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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0031514 | motile cilium | 5 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HPH8
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 4 |
GO:0005509 | calcium ion binding | 5 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 382 | 386 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.469 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.340 |
CLV_PCSK_PC7_1 | 354 | 360 | PF00082 | 0.266 |
CLV_PCSK_PC7_1 | 544 | 550 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.388 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.743 |
DOC_CYCLIN_RxL_1 | 493 | 501 | PF00134 | 0.242 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 358 | 366 | PF00069 | 0.505 |
DOC_MAPK_HePTP_8 | 88 | 100 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 13 | 20 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 333 | 341 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 359 | 368 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 398 | 406 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.544 |
DOC_MAPK_RevD_3 | 364 | 379 | PF00069 | 0.314 |
DOC_PP1_MyPhoNE_1 | 30 | 37 | PF00149 | 0.556 |
DOC_PP1_RVXF_1 | 327 | 333 | PF00149 | 0.353 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.339 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 517 | 522 | PF00244 | 0.436 |
LIG_Actin_WH2_2 | 164 | 182 | PF00022 | 0.441 |
LIG_Actin_WH2_2 | 543 | 559 | PF00022 | 0.462 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 |
LIG_BIR_III_2 | 282 | 286 | PF00653 | 0.437 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.449 |
LIG_eIF4E_1 | 14 | 20 | PF01652 | 0.420 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.383 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.640 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.500 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.440 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.410 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.536 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.456 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.535 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.621 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.527 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.515 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.385 |
LIG_LIR_Apic_2 | 210 | 216 | PF02991 | 0.572 |
LIG_LIR_Apic_2 | 501 | 505 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 479 | 487 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 491 | 499 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.437 |
LIG_Pex14_2 | 457 | 461 | PF04695 | 0.322 |
LIG_Rb_pABgroove_1 | 517 | 525 | PF01858 | 0.333 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 186 | 190 | PF00017 | 0.537 |
LIG_SH2_NCK_1 | 481 | 485 | PF00017 | 0.315 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.567 |
LIG_SH2_STAT3 | 37 | 40 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 411 | 414 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.544 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.494 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.602 |
LIG_SUMO_SIM_anti_2 | 221 | 228 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 221 | 228 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.407 |
LIG_UBA3_1 | 518 | 526 | PF00899 | 0.337 |
MOD_CDC14_SPxK_1 | 215 | 218 | PF00782 | 0.285 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.417 |
MOD_CDK_SPxxK_3 | 482 | 489 | PF00069 | 0.257 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.614 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.537 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.225 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.547 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.531 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.648 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.548 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.459 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.358 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.546 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.600 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.425 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.439 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.457 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.390 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.525 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.525 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.371 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.454 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.529 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.526 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.381 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.642 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.575 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.335 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.458 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.483 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.581 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.340 |
MOD_N-GLC_2 | 192 | 194 | PF02516 | 0.418 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.440 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.383 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.426 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.487 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.404 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.446 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.550 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.536 |
MOD_NEK2_2 | 203 | 208 | PF00069 | 0.481 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.650 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.612 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.573 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.409 |
MOD_PK_1 | 333 | 339 | PF00069 | 0.470 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.370 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.475 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.758 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.592 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.485 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.459 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.590 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.429 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.325 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.643 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.424 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.389 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.550 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.537 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.437 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.405 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.405 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.339 |
MOD_SUMO_for_1 | 269 | 272 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 419 | 429 | PF00179 | 0.444 |
TRG_DiLeu_BaEn_1 | 372 | 377 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 514 | 519 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 546 | 551 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 392 | 407 | PF08389 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 548 | 553 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW03 | Leptomonas seymouri | 62% | 99% |
A0A0S4JII0 | Bodo saltans | 27% | 97% |
A0A1X0P3R1 | Trypanosomatidae | 43% | 100% |
A0A3Q8IJI1 | Leishmania donovani | 84% | 100% |
A0A422NKK1 | Trypanosoma rangeli | 44% | 100% |
A4IDA0 | Leishmania infantum | 84% | 100% |
D0A8E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 86% |
E9AT90 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q1A7 | Leishmania major | 85% | 100% |
V5AU55 | Trypanosoma cruzi | 41% | 100% |