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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A4H8W0
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 | 66 | 70 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.812 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 158 | 164 | PF00082 | 0.510 |
CLV_PCSK_PC7_1 | 358 | 364 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.456 |
DEG_APCC_DBOX_1 | 473 | 481 | PF00400 | 0.515 |
DEG_SCF_FBW7_1 | 417 | 423 | PF00400 | 0.444 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.737 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.362 |
DOC_CKS1_1 | 417 | 422 | PF01111 | 0.463 |
DOC_MAPK_gen_1 | 161 | 171 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 471 | 479 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.484 |
DOC_PP1_RVXF_1 | 309 | 315 | PF00149 | 0.347 |
DOC_SPAK_OSR1_1 | 93 | 97 | PF12202 | 0.497 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.648 |
DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 149 | 156 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 324 | 331 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 348 | 355 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 445 | 449 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 62 | 72 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 93 | 103 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 442 | 459 | PF00022 | 0.366 |
LIG_BIR_III_2 | 367 | 371 | PF00653 | 0.477 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.491 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.475 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.487 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.491 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.508 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.642 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.650 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.571 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.497 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.653 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.329 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.580 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.682 |
LIG_LIR_Gen_1 | 150 | 160 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 266 | 274 | PF02991 | 0.432 |
LIG_LIR_LC3C_4 | 447 | 450 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.440 |
LIG_PDZ_Class_1 | 479 | 484 | PF00595 | 0.379 |
LIG_RPA_C_Plants | 208 | 219 | PF08784 | 0.529 |
LIG_SH2_STAT3 | 277 | 280 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.445 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.651 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.767 |
LIG_SUMO_SIM_anti_2 | 442 | 450 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 475 | 483 | PF11976 | 0.369 |
LIG_TRAF2_1 | 263 | 266 | PF00917 | 0.494 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.641 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.607 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.694 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.761 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.668 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.517 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.666 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.404 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.599 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.597 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.805 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.645 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.471 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.747 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.551 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.644 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.668 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.519 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.452 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.684 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.325 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.496 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.656 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.605 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.663 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.713 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.749 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.683 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.697 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.487 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.560 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.656 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.688 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.646 |
MOD_LATS_1 | 40 | 46 | PF00433 | 0.504 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.517 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.726 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.324 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.509 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.561 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.376 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.715 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.601 |
MOD_PK_1 | 53 | 59 | PF00069 | 0.520 |
MOD_PKA_1 | 348 | 354 | PF00069 | 0.460 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.754 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.435 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.324 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.569 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.455 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.651 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.440 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.530 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.679 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.730 |
MOD_PKB_1 | 51 | 59 | PF00069 | 0.681 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.555 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.435 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.518 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.597 |
MOD_Plk_2-3 | 266 | 272 | PF00069 | 0.488 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.488 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.492 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.728 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.646 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.709 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.479 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.562 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 150 | 159 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 444 | 449 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 238 | 241 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 471 | 475 | PF00026 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9K9 | Leptomonas seymouri | 56% | 95% |
A0A1X0NUG8 | Trypanosomatidae | 40% | 100% |
A0A3S7WUA9 | Leishmania donovani | 75% | 92% |
A0A422NFB5 | Trypanosoma rangeli | 38% | 100% |
A4HXA7 | Leishmania infantum | 75% | 92% |
C9ZTV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AQY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 92% |
Q4QEH7 | Leishmania major | 75% | 100% |