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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005657 | replication fork | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0033061 | DNA recombinase mediator complex | 2 | 2 |
GO:0033063 | Rad51B-Rad51C-Rad51D-XRCC2 complex | 3 | 2 |
GO:0033065 | Rad51C-XRCC3 complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q3T8
Term | Name | Level | Count |
---|---|---|---|
GO:0000707 | meiotic DNA recombinase assembly | 4 | 2 |
GO:0000730 | DNA recombinase assembly | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0007131 | reciprocal meiotic recombination | 3 | 2 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0035825 | homologous recombination | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0061982 | meiosis I cell cycle process | 3 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065004 | protein-DNA complex assembly | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:0090735 | DNA repair complex assembly | 6 | 2 |
GO:0140527 | reciprocal homologous recombination | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140299 | small molecule sensor activity | 1 | 10 |
GO:0140612 | DNA damage sensor activity | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 42 | 46 | PF00656 | 0.769 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.695 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.804 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.796 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.813 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.556 |
DOC_CYCLIN_RxL_1 | 109 | 123 | PF00134 | 0.684 |
DOC_CYCLIN_RxL_1 | 501 | 511 | PF00134 | 0.471 |
DOC_MAPK_gen_1 | 501 | 507 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 566 | 572 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 253 | 262 | PF00069 | 0.444 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.388 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 379 | 387 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 53 | 63 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 566 | 571 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.310 |
LIG_Actin_WH2_2 | 630 | 648 | PF00022 | 0.527 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.527 |
LIG_BIR_III_4 | 577 | 581 | PF00653 | 0.402 |
LIG_BIR_III_4 | 77 | 81 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.434 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.473 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.573 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.435 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.533 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.342 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.551 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.537 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.453 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.440 |
LIG_Integrin_RGD_1 | 189 | 191 | PF01839 | 0.503 |
LIG_LIR_Gen_1 | 114 | 124 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 590 | 594 | PF02991 | 0.560 |
LIG_MAD2 | 643 | 651 | PF02301 | 0.522 |
LIG_NRBOX | 382 | 388 | PF00104 | 0.426 |
LIG_PCNA_yPIPBox_3 | 634 | 645 | PF02747 | 0.424 |
LIG_Rb_LxCxE_1 | 1 | 14 | PF01857 | 0.603 |
LIG_SH2_CRK | 594 | 598 | PF00017 | 0.708 |
LIG_SH2_NCK_1 | 594 | 598 | PF00017 | 0.597 |
LIG_SH2_PTP2 | 377 | 380 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.371 |
LIG_SH3_2 | 68 | 73 | PF14604 | 0.613 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.700 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.552 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.505 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.594 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.620 |
LIG_SUMO_SIM_anti_2 | 27 | 36 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 27 | 36 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.307 |
LIG_TRAF2_1 | 548 | 551 | PF00917 | 0.527 |
LIG_TYR_ITIM | 375 | 380 | PF00017 | 0.490 |
LIG_WRC_WIRS_1 | 222 | 227 | PF05994 | 0.484 |
LIG_WRC_WIRS_1 | 588 | 593 | PF05994 | 0.444 |
LIG_WW_3 | 165 | 169 | PF00397 | 0.635 |
MOD_CDC14_SPxK_1 | 331 | 334 | PF00782 | 0.624 |
MOD_CDC14_SPxK_1 | 489 | 492 | PF00782 | 0.532 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.623 |
MOD_CDK_SPxK_1 | 328 | 334 | PF00069 | 0.625 |
MOD_CDK_SPxK_1 | 413 | 419 | PF00069 | 0.533 |
MOD_CDK_SPxK_1 | 486 | 492 | PF00069 | 0.545 |
MOD_CDK_SPxxK_3 | 328 | 335 | PF00069 | 0.627 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.762 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.417 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.670 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.461 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.652 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.556 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.716 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.706 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.572 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.656 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.533 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.687 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.529 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.580 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.437 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.434 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.442 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.669 |
MOD_DYRK1A_RPxSP_1 | 604 | 608 | PF00069 | 0.572 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.776 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.754 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.467 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.194 |
MOD_GlcNHglycan | 244 | 248 | PF01048 | 0.325 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.747 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.676 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.635 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.679 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.527 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.568 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.734 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.775 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.485 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.506 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.580 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.768 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.401 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.596 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.578 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.650 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.586 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.627 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.690 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.599 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.451 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.620 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.382 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.685 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.770 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.576 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.712 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.731 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.660 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.621 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.695 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.590 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.539 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.638 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.495 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.404 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.502 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.451 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.456 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.401 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.662 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.457 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.468 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.368 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.605 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.501 |
MOD_NEK2_2 | 481 | 486 | PF00069 | 0.491 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.442 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.549 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.550 |
MOD_PIKK_1 | 621 | 627 | PF00454 | 0.526 |
MOD_PIKK_1 | 670 | 676 | PF00454 | 0.566 |
MOD_PK_1 | 566 | 572 | PF00069 | 0.468 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.495 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.637 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.468 |
MOD_PKA_1 | 652 | 658 | PF00069 | 0.406 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.606 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.467 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.774 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.442 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.561 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.511 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.392 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.490 |
MOD_PKA_2 | 603 | 609 | PF00069 | 0.573 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.456 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.594 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.654 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.543 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.502 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.390 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.442 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.501 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.476 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.463 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.535 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.520 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.609 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.625 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.664 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.621 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.545 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.610 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.603 |
MOD_SUMO_rev_2 | 398 | 408 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 42 | 49 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_2 | 111 | 117 | PF01217 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.574 |
TRG_DiLeu_BaLyEn_6 | 501 | 506 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 633 | 635 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 651 | 653 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 680 | 683 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.781 |
TRG_ER_diArg_1 | 74 | 76 | PF00400 | 0.803 |
TRG_NLS_MonoExtC_3 | 332 | 337 | PF00514 | 0.728 |
TRG_NLS_MonoExtN_4 | 332 | 338 | PF00514 | 0.730 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 504 | 508 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE01 | Leptomonas seymouri | 42% | 100% |
A0A1X0P3T9 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGS3 | Leishmania donovani | 89% | 100% |
A4HLW0 | Leishmania braziliensis | 67% | 100% |
D0A661 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AHR7 | Leishmania infantum | 89% | 100% |
E9B488 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BTS0 | Trypanosoma cruzi | 36% | 100% |