Translation, eukaryotic release factor 3
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | yes | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 2 |
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: 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:0005737 | cytoplasm | 2 | 1 |
GO:0018444 | translation release factor complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 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: A4HV24
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003924 | GTPase activity | 7 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005525 | GTP binding | 5 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0019001 | guanyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003747 | translation release factor activity | 5 | 1 |
GO:0008079 | translation termination factor activity | 4 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.311 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.238 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.240 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.722 |
DOC_ANK_TNKS_1 | 732 | 739 | PF00023 | 0.541 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.570 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.667 |
DOC_CYCLIN_yCln2_LP_2 | 708 | 714 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 192 | 201 | PF00069 | 0.590 |
DOC_MAPK_gen_1 | 203 | 209 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 313 | 324 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 497 | 506 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 527 | 534 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 733 | 741 | PF00069 | 0.462 |
DOC_PP1_RVXF_1 | 497 | 504 | PF00149 | 0.440 |
DOC_PP1_RVXF_1 | 635 | 642 | PF00149 | 0.393 |
DOC_PP2B_LxvP_1 | 402 | 405 | PF13499 | 0.440 |
DOC_PP2B_LxvP_1 | 538 | 541 | PF13499 | 0.435 |
DOC_PP4_FxxP_1 | 550 | 553 | PF00568 | 0.415 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.695 |
DOC_USP7_MATH_2 | 214 | 220 | PF00917 | 0.670 |
DOC_USP7_UBL2_3 | 283 | 287 | PF12436 | 0.639 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.576 |
DOC_USP7_UBL2_3 | 559 | 563 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 676 | 680 | PF12436 | 0.440 |
DOC_USP7_UBL2_3 | 718 | 722 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 397 | 402 | PF00244 | 0.479 |
LIG_APCC_ABBA_1 | 714 | 719 | PF00400 | 0.480 |
LIG_APCC_ABBAyCdc20_2 | 80 | 86 | PF00400 | 0.666 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.589 |
LIG_BIR_III_2 | 234 | 238 | PF00653 | 0.637 |
LIG_BIR_III_4 | 403 | 407 | PF00653 | 0.440 |
LIG_BRCT_BRCA1_1 | 598 | 602 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_2 | 598 | 604 | PF00533 | 0.463 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.622 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.440 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.440 |
LIG_FHA_1 | 732 | 738 | PF00498 | 0.440 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.692 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.774 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.740 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.626 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.501 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.440 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.440 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.440 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.479 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.394 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.434 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.323 |
LIG_FXI_DFP_1 | 717 | 721 | PF00024 | 0.257 |
LIG_IRF3_LxIS_1 | 423 | 429 | PF10401 | 0.440 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.608 |
LIG_LIR_Apic_2 | 547 | 553 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 367 | 374 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 475 | 484 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 671 | 681 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 719 | 728 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 564 | 570 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 719 | 723 | PF02991 | 0.511 |
LIG_PCNA_APIM_2 | 723 | 729 | PF02747 | 0.440 |
LIG_Pex14_1 | 366 | 370 | PF04695 | 0.440 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.457 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.440 |
LIG_REV1ctd_RIR_1 | 639 | 649 | PF16727 | 0.511 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.682 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.440 |
LIG_SH2_GRB2like | 24 | 27 | PF00017 | 0.640 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.646 |
LIG_SH2_SRC | 368 | 371 | PF00017 | 0.440 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.698 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.440 |
LIG_SH2_STAT3 | 122 | 125 | PF00017 | 0.724 |
LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.390 |
LIG_SH2_STAT3 | 28 | 31 | PF00017 | 0.633 |
LIG_SH2_STAT3 | 49 | 52 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.345 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.571 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.587 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.714 |
LIG_SH3_3 | 710 | 716 | PF00018 | 0.480 |
LIG_SUMO_SIM_par_1 | 424 | 430 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 645 | 650 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 709 | 715 | PF11976 | 0.511 |
LIG_SxIP_EBH_1 | 625 | 637 | PF03271 | 0.382 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.701 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.661 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.503 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.480 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.440 |
LIG_UBA3_1 | 460 | 466 | PF00899 | 0.457 |
LIG_UBA3_1 | 531 | 539 | PF00899 | 0.541 |
LIG_UBA3_1 | 677 | 684 | PF00899 | 0.511 |
MOD_CDK_SPxxK_3 | 286 | 293 | PF00069 | 0.659 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.665 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.732 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.440 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.457 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.453 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.359 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.511 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.687 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.624 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.683 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.524 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.440 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.440 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.461 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.342 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.390 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.365 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.541 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.423 |
MOD_Cter_Amidation | 201 | 204 | PF01082 | 0.625 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.704 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.638 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.627 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.692 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.635 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.240 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.347 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.516 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.311 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.311 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.647 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.740 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.668 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.457 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.382 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.356 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.428 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.513 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.644 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.428 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.440 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.413 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.657 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.752 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.426 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.440 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.440 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.440 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.511 |
MOD_PKB_1 | 303 | 311 | PF00069 | 0.644 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.457 |
MOD_Plk_2-3 | 542 | 548 | PF00069 | 0.429 |
MOD_Plk_2-3 | 593 | 599 | PF00069 | 0.379 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.519 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.451 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.416 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.457 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.663 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.664 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.731 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.706 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.710 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.547 |
MOD_SUMO_for_1 | 229 | 232 | PF00179 | 0.682 |
MOD_SUMO_for_1 | 297 | 300 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 222 | 231 | PF00179 | 0.719 |
MOD_SUMO_rev_2 | 468 | 473 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 533 | 541 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 560 | 564 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.435 |
TRG_NLS_Bipartite_1 | 192 | 207 | PF00514 | 0.726 |
TRG_NLS_MonoExtN_4 | 191 | 196 | PF00514 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 616 | 620 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAZ5 | Leptomonas seymouri | 80% | 100% |
A0A1X0NV54 | Trypanosomatidae | 71% | 100% |
A0A3Q8ICH2 | Leishmania donovani | 99% | 100% |
A0A3R7MLL0 | Trypanosoma rangeli | 70% | 100% |
A0A3S7X9T0 | Leishmania donovani | 32% | 100% |
A4H6P3 | Leishmania braziliensis | 89% | 100% |
A4HN87 | Leishmania braziliensis | 31% | 100% |
A4IBV5 | Leishmania infantum | 31% | 100% |
C9ZYQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A7C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9AFP2 | Leishmania major | 32% | 100% |
E9AGP5 | Leishmania infantum | 36% | 100% |
E9ANQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B6U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O74718 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
P23637 | Ogataea pini | 40% | 100% |
Q4QGW5 | Leishmania major | 94% | 100% |
Q5R6Y0 | Pongo abelii | 37% | 100% |
Q69ZS7 | Mus musculus | 35% | 100% |
Q6AXM7 | Rattus norvegicus | 36% | 100% |
Q9HGI6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 41% | 100% |
Q9HGI7 | Candida maltosa | 38% | 100% |
Q9W074 | Drosophila melanogaster | 35% | 100% |
Q9Y450 | Homo sapiens | 37% | 100% |