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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0034451 | centriolar satellite | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4H4S1
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.423 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.537 |
CLV_Separin_Metazoa | 504 | 508 | PF03568 | 0.389 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.566 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.376 |
DEG_APCC_DBOX_1 | 80 | 88 | PF00400 | 0.557 |
DEG_SCF_FBW7_1 | 595 | 602 | PF00400 | 0.486 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.759 |
DEG_SPOP_SBC_1 | 55 | 59 | PF00917 | 0.602 |
DOC_CYCLIN_RxL_1 | 407 | 415 | PF00134 | 0.376 |
DOC_CYCLIN_RxL_1 | 507 | 519 | PF00134 | 0.467 |
DOC_MAPK_FxFP_2 | 521 | 524 | PF00069 | 0.626 |
DOC_MAPK_gen_1 | 397 | 407 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 481 | 488 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 507 | 517 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 546 | 552 | PF00069 | 0.688 |
DOC_MAPK_gen_1 | 9 | 17 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 144 | 151 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.446 |
DOC_MAPK_NFAT4_5 | 481 | 489 | PF00069 | 0.446 |
DOC_PP2B_LxvP_1 | 393 | 396 | PF13499 | 0.458 |
DOC_PP4_FxxP_1 | 521 | 524 | PF00568 | 0.669 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.551 |
DOC_USP7_UBL2_3 | 233 | 237 | PF12436 | 0.332 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 288 | 292 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 496 | 501 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 566 | 571 | PF00244 | 0.675 |
LIG_Actin_WH2_2 | 174 | 191 | PF00022 | 0.543 |
LIG_Actin_WH2_2 | 504 | 520 | PF00022 | 0.483 |
LIG_APCC_ABBAyCdc20_2 | 409 | 415 | PF00400 | 0.528 |
LIG_BRCT_BRCA1_1 | 355 | 359 | PF00533 | 0.409 |
LIG_CtBP_PxDLS_1 | 608 | 612 | PF00389 | 0.588 |
LIG_DLG_GKlike_1 | 566 | 573 | PF00625 | 0.474 |
LIG_eIF4E_1 | 500 | 506 | PF01652 | 0.294 |
LIG_EVH1_2 | 599 | 603 | PF00568 | 0.483 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.343 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.394 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.445 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.587 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.474 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.379 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.450 |
LIG_LIR_Apic_2 | 519 | 524 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 390 | 396 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 451 | 461 | PF02991 | 0.401 |
LIG_LIR_LC3C_4 | 404 | 407 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 602 | 606 | PF02991 | 0.699 |
LIG_PCNA_yPIPBox_3 | 170 | 183 | PF02747 | 0.460 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.403 |
LIG_SH2_PTP2 | 453 | 456 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 322 | 326 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.290 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 266 | 269 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.548 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.647 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.715 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.535 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.477 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 172 | 178 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 331 | 337 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 403 | 408 | PF11976 | 0.439 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.506 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.339 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.423 |
LIG_UBA3_1 | 505 | 510 | PF00899 | 0.480 |
LIG_UBA3_1 | 83 | 92 | PF00899 | 0.513 |
LIG_WW_3 | 10 | 14 | PF00397 | 0.623 |
MOD_CDK_SPK_2 | 87 | 92 | PF00069 | 0.608 |
MOD_CDK_SPxxK_3 | 559 | 566 | PF00069 | 0.480 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.389 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.518 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.710 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.638 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.640 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.656 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.490 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.456 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.343 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.500 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.404 |
MOD_Cter_Amidation | 544 | 547 | PF01082 | 0.492 |
MOD_DYRK1A_RPxSP_1 | 44 | 48 | PF00069 | 0.746 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.552 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.516 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.593 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.532 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.658 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.612 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.725 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.625 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.549 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.407 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.409 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.478 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.680 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.621 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.446 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.533 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.648 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.749 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.555 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.607 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.528 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.556 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.434 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.414 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.454 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.409 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.572 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.549 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.541 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.530 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.461 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.443 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.671 |
MOD_PKA_1 | 546 | 552 | PF00069 | 0.491 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.476 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.410 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.503 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.394 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.471 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.501 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.489 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.413 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.563 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.736 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.402 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.513 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.719 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.557 |
MOD_SUMO_for_1 | 108 | 111 | PF00179 | 0.441 |
MOD_SUMO_for_1 | 317 | 320 | PF00179 | 0.361 |
MOD_SUMO_rev_2 | 212 | 218 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 230 | 238 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 308 | 314 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 319 | 326 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 337 | 346 | PF00179 | 0.394 |
MOD_SUMO_rev_2 | 475 | 484 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_2 | 354 | 360 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_4 | 110 | 116 | PF01217 | 0.316 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.467 |
TRG_NES_CRM1_1 | 172 | 184 | PF08389 | 0.519 |
TRG_NES_CRM1_1 | 344 | 355 | PF08389 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 171 | 175 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 331 | 336 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 410 | 415 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 81 | 86 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3D2 | Leptomonas seymouri | 59% | 100% |
A0A0S4KJ48 | Bodo saltans | 38% | 100% |
A0A1X0NFW7 | Trypanosomatidae | 51% | 100% |
A0A1X0NGS8 | Trypanosomatidae | 52% | 100% |
A0A3R7KEX6 | Trypanosoma rangeli | 50% | 100% |
A0A3S7WPN7 | Leishmania donovani | 80% | 100% |
A4HT01 | Leishmania infantum | 80% | 100% |
C9ZTN3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AKY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QIW7 | Leishmania major | 80% | 97% |
V5BXW3 | Trypanosoma cruzi | 51% | 100% |