by homology
Contact email: opmn@cpqam.biocruz.br
Publication title: Translation initiation in Leishmania major: characterisation of multiple eIF4F subunit homologues
Publication 1st author(s): Dhalia
Publication Identifier(s): 15694484
Host organism: -1
Interaction detection method(s): pull down
Interaction type: physical association
Identification method participant A: autoradiography
Identification method participant B: autoradiography
ID(s) interactor A: P60842
ID(s) interactor B: Q4QEK5
Taxid interactor A: Homo sapiens
Taxid interactor B: Leishmania major
Biological role(s) interactor A: unspecified role
Biological role(s) interactor B: unspecified role
Experimental role(s) interactor A: bait
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
Related structures:
AlphaFold database: A4H8T8
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 237 | 241 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.282 |
CLV_PCSK_FUR_1 | 89 | 93 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.297 |
DEG_APCC_DBOX_1 | 475 | 483 | PF00400 | 0.565 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.331 |
DEG_SPOP_SBC_1 | 276 | 280 | PF00917 | 0.752 |
DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.563 |
DOC_MAPK_gen_1 | 177 | 185 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.476 |
DOC_PP1_RVXF_1 | 4 | 10 | PF00149 | 0.451 |
DOC_SPAK_OSR1_1 | 179 | 183 | PF12202 | 0.517 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.424 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.400 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.567 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.571 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 263 | 270 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 413 | 418 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 63 | 72 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 22 | 40 | PF00022 | 0.581 |
LIG_APCC_ABBAyCdc20_2 | 428 | 434 | PF00400 | 0.519 |
LIG_BH_BH3_1 | 133 | 149 | PF00452 | 0.581 |
LIG_Clathr_ClatBox_1 | 305 | 309 | PF01394 | 0.547 |
LIG_DLG_GKlike_1 | 413 | 420 | PF00625 | 0.528 |
LIG_EH1_1 | 179 | 187 | PF00400 | 0.487 |
LIG_EH1_1 | 451 | 459 | PF00400 | 0.420 |
LIG_eIF4E_1 | 452 | 458 | PF01652 | 0.278 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.762 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.609 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.534 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.522 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.501 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.345 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.442 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.528 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.608 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.535 |
LIG_Integrin_isoDGR_2 | 261 | 263 | PF01839 | 0.783 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 374 | 383 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 412 | 420 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 442 | 449 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 459 | 467 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 519 | 525 | PF02991 | 0.499 |
LIG_LIR_LC3C_4 | 374 | 378 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 519 | 523 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.577 |
LIG_NRBOX | 136 | 142 | PF00104 | 0.537 |
LIG_NRBOX | 494 | 500 | PF00104 | 0.504 |
LIG_PCNA_TLS_4 | 153 | 160 | PF02747 | 0.520 |
LIG_PCNA_yPIPBox_3 | 323 | 332 | PF02747 | 0.595 |
LIG_PCNA_yPIPBox_3 | 492 | 501 | PF02747 | 0.520 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.426 |
LIG_Pex14_2 | 410 | 414 | PF04695 | 0.381 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.684 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.474 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.644 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 130 | 138 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 478 | 484 | PF11976 | 0.564 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.672 |
LIG_TRAF2_1 | 469 | 472 | PF00917 | 0.652 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.521 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.447 |
LIG_UBA3_1 | 182 | 190 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 457 | 462 | PF05994 | 0.505 |
LIG_WW_3 | 174 | 178 | PF00397 | 0.517 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.555 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.510 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.522 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.574 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.582 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.560 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.385 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.505 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.587 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.494 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.591 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.679 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.688 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.671 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.621 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.514 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.372 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.361 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.559 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.539 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.460 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.742 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.513 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.475 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.546 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.571 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.732 |
MOD_N-GLC_2 | 336 | 338 | PF02516 | 0.543 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.526 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.535 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.487 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.487 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.755 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.489 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.475 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.589 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.400 |
MOD_PKA_1 | 90 | 96 | PF00069 | 0.554 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.581 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.743 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.504 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.494 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.562 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.400 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.729 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.462 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.501 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.480 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.400 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.515 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.513 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.487 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.394 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.470 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.677 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.572 |
MOD_SUMO_for_1 | 306 | 309 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 207 | 215 | PF00179 | 0.789 |
MOD_SUMO_rev_2 | 68 | 76 | PF00179 | 0.581 |
TRG_DiLeu_BaEn_1 | 132 | 137 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.495 |
TRG_NES_CRM1_1 | 455 | 470 | PF08389 | 0.586 |
TRG_NES_CRM1_1 | 515 | 527 | PF08389 | 0.545 |
TRG_NLS_MonoExtN_4 | 89 | 94 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.268 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA5 | Leptomonas seymouri | 65% | 86% |
A0A0S4IUF0 | Bodo saltans | 31% | 84% |
A0A1X0NZC7 | Trypanosomatidae | 39% | 86% |
A0A3Q8IAL0 | Leishmania donovani | 91% | 86% |
A0A422NEE1 | Trypanosoma rangeli | 40% | 88% |
A4HX58 | Leishmania infantum | 92% | 86% |
C9ZVT3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 87% |
E9AQX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 86% |
Q4QEK5 | Leishmania major | 92% | 100% |
V5DJ79 | Trypanosoma cruzi | 40% | 88% |