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:0005874 | microtubule | 6 | 18 |
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 |
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: A4HRC5
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 18 |
GO:0007018 | microtubule-based movement | 3 | 18 |
GO:0009987 | cellular process | 1 | 18 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007019 | microtubule depolymerization | 5 | 2 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 2 |
GO:0032984 | protein-containing complex disassembly | 5 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051261 | protein depolymerization | 6 | 2 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
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 | 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 | 153 | 157 | PF00656 | 0.322 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.735 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 452 | 454 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 632 | 634 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 478 | 484 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 566 | 572 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.450 |
CLV_Separin_Metazoa | 410 | 414 | PF03568 | 0.277 |
DEG_APCC_DBOX_1 | 277 | 285 | PF00400 | 0.223 |
DEG_SPOP_SBC_1 | 668 | 672 | PF00917 | 0.465 |
DOC_CKS1_1 | 528 | 533 | PF01111 | 0.530 |
DOC_CYCLIN_RxL_1 | 379 | 389 | PF00134 | 0.316 |
DOC_MAPK_gen_1 | 128 | 137 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 166 | 174 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 128 | 137 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 166 | 174 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 331 | 340 | PF00069 | 0.359 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.607 |
DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.188 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.645 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 175 | 184 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 252 | 261 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 453 | 461 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 482 | 488 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 626 | 636 | PF00244 | 0.483 |
LIG_Actin_WH2_1 | 48 | 63 | PF00022 | 0.322 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.233 |
LIG_BRCT_BRCA1_1 | 669 | 673 | PF00533 | 0.476 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.445 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.219 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.307 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.275 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.636 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.601 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.420 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.324 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.219 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.188 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.513 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.286 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.226 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.312 |
LIG_FHA_2 | 639 | 645 | PF00498 | 0.490 |
LIG_Integrin_isoDGR_2 | 276 | 278 | PF01839 | 0.230 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 248 | 256 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.461 |
LIG_NRBOX | 270 | 276 | PF00104 | 0.286 |
LIG_PCNA_TLS_4 | 633 | 640 | PF02747 | 0.483 |
LIG_PDZ_Class_1 | 668 | 673 | PF00595 | 0.470 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.277 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.473 |
LIG_RPA_C_Fungi | 621 | 633 | PF08784 | 0.483 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.371 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.619 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.532 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.429 |
LIG_SUMO_SIM_par_1 | 383 | 389 | PF11976 | 0.277 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.409 |
LIG_UBA3_1 | 133 | 139 | PF00899 | 0.405 |
LIG_UBA3_1 | 335 | 343 | PF00899 | 0.247 |
LIG_UBA3_1 | 384 | 388 | PF00899 | 0.315 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.277 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.486 |
MOD_CDK_SPK_2 | 527 | 532 | PF00069 | 0.667 |
MOD_CDK_SPxxK_3 | 91 | 98 | PF00069 | 0.648 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.499 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.316 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.445 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.284 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.363 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.233 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.316 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.599 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.594 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.607 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.585 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.697 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.540 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.431 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.187 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.316 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.247 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.316 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.498 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.610 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.390 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.471 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.694 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.311 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.234 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.310 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.267 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.631 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.572 |
MOD_GlcNHglycan | 552 | 556 | PF01048 | 0.685 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.694 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.717 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.474 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.265 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.341 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.284 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.155 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.217 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.230 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.649 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.674 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.613 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.606 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.652 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.647 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.664 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.599 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.698 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.461 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.574 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.230 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.313 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.454 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.427 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.459 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.306 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.298 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.624 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.652 |
MOD_NEK2_2 | 214 | 219 | PF00069 | 0.316 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.552 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.471 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.517 |
MOD_PIKK_1 | 663 | 669 | PF00454 | 0.670 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.396 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.342 |
MOD_PKA_1 | 343 | 349 | PF00069 | 0.363 |
MOD_PKA_1 | 482 | 488 | PF00069 | 0.664 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.453 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.388 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.410 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.433 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.230 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.310 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.293 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.657 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.573 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.650 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.540 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.501 |
MOD_PKB_1 | 138 | 146 | PF00069 | 0.305 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.316 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.286 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.219 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.445 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.303 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.316 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.305 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.375 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.316 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.259 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.653 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.649 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.475 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.316 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.668 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.675 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.680 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.646 |
MOD_SUMO_for_1 | 601 | 604 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 162 | 170 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 332 | 340 | PF00179 | 0.230 |
TRG_DiLeu_BaEn_1 | 623 | 628 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_2 | 388 | 394 | PF01217 | 0.363 |
TRG_DiLeu_LyEn_5 | 623 | 628 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 624 | 627 | PF00400 | 0.545 |
TRG_NLS_Bipartite_1 | 128 | 142 | PF00514 | 0.390 |
TRG_NLS_MonoExtC_3 | 127 | 132 | PF00514 | 0.528 |
TRG_NLS_MonoExtN_4 | 128 | 133 | PF00514 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 282 | 286 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.206 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 585 | 589 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 626 | 631 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 73% | 100% |
A0A0S4IP49 | Bodo saltans | 27% | 83% |
A0A1X0P2U1 | Trypanosomatidae | 46% | 96% |
A0A3S5H4S8 | Leishmania donovani | 100% | 100% |
A0A3S7WST0 | Leishmania donovani | 46% | 92% |
A0A3S7X9Y1 | Leishmania donovani | 34% | 100% |
A0A422NY45 | Trypanosoma rangeli | 51% | 96% |
A4H337 | Leishmania braziliensis | 88% | 100% |
A4H7F1 | Leishmania braziliensis | 46% | 100% |
A4HAQ7 | Leishmania braziliensis | 26% | 100% |
A4HDC2 | Leishmania braziliensis | 41% | 100% |
A4HND6 | Leishmania braziliensis | 34% | 100% |
A4HSA6 | Leishmania infantum | 32% | 100% |
A4HVT9 | Leishmania infantum | 46% | 92% |
A4IC09 | Leishmania infantum | 34% | 100% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 97% |
E9ABZ2 | Leishmania major | 97% | 100% |
E9AFU7 | Leishmania major | 34% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9API5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AWQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4QFZ3 | Leishmania major | 46% | 100% |
Q940Y8 | Arabidopsis thaliana | 40% | 98% |
V5D311 | Trypanosoma cruzi | 47% | 99% |