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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000159 | protein phosphatase type 2A complex | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AQ91
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016311 | dephosphorylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0019208 | phosphatase regulator activity | 3 | 1 |
GO:0019888 | protein phosphatase regulator activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.609 |
CLV_MEL_PAP_1 | 380 | 386 | PF00089 | 0.465 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 855 | 857 | PF00675 | 0.491 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 726 | 728 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 855 | 857 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 726 | 728 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 771 | 775 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 794 | 798 | PF00082 | 0.521 |
CLV_Separin_Metazoa | 606 | 610 | PF03568 | 0.513 |
DEG_APCC_DBOX_1 | 451 | 459 | PF00400 | 0.517 |
DEG_SCF_FBW7_1 | 147 | 154 | PF00400 | 0.594 |
DEG_SCF_FBW7_1 | 60 | 65 | PF00400 | 0.518 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.516 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.516 |
DEG_SPOP_SBC_1 | 492 | 496 | PF00917 | 0.545 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 664 | 668 | PF00917 | 0.606 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.716 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.502 |
DOC_CYCLIN_RxL_1 | 473 | 482 | PF00134 | 0.438 |
DOC_CYCLIN_RxL_1 | 493 | 502 | PF00134 | 0.214 |
DOC_CYCLIN_yCln2_LP_2 | 374 | 380 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 42 | 48 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 749 | 757 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.775 |
DOC_PP1_RVXF_1 | 381 | 387 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.384 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 926 | 930 | PF00917 | 0.588 |
DOC_USP7_UBL2_3 | 493 | 497 | PF12436 | 0.509 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 847 | 852 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 213 | 217 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 328 | 336 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 383 | 387 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 513 | 522 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 590 | 597 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 733 | 742 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 825 | 830 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.705 |
LIG_Actin_WH2_2 | 781 | 799 | PF00022 | 0.486 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
LIG_BIR_III_2 | 584 | 588 | PF00653 | 0.570 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.608 |
LIG_CtBP_PxDLS_1 | 45 | 49 | PF00389 | 0.497 |
LIG_EH1_1 | 334 | 342 | PF00400 | 0.447 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.451 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.467 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.512 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.487 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.513 |
LIG_FHA_1 | 735 | 741 | PF00498 | 0.566 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.462 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.456 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.432 |
LIG_FHA_1 | 861 | 867 | PF00498 | 0.455 |
LIG_FHA_1 | 870 | 876 | PF00498 | 0.417 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.729 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.486 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.567 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.548 |
LIG_FHA_2 | 809 | 815 | PF00498 | 0.342 |
LIG_FHA_2 | 894 | 900 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 351 | 359 | PF00786 | 0.476 |
LIG_GBD_Chelix_1 | 393 | 401 | PF00786 | 0.453 |
LIG_LIR_Apic_2 | 156 | 161 | PF02991 | 0.748 |
LIG_LIR_Apic_2 | 385 | 390 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 443 | 450 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 474 | 484 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 768 | 773 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 828 | 834 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 891 | 895 | PF02991 | 0.423 |
LIG_LYPXL_SIV_4 | 902 | 910 | PF13949 | 0.523 |
LIG_MYND_3 | 638 | 642 | PF01753 | 0.459 |
LIG_PCNA_yPIPBox_3 | 280 | 291 | PF02747 | 0.397 |
LIG_PDZ_Class_3 | 936 | 941 | PF00595 | 0.489 |
LIG_Pex14_1 | 512 | 516 | PF04695 | 0.369 |
LIG_Pex14_1 | 889 | 893 | PF04695 | 0.494 |
LIG_Pex3_1 | 287 | 298 | PF04882 | 0.546 |
LIG_SH2_GRB2like | 257 | 260 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 516 | 520 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.485 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.674 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.814 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.573 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.729 |
LIG_SH3_3 | 761 | 767 | PF00018 | 0.473 |
LIG_SH3_3 | 838 | 844 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 533 | 541 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 915 | 920 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 141 | 146 | PF11976 | 0.731 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.542 |
LIG_TRAF2_1 | 625 | 628 | PF00917 | 0.548 |
LIG_TRFH_1 | 220 | 224 | PF08558 | 0.671 |
LIG_TYR_ITIM | 398 | 403 | PF00017 | 0.307 |
LIG_TYR_ITIM | 475 | 480 | PF00017 | 0.394 |
LIG_WRC_WIRS_1 | 500 | 505 | PF05994 | 0.485 |
LIG_WRC_WIRS_1 | 732 | 737 | PF05994 | 0.572 |
MOD_CDK_SPK_2 | 220 | 225 | PF00069 | 0.643 |
MOD_CDK_SPK_2 | 58 | 63 | PF00069 | 0.515 |
MOD_CDK_SPK_2 | 847 | 852 | PF00069 | 0.513 |
MOD_CDK_SPxK_1 | 114 | 120 | PF00069 | 0.799 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 76 | 83 | PF00069 | 0.599 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.664 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.677 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.670 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.729 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.560 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.396 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.428 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.526 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.546 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.803 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.656 |
MOD_CK1_1 | 734 | 740 | PF00069 | 0.559 |
MOD_CK1_1 | 847 | 853 | PF00069 | 0.434 |
MOD_CK1_1 | 929 | 935 | PF00069 | 0.734 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.680 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.810 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.738 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.545 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.473 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.567 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.484 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.465 |
MOD_CK2_1 | 792 | 798 | PF00069 | 0.503 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.514 |
MOD_CK2_1 | 893 | 899 | PF00069 | 0.482 |
MOD_CMANNOS | 889 | 892 | PF00535 | 0.499 |
MOD_DYRK1A_RPxSP_1 | 56 | 60 | PF00069 | 0.656 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.709 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.749 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.816 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.665 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.713 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.688 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.726 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.466 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.431 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.418 |
MOD_GlcNHglycan | 428 | 432 | PF01048 | 0.473 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.710 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.466 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.643 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.686 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.698 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.635 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.775 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.755 |
MOD_GlcNHglycan | 928 | 931 | PF01048 | 0.668 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.747 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.724 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.685 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.705 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.686 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.660 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.651 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.481 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.385 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.504 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.669 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.441 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.705 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.749 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.620 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.641 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.393 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.462 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.554 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.730 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.798 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.776 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.491 |
MOD_N-GLC_1 | 668 | 673 | PF02516 | 0.804 |
MOD_N-GLC_1 | 719 | 724 | PF02516 | 0.564 |
MOD_N-GLC_1 | 919 | 924 | PF02516 | 0.568 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.737 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.734 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.558 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.358 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.504 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.644 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.487 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.463 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.373 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.479 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.363 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.488 |
MOD_NEK2_1 | 859 | 864 | PF00069 | 0.508 |
MOD_NEK2_1 | 919 | 924 | PF00069 | 0.526 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.646 |
MOD_NEK2_2 | 784 | 789 | PF00069 | 0.539 |
MOD_NEK2_2 | 792 | 797 | PF00069 | 0.469 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.457 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.570 |
MOD_PIKK_1 | 787 | 793 | PF00454 | 0.498 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.678 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.544 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.505 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.520 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.396 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.452 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.713 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.682 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.798 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.593 |
MOD_PKB_1 | 725 | 733 | PF00069 | 0.292 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.798 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.798 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.735 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.663 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.422 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.510 |
MOD_Plk_1 | 719 | 725 | PF00069 | 0.417 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.435 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.404 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.372 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.318 |
MOD_Plk_4 | 825 | 831 | PF00069 | 0.525 |
MOD_Plk_4 | 888 | 894 | PF00069 | 0.448 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.615 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.789 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.750 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.635 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.697 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.728 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.631 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.773 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.739 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.701 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.675 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.508 |
MOD_ProDKin_1 | 847 | 853 | PF00069 | 0.485 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.605 |
TRG_DiLeu_BaEn_1 | 367 | 372 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_3 | 264 | 270 | PF01217 | 0.529 |
TRG_DiLeu_BaEn_4 | 481 | 487 | PF01217 | 0.473 |
TRG_DiLeu_BaEn_4 | 87 | 93 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.710 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 458 | 463 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 862 | 867 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 890 | 893 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 512 | 515 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 748 | 751 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 854 | 856 | PF00400 | 0.492 |
TRG_NES_CRM1_1 | 360 | 373 | PF08389 | 0.490 |
TRG_NES_CRM1_1 | 469 | 482 | PF08389 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 316 | 320 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 476 | 481 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 616 | 620 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 794 | 798 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA72 | Leptomonas seymouri | 65% | 96% |
A0A3Q8IDF8 | Leishmania donovani | 94% | 100% |
A0A3R7N5C8 | Trypanosoma rangeli | 36% | 100% |
A4H865 | Leishmania braziliensis | 79% | 98% |
A4HWJ0 | Leishmania infantum | 94% | 100% |
C9ZXV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
Q4QF92 | Leishmania major | 93% | 100% |
V5DL61 | Trypanosoma cruzi | 37% | 100% |