A large and likely artifical grouping of protease domain carrying proteins related to proteasomal proteases. Only a tiny subgroup (the AFG3-related mitochondrail proteins) seem to have a TM segment.. Localization: Cytoplasmic (by homology) / Mitochondrial (by homology)
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HGJ8
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0051301 | cell division | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 665 | 669 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.490 |
DEG_SCF_FBW7_2 | 171 | 178 | PF00400 | 0.422 |
DOC_CDC14_PxL_1 | 478 | 486 | PF14671 | 0.279 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 592 | 598 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 114 | 121 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 400 | 408 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 504 | 512 | PF00069 | 0.279 |
DOC_MAPK_gen_1 | 599 | 609 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 504 | 512 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 602 | 611 | PF00069 | 0.215 |
DOC_PP2B_LxvP_1 | 291 | 294 | PF13499 | 0.419 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.418 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.642 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.317 |
LIG_14-3-3_CanoR_1 | 117 | 122 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 400 | 408 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 547 | 552 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 561 | 570 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 685 | 691 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 509 | 525 | PF00022 | 0.410 |
LIG_Actin_WH2_2 | 585 | 601 | PF00022 | 0.280 |
LIG_APCC_ABBAyCdc20_2 | 622 | 628 | PF00400 | 0.445 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 508 | 512 | PF00533 | 0.279 |
LIG_BRCT_BRCA1_1 | 675 | 679 | PF00533 | 0.453 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.406 |
LIG_Clathr_ClatBox_1 | 510 | 514 | PF01394 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 628 | 632 | PF00928 | 0.388 |
LIG_eIF4E_1 | 755 | 761 | PF01652 | 0.297 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.409 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.623 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.505 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.237 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.398 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.511 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.264 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.302 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.579 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.467 |
LIG_FHA_1 | 738 | 744 | PF00498 | 0.495 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.399 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.513 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.483 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.355 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.279 |
LIG_GBD_Chelix_1 | 562 | 570 | PF00786 | 0.322 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 402 | 410 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 411 | 420 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 475 | 485 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 577 | 586 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 754 | 763 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 754 | 758 | PF02991 | 0.308 |
LIG_LYPXL_S_1 | 233 | 237 | PF13949 | 0.465 |
LIG_NRBOX | 140 | 146 | PF00104 | 0.509 |
LIG_NRBOX | 27 | 33 | PF00104 | 0.466 |
LIG_NRBOX | 565 | 571 | PF00104 | 0.322 |
LIG_NRBOX | 602 | 608 | PF00104 | 0.355 |
LIG_Pex14_2 | 687 | 691 | PF04695 | 0.349 |
LIG_Rb_LxCxE_1 | 712 | 730 | PF01857 | 0.434 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.353 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.354 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.201 |
LIG_SH2_CRK | 755 | 759 | PF00017 | 0.314 |
LIG_SH2_GRB2like | 499 | 502 | PF00017 | 0.197 |
LIG_SH2_GRB2like | 524 | 527 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 524 | 528 | PF00017 | 0.258 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.437 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 755 | 759 | PF00017 | 0.314 |
LIG_SH2_STAT3 | 191 | 194 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.410 |
LIG_SH3_1 | 33 | 39 | PF00018 | 0.430 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.452 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.759 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.537 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.376 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.302 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.565 |
LIG_Sin3_3 | 757 | 764 | PF02671 | 0.431 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.431 |
LIG_SUMO_SIM_anti_2 | 276 | 283 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 756 | 762 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 180 | 186 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 25 | 30 | PF11976 | 0.350 |
LIG_SxIP_EBH_1 | 114 | 128 | PF03271 | 0.467 |
LIG_TYR_ITIM | 336 | 341 | PF00017 | 0.341 |
LIG_TYR_ITIM | 753 | 758 | PF00017 | 0.305 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.528 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.753 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.369 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.676 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.697 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.507 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.614 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.568 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.517 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.398 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.523 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.279 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.445 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.622 |
MOD_CMANNOS | 629 | 632 | PF00535 | 0.386 |
MOD_DYRK1A_RPxSP_1 | 12 | 16 | PF00069 | 0.596 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.414 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.488 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.759 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.464 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.385 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.431 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.517 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.689 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.397 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.595 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.612 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.538 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.613 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.681 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.489 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.511 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.448 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.464 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.466 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.333 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.783 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.467 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.492 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.381 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.358 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.597 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.524 |
MOD_LATS_1 | 444 | 450 | PF00433 | 0.427 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.550 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.279 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.197 |
MOD_N-GLC_1 | 637 | 642 | PF02516 | 0.626 |
MOD_N-GLC_1 | 685 | 690 | PF02516 | 0.429 |
MOD_N-GLC_2 | 68 | 70 | PF02516 | 0.468 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.529 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.272 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.460 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.279 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.378 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.582 |
MOD_NEK2_2 | 167 | 172 | PF00069 | 0.455 |
MOD_NEK2_2 | 229 | 234 | PF00069 | 0.366 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.462 |
MOD_PK_1 | 264 | 270 | PF00069 | 0.452 |
MOD_PK_1 | 534 | 540 | PF00069 | 0.476 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.478 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.549 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.736 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.663 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.441 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.495 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.377 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.380 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.446 |
MOD_PKB_1 | 115 | 123 | PF00069 | 0.302 |
MOD_PKB_1 | 504 | 512 | PF00069 | 0.279 |
MOD_PKB_1 | 532 | 540 | PF00069 | 0.444 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.654 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.279 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.424 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.692 |
MOD_Plk_2-3 | 72 | 78 | PF00069 | 0.456 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.586 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.558 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.375 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.405 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.334 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.633 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.319 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.279 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.279 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.279 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.308 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.441 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.471 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.591 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.589 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.434 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.670 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.318 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.317 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_1 | 22 | 27 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.510 |
TRG_DiLeu_BaLyEn_6 | 592 | 597 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 755 | 758 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 621 | 623 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 673 | 675 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 724 | 726 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 735 | 737 | PF00400 | 0.564 |
TRG_ER_diLys_1 | 766 | 770 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 660 | 670 | PF08389 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 494 | 498 | PF00026 | 0.322 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9Q8 | Leptomonas seymouri | 56% | 100% |
A0A1X0NZ99 | Trypanosomatidae | 41% | 100% |
A0A3Q8II41 | Leishmania donovani | 77% | 100% |
A0A422MTD5 | Trypanosoma rangeli | 41% | 100% |
A4I3M5 | Leishmania infantum | 77% | 100% |
D0A856 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AZW6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q8C0 | Leishmania major | 76% | 100% |
V5BCT3 | Trypanosoma cruzi | 37% | 100% |