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 | 2 |
GO:0031514 | motile cilium | 5 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q1A7
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
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 | 278 | 282 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.459 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.573 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 548 | 550 | PF00082 | 0.597 |
CLV_PCSK_PC7_1 | 544 | 550 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.456 |
DOC_MAPK_FxFP_2 | 213 | 216 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 358 | 366 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 544 | 552 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 88 | 100 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 333 | 341 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 359 | 368 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 80 | 88 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.551 |
DOC_PP1_MyPhoNE_1 | 30 | 37 | PF00149 | 0.578 |
DOC_PP1_RVXF_1 | 327 | 333 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.606 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.390 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 517 | 522 | PF00244 | 0.492 |
LIG_Actin_WH2_2 | 164 | 182 | PF00022 | 0.556 |
LIG_Actin_WH2_2 | 543 | 559 | PF00022 | 0.605 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.493 |
LIG_eIF4E_1 | 14 | 20 | PF01652 | 0.471 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.440 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.668 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.505 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.555 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.463 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.559 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.515 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.610 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.287 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.524 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.428 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.636 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.438 |
LIG_LIR_Apic_2 | 210 | 216 | PF02991 | 0.591 |
LIG_LIR_Apic_2 | 501 | 505 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 479 | 487 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 491 | 498 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.349 |
LIG_NRBOX | 363 | 369 | PF00104 | 0.481 |
LIG_Pex14_2 | 457 | 461 | PF04695 | 0.375 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.510 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.467 |
LIG_SH2_GRB2like | 8 | 11 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 186 | 190 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 481 | 485 | PF00017 | 0.376 |
LIG_SH2_NCK_1 | 8 | 12 | PF00017 | 0.584 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 37 | 40 | PF00017 | 0.623 |
LIG_SH2_STAT3 | 411 | 414 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.474 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.565 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.652 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.604 |
LIG_SUMO_SIM_anti_2 | 221 | 228 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 221 | 228 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 517 | 522 | PF11976 | 0.561 |
LIG_TRAF2_1 | 486 | 489 | PF00917 | 0.512 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.645 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.219 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.571 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.662 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.500 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.281 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.543 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.504 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.398 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.569 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.558 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.627 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.480 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.481 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.496 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.616 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.550 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.555 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.580 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.495 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.552 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.429 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.647 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.440 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.422 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.524 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.526 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.628 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.624 |
MOD_N-GLC_2 | 192 | 194 | PF02516 | 0.554 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.494 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.537 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.477 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.498 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.544 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.507 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.460 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.483 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.678 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.572 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.650 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.657 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.553 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.597 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.547 |
MOD_PK_1 | 333 | 339 | PF00069 | 0.494 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.426 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.605 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.722 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.564 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.515 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.514 |
MOD_PKB_1 | 289 | 297 | PF00069 | 0.687 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.636 |
MOD_Plk_1 | 560 | 566 | PF00069 | 0.635 |
MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.373 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.510 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.576 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.485 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.543 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.402 |
MOD_SUMO_for_1 | 269 | 272 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 419 | 429 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 540 | 547 | PF00179 | 0.538 |
TRG_DiLeu_BaEn_1 | 372 | 377 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_1 | 514 | 519 | PF01217 | 0.554 |
TRG_DiLeu_BaLyEn_6 | 546 | 551 | PF01217 | 0.557 |
TRG_DiLeu_LyEn_5 | 514 | 519 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.769 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.588 |
TRG_NES_CRM1_1 | 392 | 407 | PF08389 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 549 | 553 | PF00026 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW03 | Leptomonas seymouri | 61% | 99% |
A0A0S4JII0 | Bodo saltans | 28% | 97% |
A0A1X0P3R1 | Trypanosomatidae | 44% | 100% |
A0A3Q8IJI1 | Leishmania donovani | 95% | 100% |
A0A422NKK1 | Trypanosoma rangeli | 43% | 100% |
A4HPH8 | Leishmania braziliensis | 85% | 100% |
A4IDA0 | Leishmania infantum | 95% | 100% |
D0A8E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 86% |
E9AT90 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5AU55 | Trypanosoma cruzi | 41% | 100% |