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: A0A3S7WUA9
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 | 0.495 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.563 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.515 |
CLV_PCSK_PC7_1 | 176 | 182 | PF00082 | 0.502 |
CLV_PCSK_PC7_1 | 376 | 382 | PF00082 | 0.583 |
CLV_PCSK_PC7_1 | 39 | 45 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.697 |
CLV_Separin_Metazoa | 443 | 447 | PF03568 | 0.426 |
DEG_APCC_DBOX_1 | 491 | 499 | PF00400 | 0.484 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.688 |
DOC_ANK_TNKS_1 | 506 | 513 | PF00023 | 0.499 |
DOC_CKS1_1 | 86 | 91 | PF01111 | 0.758 |
DOC_CYCLIN_RxL_1 | 457 | 470 | PF00134 | 0.374 |
DOC_MAPK_gen_1 | 179 | 189 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 489 | 497 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 69 | 78 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.635 |
DOC_MAPK_RevD_3 | 486 | 502 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 165 | 172 | PF00149 | 0.403 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.625 |
DOC_USP7_UBL2_3 | 161 | 165 | PF12436 | 0.610 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 111 | 121 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 13 | 20 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 346 | 354 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 81 | 85 | PF00244 | 0.773 |
LIG_ActinCP_TwfCPI_2 | 104 | 111 | PF01115 | 0.575 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.547 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.532 |
LIG_CaM_IQ_9 | 351 | 366 | PF13499 | 0.466 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.701 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.496 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.487 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.514 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.603 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.524 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.582 |
LIG_LIR_Apic_2 | 103 | 107 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 284 | 292 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.411 |
LIG_RPA_C_Plants | 226 | 237 | PF08784 | 0.526 |
LIG_SH2_STAT3 | 295 | 298 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.399 |
LIG_SH3_2 | 86 | 91 | PF14604 | 0.629 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.729 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.704 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.712 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.477 |
LIG_WRC_WIRS_1 | 101 | 106 | PF05994 | 0.571 |
LIG_WW_2 | 389 | 392 | PF00397 | 0.618 |
MOD_CDK_SPxK_1 | 85 | 91 | PF00069 | 0.749 |
MOD_CDK_SPxxK_3 | 85 | 92 | PF00069 | 0.628 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.632 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.677 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.693 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.617 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.639 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.701 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.705 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.704 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.664 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.450 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.594 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.666 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.593 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.397 |
MOD_DYRK1A_RPxSP_1 | 81 | 85 | PF00069 | 0.571 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.701 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.650 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.668 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.633 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.707 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.584 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.658 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.549 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.686 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.605 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.681 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.643 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.492 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.563 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.636 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.642 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.726 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.758 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.452 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.739 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.565 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.649 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.680 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.655 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.522 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.630 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.735 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.737 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.692 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.492 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.723 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.562 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.686 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.609 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.459 |
MOD_PKA_1 | 44 | 50 | PF00069 | 0.722 |
MOD_PKA_1 | 91 | 97 | PF00069 | 0.631 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.727 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.431 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.516 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.461 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.768 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.446 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.703 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.505 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.537 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.681 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.739 |
MOD_PKB_1 | 43 | 51 | PF00069 | 0.718 |
MOD_PKB_1 | 518 | 526 | PF00069 | 0.527 |
MOD_PKB_1 | 70 | 78 | PF00069 | 0.685 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.569 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.430 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.523 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.424 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.475 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.475 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.582 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.316 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.737 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.637 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.718 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.740 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.667 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_2 | 492 | 498 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 359 | 363 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 463 | 468 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9K9 | Leptomonas seymouri | 52% | 100% |
A0A1X0NUG8 | Trypanosomatidae | 38% | 100% |
A0A422NFB5 | Trypanosoma rangeli | 39% | 100% |
A4H8W0 | Leishmania braziliensis | 75% | 100% |
A4HXA7 | Leishmania infantum | 100% | 100% |
C9ZTV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AQY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QEH7 | Leishmania major | 91% | 100% |