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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005819 | spindle | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJ35
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007018 | microtubule-based movement | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003774 | cytoskeletal motor activity | 1 | 2 |
GO:0003777 | microtubule motor activity | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0008017 | microtubule binding | 5 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 189 | 193 | PF00656 | 0.739 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.560 |
CLV_PCSK_FUR_1 | 421 | 425 | PF00082 | 0.485 |
CLV_PCSK_FUR_1 | 634 | 638 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 608 | 610 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.576 |
DEG_APCC_KENBOX_2 | 195 | 199 | PF00400 | 0.755 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.593 |
DEG_SPOP_SBC_1 | 13 | 17 | PF00917 | 0.825 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.383 |
DOC_MAPK_DCC_7 | 351 | 361 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 608 | 618 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 539 | 547 | PF00069 | 0.425 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.640 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 112 | 120 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 149 | 154 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 387 | 395 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 6 | 11 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 60 | 70 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 625 | 632 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 642 | 650 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.530 |
LIG_14-3-3_CterR_2 | 685 | 690 | PF00244 | 0.596 |
LIG_Actin_WH2_2 | 561 | 576 | PF00022 | 0.477 |
LIG_BIR_III_4 | 192 | 196 | PF00653 | 0.679 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_1 | 508 | 512 | PF00533 | 0.546 |
LIG_EH1_1 | 395 | 403 | PF00400 | 0.395 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.595 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.350 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.362 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.429 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.504 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.411 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.552 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.773 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.327 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.353 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.579 |
LIG_LIR_Apic_2 | 152 | 157 | PF02991 | 0.417 |
LIG_LIR_Apic_2 | 253 | 257 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 136 | 145 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 509 | 515 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.473 |
LIG_NRBOX | 351 | 357 | PF00104 | 0.326 |
LIG_Pex14_1 | 101 | 105 | PF04695 | 0.443 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.445 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 10 | 14 | PF00017 | 0.720 |
LIG_SH2_NCK_1 | 295 | 299 | PF00017 | 0.437 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.491 |
LIG_SH2_PTP2 | 363 | 366 | PF00017 | 0.355 |
LIG_SH2_SRC | 120 | 123 | PF00017 | 0.441 |
LIG_SH2_SRC | 295 | 298 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.631 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.495 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.402 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.349 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.437 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.404 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.321 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.370 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.640 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.601 |
LIG_SUMO_SIM_par_1 | 365 | 371 | PF11976 | 0.449 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.379 |
LIG_UBA3_1 | 602 | 610 | PF00899 | 0.493 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.462 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.346 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.748 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.675 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.354 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.356 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.406 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.516 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.552 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.507 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.471 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.663 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.795 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.792 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.485 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.357 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.505 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.475 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.422 |
MOD_Cter_Amidation | 301 | 304 | PF01082 | 0.443 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.427 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.394 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.630 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.784 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.788 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.616 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.346 |
MOD_GlcNHglycan | 546 | 550 | PF01048 | 0.533 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.579 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.600 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.622 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.655 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.613 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.554 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.466 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.437 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.772 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.671 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.652 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.518 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.493 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.388 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.487 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.481 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.585 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.590 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.602 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.644 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.747 |
MOD_LATS_1 | 51 | 57 | PF00433 | 0.472 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.408 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.508 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.511 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.423 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.398 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.397 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.683 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.552 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.525 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.492 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.628 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.419 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.683 |
MOD_PIKK_1 | 506 | 512 | PF00454 | 0.461 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.509 |
MOD_PIKK_1 | 534 | 540 | PF00454 | 0.448 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.580 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.669 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.742 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.695 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.459 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.386 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.461 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.552 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.521 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.485 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.489 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.441 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.350 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.407 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.422 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.605 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.407 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.447 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.479 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.377 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.329 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.802 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.485 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.573 |
MOD_SUMO_rev_2 | 275 | 284 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 344 | 353 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 546 | 554 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 324 | 329 | PF01217 | 0.340 |
TRG_DiLeu_BaEn_4 | 513 | 519 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 609 | 612 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 636 | 639 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 70 | 73 | PF00400 | 0.495 |
TRG_NLS_MonoCore_2 | 607 | 612 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 607 | 613 | PF00514 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 516 | 520 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC06 | Leptomonas seymouri | 72% | 99% |
A0A0S4KIG4 | Bodo saltans | 28% | 94% |
A0A1X0NKL3 | Trypanosomatidae | 54% | 100% |
A0A3R7LWH4 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H5Q4 | Leishmania donovani | 97% | 100% |
A4H4K9 | Leishmania braziliensis | 88% | 100% |
A4HST5 | Leishmania infantum | 97% | 100% |
C9ZTE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AKS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5DPG4 | Trypanosoma cruzi | 52% | 100% |