Translation, eukaryotic translation initation factor 4 gamma 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. | 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0016281 | eukaryotic translation initiation factor 4F 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: A4IE18
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 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:0016070 | RNA metabolic process | 5 | 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:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 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:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0003743 | translation initiation factor activity | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008135 | translation factor activity, RNA binding | 3 | 7 |
GO:0045182 | translation regulator activity | 1 | 7 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.288 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.387 |
DEG_MDM2_SWIB_1 | 28 | 35 | PF02201 | 0.520 |
DEG_MDM2_SWIB_1 | 670 | 678 | PF02201 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.535 |
DOC_ANK_TNKS_1 | 445 | 452 | PF00023 | 0.787 |
DOC_CKS1_1 | 513 | 518 | PF01111 | 0.590 |
DOC_CYCLIN_RxL_1 | 41 | 48 | PF00134 | 0.502 |
DOC_MAPK_DCC_7 | 55 | 64 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 12 | 22 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 217 | 226 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 55 | 64 | PF00069 | 0.529 |
DOC_MAPK_RevD_3 | 264 | 279 | PF00069 | 0.488 |
DOC_MAPK_RevD_3 | 60 | 75 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.488 |
DOC_PP2B_LxvP_1 | 655 | 658 | PF13499 | 0.467 |
DOC_PP4_FxxP_1 | 381 | 384 | PF00568 | 0.696 |
DOC_PP4_MxPP_1 | 474 | 477 | PF00568 | 0.682 |
DOC_PP4_MxPP_1 | 486 | 489 | PF00568 | 0.602 |
DOC_SPAK_OSR1_1 | 323 | 327 | PF12202 | 0.488 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.407 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.488 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 307 | 316 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 432 | 437 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 600 | 605 | PF00244 | 0.380 |
LIG_AP2alpha_1 | 197 | 201 | PF02296 | 0.488 |
LIG_APCC_ABBAyCdc20_2 | 742 | 748 | PF00400 | 0.592 |
LIG_BRCT_BRCA1_1 | 589 | 593 | PF00533 | 0.474 |
LIG_BRCT_BRCA1_1 | 633 | 637 | PF00533 | 0.412 |
LIG_deltaCOP1_diTrp_1 | 331 | 337 | PF00928 | 0.488 |
LIG_deltaCOP1_diTrp_1 | 665 | 670 | PF00928 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 672 | 681 | PF00928 | 0.407 |
LIG_EH1_1 | 323 | 331 | PF00400 | 0.488 |
LIG_EVH1_2 | 477 | 481 | PF00568 | 0.664 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.510 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.488 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.602 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.385 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.364 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.523 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.460 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.693 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.494 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.456 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.511 |
LIG_Integrin_isoDGR_2 | 183 | 185 | PF01839 | 0.361 |
LIG_Integrin_RGD_1 | 439 | 441 | PF01839 | 0.784 |
LIG_LIR_Apic_2 | 378 | 384 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 30 | 40 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 459 | 469 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 634 | 645 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 667 | 678 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 96 | 107 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 616 | 621 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 667 | 673 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 741 | 746 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.464 |
LIG_PCNA_yPIPBox_3 | 39 | 53 | PF02747 | 0.507 |
LIG_PDZ_Class_3 | 753 | 758 | PF00595 | 0.639 |
LIG_Pex14_1 | 666 | 670 | PF04695 | 0.425 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.488 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.513 |
LIG_Pex14_2 | 670 | 674 | PF04695 | 0.406 |
LIG_PTB_Apo_2 | 220 | 227 | PF02174 | 0.446 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 656 | 659 | PF00017 | 0.474 |
LIG_SH2_SRC | 651 | 654 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 602 | 606 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 622 | 626 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.570 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.488 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.488 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.488 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.679 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.581 |
LIG_Sin3_3 | 99 | 106 | PF02671 | 0.560 |
LIG_SUMO_SIM_par_1 | 240 | 247 | PF11976 | 0.488 |
LIG_UBA3_1 | 272 | 278 | PF00899 | 0.488 |
LIG_UBA3_1 | 510 | 518 | PF00899 | 0.497 |
LIG_UBA3_1 | 592 | 596 | PF00899 | 0.451 |
LIG_UBA3_1 | 695 | 703 | PF00899 | 0.446 |
LIG_WRC_WIRS_1 | 458 | 463 | PF05994 | 0.631 |
LIG_WW_3 | 205 | 209 | PF00397 | 0.505 |
MOD_CDK_SPK_2 | 253 | 258 | PF00069 | 0.560 |
MOD_CDK_SPxK_1 | 512 | 518 | PF00069 | 0.498 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.505 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.748 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.664 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.722 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.507 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.422 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.402 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.514 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.674 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.442 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.445 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.288 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.288 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.671 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.673 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.774 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.503 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.549 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.728 |
MOD_GlcNHglycan | 523 | 527 | PF01048 | 0.407 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.441 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.748 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.701 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.680 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.779 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.603 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.433 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.423 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.490 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.438 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.361 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.680 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.519 |
MOD_N-GLC_1 | 736 | 741 | PF02516 | 0.462 |
MOD_N-GLC_2 | 371 | 373 | PF02516 | 0.650 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.560 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.479 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.514 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.560 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.608 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.417 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.394 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.554 |
MOD_NEK2_2 | 698 | 703 | PF00069 | 0.426 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.662 |
MOD_PIKK_1 | 498 | 504 | PF00454 | 0.662 |
MOD_PIKK_1 | 717 | 723 | PF00454 | 0.560 |
MOD_PKA_1 | 570 | 576 | PF00069 | 0.427 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.512 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.488 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.687 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.597 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.560 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.515 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.662 |
MOD_Plk_2-3 | 534 | 540 | PF00069 | 0.497 |
MOD_Plk_2-3 | 574 | 580 | PF00069 | 0.464 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.560 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.505 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.488 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.414 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.411 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.426 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.458 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.500 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.602 |
MOD_SUMO_rev_2 | 176 | 182 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 501 | 511 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 590 | 598 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_1 | 506 | 511 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 743 | 746 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 320 | 323 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL6 | Leptomonas seymouri | 68% | 100% |
A0A3Q8IJA9 | Leishmania donovani | 100% | 100% |
A4HQC5 | Leishmania braziliensis | 83% | 99% |
E9AU41 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q0F4 | Leishmania major | 95% | 100% |