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 | 2 |
GO:0005814 | centriole | 5 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QEH7
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007098 | centrosome cycle | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010638 | positive regulation of organelle organization | 6 | 2 |
GO:0010824 | regulation of centrosome duplication | 6 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0031023 | microtubule organizing center organization | 3 | 2 |
GO:0032886 | regulation of microtubule-based process | 4 | 2 |
GO:0033043 | regulation of organelle organization | 5 | 2 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 2 |
GO:0044089 | positive regulation of cellular component biogenesis | 5 | 2 |
GO:0045787 | positive regulation of cell cycle | 5 | 2 |
GO:0046599 | regulation of centriole replication | 6 | 2 |
GO:0046601 | positive regulation of centriole replication | 7 | 2 |
GO:0046605 | regulation of centrosome cycle | 5 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051130 | positive regulation of cellular component organization | 5 | 2 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 2 |
GO:0051495 | positive regulation of cytoskeleton organization | 7 | 2 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090068 | positive regulation of cell cycle process | 6 | 2 |
GO:1902115 | regulation of organelle assembly | 5 | 2 |
GO:1902117 | positive regulation of organelle assembly | 6 | 2 |
GO:1903722 | regulation of centriole elongation | 6 | 2 |
GO:1903724 | positive regulation of centriole elongation | 7 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 500 | 504 | PF00656 | 0.415 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.455 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.538 |
CLV_PCSK_PC7_1 | 177 | 183 | PF00082 | 0.493 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.571 |
CLV_PCSK_PC7_1 | 40 | 46 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 491 | 499 | PF00400 | 0.450 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 418 | 422 | PF00917 | 0.662 |
DOC_ANK_TNKS_1 | 506 | 513 | PF00023 | 0.457 |
DOC_CKS1_1 | 87 | 92 | PF01111 | 0.728 |
DOC_MAPK_gen_1 | 180 | 190 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 71 | 79 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 71 | 79 | PF00069 | 0.609 |
DOC_PP1_RVXF_1 | 166 | 173 | PF00149 | 0.385 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.603 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.609 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 45 | 55 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 463 | 467 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.694 |
LIG_ActinCP_TwfCPI_2 | 105 | 112 | PF01115 | 0.543 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.538 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.648 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.456 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.467 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.548 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.638 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.498 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.366 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.483 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.586 |
LIG_LIR_Apic_2 | 104 | 108 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 285 | 293 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.439 |
LIG_RPA_C_Plants | 227 | 238 | PF08784 | 0.523 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.391 |
LIG_SH3_2 | 87 | 92 | PF14604 | 0.590 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.601 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.691 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.635 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.457 |
LIG_WRC_WIRS_1 | 102 | 107 | PF05994 | 0.544 |
LIG_WW_2 | 390 | 393 | PF00397 | 0.581 |
MOD_CDK_SPxK_1 | 86 | 92 | PF00069 | 0.721 |
MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.591 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.644 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.625 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.674 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.617 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.729 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.644 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.696 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.680 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.453 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.602 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.369 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.597 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.446 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.642 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.723 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.612 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.658 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.704 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.589 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.637 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.510 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.317 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.664 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.601 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.646 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.626 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.678 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.714 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.475 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.565 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.607 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.646 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.693 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.739 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.471 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.427 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.692 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.578 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.546 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.636 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.505 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.604 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.722 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.540 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.398 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.653 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.587 |
MOD_PK_1 | 166 | 172 | PF00069 | 0.323 |
MOD_PKA_1 | 14 | 20 | PF00069 | 0.586 |
MOD_PKA_1 | 367 | 373 | PF00069 | 0.459 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.590 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.594 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.426 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.744 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.496 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.723 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.446 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.607 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.505 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.472 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.512 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.695 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.539 |
MOD_PKB_1 | 44 | 52 | PF00069 | 0.589 |
MOD_PKB_1 | 518 | 526 | PF00069 | 0.510 |
MOD_PKB_1 | 71 | 79 | PF00069 | 0.656 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.506 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.412 |
MOD_Plk_2-3 | 285 | 291 | PF00069 | 0.453 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.460 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.574 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.490 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.559 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.713 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.592 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.632 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.674 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.737 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.611 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 44 | 46 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 70 | 73 | PF00400 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 51 | 56 | PF00026 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9K9 | Leptomonas seymouri | 54% | 100% |
A0A1X0NUG8 | Trypanosomatidae | 36% | 100% |
A0A3S7WUA9 | Leishmania donovani | 91% | 100% |
A0A422NFB5 | Trypanosoma rangeli | 40% | 100% |
A4H8W0 | Leishmania braziliensis | 75% | 100% |
A4HXA7 | Leishmania infantum | 91% | 100% |
C9ZTV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AQY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |