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. | yes | 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: A0A3S7X7X7
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 | 826 | 830 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 834 | 838 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 874 | 878 | PF00656 | 0.517 |
CLV_MEL_PAP_1 | 692 | 698 | PF00089 | 0.329 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.767 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.302 |
CLV_PCSK_FUR_1 | 173 | 177 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.767 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 726 | 728 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 832 | 834 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 656 | 658 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 726 | 728 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 832 | 834 | PF00082 | 0.396 |
CLV_PCSK_PC7_1 | 652 | 658 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.659 |
CLV_Separin_Metazoa | 578 | 582 | PF03568 | 0.568 |
DEG_APCC_DBOX_1 | 575 | 583 | PF00400 | 0.510 |
DEG_SCF_FBW7_1 | 190 | 197 | PF00400 | 0.612 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.602 |
DOC_CKS1_1 | 191 | 196 | PF01111 | 0.616 |
DOC_CYCLIN_yCln2_LP_2 | 107 | 113 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 165 | 171 | PF00134 | 0.649 |
DOC_CYCLIN_yCln2_LP_2 | 522 | 528 | PF00134 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.587 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 367 | 376 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 470 | 479 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 574 | 582 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 730 | 740 | PF00069 | 0.492 |
DOC_MAPK_RevD_3 | 163 | 176 | PF00069 | 0.637 |
DOC_PP1_RVXF_1 | 862 | 869 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.783 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.716 |
DOC_PP2B_LxvP_1 | 522 | 525 | PF13499 | 0.502 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 722 | 726 | PF12436 | 0.500 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.792 |
LIG_14-3-3_CanoR_1 | 148 | 157 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 173 | 179 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 657 | 665 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.763 |
LIG_Actin_WH2_2 | 372 | 388 | PF00022 | 0.559 |
LIG_APCC_ABBA_1 | 580 | 585 | PF00400 | 0.506 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.492 |
LIG_eIF4E_1 | 822 | 828 | PF01652 | 0.596 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.607 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.492 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.618 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.455 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.824 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.605 |
LIG_FHA_1 | 633 | 639 | PF00498 | 0.512 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.492 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.621 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.623 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.499 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.483 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.502 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.616 |
LIG_FHA_2 | 797 | 803 | PF00498 | 0.516 |
LIG_GBD_Chelix_1 | 198 | 206 | PF00786 | 0.561 |
LIG_LIR_Gen_1 | 478 | 484 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 532 | 540 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 609 | 617 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 660 | 669 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 673 | 681 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 682 | 693 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 775 | 784 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 436 | 441 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 478 | 482 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 532 | 536 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 660 | 665 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 673 | 677 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 839 | 844 | PF02991 | 0.511 |
LIG_MYND_1 | 86 | 90 | PF01753 | 0.613 |
LIG_Pex14_1 | 588 | 592 | PF04695 | 0.596 |
LIG_Pex14_2 | 583 | 587 | PF04695 | 0.502 |
LIG_Pex14_2 | 778 | 782 | PF04695 | 0.534 |
LIG_Rb_pABgroove_1 | 551 | 559 | PF01858 | 0.471 |
LIG_RPA_C_Fungi | 340 | 352 | PF08784 | 0.346 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 533 | 537 | PF00017 | 0.408 |
LIG_SH2_SRC | 630 | 633 | PF00017 | 0.453 |
LIG_SH2_SRC | 734 | 737 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 734 | 738 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 824 | 828 | PF00017 | 0.345 |
LIG_SH2_STAT3 | 622 | 625 | PF00017 | 0.397 |
LIG_SH2_STAT3 | 844 | 847 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.206 |
LIG_SH2_STAT5 | 844 | 847 | PF00017 | 0.326 |
LIG_SH3_1 | 722 | 728 | PF00018 | 0.333 |
LIG_SH3_2 | 725 | 730 | PF14604 | 0.326 |
LIG_SH3_2 | 87 | 92 | PF14604 | 0.663 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.540 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.753 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.424 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.568 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.326 |
LIG_SH3_3 | 712 | 718 | PF00018 | 0.345 |
LIG_SH3_3 | 722 | 728 | PF00018 | 0.413 |
LIG_SH3_3 | 792 | 798 | PF00018 | 0.397 |
LIG_SH3_3 | 803 | 809 | PF00018 | 0.341 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.663 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.509 |
LIG_SUMO_SIM_anti_2 | 801 | 808 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.603 |
LIG_TRAF2_2 | 705 | 710 | PF00917 | 0.397 |
LIG_UBA3_1 | 611 | 620 | PF00899 | 0.294 |
LIG_UBA3_1 | 869 | 876 | PF00899 | 0.471 |
LIG_WRC_WIRS_1 | 671 | 676 | PF05994 | 0.471 |
LIG_WRC_WIRS_1 | 786 | 791 | PF05994 | 0.326 |
LIG_WW_2 | 109 | 112 | PF00397 | 0.517 |
MOD_CDK_SPK_2 | 183 | 188 | PF00069 | 0.770 |
MOD_CDK_SPK_2 | 271 | 276 | PF00069 | 0.326 |
MOD_CDK_SPK_2 | 721 | 726 | PF00069 | 0.346 |
MOD_CDK_SPxK_1 | 190 | 196 | PF00069 | 0.719 |
MOD_CDK_SPxK_1 | 721 | 727 | PF00069 | 0.471 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.654 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.741 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.678 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.736 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.341 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.496 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.335 |
MOD_CK1_1 | 785 | 791 | PF00069 | 0.346 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.766 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.320 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.320 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.619 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.490 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.360 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.360 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.326 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.397 |
MOD_CK2_1 | 796 | 802 | PF00069 | 0.377 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.735 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.808 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.809 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.774 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.676 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.687 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.480 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.500 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.404 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.430 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.436 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.829 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.373 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.822 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.716 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.341 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.413 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.374 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.357 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.737 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.398 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.626 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.346 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.388 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.705 |
MOD_NEK2_2 | 607 | 612 | PF00069 | 0.326 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.326 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.375 |
MOD_PIKK_1 | 621 | 627 | PF00454 | 0.362 |
MOD_PIKK_1 | 703 | 709 | PF00454 | 0.388 |
MOD_PK_1 | 18 | 24 | PF00069 | 0.552 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.614 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.341 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.326 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.326 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.327 |
MOD_PKB_1 | 16 | 24 | PF00069 | 0.756 |
MOD_PKB_1 | 470 | 478 | PF00069 | 0.332 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.644 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.580 |
MOD_Plk_1 | 660 | 666 | PF00069 | 0.370 |
MOD_Plk_1 | 836 | 842 | PF00069 | 0.451 |
MOD_Plk_2-3 | 670 | 676 | PF00069 | 0.433 |
MOD_Plk_2-3 | 796 | 802 | PF00069 | 0.362 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.710 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.419 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.595 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.419 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.348 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.326 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.405 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.355 |
MOD_Plk_4 | 837 | 843 | PF00069 | 0.365 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.796 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.691 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.685 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.332 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.608 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.341 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.586 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.489 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.795 |
MOD_SUMO_for_1 | 417 | 420 | PF00179 | 0.723 |
MOD_SUMO_for_1 | 425 | 428 | PF00179 | 0.735 |
MOD_SUMO_for_1 | 518 | 521 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 271 | 281 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 407 | 415 | PF00179 | 0.628 |
TRG_DiLeu_BaLyEn_6 | 861 | 866 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 824 | 827 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.763 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 729 | 731 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 848 | 850 | PF00400 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 657 | 661 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMR3 | Leptomonas seymouri | 77% | 100% |
A0A0S4JDH2 | Bodo saltans | 60% | 100% |
A0A1X0P9Y4 | Trypanosomatidae | 62% | 100% |
A0A3R7P1H1 | Trypanosoma rangeli | 63% | 100% |
A4HAU6 | Leishmania braziliensis | 76% | 100% |
A4IA13 | Leishmania infantum | 100% | 100% |
C9ZMM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AV72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B520 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
Q4Q2W6 | Leishmania major | 94% | 100% |
Q554D9 | Dictyostelium discoideum | 39% | 100% |
V5DGS5 | Trypanosoma cruzi | 63% | 100% |