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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0010494 | cytoplasmic stress granule | 5 | 2 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0035770 | ribonucleoprotein granule | 3 | 2 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QEK5
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003723 | RNA binding | 4 | 13 |
GO:0003729 | mRNA binding | 5 | 2 |
GO:0003743 | translation initiation factor activity | 4 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008135 | translation factor activity, RNA binding | 3 | 13 |
GO:0045182 | translation regulator activity | 1 | 13 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 329 | 333 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.502 |
CLV_PCSK_FUR_1 | 182 | 186 | PF00082 | 0.285 |
CLV_PCSK_FUR_1 | 30 | 34 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 184 | 186 | PF00082 | 0.256 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.342 |
CLV_Separin_Metazoa | 27 | 31 | PF03568 | 0.503 |
DEG_APCC_DBOX_1 | 567 | 575 | PF00400 | 0.536 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.635 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.642 |
DEG_SPOP_SBC_1 | 452 | 456 | PF00917 | 0.441 |
DOC_CYCLIN_RxL_1 | 81 | 92 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 270 | 278 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.635 |
DOC_PP1_RVXF_1 | 268 | 274 | PF00149 | 0.434 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.500 |
DOC_SPAK_OSR1_1 | 272 | 276 | PF12202 | 0.485 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.382 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.481 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.401 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 355 | 362 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 532 | 536 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 593 | 599 | PF00244 | 0.367 |
LIG_Actin_WH2_2 | 115 | 133 | PF00022 | 0.579 |
LIG_APCC_ABBAyCdc20_2 | 520 | 526 | PF00400 | 0.475 |
LIG_BH_BH3_1 | 226 | 242 | PF00452 | 0.488 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.531 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.532 |
LIG_DLG_GKlike_1 | 505 | 512 | PF00625 | 0.500 |
LIG_Dynein_DLC8_1 | 31 | 37 | PF01221 | 0.529 |
LIG_EH1_1 | 272 | 280 | PF00400 | 0.454 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.507 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.659 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.584 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.462 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.518 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.492 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.488 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.399 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.470 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.435 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.585 |
LIG_GBD_Chelix_1 | 487 | 495 | PF00786 | 0.409 |
LIG_Integrin_isoDGR_2 | 353 | 355 | PF01839 | 0.676 |
LIG_LIR_Gen_1 | 203 | 213 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 463 | 473 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 504 | 512 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 534 | 541 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 551 | 559 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 610 | 617 | PF02991 | 0.463 |
LIG_LIR_LC3C_4 | 466 | 470 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 534 | 538 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 551 | 556 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 610 | 615 | PF02991 | 0.453 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.509 |
LIG_NRBOX | 586 | 592 | PF00104 | 0.474 |
LIG_PCNA_yPIPBox_3 | 415 | 424 | PF02747 | 0.550 |
LIG_PCNA_yPIPBox_3 | 584 | 593 | PF02747 | 0.449 |
LIG_Pex14_1 | 423 | 427 | PF04695 | 0.361 |
LIG_Pex14_2 | 502 | 506 | PF04695 | 0.325 |
LIG_PTB_Apo_2 | 96 | 103 | PF02174 | 0.531 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.433 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.605 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.409 |
LIG_SH3_1 | 15 | 21 | PF00018 | 0.513 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.514 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.486 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.649 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.463 |
LIG_SUMO_SIM_anti_2 | 223 | 231 | PF11976 | 0.494 |
LIG_SUMO_SIM_anti_2 | 570 | 576 | PF11976 | 0.528 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.491 |
LIG_TRAF2_1 | 515 | 518 | PF00917 | 0.628 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.494 |
LIG_TRAF2_1 | 561 | 564 | PF00917 | 0.634 |
LIG_TYR_ITIM | 533 | 538 | PF00017 | 0.417 |
LIG_UBA3_1 | 275 | 283 | PF00899 | 0.468 |
LIG_UBA3_1 | 78 | 85 | PF00899 | 0.455 |
LIG_WRC_WIRS_1 | 549 | 554 | PF05994 | 0.492 |
LIG_WW_3 | 267 | 271 | PF00397 | 0.485 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.577 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.678 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.571 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.460 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.468 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.488 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.545 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.342 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.431 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.452 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.564 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.664 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.699 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.699 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.679 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.496 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.315 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.305 |
MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.567 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.540 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.561 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.540 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.728 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.756 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.581 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.449 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.477 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.450 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.484 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.533 |
MOD_N-GLC_2 | 428 | 430 | PF02516 | 0.520 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.498 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.522 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.459 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.522 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.643 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.417 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.421 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.543 |
MOD_NEK2_2 | 383 | 388 | PF00069 | 0.569 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.584 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.509 |
MOD_PKA_1 | 183 | 189 | PF00069 | 0.531 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.491 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.488 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.513 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.737 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.451 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.475 |
MOD_PKB_1 | 30 | 38 | PF00069 | 0.509 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.550 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.417 |
MOD_Plk_2-3 | 166 | 172 | PF00069 | 0.468 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.462 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.451 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.449 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.366 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.433 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.691 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.459 |
MOD_SUMO_for_1 | 398 | 401 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 121 | 130 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 161 | 169 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 300 | 308 | PF00179 | 0.664 |
MOD_SUMO_rev_2 | 72 | 77 | PF00179 | 0.563 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_2 | 462 | 468 | PF01217 | 0.326 |
TRG_DiLeu_BaEn_3 | 72 | 78 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 58 | 63 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.343 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.502 |
TRG_NES_CRM1_1 | 547 | 562 | PF08389 | 0.591 |
TRG_NES_CRM1_1 | 607 | 619 | PF08389 | 0.518 |
TRG_NLS_MonoExtN_4 | 182 | 187 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.233 |
TRG_Pf-PMV_PEXEL_1 | 156 | 161 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA5 | Leptomonas seymouri | 67% | 100% |
A0A0S4IUF0 | Bodo saltans | 34% | 98% |
A0A0S4KJH6 | Bodo saltans | 25% | 100% |
A0A1X0NZC7 | Trypanosomatidae | 41% | 100% |
A0A3Q8IAL0 | Leishmania donovani | 96% | 100% |
A0A422NEE1 | Trypanosoma rangeli | 42% | 100% |
A4H8T8 | Leishmania braziliensis | 92% | 100% |
A4HX58 | Leishmania infantum | 97% | 100% |
C9ZVT3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AQX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5DJ79 | Trypanosoma cruzi | 43% | 100% |