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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005813 | centrosome | 3 | 1 |
GO:0005814 | centriole | 5 | 1 |
GO:0005815 | microtubule organizing center | 2 | 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: E9AQY6
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 | 508 | 512 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.560 |
CLV_PCSK_PC7_1 | 176 | 182 | PF00082 | 0.499 |
CLV_PCSK_PC7_1 | 376 | 382 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.485 |
CLV_Separin_Metazoa | 443 | 447 | PF03568 | 0.418 |
DEG_APCC_DBOX_1 | 491 | 499 | PF00400 | 0.524 |
DEG_SCF_TRCP1_1 | 23 | 29 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 418 | 422 | PF00917 | 0.786 |
DOC_CKS1_1 | 86 | 91 | PF01111 | 0.626 |
DOC_MAPK_gen_1 | 179 | 189 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 489 | 499 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 70 | 78 | PF00069 | 0.641 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 492 | 499 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 70 | 78 | PF00069 | 0.641 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.476 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 161 | 165 | PF12436 | 0.618 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 111 | 121 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 209 | 217 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 380 | 389 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 463 | 467 | PF00244 | 0.427 |
LIG_Actin_WH2_2 | 460 | 477 | PF00022 | 0.390 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.549 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.615 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.493 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.495 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.522 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.647 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.654 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.563 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.566 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.490 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.463 |
LIG_LIR_Gen_1 | 168 | 178 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 284 | 292 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.410 |
LIG_RPA_C_Plants | 226 | 237 | PF08784 | 0.517 |
LIG_SH2_STAT3 | 295 | 298 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.408 |
LIG_SH3_2 | 86 | 91 | PF14604 | 0.626 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.632 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.615 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.349 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.690 |
LIG_SUMO_SIM_anti_2 | 460 | 468 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 493 | 499 | PF11976 | 0.363 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.492 |
LIG_WW_2 | 389 | 392 | PF00397 | 0.601 |
MOD_CDK_SPxK_1 | 85 | 91 | PF00069 | 0.623 |
MOD_CDK_SPxxK_3 | 85 | 92 | PF00069 | 0.625 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.565 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.669 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.646 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.685 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.617 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.700 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.713 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.646 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.516 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.584 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.493 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.380 |
MOD_DYRK1A_RPxSP_1 | 81 | 85 | PF00069 | 0.566 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.707 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.660 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.451 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.711 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.657 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.720 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.631 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.524 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.672 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.724 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.626 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.625 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.554 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.609 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.631 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.573 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.742 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.790 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.471 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.734 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.645 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.635 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.677 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.501 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.430 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.766 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.623 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.625 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.551 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.660 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.558 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.719 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.599 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.490 |
MOD_PKA_1 | 380 | 386 | PF00069 | 0.576 |
MOD_PKA_1 | 91 | 97 | PF00069 | 0.627 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.457 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.446 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.493 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.386 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.718 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.479 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.573 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.585 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.504 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.517 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.574 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.489 |
MOD_PKB_1 | 507 | 515 | PF00069 | 0.459 |
MOD_PKB_1 | 518 | 526 | PF00069 | 0.531 |
MOD_PKB_1 | 70 | 78 | PF00069 | 0.695 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.451 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.502 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.489 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.380 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.489 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.499 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.559 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.388 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.616 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.724 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.665 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.643 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.622 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 359 | 363 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9K9 | Leptomonas seymouri | 51% | 100% |
A0A3S7WUA9 | Leishmania donovani | 86% | 100% |
A0A422NFB5 | Trypanosoma rangeli | 38% | 100% |
A4H8W0 | Leishmania braziliensis | 75% | 100% |
A4HXA7 | Leishmania infantum | 87% | 100% |
C9ZTV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4QEH7 | Leishmania major | 87% | 100% |