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: 1, no: 13 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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: A0A3S7X658
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 15 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 15 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009451 | RNA modification | 5 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016070 | RNA metabolic process | 5 | 15 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 15 |
GO:0043170 | macromolecule metabolic process | 3 | 15 |
GO:0043412 | macromolecule modification | 4 | 15 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 15 |
GO:0046483 | heterocycle metabolic process | 3 | 15 |
GO:0071704 | organic substance metabolic process | 2 | 15 |
GO:0090304 | nucleic acid metabolic process | 4 | 15 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 15 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006399 | tRNA metabolic process | 7 | 3 |
GO:0008033 | tRNA processing | 8 | 3 |
GO:0034470 | ncRNA processing | 7 | 3 |
GO:0034660 | ncRNA metabolic process | 6 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 15 |
GO:0003723 | RNA binding | 4 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0009982 | pseudouridine synthase activity | 4 | 15 |
GO:0016853 | isomerase activity | 2 | 15 |
GO:0016866 | intramolecular transferase activity | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:0016829 | lyase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.568 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.707 |
CLV_PCSK_FUR_1 | 194 | 198 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.451 |
CLV_Separin_Metazoa | 154 | 158 | PF03568 | 0.447 |
DEG_APCC_DBOX_1 | 592 | 600 | PF00400 | 0.348 |
DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.446 |
DEG_MDM2_SWIB_1 | 422 | 430 | PF02201 | 0.382 |
DEG_ODPH_VHL_1 | 571 | 584 | PF01847 | 0.275 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.535 |
DOC_CYCLIN_RxL_1 | 293 | 302 | PF00134 | 0.273 |
DOC_CYCLIN_yCln2_LP_2 | 311 | 317 | PF00134 | 0.355 |
DOC_CYCLIN_yCln2_LP_2 | 601 | 607 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 271 | 278 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 636 | 643 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 688 | 695 | PF00069 | 0.270 |
DOC_MAPK_NFAT4_5 | 688 | 696 | PF00069 | 0.267 |
DOC_PP1_RVXF_1 | 347 | 354 | PF00149 | 0.382 |
DOC_PP1_RVXF_1 | 621 | 628 | PF00149 | 0.438 |
DOC_PP4_FxxP_1 | 695 | 698 | PF00568 | 0.319 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.266 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.568 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 297 | 306 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 326 | 336 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 405 | 413 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 468 | 472 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 626 | 633 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 688 | 692 | PF00244 | 0.444 |
LIG_BIR_III_2 | 17 | 21 | PF00653 | 0.478 |
LIG_BIR_III_2 | 218 | 222 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 517 | 521 | PF00533 | 0.235 |
LIG_deltaCOP1_diTrp_1 | 624 | 633 | PF00928 | 0.360 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.386 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.479 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.437 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.245 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.617 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.633 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.740 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.347 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.388 |
LIG_LIR_Apic_2 | 694 | 698 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 320 | 329 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 439 | 448 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 489 | 500 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 575 | 584 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 700 | 710 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 320 | 324 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 575 | 579 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 646 | 650 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 700 | 705 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.507 |
LIG_LYPXL_S_1 | 159 | 163 | PF13949 | 0.540 |
LIG_LYPXL_yS_3 | 160 | 163 | PF13949 | 0.397 |
LIG_MLH1_MIPbox_1 | 517 | 521 | PF16413 | 0.382 |
LIG_NRBOX | 84 | 90 | PF00104 | 0.399 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.248 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.375 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.382 |
LIG_SH2_CRK | 576 | 580 | PF00017 | 0.477 |
LIG_SH2_CRK | 702 | 706 | PF00017 | 0.258 |
LIG_SH2_NCK_1 | 702 | 706 | PF00017 | 0.285 |
LIG_SH2_PTP2 | 235 | 238 | PF00017 | 0.276 |
LIG_SH2_SRC | 235 | 238 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 576 | 580 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 702 | 706 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.159 |
LIG_SH3_1 | 125 | 131 | PF00018 | 0.520 |
LIG_SH3_2 | 128 | 133 | PF14604 | 0.495 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.590 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.526 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.240 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.475 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.451 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.338 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.296 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.432 |
LIG_TRFH_1 | 695 | 699 | PF08558 | 0.402 |
LIG_TYR_ITIM | 574 | 579 | PF00017 | 0.280 |
LIG_WW_2 | 19 | 22 | PF00397 | 0.486 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.520 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.625 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.337 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.666 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.257 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.259 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.722 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.439 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.474 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.615 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.591 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.347 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.377 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.542 |
MOD_CMANNOS | 610 | 613 | PF00535 | 0.459 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.619 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.267 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.663 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.303 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.320 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.386 |
MOD_GlcNHglycan | 546 | 550 | PF01048 | 0.777 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.643 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.661 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.506 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.514 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.529 |
MOD_GlcNHglycan | 680 | 684 | PF01048 | 0.728 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.541 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.476 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.370 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.403 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.723 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.536 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.641 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.380 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.327 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.564 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.527 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.362 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.517 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.320 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.447 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.400 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.217 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.408 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.310 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.373 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.304 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.484 |
MOD_NEK2_2 | 429 | 434 | PF00069 | 0.382 |
MOD_NEK2_2 | 515 | 520 | PF00069 | 0.382 |
MOD_NEK2_2 | 595 | 600 | PF00069 | 0.353 |
MOD_NEK2_2 | 701 | 706 | PF00069 | 0.387 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.412 |
MOD_PK_1 | 261 | 267 | PF00069 | 0.243 |
MOD_PK_1 | 274 | 280 | PF00069 | 0.216 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.703 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.270 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.435 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.266 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.303 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.610 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.469 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.372 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.469 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.564 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.226 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.522 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.428 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.613 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.653 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.293 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.293 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.310 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.552 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.359 |
TRG_DiLeu_BaEn_1 | 249 | 254 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_3 | 379 | 385 | PF01217 | 0.226 |
TRG_DiLeu_BaEn_4 | 376 | 382 | PF01217 | 0.198 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.262 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 636 | 638 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 671 | 673 | PF00400 | 0.441 |
TRG_NES_CRM1_1 | 249 | 262 | PF08389 | 0.291 |
TRG_NLS_MonoExtC_3 | 240 | 246 | PF00514 | 0.248 |
TRG_Pf-PMV_PEXEL_1 | 251 | 256 | PF00026 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 297 | 302 | PF00026 | 0.184 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F4 | Leptomonas seymouri | 51% | 75% |
A0A0S4JDL8 | Bodo saltans | 27% | 100% |
A0A1X0NRV3 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJ87 | Leishmania donovani | 23% | 100% |
A0A3R7LD82 | Trypanosoma rangeli | 33% | 100% |
A4HKY3 | Leishmania braziliensis | 74% | 100% |
A4I8G2 | Leishmania infantum | 100% | 100% |
A4IDY9 | Leishmania infantum | 23% | 100% |
D0AAQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B3C1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q08647 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
Q1L8I0 | Danio rerio | 23% | 100% |
Q4Q0I6 | Leishmania major | 23% | 100% |
Q4Q4T4 | Leishmania major | 92% | 99% |
V5BLA6 | Trypanosoma cruzi | 32% | 100% |