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:0005730 | nucleolus | 5 | 11 |
GO:0005786 | signal recognition particle, endoplasmic reticulum targeting | 4 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0048500 | signal recognition particle | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: A4HAZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 11 |
GO:0006612 | protein targeting to membrane | 5 | 11 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 11 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0033365 | protein localization to organelle | 5 | 11 |
GO:0045047 | protein targeting to ER | 6 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0051668 | localization within membrane | 3 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0072594 | establishment of protein localization to organelle | 4 | 11 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 11 |
GO:0072657 | protein localization to membrane | 4 | 11 |
GO:0090150 | establishment of protein localization to membrane | 4 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005047 | signal recognition particle binding | 4 | 11 |
GO:0005048 | signal sequence binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008312 | 7S RNA binding | 5 | 11 |
GO:0030942 | endoplasmic reticulum signal peptide binding | 5 | 11 |
GO:0033218 | amide binding | 2 | 11 |
GO:0042277 | peptide binding | 3 | 11 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 11 |
GO:0044877 | protein-containing complex binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.206 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.183 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.246 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.183 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.200 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.167 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.126 |
CLV_Separin_Metazoa | 401 | 405 | PF03568 | 0.431 |
DOC_ANK_TNKS_1 | 313 | 320 | PF00023 | 0.472 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.360 |
DOC_MAPK_MEF2A_6 | 66 | 73 | PF00069 | 0.422 |
DOC_MAPK_NFAT4_5 | 66 | 74 | PF00069 | 0.512 |
DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.418 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.360 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.563 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.418 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.418 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.474 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 360 | 369 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 448 | 455 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 522 | 530 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 326 | 344 | PF00022 | 0.512 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.449 |
LIG_APCC_ABBAyCdc20_2 | 50 | 56 | PF00400 | 0.447 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.486 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.395 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.554 |
LIG_deltaCOP1_diTrp_1 | 445 | 453 | PF00928 | 0.532 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.453 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.483 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.554 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.431 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.521 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.491 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.454 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.521 |
LIG_Integrin_RGD_1 | 97 | 99 | PF01839 | 0.160 |
LIG_LIR_Gen_1 | 173 | 181 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 4 | 11 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 536 | 545 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 4 | 8 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 536 | 540 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 551 | 556 | PF02991 | 0.421 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.515 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.421 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.401 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.363 |
LIG_SH2_GRB2like | 301 | 304 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.403 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.431 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.461 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.382 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.348 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 398 | 404 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.431 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.360 |
LIG_TYR_ITSM | 321 | 328 | PF00017 | 0.421 |
LIG_UBA3_1 | 7 | 12 | PF00899 | 0.262 |
LIG_WW_1 | 534 | 537 | PF00397 | 0.418 |
MOD_CDK_SPxxK_3 | 585 | 592 | PF00069 | 0.467 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.561 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.464 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.363 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.376 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.446 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.433 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.441 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.528 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.346 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.311 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.301 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.655 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.418 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.469 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.421 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.462 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.522 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.579 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.231 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.246 |
MOD_N-GLC_2 | 567 | 569 | PF02516 | 0.468 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.431 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.472 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.418 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.474 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.471 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.512 |
MOD_NEK2_2 | 474 | 479 | PF00069 | 0.382 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.414 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.512 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.360 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.546 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.472 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.461 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.508 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.487 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.431 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.383 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.507 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.431 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.474 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.360 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.474 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.404 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.512 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.528 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.431 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.429 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.525 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.467 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.597 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.649 |
MOD_SUMO_for_1 | 139 | 142 | PF00179 | 0.453 |
MOD_SUMO_for_1 | 572 | 575 | PF00179 | 0.728 |
MOD_SUMO_for_1 | 91 | 94 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 157 | 167 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 44 | 52 | PF00179 | 0.477 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.379 |
TRG_NLS_Bipartite_1 | 96 | 118 | PF00514 | 0.360 |
TRG_NLS_MonoExtN_4 | 377 | 382 | PF00514 | 0.391 |
TRG_NLS_MonoExtN_4 | 589 | 596 | PF00514 | 0.615 |
TRG_PTS2 | 1 | 43 | PF00400 | 0.260 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH42 | Leptomonas seymouri | 68% | 100% |
A0A0S4J2Z5 | Bodo saltans | 45% | 100% |
A0A1X0PAR6 | Trypanosomatidae | 47% | 100% |
A0A3S7X839 | Leishmania donovani | 81% | 100% |
A4IA56 | Leishmania infantum | 81% | 100% |
C9ZM46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9B570 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q00004 | Canis lupus familiaris | 24% | 97% |
Q4Q2R5 | Leishmania major | 81% | 100% |
Q8BMA6 | Mus musculus | 24% | 96% |
Q9UHB9 | Homo sapiens | 24% | 96% |
Q9VSS2 | Drosophila melanogaster | 24% | 100% |
V5BV06 | Trypanosoma cruzi | 48% | 100% |