Translation, Eukaryotic translation initiation factor 3 subunit L
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | yes | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 12 |
GO:0016282 | eukaryotic 43S preinitiation complex | 4 | 6 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0033290 | eukaryotic 48S preinitiation complex | 4 | 6 |
GO:0070993 | translation preinitiation complex | 3 | 6 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
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: A4ICW2
Term | Name | Level | Count |
---|---|---|---|
GO:0001732 | formation of cytoplasmic translation initiation complex | 7 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0022607 | cellular component assembly | 4 | 6 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 6 |
GO:0043933 | protein-containing complex organization | 4 | 6 |
GO:0065003 | protein-containing complex assembly | 5 | 6 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.531 |
CLV_MEL_PAP_1 | 229 | 235 | PF00089 | 0.272 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.238 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 472 | 474 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.752 |
CLV_PCSK_PC7_1 | 24 | 30 | PF00082 | 0.484 |
CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.281 |
DEG_APCC_DBOX_1 | 226 | 234 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.472 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.302 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 295 | 304 | PF00134 | 0.472 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 386 | 393 | PF00134 | 0.472 |
DOC_MAPK_gen_1 | 200 | 207 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 200 | 207 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 262 | 269 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 58 | 65 | PF00069 | 0.362 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.424 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 446 | 461 | PF00022 | 0.602 |
LIG_AP2alpha_1 | 327 | 331 | PF02296 | 0.474 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_BIR_III_4 | 101 | 105 | PF00653 | 0.454 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.501 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.401 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_2 | 82 | 88 | PF00533 | 0.416 |
LIG_Clathr_ClatBox_1 | 393 | 397 | PF01394 | 0.515 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.453 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.513 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.515 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.472 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.501 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.625 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.517 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.560 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.472 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.480 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.448 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.534 |
LIG_Integrin_isoDGR_2 | 270 | 272 | PF01839 | 0.315 |
LIG_LIR_Apic_2 | 118 | 122 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 14 | 22 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 192 | 203 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 247 | 254 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 281 | 292 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 335 | 343 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 430 | 437 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.138 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.480 |
LIG_NRBOX | 389 | 395 | PF00104 | 0.515 |
LIG_PCNA_yPIPBox_3 | 166 | 174 | PF02747 | 0.472 |
LIG_PCNA_yPIPBox_3 | 200 | 211 | PF02747 | 0.451 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.421 |
LIG_REV1ctd_RIR_1 | 16 | 24 | PF16727 | 0.352 |
LIG_SH2_CRK | 141 | 145 | PF00017 | 0.515 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.555 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.424 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.480 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.538 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.271 |
LIG_SH2_GRB2like | 382 | 385 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.515 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.472 |
LIG_SH2_SRC | 303 | 306 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.361 |
LIG_SH2_STAT3 | 524 | 527 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.438 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.443 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 439 | 447 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 391 | 398 | PF11976 | 0.421 |
LIG_TYR_ITIM | 139 | 144 | PF00017 | 0.515 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.362 |
LIG_UBA3_1 | 112 | 117 | PF00899 | 0.472 |
LIG_UBA3_1 | 169 | 174 | PF00899 | 0.515 |
LIG_UBA3_1 | 372 | 380 | PF00899 | 0.515 |
LIG_UBA3_1 | 403 | 407 | PF00899 | 0.438 |
LIG_UBA3_1 | 457 | 462 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.286 |
MOD_CDC14_SPxK_1 | 347 | 350 | PF00782 | 0.506 |
MOD_CDK_SPK_2 | 332 | 337 | PF00069 | 0.413 |
MOD_CDK_SPxK_1 | 344 | 350 | PF00069 | 0.506 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.505 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.504 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.489 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.491 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.515 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.449 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.462 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.472 |
MOD_CMANNOS | 124 | 127 | PF00535 | 0.224 |
MOD_Cter_Amidation | 270 | 273 | PF01082 | 0.315 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.306 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.118 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.762 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.525 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.531 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.515 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.224 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.494 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.428 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.440 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.427 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.494 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.410 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.480 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.369 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.497 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.424 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.460 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.515 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.467 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.480 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.437 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.493 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.421 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.420 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.439 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.424 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.310 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.526 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.424 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.463 |
TRG_DiLeu_BaEn_1 | 155 | 160 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.443 |
TRG_DiLeu_LyEn_5 | 155 | 160 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.278 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.653 |
TRG_NES_CRM1_1 | 128 | 142 | PF08389 | 0.443 |
TRG_NES_CRM1_1 | 371 | 383 | PF08389 | 0.441 |
TRG_NLS_MonoExtN_4 | 492 | 499 | PF00514 | 0.689 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 411 | 416 | PF00026 | 0.224 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA7 | Leptomonas seymouri | 79% | 100% |
A0A0S4KNQ8 | Bodo saltans | 35% | 100% |
A0A1X0P8D7 | Trypanosomatidae | 53% | 100% |
A0A3Q8IIN0 | Leishmania donovani | 100% | 100% |
A0A3R7KQY4 | Trypanosoma rangeli | 53% | 100% |
A1C690 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 23% | 100% |
A1DGW6 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 23% | 100% |
A2R7S7 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 23% | 100% |
A4HNN3 | Leishmania braziliensis | 97% | 100% |
A5A6M4 | Pan troglodytes | 25% | 96% |
A7SDW5 | Nematostella vectensis | 24% | 100% |
A8PHP4 | Brugia malayi | 22% | 99% |
A8X419 | Caenorhabditis briggsae | 24% | 100% |
A9VCY6 | Monosiga brevicollis | 24% | 100% |
B0WR18 | Culex quinquefasciatus | 22% | 100% |
B0XS74 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 23% | 100% |
B3M7W0 | Drosophila ananassae | 23% | 100% |
B3NH71 | Drosophila erecta | 23% | 100% |
B4GR63 | Drosophila persimilis | 24% | 100% |
B4HFJ3 | Drosophila sechellia | 23% | 100% |
B4IWN1 | Drosophila grimshawi | 23% | 100% |
B4KZ45 | Drosophila mojavensis | 23% | 100% |
B4LEJ0 | Drosophila virilis | 23% | 100% |
B4MX71 | Drosophila willistoni | 23% | 100% |
B4PG99 | Drosophila yakuba | 23% | 100% |
B4QR64 | Drosophila simulans | 23% | 100% |
D0A2I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ASE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
P0CN56 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 23% | 86% |
P0CN57 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 23% | 86% |
Q0CPA8 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 23% | 100% |
Q16FL6 | Aedes aegypti | 23% | 100% |
Q2M0S3 | Drosophila pseudoobscura pseudoobscura | 24% | 100% |
Q2U041 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 100% |
Q3ZCK1 | Bos taurus | 25% | 96% |
Q4PF85 | Ustilago maydis (strain 521 / FGSC 9021) | 22% | 81% |
Q4Q253 | Leishmania major | 98% | 100% |
Q4X1D2 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 23% | 100% |
Q5B0H6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 100% |
Q5F428 | Gallus gallus | 25% | 96% |
Q6CAE9 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 100% |
Q6P878 | Xenopus tropicalis | 25% | 97% |
Q7Q5Y8 | Anopheles gambiae | 22% | 100% |
Q7T2A5 | Danio rerio | 25% | 94% |
Q8AVJ0 | Xenopus laevis | 24% | 97% |
Q8QZY1 | Mus musculus | 25% | 96% |
Q95QW0 | Caenorhabditis elegans | 24% | 100% |
Q9VTU4 | Drosophila melanogaster | 23% | 100% |
Q9Y262 | Homo sapiens | 25% | 96% |
V5BV76 | Trypanosoma cruzi | 53% | 100% |