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 | 1 |
GO:0005657 | replication fork | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0033061 | DNA recombinase mediator complex | 2 | 1 |
GO:0033063 | Rad51B-Rad51C-Rad51D-XRCC2 complex | 3 | 1 |
GO:0033065 | Rad51C-XRCC3 complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9B488
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 9 |
GO:0006974 | DNA damage response | 4 | 9 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0033554 | cellular response to stress | 3 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
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:0050896 | response to stimulus | 1 | 9 |
GO:0051716 | cellular response to stimulus | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0000707 | meiotic DNA recombinase assembly | 4 | 1 |
GO:0000730 | DNA recombinase assembly | 7 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0035825 | homologous recombination | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065004 | protein-DNA complex assembly | 6 | 1 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090735 | DNA repair complex assembly | 6 | 1 |
GO:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
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 | 0.786 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.662 |
CLV_MEL_PAP_1 | 668 | 674 | PF00089 | 0.428 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.815 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.818 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.835 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.402 |
DEG_SPOP_SBC_1 | 161 | 165 | PF00917 | 0.624 |
DOC_CYCLIN_RxL_1 | 109 | 123 | PF00134 | 0.685 |
DOC_CYCLIN_RxL_1 | 501 | 511 | PF00134 | 0.502 |
DOC_CYCLIN_yClb3_PxF_3 | 166 | 172 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 501 | 507 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 253 | 262 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.494 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.705 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 379 | 387 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 410 | 417 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 563 | 567 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 582 | 588 | PF00244 | 0.416 |
LIG_Actin_WH2_2 | 626 | 644 | PF00022 | 0.547 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.554 |
LIG_BIR_III_4 | 573 | 577 | PF00653 | 0.463 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.471 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.570 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.568 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.469 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.459 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.555 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.465 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.528 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.372 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.575 |
LIG_LIR_Apic_2 | 548 | 553 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 114 | 124 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 449 | 453 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 586 | 590 | PF02991 | 0.543 |
LIG_MAD2 | 639 | 647 | PF02301 | 0.526 |
LIG_NRBOX | 382 | 388 | PF00104 | 0.390 |
LIG_PCNA_yPIPBox_3 | 630 | 641 | PF02747 | 0.441 |
LIG_Rb_LxCxE_1 | 1 | 14 | PF01857 | 0.629 |
LIG_SH2_CRK | 550 | 554 | PF00017 | 0.372 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 550 | 554 | PF00017 | 0.372 |
LIG_SH2_NCK_1 | 590 | 594 | PF00017 | 0.514 |
LIG_SH2_PTP2 | 377 | 380 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.516 |
LIG_SH3_1 | 337 | 343 | PF00018 | 0.637 |
LIG_SH3_1 | 62 | 68 | PF00018 | 0.501 |
LIG_SH3_2 | 340 | 345 | PF14604 | 0.593 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.726 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.566 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.637 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.505 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.490 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.629 |
LIG_SUMO_SIM_anti_2 | 27 | 36 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 27 | 36 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.310 |
LIG_TYR_ITIM | 375 | 380 | PF00017 | 0.468 |
LIG_WRC_WIRS_1 | 222 | 227 | PF05994 | 0.488 |
LIG_WRC_WIRS_1 | 447 | 452 | PF05994 | 0.330 |
LIG_WRC_WIRS_1 | 584 | 589 | PF05994 | 0.497 |
LIG_WW_3 | 165 | 169 | PF00397 | 0.674 |
LIG_WW_3 | 338 | 342 | PF00397 | 0.520 |
MOD_CDC14_SPxK_1 | 165 | 168 | PF00782 | 0.546 |
MOD_CDC14_SPxK_1 | 331 | 334 | PF00782 | 0.637 |
MOD_CDC14_SPxK_1 | 338 | 341 | PF00782 | 0.568 |
MOD_CDC14_SPxK_1 | 489 | 492 | PF00782 | 0.547 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.639 |
MOD_CDK_SPxK_1 | 162 | 168 | PF00069 | 0.538 |
MOD_CDK_SPxK_1 | 328 | 334 | PF00069 | 0.641 |
MOD_CDK_SPxK_1 | 335 | 341 | PF00069 | 0.573 |
MOD_CDK_SPxK_1 | 486 | 492 | PF00069 | 0.557 |
MOD_CDK_SPxxK_3 | 328 | 335 | PF00069 | 0.644 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.761 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.433 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.623 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.734 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.526 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.642 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.541 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.556 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.543 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.582 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.481 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.516 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.528 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.473 |
MOD_DYRK1A_RPxSP_1 | 600 | 604 | PF00069 | 0.463 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.755 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.755 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.567 |
MOD_GlcNHglycan | 244 | 248 | PF01048 | 0.329 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.676 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.667 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.679 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.564 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.707 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.544 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.601 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.360 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.366 |
MOD_GlcNHglycan | 556 | 560 | PF01048 | 0.174 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.509 |
MOD_GlcNHglycan | 77 | 81 | PF01048 | 0.618 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.726 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.649 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.413 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.575 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.676 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.656 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.622 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.655 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.471 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.488 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.567 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.621 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.544 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.739 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.655 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.561 |
MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.482 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.323 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.586 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.522 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.587 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.466 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.421 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.697 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.604 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.507 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.471 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.514 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.459 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.522 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.453 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.344 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.504 |
MOD_NEK2_2 | 625 | 630 | PF00069 | 0.455 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.445 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.492 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.656 |
MOD_PKA_1 | 648 | 654 | PF00069 | 0.418 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.693 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.422 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.447 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.463 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.493 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.463 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.418 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.433 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.594 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.641 |
MOD_PKB_1 | 312 | 320 | PF00069 | 0.485 |
MOD_PKB_1 | 73 | 81 | PF00069 | 0.522 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.589 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.618 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.566 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.445 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.363 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.508 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.498 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.568 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.535 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.514 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.455 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.538 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.694 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.692 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.651 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.557 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.497 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 398 | 408 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 42 | 49 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.504 |
TRG_DiLeu_BaEn_2 | 111 | 117 | PF01217 | 0.579 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 501 | 506 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 579 | 584 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 72 | 75 | PF00400 | 0.798 |
TRG_NLS_MonoExtC_3 | 332 | 337 | PF00514 | 0.738 |
TRG_NLS_MonoExtN_4 | 332 | 338 | PF00514 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.725 |
TRG_Pf-PMV_PEXEL_1 | 504 | 508 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE01 | Leptomonas seymouri | 40% | 100% |
A0A1X0P3T9 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGS3 | Leishmania donovani | 84% | 99% |
A4HLW0 | Leishmania braziliensis | 67% | 100% |
D0A661 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AHR7 | Leishmania infantum | 84% | 99% |
Q4Q3T8 | Leishmania major | 83% | 100% |
V5BTS0 | Trypanosoma cruzi | 36% | 100% |