| 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: 5 | 
| 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: 13 | 
| NetGPI | no | yes: 0, no: 13 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005874 | microtubule | 6 | 12 | 
| GO:0099080 | supramolecular complex | 2 | 12 | 
| GO:0099081 | supramolecular polymer | 3 | 12 | 
| GO:0099512 | supramolecular fiber | 4 | 12 | 
| GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 | 
| GO:0110165 | cellular anatomical entity | 1 | 12 | 
| GO:0005737 | cytoplasm | 2 | 1 | 
| GO:0005871 | kinesin complex | 3 | 2 | 
| GO:0005875 | microtubule associated complex | 2 | 2 | 
| GO:0032991 | protein-containing complex | 1 | 2 | 
| GO:0051286 | cell tip | 3 | 1 | 
| GO:0060187 | cell pole | 2 | 1 | 
Related structures:
AlphaFold database: A4H4I4
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0007017 | microtubule-based process | 2 | 14 | 
| GO:0007018 | microtubule-based movement | 3 | 14 | 
| GO:0009987 | cellular process | 1 | 14 | 
| 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 | 
| GO:0003824 | catalytic activity | 1 | 3 | 
| GO:0016462 | pyrophosphatase activity | 5 | 2 | 
| GO:0016787 | hydrolase activity | 2 | 3 | 
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 | 
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 | 
| GO:0016887 | ATP hydrolysis activity | 7 | 2 | 
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.326 | 
| CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.374 | 
| CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.356 | 
| CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.354 | 
| CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.310 | 
| CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.458 | 
| CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.505 | 
| CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.374 | 
| CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.356 | 
| CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.340 | 
| CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.529 | 
| CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.427 | 
| CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.423 | 
| CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.390 | 
| CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.307 | 
| CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.289 | 
| CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.572 | 
| CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.376 | 
| CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.576 | 
| CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.661 | 
| CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.578 | 
| DEG_APCC_KENBOX_2 | 512 | 516 | PF00400 | 0.404 | 
| DEG_SCF_FBW7_1 | 20 | 27 | PF00400 | 0.491 | 
| DEG_SPOP_SBC_1 | 613 | 617 | PF00917 | 0.682 | 
| DOC_CKS1_1 | 185 | 190 | PF01111 | 0.305 | 
| DOC_CYCLIN_RxL_1 | 387 | 395 | PF00134 | 0.409 | 
| DOC_CYCLIN_RxL_1 | 517 | 525 | PF00134 | 0.389 | 
| DOC_CYCLIN_yCln2_LP_2 | 173 | 179 | PF00134 | 0.326 | 
| DOC_MAPK_DCC_7 | 484 | 494 | PF00069 | 0.294 | 
| DOC_MAPK_gen_1 | 287 | 296 | PF00069 | 0.397 | 
| DOC_MAPK_gen_1 | 303 | 312 | PF00069 | 0.248 | 
| DOC_MAPK_gen_1 | 360 | 369 | PF00069 | 0.340 | 
| DOC_MAPK_gen_1 | 482 | 491 | PF00069 | 0.507 | 
| DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.578 | 
| DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.356 | 
| DOC_MAPK_MEF2A_6 | 487 | 494 | PF00069 | 0.540 | 
| DOC_PP1_RVXF_1 | 361 | 367 | PF00149 | 0.334 | 
| DOC_PP2B_LxvP_1 | 137 | 140 | PF13499 | 0.326 | 
| DOC_PP2B_LxvP_1 | 173 | 176 | PF13499 | 0.302 | 
| DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.169 | 
| DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.169 | 
| DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.592 | 
| DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.464 | 
| DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.759 | 
| DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.437 | 
| DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.326 | 
| DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.793 | 
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.266 | 
| DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.442 | 
| DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.265 | 
| DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.693 | 
| DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.725 | 
| DOC_USP7_MATH_2 | 555 | 561 | PF00917 | 0.437 | 
| DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.378 | 
| DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.409 | 
| DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.610 | 
| DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.410 | 
| DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.396 | 
| DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.301 | 
| DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.714 | 
| DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.489 | 
| DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.755 | 
| LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.440 | 
| LIG_14-3-3_CanoR_1 | 268 | 276 | PF00244 | 0.411 | 
| LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.393 | 
| LIG_14-3-3_CanoR_1 | 439 | 443 | PF00244 | 0.334 | 
| LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.611 | 
| LIG_14-3-3_CanoR_1 | 605 | 609 | PF00244 | 0.734 | 
| LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.645 | 
| LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.524 | 
| LIG_14-3-3_CterR_2 | 657 | 661 | PF00244 | 0.608 | 
| LIG_Actin_WH2_2 | 196 | 213 | PF00022 | 0.450 | 
| LIG_Actin_WH2_2 | 362 | 378 | PF00022 | 0.367 | 
| LIG_Actin_WH2_2 | 504 | 521 | PF00022 | 0.522 | 
| LIG_APCC_ABBA_1 | 246 | 251 | PF00400 | 0.301 | 
| LIG_APCC_ABBA_1 | 321 | 326 | PF00400 | 0.367 | 
| LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.326 | 
| LIG_Clathr_ClatBox_1 | 15 | 19 | PF01394 | 0.455 | 
| LIG_Clathr_ClatBox_1 | 364 | 368 | PF01394 | 0.410 | 
| LIG_EVH1_2 | 431 | 435 | PF00568 | 0.169 | 
| LIG_FHA_1 | 1 | 7 | PF00498 | 0.564 | 
| LIG_FHA_1 | 163 | 169 | PF00498 | 0.319 | 
| LIG_FHA_1 | 185 | 191 | PF00498 | 0.326 | 
| LIG_FHA_1 | 384 | 390 | PF00498 | 0.296 | 
| LIG_FHA_1 | 410 | 416 | PF00498 | 0.169 | 
| LIG_FHA_1 | 442 | 448 | PF00498 | 0.301 | 
| LIG_FHA_1 | 455 | 461 | PF00498 | 0.301 | 
| LIG_FHA_1 | 627 | 633 | PF00498 | 0.747 | 
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.645 | 
| LIG_FHA_2 | 126 | 132 | PF00498 | 0.339 | 
| LIG_FHA_2 | 615 | 621 | PF00498 | 0.663 | 
| LIG_LIR_Gen_1 | 131 | 142 | PF02991 | 0.375 | 
| LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.281 | 
| LIG_LIR_Gen_1 | 290 | 296 | PF02991 | 0.367 | 
| LIG_LIR_Gen_1 | 47 | 55 | PF02991 | 0.439 | 
| LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.346 | 
| LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.281 | 
| LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.269 | 
| LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.348 | 
| LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.387 | 
| LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.462 | 
| LIG_MAD2 | 398 | 406 | PF02301 | 0.169 | 
| LIG_MLH1_MIPbox_1 | 273 | 277 | PF16413 | 0.326 | 
| LIG_NRBOX | 252 | 258 | PF00104 | 0.367 | 
| LIG_NRBOX | 442 | 448 | PF00104 | 0.330 | 
| LIG_Pex14_2 | 321 | 325 | PF04695 | 0.410 | 
| LIG_REV1ctd_RIR_1 | 322 | 332 | PF16727 | 0.326 | 
| LIG_SH2_CRK | 197 | 201 | PF00017 | 0.326 | 
| LIG_SH2_CRK | 254 | 258 | PF00017 | 0.367 | 
| LIG_SH2_CRK | 361 | 365 | PF00017 | 0.403 | 
| LIG_SH2_NCK_1 | 556 | 560 | PF00017 | 0.434 | 
| LIG_SH2_PTP2 | 245 | 248 | PF00017 | 0.357 | 
| LIG_SH2_SRC | 249 | 252 | PF00017 | 0.444 | 
| LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.403 | 
| LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.397 | 
| LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.529 | 
| LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.381 | 
| LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.375 | 
| LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.367 | 
| LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.324 | 
| LIG_SH3_1 | 580 | 586 | PF00018 | 0.562 | 
| LIG_SH3_2 | 434 | 439 | PF14604 | 0.410 | 
| LIG_SH3_3 | 182 | 188 | PF00018 | 0.300 | 
| LIG_SH3_3 | 26 | 32 | PF00018 | 0.631 | 
| LIG_SH3_3 | 343 | 349 | PF00018 | 0.324 | 
| LIG_SH3_3 | 404 | 410 | PF00018 | 0.302 | 
| LIG_SH3_3 | 428 | 434 | PF00018 | 0.369 | 
| LIG_SH3_3 | 563 | 569 | PF00018 | 0.632 | 
| LIG_SH3_3 | 580 | 586 | PF00018 | 0.706 | 
| LIG_SH3_3 | 70 | 76 | PF00018 | 0.658 | 
| LIG_SUMO_SIM_anti_2 | 150 | 156 | PF11976 | 0.302 | 
| LIG_SUMO_SIM_anti_2 | 290 | 298 | PF11976 | 0.372 | 
| LIG_SUMO_SIM_par_1 | 290 | 298 | PF11976 | 0.342 | 
| LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.410 | 
| LIG_SUMO_SIM_par_1 | 645 | 652 | PF11976 | 0.565 | 
| LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.410 | 
| LIG_TRAF2_1 | 497 | 500 | PF00917 | 0.466 | 
| LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.516 | 
| LIG_TYR_ITIM | 195 | 200 | PF00017 | 0.326 | 
| LIG_TYR_ITIM | 46 | 51 | PF00017 | 0.488 | 
| LIG_WRC_WIRS_1 | 117 | 122 | PF05994 | 0.314 | 
| MOD_CDK_SPxK_1 | 421 | 427 | PF00069 | 0.169 | 
| MOD_CK1_1 | 162 | 168 | PF00069 | 0.301 | 
| MOD_CK1_1 | 169 | 175 | PF00069 | 0.301 | 
| MOD_CK1_1 | 232 | 238 | PF00069 | 0.402 | 
| MOD_CK1_1 | 241 | 247 | PF00069 | 0.350 | 
| MOD_CK1_1 | 25 | 31 | PF00069 | 0.796 | 
| MOD_CK1_1 | 314 | 320 | PF00069 | 0.295 | 
| MOD_CK1_1 | 38 | 44 | PF00069 | 0.694 | 
| MOD_CK1_1 | 380 | 386 | PF00069 | 0.355 | 
| MOD_CK1_1 | 392 | 398 | PF00069 | 0.440 | 
| MOD_CK1_1 | 417 | 423 | PF00069 | 0.404 | 
| MOD_CK1_1 | 441 | 447 | PF00069 | 0.301 | 
| MOD_CK1_1 | 473 | 479 | PF00069 | 0.367 | 
| MOD_CK1_1 | 567 | 573 | PF00069 | 0.632 | 
| MOD_CK1_1 | 616 | 622 | PF00069 | 0.749 | 
| MOD_CK1_1 | 91 | 97 | PF00069 | 0.764 | 
| MOD_CK2_1 | 125 | 131 | PF00069 | 0.337 | 
| MOD_CK2_1 | 241 | 247 | PF00069 | 0.348 | 
| MOD_CK2_1 | 379 | 385 | PF00069 | 0.367 | 
| MOD_CK2_1 | 44 | 50 | PF00069 | 0.654 | 
| MOD_CK2_1 | 612 | 618 | PF00069 | 0.654 | 
| MOD_DYRK1A_RPxSP_1 | 605 | 609 | PF00069 | 0.499 | 
| MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.312 | 
| MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.304 | 
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.308 | 
| MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.304 | 
| MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.656 | 
| MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.400 | 
| MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.431 | 
| MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.424 | 
| MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.376 | 
| MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.323 | 
| MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.410 | 
| MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.673 | 
| MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.629 | 
| MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.630 | 
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.310 | 
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.310 | 
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.764 | 
| MOD_GSK3_1 | 221 | 228 | PF00069 | 0.275 | 
| MOD_GSK3_1 | 234 | 241 | PF00069 | 0.380 | 
| MOD_GSK3_1 | 267 | 274 | PF00069 | 0.412 | 
| MOD_GSK3_1 | 375 | 382 | PF00069 | 0.339 | 
| MOD_GSK3_1 | 385 | 392 | PF00069 | 0.293 | 
| MOD_GSK3_1 | 409 | 416 | PF00069 | 0.306 | 
| MOD_GSK3_1 | 417 | 424 | PF00069 | 0.348 | 
| MOD_GSK3_1 | 437 | 444 | PF00069 | 0.347 | 
| MOD_GSK3_1 | 522 | 529 | PF00069 | 0.414 | 
| MOD_GSK3_1 | 564 | 571 | PF00069 | 0.560 | 
| MOD_GSK3_1 | 59 | 66 | PF00069 | 0.610 | 
| MOD_GSK3_1 | 604 | 611 | PF00069 | 0.594 | 
| MOD_GSK3_1 | 612 | 619 | PF00069 | 0.640 | 
| MOD_GSK3_1 | 622 | 629 | PF00069 | 0.684 | 
| MOD_GSK3_1 | 649 | 656 | PF00069 | 0.631 | 
| MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.301 | 
| MOD_NEK2_1 | 157 | 162 | PF00069 | 0.293 | 
| MOD_NEK2_1 | 210 | 215 | PF00069 | 0.400 | 
| MOD_NEK2_1 | 312 | 317 | PF00069 | 0.370 | 
| MOD_NEK2_1 | 350 | 355 | PF00069 | 0.228 | 
| MOD_NEK2_1 | 356 | 361 | PF00069 | 0.453 | 
| MOD_NEK2_1 | 375 | 380 | PF00069 | 0.232 | 
| MOD_NEK2_1 | 470 | 475 | PF00069 | 0.384 | 
| MOD_NEK2_1 | 522 | 527 | PF00069 | 0.525 | 
| MOD_NEK2_1 | 590 | 595 | PF00069 | 0.665 | 
| MOD_NEK2_1 | 604 | 609 | PF00069 | 0.741 | 
| MOD_NEK2_1 | 649 | 654 | PF00069 | 0.671 | 
| MOD_NEK2_2 | 249 | 254 | PF00069 | 0.404 | 
| MOD_NEK2_2 | 272 | 277 | PF00069 | 0.410 | 
| MOD_PIKK_1 | 126 | 132 | PF00454 | 0.287 | 
| MOD_PIKK_1 | 441 | 447 | PF00454 | 0.282 | 
| MOD_PIKK_1 | 495 | 501 | PF00454 | 0.463 | 
| MOD_PIKK_1 | 557 | 563 | PF00454 | 0.696 | 
| MOD_PKA_1 | 211 | 217 | PF00069 | 0.326 | 
| MOD_PKA_2 | 210 | 216 | PF00069 | 0.440 | 
| MOD_PKA_2 | 267 | 273 | PF00069 | 0.310 | 
| MOD_PKA_2 | 304 | 310 | PF00069 | 0.398 | 
| MOD_PKA_2 | 438 | 444 | PF00069 | 0.301 | 
| MOD_PKA_2 | 59 | 65 | PF00069 | 0.608 | 
| MOD_PKA_2 | 604 | 610 | PF00069 | 0.726 | 
| MOD_PKA_2 | 88 | 94 | PF00069 | 0.748 | 
| MOD_Plk_1 | 389 | 395 | PF00069 | 0.305 | 
| MOD_Plk_1 | 470 | 476 | PF00069 | 0.320 | 
| MOD_Plk_4 | 113 | 119 | PF00069 | 0.248 | 
| MOD_Plk_4 | 150 | 156 | PF00069 | 0.300 | 
| MOD_Plk_4 | 234 | 240 | PF00069 | 0.340 | 
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.293 | 
| MOD_Plk_4 | 249 | 255 | PF00069 | 0.275 | 
| MOD_Plk_4 | 272 | 278 | PF00069 | 0.334 | 
| MOD_Plk_4 | 389 | 395 | PF00069 | 0.351 | 
| MOD_Plk_4 | 438 | 444 | PF00069 | 0.299 | 
| MOD_Plk_4 | 592 | 598 | PF00069 | 0.757 | 
| MOD_Plk_4 | 608 | 614 | PF00069 | 0.705 | 
| MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.409 | 
| MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.612 | 
| MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.410 | 
| MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.396 | 
| MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.301 | 
| MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.712 | 
| MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.489 | 
| MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.755 | 
| MOD_SUMO_rev_2 | 380 | 389 | PF00179 | 0.286 | 
| MOD_SUMO_rev_2 | 500 | 508 | PF00179 | 0.564 | 
| TRG_DiLeu_BaEn_1 | 290 | 295 | PF01217 | 0.444 | 
| TRG_DiLeu_BaEn_3 | 131 | 137 | PF01217 | 0.326 | 
| TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.326 | 
| TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.294 | 
| TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.285 | 
| TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.403 | 
| TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.540 | 
| TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.470 | 
| TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.374 | 
| TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.357 | 
| TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.520 | 
| TRG_NLS_Bipartite_1 | 205 | 219 | PF00514 | 0.390 | 
| TRG_NLS_MonoExtN_4 | 212 | 219 | PF00514 | 0.266 | 
| TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.603 | 
| TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.359 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P569 | Leptomonas seymouri | 27% | 75% | 
| A0A0N1HVM1 | Leptomonas seymouri | 27% | 71% | 
| A0A0N1HY56 | Leptomonas seymouri | 54% | 96% | 
| A0A0N1I0Y5 | Leptomonas seymouri | 26% | 100% | 
| A0A0N1I2F8 | Leptomonas seymouri | 25% | 79% | 
| A0A0S4ILK1 | Bodo saltans | 30% | 77% | 
| A0A0S4ILY1 | Bodo saltans | 28% | 73% | 
| A0A0S4JBC0 | Bodo saltans | 23% | 71% | 
| A0A0S4JIG8 | Bodo saltans | 27% | 69% | 
| A0A0S4JJ54 | Bodo saltans | 27% | 94% | 
| A0A1X0NJN6 | Trypanosomatidae | 39% | 100% | 
| A0A1X0NQ03 | Trypanosomatidae | 27% | 80% | 
| A0A1X0P0C2 | Trypanosomatidae | 27% | 81% | 
| A0A1X0P2B6 | Trypanosomatidae | 26% | 100% | 
| A0A1X0P9E3 | Trypanosomatidae | 28% | 100% | 
| A0A3Q8IBS7 | Leishmania donovani | 25% | 100% | 
| A0A3R7KHX7 | Trypanosoma rangeli | 27% | 89% | 
| A0A3R7MC35 | Trypanosoma rangeli | 38% | 100% | 
| A0A3R7RD86 | Trypanosoma rangeli | 27% | 82% | 
| A0A3S5H5N6 | Leishmania donovani | 76% | 100% | 
| A0A3S5IRH3 | Trypanosoma rangeli | 26% | 100% | 
| A0A3S7WX05 | Leishmania donovani | 25% | 74% | 
| A4HAQ7 | Leishmania braziliensis | 28% | 100% | 
| A4HCA1 | Leishmania braziliensis | 26% | 74% | 
| A4HSA6 | Leishmania infantum | 26% | 100% | 
| A4HSQ9 | Leishmania infantum | 75% | 100% | 
| A4HZT3 | Leishmania infantum | 25% | 74% | 
| A4I562 | Leishmania infantum | 25% | 100% | 
| C9ZL08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% | 
| C9ZQI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% | 
| C9ZTV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 74% | 
| C9ZU98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 82% | 
| E9AEA1 | Leishmania major | 28% | 100% | 
| E9AKP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% | 
| E9AVN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 74% | 
| E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% | 
| O14343 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 75% | 
| O59751 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 84% | 
| Q4Q7S4 | Leishmania major | 26% | 100% | 
| Q4QBU1 | Leishmania major | 24% | 74% | 
| Q4QJ61 | Leishmania major | 76% | 100% | 
| Q5E913 | Arabidopsis thaliana | 25% | 100% | 
| Q8S905 | Arabidopsis thaliana | 28% | 68% | 
| Q8S950 | Nicotiana tabacum | 27% | 69% | 
| Q9AWM8 | Oryza sativa subsp. japonica | 24% | 69% | 
| Q9S7P3 | Arabidopsis thaliana | 27% | 80% | 
| V5B325 | Trypanosoma cruzi | 26% | 80% | 
| V5BCN9 | Trypanosoma cruzi | 25% | 92% |