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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005929 | cilium | 4 | 6 |
GO:0031514 | motile cilium | 5 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
Related structures:
AlphaFold database: Q4Q0Z9
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 575 | 579 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.614 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.573 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.592 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.768 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.429 |
DEG_APCC_DBOX_1 | 248 | 256 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.443 |
DEG_SCF_FBW7_2 | 84 | 89 | PF00400 | 0.620 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.627 |
DOC_CYCLIN_RxL_1 | 207 | 218 | PF00134 | 0.582 |
DOC_MAPK_gen_1 | 427 | 436 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 430 | 438 | PF00069 | 0.399 |
DOC_MAPK_RevD_3 | 158 | 173 | PF00069 | 0.510 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.559 |
DOC_USP7_UBL2_3 | 524 | 528 | PF12436 | 0.552 |
DOC_USP7_UBL2_3 | 605 | 609 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 292 | 300 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 7 | 14 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 99 | 107 | PF00244 | 0.665 |
LIG_Actin_WH2_2 | 207 | 224 | PF00022 | 0.474 |
LIG_BIR_III_4 | 530 | 534 | PF00653 | 0.486 |
LIG_BIR_III_4 | 80 | 84 | PF00653 | 0.638 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.650 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.525 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.483 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.390 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.651 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.583 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.555 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.495 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.651 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.473 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.469 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.577 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.522 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.460 |
LIG_Integrin_isoDGR_2 | 247 | 249 | PF01839 | 0.434 |
LIG_LIR_Gen_1 | 303 | 311 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.649 |
LIG_MYND_1 | 192 | 196 | PF01753 | 0.515 |
LIG_NRBOX | 251 | 257 | PF00104 | 0.412 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.455 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.594 |
LIG_SH2_NCK_1 | 581 | 585 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.480 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.553 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.528 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.489 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 159 | 166 | PF11976 | 0.498 |
LIG_SUMO_SIM_anti_2 | 213 | 218 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 71 | 77 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 144 | 149 | PF11976 | 0.577 |
LIG_SUMO_SIM_par_1 | 74 | 80 | PF11976 | 0.532 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.609 |
MOD_CDK_SPK_2 | 117 | 122 | PF00069 | 0.529 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.484 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.651 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.674 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.486 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.631 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.624 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.319 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.616 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.478 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.763 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.625 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.420 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.511 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.459 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.520 |
MOD_Cter_Amidation | 247 | 250 | PF01082 | 0.419 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.694 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.702 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.767 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.606 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.520 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.714 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.620 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.649 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.541 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.324 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.464 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.647 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.630 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.730 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.704 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.551 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.455 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.530 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.693 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.518 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.533 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.498 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.580 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.586 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.527 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.540 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.570 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.545 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.474 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.596 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.690 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.472 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.662 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.641 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.548 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.636 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.407 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.531 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.386 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.615 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.634 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.600 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.460 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.461 |
MOD_Plk_2-3 | 514 | 520 | PF00069 | 0.485 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.499 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.719 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.554 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.671 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.599 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.500 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.508 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.578 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.511 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.675 |
MOD_SUMO_for_1 | 434 | 437 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 508 | 518 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 548 | 557 | PF00179 | 0.427 |
TRG_DiLeu_BaEn_1 | 251 | 256 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 223 | 228 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 570 | 572 | PF00400 | 0.572 |
TRG_ER_diLys_1 | 610 | 615 | PF00400 | 0.657 |
TRG_NES_CRM1_1 | 426 | 437 | PF08389 | 0.482 |
TRG_NLS_MonoCore_2 | 607 | 612 | PF00514 | 0.589 |
TRG_NLS_MonoExtC_3 | 607 | 612 | PF00514 | 0.603 |
TRG_NLS_MonoExtN_4 | 605 | 612 | PF00514 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 226 | 231 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 381 | 385 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 516 | 520 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCM9 | Leptomonas seymouri | 58% | 92% |
A0A1X0P338 | Trypanosomatidae | 36% | 100% |
A0A3R7NMF4 | Trypanosoma rangeli | 37% | 100% |
A0A3S7XBE2 | Leishmania donovani | 94% | 100% |
A4HPT4 | Leishmania braziliensis | 78% | 93% |
A4IE58 | Leishmania infantum | 94% | 100% |
D0A8P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9ATJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BS07 | Trypanosoma cruzi | 38% | 100% |