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:0005813 | centrosome | 3 | 1 |
GO:0005814 | centriole | 5 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B022
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007098 | centrosome cycle | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010638 | positive regulation of organelle organization | 6 | 1 |
GO:0010824 | regulation of centrosome duplication | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031023 | microtubule organizing center organization | 3 | 1 |
GO:0032886 | regulation of microtubule-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 1 |
GO:0044089 | positive regulation of cellular component biogenesis | 5 | 1 |
GO:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0046599 | regulation of centriole replication | 6 | 1 |
GO:0046601 | positive regulation of centriole replication | 7 | 1 |
GO:0046605 | regulation of centrosome cycle | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051130 | positive regulation of cellular component organization | 5 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0051495 | positive regulation of cytoskeleton organization | 7 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 1 |
GO:1902115 | regulation of organelle assembly | 5 | 1 |
GO:1902117 | positive regulation of organelle assembly | 6 | 1 |
GO:1903722 | regulation of centriole elongation | 6 | 1 |
GO:1903724 | positive regulation of centriole elongation | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.749 |
CLV_MEL_PAP_1 | 152 | 158 | PF00089 | 0.601 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.573 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.543 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.489 |
DEG_SCF_TRCP1_1 | 428 | 434 | PF00400 | 0.713 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.696 |
DOC_MAPK_DCC_7 | 336 | 345 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 145 | 152 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 207 | 216 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 336 | 345 | PF00069 | 0.709 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.650 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.624 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 475 | 480 | PF00244 | 0.731 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.721 |
LIG_BRCT_BRCA1_1 | 285 | 289 | PF00533 | 0.698 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.725 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.640 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.762 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.732 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.612 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.540 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.479 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.421 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.782 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.609 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.810 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.720 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.700 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.701 |
LIG_LIR_Gen_1 | 162 | 171 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 314 | 323 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.572 |
LIG_LYPXL_yS_3 | 448 | 451 | PF13949 | 0.701 |
LIG_MAD2 | 410 | 418 | PF02301 | 0.602 |
LIG_MYND_1 | 480 | 484 | PF01753 | 0.668 |
LIG_PCNA_PIPBox_1 | 282 | 291 | PF02747 | 0.470 |
LIG_PCNA_yPIPBox_3 | 276 | 289 | PF02747 | 0.480 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.525 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.583 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 37 | 40 | PF00017 | 0.574 |
LIG_SH2_STAT3 | 573 | 576 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.586 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.750 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.642 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.588 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.597 |
LIG_TRAF2_1 | 462 | 465 | PF00917 | 0.697 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.729 |
LIG_UBA3_1 | 319 | 324 | PF00899 | 0.530 |
LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.532 |
MOD_CDC14_SPxK_1 | 264 | 267 | PF00782 | 0.680 |
MOD_CDK_SPxK_1 | 261 | 267 | PF00069 | 0.662 |
MOD_CDK_SPxxK_3 | 261 | 268 | PF00069 | 0.668 |
MOD_CDK_SPxxK_3 | 366 | 373 | PF00069 | 0.796 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.559 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.768 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.647 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.665 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.777 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.699 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.500 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.586 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.779 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.768 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.715 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.725 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.742 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.598 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.515 |
MOD_GlcNHglycan | 208 | 212 | PF01048 | 0.591 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.737 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.801 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.756 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.769 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.655 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.616 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.674 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.572 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.746 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.714 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.557 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.622 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.650 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.760 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.650 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.718 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.613 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.505 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.582 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.700 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.569 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.584 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.598 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.511 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.803 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.738 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.709 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.689 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.489 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.609 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.601 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.509 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.534 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.722 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.586 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.508 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.524 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.737 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.738 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.608 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.411 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.699 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.733 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.697 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.722 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.685 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.539 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.731 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.755 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.808 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.654 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.726 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.577 |
MOD_SUMO_for_1 | 323 | 326 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 55 | 64 | PF00179 | 0.575 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.584 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.808 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.562 |
TRG_NES_CRM1_1 | 532 | 545 | PF08389 | 0.539 |
TRG_NES_CRM1_1 | 72 | 86 | PF08389 | 0.480 |
TRG_NLS_Bipartite_1 | 90 | 109 | PF00514 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 172 | 176 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 487 | 491 | PF00026 | 0.774 |
TRG_Pf-PMV_PEXEL_1 | 50 | 55 | PF00026 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYF9 | Leptomonas seymouri | 55% | 93% |
A0A1X0NR42 | Trypanosomatidae | 32% | 99% |
A0A3S5IQW4 | Trypanosoma rangeli | 33% | 95% |
A0A3S7X1P3 | Leishmania donovani | 93% | 100% |
A4HGQ6 | Leishmania braziliensis | 83% | 100% |
A4I3T0 | Leishmania infantum | 93% | 100% |
D0A877 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q864 | Leishmania major | 93% | 100% |
V5AWM8 | Trypanosoma cruzi | 31% | 100% |