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: A4HGQ6
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 | 178 | 182 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.768 |
CLV_MEL_PAP_1 | 152 | 158 | PF00089 | 0.606 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.563 |
CLV_PCSK_FUR_1 | 255 | 259 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.544 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.498 |
DOC_MAPK_gen_1 | 335 | 344 | PF00069 | 0.697 |
DOC_MAPK_gen_1 | 372 | 380 | PF00069 | 0.720 |
DOC_MAPK_gen_1 | 528 | 535 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 372 | 380 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 528 | 535 | PF00069 | 0.360 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.624 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 409 | 417 | PF00244 | 0.543 |
LIG_Actin_WH2_2 | 339 | 357 | PF00022 | 0.638 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.731 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.672 |
LIG_EVH1_2 | 448 | 452 | PF00568 | 0.504 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.763 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.606 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.417 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.366 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.766 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.596 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.786 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.714 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.706 |
LIG_LIR_Gen_1 | 162 | 171 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 341 | 351 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.633 |
LIG_MYND_1 | 479 | 483 | PF01753 | 0.670 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.524 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.561 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 299 | 303 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.467 |
LIG_SH2_STAT3 | 37 | 40 | PF00017 | 0.577 |
LIG_SH2_STAT3 | 571 | 574 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.595 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.733 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.689 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.645 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.582 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.601 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.736 |
LIG_UBA3_1 | 318 | 323 | PF00899 | 0.530 |
LIG_WW_3 | 415 | 419 | PF00397 | 0.663 |
MOD_CDK_SPxxK_3 | 2 | 9 | PF00069 | 0.713 |
MOD_CDK_SPxxK_3 | 365 | 372 | PF00069 | 0.781 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.574 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.543 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.763 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.664 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.681 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.578 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.427 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.746 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.766 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.743 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.713 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.548 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.744 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.623 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.522 |
MOD_GlcNHglycan | 208 | 212 | PF01048 | 0.580 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.692 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.519 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.536 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.781 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.772 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.756 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.713 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.627 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.668 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.557 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.585 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.432 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.538 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.724 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.675 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.622 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.649 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.748 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.665 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.630 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.609 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.503 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.620 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.681 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.722 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.571 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.503 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.604 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.592 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.787 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.754 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.721 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.694 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.487 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.425 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.567 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.708 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.655 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.763 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.468 |
MOD_PK_1 | 374 | 380 | PF00069 | 0.531 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.578 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.525 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.529 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.722 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.715 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.626 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.608 |
MOD_PKB_1 | 372 | 380 | PF00069 | 0.529 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.415 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.695 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.711 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.595 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.680 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.752 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.794 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.686 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.615 |
MOD_SUMO_for_1 | 322 | 325 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 212 | 222 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 55 | 64 | PF00179 | 0.576 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.563 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 530 | 543 | PF08389 | 0.528 |
TRG_NES_CRM1_1 | 72 | 86 | PF08389 | 0.484 |
TRG_NLS_Bipartite_1 | 90 | 109 | PF00514 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 172 | 176 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 486 | 490 | PF00026 | 0.766 |
TRG_Pf-PMV_PEXEL_1 | 50 | 55 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYF9 | Leptomonas seymouri | 55% | 93% |
A0A1X0NR42 | Trypanosomatidae | 32% | 98% |
A0A3S5IQW4 | Trypanosoma rangeli | 32% | 94% |
A0A3S7X1P3 | Leishmania donovani | 81% | 100% |
A4I3T0 | Leishmania infantum | 81% | 100% |
D0A877 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B022 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q864 | Leishmania major | 81% | 100% |
V5AWM8 | Trypanosoma cruzi | 31% | 100% |