Translation, translation initiation factor EIF-2B gamma subunit
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 27 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005850 | eukaryotic translation initiation factor 2 complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HU30
Term | Name | Level | Count |
---|---|---|---|
GO:0001731 | formation of translation preinitiation complex | 7 | 2 |
GO:0006417 | regulation of translation | 6 | 2 |
GO:0006450 | regulation of translational fidelity | 3 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0010628 | positive regulation of gene expression | 6 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0034250 | positive regulation of amide metabolic process | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0045727 | positive regulation of translation | 7 | 2 |
GO:0045903 | positive regulation of translational fidelity | 4 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003924 | GTPase activity | 7 | 10 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
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 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0000049 | tRNA binding | 5 | 5 |
GO:0003723 | RNA binding | 4 | 5 |
GO:0003746 | translation elongation factor activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.649 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.456 |
CLV_PCSK_PC7_1 | 404 | 410 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.326 |
DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.642 |
DOC_CDC14_PxL_1 | 301 | 309 | PF14671 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 556 | 562 | PF00134 | 0.326 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 524 | 533 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 79 | 87 | PF00069 | 0.656 |
DOC_MAPK_RevD_3 | 305 | 320 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 578 | 585 | PF00149 | 0.386 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.521 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.656 |
DOC_PP4_FxxP_1 | 361 | 364 | PF00568 | 0.380 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.523 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.373 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.378 |
LIG_Actin_WH2_2 | 460 | 477 | PF00022 | 0.401 |
LIG_Actin_WH2_2 | 529 | 546 | PF00022 | 0.326 |
LIG_Actin_WH2_2 | 575 | 591 | PF00022 | 0.331 |
LIG_APCC_ABBA_1 | 461 | 466 | PF00400 | 0.397 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.749 |
LIG_BIR_III_2 | 433 | 437 | PF00653 | 0.579 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.656 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.482 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.646 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.416 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.656 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.476 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.649 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.763 |
LIG_LIR_Apic_2 | 167 | 172 | PF02991 | 0.656 |
LIG_LIR_Apic_2 | 339 | 344 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 358 | 364 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 27 | 36 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.593 |
LIG_PCNA_PIPBox_1 | 207 | 216 | PF02747 | 0.494 |
LIG_PCNA_PIPBox_1 | 465 | 474 | PF02747 | 0.434 |
LIG_PCNA_yPIPBox_3 | 465 | 475 | PF02747 | 0.426 |
LIG_REV1ctd_RIR_1 | 469 | 479 | PF16727 | 0.404 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.388 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 259 | 262 | PF00017 | 0.384 |
LIG_SH2_GRB2like | 91 | 94 | PF00017 | 0.656 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.494 |
LIG_SH2_SRC | 464 | 467 | PF00017 | 0.373 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.326 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.656 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.537 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.415 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.434 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.465 |
LIG_Sin3_3 | 158 | 165 | PF02671 | 0.656 |
LIG_SUMO_SIM_anti_2 | 187 | 193 | PF11976 | 0.496 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 366 | 373 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 451 | 456 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 525 | 535 | PF11976 | 0.331 |
LIG_UBA3_1 | 189 | 195 | PF00899 | 0.494 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.466 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.632 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.568 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.840 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.531 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.302 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.483 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.485 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.670 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.717 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.326 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.456 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.630 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.586 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.453 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.482 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.636 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.589 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.649 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.363 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.417 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.656 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.456 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.331 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.456 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.656 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.430 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.425 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.326 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.656 |
MOD_OFUCOSY | 102 | 107 | PF10250 | 0.456 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.656 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.656 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.656 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.465 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.498 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.326 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.656 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.531 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.450 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.331 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.764 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.656 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.656 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.494 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.477 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.598 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.351 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.443 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.331 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.656 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.656 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.503 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.637 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.615 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.600 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.538 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.373 |
MOD_SUMO_rev_2 | 8 | 17 | PF00179 | 0.694 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.326 |
TRG_NES_CRM1_1 | 182 | 193 | PF08389 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 594 | 598 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M5 | Leptomonas seymouri | 63% | 100% |
A0A3S7WQT0 | Leishmania donovani | 70% | 100% |
A4H5T6 | Leishmania braziliensis | 68% | 100% |
A4H5T7 | Leishmania braziliensis | 85% | 100% |
A4HU29 | Leishmania infantum | 70% | 100% |
E9AMV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9AMW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
Q4QHR6 | Leishmania major | 95% | 100% |
Q4QHR7 | Leishmania major | 69% | 100% |