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:0005737 | cytoplasm | 2 | 1 |
GO:0005929 | cilium | 4 | 4 |
GO:0031514 | motile cilium | 5 | 4 |
GO:0042995 | cell projection | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 4 |
Related structures:
AlphaFold database: A4HPT4
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 606 | 610 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 624 | 628 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.481 |
CLV_PCSK_PC7_1 | 208 | 214 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.497 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 288 | 296 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 645 | 653 | PF00400 | 0.488 |
DEG_SCF_FBW7_2 | 124 | 129 | PF00400 | 0.721 |
DEG_SPOP_SBC_1 | 419 | 423 | PF00917 | 0.688 |
DOC_CYCLIN_RxL_1 | 249 | 258 | PF00134 | 0.576 |
DOC_MAPK_RevD_3 | 198 | 213 | PF00069 | 0.552 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.612 |
DOC_USP7_UBL2_3 | 573 | 577 | PF12436 | 0.582 |
DOC_USP7_UBL2_3 | 654 | 658 | PF12436 | 0.638 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 266 | 276 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 333 | 337 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 34 | 41 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 374 | 383 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 417 | 427 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 524 | 533 | PF00244 | 0.373 |
LIG_Actin_WH2_2 | 247 | 264 | PF00022 | 0.521 |
LIG_BIR_III_4 | 120 | 124 | PF00653 | 0.652 |
LIG_BIR_III_4 | 579 | 583 | PF00653 | 0.620 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.463 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.642 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.667 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.557 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.521 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.600 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.600 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.692 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.609 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.554 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.629 |
LIG_LIR_Gen_1 | 280 | 288 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 421 | 432 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 95 | 104 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.645 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.503 |
LIG_NRBOX | 291 | 297 | PF00104 | 0.454 |
LIG_Pex14_2 | 395 | 399 | PF04695 | 0.763 |
LIG_SH2_NCK_1 | 630 | 634 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.622 |
LIG_SH3_2 | 29 | 34 | PF14604 | 0.494 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.597 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.544 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.687 |
LIG_SUMO_SIM_anti_2 | 111 | 117 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 253 | 258 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 291 | 298 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 114 | 120 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.481 |
MOD_CDK_SPxxK_3 | 390 | 397 | PF00069 | 0.505 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.741 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.732 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.543 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.488 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.661 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.671 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.644 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.650 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.709 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.643 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.513 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.510 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.561 |
MOD_DYRK1A_RPxSP_1 | 333 | 337 | PF00069 | 0.497 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.704 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.755 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.682 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.686 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.699 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.754 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.673 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.568 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.563 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.670 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.735 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.558 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.422 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.692 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.587 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.662 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.592 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.638 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.695 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.561 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.579 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.711 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.721 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.664 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.635 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.478 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.635 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.455 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.504 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.760 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.619 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.731 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.656 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.357 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.576 |
MOD_NEK2_2 | 223 | 228 | PF00069 | 0.562 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.574 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.573 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.545 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.543 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.620 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.478 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.646 |
MOD_PKA_1 | 332 | 338 | PF00069 | 0.684 |
MOD_PKA_1 | 619 | 625 | PF00069 | 0.560 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.527 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.464 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.524 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.663 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.650 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.772 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.595 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.611 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.442 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.566 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.512 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.640 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.487 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.560 |
MOD_Plk_2-3 | 563 | 569 | PF00069 | 0.611 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.571 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.594 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.685 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.357 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.575 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.661 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.648 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.639 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.506 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 560 | 567 | PF00179 | 0.474 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.346 |
TRG_DiLeu_BaEn_1 | 288 | 293 | PF01217 | 0.455 |
TRG_DiLeu_LyEn_5 | 263 | 268 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.613 |
TRG_ER_diLys_1 | 659 | 664 | PF00400 | 0.700 |
TRG_NES_CRM1_1 | 475 | 486 | PF08389 | 0.528 |
TRG_NLS_MonoCore_2 | 656 | 661 | PF00514 | 0.660 |
TRG_NLS_MonoExtC_3 | 656 | 661 | PF00514 | 0.673 |
TRG_NLS_MonoExtN_4 | 654 | 661 | PF00514 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 266 | 271 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 430 | 434 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 449 | 453 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCM9 | Leptomonas seymouri | 57% | 99% |
A0A3R7NMF4 | Trypanosoma rangeli | 36% | 100% |
A0A3S7XBE2 | Leishmania donovani | 78% | 100% |
A4IE58 | Leishmania infantum | 78% | 100% |
D0A8P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9ATJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q0Z9 | Leishmania major | 78% | 100% |
V5BS07 | Trypanosoma cruzi | 38% | 100% |