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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IS46
Term | Name | Level | Count |
---|---|---|---|
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051054 | positive regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0051972 | regulation of telomerase activity | 5 | 1 |
GO:0051973 | positive regulation of telomerase activity | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000278 | regulation of DNA biosynthetic process | 6 | 1 |
GO:2000573 | positive regulation of DNA biosynthetic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:1990275 | preribosome binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 322 | 326 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 802 | 806 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 826 | 830 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 852 | 856 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 902 | 906 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 866 | 868 | PF00675 | 0.290 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 689 | 691 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 866 | 868 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 689 | 691 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 749 | 753 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 839 | 843 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.429 |
DEG_APCC_DBOX_1 | 613 | 621 | PF00400 | 0.595 |
DEG_COP1_1 | 322 | 331 | PF00400 | 0.508 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.427 |
DEG_SPOP_SBC_1 | 68 | 72 | PF00917 | 0.720 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.690 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.570 |
DOC_CDC14_PxL_1 | 299 | 307 | PF14671 | 0.344 |
DOC_CDC14_PxL_1 | 869 | 877 | PF14671 | 0.500 |
DOC_CYCLIN_yClb1_LxF_4 | 839 | 845 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 117 | 120 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 34 | 37 | PF00134 | 0.661 |
DOC_MAPK_gen_1 | 567 | 573 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 689 | 695 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 838 | 845 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 860 | 870 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 348 | 356 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 792 | 800 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 863 | 872 | PF00069 | 0.352 |
DOC_PP1_RVXF_1 | 487 | 494 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.574 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.661 |
DOC_PP2B_LxvP_1 | 600 | 603 | PF13499 | 0.528 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.545 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.552 |
DOC_SPAK_OSR1_1 | 690 | 694 | PF12202 | 0.575 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 757 | 761 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 928 | 932 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.718 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 792 | 797 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 125 | 133 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 21 | 26 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 364 | 368 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 419 | 423 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 519 | 525 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 547 | 553 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 666 | 671 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 677 | 685 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 813 | 821 | PF00244 | 0.333 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 724 | 728 | PF00533 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 336 | 341 | PF00928 | 0.542 |
LIG_deltaCOP1_diTrp_1 | 718 | 726 | PF00928 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 952 | 960 | PF00928 | 0.410 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.445 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.544 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.516 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.553 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.476 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.499 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.423 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.621 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.624 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.640 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.369 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.585 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.405 |
LIG_FHA_2 | 710 | 716 | PF00498 | 0.321 |
LIG_FHA_2 | 824 | 830 | PF00498 | 0.352 |
LIG_FHA_2 | 872 | 878 | PF00498 | 0.588 |
LIG_FHA_2 | 906 | 912 | PF00498 | 0.359 |
LIG_FHA_2 | 932 | 938 | PF00498 | 0.305 |
LIG_HCF-1_HBM_1 | 431 | 434 | PF13415 | 0.511 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 334 | 345 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 492 | 500 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 699 | 707 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 725 | 736 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 918 | 928 | PF02991 | 0.287 |
LIG_LIR_LC3C_4 | 445 | 448 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 699 | 703 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 725 | 731 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 918 | 924 | PF02991 | 0.287 |
LIG_MYND_1 | 294 | 298 | PF01753 | 0.471 |
LIG_MYND_1 | 36 | 40 | PF01753 | 0.546 |
LIG_PCNA_yPIPBox_3 | 642 | 655 | PF02747 | 0.403 |
LIG_Pex14_1 | 337 | 341 | PF04695 | 0.534 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.407 |
LIG_PTB_Apo_2 | 880 | 887 | PF02174 | 0.283 |
LIG_REV1ctd_RIR_1 | 2 | 12 | PF16727 | 0.412 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.406 |
LIG_SH2_CRK | 742 | 746 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 351 | 354 | PF00017 | 0.513 |
LIG_SH2_PTP2 | 869 | 872 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 869 | 872 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 899 | 902 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 907 | 910 | PF00017 | 0.281 |
LIG_SH3_2 | 873 | 878 | PF14604 | 0.399 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.423 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.552 |
LIG_SH3_3 | 690 | 696 | PF00018 | 0.441 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.332 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.287 |
LIG_SH3_3 | 855 | 861 | PF00018 | 0.318 |
LIG_SH3_3 | 867 | 873 | PF00018 | 0.400 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 366 | 371 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 911 | 918 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 365 | 371 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 444 | 450 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 560 | 566 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 596 | 601 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 632 | 641 | PF11976 | 0.509 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.686 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.493 |
LIG_TYR_ITSM | 250 | 257 | PF00017 | 0.530 |
MOD_CDK_SPK_2 | 174 | 179 | PF00069 | 0.700 |
MOD_CDK_SPxK_1 | 731 | 737 | PF00069 | 0.450 |
MOD_CDK_SPxxK_3 | 174 | 181 | PF00069 | 0.569 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.692 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.639 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.577 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.431 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.492 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.532 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.355 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.709 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.712 |
MOD_CK1_1 | 931 | 937 | PF00069 | 0.434 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.643 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.694 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.466 |
MOD_CK2_1 | 871 | 877 | PF00069 | 0.504 |
MOD_CK2_1 | 905 | 911 | PF00069 | 0.294 |
MOD_DYRK1A_RPxSP_1 | 419 | 423 | PF00069 | 0.581 |
MOD_DYRK1A_RPxSP_1 | 792 | 796 | PF00069 | 0.420 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.729 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.421 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.688 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.570 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.433 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.664 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.666 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.711 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.665 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.479 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.569 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.542 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.355 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.340 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.406 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.404 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.487 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.469 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.534 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.827 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.549 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.640 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.514 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.432 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.670 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.699 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.738 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.463 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.399 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.345 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.548 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.716 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.521 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.711 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.287 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.287 |
MOD_LATS_1 | 19 | 25 | PF00433 | 0.437 |
MOD_LATS_1 | 962 | 968 | PF00433 | 0.524 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.581 |
MOD_N-GLC_1 | 696 | 701 | PF02516 | 0.475 |
MOD_N-GLC_1 | 731 | 736 | PF02516 | 0.542 |
MOD_N-GLC_1 | 757 | 762 | PF02516 | 0.352 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.528 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.315 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.413 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.587 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.344 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.546 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.605 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.364 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.515 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.420 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.384 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.556 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.455 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.459 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.646 |
MOD_PIKK_1 | 644 | 650 | PF00454 | 0.384 |
MOD_PIKK_1 | 819 | 825 | PF00454 | 0.287 |
MOD_PKA_1 | 964 | 970 | PF00069 | 0.721 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.793 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.587 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.437 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.288 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.338 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.495 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.781 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.520 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.658 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.562 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.486 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.575 |
MOD_Plk_1 | 691 | 697 | PF00069 | 0.532 |
MOD_Plk_1 | 757 | 763 | PF00069 | 0.420 |
MOD_Plk_2-3 | 426 | 432 | PF00069 | 0.587 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.514 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.445 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.525 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.446 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.460 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.487 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.352 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.573 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.590 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.749 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.407 |
MOD_ProDKin_1 | 792 | 798 | PF00069 | 0.420 |
MOD_SUMO_rev_2 | 131 | 135 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 702 | 712 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 836 | 841 | PF00179 | 0.279 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 869 | 872 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 866 | 868 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 945 | 948 | PF00400 | 0.428 |
TRG_NLS_MonoExtN_4 | 29 | 35 | PF00514 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 567 | 572 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 785 | 789 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 819 | 823 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H1 | Leptomonas seymouri | 59% | 100% |
A0A1X0P1J4 | Trypanosomatidae | 49% | 100% |
A0A3R7M308 | Trypanosoma rangeli | 50% | 100% |
A0A3S7X0L3 | Leishmania donovani | 32% | 100% |
A4HFM9 | Leishmania braziliensis | 32% | 100% |
A4HII5 | Leishmania braziliensis | 76% | 100% |
A4I2Q7 | Leishmania infantum | 32% | 100% |
A4I5S8 | Leishmania infantum | 99% | 100% |
C9ZR48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AD83 | Leishmania major | 33% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B124 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q741 | Leishmania major | 92% | 100% |
V5AUZ1 | Trypanosoma cruzi | 48% | 100% |