Translation, translation initiation factor
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: 4 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
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:0032991 | protein-containing complex | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 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: A4HXK6
Term | Name | Level | Count |
---|---|---|---|
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0031369 | translation initiation factor 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 | 128 | 132 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 699 | 701 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 642 | 644 | PF00082 | 0.389 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.476 |
CLV_PCSK_PC7_1 | 432 | 438 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.180 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.398 |
DOC_CKS1_1 | 250 | 255 | PF01111 | 0.420 |
DOC_MAPK_gen_1 | 265 | 275 | PF00069 | 0.321 |
DOC_PP1_RVXF_1 | 225 | 231 | PF00149 | 0.436 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.376 |
DOC_PP4_FxxP_1 | 496 | 499 | PF00568 | 0.390 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.393 |
DOC_USP7_UBL2_3 | 479 | 483 | PF12436 | 0.393 |
DOC_USP7_UBL2_3 | 576 | 580 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.253 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.270 |
LIG_14-3-3_CanoR_1 | 285 | 293 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 92 | 97 | PF00244 | 0.397 |
LIG_APCC_ABBA_1 | 226 | 231 | PF00400 | 0.437 |
LIG_APCC_ABBA_1 | 273 | 278 | PF00400 | 0.460 |
LIG_BIR_III_2 | 131 | 135 | PF00653 | 0.332 |
LIG_CSL_BTD_1 | 398 | 401 | PF09270 | 0.380 |
LIG_deltaCOP1_diTrp_1 | 145 | 153 | PF00928 | 0.268 |
LIG_deltaCOP1_diTrp_1 | 278 | 286 | PF00928 | 0.290 |
LIG_deltaCOP1_diTrp_1 | 396 | 405 | PF00928 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 540 | 548 | PF00928 | 0.385 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.379 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.339 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.405 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.386 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.331 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.431 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.470 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.477 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.445 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.339 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.482 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.361 |
LIG_FHA_2 | 657 | 663 | PF00498 | 0.484 |
LIG_LIR_Apic_2 | 103 | 109 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 333 | 337 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 493 | 499 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 245 | 253 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 404 | 411 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 451 | 457 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 692 | 702 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.340 |
LIG_LIR_LC3C_4 | 289 | 294 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 544 | 550 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 667 | 672 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 692 | 697 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.322 |
LIG_Pex14_2 | 144 | 148 | PF04695 | 0.277 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.416 |
LIG_SH2_CRK | 694 | 698 | PF00017 | 0.567 |
LIG_SH2_PTP2 | 106 | 109 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 247 | 250 | PF00017 | 0.348 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.573 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.410 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.568 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.374 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.345 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 255 | 260 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 289 | 296 | PF11976 | 0.400 |
LIG_TRAF2_1 | 635 | 638 | PF00917 | 0.512 |
LIG_TRAF2_1 | 659 | 662 | PF00917 | 0.485 |
LIG_TRAF2_1 | 681 | 684 | PF00917 | 0.441 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.418 |
LIG_TYR_ITSM | 690 | 697 | PF00017 | 0.561 |
LIG_UBA3_1 | 258 | 266 | PF00899 | 0.444 |
LIG_UBA3_1 | 474 | 479 | PF00899 | 0.489 |
MOD_CDK_SPK_2 | 249 | 254 | PF00069 | 0.363 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.373 |
MOD_CDK_SPxxK_3 | 17 | 24 | PF00069 | 0.371 |
MOD_CDK_SPxxK_3 | 239 | 246 | PF00069 | 0.274 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.364 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.347 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.416 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.334 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.426 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.253 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.403 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.482 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.374 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.427 |
MOD_CK2_1 | 632 | 638 | PF00069 | 0.570 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.466 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.414 |
MOD_CMANNOS | 150 | 153 | PF00535 | 0.397 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.438 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.422 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.406 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.374 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.402 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.204 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.213 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.426 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.426 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.372 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.398 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.345 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.404 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.427 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.318 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.391 |
MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.203 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.379 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.390 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.283 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.482 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.466 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.417 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.459 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.530 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.430 |
MOD_NEK2_2 | 222 | 227 | PF00069 | 0.436 |
MOD_NEK2_2 | 551 | 556 | PF00069 | 0.482 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.282 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.365 |
MOD_PIKK_1 | 593 | 599 | PF00454 | 0.498 |
MOD_PK_1 | 254 | 260 | PF00069 | 0.353 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.496 |
MOD_PKA_1 | 183 | 189 | PF00069 | 0.501 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.495 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.393 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.475 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.482 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.433 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.387 |
MOD_PKB_1 | 162 | 170 | PF00069 | 0.531 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.356 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.292 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.290 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.403 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.404 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.450 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.458 |
MOD_Plk_2-3 | 521 | 527 | PF00069 | 0.482 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.359 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.271 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.482 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.404 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.479 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.346 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.373 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.253 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.271 |
MOD_SUMO_rev_2 | 176 | 185 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 598 | 603 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 627 | 635 | PF00179 | 0.483 |
TRG_DiLeu_BaEn_1 | 118 | 123 | PF01217 | 0.574 |
TRG_DiLeu_BaEn_1 | 319 | 324 | PF01217 | 0.391 |
TRG_DiLeu_BaEn_1 | 386 | 391 | PF01217 | 0.277 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 694 | 697 | PF00928 | 0.570 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.455 |
TRG_NES_CRM1_1 | 231 | 245 | PF08389 | 0.412 |
TRG_NLS_MonoExtN_4 | 262 | 269 | PF00514 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 24 | 28 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 483 | 487 | PF00026 | 0.231 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P842 | Leptomonas seymouri | 80% | 100% |
A0A0S4JDX9 | Bodo saltans | 33% | 97% |
A0A1X0NUD9 | Trypanosomatidae | 45% | 100% |
A0A3R7NH08 | Trypanosoma rangeli | 46% | 100% |
A0A3S7WUM3 | Leishmania donovani | 100% | 100% |
A1CS92 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 21% | 96% |
A1D558 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 21% | 96% |
A2Q908 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 21% | 96% |
A3LY29 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 21% | 100% |
A4H988 | Leishmania braziliensis | 94% | 100% |
A4QZL9 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 23% | 95% |
A5E5Y8 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 25% | 100% |
A6SFQ6 | Botryotinia fuckeliana (strain B05.10) | 22% | 95% |
A6ZPJ1 | Saccharomyces cerevisiae (strain YJM789) | 24% | 93% |
A7EHM8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 22% | 95% |
A7TKF2 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 25% | 98% |
B0W562 | Culex quinquefasciatus | 23% | 100% |
B0XRG7 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 21% | 96% |
B3ME25 | Drosophila ananassae | 22% | 100% |
B3NMI5 | Drosophila erecta | 22% | 100% |
B4GAY7 | Drosophila persimilis | 23% | 100% |
B4HMV9 | Drosophila sechellia | 22% | 100% |
B4J6D5 | Drosophila grimshawi | 22% | 100% |
B4KNN9 | Drosophila mojavensis | 22% | 100% |
B4LM71 | Drosophila virilis | 22% | 100% |
B4MQL8 | Drosophila willistoni | 22% | 100% |
B4P5F7 | Drosophila yakuba | 22% | 100% |
B4QB88 | Drosophila simulans | 22% | 100% |
B5E081 | Drosophila pseudoobscura pseudoobscura | 23% | 100% |
C9ZP96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ARA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
P06103 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 93% |
P0CN44 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 94% |
P0CN45 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 94% |
P56821 | Nicotiana tabacum | 22% | 99% |
Q0CN46 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 21% | 96% |
Q0E940 | Drosophila melanogaster | 22% | 100% |
Q0IEY3 | Aedes aegypti | 23% | 100% |
Q10425 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 98% |
Q1DI97 | Coccidioides immitis (strain RS) | 23% | 96% |
Q1HDZ5 | Bombyx mori | 25% | 100% |
Q2GM53 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 22% | 95% |
Q2URB7 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 22% | 96% |
Q4P6G4 | Ustilago maydis (strain 521 / FGSC 9021) | 24% | 95% |
Q4QE62 | Leishmania major | 99% | 100% |
Q4WKL7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 21% | 96% |
Q54QW1 | Dictyostelium discoideum | 22% | 100% |
Q569Z1 | Xenopus laevis | 24% | 100% |
Q5AGV4 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 96% |
Q5BGH1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 22% | 96% |
Q6BLY5 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 24% | 99% |
Q6C1H8 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 99% |
Q6CY34 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 97% |
Q6FM92 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 22% | 99% |
Q758X9 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 23% | 96% |
Q7PZY1 | Anopheles gambiae | 23% | 100% |
Q7S464 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 95% |
Q9C5Z1 | Arabidopsis thaliana | 23% | 100% |
Q9XWI6 | Caenorhabditis elegans | 25% | 98% |
V5AZD7 | Trypanosoma cruzi | 46% | 100% |