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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q427
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0009982 | pseudouridine synthase activity | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016866 | intramolecular transferase activity | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 893 | 897 | PF00656 | 0.579 |
CLV_MEL_PAP_1 | 875 | 881 | PF00089 | 0.341 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.665 |
CLV_PCSK_FUR_1 | 274 | 278 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 830 | 832 | PF00082 | 0.763 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 545 | 547 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 830 | 832 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 833 | 837 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.573 |
CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.588 |
DEG_APCC_DBOX_1 | 456 | 464 | PF00400 | 0.506 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.667 |
DEG_SCF_TRCP1_1 | 657 | 662 | PF00400 | 0.534 |
DEG_SIAH_1 | 820 | 828 | PF03145 | 0.646 |
DOC_CDC14_PxL_1 | 70 | 78 | PF14671 | 0.588 |
DOC_CKS1_1 | 345 | 350 | PF01111 | 0.484 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.581 |
DOC_CYCLIN_RxL_1 | 720 | 731 | PF00134 | 0.554 |
DOC_CYCLIN_RxL_1 | 750 | 760 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 670 | 676 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 485 | 493 | PF00069 | 0.262 |
DOC_MAPK_gen_1 | 722 | 728 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 444 | 451 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.311 |
DOC_PP2B_LxvP_1 | 670 | 673 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 773 | 776 | PF00568 | 0.529 |
DOC_PP4_FxxP_1 | 782 | 785 | PF00568 | 0.674 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 774 | 778 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 788 | 792 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 849 | 853 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 877 | 881 | PF00917 | 0.438 |
DOC_USP7_MATH_2 | 310 | 316 | PF00917 | 0.458 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 285 | 292 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 685 | 689 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 723 | 729 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 733 | 742 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 833 | 840 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 878 | 882 | PF00244 | 0.373 |
LIG_Actin_WH2_2 | 881 | 897 | PF00022 | 0.400 |
LIG_BIR_III_4 | 468 | 472 | PF00653 | 0.393 |
LIG_BRCT_BRCA1_1 | 699 | 703 | PF00533 | 0.494 |
LIG_deltaCOP1_diTrp_1 | 588 | 595 | PF00928 | 0.423 |
LIG_DLG_GKlike_1 | 375 | 383 | PF00625 | 0.342 |
LIG_EVH1_1 | 131 | 135 | PF00568 | 0.575 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.417 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.458 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.352 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.546 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.464 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.628 |
LIG_FHA_1 | 834 | 840 | PF00498 | 0.606 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.450 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.572 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.472 |
LIG_FHA_2 | 798 | 804 | PF00498 | 0.337 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.659 |
LIG_GBD_Chelix_1 | 162 | 170 | PF00786 | 0.409 |
LIG_GBD_Chelix_1 | 178 | 186 | PF00786 | 0.370 |
LIG_HP1_1 | 456 | 460 | PF01393 | 0.362 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.656 |
LIG_LIR_Apic_2 | 772 | 776 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 613 | 624 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 749 | 755 | PF02991 | 0.439 |
LIG_PDZ_Class_1 | 894 | 899 | PF00595 | 0.504 |
LIG_Pex14_1 | 769 | 773 | PF04695 | 0.501 |
LIG_REV1ctd_RIR_1 | 531 | 539 | PF16727 | 0.438 |
LIG_RPA_C_Fungi | 175 | 187 | PF08784 | 0.397 |
LIG_RPA_C_Fungi | 370 | 382 | PF08784 | 0.270 |
LIG_RPA_C_Fungi | 680 | 692 | PF08784 | 0.362 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 548 | 552 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 678 | 682 | PF00017 | 0.391 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.560 |
LIG_SH2_SRC | 548 | 551 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.624 |
LIG_SH3_1 | 129 | 135 | PF00018 | 0.579 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.579 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.575 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.365 |
LIG_SH3_3 | 748 | 754 | PF00018 | 0.418 |
LIG_Sin3_3 | 212 | 219 | PF02671 | 0.346 |
LIG_SUMO_SIM_anti_2 | 707 | 713 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 666 | 671 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 693 | 698 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 753 | 758 | PF11976 | 0.361 |
LIG_TYR_ITIM | 487 | 492 | PF00017 | 0.448 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.586 |
LIG_WRC_WIRS_1 | 301 | 306 | PF05994 | 0.392 |
MOD_CDC14_SPxK_1 | 483 | 486 | PF00782 | 0.440 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.513 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.595 |
MOD_CDK_SPK_2 | 452 | 457 | PF00069 | 0.408 |
MOD_CDK_SPK_2 | 480 | 485 | PF00069 | 0.388 |
MOD_CDK_SPxK_1 | 480 | 486 | PF00069 | 0.483 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.599 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.502 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.494 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.558 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.497 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.509 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.472 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.680 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.503 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.571 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.448 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.460 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.666 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.600 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.461 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.729 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.549 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.456 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.616 |
MOD_CMANNOS | 591 | 594 | PF00535 | 0.462 |
MOD_DYRK1A_RPxSP_1 | 239 | 243 | PF00069 | 0.547 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.689 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.567 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.654 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.413 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.449 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.573 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.706 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.530 |
MOD_GlcNHglycan | 656 | 660 | PF01048 | 0.661 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.683 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.478 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.585 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.593 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.390 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.545 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.552 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.650 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.529 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.370 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.734 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.468 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.679 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.484 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.601 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.755 |
MOD_N-GLC_1 | 747 | 752 | PF02516 | 0.479 |
MOD_N-GLC_1 | 791 | 796 | PF02516 | 0.619 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.587 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.542 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.423 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.388 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.335 |
MOD_NEK2_1 | 894 | 899 | PF00069 | 0.531 |
MOD_NEK2_2 | 684 | 689 | PF00069 | 0.423 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.575 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.553 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.587 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.413 |
MOD_PIKK_1 | 676 | 682 | PF00454 | 0.428 |
MOD_PIKK_1 | 728 | 734 | PF00454 | 0.689 |
MOD_PIKK_1 | 803 | 809 | PF00454 | 0.395 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.666 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.569 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.402 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.443 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.482 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.719 |
MOD_PKA_2 | 684 | 690 | PF00069 | 0.459 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.449 |
MOD_PKA_2 | 877 | 883 | PF00069 | 0.483 |
MOD_PKB_1 | 722 | 730 | PF00069 | 0.540 |
MOD_PKB_1 | 831 | 839 | PF00069 | 0.627 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.617 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.410 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.347 |
MOD_Plk_1 | 747 | 753 | PF00069 | 0.466 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.502 |
MOD_Plk_1 | 791 | 797 | PF00069 | 0.611 |
MOD_Plk_2-3 | 559 | 565 | PF00069 | 0.389 |
MOD_Plk_2-3 | 698 | 704 | PF00069 | 0.487 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.551 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.435 |
MOD_Plk_4 | 791 | 797 | PF00069 | 0.540 |
MOD_Plk_4 | 850 | 856 | PF00069 | 0.611 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.718 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.583 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.560 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.477 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.599 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.394 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.634 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.362 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.759 |
MOD_SUMO_rev_2 | 315 | 325 | PF00179 | 0.633 |
TRG_DiLeu_BaLyEn_6 | 751 | 756 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 546 | 548 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 722 | 724 | PF00400 | 0.630 |
TRG_NLS_MonoExtC_3 | 544 | 550 | PF00514 | 0.357 |
TRG_NLS_MonoExtN_4 | 827 | 834 | PF00514 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 444 | 448 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 753 | 758 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 833 | 837 | PF00026 | 0.620 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E0 | Leptomonas seymouri | 47% | 99% |
A0A1X0P134 | Trypanosomatidae | 24% | 100% |
A0A3Q8IEW6 | Leishmania donovani | 93% | 100% |
A0A3R7KAP3 | Trypanosoma rangeli | 29% | 100% |
A4HLM1 | Leishmania braziliensis | 78% | 100% |
A4I932 | Leishmania infantum | 93% | 100% |
D0A535 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B3Z7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BLS1 | Trypanosoma cruzi | 29% | 100% |