Translation, eukaryotic translation initiation factor 3 subunit 8
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) | yes | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4ICD8
Term | Name | Level | Count |
---|---|---|---|
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003743 | translation initiation factor activity | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008135 | translation factor activity, RNA binding | 3 | 10 |
GO:0031369 | translation initiation factor binding | 3 | 10 |
GO:0045182 | translation regulator activity | 1 | 10 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.575 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.262 |
CLV_PCSK_PC1ET2_1 | 600 | 602 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.182 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.488 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.621 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.705 |
DOC_CYCLIN_yClb1_LxF_4 | 126 | 131 | PF00134 | 0.590 |
DOC_CYCLIN_yCln2_LP_2 | 501 | 504 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 132 | 140 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 209 | 217 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 229 | 237 | PF00069 | 0.257 |
DOC_MAPK_MEF2A_6 | 338 | 345 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 381 | 390 | PF00069 | 0.535 |
DOC_MAPK_RevD_3 | 339 | 352 | PF00069 | 0.545 |
DOC_PP1_RVXF_1 | 126 | 132 | PF00149 | 0.586 |
DOC_PP1_RVXF_1 | 307 | 314 | PF00149 | 0.516 |
DOC_PP2B_LxvP_1 | 500 | 503 | PF13499 | 0.445 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.507 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.475 |
DOC_USP7_UBL2_3 | 596 | 600 | PF12436 | 0.500 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 601 | 607 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 619 | 628 | PF00244 | 0.435 |
LIG_Actin_WH2_2 | 295 | 311 | PF00022 | 0.516 |
LIG_Actin_WH2_2 | 376 | 393 | PF00022 | 0.501 |
LIG_Actin_WH2_2 | 451 | 468 | PF00022 | 0.485 |
LIG_Actin_WH2_2 | 557 | 574 | PF00022 | 0.381 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.501 |
LIG_deltaCOP1_diTrp_1 | 240 | 248 | PF00928 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 73 | 82 | PF00928 | 0.400 |
LIG_EH_1 | 29 | 33 | PF12763 | 0.662 |
LIG_eIF4E_1 | 288 | 294 | PF01652 | 0.545 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.522 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.538 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.452 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.471 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.597 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.402 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.504 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.491 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.565 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.521 |
LIG_GBD_Chelix_1 | 515 | 523 | PF00786 | 0.300 |
LIG_IBAR_NPY_1 | 532 | 534 | PF08397 | 0.532 |
LIG_LIR_Gen_1 | 178 | 188 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 374 | 383 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 587 | 593 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 620 | 630 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 662 | 673 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.377 |
LIG_NRBOX | 518 | 524 | PF00104 | 0.508 |
LIG_NRP_CendR_1 | 728 | 731 | PF00754 | 0.688 |
LIG_PCNA_PIPBox_1 | 110 | 119 | PF02747 | 0.593 |
LIG_PCNA_PIPBox_1 | 407 | 416 | PF02747 | 0.516 |
LIG_PCNA_yPIPBox_3 | 407 | 418 | PF02747 | 0.516 |
LIG_PCNA_yPIPBox_3 | 443 | 454 | PF02747 | 0.516 |
LIG_PCNA_yPIPBox_3 | 652 | 661 | PF02747 | 0.444 |
LIG_Pex14_1 | 242 | 246 | PF04695 | 0.357 |
LIG_Pex14_1 | 248 | 252 | PF04695 | 0.363 |
LIG_Pex14_2 | 32 | 36 | PF04695 | 0.682 |
LIG_Rb_pABgroove_1 | 339 | 347 | PF01858 | 0.545 |
LIG_REV1ctd_RIR_1 | 250 | 259 | PF16727 | 0.525 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.523 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.516 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.480 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.418 |
LIG_SH2_GRB2like | 212 | 215 | PF00017 | 0.494 |
LIG_SH2_GRB2like | 616 | 619 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 544 | 548 | PF00017 | 0.530 |
LIG_SH2_SRC | 406 | 409 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.372 |
LIG_SUMO_SIM_anti_2 | 136 | 145 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 316 | 322 | PF11976 | 0.516 |
LIG_SUMO_SIM_anti_2 | 364 | 375 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 608 | 613 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 136 | 145 | PF11976 | 0.499 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.545 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.631 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.516 |
LIG_TYR_ITIM | 566 | 571 | PF00017 | 0.461 |
LIG_TYR_ITSM | 177 | 184 | PF00017 | 0.389 |
LIG_WRC_WIRS_1 | 310 | 315 | PF05994 | 0.501 |
LIG_WRC_WIRS_1 | 586 | 591 | PF05994 | 0.504 |
MOD_CDK_SPxxK_3 | 478 | 485 | PF00069 | 0.545 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.593 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.459 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.516 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.545 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.479 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.466 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.568 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.479 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.602 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.546 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.516 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.540 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.568 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.559 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.555 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.276 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.427 |
MOD_CMANNOS | 33 | 36 | PF00535 | 0.685 |
MOD_GlcNHglycan | 186 | 191 | PF01048 | 0.539 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.458 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.466 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.288 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.316 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.438 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.500 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.550 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.484 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.392 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.445 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.651 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.479 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.500 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.476 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.499 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.433 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.569 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.316 |
MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.198 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.495 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.461 |
MOD_N-GLC_1 | 671 | 676 | PF02516 | 0.440 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.524 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.360 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.502 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.519 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.653 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.486 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.549 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.432 |
MOD_NEK2_2 | 602 | 607 | PF00069 | 0.398 |
MOD_PIKK_1 | 301 | 307 | PF00454 | 0.495 |
MOD_PKA_1 | 229 | 235 | PF00069 | 0.559 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.531 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.501 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.619 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.432 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.357 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.469 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.487 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.467 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.440 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.520 |
MOD_Plk_2-3 | 10 | 16 | PF00069 | 0.711 |
MOD_Plk_2-3 | 130 | 136 | PF00069 | 0.541 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.738 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.557 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.455 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.545 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.455 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.460 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.519 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 50 | 53 | PF00179 | 0.604 |
MOD_SUMO_for_1 | 526 | 529 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 124 | 134 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_1 | 136 | 141 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_1 | 496 | 501 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_1 | 608 | 613 | PF01217 | 0.439 |
TRG_DiLeu_BaEn_2 | 87 | 93 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_4 | 142 | 148 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 599 | 602 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 641 | 643 | PF00400 | 0.500 |
TRG_NLS_Bipartite_1 | 83 | 98 | PF00514 | 0.489 |
TRG_NLS_MonoExtN_4 | 596 | 603 | PF00514 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 443 | 447 | PF00026 | 0.245 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I262 | Leptomonas seymouri | 76% | 99% |
A0A1X0NL84 | Trypanosomatidae | 38% | 100% |
A0A3Q8IWP7 | Leishmania donovani | 100% | 100% |
A0A422NVW4 | Trypanosoma rangeli | 39% | 100% |
A4HQM0 | Leishmania braziliensis | 93% | 100% |
A7E471 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 22% | 84% |
E9AUD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4Q055 | Leishmania major | 98% | 100% |
Q54X97 | Dictyostelium discoideum | 23% | 78% |
Q6BJF7 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 22% | 86% |
Q6P1V4 | Xenopus tropicalis | 23% | 79% |
Q6PFQ2 | Danio rerio | 22% | 79% |
V5DDW8 | Trypanosoma cruzi | 39% | 100% |