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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 14 |
GO:0099080 | supramolecular complex | 2 | 14 |
GO:0099081 | supramolecular polymer | 3 | 14 |
GO:0099512 | supramolecular fiber | 4 | 14 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0000922 | spindle pole | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005819 | spindle | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H337
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 14 |
GO:0007018 | microtubule-based movement | 3 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007019 | microtubule depolymerization | 5 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051261 | protein depolymerization | 6 | 1 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003774 | cytoskeletal motor activity | 1 | 14 |
GO:0003777 | microtubule motor activity | 2 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005515 | protein binding | 2 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008017 | microtubule binding | 5 | 14 |
GO:0008092 | cytoskeletal protein binding | 3 | 14 |
GO:0015631 | tubulin binding | 4 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.289 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.718 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.147 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.147 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 567 | 569 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 629 | 631 | PF00082 | 0.452 |
CLV_PCSK_PC7_1 | 474 | 480 | PF00082 | 0.549 |
CLV_PCSK_PC7_1 | 563 | 569 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.409 |
CLV_Separin_Metazoa | 406 | 410 | PF03568 | 0.203 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.203 |
DOC_CYCLIN_RxL_1 | 375 | 385 | PF00134 | 0.249 |
DOC_MAPK_gen_1 | 124 | 133 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 162 | 170 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 253 | 259 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 124 | 133 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 162 | 170 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.292 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.282 |
DOC_USP7_UBL2_3 | 343 | 347 | PF12436 | 0.203 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 102 | 112 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 449 | 457 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 478 | 484 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 509 | 515 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 623 | 633 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 48 | 63 | PF00022 | 0.321 |
LIG_AP2alpha_2 | 488 | 490 | PF02296 | 0.442 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.215 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.452 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.254 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.249 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.249 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.605 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.611 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.468 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.290 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.489 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.249 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.122 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.456 |
LIG_Integrin_isoDGR_2 | 272 | 274 | PF01839 | 0.203 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 244 | 252 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 585 | 590 | PF02991 | 0.456 |
LIG_LRP6_Inhibitor_1 | 593 | 599 | PF00058 | 0.251 |
LIG_NRBOX | 266 | 272 | PF00104 | 0.249 |
LIG_PCNA_TLS_4 | 630 | 637 | PF02747 | 0.454 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.203 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.446 |
LIG_RPA_C_Fungi | 618 | 630 | PF08784 | 0.455 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.203 |
LIG_SH2_PTP2 | 173 | 176 | PF00017 | 0.147 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.147 |
LIG_SH2_SRC | 590 | 593 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.203 |
LIG_SH2_STAP1 | 440 | 444 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.346 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.567 |
LIG_SUMO_SIM_par_1 | 379 | 385 | PF11976 | 0.220 |
LIG_UBA3_1 | 331 | 339 | PF00899 | 0.218 |
LIG_UBA3_1 | 380 | 384 | PF00899 | 0.278 |
LIG_WRC_WIRS_1 | 256 | 261 | PF05994 | 0.203 |
LIG_WRC_WIRS_1 | 633 | 638 | PF05994 | 0.456 |
MOD_CDK_SPxxK_3 | 87 | 94 | PF00069 | 0.628 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.249 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.429 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.230 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.287 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.249 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.249 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.618 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.615 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.598 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.532 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.514 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.167 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.255 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.228 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.249 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.435 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.599 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.333 |
MOD_Cter_Amidation | 99 | 102 | PF01082 | 0.523 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.228 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.143 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.556 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.284 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.291 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.221 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.215 |
MOD_GlcNHglycan | 44 | 49 | PF01048 | 0.477 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.657 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.621 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.682 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.469 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.242 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.329 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.252 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.223 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.192 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.203 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.604 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.673 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.536 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.538 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.619 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.580 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.483 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.652 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.515 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.147 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.203 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.249 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.399 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.448 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.288 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.288 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.623 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.633 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.456 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.506 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.249 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.529 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.400 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.484 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.367 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.333 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.645 |
MOD_PKA_1 | 501 | 507 | PF00069 | 0.537 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.453 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.358 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.381 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.375 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.203 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.249 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.265 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.625 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.591 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.520 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.592 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.492 |
MOD_PKB_1 | 101 | 109 | PF00069 | 0.491 |
MOD_PKB_1 | 134 | 142 | PF00069 | 0.273 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.249 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.249 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.452 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.252 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.249 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.282 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.346 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.249 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.203 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.626 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.329 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.416 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.249 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.580 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 598 | 601 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 328 | 336 | PF00179 | 0.203 |
MOD_SUMO_rev_2 | 442 | 450 | PF00179 | 0.190 |
TRG_AP2beta_CARGO_1 | 244 | 253 | PF09066 | 0.147 |
TRG_DiLeu_BaEn_1 | 620 | 625 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_2 | 384 | 390 | PF01217 | 0.389 |
TRG_DiLeu_LyEn_5 | 620 | 625 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.228 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.147 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 580 | 583 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 621 | 624 | PF00400 | 0.453 |
TRG_NLS_Bipartite_1 | 124 | 138 | PF00514 | 0.355 |
TRG_NLS_MonoCore_2 | 542 | 547 | PF00514 | 0.435 |
TRG_NLS_MonoExtC_3 | 123 | 128 | PF00514 | 0.507 |
TRG_NLS_MonoExtN_4 | 124 | 129 | PF00514 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.203 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.203 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 582 | 586 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 623 | 628 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 72% | 100% |
A0A0S4IP49 | Bodo saltans | 26% | 82% |
A0A1X0NJN6 | Trypanosomatidae | 27% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 27% | 80% |
A0A1X0P2U1 | Trypanosomatidae | 47% | 94% |
A0A3S5H4S8 | Leishmania donovani | 88% | 99% |
A0A3S7WST0 | Leishmania donovani | 46% | 100% |
A0A3S7X9Y1 | Leishmania donovani | 34% | 100% |
A0A422NY45 | Trypanosoma rangeli | 57% | 95% |
A4H7F1 | Leishmania braziliensis | 45% | 91% |
A4HAQ7 | Leishmania braziliensis | 26% | 100% |
A4HND6 | Leishmania braziliensis | 34% | 100% |
A4HRC5 | Leishmania infantum | 88% | 99% |
A4HSA6 | Leishmania infantum | 33% | 100% |
A4HVT9 | Leishmania infantum | 46% | 100% |
A4IC09 | Leishmania infantum | 34% | 100% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 96% |
E9ABZ2 | Leishmania major | 88% | 100% |
E9AFU7 | Leishmania major | 34% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q5R9Y9 | Pongo abelii | 40% | 89% |
Q940Y8 | Arabidopsis thaliana | 39% | 97% |
V5D311 | Trypanosoma cruzi | 47% | 98% |