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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WV22
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009451 | RNA modification | 5 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016070 | RNA metabolic process | 5 | 13 |
GO:0032259 | methylation | 2 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0043414 | macromolecule methylation | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003723 | RNA binding | 4 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008168 | methyltransferase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 688 | 694 | PF00089 | 0.486 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.500 |
CLV_PCSK_FUR_1 | 356 | 360 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 270 | 272 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.286 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.639 |
CLV_PCSK_PC7_1 | 682 | 688 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 696 | 700 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.490 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.687 |
DEG_ODPH_VHL_1 | 679 | 692 | PF01847 | 0.506 |
DEG_SIAH_1 | 730 | 738 | PF03145 | 0.640 |
DEG_SPOP_SBC_1 | 597 | 601 | PF00917 | 0.550 |
DOC_CKS1_1 | 212 | 217 | PF01111 | 0.499 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.560 |
DOC_CKS1_1 | 624 | 629 | PF01111 | 0.489 |
DOC_CYCLIN_RxL_1 | 433 | 445 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 682 | 693 | PF00134 | 0.533 |
DOC_CYCLIN_yCln2_LP_2 | 564 | 570 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 624 | 630 | PF00134 | 0.490 |
DOC_MAPK_gen_1 | 561 | 570 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 637 | 646 | PF00069 | 0.426 |
DOC_MAPK_HePTP_8 | 634 | 646 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 637 | 646 | PF00069 | 0.426 |
DOC_PP1_RVXF_1 | 684 | 691 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.563 |
DOC_PP2B_LxvP_1 | 564 | 567 | PF13499 | 0.481 |
DOC_PP4_FxxP_1 | 678 | 681 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.598 |
DOC_USP7_UBL2_3 | 344 | 348 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 346 | 354 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 414 | 424 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 621 | 627 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 682 | 690 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 824 | 828 | PF00244 | 0.614 |
LIG_APCC_ABBA_1 | 523 | 528 | PF00400 | 0.480 |
LIG_BRCT_BRCA1_1 | 674 | 678 | PF00533 | 0.499 |
LIG_deltaCOP1_diTrp_1 | 202 | 208 | PF00928 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 571 | 581 | PF00928 | 0.404 |
LIG_Dynein_DLC8_1 | 346 | 352 | PF01221 | 0.520 |
LIG_FAT_LD_1 | 75 | 83 | PF03623 | 0.537 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.569 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.552 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.390 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.418 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.520 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.489 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.547 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.428 |
LIG_FHA_1 | 762 | 768 | PF00498 | 0.559 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.586 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.546 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.539 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.491 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.689 |
LIG_FHA_2 | 751 | 757 | PF00498 | 0.705 |
LIG_LIR_Apic_2 | 545 | 549 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 636 | 642 | PF02991 | 0.434 |
LIG_LIR_Apic_2 | 675 | 681 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 156 | 162 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 202 | 212 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 39 | 47 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 572 | 582 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 89 | 97 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 712 | 717 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 815 | 819 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.578 |
LIG_MYND_1 | 509 | 513 | PF01753 | 0.577 |
LIG_NRBOX | 698 | 704 | PF00104 | 0.534 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.532 |
LIG_NRBOX | 740 | 746 | PF00104 | 0.680 |
LIG_Pex14_1 | 375 | 379 | PF04695 | 0.491 |
LIG_Pex14_1 | 420 | 424 | PF04695 | 0.480 |
LIG_Pex14_2 | 534 | 538 | PF04695 | 0.475 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.504 |
LIG_SH2_CRK | 639 | 643 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 709 | 712 | PF00017 | 0.656 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.465 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.502 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.532 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 474 | 480 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 755 | 765 | PF11976 | 0.661 |
LIG_SUMO_SIM_par_1 | 124 | 131 | PF11976 | 0.585 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.367 |
LIG_TRAF2_1 | 755 | 758 | PF00917 | 0.694 |
LIG_TRAF2_1 | 840 | 843 | PF00917 | 0.795 |
LIG_TRFH_1 | 610 | 614 | PF08558 | 0.451 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.512 |
LIG_WRC_WIRS_1 | 813 | 818 | PF05994 | 0.456 |
LIG_WW_1 | 512 | 515 | PF00397 | 0.472 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.428 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.470 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.492 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.472 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.378 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.373 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.320 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.595 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.692 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.725 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.369 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.307 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.626 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.549 |
MOD_CK2_1 | 736 | 742 | PF00069 | 0.692 |
MOD_CK2_1 | 752 | 758 | PF00069 | 0.586 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.558 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.592 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.656 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.575 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.769 |
MOD_GlcNHglycan | 204 | 208 | PF01048 | 0.457 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.527 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.398 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.363 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.415 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.383 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.323 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.323 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.396 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.756 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.719 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.598 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.380 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.370 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.511 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.409 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.473 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.747 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.693 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.515 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.535 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.509 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.411 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.452 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.323 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.323 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.323 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.755 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.551 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.651 |
MOD_GSK3_1 | 775 | 782 | PF00069 | 0.502 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.388 |
MOD_LATS_1 | 130 | 136 | PF00433 | 0.699 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.727 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.680 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.258 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.429 |
MOD_N-GLC_1 | 829 | 834 | PF02516 | 0.736 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.551 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.589 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.464 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.379 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.299 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.541 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.594 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.409 |
MOD_NEK2_2 | 406 | 411 | PF00069 | 0.323 |
MOD_NEK2_2 | 812 | 817 | PF00069 | 0.499 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.486 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.425 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.336 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.640 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.336 |
MOD_PIKK_1 | 762 | 768 | PF00454 | 0.625 |
MOD_PK_1 | 412 | 418 | PF00069 | 0.418 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.526 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.710 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.710 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.544 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.534 |
MOD_PKA_2 | 690 | 696 | PF00069 | 0.472 |
MOD_PKA_2 | 823 | 829 | PF00069 | 0.711 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.569 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.567 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.433 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.418 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.464 |
MOD_Plk_1 | 750 | 756 | PF00069 | 0.641 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.545 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.344 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.370 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.352 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.600 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.452 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.413 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.518 |
MOD_Plk_4 | 812 | 818 | PF00069 | 0.477 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.665 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.419 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.529 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.335 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.489 |
MOD_SUMO_rev_2 | 655 | 662 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 758 | 763 | PF01217 | 0.693 |
TRG_DiLeu_BaEn_1 | 823 | 828 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_2 | 203 | 209 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_2 | 673 | 679 | PF01217 | 0.499 |
TRG_DiLeu_LyEn_5 | 145 | 150 | PF01217 | 0.463 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 634 | 637 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 686 | 688 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.519 |
TRG_NES_CRM1_1 | 13 | 29 | PF08389 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 696 | 700 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H1 | Leptomonas seymouri | 72% | 98% |
A0A0S4KJ12 | Bodo saltans | 42% | 100% |
A0A1X0P6Y3 | Trypanosomatidae | 54% | 100% |
A0A3R7M922 | Trypanosoma rangeli | 52% | 100% |
A4H9M1 | Leishmania braziliensis | 83% | 99% |
A4HXY5 | Leishmania infantum | 99% | 100% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A5C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ARP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QDT1 | Leishmania major | 94% | 100% |
V5DFH6 | Trypanosoma cruzi | 52% | 100% |