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:0005634 | nucleus | 5 | 2 |
GO:0016592 | mediator complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9ADH4
Term | Name | Level | Count |
---|---|---|---|
GO:0000086 | G2/M transition of mitotic cell cycle | 5 | 2 |
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 2 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044770 | cell cycle phase transition | 3 | 2 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 2 |
GO:0044839 | cell cycle G2/M phase transition | 4 | 2 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 2 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 476 | 480 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 905 | 909 | PF00656 | 0.689 |
CLV_C14_Caspase3-7 | 937 | 941 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 752 | 754 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 804 | 806 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 926 | 928 | PF00675 | 0.689 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 804 | 806 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 926 | 928 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.393 |
CLV_Separin_Metazoa | 776 | 780 | PF03568 | 0.480 |
DEG_APCC_DBOX_1 | 200 | 208 | PF00400 | 0.494 |
DEG_APCC_KENBOX_2 | 185 | 189 | PF00400 | 0.430 |
DEG_COP1_1 | 216 | 224 | PF00400 | 0.534 |
DEG_COP1_1 | 318 | 328 | PF00400 | 0.463 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.595 |
DEG_SPOP_SBC_1 | 396 | 400 | PF00917 | 0.649 |
DEG_SPOP_SBC_1 | 69 | 73 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 824 | 828 | PF00917 | 0.592 |
DOC_CDC14_PxL_1 | 622 | 630 | PF14671 | 0.276 |
DOC_CYCLIN_RxL_1 | 652 | 662 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 653 | 659 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 582 | 591 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 356 | 364 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 494 | 502 | PF00069 | 0.501 |
DOC_MAPK_RevD_3 | 639 | 655 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 567 | 574 | PF00149 | 0.335 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.560 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 674 | 677 | PF13499 | 0.341 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 793 | 797 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.678 |
DOC_USP7_UBL2_3 | 336 | 340 | PF12436 | 0.415 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 865 | 870 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 871 | 876 | PF00397 | 0.814 |
LIG_14-3-3_CanoR_1 | 241 | 248 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 283 | 291 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 294 | 301 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 329 | 334 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 463 | 470 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 514 | 522 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 533 | 541 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 700 | 710 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 830 | 838 | PF00244 | 0.721 |
LIG_BIR_III_4 | 157 | 161 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.496 |
LIG_Clathr_ClatBox_1 | 375 | 379 | PF01394 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 640 | 648 | PF00928 | 0.341 |
LIG_EVH1_2 | 83 | 87 | PF00568 | 0.687 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.743 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.377 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.669 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.710 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.278 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.276 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.483 |
LIG_FHA_1 | 941 | 947 | PF00498 | 0.571 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.763 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.567 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.429 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.771 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.692 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.728 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.547 |
LIG_LIR_Apic_2 | 620 | 626 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 497 | 507 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 562 | 573 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 562 | 568 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 679 | 685 | PF02991 | 0.309 |
LIG_NRBOX | 117 | 123 | PF00104 | 0.490 |
LIG_Pex14_2 | 648 | 652 | PF04695 | 0.341 |
LIG_REV1ctd_RIR_1 | 762 | 768 | PF16727 | 0.297 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.407 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.314 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.341 |
LIG_SH2_CRK | 686 | 690 | PF00017 | 0.393 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 516 | 520 | PF00017 | 0.487 |
LIG_SH2_PTP2 | 596 | 599 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 516 | 520 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.276 |
LIG_SH2_STAT3 | 301 | 304 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.366 |
LIG_SH3_2 | 210 | 215 | PF14604 | 0.602 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.777 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.724 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.456 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.686 |
LIG_SH3_3 | 768 | 774 | PF00018 | 0.415 |
LIG_SH3_CIN85_PxpxPR_1 | 380 | 385 | PF14604 | 0.673 |
LIG_SUMO_SIM_anti_2 | 357 | 362 | PF11976 | 0.455 |
LIG_SUMO_SIM_anti_2 | 374 | 379 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 617 | 623 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 736 | 744 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 32 | 37 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 374 | 379 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 666 | 672 | PF11976 | 0.393 |
LIG_TRAF2_1 | 677 | 680 | PF00917 | 0.324 |
LIG_TYR_ITIM | 538 | 543 | PF00017 | 0.534 |
LIG_TYR_ITIM | 563 | 568 | PF00017 | 0.341 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.581 |
MOD_CDK_SPK_2 | 541 | 546 | PF00069 | 0.524 |
MOD_CDK_SPxxK_3 | 378 | 385 | PF00069 | 0.647 |
MOD_CDK_SPxxK_3 | 865 | 872 | PF00069 | 0.536 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.683 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.695 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.659 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.518 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.533 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.682 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.791 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.603 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.519 |
MOD_CK1_1 | 661 | 667 | PF00069 | 0.393 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.599 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.669 |
MOD_CK1_1 | 818 | 824 | PF00069 | 0.665 |
MOD_CK1_1 | 832 | 838 | PF00069 | 0.577 |
MOD_CK1_1 | 858 | 864 | PF00069 | 0.628 |
MOD_CK1_1 | 874 | 880 | PF00069 | 0.525 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.519 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.667 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.602 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.561 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.664 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.695 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.700 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.727 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.534 |
MOD_CK2_1 | 752 | 758 | PF00069 | 0.335 |
MOD_CK2_1 | 845 | 851 | PF00069 | 0.609 |
MOD_CK2_1 | 856 | 862 | PF00069 | 0.607 |
MOD_CK2_1 | 936 | 942 | PF00069 | 0.587 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.744 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.632 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.553 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.667 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.644 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.568 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.641 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.646 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.612 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.657 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.695 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.312 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.294 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.579 |
MOD_GlcNHglycan | 858 | 861 | PF01048 | 0.768 |
MOD_GlcNHglycan | 903 | 907 | PF01048 | 0.659 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.685 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.699 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.452 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.743 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.705 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.616 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.654 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.678 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.693 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.561 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.625 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.671 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.638 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.425 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.451 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.779 |
MOD_GSK3_1 | 858 | 865 | PF00069 | 0.708 |
MOD_GSK3_1 | 881 | 888 | PF00069 | 0.647 |
MOD_GSK3_1 | 898 | 905 | PF00069 | 0.525 |
MOD_GSK3_1 | 922 | 929 | PF00069 | 0.628 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.514 |
MOD_LATS_1 | 125 | 131 | PF00433 | 0.450 |
MOD_LATS_1 | 924 | 930 | PF00433 | 0.631 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.678 |
MOD_N-GLC_1 | 701 | 706 | PF02516 | 0.455 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.573 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.530 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.427 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.289 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.335 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.345 |
MOD_OFUCOSY | 106 | 111 | PF10250 | 0.508 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.513 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.515 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.672 |
MOD_PIKK_1 | 810 | 816 | PF00454 | 0.842 |
MOD_PIKK_1 | 818 | 824 | PF00454 | 0.604 |
MOD_PK_1 | 559 | 565 | PF00069 | 0.393 |
MOD_PKA_1 | 752 | 758 | PF00069 | 0.393 |
MOD_PKA_1 | 926 | 932 | PF00069 | 0.632 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.726 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.657 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.621 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.582 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.648 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.460 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.393 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.276 |
MOD_PKA_2 | 810 | 816 | PF00069 | 0.840 |
MOD_PKA_2 | 829 | 835 | PF00069 | 0.489 |
MOD_PKA_2 | 925 | 931 | PF00069 | 0.629 |
MOD_PKB_1 | 430 | 438 | PF00069 | 0.527 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.573 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.608 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.276 |
MOD_Plk_1 | 850 | 856 | PF00069 | 0.752 |
MOD_Plk_2-3 | 419 | 425 | PF00069 | 0.581 |
MOD_Plk_2-3 | 936 | 942 | PF00069 | 0.655 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.602 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.551 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.375 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.574 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.419 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.286 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.297 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.585 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.437 |
MOD_Plk_4 | 741 | 747 | PF00069 | 0.455 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.618 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.636 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.723 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.609 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.518 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.393 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.570 |
MOD_ProDKin_1 | 865 | 871 | PF00069 | 0.644 |
MOD_SUMO_for_1 | 765 | 768 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 525 | 532 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 577 | 587 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 357 | 362 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 916 | 922 | PF01217 | 0.597 |
TRG_DiLeu_BaLyEn_6 | 948 | 953 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 513 | 515 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 750 | 753 | PF00400 | 0.393 |
TRG_NLS_Bipartite_1 | 429 | 449 | PF00514 | 0.641 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.565 |
TRG_NLS_MonoExtC_3 | 444 | 450 | PF00514 | 0.648 |
TRG_NLS_MonoExtN_4 | 9 | 15 | PF00514 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 578 | 583 | PF00026 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 951 | 956 | PF00026 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6G8 | Leptomonas seymouri | 48% | 100% |
A0A3R7KFZ3 | Trypanosoma rangeli | 39% | 100% |
A0A3S5H7I2 | Leishmania donovani | 92% | 100% |
A4HFW9 | Leishmania braziliensis | 77% | 100% |
A4I302 | Leishmania infantum | 92% | 100% |
C9ZJF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AZ98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BIQ0 | Trypanosoma cruzi | 37% | 100% |