regulation of molecular function | 2 | 6 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 6 |
GO:0080090 | regulation of primary metabolic process | 4 | 6 |
GO:1904029 | regulation of cyclin-dependent protein kinase activity | 5 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0005515 | protein binding | 2 | 6 |
GO:0019899 | enzyme binding | 3 | 6 |
GO:0019900 | kinase binding | 4 | 6 |
GO:0019901 | protein kinase binding | 5 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 835 | 839 | PF00656 | 0.520 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.776 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.776 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.646 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 632 | 640 | PF00400 | 0.711 |
DEG_SCF_FBW7_1 | 307 | 313 | PF00400 | 0.592 |
DEG_SPOP_SBC_1 | 777 | 781 | PF00917 | 0.661 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.587 |
DOC_CKS1_1 | 747 | 752 | PF01111 | 0.699 |
DOC_CYCLIN_RxL_1 | 490 | 500 | PF00134 | 0.656 |
DOC_MAPK_DCC_7 | 474 | 483 | PF00069 | 0.636 |
DOC_MAPK_HePTP_8 | 471 | 483 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 199 | 206 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 474 | 483 | PF00069 | 0.636 |
DOC_PP2B_LxvP_1 | 153 | 156 | PF13499 | 0.673 |
DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.667 |
DOC_PP2B_LxvP_1 | 489 | 492 | PF13499 | 0.782 |
DOC_PP2B_LxvP_1 | 528 | 531 | PF13499 | 0.769 |
DOC_PP2B_LxvP_1 | 651 | 654 | PF13499 | 0.768 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.784 |
DOC_PP4_FxxP_1 | 477 | 480 | PF00568 | 0.630 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.604 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 777 | 781 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.726 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.236 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 875 | 880 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 438 | 447 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 466 | 472 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 496 | 502 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 579 | 586 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 667 | 673 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 676 | 684 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 726 | 735 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 872 | 882 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 96 | 103 | PF00244 | 0.734 |
LIG_Actin_WH2_2 | 272 | 289 | PF00022 | 0.439 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.691 |
LIG_BRCT_BRCA1_2 | 537 | 543 | PF00533 | 0.694 |
LIG_Clathr_ClatBox_1 | 279 | 283 | PF01394 | 0.439 |
LIG_Clathr_ClatBox_1 | 295 | 299 | PF01394 | 0.313 |
LIG_deltaCOP1_diTrp_1 | 292 | 297 | PF00928 | 0.508 |
LIG_EVH1_1 | 700 | 704 | PF00568 | 0.758 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.505 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.494 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.477 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.564 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.632 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.671 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.712 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.659 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.706 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.552 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.681 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.439 |
LIG_FXI_DFP_1 | 279 | 283 | PF00024 | 0.439 |
LIG_IRF3_LxIS_1 | 14 | 21 | PF10401 | 0.531 |
LIG_LIR_Apic_2 | 120 | 126 | PF02991 | 0.657 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 221 | 229 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 273 | 284 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 376 | 387 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 41 | 51 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 452 | 463 | PF02991 | 0.751 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.782 |
LIG_LIR_Nem_3 | 699 | 703 | PF02991 | 0.764 |
LIG_LIR_Nem_3 | 816 | 822 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 824 | 830 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 838 | 844 | PF02991 | 0.586 |
LIG_Pex14_2 | 703 | 707 | PF04695 | 0.554 |
LIG_PTAP_UEV_1 | 736 | 741 | PF05743 | 0.569 |
LIG_REV1ctd_RIR_1 | 539 | 547 | PF16727 | 0.755 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.651 |
LIG_SH2_NCK_1 | 7 | 11 | PF00017 | 0.651 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.439 |
LIG_SH2_SRC | 800 | 803 | PF00017 | 0.768 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 778 | 782 | PF00017 | 0.746 |
LIG_SH2_STAP1 | 841 | 845 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 822 | 825 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 827 | 830 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.714 |
LIG_SH3_1 | 744 | 750 | PF00018 | 0.635 |
LIG_SH3_2 | 524 | 529 | PF14604 | 0.634 |
LIG_SH3_2 | 737 | 742 | PF14604 | 0.607 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.674 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.729 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.616 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.616 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.594 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.485 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.600 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.798 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.762 |
LIG_SH3_3 | 734 | 740 | PF00018 | 0.752 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.630 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.642 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.536 |
LIG_WW_2 | 479 | 482 | PF00397 | 0.582 |
LIG_WW_3 | 435 | 439 | PF00397 | 0.707 |
LIG_WW_3 | 689 | 693 | PF00397 | 0.773 |
MOD_CDC14_SPxK_1 | 526 | 529 | PF00782 | 0.770 |
MOD_CDK_SPK_2 | 117 | 122 | PF00069 | 0.654 |
MOD_CDK_SPK_2 | 248 | 253 | PF00069 | 0.236 |
MOD_CDK_SPK_2 | 327 | 332 | PF00069 | 0.620 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.623 |
MOD_CDK_SPxK_1 | 523 | 529 | PF00069 | 0.762 |
MOD_CDK_SPxxK_3 | 754 | 761 | PF00069 | 0.710 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.560 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.641 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.450 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.643 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.564 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.700 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.737 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.714 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.739 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.669 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.758 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.707 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.759 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.629 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.615 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.741 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.587 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.439 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.513 |
MOD_CK2_1 | 803 | 809 | PF00069 | 0.754 |
MOD_CMANNOS | 294 | 297 | PF00535 | 0.496 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.700 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.439 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.739 |
MOD_GlcNHglycan | 317 | 321 | PF01048 | 0.668 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.663 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.637 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.786 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.677 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.773 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.730 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.768 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.728 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.610 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.693 |
MOD_GlcNHglycan | 771 | 774 | PF01048 | 0.680 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.702 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.598 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.659 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.616 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.581 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.439 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.534 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.592 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.591 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.650 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.682 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.554 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.680 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.660 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.569 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.717 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.736 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.744 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.760 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.706 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.632 |
MOD_LATS_1 | 134 | 140 | PF00433 | 0.712 |
MOD_LATS_1 | 409 | 415 | PF00433 | 0.503 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.439 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.537 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.439 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.319 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.439 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.651 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.703 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.757 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.651 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.604 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.624 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.720 |
MOD_PIKK_1 | 660 | 666 | PF00454 | 0.772 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.642 |
MOD_PIKK_1 | 772 | 778 | PF00454 | 0.744 |
MOD_PK_1 | 497 | 503 | PF00069 | 0.721 |
MOD_PK_1 | 529 | 535 | PF00069 | 0.758 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.687 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.442 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.490 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.564 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.365 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.660 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.597 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.702 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.722 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.628 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.617 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.696 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.720 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.726 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.494 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.611 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.552 |
MOD_Plk_1 | 646 | 652 | PF00069 | 0.781 |
MOD_Plk_2-3 | 36 | 42 | PF00069 | 0.607 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.557 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.508 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.301 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.603 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.631 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.720 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.667 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.560 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.745 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.236 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.588 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.543 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.609 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.768 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.718 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.599 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.644 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.641 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.681 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.682 |
MOD_ProDKin_1 | 875 | 881 | PF00069 | 0.716 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.638 |
MOD_SUMO_rev_2 | 705 | 713 | PF00179 | 0.666 |
TRG_DiLeu_BaEn_4 | 646 | 652 | PF01217 | 0.781 |
TRG_ENDOCYTIC_2 | 700 | 703 | PF00928 | 0.761 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 691 | 693 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 870 | 873 | PF00400 | 0.719 |
TRG_NES_CRM1_1 | 275 | 290 | PF08389 | 0.439 |
TRG_NES_CRM1_1 | 293 | 306 | PF08389 | 0.521 |
TRG_NLS_MonoExtN_4 | 492 | 499 | PF00514 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDM6 | Leishmania donovani | 88% | 100% |
A4HLB8 | Leishmania braziliensis | 70% | 100% |
A4I8U4 | Leishmania infantum | 88% | 100% |
E9B3R0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |