LeishMANIAdb
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Translation initiation factor eIF2B delta subunit, putative

Quick info Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Translation initiation factor eIF2B delta subunit, putative
Gene product:
translation initiation factor eIF2B delta subunit, putative
Species:
Leishmania donovani
UniProt:
A0A3Q8IE91_LEIDO
TriTrypDb:
LdBPK_271090.1 , LdCL_270017400 , LDHU3_27.1720
Length:
669

Localization

Secreted promastigote
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
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 8
NetGPI no yes: 0, no: 8
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A0A3Q8IE91
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3Q8IE91

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003676 nucleic acid binding 3 9
GO:0003743 translation initiation factor activity 4 9
GO:0005488 binding 1 9
GO:0008135 translation factor activity, RNA binding 3 9
GO:0045182 translation regulator activity 1 9
GO:0090079 translation regulator activity, nucleic acid binding 2 9
GO:0097159 organic cyclic compound binding 2 9
GO:1901363 heterocyclic compound binding 2 9

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 156 158 PF00675 0.450
CLV_NRD_NRD_1 348 350 PF00675 0.425
CLV_NRD_NRD_1 366 368 PF00675 0.250
CLV_NRD_NRD_1 42 44 PF00675 0.438
CLV_NRD_NRD_1 528 530 PF00675 0.248
CLV_NRD_NRD_1 80 82 PF00675 0.431
CLV_PCSK_FUR_1 348 352 PF00082 0.466
CLV_PCSK_KEX2_1 152 154 PF00082 0.432
CLV_PCSK_KEX2_1 256 258 PF00082 0.665
CLV_PCSK_KEX2_1 348 350 PF00082 0.421
CLV_PCSK_KEX2_1 366 368 PF00082 0.253
CLV_PCSK_KEX2_1 38 40 PF00082 0.434
CLV_PCSK_KEX2_1 454 456 PF00082 0.310
CLV_PCSK_KEX2_1 47 49 PF00082 0.444
CLV_PCSK_PC1ET2_1 152 154 PF00082 0.432
CLV_PCSK_PC1ET2_1 256 258 PF00082 0.512
CLV_PCSK_PC1ET2_1 350 352 PF00082 0.428
CLV_PCSK_PC1ET2_1 38 40 PF00082 0.434
CLV_PCSK_PC1ET2_1 454 456 PF00082 0.315
CLV_PCSK_PC1ET2_1 47 49 PF00082 0.444
CLV_PCSK_PC7_1 43 49 PF00082 0.381
CLV_PCSK_SKI1_1 147 151 PF00082 0.444
CLV_PCSK_SKI1_1 153 157 PF00082 0.424
CLV_PCSK_SKI1_1 244 248 PF00082 0.564
CLV_PCSK_SKI1_1 33 37 PF00082 0.444
CLV_PCSK_SKI1_1 358 362 PF00082 0.427
CLV_PCSK_SKI1_1 393 397 PF00082 0.437
CLV_PCSK_SKI1_1 47 51 PF00082 0.457
CLV_PCSK_SKI1_1 530 534 PF00082 0.248
CLV_PCSK_SKI1_1 7 11 PF00082 0.539
DEG_APCC_DBOX_1 152 160 PF00400 0.488
DEG_COP1_1 320 328 PF00400 0.484
DEG_COP1_1 536 545 PF00400 0.474
DEG_SPOP_SBC_1 615 619 PF00917 0.506
DOC_CKS1_1 578 583 PF01111 0.590
DOC_CKS1_1 595 600 PF01111 0.410
DOC_MAPK_gen_1 452 459 PF00069 0.517
DOC_MAPK_gen_1 526 535 PF00069 0.448
DOC_MAPK_gen_1 7 17 PF00069 0.533
DOC_MAPK_MEF2A_6 286 294 PF00069 0.439
DOC_MAPK_MEF2A_6 526 535 PF00069 0.448
DOC_MAPK_MEF2A_6 540 547 PF00069 0.448
DOC_MIT_MIM_1 362 372 PF04212 0.429
DOC_PP2B_LxvP_1 323 326 PF13499 0.498
DOC_PP2B_LxvP_1 584 587 PF13499 0.512
DOC_PP4_FxxP_1 528 531 PF00568 0.473
DOC_USP7_MATH_1 103 107 PF00917 0.547
DOC_USP7_MATH_1 124 128 PF00917 0.564
DOC_USP7_MATH_1 206 210 PF00917 0.805
DOC_USP7_MATH_1 324 328 PF00917 0.470
DOC_USP7_MATH_1 378 382 PF00917 0.632
DOC_USP7_MATH_1 421 425 PF00917 0.516
DOC_USP7_MATH_1 615 619 PF00917 0.484
DOC_USP7_MATH_1 90 94 PF00917 0.466
DOC_USP7_UBL2_3 121 125 PF12436 0.636
DOC_USP7_UBL2_3 158 162 PF12436 0.461
DOC_USP7_UBL2_3 408 412 PF12436 0.477
DOC_USP7_UBL2_3 526 530 PF12436 0.448
DOC_USP7_UBL2_3 7 11 PF12436 0.539
DOC_WW_Pin1_4 101 106 PF00397 0.627
DOC_WW_Pin1_4 209 214 PF00397 0.725
DOC_WW_Pin1_4 216 221 PF00397 0.710
DOC_WW_Pin1_4 571 576 PF00397 0.448
DOC_WW_Pin1_4 577 582 PF00397 0.448
DOC_WW_Pin1_4 594 599 PF00397 0.516
DOC_WW_Pin1_4 625 630 PF00397 0.444
LIG_14-3-3_CanoR_1 251 258 PF00244 0.639
LIG_14-3-3_CanoR_1 318 323 PF00244 0.471
LIG_14-3-3_CanoR_1 434 438 PF00244 0.448
LIG_Actin_WH2_2 392 410 PF00022 0.404
LIG_BIR_II_1 1 5 PF00653 0.580
LIG_BRCT_BRCA1_1 537 541 PF00533 0.448
LIG_CtBP_PxDLS_1 108 112 PF00389 0.541
LIG_FHA_1 199 205 PF00498 0.795
LIG_FHA_1 219 225 PF00498 0.587
LIG_FHA_1 318 324 PF00498 0.427
LIG_FHA_1 394 400 PF00498 0.396
LIG_FHA_1 426 432 PF00498 0.450
LIG_FHA_1 480 486 PF00498 0.448
LIG_FHA_1 643 649 PF00498 0.508
LIG_FHA_1 658 664 PF00498 0.468
LIG_FHA_2 117 123 PF00498 0.539
LIG_FHA_2 143 149 PF00498 0.421
LIG_FHA_2 245 251 PF00498 0.579
LIG_FHA_2 332 338 PF00498 0.455
LIG_LIR_Apic_2 592 598 PF02991 0.516
LIG_LIR_Gen_1 333 344 PF02991 0.383
LIG_LIR_Gen_1 631 640 PF02991 0.499
LIG_LIR_Nem_3 311 316 PF02991 0.377
LIG_LIR_Nem_3 333 339 PF02991 0.392
LIG_LIR_Nem_3 410 414 PF02991 0.425
LIG_LIR_Nem_3 439 443 PF02991 0.516
LIG_LIR_Nem_3 482 486 PF02991 0.451
LIG_LIR_Nem_3 536 542 PF02991 0.474
LIG_MYND_1 582 586 PF01753 0.479
LIG_SH2_CRK 483 487 PF00017 0.448
LIG_SH2_CRK 539 543 PF00017 0.493
LIG_SH2_CRK 578 582 PF00017 0.409
LIG_SH2_PTP2 440 443 PF00017 0.516
LIG_SH2_STAT5 422 425 PF00017 0.475
LIG_SH2_STAT5 440 443 PF00017 0.473
LIG_SH2_STAT5 623 626 PF00017 0.448
LIG_SH2_STAT5 632 635 PF00017 0.448
LIG_SH3_3 102 108 PF00018 0.605
LIG_SH3_3 279 285 PF00018 0.529
LIG_SH3_3 372 378 PF00018 0.479
LIG_SUMO_SIM_anti_2 289 295 PF11976 0.379
LIG_SUMO_SIM_anti_2 381 388 PF11976 0.399
LIG_SUMO_SIM_par_1 106 113 PF11976 0.544
LIG_SUMO_SIM_par_1 221 228 PF11976 0.578
LIG_SUMO_SIM_par_1 320 327 PF11976 0.576
LIG_SUMO_SIM_par_1 398 404 PF11976 0.344
LIG_SUMO_SIM_par_1 455 461 PF11976 0.459
LIG_TRAF2_1 247 250 PF00917 0.588
LIG_TRFH_1 625 629 PF08558 0.448
LIG_TYR_ITIM 438 443 PF00017 0.516
LIG_TYR_ITIM 481 486 PF00017 0.448
LIG_UBA3_1 399 408 PF00899 0.399
MOD_CDK_SPxK_1 594 600 PF00069 0.516
MOD_CK1_1 104 110 PF00069 0.693
MOD_CK1_1 165 171 PF00069 0.533
MOD_CK1_1 193 199 PF00069 0.596
MOD_CK1_1 2 8 PF00069 0.498
MOD_CK1_1 209 215 PF00069 0.551
MOD_CK1_1 317 323 PF00069 0.424
MOD_CK1_1 410 416 PF00069 0.336
MOD_CK1_1 425 431 PF00069 0.456
MOD_CK1_1 618 624 PF00069 0.531
MOD_CK2_1 116 122 PF00069 0.621
MOD_CK2_1 132 138 PF00069 0.506
MOD_CK2_1 142 148 PF00069 0.443
MOD_CK2_1 165 171 PF00069 0.532
MOD_CK2_1 17 23 PF00069 0.398
MOD_CK2_1 2 8 PF00069 0.498
MOD_CK2_1 244 250 PF00069 0.565
MOD_CK2_1 324 330 PF00069 0.500
MOD_CK2_1 331 337 PF00069 0.448
MOD_CK2_1 410 416 PF00069 0.336
MOD_CK2_1 433 439 PF00069 0.471
MOD_GlcNHglycan 112 115 PF01048 0.602
MOD_GlcNHglycan 134 137 PF01048 0.606
MOD_GlcNHglycan 140 143 PF01048 0.638
MOD_GlcNHglycan 192 195 PF01048 0.611
MOD_GlcNHglycan 196 199 PF01048 0.650
MOD_GlcNHglycan 208 211 PF01048 0.533
MOD_GlcNHglycan 231 234 PF01048 0.585
MOD_GlcNHglycan 238 241 PF01048 0.627
MOD_GlcNHglycan 253 256 PF01048 0.609
MOD_GlcNHglycan 302 305 PF01048 0.421
MOD_GlcNHglycan 310 313 PF01048 0.348
MOD_GlcNHglycan 352 356 PF01048 0.338
MOD_GlcNHglycan 460 463 PF01048 0.265
MOD_GlcNHglycan 475 478 PF01048 0.214
MOD_GlcNHglycan 503 506 PF01048 0.315
MOD_GlcNHglycan 591 594 PF01048 0.279
MOD_GlcNHglycan 607 610 PF01048 0.227
MOD_GlcNHglycan 618 621 PF01048 0.251
MOD_GlcNHglycan 645 648 PF01048 0.350
MOD_GlcNHglycan 92 95 PF01048 0.581
MOD_GSK3_1 103 110 PF00069 0.633
MOD_GSK3_1 112 119 PF00069 0.585
MOD_GSK3_1 138 145 PF00069 0.658
MOD_GSK3_1 190 197 PF00069 0.572
MOD_GSK3_1 208 215 PF00069 0.717
MOD_GSK3_1 218 225 PF00069 0.585
MOD_GSK3_1 314 321 PF00069 0.441
MOD_GSK3_1 421 428 PF00069 0.479
MOD_GSK3_1 484 491 PF00069 0.473
MOD_GSK3_1 565 572 PF00069 0.528
MOD_GSK3_1 614 621 PF00069 0.483
MOD_N-GLC_1 228 233 PF02516 0.580
MOD_NEK2_1 407 412 PF00069 0.379
MOD_NEK2_1 432 437 PF00069 0.470
MOD_NEK2_1 501 506 PF00069 0.505
MOD_NEK2_1 535 540 PF00069 0.448
MOD_NEK2_1 589 594 PF00069 0.567
MOD_NEK2_1 605 610 PF00069 0.389
MOD_NEK2_1 616 621 PF00069 0.522
MOD_NEK2_1 643 648 PF00069 0.495
MOD_PIKK_1 124 130 PF00454 0.548
MOD_PIKK_1 142 148 PF00454 0.373
MOD_PIKK_1 658 664 PF00454 0.548
MOD_PKA_2 317 323 PF00069 0.430
MOD_PKA_2 433 439 PF00069 0.448
MOD_PKA_2 589 595 PF00069 0.505
MOD_PKA_2 657 663 PF00069 0.556
MOD_PKB_1 349 357 PF00069 0.348
MOD_Plk_1 331 337 PF00069 0.448
MOD_Plk_1 393 399 PF00069 0.378
MOD_Plk_1 416 422 PF00069 0.458
MOD_Plk_1 658 664 PF00069 0.548
MOD_Plk_4 318 324 PF00069 0.478
MOD_Plk_4 378 384 PF00069 0.608
MOD_Plk_4 410 416 PF00069 0.336
MOD_Plk_4 425 431 PF00069 0.448
MOD_Plk_4 433 439 PF00069 0.448
MOD_Plk_4 488 494 PF00069 0.448
MOD_Plk_4 628 634 PF00069 0.501
MOD_ProDKin_1 101 107 PF00069 0.627
MOD_ProDKin_1 209 215 PF00069 0.724
MOD_ProDKin_1 216 222 PF00069 0.710
MOD_ProDKin_1 571 577 PF00069 0.448
MOD_ProDKin_1 582 588 PF00069 0.448
MOD_ProDKin_1 594 600 PF00069 0.459
MOD_ProDKin_1 625 631 PF00069 0.444
MOD_SUMO_rev_2 401 410 PF00179 0.436
MOD_SUMO_rev_2 75 84 PF00179 0.350
TRG_DiLeu_BaEn_1 289 294 PF01217 0.437
TRG_DiLeu_BaEn_1 295 300 PF01217 0.459
TRG_DiLeu_BaEn_2 536 542 PF01217 0.448
TRG_ENDOCYTIC_2 440 443 PF00928 0.516
TRG_ENDOCYTIC_2 483 486 PF00928 0.448
TRG_ENDOCYTIC_2 539 542 PF00928 0.516
TRG_ENDOCYTIC_2 632 635 PF00928 0.499
TRG_ER_diArg_1 347 349 PF00400 0.394
TRG_ER_diArg_1 365 367 PF00400 0.254
TRG_NLS_Bipartite_1 150 165 PF00514 0.483
TRG_NLS_MonoExtN_4 158 165 PF00514 0.492
TRG_Pf-PMV_PEXEL_1 468 472 PF00026 0.315
TRG_Pf-PMV_PEXEL_1 81 85 PF00026 0.433

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I1D4 Leptomonas seymouri 67% 99%
A0A1X0P4F2 Trypanosomatidae 44% 100%
A4HFP5 Leishmania braziliensis 87% 100%
A4I2S1 Leishmania infantum 100% 100%
D0A5X8 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 43% 100%
E9AD99 Leishmania major 93% 100%
E9AZ24 Leishmania mexicana (strain MHOM/GT/2001/U1103) 95% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS