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: 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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 4 |
GO:0005868 | cytoplasmic dynein complex | 4 | 4 |
GO:0005874 | microtubule | 6 | 4 |
GO:0005875 | microtubule associated complex | 2 | 4 |
GO:0030286 | dynein complex | 3 | 4 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0099080 | supramolecular complex | 2 | 4 |
GO:0099081 | supramolecular polymer | 3 | 4 |
GO:0099512 | supramolecular fiber | 4 | 4 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:1902494 | catalytic complex | 2 | 4 |
Related structures:
AlphaFold database: A0A3Q8I9X0
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 4 |
GO:0007018 | microtubule-based movement | 3 | 4 |
GO:0009987 | cellular process | 1 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0036094 | small molecule binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.757 |
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 563 | 567 | PF00656 | 0.776 |
CLV_MEL_PAP_1 | 467 | 473 | PF00089 | 0.623 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.469 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.463 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.535 |
DEG_APCC_DBOX_1 | 441 | 449 | PF00400 | 0.520 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.278 |
DEG_SPOP_SBC_1 | 335 | 339 | PF00917 | 0.496 |
DEG_SPOP_SBC_1 | 349 | 353 | PF00917 | 0.566 |
DEG_SPOP_SBC_1 | 375 | 379 | PF00917 | 0.525 |
DOC_CKS1_1 | 228 | 233 | PF01111 | 0.657 |
DOC_CKS1_1 | 576 | 581 | PF01111 | 0.691 |
DOC_CYCLIN_RxL_1 | 406 | 416 | PF00134 | 0.553 |
DOC_CYCLIN_RxL_1 | 97 | 109 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 428 | 434 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.714 |
DOC_MAPK_gen_1 | 439 | 448 | PF00069 | 0.537 |
DOC_MAPK_HePTP_8 | 424 | 436 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 357 | 365 | PF00069 | 0.623 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.504 |
DOC_PP1_RVXF_1 | 100 | 107 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.561 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.687 |
DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.631 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.621 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.584 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 173 | 179 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 222 | 229 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 28 | 38 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 519 | 527 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 570 | 579 | PF00244 | 0.695 |
LIG_Actin_WH2_2 | 421 | 437 | PF00022 | 0.581 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.768 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_2 | 351 | 357 | PF00533 | 0.570 |
LIG_Clathr_ClatBox_1 | 267 | 271 | PF01394 | 0.392 |
LIG_EH_1 | 488 | 492 | PF12763 | 0.517 |
LIG_eIF4E_1 | 260 | 266 | PF01652 | 0.358 |
LIG_eIF4E_1 | 482 | 488 | PF01652 | 0.637 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.580 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.580 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.647 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.410 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.731 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.706 |
LIG_LIR_Apic_2 | 362 | 368 | PF02991 | 0.632 |
LIG_LIR_Apic_2 | 377 | 383 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.505 |
LIG_PTB_Apo_2 | 486 | 493 | PF02174 | 0.545 |
LIG_PTB_Phospho_1 | 486 | 492 | PF10480 | 0.546 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.533 |
LIG_SH2_GRB2like | 482 | 485 | PF00017 | 0.704 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.535 |
LIG_SH2_SRC | 260 | 263 | PF00017 | 0.376 |
LIG_SH2_SRC | 482 | 485 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.668 |
LIG_SH2_STAT3 | 196 | 199 | PF00017 | 0.540 |
LIG_SH2_STAT3 | 589 | 592 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.579 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.751 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.719 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.703 |
LIG_SH3_5 | 256 | 260 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 262 | 269 | PF11976 | 0.379 |
LIG_SUMO_SIM_anti_2 | 536 | 542 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 265 | 271 | PF11976 | 0.390 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.538 |
LIG_TRAF2_1 | 606 | 609 | PF00917 | 0.713 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.540 |
LIG_WW_3 | 36 | 40 | PF00397 | 0.724 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.630 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.594 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.516 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.761 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.686 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.613 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.563 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.682 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.488 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.530 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.573 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.804 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.648 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.518 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.480 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.599 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.759 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.676 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.751 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.426 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.666 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.631 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.679 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.673 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.641 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.543 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.697 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.614 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.593 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.624 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.243 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.460 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.693 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.671 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.466 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.718 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.677 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.695 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.750 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.496 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.598 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.706 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.726 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.708 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.566 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.420 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.717 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.671 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.383 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.641 |
MOD_N-GLC_1 | 509 | 514 | PF02516 | 0.612 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.573 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.597 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.610 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.631 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.508 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.666 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.676 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.705 |
MOD_NEK2_2 | 581 | 586 | PF00069 | 0.615 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.697 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.500 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.767 |
MOD_PIKK_1 | 608 | 614 | PF00454 | 0.660 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.679 |
MOD_PKA_1 | 237 | 243 | PF00069 | 0.513 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.695 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.767 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.295 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.770 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.736 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.504 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.470 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.621 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.711 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.494 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.595 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.614 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.439 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.726 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.665 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.761 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.783 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.620 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.566 |
MOD_SUMO_rev_2 | 318 | 327 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.584 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 588 | 592 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAQ5 | Leptomonas seymouri | 58% | 100% |
A0A1X0NMR8 | Trypanosomatidae | 28% | 100% |
A0A422NDE3 | Trypanosoma rangeli | 27% | 87% |
A4H7V5 | Leishmania braziliensis | 77% | 100% |
A4HW81 | Leishmania infantum | 99% | 100% |
D0A9A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9APY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QFJ9 | Leishmania major | 92% | 100% |
V5BID0 | Trypanosoma cruzi | 27% | 100% |