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: E9APY3
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 | 0.763 |
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.717 |
CLV_C14_Caspase3-7 | 565 | 569 | PF00656 | 0.703 |
CLV_MEL_PAP_1 | 469 | 475 | PF00089 | 0.617 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.457 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.538 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.275 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 351 | 355 | PF00917 | 0.567 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.353 |
DOC_CKS1_1 | 228 | 233 | PF01111 | 0.670 |
DOC_CKS1_1 | 578 | 583 | PF01111 | 0.674 |
DOC_CYCLIN_RxL_1 | 408 | 418 | PF00134 | 0.548 |
DOC_CYCLIN_RxL_1 | 97 | 109 | PF00134 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 430 | 436 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.712 |
DOC_MAPK_gen_1 | 441 | 450 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 82 | 90 | PF00069 | 0.428 |
DOC_MAPK_HePTP_8 | 426 | 438 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 359 | 367 | PF00069 | 0.686 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 100 | 107 | PF00149 | 0.532 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.574 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.674 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.624 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.606 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.745 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 173 | 179 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 222 | 229 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 383 | 391 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 444 | 448 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 472 | 476 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 521 | 529 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 572 | 581 | PF00244 | 0.681 |
LIG_Actin_WH2_2 | 423 | 439 | PF00022 | 0.584 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.751 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.670 |
LIG_BRCT_BRCA1_1 | 378 | 382 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_2 | 353 | 359 | PF00533 | 0.580 |
LIG_Clathr_ClatBox_1 | 267 | 271 | PF01394 | 0.392 |
LIG_EH_1 | 490 | 494 | PF12763 | 0.521 |
LIG_eIF4E_1 | 260 | 266 | PF01652 | 0.360 |
LIG_eIF4E_1 | 484 | 490 | PF01652 | 0.641 |
LIG_EVH1_2 | 37 | 41 | PF00568 | 0.499 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.658 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.567 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.408 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.772 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.692 |
LIG_LIR_Apic_2 | 364 | 370 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 379 | 385 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 40 | 44 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.508 |
LIG_PTB_Apo_2 | 488 | 495 | PF02174 | 0.547 |
LIG_PTB_Phospho_1 | 488 | 494 | PF10480 | 0.549 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.589 |
LIG_SH2_GRB2like | 484 | 487 | PF00017 | 0.711 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.598 |
LIG_SH2_SRC | 260 | 263 | PF00017 | 0.376 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 484 | 488 | PF00017 | 0.671 |
LIG_SH2_STAT3 | 196 | 199 | PF00017 | 0.603 |
LIG_SH2_STAT3 | 591 | 594 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.541 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.755 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.666 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.687 |
LIG_SH3_5 | 256 | 260 | PF00018 | 0.395 |
LIG_SUMO_SIM_anti_2 | 262 | 269 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 538 | 544 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 265 | 271 | PF11976 | 0.390 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.536 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.702 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.598 |
LIG_WW_3 | 36 | 40 | PF00397 | 0.730 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.657 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.516 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.761 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.660 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.622 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.564 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.468 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.584 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.582 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.790 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.486 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.650 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.506 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.523 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.479 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.570 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.777 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.681 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.741 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.427 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.775 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.702 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.656 |
MOD_GlcNHglycan | 20 | 25 | PF01048 | 0.720 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.666 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.662 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.545 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.659 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.687 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.602 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.576 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.629 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.441 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.520 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.685 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.467 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.663 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.683 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.509 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.805 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.497 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.475 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.595 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.692 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.708 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.551 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.726 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.656 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.675 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.375 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.641 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.616 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.608 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.553 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.612 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.489 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.649 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.661 |
MOD_NEK2_2 | 583 | 588 | PF00069 | 0.592 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.696 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.659 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.466 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.489 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.763 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.682 |
MOD_PKA_1 | 237 | 243 | PF00069 | 0.534 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.686 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.757 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.374 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.510 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.453 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.617 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.698 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.357 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.493 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.593 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.620 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.449 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.419 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.701 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.558 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.669 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.761 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.791 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.603 |
MOD_SUMO_rev_2 | 318 | 327 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_1 | 422 | 427 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.665 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 590 | 594 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAQ5 | Leptomonas seymouri | 56% | 100% |
A0A1X0NMR8 | Trypanosomatidae | 27% | 100% |
A0A3Q8I9X0 | Leishmania donovani | 92% | 100% |
A0A422NDE3 | Trypanosoma rangeli | 28% | 87% |
A4H7V5 | Leishmania braziliensis | 75% | 100% |
A4HW81 | Leishmania infantum | 92% | 100% |
D0A9A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4QFJ9 | Leishmania major | 92% | 100% |
V5BID0 | Trypanosoma cruzi | 28% | 100% |