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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HAU6
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 12 |
GO:0006421 | asparaginyl-tRNA aminoacylation | 7 | 10 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043038 | amino acid activation | 4 | 12 |
GO:0043039 | tRNA aminoacylation | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 12 |
GO:0004816 | asparagine-tRNA ligase activity | 5 | 10 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 719 | 723 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 831 | 835 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 839 | 843 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 853 | 855 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.753 |
CLV_PCSK_FUR_1 | 174 | 178 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 661 | 663 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 731 | 733 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 837 | 839 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 853 | 855 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 661 | 663 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 731 | 733 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 837 | 839 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.757 |
CLV_Separin_Metazoa | 583 | 587 | PF03568 | 0.528 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 527 | 533 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 367 | 376 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 475 | 484 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 735 | 745 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 97 | 103 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 45 | 54 | PF00069 | 0.489 |
DOC_MAPK_RevD_3 | 162 | 177 | PF00069 | 0.715 |
DOC_MAPK_RevD_3 | 280 | 296 | PF00069 | 0.410 |
DOC_PP1_RVXF_1 | 867 | 874 | PF00149 | 0.487 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 166 | 169 | PF13499 | 0.700 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 527 | 530 | PF13499 | 0.498 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.496 |
DOC_USP7_MATH_2 | 181 | 187 | PF00917 | 0.503 |
DOC_USP7_UBL2_3 | 657 | 661 | PF12436 | 0.464 |
DOC_USP7_UBL2_3 | 727 | 731 | PF12436 | 0.496 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 114 | 119 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 444 | 451 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 481 | 485 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 662 | 670 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.743 |
LIG_Actin_WH2_2 | 100 | 116 | PF00022 | 0.496 |
LIG_Actin_WH2_2 | 372 | 388 | PF00022 | 0.548 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.487 |
LIG_eIF4E_1 | 827 | 833 | PF01652 | 0.573 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.673 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.497 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.475 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.453 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.497 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.508 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.544 |
LIG_FHA_1 | 804 | 810 | PF00498 | 0.487 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.626 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.520 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.693 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.503 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.494 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.476 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.498 |
LIG_FHA_2 | 694 | 700 | PF00498 | 0.586 |
LIG_FHA_2 | 802 | 808 | PF00498 | 0.499 |
LIG_LIR_Gen_1 | 483 | 489 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 537 | 545 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 614 | 622 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 665 | 674 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 678 | 686 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 780 | 789 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 483 | 487 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 665 | 670 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 678 | 682 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 844 | 849 | PF02991 | 0.506 |
LIG_Pex14_1 | 593 | 597 | PF04695 | 0.573 |
LIG_Pex14_2 | 588 | 592 | PF04695 | 0.498 |
LIG_Pex14_2 | 783 | 787 | PF04695 | 0.528 |
LIG_Rb_pABgroove_1 | 556 | 564 | PF01858 | 0.460 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.634 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.410 |
LIG_SH2_CRK | 647 | 651 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 538 | 542 | PF00017 | 0.410 |
LIG_SH2_SRC | 538 | 541 | PF00017 | 0.311 |
LIG_SH2_SRC | 739 | 742 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 739 | 743 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 829 | 833 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 627 | 630 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 849 | 852 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 849 | 852 | PF00017 | 0.487 |
LIG_SH3_1 | 727 | 733 | PF00018 | 0.492 |
LIG_SH3_2 | 730 | 735 | PF14604 | 0.487 |
LIG_SH3_2 | 87 | 92 | PF14604 | 0.749 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.576 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.487 |
LIG_SH3_3 | 727 | 733 | PF00018 | 0.500 |
LIG_SH3_3 | 808 | 814 | PF00018 | 0.476 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.749 |
LIG_SH3_CIN85_PxpxPR_1 | 133 | 138 | PF14604 | 0.488 |
LIG_SUMO_SIM_anti_2 | 141 | 149 | PF11976 | 0.485 |
LIG_SUMO_SIM_anti_2 | 51 | 57 | PF11976 | 0.485 |
LIG_SUMO_SIM_anti_2 | 806 | 813 | PF11976 | 0.487 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.795 |
LIG_TYR_ITSM | 191 | 198 | PF00017 | 0.480 |
LIG_UBA3_1 | 404 | 413 | PF00899 | 0.408 |
LIG_UBA3_1 | 874 | 881 | PF00899 | 0.573 |
LIG_WRC_WIRS_1 | 298 | 303 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 676 | 681 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 791 | 796 | PF05994 | 0.487 |
LIG_WW_3 | 215 | 219 | PF00397 | 0.524 |
MOD_CDK_SPK_2 | 271 | 276 | PF00069 | 0.487 |
MOD_CDK_SPK_2 | 726 | 731 | PF00069 | 0.535 |
MOD_CDK_SPxK_1 | 726 | 732 | PF00069 | 0.573 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.484 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.684 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.646 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.498 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.476 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.487 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.735 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.632 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.692 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.510 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.465 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.485 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.512 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.487 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.535 |
MOD_CK2_1 | 801 | 807 | PF00069 | 0.491 |
MOD_CMANNOS | 25 | 28 | PF00535 | 0.472 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.726 |
MOD_GlcNHglycan | 359 | 364 | PF01048 | 0.210 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.323 |
MOD_GlcNHglycan | 489 | 493 | PF01048 | 0.225 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.642 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.656 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.663 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.513 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.496 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.448 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.416 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.519 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.525 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.548 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.786 |
MOD_GSK3_1 | 801 | 808 | PF00069 | 0.513 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.754 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.210 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.677 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.702 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.744 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.527 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.532 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.656 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.498 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.502 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.487 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.535 |
MOD_NEK2_1 | 841 | 846 | PF00069 | 0.576 |
MOD_NEK2_2 | 612 | 617 | PF00069 | 0.487 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.519 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.487 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.410 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.538 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.412 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.512 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.631 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.487 |
MOD_PIKK_1 | 708 | 714 | PF00454 | 0.589 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.507 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.586 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.665 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.686 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.498 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.487 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.487 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.478 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.410 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.582 |
MOD_PKB_1 | 475 | 483 | PF00069 | 0.487 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.449 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.440 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.564 |
MOD_Plk_1 | 665 | 671 | PF00069 | 0.487 |
MOD_Plk_1 | 801 | 807 | PF00069 | 0.464 |
MOD_Plk_1 | 841 | 847 | PF00069 | 0.589 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.690 |
MOD_Plk_2-3 | 675 | 681 | PF00069 | 0.555 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.554 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.704 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.507 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.557 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.569 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.547 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.548 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.487 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.487 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.538 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.487 |
MOD_Plk_4 | 842 | 848 | PF00069 | 0.499 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.701 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.616 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.492 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.498 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.565 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.758 |
MOD_SUMO_for_1 | 422 | 425 | PF00179 | 0.746 |
MOD_SUMO_for_1 | 523 | 526 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 272 | 281 | PF00179 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 866 | 871 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 829 | 832 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 595 | 597 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 853 | 855 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMR3 | Leptomonas seymouri | 77% | 100% |
A0A0S4JDH2 | Bodo saltans | 61% | 100% |
A0A1X0P9Y4 | Trypanosomatidae | 64% | 100% |
A0A3R7P1H1 | Trypanosoma rangeli | 62% | 100% |
A0A3S7WWM6 | Leishmania donovani | 26% | 100% |
A0A3S7X7X7 | Leishmania donovani | 76% | 100% |
A4HBV0 | Leishmania braziliensis | 24% | 100% |
A4IA13 | Leishmania infantum | 76% | 100% |
C9ZMM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9AGV6 | Leishmania infantum | 26% | 100% |
E9B520 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q2W6 | Leishmania major | 76% | 99% |
Q4QCA9 | Leishmania major | 24% | 100% |
Q554D9 | Dictyostelium discoideum | 38% | 100% |
V5DGS5 | Trypanosoma cruzi | 62% | 100% |