Translation, Uncharacterized
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: A4IA56
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_C14_Caspase3-7 | 562 | 566 | PF00656 | 0.750 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.665 |
CLV_Separin_Metazoa | 401 | 405 | PF03568 | 0.475 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.429 |
DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.503 |
DOC_ANK_TNKS_1 | 313 | 320 | PF00023 | 0.565 |
DOC_CYCLIN_RxL_1 | 340 | 349 | PF00134 | 0.466 |
DOC_CYCLIN_RxL_1 | 35 | 48 | PF00134 | 0.525 |
DOC_MAPK_MEF2A_6 | 66 | 73 | PF00069 | 0.465 |
DOC_MAPK_NFAT4_5 | 66 | 74 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.461 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.644 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.412 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.634 |
LIG_Actin_WH2_2 | 326 | 344 | PF00022 | 0.541 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 445 | 453 | PF00928 | 0.541 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.496 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.562 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.473 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.528 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.576 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.527 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.776 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.457 |
LIG_Integrin_isoDGR_2 | 246 | 248 | PF01839 | 0.276 |
LIG_LIR_Apic_2 | 394 | 399 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 173 | 181 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 551 | 556 | PF02991 | 0.506 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.514 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.442 |
LIG_SH2_GRB2like | 301 | 304 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.528 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.481 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.441 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.571 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 398 | 404 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 462 | 468 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 248 | 254 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.466 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.481 |
LIG_TRAF2_1 | 477 | 480 | PF00917 | 0.525 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.553 |
LIG_WW_1 | 534 | 537 | PF00397 | 0.472 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.492 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.539 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.536 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.501 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.509 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.480 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.450 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.551 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.683 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.303 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.316 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.372 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.308 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.727 |
MOD_GlcNHglycan | 567 | 572 | PF01048 | 0.750 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.654 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.461 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.516 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.466 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.459 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.480 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.569 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.740 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.555 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.275 |
MOD_N-GLC_1 | 582 | 587 | PF02516 | 0.780 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.275 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.464 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.572 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.527 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.461 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.497 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.507 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.344 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.563 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.541 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.462 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.481 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.541 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.459 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.650 |
MOD_PK_1 | 248 | 254 | PF00069 | 0.412 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.565 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.502 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.535 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.541 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.475 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.630 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.570 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.475 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.513 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.513 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.372 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.575 |
MOD_Plk_2-3 | 563 | 569 | PF00069 | 0.683 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.412 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.472 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.405 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.631 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.463 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.541 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.472 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.649 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.507 |
MOD_SUMO_for_1 | 139 | 142 | PF00179 | 0.495 |
MOD_SUMO_for_1 | 91 | 94 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 157 | 167 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 268 | 276 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 44 | 52 | PF00179 | 0.521 |
TRG_DiLeu_BaEn_1 | 414 | 419 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_4 | 414 | 420 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.561 |
TRG_NLS_MonoCore_2 | 384 | 389 | PF00514 | 0.440 |
TRG_NLS_MonoExtC_3 | 384 | 390 | PF00514 | 0.440 |
TRG_NLS_MonoExtN_4 | 383 | 389 | PF00514 | 0.445 |
TRG_NLS_MonoExtN_4 | 591 | 596 | PF00514 | 0.680 |
TRG_PTS2 | 1 | 43 | PF00400 | 0.320 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH42 | Leptomonas seymouri | 69% | 100% |
A0A0S4J2Z5 | Bodo saltans | 43% | 100% |
A0A1X0PAR6 | Trypanosomatidae | 48% | 100% |
A0A3S7X839 | Leishmania donovani | 99% | 100% |
A4HAZ6 | Leishmania braziliensis | 81% | 100% |
C9ZM46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9B570 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q00004 | Canis lupus familiaris | 25% | 97% |
Q1ZXE8 | Dictyostelium discoideum | 21% | 98% |
Q4Q2R5 | Leishmania major | 93% | 100% |
Q8BMA6 | Mus musculus | 25% | 96% |
Q9UHB9 | Homo sapiens | 25% | 96% |
Q9VSS2 | Drosophila melanogaster | 24% | 100% |
V5BV06 | Trypanosoma cruzi | 49% | 100% |