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. | yes | yes: 30 |
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005874 | microtubule | 6 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HHN7
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 16 |
GO:0007018 | microtubule-based movement | 3 | 16 |
GO:0009987 | cellular process | 1 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003774 | cytoskeletal motor activity | 1 | 16 |
GO:0003777 | microtubule motor activity | 2 | 16 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 16 |
GO:0005515 | protein binding | 2 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008017 | microtubule binding | 5 | 16 |
GO:0008092 | cytoskeletal protein binding | 3 | 16 |
GO:0015631 | tubulin binding | 4 | 16 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.385 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.366 |
CLV_Separin_Metazoa | 121 | 125 | PF03568 | 0.422 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.210 |
DEG_SCF_FBW7_1 | 454 | 460 | PF00400 | 0.470 |
DOC_CKS1_1 | 454 | 459 | PF01111 | 0.485 |
DOC_CYCLIN_RxL_1 | 42 | 50 | PF00134 | 0.490 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 405 | 414 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 212 | 219 | PF00069 | 0.406 |
DOC_MAPK_HePTP_8 | 359 | 371 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 143 | 152 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 362 | 371 | PF00069 | 0.384 |
DOC_PP2B_LxvP_1 | 392 | 395 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.366 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.505 |
DOC_USP7_UBL2_3 | 467 | 471 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 106 | 111 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 130 | 137 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 204 | 210 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 485 | 494 | PF00244 | 0.506 |
LIG_Actin_WH2_2 | 346 | 364 | PF00022 | 0.414 |
LIG_APCC_ABBA_1 | 70 | 75 | PF00400 | 0.366 |
LIG_APCC_ABBA_1 | 93 | 98 | PF00400 | 0.366 |
LIG_BRCT_BRCA1_1 | 152 | 156 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.263 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.370 |
LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.515 |
LIG_EH1_1 | 386 | 394 | PF00400 | 0.539 |
LIG_eIF4E_1 | 387 | 393 | PF01652 | 0.544 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.357 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.352 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.352 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.352 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.421 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.429 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.419 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.535 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.529 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.490 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.457 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.490 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.455 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.454 |
LIG_LIR_Gen_1 | 153 | 164 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 215 | 226 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 24 | 31 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.468 |
LIG_LIR_LC3C_4 | 391 | 394 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.482 |
LIG_MAD2 | 453 | 461 | PF02301 | 0.331 |
LIG_NRBOX | 225 | 231 | PF00104 | 0.381 |
LIG_PTB_Apo_2 | 462 | 469 | PF02174 | 0.534 |
LIG_Rb_pABgroove_1 | 391 | 399 | PF01858 | 0.464 |
LIG_Rb_pABgroove_1 | 42 | 50 | PF01858 | 0.490 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.490 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.612 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.410 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.603 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 419 | 425 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 165 | 172 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 325 | 332 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 419 | 425 | PF11976 | 0.516 |
LIG_TYR_ITIM | 491 | 496 | PF00017 | 0.487 |
LIG_UBA3_1 | 119 | 125 | PF00899 | 0.381 |
LIG_UBA3_1 | 287 | 292 | PF00899 | 0.497 |
LIG_WRC_WIRS_1 | 206 | 211 | PF05994 | 0.352 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.397 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.337 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.399 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.352 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.464 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.469 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.342 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.315 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.429 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.499 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.561 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.542 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.366 |
MOD_DYRK1A_RPxSP_1 | 453 | 457 | PF00069 | 0.462 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.490 |
MOD_GlcNHglycan | 183 | 187 | PF01048 | 0.455 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.385 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.499 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.598 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.352 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.331 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.348 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.355 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.339 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.533 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.553 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.586 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.448 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.469 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.433 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.376 |
MOD_N-GLC_1 | 137 | 142 | PF02516 | 0.339 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.352 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.352 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.493 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.623 |
MOD_N-GLC_2 | 10 | 12 | PF02516 | 0.359 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.352 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.352 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.352 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.352 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.352 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.492 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.463 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.531 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.472 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.490 |
MOD_OFUCOSY | 370 | 375 | PF10250 | 0.472 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.352 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.610 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.636 |
MOD_PK_1 | 106 | 112 | PF00069 | 0.490 |
MOD_PKA_1 | 212 | 218 | PF00069 | 0.477 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.370 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.342 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.348 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.546 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.517 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.352 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.360 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.600 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.490 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.256 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.256 |
MOD_Plk_2-3 | 325 | 331 | PF00069 | 0.452 |
MOD_Plk_2-3 | 340 | 346 | PF00069 | 0.389 |
MOD_Plk_2-3 | 89 | 95 | PF00069 | 0.399 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.385 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.352 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.366 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.352 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.574 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.424 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.460 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.366 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.356 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.457 |
MOD_SUMO_for_1 | 315 | 318 | PF00179 | 0.628 |
MOD_SUMO_rev_2 | 155 | 164 | PF00179 | 0.291 |
MOD_SUMO_rev_2 | 208 | 215 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 220 | 227 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 283 | 288 | PF01217 | 0.608 |
TRG_DiLeu_BaEn_1 | 344 | 349 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.356 |
TRG_NES_CRM1_1 | 163 | 177 | PF08389 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 228 | 232 | PF00026 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY56 | Leptomonas seymouri | 28% | 76% |
A0A0N1IH46 | Leptomonas seymouri | 33% | 73% |
A0A0S4J1I2 | Bodo saltans | 32% | 78% |
A0A0S4J3A4 | Bodo saltans | 29% | 85% |
A0A0S4JJ54 | Bodo saltans | 31% | 74% |
A0A0S4KL43 | Bodo saltans | 28% | 100% |
A0A1X0P9E3 | Trypanosomatidae | 63% | 87% |
A0A1X0PAG9 | Trypanosomatidae | 51% | 87% |
A0A3Q8IEL2 | Leishmania donovani | 67% | 88% |
A0A3Q8IHG6 | Leishmania donovani | 88% | 88% |
A0A3R7KHX7 | Trypanosoma rangeli | 34% | 70% |
A0A3R7MDH9 | Trypanosoma rangeli | 29% | 73% |
A0A3R7R330 | Trypanosoma rangeli | 64% | 99% |
A0A3S7X2P9 | Leishmania donovani | 88% | 88% |
A0A422NXU3 | Trypanosoma rangeli | 44% | 100% |
A4I4V2 | Leishmania infantum | 88% | 88% |
A4I4V3 | Leishmania infantum | 67% | 88% |
B9G2X9 | Oryza sativa subsp. japonica | 33% | 86% |
C9ZL08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 88% |
C9ZL09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 90% |
E9AEA0 | Leishmania major | 87% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 88% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 85% |
Q10E64 | Oryza sativa subsp. japonica | 36% | 70% |
Q4Q7S4 | Leishmania major | 32% | 85% |
Q5E913 | Arabidopsis thaliana | 28% | 82% |
Q6S001 | Dictyostelium discoideum | 32% | 76% |
Q8J1G1 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 29% | 76% |
Q965T6 | Caenorhabditis elegans | 38% | 80% |
Q9D2Z8 | Mus musculus | 33% | 81% |
Q9V877 | Drosophila melanogaster | 29% | 82% |
V5B8M1 | Trypanosoma cruzi | 35% | 84% |
V5BK25 | Trypanosoma cruzi | 30% | 72% |
V5BMP0 | Trypanosoma cruzi | 34% | 67% |
V5DMS2 | Trypanosoma cruzi | 34% | 97% |
V5DTU1 | Trypanosoma cruzi | 48% | 90% |