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:0005634 | nucleus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0032993 | protein-DNA complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097550 | transcription preinitiation complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HDY6
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0022607 | cellular component assembly | 4 | 10 |
GO:0043933 | protein-containing complex organization | 4 | 10 |
GO:0065003 | protein-containing complex assembly | 5 | 10 |
GO:0065004 | protein-DNA complex assembly | 6 | 10 |
GO:0070897 | transcription preinitiation complex assembly | 7 | 10 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006352 | DNA-templated transcription initiation | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008134 | transcription factor binding | 3 | 10 |
GO:0017025 | TBP-class protein binding | 5 | 10 |
GO:0140296 | general transcription initiation factor binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.247 |
CLV_PCSK_FUR_1 | 570 | 574 | PF00082 | 0.565 |
CLV_PCSK_FUR_1 | 605 | 609 | PF00082 | 0.491 |
CLV_PCSK_FUR_1 | 642 | 646 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 621 | 623 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 641 | 643 | PF00082 | 0.488 |
CLV_PCSK_PC7_1 | 389 | 395 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 638 | 644 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.290 |
DEG_APCC_DBOX_1 | 559 | 567 | PF00400 | 0.624 |
DEG_SCF_FBW7_2 | 345 | 350 | PF00400 | 0.618 |
DEG_SCF_FBW7_2 | 539 | 546 | PF00400 | 0.599 |
DOC_CKS1_1 | 323 | 328 | PF01111 | 0.474 |
DOC_CKS1_1 | 540 | 545 | PF01111 | 0.670 |
DOC_CYCLIN_RxL_1 | 361 | 371 | PF00134 | 0.364 |
DOC_MAPK_gen_1 | 605 | 615 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 664 | 673 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 85 | 93 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 442 | 449 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 607 | 615 | PF00069 | 0.594 |
DOC_MAPK_NFAT4_5 | 112 | 120 | PF00069 | 0.389 |
DOC_PP2B_LxvP_1 | 366 | 369 | PF13499 | 0.439 |
DOC_PP2B_LxvP_1 | 581 | 584 | PF13499 | 0.602 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.580 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 259 | 267 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 293 | 300 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 408 | 416 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 610 | 616 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 62 | 68 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 624 | 631 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 642 | 648 | PF00244 | 0.736 |
LIG_Actin_WH2_2 | 361 | 379 | PF00022 | 0.370 |
LIG_APCC_ABBA_1 | 613 | 618 | PF00400 | 0.604 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 330 | 335 | PF00928 | 0.417 |
LIG_EH1_1 | 673 | 681 | PF00400 | 0.370 |
LIG_eIF4E_1 | 674 | 680 | PF01652 | 0.362 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.530 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.356 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.447 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.433 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.516 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.507 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.562 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.594 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.510 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.677 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.623 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.357 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.564 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.525 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.438 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.809 |
LIG_FHA_2 | 625 | 631 | PF00498 | 0.512 |
LIG_Integrin_isoDGR_2 | 17 | 19 | PF01839 | 0.421 |
LIG_IRF3_LxIS_1 | 93 | 100 | PF10401 | 0.465 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 579 | 586 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 579 | 583 | PF02991 | 0.532 |
LIG_OCRL_FandH_1 | 334 | 346 | PF00620 | 0.467 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.379 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.443 |
LIG_SH2_SRC | 277 | 280 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.496 |
LIG_SH3_2 | 323 | 328 | PF14604 | 0.470 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.447 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.477 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.708 |
LIG_SH3_3 | 650 | 656 | PF00018 | 0.547 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.637 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.568 |
LIG_TRAF2_1 | 543 | 546 | PF00917 | 0.692 |
LIG_TRAF2_1 | 627 | 630 | PF00917 | 0.530 |
LIG_TRFH_1 | 34 | 38 | PF08558 | 0.543 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.514 |
LIG_TYR_ITIM | 595 | 600 | PF00017 | 0.617 |
LIG_UBA3_1 | 159 | 164 | PF00899 | 0.473 |
LIG_UBA3_1 | 310 | 319 | PF00899 | 0.524 |
LIG_UBA3_1 | 365 | 372 | PF00899 | 0.456 |
MOD_CDK_SPxK_1 | 322 | 328 | PF00069 | 0.470 |
MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.588 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.530 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.528 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.530 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.449 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.743 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.694 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.585 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.423 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.395 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.611 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.467 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.553 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.394 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.801 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.508 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.612 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.247 |
MOD_Cter_Amidation | 256 | 259 | PF01082 | 0.302 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.247 |
MOD_GlcNHglycan | 306 | 310 | PF01048 | 0.428 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.804 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.746 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.602 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.440 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.471 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.565 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.439 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.488 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.726 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.642 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.632 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.592 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.601 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.475 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.611 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.490 |
MOD_N-GLC_1 | 522 | 527 | PF02516 | 0.726 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.570 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.302 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.389 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.502 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.537 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.543 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.719 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.681 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.549 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.414 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.475 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.572 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.730 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.706 |
MOD_PK_1 | 643 | 649 | PF00069 | 0.652 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.502 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.591 |
MOD_PKA_1 | 643 | 649 | PF00069 | 0.652 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.504 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.387 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.457 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.447 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.447 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.627 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.539 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.520 |
MOD_PKB_1 | 622 | 630 | PF00069 | 0.630 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.530 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.358 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.523 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.676 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.628 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.559 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.627 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.571 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.530 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.407 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.674 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.498 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.447 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.611 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.473 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.524 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.421 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.608 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.556 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.712 |
MOD_SUMO_for_1 | 383 | 386 | PF00179 | 0.473 |
MOD_SUMO_for_1 | 392 | 395 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 313 | 321 | PF00179 | 0.420 |
TRG_DiLeu_BaEn_1 | 386 | 391 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_1 | 480 | 485 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_4 | 349 | 355 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_4 | 629 | 635 | PF01217 | 0.521 |
TRG_DiLeu_LyEn_5 | 386 | 391 | PF01217 | 0.535 |
TRG_DiLeu_LyEn_5 | 480 | 485 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 605 | 608 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 642 | 645 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 663 | 666 | PF00400 | 0.496 |
TRG_NES_CRM1_1 | 89 | 102 | PF08389 | 0.530 |
TRG_NLS_Bipartite_1 | 607 | 625 | PF00514 | 0.569 |
TRG_NLS_MonoCore_2 | 640 | 645 | PF00514 | 0.532 |
TRG_NLS_MonoExtC_3 | 640 | 645 | PF00514 | 0.532 |
TRG_NLS_MonoExtN_4 | 619 | 625 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 638 | 645 | PF00514 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.247 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM92 | Leptomonas seymouri | 70% | 99% |
A0A3R7L9Y8 | Trypanosoma rangeli | 48% | 100% |
A0A3S7WYT5 | Leishmania donovani | 86% | 99% |
A4I187 | Leishmania infantum | 86% | 99% |
D0A5H2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AXC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4QA51 | Leishmania major | 85% | 100% |
V5DPA1 | Trypanosoma cruzi | 49% | 100% |