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: E9B520
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 | 820 | 824 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 828 | 832 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 868 | 872 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 842 | 844 | PF00675 | 0.297 |
CLV_PCSK_FUR_1 | 165 | 169 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 826 | 828 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 842 | 844 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 650 | 652 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 720 | 722 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 826 | 828 | PF00082 | 0.373 |
CLV_PCSK_PC7_1 | 646 | 652 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.764 |
CLV_Separin_Metazoa | 572 | 576 | PF03568 | 0.527 |
DEG_APCC_DBOX_1 | 569 | 577 | PF00400 | 0.535 |
DEG_SCF_FBW7_1 | 184 | 191 | PF00400 | 0.681 |
DEG_SPOP_SBC_1 | 121 | 125 | PF00917 | 0.653 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.683 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.662 |
DOC_CYCLIN_yCln2_LP_2 | 516 | 522 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.616 |
DOC_MAPK_gen_1 | 248 | 258 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 361 | 370 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 464 | 473 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 568 | 576 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 724 | 734 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 151 | 159 | PF00069 | 0.646 |
DOC_MAPK_RevD_3 | 153 | 168 | PF00069 | 0.719 |
DOC_PP1_RVXF_1 | 856 | 863 | PF00149 | 0.486 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.709 |
DOC_PP2B_LxvP_1 | 516 | 519 | PF13499 | 0.497 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.495 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 716 | 720 | PF12436 | 0.495 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.770 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 140 | 149 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 165 | 171 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 211 | 218 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 651 | 659 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.758 |
LIG_Actin_WH2_2 | 366 | 382 | PF00022 | 0.547 |
LIG_APCC_ABBA_1 | 574 | 579 | PF00400 | 0.535 |
LIG_APCC_ABBAyCdc20_2 | 284 | 290 | PF00400 | 0.392 |
LIG_BRCT_BRCA1_1 | 602 | 606 | PF00533 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 15 | 21 | PF00928 | 0.417 |
LIG_eIF4E_1 | 816 | 822 | PF01652 | 0.573 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.662 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.546 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.525 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.452 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.564 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.507 |
LIG_FHA_1 | 793 | 799 | PF00498 | 0.486 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.392 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.589 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.494 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.476 |
LIG_FHA_2 | 655 | 661 | PF00498 | 0.497 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.585 |
LIG_FHA_2 | 791 | 797 | PF00498 | 0.498 |
LIG_GBD_Chelix_1 | 192 | 200 | PF00786 | 0.579 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 472 | 478 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 526 | 534 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 603 | 611 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 654 | 663 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 667 | 675 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 769 | 778 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 526 | 530 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 583 | 589 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 654 | 659 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 667 | 671 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 833 | 838 | PF02991 | 0.505 |
LIG_MYND_1 | 78 | 82 | PF01753 | 0.679 |
LIG_Pex14_1 | 582 | 586 | PF04695 | 0.573 |
LIG_Pex14_2 | 577 | 581 | PF04695 | 0.497 |
LIG_Pex14_2 | 772 | 776 | PF04695 | 0.527 |
LIG_Rb_pABgroove_1 | 545 | 553 | PF01858 | 0.459 |
LIG_RPA_C_Fungi | 334 | 346 | PF08784 | 0.406 |
LIG_SH2_CRK | 527 | 531 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.417 |
LIG_SH2_SRC | 624 | 627 | PF00017 | 0.448 |
LIG_SH2_SRC | 728 | 731 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 728 | 732 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 616 | 619 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 838 | 841 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.156 |
LIG_SH2_STAT5 | 838 | 841 | PF00017 | 0.338 |
LIG_SH3_1 | 716 | 722 | PF00018 | 0.345 |
LIG_SH3_2 | 719 | 724 | PF14604 | 0.338 |
LIG_SH3_2 | 79 | 84 | PF14604 | 0.759 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.763 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.427 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.338 |
LIG_SH3_3 | 706 | 712 | PF00018 | 0.327 |
LIG_SH3_3 | 716 | 722 | PF00018 | 0.356 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.764 |
LIG_SH3_3 | 786 | 792 | PF00018 | 0.376 |
LIG_SH3_3 | 797 | 803 | PF00018 | 0.323 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.513 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 795 | 802 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 95 | 100 | PF11976 | 0.687 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.206 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.783 |
LIG_TRAF2_2 | 699 | 704 | PF00917 | 0.406 |
LIG_UBA3_1 | 605 | 614 | PF00899 | 0.300 |
LIG_UBA3_1 | 863 | 870 | PF00899 | 0.459 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.356 |
LIG_WRC_WIRS_1 | 665 | 670 | PF05994 | 0.459 |
LIG_WRC_WIRS_1 | 780 | 785 | PF05994 | 0.338 |
MOD_CDK_SPK_2 | 177 | 182 | PF00069 | 0.776 |
MOD_CDK_SPK_2 | 265 | 270 | PF00069 | 0.338 |
MOD_CDK_SPK_2 | 715 | 720 | PF00069 | 0.406 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.725 |
MOD_CDK_SPxK_1 | 715 | 721 | PF00069 | 0.459 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.748 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.734 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.667 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.354 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.477 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.338 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.406 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.331 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.319 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.482 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.373 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.373 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.338 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.406 |
MOD_CK2_1 | 790 | 796 | PF00069 | 0.344 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.759 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.413 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.772 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.692 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.667 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.653 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.355 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.450 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.239 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.384 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.391 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.423 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.788 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.375 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.704 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.444 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.767 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.354 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.731 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.392 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.730 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.360 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.338 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.406 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.643 |
MOD_NEK2_1 | 809 | 814 | PF00069 | 0.503 |
MOD_NEK2_1 | 830 | 835 | PF00069 | 0.463 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.719 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.652 |
MOD_NEK2_2 | 601 | 606 | PF00069 | 0.338 |
MOD_PIKK_1 | 301 | 307 | PF00454 | 0.338 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.373 |
MOD_PIKK_1 | 615 | 621 | PF00454 | 0.338 |
MOD_PIKK_1 | 697 | 703 | PF00454 | 0.481 |
MOD_PKA_1 | 211 | 217 | PF00069 | 0.607 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.632 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.354 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.338 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.338 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.326 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.594 |
MOD_PKB_1 | 464 | 472 | PF00069 | 0.338 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.568 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.338 |
MOD_Plk_1 | 830 | 836 | PF00069 | 0.481 |
MOD_Plk_2-3 | 664 | 670 | PF00069 | 0.433 |
MOD_Plk_2-3 | 790 | 796 | PF00069 | 0.375 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.695 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.436 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.453 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.546 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.423 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.338 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.338 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.410 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.338 |
MOD_Plk_4 | 831 | 837 | PF00069 | 0.356 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.612 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.715 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.701 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.345 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.554 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.614 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.354 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.448 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.772 |
MOD_SUMO_for_1 | 411 | 414 | PF00179 | 0.734 |
MOD_SUMO_for_1 | 419 | 422 | PF00179 | 0.732 |
MOD_SUMO_for_1 | 512 | 515 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 205 | 210 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 265 | 275 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 294 | 301 | PF00179 | 0.206 |
MOD_SUMO_rev_2 | 401 | 409 | PF00179 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 855 | 860 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 723 | 725 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 842 | 844 | PF00400 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 651 | 655 | PF00026 | 0.338 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMR3 | Leptomonas seymouri | 78% | 100% |
A0A0S4JDH2 | Bodo saltans | 60% | 100% |
A0A1X0P9Y4 | Trypanosomatidae | 65% | 100% |
A0A3R7P1H1 | Trypanosoma rangeli | 63% | 100% |
A0A3S7X7X7 | Leishmania donovani | 92% | 99% |
A4HAU6 | Leishmania braziliensis | 77% | 100% |
A4IA13 | Leishmania infantum | 92% | 99% |
C9ZMM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AV72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q2W6 | Leishmania major | 90% | 100% |
Q554D9 | Dictyostelium discoideum | 39% | 100% |
V5DGS5 | Trypanosoma cruzi | 63% | 100% |