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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 6 |
GO:0099080 | supramolecular complex | 2 | 6 |
GO:0099081 | supramolecular polymer | 3 | 6 |
GO:0099512 | supramolecular fiber | 4 | 6 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 4 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: A4HMM9
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 22 |
GO:0007018 | microtubule-based movement | 3 | 22 |
GO:0009987 | cellular process | 1 | 22 |
GO:0006810 | transport | 3 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 22 |
GO:0003774 | cytoskeletal motor activity | 1 | 22 |
GO:0003777 | microtubule motor activity | 2 | 22 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 22 |
GO:0005515 | protein binding | 2 | 22 |
GO:0005524 | ATP binding | 5 | 22 |
GO:0008017 | microtubule binding | 5 | 22 |
GO:0008092 | cytoskeletal protein binding | 3 | 22 |
GO:0015631 | tubulin binding | 4 | 22 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0030554 | adenyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 1 |
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 | 82 | 86 | PF00656 | 0.263 |
CLV_MEL_PAP_1 | 364 | 370 | PF00089 | 0.211 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.399 |
CLV_PCSK_FUR_1 | 488 | 492 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.199 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 648 | 650 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.409 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.359 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 367 | 375 | PF00134 | 0.260 |
DOC_MAPK_gen_1 | 143 | 153 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 146 | 155 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 8 | 15 | PF00069 | 0.314 |
DOC_PP1_RVXF_1 | 425 | 431 | PF00149 | 0.471 |
DOC_PP4_FxxP_1 | 379 | 382 | PF00568 | 0.232 |
DOC_SPAK_OSR1_1 | 491 | 495 | PF12202 | 0.352 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.175 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.257 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.247 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 490 | 495 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 649 | 654 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.386 |
LIG_Actin_WH2_2 | 361 | 378 | PF00022 | 0.387 |
LIG_Actin_WH2_2 | 6 | 22 | PF00022 | 0.245 |
LIG_APCC_ABBA_1 | 158 | 163 | PF00400 | 0.241 |
LIG_APCC_ABBA_1 | 655 | 660 | PF00400 | 0.266 |
LIG_APCC_ABBA_1 | 73 | 78 | PF00400 | 0.232 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.245 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.215 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.245 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.214 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.279 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.149 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.620 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.468 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.182 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.453 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.625 |
LIG_FHA_2 | 625 | 631 | PF00498 | 0.557 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.271 |
LIG_IRF3_LxIS_1 | 209 | 214 | PF10401 | 0.163 |
LIG_LIR_Apic_2 | 301 | 306 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 378 | 382 | PF02991 | 0.189 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 127 | 138 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 583 | 593 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 61 | 66 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 659 | 665 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 583 | 588 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 656 | 661 | PF02991 | 0.534 |
LIG_NRBOX | 370 | 376 | PF00104 | 0.261 |
LIG_PCNA_yPIPBox_3 | 162 | 172 | PF02747 | 0.362 |
LIG_PDZ_Class_1 | 689 | 694 | PF00595 | 0.326 |
LIG_Pex14_1 | 294 | 298 | PF04695 | 0.403 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.249 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.332 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.414 |
LIG_SH2_PTP2 | 661 | 664 | PF00017 | 0.267 |
LIG_SH2_SRC | 76 | 79 | PF00017 | 0.245 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.217 |
LIG_SH2_STAP1 | 472 | 476 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 637 | 641 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 658 | 662 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.267 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.224 |
LIG_SUMO_SIM_anti_2 | 235 | 240 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 383 | 390 | PF11976 | 0.229 |
LIG_SUMO_SIM_anti_2 | 587 | 592 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 659 | 668 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 659 | 668 | PF11976 | 0.271 |
LIG_TRAF2_1 | 502 | 505 | PF00917 | 0.424 |
LIG_TRAF2_1 | 550 | 553 | PF00917 | 0.446 |
LIG_TRAF2_1 | 627 | 630 | PF00917 | 0.480 |
LIG_TYR_ITIM | 470 | 475 | PF00017 | 0.421 |
LIG_UBA3_1 | 510 | 516 | PF00899 | 0.350 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.243 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.254 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.229 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.632 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.639 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.273 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.246 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.261 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.282 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.587 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.264 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.522 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.532 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.233 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.456 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.244 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.460 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.518 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.273 |
MOD_Cter_Amidation | 573 | 576 | PF01082 | 0.302 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.267 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.232 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.452 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.342 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.612 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.601 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.277 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.515 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.436 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.217 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.474 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.508 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.248 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.258 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.273 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.150 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.214 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.207 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.245 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.600 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.253 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.595 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.251 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.303 |
MOD_N-GLC_1 | 680 | 685 | PF02516 | 0.473 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.237 |
MOD_N-GLC_2 | 530 | 532 | PF02516 | 0.267 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.196 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.511 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.413 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.369 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.473 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.479 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.507 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.457 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.477 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.274 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.541 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.365 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.264 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.508 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.218 |
MOD_PK_1 | 490 | 496 | PF00069 | 0.433 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.232 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.544 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.247 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.280 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.492 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.461 |
MOD_PKB_1 | 488 | 496 | PF00069 | 0.355 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.245 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.251 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.200 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.235 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.245 |
MOD_Plk_1 | 680 | 686 | PF00069 | 0.397 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.216 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.241 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.301 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.397 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.478 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.311 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.241 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.543 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.247 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.661 |
MOD_SUMO_for_1 | 44 | 47 | PF00179 | 0.279 |
MOD_SUMO_rev_2 | 135 | 142 | PF00179 | 0.290 |
MOD_SUMO_rev_2 | 256 | 265 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 268 | 273 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 542 | 550 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_1 | 506 | 511 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_4 | 552 | 558 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.279 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.240 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 460 | 462 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.408 |
TRG_NES_CRM1_1 | 440 | 452 | PF08389 | 0.401 |
TRG_NLS_MonoExtN_4 | 676 | 682 | PF00514 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.200 |
TRG_Pf-PMV_PEXEL_1 | 575 | 579 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 609 | 613 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVM1 | Leptomonas seymouri | 29% | 75% |
A0A0N1IM30 | Leptomonas seymouri | 73% | 99% |
A0A0S4IXS6 | Bodo saltans | 37% | 67% |
A0A0S4JN49 | Bodo saltans | 51% | 96% |
A0A0S4KM02 | Bodo saltans | 27% | 68% |
A0A1X0NYU1 | Trypanosomatidae | 34% | 68% |
A0A1X0P5Y8 | Trypanosomatidae | 59% | 100% |
A0A3Q8IG88 | Leishmania donovani | 77% | 99% |
A0A422MZ05 | Trypanosoma rangeli | 57% | 100% |
A0A422NEF2 | Trypanosoma rangeli | 34% | 69% |
A0A422NEQ8 | Trypanosoma rangeli | 26% | 92% |
A4HCA1 | Leishmania braziliensis | 31% | 78% |
A4HHY2 | Leishmania braziliensis | 27% | 100% |
A4IBA7 | Leishmania infantum | 76% | 99% |
C9ZVT5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 68% |
C9ZZN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AF32 | Leishmania major | 75% | 100% |
E9AVN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 78% |
E9B687 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
O43093 | Syncephalastrum racemosum | 26% | 74% |
Q7X7H4 | Oryza sativa subsp. japonica | 26% | 73% |
V5B8X9 | Trypanosoma cruzi | 56% | 99% |
V5DFA7 | Trypanosoma cruzi | 29% | 100% |