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: 5 |
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:0005783 | endoplasmic reticulum | 5 | 12 |
GO:0005786 | signal recognition particle, endoplasmic reticulum targeting | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0048500 | signal recognition particle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IDA7
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 12 |
GO:0006612 | protein targeting to membrane | 5 | 12 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 12 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0045047 | protein targeting to ER | 6 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0051668 | localization within membrane | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 12 |
GO:0072657 | protein localization to membrane | 4 | 12 |
GO:0090150 | establishment of protein localization to membrane | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008312 | 7S RNA binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.671 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 663 | 665 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 699 | 701 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.537 |
CLV_PCSK_FUR_1 | 657 | 661 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 663 | 665 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 709 | 711 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 709 | 711 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 659 | 665 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.315 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.515 |
DEG_SCF_SKP2-CKS1_1 | 67 | 74 | PF00560 | 0.476 |
DOC_CYCLIN_RxL_1 | 446 | 456 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 287 | 294 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 325 | 335 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 446 | 454 | PF00069 | 0.588 |
DOC_MAPK_gen_1 | 561 | 570 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 287 | 294 | PF00069 | 0.406 |
DOC_MAPK_RevD_3 | 384 | 397 | PF00069 | 0.561 |
DOC_PP2B_LxvP_1 | 242 | 245 | PF13499 | 0.650 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.734 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 732 | 737 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 31 | 36 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 338 | 345 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 511 | 521 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 583 | 589 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 631 | 636 | PF00244 | 0.586 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.451 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.559 |
LIG_CtBP_PxDLS_1 | 680 | 684 | PF00389 | 0.504 |
LIG_eIF4E_1 | 85 | 91 | PF01652 | 0.515 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.412 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.449 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.334 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.401 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.376 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.420 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.397 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.535 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.517 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.504 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.567 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.491 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.629 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.654 |
LIG_GBD_Chelix_1 | 306 | 314 | PF00786 | 0.469 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.642 |
LIG_PDZ_Class_1 | 736 | 741 | PF00595 | 0.674 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.470 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.504 |
LIG_SH2_CRK | 630 | 634 | PF00017 | 0.563 |
LIG_SH2_NCK_1 | 127 | 131 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 197 | 201 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 542 | 546 | PF00017 | 0.477 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.454 |
LIG_Sin3_3 | 567 | 574 | PF02671 | 0.490 |
LIG_SUMO_SIM_anti_2 | 47 | 53 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 566 | 572 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 386 | 392 | PF11976 | 0.525 |
LIG_TYR_ITIM | 309 | 314 | PF00017 | 0.499 |
LIG_TYR_ITIM | 628 | 633 | PF00017 | 0.591 |
MOD_CDC14_SPxK_1 | 257 | 260 | PF00782 | 0.408 |
MOD_CDK_SPxK_1 | 254 | 260 | PF00069 | 0.456 |
MOD_CDK_SPxK_1 | 68 | 74 | PF00069 | 0.532 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.559 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.377 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.727 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.479 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.451 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.575 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.540 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.207 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.426 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.421 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.391 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.448 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.561 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.736 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.635 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.339 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.646 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.765 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.748 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.371 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.382 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.508 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.389 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.683 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.456 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.667 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.548 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.497 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.560 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.728 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.418 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.480 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.418 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.413 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.427 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.542 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.543 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.501 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.537 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.540 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.379 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.555 |
MOD_PKA_1 | 483 | 489 | PF00069 | 0.454 |
MOD_PKA_1 | 631 | 637 | PF00069 | 0.655 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.416 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.476 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.712 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.570 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.522 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.580 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.556 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.538 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.425 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.514 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.470 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.435 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.493 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.448 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.529 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.446 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.748 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.559 |
MOD_ProDKin_1 | 732 | 738 | PF00069 | 0.656 |
MOD_SUMO_for_1 | 5 | 8 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 174 | 181 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 564 | 569 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 448 | 451 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 630 | 632 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 657 | 660 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 662 | 664 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 698 | 700 | PF00400 | 0.559 |
TRG_NES_CRM1_1 | 379 | 392 | PF08389 | 0.423 |
TRG_NES_CRM1_1 | 497 | 510 | PF08389 | 0.540 |
TRG_NLS_Bipartite_1 | 693 | 713 | PF00514 | 0.598 |
TRG_NLS_MonoCore_2 | 393 | 398 | PF00514 | 0.536 |
TRG_NLS_MonoExtC_3 | 393 | 398 | PF00514 | 0.439 |
TRG_NLS_MonoExtC_3 | 445 | 450 | PF00514 | 0.500 |
TRG_NLS_MonoExtN_4 | 391 | 398 | PF00514 | 0.521 |
TRG_NLS_MonoExtN_4 | 446 | 451 | PF00514 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 114 | 119 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 287 | 291 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 688 | 692 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I027 | Leptomonas seymouri | 63% | 100% |
A0A0S4J0A8 | Bodo saltans | 34% | 100% |
A0A1X0P6G4 | Trypanosomatidae | 41% | 100% |
A0A422NHC6 | Trypanosoma rangeli | 42% | 100% |
A4HA36 | Leishmania braziliensis | 83% | 100% |
A4HY99 | Leishmania infantum | 99% | 100% |
D0A0N5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AS31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O76094 | Homo sapiens | 23% | 100% |
P33731 | Canis lupus familiaris | 23% | 100% |
Q4QDE2 | Leishmania major | 93% | 100% |
Q54EP7 | Dictyostelium discoideum | 22% | 100% |
V5BJ44 | Trypanosoma cruzi | 43% | 100% |