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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0042579 | microbody | 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 | 1 |
Related structures:
AlphaFold database: E9B4A0
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 11 |
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006631 | fatty acid metabolic process | 4 | 11 |
GO:0006635 | fatty acid beta-oxidation | 6 | 10 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009062 | fatty acid catabolic process | 5 | 10 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016042 | lipid catabolic process | 4 | 10 |
GO:0016054 | organic acid catabolic process | 4 | 10 |
GO:0019395 | fatty acid oxidation | 5 | 10 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0030258 | lipid modification | 4 | 10 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 11 |
GO:0034440 | lipid oxidation | 5 | 10 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044242 | cellular lipid catabolic process | 4 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044282 | small molecule catabolic process | 3 | 10 |
GO:0046395 | carboxylic acid catabolic process | 5 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003857 | 3-hydroxyacyl-CoA dehydrogenase activity | 5 | 7 |
GO:0004300 | enoyl-CoA hydratase activity | 5 | 6 |
GO:0005488 | binding | 1 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 11 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 11 |
GO:0016829 | lyase activity | 2 | 6 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 6 |
GO:0016836 | hydro-lyase activity | 4 | 6 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0051287 | NAD binding | 4 | 11 |
GO:0070403 | NAD+ binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 827 | 829 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 831 | 833 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 897 | 899 | PF00675 | 0.383 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 764 | 766 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 825 | 827 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 831 | 833 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 678 | 680 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 825 | 827 | PF00082 | 0.527 |
CLV_PCSK_PC7_1 | 827 | 833 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 827 | 831 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 842 | 846 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 898 | 902 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 925 | 929 | PF00082 | 0.323 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.380 |
DEG_APCC_DBOX_1 | 606 | 614 | PF00400 | 0.404 |
DEG_APCC_DBOX_1 | 798 | 806 | PF00400 | 0.476 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.580 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.392 |
DOC_CDC14_PxL_1 | 590 | 598 | PF14671 | 0.396 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.572 |
DOC_CKS1_1 | 727 | 732 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 330 | 338 | PF00134 | 0.477 |
DOC_CYCLIN_RxL_1 | 635 | 648 | PF00134 | 0.404 |
DOC_CYCLIN_yCln2_LP_2 | 45 | 51 | PF00134 | 0.392 |
DOC_MAPK_FxFP_2 | 149 | 152 | PF00069 | 0.281 |
DOC_MAPK_FxFP_2 | 874 | 877 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 18 | 27 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 380 | 388 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 797 | 805 | PF00069 | 0.410 |
DOC_MAPK_HePTP_8 | 545 | 557 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 292 | 301 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 382 | 390 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 548 | 557 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 797 | 805 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 840 | 846 | PF00149 | 0.313 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.370 |
DOC_PP4_FxxP_1 | 149 | 152 | PF00568 | 0.261 |
DOC_PP4_FxxP_1 | 557 | 560 | PF00568 | 0.278 |
DOC_PP4_FxxP_1 | 874 | 877 | PF00568 | 0.484 |
DOC_PP4_FxxP_1 | 912 | 915 | PF00568 | 0.329 |
DOC_SPAK_OSR1_1 | 155 | 159 | PF12202 | 0.285 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 742 | 746 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 801 | 805 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 906 | 910 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 895 | 899 | PF12436 | 0.433 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 254 | 261 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 353 | 360 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 571 | 580 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 607 | 617 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 659 | 663 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.330 |
LIG_BIR_III_2 | 281 | 285 | PF00653 | 0.299 |
LIG_BRCT_BRCA1_1 | 526 | 530 | PF00533 | 0.235 |
LIG_BRCT_BRCA1_1 | 74 | 78 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 908 | 912 | PF00533 | 0.452 |
LIG_Clathr_ClatBox_1 | 643 | 647 | PF01394 | 0.404 |
LIG_eIF4E_1 | 603 | 609 | PF01652 | 0.332 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.276 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.287 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.373 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.598 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.292 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.307 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.378 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.126 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.370 |
LIG_FHA_1 | 784 | 790 | PF00498 | 0.732 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.422 |
LIG_FHA_2 | 727 | 733 | PF00498 | 0.498 |
LIG_HP1_1 | 801 | 805 | PF01393 | 0.464 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 693 | 699 | PF02991 | 0.439 |
LIG_LIR_Apic_2 | 909 | 915 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 13 | 20 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 837 | 848 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 928 | 933 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 591 | 596 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 611 | 617 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 722 | 728 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 815 | 821 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 837 | 843 | PF02991 | 0.445 |
LIG_LYPXL_SIV_4 | 327 | 335 | PF13949 | 0.474 |
LIG_LYPXL_yS_3 | 593 | 596 | PF13949 | 0.396 |
LIG_PCNA_TLS_4 | 454 | 461 | PF02747 | 0.396 |
LIG_Pex14_2 | 88 | 92 | PF04695 | 0.392 |
LIG_Pex14_2 | 929 | 933 | PF04695 | 0.379 |
LIG_PTB_Apo_2 | 691 | 698 | PF02174 | 0.235 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.428 |
LIG_SH2_CRK | 725 | 729 | PF00017 | 0.474 |
LIG_SH2_SRC | 886 | 889 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 814 | 818 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 886 | 890 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 727 | 730 | PF00017 | 0.500 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.392 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.521 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.413 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.703 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.407 |
LIG_SH3_3 | 671 | 677 | PF00018 | 0.663 |
LIG_SH3_3 | 681 | 687 | PF00018 | 0.679 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.368 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.307 |
LIG_SUMO_SIM_anti_2 | 426 | 432 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 436 | 442 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 439 | 444 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 594 | 599 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 67 | 75 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 801 | 807 | PF11976 | 0.443 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.396 |
LIG_TRAF2_1 | 729 | 732 | PF00917 | 0.462 |
LIG_TYR_ITIM | 816 | 821 | PF00017 | 0.392 |
LIG_UBA3_1 | 516 | 525 | PF00899 | 0.404 |
LIG_UBA3_1 | 586 | 592 | PF00899 | 0.401 |
LIG_WW_3 | 34 | 38 | PF00397 | 0.513 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.230 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.521 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.534 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.638 |
MOD_CK1_1 | 804 | 810 | PF00069 | 0.330 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.350 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.326 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.646 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.338 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.434 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.157 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.542 |
MOD_CK2_1 | 726 | 732 | PF00069 | 0.484 |
MOD_CMANNOS | 271 | 274 | PF00535 | 0.485 |
MOD_Cter_Amidation | 183 | 186 | PF01082 | 0.369 |
MOD_Cter_Amidation | 716 | 719 | PF01082 | 0.446 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.522 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.492 |
MOD_GlcNHglycan | 381 | 385 | PF01048 | 0.681 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.553 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.319 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.616 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.638 |
MOD_GlcNHglycan | 765 | 768 | PF01048 | 0.613 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.608 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.614 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.323 |
MOD_GlcNHglycan | 862 | 865 | PF01048 | 0.307 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.529 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.569 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.409 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.157 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.341 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.620 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.707 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.673 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.674 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.478 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.404 |
MOD_N-GLC_1 | 669 | 674 | PF02516 | 0.476 |
MOD_N-GLC_1 | 812 | 817 | PF02516 | 0.466 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.393 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.312 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.519 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.462 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.417 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.310 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.349 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.501 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.338 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.387 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.126 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.534 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.348 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.348 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.287 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.327 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.550 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.483 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.542 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.387 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.291 |
MOD_PKA_1 | 254 | 260 | PF00069 | 0.413 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.396 |
MOD_PKA_1 | 827 | 833 | PF00069 | 0.515 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.444 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.450 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.457 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.284 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.387 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.396 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.467 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.591 |
MOD_PKA_2 | 827 | 833 | PF00069 | 0.531 |
MOD_PKB_1 | 254 | 262 | PF00069 | 0.288 |
MOD_PKB_1 | 462 | 470 | PF00069 | 0.157 |
MOD_Plk_1 | 731 | 737 | PF00069 | 0.502 |
MOD_Plk_1 | 812 | 818 | PF00069 | 0.387 |
MOD_Plk_1 | 866 | 872 | PF00069 | 0.345 |
MOD_Plk_2-3 | 401 | 407 | PF00069 | 0.598 |
MOD_Plk_2-3 | 817 | 823 | PF00069 | 0.531 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.438 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.355 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.457 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.396 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.623 |
MOD_Plk_4 | 804 | 810 | PF00069 | 0.525 |
MOD_Plk_4 | 867 | 873 | PF00069 | 0.329 |
MOD_Plk_4 | 928 | 934 | PF00069 | 0.477 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.349 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.678 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.292 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.579 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.510 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_2 | 840 | 846 | PF01217 | 0.356 |
TRG_DiLeu_BaLyEn_6 | 604 | 609 | PF01217 | 0.356 |
TRG_DiLeu_BaLyEn_6 | 64 | 69 | PF01217 | 0.262 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 725 | 728 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 818 | 821 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 737 | 740 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 797 | 800 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 826 | 828 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 831 | 833 | PF00400 | 0.386 |
TRG_NES_CRM1_1 | 837 | 850 | PF08389 | 0.366 |
TRG_NLS_MonoCore_2 | 824 | 829 | PF00514 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 641 | 645 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 905 | 910 | PF00026 | 0.440 |
TRG_PTS2 | 1 | 11 | PF00400 | 0.636 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVX9 | Leptomonas seymouri | 58% | 100% |
A0A0N1PD28 | Leptomonas seymouri | 23% | 100% |
A0A0S4JJU7 | Bodo saltans | 25% | 100% |
A0A1X0NSP5 | Trypanosomatidae | 30% | 100% |
A0A3R7KS65 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X716 | Leishmania donovani | 88% | 100% |
A4HF10 | Leishmania braziliensis | 24% | 100% |
A4HLX1 | Leishmania braziliensis | 77% | 100% |
A4I9A0 | Leishmania infantum | 87% | 100% |
A4WCW6 | Enterobacter sp. (strain 638) | 26% | 100% |
A8A2L0 | Escherichia coli O9:H4 (strain HS) | 26% | 100% |
B5XVW2 | Klebsiella pneumoniae (strain 342) | 25% | 100% |
C9ZJC6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
P07896 | Rattus norvegicus | 27% | 100% |
P40939 | Homo sapiens | 24% | 100% |
P55100 | Cavia porcellus | 28% | 100% |
Q08426 | Homo sapiens | 27% | 100% |
Q29554 | Sus scrofa | 24% | 100% |
Q4Q3S6 | Leishmania major | 87% | 100% |
Q5R5M8 | Pongo abelii | 27% | 100% |
Q64428 | Rattus norvegicus | 24% | 100% |
Q6NYL3 | Danio rerio | 29% | 100% |
Q8BMS1 | Mus musculus | 24% | 100% |
Q9DBM2 | Mus musculus | 27% | 100% |
Q9ZPI6 | Arabidopsis thaliana | 24% | 100% |
V5BN63 | Trypanosoma cruzi | 30% | 100% |