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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0016592 | mediator complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H7I2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0000086 | G2/M transition of mitotic cell cycle | 5 | 1 |
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 1 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044839 | cell cycle G2/M phase transition | 4 | 1 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 903 | 907 | PF00656 | 0.778 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.760 |
CLV_C14_Caspase3-7 | 935 | 939 | PF00656 | 0.788 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 924 | 926 | PF00675 | 0.776 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 924 | 926 | PF00082 | 0.776 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.765 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 881 | 885 | PF00082 | 0.580 |
CLV_Separin_Metazoa | 774 | 778 | PF03568 | 0.500 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.753 |
DEG_SPOP_SBC_1 | 391 | 395 | PF00917 | 0.777 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.733 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.742 |
DEG_SPOP_SBC_1 | 822 | 826 | PF00917 | 0.702 |
DOC_CDC14_PxL_1 | 620 | 628 | PF14671 | 0.357 |
DOC_CYCLIN_RxL_1 | 650 | 660 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 651 | 657 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 580 | 589 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 351 | 359 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 492 | 500 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 97 | 104 | PF00069 | 0.633 |
DOC_MAPK_RevD_3 | 637 | 653 | PF00069 | 0.438 |
DOC_PP1_RVXF_1 | 565 | 572 | PF00149 | 0.438 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.648 |
DOC_PP2B_LxvP_1 | 672 | 675 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.652 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 867 | 871 | PF00917 | 0.646 |
DOC_USP7_UBL2_3 | 331 | 335 | PF12436 | 0.479 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 863 | 868 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 869 | 874 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 236 | 243 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 278 | 286 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 289 | 296 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 512 | 521 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 698 | 708 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 828 | 836 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 924 | 931 | PF00244 | 0.687 |
LIG_BIR_III_4 | 152 | 156 | PF00653 | 0.659 |
LIG_Clathr_ClatBox_1 | 370 | 374 | PF01394 | 0.576 |
LIG_deltaCOP1_diTrp_1 | 638 | 646 | PF00928 | 0.492 |
LIG_EVH1_2 | 78 | 82 | PF00568 | 0.720 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.790 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.766 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.595 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.500 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.735 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.745 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.369 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.357 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.492 |
LIG_FHA_1 | 939 | 945 | PF00498 | 0.731 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.713 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.582 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.716 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.753 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.663 |
LIG_LIR_Apic_2 | 618 | 624 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 495 | 505 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 560 | 571 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 591 | 602 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 501 | 505 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 591 | 597 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 625 | 631 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 677 | 683 | PF02991 | 0.369 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.701 |
LIG_Pex14_2 | 646 | 650 | PF04695 | 0.492 |
LIG_REV1ctd_RIR_1 | 760 | 766 | PF16727 | 0.415 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.478 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.378 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.492 |
LIG_SH2_CRK | 684 | 688 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 514 | 518 | PF00017 | 0.580 |
LIG_SH2_PTP2 | 594 | 597 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 633 | 637 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.417 |
LIG_SH3_2 | 205 | 210 | PF14604 | 0.720 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.708 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.763 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.523 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.732 |
LIG_SH3_3 | 766 | 772 | PF00018 | 0.474 |
LIG_SH3_CIN85_PxpxPR_1 | 375 | 380 | PF14604 | 0.717 |
LIG_SUMO_SIM_anti_2 | 352 | 357 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 369 | 374 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 615 | 621 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 734 | 742 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 369 | 374 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 664 | 670 | PF11976 | 0.438 |
LIG_TRAF2_1 | 675 | 678 | PF00917 | 0.422 |
LIG_TYR_ITIM | 536 | 541 | PF00017 | 0.534 |
LIG_TYR_ITIM | 561 | 566 | PF00017 | 0.492 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.646 |
MOD_CDC14_SPxK_1 | 384 | 387 | PF00782 | 0.724 |
MOD_CDK_SPK_2 | 539 | 544 | PF00069 | 0.624 |
MOD_CDK_SPxK_1 | 381 | 387 | PF00069 | 0.718 |
MOD_CDK_SPxxK_3 | 373 | 380 | PF00069 | 0.692 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.735 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.807 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.793 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.629 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.739 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.813 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.677 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.552 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.438 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.682 |
MOD_CK1_1 | 808 | 814 | PF00069 | 0.717 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.715 |
MOD_CK1_1 | 830 | 836 | PF00069 | 0.666 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.595 |
MOD_CK1_1 | 856 | 862 | PF00069 | 0.757 |
MOD_CK1_1 | 872 | 878 | PF00069 | 0.564 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.753 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.666 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.758 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.736 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.657 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.657 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.391 |
MOD_CK2_1 | 843 | 849 | PF00069 | 0.725 |
MOD_CK2_1 | 854 | 860 | PF00069 | 0.736 |
MOD_CK2_1 | 934 | 940 | PF00069 | 0.726 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.771 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.811 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.736 |
MOD_GlcNHglycan | 177 | 181 | PF01048 | 0.686 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.705 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.416 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.711 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.710 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.750 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.640 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.403 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.246 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.771 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.727 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.774 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.792 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.741 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.642 |
MOD_GlcNHglycan | 901 | 905 | PF01048 | 0.781 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.715 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.705 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.614 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.742 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.701 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.731 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.726 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.741 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.769 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.716 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.718 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.723 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.741 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.446 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.455 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.813 |
MOD_GSK3_1 | 856 | 863 | PF00069 | 0.695 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.753 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.565 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.817 |
MOD_GSK3_1 | 934 | 941 | PF00069 | 0.569 |
MOD_LATS_1 | 922 | 928 | PF00433 | 0.822 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.723 |
MOD_N-GLC_1 | 699 | 704 | PF02516 | 0.482 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.579 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.427 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.346 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.385 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.464 |
MOD_NEK2_1 | 877 | 882 | PF00069 | 0.584 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.719 |
MOD_NEK2_2 | 879 | 884 | PF00069 | 0.580 |
MOD_OFUCOSY | 101 | 106 | PF10250 | 0.704 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.723 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.551 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.569 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.817 |
MOD_PIKK_1 | 808 | 814 | PF00454 | 0.845 |
MOD_PK_1 | 557 | 563 | PF00069 | 0.438 |
MOD_PKA_1 | 750 | 756 | PF00069 | 0.438 |
MOD_PKA_1 | 924 | 930 | PF00069 | 0.825 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.716 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.687 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.605 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.782 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.753 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.438 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.357 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.752 |
MOD_PKA_2 | 827 | 833 | PF00069 | 0.507 |
MOD_PKA_2 | 923 | 929 | PF00069 | 0.771 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.679 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.617 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.357 |
MOD_Plk_1 | 848 | 854 | PF00069 | 0.723 |
MOD_Plk_2-3 | 934 | 940 | PF00069 | 0.772 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.609 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.666 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.616 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.453 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.561 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.452 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.366 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.705 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.458 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.404 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.436 |
MOD_Plk_4 | 872 | 878 | PF00069 | 0.580 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.683 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.761 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.592 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.700 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.617 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.438 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.649 |
MOD_ProDKin_1 | 863 | 869 | PF00069 | 0.770 |
MOD_SUMO_for_1 | 763 | 766 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 523 | 530 | PF00179 | 0.733 |
MOD_SUMO_rev_2 | 575 | 585 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_4 | 914 | 920 | PF01217 | 0.765 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.794 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 651 | 653 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 748 | 751 | PF00400 | 0.438 |
TRG_NLS_Bipartite_1 | 427 | 447 | PF00514 | 0.751 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.626 |
TRG_NLS_MonoExtC_3 | 442 | 448 | PF00514 | 0.770 |
TRG_NLS_MonoExtN_4 | 9 | 15 | PF00514 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 576 | 581 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 949 | 954 | PF00026 | 0.766 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6G8 | Leptomonas seymouri | 49% | 100% |
A0A3R7KFZ3 | Trypanosoma rangeli | 38% | 100% |
A4HFW9 | Leishmania braziliensis | 77% | 100% |
A4I302 | Leishmania infantum | 99% | 100% |
C9ZJF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ADH4 | Leishmania major | 92% | 100% |
E9AZ98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |