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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
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 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9ACY2
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 2 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 2 |
GO:0042254 | ribosome biogenesis | 5 | 2 |
GO:0044085 | cellular component biogenesis | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 385 | 389 | PF00656 | 0.390 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.276 |
CLV_C14_Caspase3-7 | 463 | 467 | PF00656 | 0.647 |
CLV_C14_Caspase3-7 | 469 | 473 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 760 | 762 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 771 | 773 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 740 | 742 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.250 |
CLV_PCSK_PC1ET2_1 | 740 | 742 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 770 | 772 | PF00082 | 0.613 |
CLV_PCSK_PC7_1 | 736 | 742 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 679 | 683 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 761 | 765 | PF00082 | 0.553 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.527 |
DEG_APCC_KENBOX_2 | 652 | 656 | PF00400 | 0.216 |
DOC_CDC14_PxL_1 | 127 | 135 | PF14671 | 0.521 |
DOC_CKS1_1 | 264 | 269 | PF01111 | 0.461 |
DOC_CYCLIN_RxL_1 | 215 | 226 | PF00134 | 0.536 |
DOC_CYCLIN_RxL_1 | 676 | 686 | PF00134 | 0.411 |
DOC_CYCLIN_RxL_1 | 773 | 787 | PF00134 | 0.652 |
DOC_MAPK_DCC_7 | 773 | 783 | PF00069 | 0.720 |
DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 373 | 382 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 514 | 524 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 738 | 746 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 83 | 91 | PF00069 | 0.707 |
DOC_MAPK_MEF2A_6 | 205 | 214 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 364 | 372 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.421 |
DOC_PP1_RVXF_1 | 157 | 163 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 391 | 398 | PF00149 | 0.341 |
DOC_PP1_RVXF_1 | 518 | 525 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 535 | 541 | PF00149 | 0.415 |
DOC_PP1_RVXF_1 | 677 | 684 | PF00149 | 0.360 |
DOC_PP1_RVXF_1 | 777 | 784 | PF00149 | 0.585 |
DOC_PP2B_LxvP_1 | 533 | 536 | PF13499 | 0.450 |
DOC_PP4_FxxP_1 | 357 | 360 | PF00568 | 0.454 |
DOC_PP4_FxxP_1 | 572 | 575 | PF00568 | 0.349 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.260 |
DOC_USP7_UBL2_3 | 617 | 621 | PF12436 | 0.383 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.688 |
DOC_USP7_UBL2_3 | 773 | 777 | PF12436 | 0.701 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 337 | 343 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 375 | 379 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 432 | 437 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 514 | 524 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 676 | 682 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 751 | 756 | PF00244 | 0.508 |
LIG_Actin_WH2_2 | 292 | 308 | PF00022 | 0.536 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.612 |
LIG_BRCT_BRCA1_1 | 402 | 406 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 568 | 572 | PF00533 | 0.345 |
LIG_BRCT_BRCA1_1 | 679 | 683 | PF00533 | 0.423 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.770 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.466 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.472 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.417 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.450 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.485 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.439 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.705 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.495 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.468 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.433 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.514 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.361 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.372 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.271 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.566 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.509 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.588 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.582 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.450 |
LIG_LIR_Apic_2 | 355 | 360 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 569 | 575 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 403 | 414 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 460 | 468 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 605 | 615 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 749 | 756 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 605 | 611 | PF02991 | 0.382 |
LIG_MLH1_MIPbox_1 | 679 | 683 | PF16413 | 0.423 |
LIG_NRBOX | 18 | 24 | PF00104 | 0.604 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.450 |
LIG_NRBOX | 375 | 381 | PF00104 | 0.442 |
LIG_PCNA_yPIPBox_3 | 700 | 713 | PF02747 | 0.519 |
LIG_PDZ_Class_2 | 783 | 788 | PF00595 | 0.584 |
LIG_Pex14_1 | 540 | 544 | PF04695 | 0.450 |
LIG_RPA_C_Fungi | 767 | 779 | PF08784 | 0.653 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.300 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 186 | 190 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 367 | 370 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.654 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.251 |
LIG_SH2_SRC | 544 | 547 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.589 |
LIG_SH3_1 | 544 | 550 | PF00018 | 0.360 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.388 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.431 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.360 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.637 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.684 |
LIG_SUMO_SIM_anti_2 | 209 | 215 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 260 | 266 | PF11976 | 0.337 |
LIG_UBA3_1 | 141 | 150 | PF00899 | 0.532 |
LIG_UBA3_1 | 270 | 275 | PF00899 | 0.327 |
LIG_UBA3_1 | 296 | 303 | PF00899 | 0.341 |
LIG_UBA3_1 | 308 | 315 | PF00899 | 0.277 |
LIG_UBA3_1 | 36 | 42 | PF00899 | 0.669 |
LIG_UBA3_1 | 612 | 617 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 379 | 384 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 458 | 463 | PF05994 | 0.586 |
LIG_WRC_WIRS_1 | 608 | 613 | PF05994 | 0.377 |
MOD_CDK_SPxK_1 | 263 | 269 | PF00069 | 0.303 |
MOD_CDK_SPxxK_3 | 198 | 205 | PF00069 | 0.450 |
MOD_CDK_SPxxK_3 | 413 | 420 | PF00069 | 0.506 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.295 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.652 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.474 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.429 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.464 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.674 |
MOD_CK1_1 | 754 | 760 | PF00069 | 0.673 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.699 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.646 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.588 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.700 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.450 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.724 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.659 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.309 |
MOD_GlcNHglycan | 27 | 31 | PF01048 | 0.674 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.298 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.698 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.513 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.674 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.744 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.773 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.431 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.290 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.604 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.314 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.407 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.303 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.496 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.186 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.351 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.402 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.611 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.690 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.609 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.411 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.616 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.681 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.607 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.725 |
MOD_N-GLC_2 | 730 | 732 | PF02516 | 0.512 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.684 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.553 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.516 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.303 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.347 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.436 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.540 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.548 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.417 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.351 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.407 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.577 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.353 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.548 |
MOD_PIKK_1 | 754 | 760 | PF00454 | 0.656 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.652 |
MOD_PKA_1 | 724 | 730 | PF00069 | 0.688 |
MOD_PKA_1 | 761 | 767 | PF00069 | 0.570 |
MOD_PKA_1 | 772 | 778 | PF00069 | 0.593 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.728 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.615 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.373 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.358 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.590 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.379 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.333 |
MOD_PKB_1 | 430 | 438 | PF00069 | 0.683 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.443 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.547 |
MOD_Plk_2-3 | 457 | 463 | PF00069 | 0.593 |
MOD_Plk_2-3 | 466 | 472 | PF00069 | 0.591 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.299 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.327 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.303 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.343 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.450 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.396 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.232 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.370 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.268 |
MOD_Plk_4 | 677 | 683 | PF00069 | 0.303 |
MOD_Plk_4 | 751 | 757 | PF00069 | 0.571 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.450 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.303 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.409 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.563 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.419 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.676 |
MOD_SUMO_for_1 | 149 | 152 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 320 | 325 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 422 | 428 | PF00179 | 0.690 |
MOD_SUMO_rev_2 | 590 | 600 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 90 | 97 | PF00179 | 0.744 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_1 | 307 | 312 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_1 | 405 | 410 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.664 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.309 |
TRG_DiLeu_LyEn_5 | 292 | 297 | PF01217 | 0.303 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.658 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 741 | 744 | PF00400 | 0.662 |
TRG_NLS_Bipartite_1 | 724 | 744 | PF00514 | 0.709 |
TRG_NLS_MonoExtC_3 | 513 | 519 | PF00514 | 0.255 |
TRG_NLS_MonoExtC_3 | 739 | 745 | PF00514 | 0.681 |
TRG_NLS_MonoExtN_4 | 738 | 744 | PF00514 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 218 | 223 | PF00026 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 303 | 307 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 717 | 722 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 761 | 766 | PF00026 | 0.681 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U1 | Leptomonas seymouri | 78% | 100% |
A0A0N1PCZ7 | Leptomonas seymouri | 22% | 100% |
A0A0S4ISP4 | Bodo saltans | 49% | 100% |
A0A1X0NMD6 | Trypanosomatidae | 53% | 96% |
A0A1X0NPK0 | Trypanosomatidae | 25% | 79% |
A0A3Q8IE53 | Leishmania donovani | 93% | 100% |
A0A3R7N587 | Trypanosoma rangeli | 54% | 96% |
A0A3R7NJH7 | Trypanosoma rangeli | 23% | 100% |
A0A3S5H7C7 | Leishmania donovani | 24% | 100% |
A1CB55 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 32% | 100% |
A1DE84 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 30% | 100% |
A2RA55 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 32% | 100% |
A2XVF7 | Oryza sativa subsp. indica | 27% | 95% |
A3AVH5 | Oryza sativa subsp. japonica | 27% | 95% |
A3LWH3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 30% | 100% |
A4H481 | Leishmania braziliensis | 27% | 100% |
A4HD81 | Leishmania braziliensis | 22% | 100% |
A4HFC4 | Leishmania braziliensis | 87% | 100% |
A4I2K1 | Leishmania infantum | 93% | 100% |
A5DAR2 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 34% | 100% |
A6RSH5 | Botryotinia fuckeliana (strain B05.10) | 32% | 90% |
A6ZZY8 | Saccharomyces cerevisiae (strain YJM789) | 31% | 100% |
A7F8V8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 32% | 90% |
A7TNT1 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 31% | 100% |
C9ZKU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 89% |
E9AH36 | Leishmania infantum | 24% | 100% |
E9AWL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AYQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O60173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
P0CQ94 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 28% | 83% |
P0CQ95 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 28% | 83% |
P36120 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q0CF43 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 32% | 100% |
Q0UHM7 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 32% | 95% |
Q0UZ59 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 26% | 100% |
Q1E9T9 | Coccidioides immitis (strain RS) | 32% | 100% |
Q2GZU7 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 30% | 98% |
Q2UE66 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 33% | 100% |
Q4HZ68 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 31% | 100% |
Q4P0Y5 | Ustilago maydis (strain 521 / FGSC 9021) | 30% | 81% |
Q4QAV6 | Leishmania major | 23% | 100% |
Q4WV71 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 30% | 100% |
Q59S50 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 100% |
Q5BGX6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 32% | 100% |
Q6BKH3 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 31% | 99% |
Q6C835 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 32% | 99% |
Q6CK32 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |
Q6NZQ2 | Mus musculus | 34% | 100% |
Q754J2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 34% | 100% |
Q7S873 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 97% |
Q7XJN0 | Arabidopsis thaliana | 33% | 100% |
Q869P0 | Dictyostelium discoideum | 35% | 87% |
Q86B47 | Drosophila melanogaster | 33% | 81% |
Q8TFL3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 31% | 100% |
Q9H8H2 | Homo sapiens | 34% | 93% |
V5BG99 | Trypanosoma cruzi | 53% | 95% |