Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 38 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 106 |
NetGPI | no | yes: 0, no: 108 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QCS6
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 109 |
GO:0006807 | nitrogen compound metabolic process | 2 | 109 |
GO:0008152 | metabolic process | 1 | 109 |
GO:0019538 | protein metabolic process | 3 | 109 |
GO:0043170 | macromolecule metabolic process | 3 | 109 |
GO:0044238 | primary metabolic process | 2 | 109 |
GO:0071704 | organic substance metabolic process | 2 | 109 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 109 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 109 |
GO:0004175 | endopeptidase activity | 4 | 109 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 109 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 109 |
GO:0008233 | peptidase activity | 3 | 109 |
GO:0008234 | cysteine-type peptidase activity | 4 | 109 |
GO:0016787 | hydrolase activity | 2 | 109 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 109 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 482 | 486 | PF00656 | 0.451 |
CLV_C14_Caspase3-7 | 544 | 548 | PF00656 | 0.431 |
CLV_C14_Caspase3-7 | 610 | 614 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.778 |
CLV_PCSK_PC1ET2_1 | 728 | 730 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.485 |
DEG_MDM2_SWIB_1 | 488 | 496 | PF02201 | 0.467 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.594 |
DEG_SCF_FBW7_1 | 234 | 239 | PF00400 | 0.534 |
DOC_CDC14_PxL_1 | 642 | 650 | PF14671 | 0.374 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.477 |
DOC_MAPK_DCC_7 | 435 | 444 | PF00069 | 0.578 |
DOC_MAPK_DCC_7 | 521 | 529 | PF00069 | 0.421 |
DOC_MAPK_DCC_7 | 6 | 15 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 182 | 189 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 435 | 444 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 521 | 529 | PF00069 | 0.392 |
DOC_PP1_RVXF_1 | 183 | 189 | PF00149 | 0.442 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.555 |
DOC_PP2B_LxvP_1 | 643 | 646 | PF13499 | 0.362 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.481 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.391 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 166 | 174 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 335 | 340 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 660 | 666 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 729 | 735 | PF00244 | 0.435 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_1 | 617 | 621 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 704 | 708 | PF00533 | 0.455 |
LIG_Clathr_ClatBox_1 | 186 | 190 | PF01394 | 0.169 |
LIG_deltaCOP1_diTrp_1 | 491 | 499 | PF00928 | 0.488 |
LIG_eIF4E_1 | 387 | 393 | PF01652 | 0.377 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.523 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.470 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.504 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.467 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.591 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.755 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.382 |
LIG_FHA_1 | 730 | 736 | PF00498 | 0.364 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.441 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.464 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.524 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.424 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.492 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.516 |
LIG_Integrin_RGD_1 | 126 | 128 | PF01839 | 0.433 |
LIG_LIR_Apic_2 | 210 | 215 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 265 | 270 | PF02991 | 0.482 |
LIG_LIR_Apic_2 | 512 | 517 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 377 | 387 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 491 | 500 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 603 | 612 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 618 | 629 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 640 | 650 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 709 | 719 | PF02991 | 0.480 |
LIG_LIR_LC3C_4 | 640 | 645 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 353 | 357 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 491 | 495 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 555 | 561 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 618 | 624 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 640 | 645 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 675 | 679 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 705 | 711 | PF02991 | 0.421 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.384 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.475 |
LIG_PTB_Apo_2 | 57 | 64 | PF02174 | 0.384 |
LIG_REV1ctd_RIR_1 | 377 | 386 | PF16727 | 0.498 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.479 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.360 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.415 |
LIG_SH2_CRK | 604 | 608 | PF00017 | 0.453 |
LIG_SH2_GRB2like | 339 | 342 | PF00017 | 0.468 |
LIG_SH2_GRB2like | 387 | 390 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.493 |
LIG_SH2_SRC | 303 | 306 | PF00017 | 0.490 |
LIG_SH2_SRC | 387 | 390 | PF00017 | 0.430 |
LIG_SH2_SRC | 419 | 422 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 604 | 608 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.472 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.318 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.523 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.514 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.400 |
LIG_SH3_3 | 671 | 677 | PF00018 | 0.574 |
LIG_SH3_4 | 139 | 146 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 537 | 544 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 537 | 544 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 559 | 564 | PF11976 | 0.389 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.430 |
LIG_WRC_WIRS_1 | 711 | 716 | PF05994 | 0.435 |
MOD_CDK_SPxxK_3 | 34 | 41 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 428 | 435 | PF00069 | 0.397 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.595 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.345 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.342 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.303 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.593 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.570 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.629 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.625 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.629 |
MOD_CK1_1 | 672 | 678 | PF00069 | 0.544 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.488 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.392 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.499 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.278 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.316 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.357 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.566 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.484 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.291 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.312 |
MOD_CMANNOS | 25 | 28 | PF00535 | 0.555 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.406 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.353 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.296 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.426 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.341 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.343 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.395 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.386 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.543 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.655 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.669 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.456 |
MOD_GlcNHglycan | 628 | 632 | PF01048 | 0.311 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.572 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.761 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.704 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.603 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.516 |
MOD_GlcNHglycan | 736 | 740 | PF01048 | 0.526 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.320 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.323 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.470 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.290 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.305 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.301 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.319 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.338 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.346 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.300 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.457 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.481 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.426 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.595 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.636 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.425 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.354 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.590 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.630 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.369 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.325 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.469 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.727 |
MOD_N-GLC_1 | 715 | 720 | PF02516 | 0.459 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.386 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.608 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.566 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.353 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.353 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.329 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.461 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.396 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.671 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.366 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.314 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.377 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.272 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.407 |
MOD_PIKK_1 | 574 | 580 | PF00454 | 0.733 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.661 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.520 |
MOD_PK_1 | 6 | 12 | PF00069 | 0.561 |
MOD_PKA_1 | 582 | 588 | PF00069 | 0.496 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.498 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.386 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.495 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.749 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.471 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.384 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.378 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.338 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.435 |
MOD_Plk_1 | 602 | 608 | PF00069 | 0.459 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.393 |
MOD_Plk_1 | 715 | 721 | PF00069 | 0.411 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.338 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.378 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.287 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.418 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.338 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.423 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.726 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.329 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.446 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.465 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.294 |
MOD_Plk_4 | 702 | 708 | PF00069 | 0.448 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.504 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.475 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.574 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.301 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.355 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.342 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.338 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.640 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.341 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.387 |
MOD_SUMO_rev_2 | 544 | 551 | PF00179 | 0.492 |
TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.437 |
TRG_DiLeu_BaEn_2 | 411 | 417 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 440 | 445 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 644 | 649 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.170 |
TRG_NLS_MonoExtC_3 | 435 | 440 | PF00514 | 0.415 |
TRG_NLS_MonoExtN_4 | 435 | 440 | PF00514 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 647 | 651 | PF00026 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 29% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 75% |
A0A0N1IGQ2 | Leptomonas seymouri | 27% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 31% | 95% |
A0A0N1P9P1 | Leptomonas seymouri | 31% | 87% |
A0A0N1PCA9 | Leptomonas seymouri | 74% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 25% | 83% |
A0A0N1PFI4 | Leptomonas seymouri | 31% | 96% |
A0A0S4JLK6 | Bodo saltans | 29% | 92% |
A0A0S4JS70 | Bodo saltans | 27% | 97% |
A0A0S4KGT2 | Bodo saltans | 34% | 98% |
A0A0S4KKP7 | Bodo saltans | 24% | 100% |
A0A1X0NJ61 | Trypanosomatidae | 31% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 98% |
A0A1X0NJX8 | Trypanosomatidae | 31% | 96% |
A0A1X0NKT7 | Trypanosomatidae | 30% | 93% |
A0A1X0NKX8 | Trypanosomatidae | 30% | 91% |
A0A1X0NMT3 | Trypanosomatidae | 33% | 87% |
A0A1X0NW84 | Trypanosomatidae | 32% | 100% |
A0A1X0NW85 | Trypanosomatidae | 41% | 100% |
A0A1X0NW89 | Trypanosomatidae | 35% | 86% |
A0A1X0NWA6 | Trypanosomatidae | 27% | 85% |
A0A1X0NWW1 | Trypanosomatidae | 34% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 36% | 82% |
A0A3Q8IDD4 | Leishmania donovani | 29% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 24% | 99% |
A0A3S5H5A5 | Leishmania donovani | 33% | 87% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 96% |
A0A3S7WW13 | Leishmania donovani | 27% | 67% |
A0A3S7WW18 | Leishmania donovani | 36% | 90% |
A0A3S7WW41 | Leishmania donovani | 94% | 100% |
A0A3S7WW71 | Leishmania donovani | 33% | 100% |
A0A3S7X430 | Leishmania donovani | 31% | 95% |
A0A3S7X438 | Leishmania donovani | 29% | 79% |
A0A3S7X460 | Leishmania donovani | 30% | 96% |
A0A3S7X463 | Leishmania donovani | 28% | 79% |
A0A3S7X470 | Leishmania donovani | 29% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 36% | 81% |
A0A422MYX0 | Trypanosoma rangeli | 35% | 100% |
A4H3W4 | Leishmania braziliensis | 30% | 87% |
A4HE81 | Leishmania braziliensis | 29% | 100% |
A4HJ14 | Leishmania braziliensis | 30% | 95% |
A4HJ21 | Leishmania braziliensis | 25% | 83% |
A4HJ22 | Leishmania braziliensis | 28% | 78% |
A4HJ24 | Leishmania braziliensis | 31% | 100% |
A4HS39 | Leishmania infantum | 32% | 87% |
A4HYN0 | Leishmania infantum | 36% | 90% |
A4HYW1 | Leishmania infantum | 36% | 73% |
A4HYW2 | Leishmania infantum | 33% | 100% |
A4HYW3 | Leishmania infantum | 95% | 100% |
A4HYW4 | Leishmania infantum | 27% | 74% |
A4I1J4 | Leishmania infantum | 29% | 100% |
A4I6E4 | Leishmania infantum | 30% | 100% |
A4I6E6 | Leishmania infantum | 30% | 96% |
A4I6F0 | Leishmania infantum | 29% | 79% |
A4I6K4 | Leishmania infantum | 31% | 95% |
A4I6K5 | Leishmania infantum | 29% | 79% |
A4I6K6 | Leishmania infantum | 25% | 99% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 69% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 94% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 87% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 87% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 79% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 95% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AIH1 | Leishmania braziliensis | 36% | 91% |
E9AIH3 | Leishmania braziliensis | 33% | 100% |
E9AIH4 | Leishmania braziliensis | 82% | 100% |
E9AIH6 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 93% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 80% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 95% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 79% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 99% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q6L7 | Leishmania major | 31% | 100% |
Q4Q6L9 | Leishmania major | 30% | 100% |
Q4Q6M0 | Leishmania major | 29% | 100% |
Q4Q6M2 | Leishmania major | 25% | 100% |
Q4Q6M3 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 30% | 100% |
Q4Q9U3 | Leishmania major | 29% | 96% |
Q4QCS7 | Leishmania major | 33% | 100% |
Q4QCS8 | Leishmania major | 35% | 90% |
Q4QCS9 | Leishmania major | 35% | 100% |
Q9U0T9 | Leishmania major | 31% | 87% |
V5AYJ1 | Trypanosoma cruzi | 32% | 100% |
V5B5I4 | Trypanosoma cruzi | 37% | 89% |
V5BA05 | Trypanosoma cruzi | 37% | 100% |
V5BEL3 | Trypanosoma cruzi | 32% | 100% |
V5BN20 | Trypanosoma cruzi | 32% | 96% |
V5D5V8 | Trypanosoma cruzi | 30% | 100% |
V5D9Y2 | Trypanosoma cruzi | 32% | 87% |
V5DES7 | Trypanosoma cruzi | 31% | 94% |