Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000922 | spindle pole | 2 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005819 | spindle | 5 | 2 |
GO:0005874 | microtubule | 6 | 18 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0099080 | supramolecular complex | 2 | 18 |
GO:0099081 | supramolecular polymer | 3 | 18 |
GO:0099512 | supramolecular fiber | 4 | 18 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: E9ABZ2
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 3 |
GO:0006996 | organelle organization | 4 | 3 |
GO:0007010 | cytoskeleton organization | 5 | 3 |
GO:0007017 | microtubule-based process | 2 | 18 |
GO:0007018 | microtubule-based movement | 3 | 18 |
GO:0007019 | microtubule depolymerization | 5 | 3 |
GO:0007051 | spindle organization | 3 | 2 |
GO:0007052 | mitotic spindle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 18 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022411 | cellular component disassembly | 4 | 3 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 3 |
GO:0032984 | protein-containing complex disassembly | 5 | 3 |
GO:0043933 | protein-containing complex organization | 4 | 3 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051261 | protein depolymerization | 6 | 3 |
GO:0051983 | regulation of chromosome segregation | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
GO:0097435 | supramolecular fiber organization | 4 | 3 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003774 | cytoskeletal motor activity | 1 | 18 |
GO:0003777 | microtubule motor activity | 2 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0005515 | protein binding | 2 | 18 |
GO:0005524 | ATP binding | 5 | 18 |
GO:0008017 | microtubule binding | 5 | 18 |
GO:0008092 | cytoskeletal protein binding | 3 | 18 |
GO:0015631 | tubulin binding | 4 | 18 |
GO:0017076 | purine nucleotide binding | 4 | 18 |
GO:0030554 | adenyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:0140657 | ATP-dependent activity | 1 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.768 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.540 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.254 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 548 | 550 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 572 | 574 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 634 | 636 | PF00082 | 0.515 |
CLV_PCSK_PC7_1 | 480 | 486 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 568 | 574 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.461 |
CLV_Separin_Metazoa | 412 | 416 | PF03568 | 0.294 |
DEG_APCC_DBOX_1 | 279 | 287 | PF00400 | 0.248 |
DOC_CKS1_1 | 530 | 535 | PF01111 | 0.553 |
DOC_CYCLIN_RxL_1 | 381 | 391 | PF00134 | 0.318 |
DOC_MAPK_gen_1 | 130 | 139 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 168 | 176 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 168 | 176 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 333 | 342 | PF00069 | 0.352 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.609 |
DOC_USP7_UBL2_3 | 341 | 345 | PF12436 | 0.389 |
DOC_USP7_UBL2_3 | 349 | 353 | PF12436 | 0.202 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 177 | 186 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 455 | 463 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 484 | 490 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 508 | 512 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 628 | 638 | PF00244 | 0.515 |
LIG_Actin_WH2_1 | 48 | 63 | PF00022 | 0.337 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.240 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.515 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.226 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.318 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.318 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.641 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.599 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.309 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.226 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.194 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.501 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.282 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.313 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.528 |
LIG_Integrin_isoDGR_2 | 278 | 280 | PF01839 | 0.248 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 250 | 258 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 351 | 360 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 570 | 574 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.475 |
LIG_NRBOX | 272 | 278 | PF00104 | 0.290 |
LIG_PCNA_TLS_4 | 635 | 642 | PF02747 | 0.518 |
LIG_Pex14_2 | 187 | 191 | PF04695 | 0.294 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.491 |
LIG_RPA_C_Fungi | 623 | 635 | PF08784 | 0.517 |
LIG_SH2_NCK_1 | 201 | 205 | PF00017 | 0.226 |
LIG_SH2_NCK_1 | 244 | 248 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.382 |
LIG_SH3_2 | 533 | 538 | PF14604 | 0.706 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.663 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.653 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.544 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.279 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.420 |
LIG_UBA3_1 | 135 | 141 | PF00899 | 0.422 |
LIG_UBA3_1 | 337 | 345 | PF00899 | 0.265 |
LIG_UBA3_1 | 386 | 390 | PF00899 | 0.318 |
LIG_WRC_WIRS_1 | 262 | 267 | PF05994 | 0.279 |
LIG_WRC_WIRS_1 | 638 | 643 | PF05994 | 0.523 |
MOD_CDK_SPK_2 | 529 | 534 | PF00069 | 0.701 |
MOD_CDK_SPxxK_3 | 93 | 100 | PF00069 | 0.670 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.518 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.313 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.457 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.250 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.372 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.240 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.318 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.749 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.753 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.583 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.626 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.696 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.573 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.443 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.201 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.311 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.254 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.318 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.478 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.535 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.314 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.803 |
MOD_Cter_Amidation | 278 | 281 | PF01082 | 0.405 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.254 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.159 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.711 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.311 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.259 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.327 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.271 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.620 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.716 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.704 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.535 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.696 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.521 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.293 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.321 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.279 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.234 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.397 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.671 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.648 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.668 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.616 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.627 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.673 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.693 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.644 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.713 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.569 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.248 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.318 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.467 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.382 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.496 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.306 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.301 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.679 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.638 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.522 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.318 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.566 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.482 |
MOD_PIKK_1 | 640 | 646 | PF00454 | 0.552 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.403 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.361 |
MOD_PKA_1 | 345 | 351 | PF00069 | 0.381 |
MOD_PKA_1 | 484 | 490 | PF00069 | 0.659 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.528 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.577 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.394 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.424 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.412 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.318 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.314 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.301 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.701 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.643 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.579 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.686 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.560 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.549 |
MOD_PKB_1 | 140 | 148 | PF00069 | 0.325 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.318 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.290 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.359 |
MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.226 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.515 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.320 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.318 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.318 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.392 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.313 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.276 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.680 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.542 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.492 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.318 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.688 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.712 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.728 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.669 |
MOD_SUMO_for_1 | 603 | 606 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 164 | 172 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 334 | 342 | PF00179 | 0.248 |
TRG_DiLeu_BaEn_1 | 625 | 630 | PF01217 | 0.394 |
TRG_DiLeu_BaEn_2 | 390 | 396 | PF01217 | 0.381 |
TRG_DiLeu_LyEn_5 | 625 | 630 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 107 | 109 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.571 |
TRG_NLS_Bipartite_1 | 130 | 144 | PF00514 | 0.395 |
TRG_NLS_MonoExtC_3 | 129 | 134 | PF00514 | 0.552 |
TRG_NLS_MonoExtN_4 | 130 | 135 | PF00514 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.248 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 587 | 591 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 628 | 633 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 74% | 100% |
A0A0S4IP49 | Bodo saltans | 27% | 83% |
A0A1X0NL76 | Trypanosomatidae | 48% | 93% |
A0A1X0NQ03 | Trypanosomatidae | 27% | 81% |
A0A1X0P2U1 | Trypanosomatidae | 59% | 95% |
A0A3S5H4S8 | Leishmania donovani | 97% | 99% |
A0A3S7WST0 | Leishmania donovani | 46% | 92% |
A0A3S7X9Y1 | Leishmania donovani | 34% | 100% |
A0A422NY45 | Trypanosoma rangeli | 55% | 96% |
A4H337 | Leishmania braziliensis | 88% | 100% |
A4H7F1 | Leishmania braziliensis | 46% | 92% |
A4HAQ7 | Leishmania braziliensis | 26% | 100% |
A4HDC2 | Leishmania braziliensis | 40% | 99% |
A4HND6 | Leishmania braziliensis | 33% | 100% |
A4HRC5 | Leishmania infantum | 97% | 99% |
A4HSA6 | Leishmania infantum | 34% | 100% |
A4HVT9 | Leishmania infantum | 46% | 92% |
A4IC09 | Leishmania infantum | 34% | 100% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 97% |
E9AFU7 | Leishmania major | 34% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 99% |
E9API5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 92% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
P48467 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 72% |
Q4QFZ3 | Leishmania major | 46% | 92% |
Q5R9Y9 | Pongo abelii | 39% | 90% |
Q940Y8 | Arabidopsis thaliana | 39% | 98% |
V5D311 | Trypanosoma cruzi | 47% | 99% |