ER-associated chaperone protein
Chaperone/Protein Folding, heat shock
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 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: E9AGQ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0044183 | protein folding chaperone | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.504 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.248 |
DEG_APCC_DBOX_1 | 267 | 275 | PF00400 | 0.279 |
DEG_APCC_KENBOX_2 | 540 | 544 | PF00400 | 0.766 |
DOC_CDC14_PxL_1 | 403 | 411 | PF14671 | 0.451 |
DOC_CYCLIN_RxL_1 | 278 | 285 | PF00134 | 0.264 |
DOC_CYCLIN_RxL_1 | 79 | 88 | PF00134 | 0.263 |
DOC_MAPK_gen_1 | 256 | 263 | PF00069 | 0.267 |
DOC_MAPK_gen_1 | 267 | 273 | PF00069 | 0.261 |
DOC_MAPK_gen_1 | 444 | 450 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 558 | 567 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 679 | 688 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 561 | 569 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 701 | 708 | PF00149 | 0.490 |
DOC_PP1_RVXF_1 | 80 | 87 | PF00149 | 0.373 |
DOC_PP1_RVXF_1 | 96 | 102 | PF00149 | 0.214 |
DOC_PP2B_LxvP_1 | 741 | 744 | PF13499 | 0.544 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.209 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 779 | 783 | PF00917 | 0.665 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.478 |
DOC_USP7_UBL2_3 | 769 | 773 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.264 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.264 |
LIG_14-3-3_CanoR_1 | 309 | 313 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 449 | 459 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 618 | 628 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 664 | 670 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.389 |
LIG_Actin_WH2_2 | 182 | 198 | PF00022 | 0.410 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.279 |
LIG_BIR_III_2 | 528 | 532 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 389 | 393 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.471 |
LIG_Clathr_ClatBox_1 | 297 | 301 | PF01394 | 0.324 |
LIG_deltaCOP1_diTrp_1 | 644 | 656 | PF00928 | 0.384 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.264 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.264 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.256 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.441 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.279 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.324 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.322 |
LIG_FHA_2 | 656 | 662 | PF00498 | 0.472 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.543 |
LIG_FHA_2 | 713 | 719 | PF00498 | 0.456 |
LIG_LIR_Apic_2 | 629 | 633 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 339 | 347 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 653 | 662 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 674 | 684 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 405 | 409 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 674 | 680 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.274 |
LIG_LYPXL_yS_3 | 406 | 409 | PF13949 | 0.447 |
LIG_NRBOX | 279 | 285 | PF00104 | 0.279 |
LIG_PCNA_TLS_4 | 607 | 614 | PF02747 | 0.331 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.279 |
LIG_Pex14_2 | 66 | 70 | PF04695 | 0.209 |
LIG_REV1ctd_RIR_1 | 63 | 73 | PF16727 | 0.209 |
LIG_SH2_CRK | 677 | 681 | PF00017 | 0.482 |
LIG_SH2_GRB2like | 128 | 131 | PF00017 | 0.264 |
LIG_SH2_GRB2like | 464 | 467 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 630 | 634 | PF00017 | 0.426 |
LIG_SH2_SRC | 478 | 481 | PF00017 | 0.493 |
LIG_SH2_SRC | 651 | 654 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.349 |
LIG_SH3_1 | 773 | 779 | PF00018 | 0.519 |
LIG_SH3_2 | 550 | 555 | PF14604 | 0.707 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.358 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.344 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.392 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.251 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.481 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.621 |
LIG_SH3_3 | 771 | 777 | PF00018 | 0.542 |
LIG_SH3_3 | 809 | 815 | PF00018 | 0.789 |
LIG_SH3_4 | 555 | 562 | PF00018 | 0.590 |
LIG_SUMO_SIM_par_1 | 13 | 18 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.375 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.335 |
LIG_TRAF2_1 | 658 | 661 | PF00917 | 0.413 |
LIG_TRAF2_1 | 682 | 685 | PF00917 | 0.397 |
LIG_TRAF2_1 | 715 | 718 | PF00917 | 0.443 |
LIG_TYR_ITSM | 16 | 23 | PF00017 | 0.391 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.279 |
LIG_WRC_WIRS_1 | 656 | 661 | PF05994 | 0.384 |
MOD_CDK_SPK_2 | 387 | 392 | PF00069 | 0.279 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.419 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.410 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.448 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.502 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.264 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.264 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.284 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.333 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.418 |
MOD_CK2_1 | 679 | 685 | PF00069 | 0.514 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.471 |
MOD_CK2_1 | 758 | 764 | PF00069 | 0.469 |
MOD_Cter_Amidation | 708 | 711 | PF01082 | 0.582 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.482 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.264 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.264 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.520 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.560 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.494 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.264 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.292 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.264 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.410 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.260 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.267 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.255 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.396 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.278 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.264 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.386 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.270 |
MOD_N-GLC_2 | 104 | 106 | PF02516 | 0.279 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.386 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.410 |
MOD_NEK2_2 | 212 | 217 | PF00069 | 0.276 |
MOD_NEK2_2 | 60 | 65 | PF00069 | 0.298 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.467 |
MOD_PIKK_1 | 743 | 749 | PF00454 | 0.598 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.264 |
MOD_PKA_1 | 758 | 764 | PF00069 | 0.462 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.285 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.298 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.264 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.437 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.403 |
MOD_PKB_1 | 618 | 626 | PF00069 | 0.322 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.273 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.329 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.264 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.434 |
MOD_Plk_1 | 747 | 753 | PF00069 | 0.368 |
MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.410 |
MOD_Plk_2-3 | 340 | 346 | PF00069 | 0.329 |
MOD_Plk_2-3 | 655 | 661 | PF00069 | 0.431 |
MOD_Plk_2-3 | 712 | 718 | PF00069 | 0.472 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.264 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.276 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.353 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.266 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.437 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.279 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.353 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.264 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.555 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.501 |
MOD_SUMO_rev_2 | 102 | 112 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 249 | 257 | PF00179 | 0.314 |
MOD_SUMO_rev_2 | 712 | 722 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 752 | 761 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 77 | 87 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 157 | 162 | PF01217 | 0.264 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.238 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 677 | 680 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 601 | 604 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 664 | 666 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 680 | 683 | PF00400 | 0.262 |
TRG_Pf-PMV_PEXEL_1 | 159 | 164 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 670 | 674 | PF00026 | 0.365 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDD3 | Leptomonas seymouri | 73% | 98% |
A0A0S4JJU2 | Bodo saltans | 24% | 100% |
A0A0S4JRV7 | Bodo saltans | 50% | 99% |
A0A1X0NER7 | Trypanosomatidae | 25% | 100% |
A0A1X0P8H2 | Trypanosomatidae | 59% | 100% |
A0A3Q8IB80 | Leishmania donovani | 25% | 100% |
A0A3Q8IQX0 | Leishmania donovani | 25% | 100% |
A0A3R7L0X2 | Trypanosoma rangeli | 56% | 99% |
A0A3S5H744 | Leishmania donovani | 100% | 100% |
A0A3S5H808 | Leishmania donovani | 24% | 100% |
A0A3S7X203 | Leishmania donovani | 25% | 100% |
A0A422MQ05 | Trypanosoma rangeli | 25% | 100% |
A4H9P0 | Leishmania braziliensis | 83% | 100% |
A4HGY1 | Leishmania braziliensis | 25% | 96% |
A4HGY5 | Leishmania braziliensis | 26% | 100% |
A4HND7 | Leishmania braziliensis | 27% | 100% |
A4I412 | Leishmania infantum | 25% | 96% |
A4I417 | Leishmania infantum | 25% | 100% |
A4IC10 | Leishmania infantum | 24% | 100% |
C9ZYJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A590 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AFU8 | Leishmania major | 25% | 100% |
E9AHH1 | Leishmania infantum | 25% | 100% |
E9ARS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B099 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 96% |
E9B0A4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B700 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
F4HQD4 | Arabidopsis thaliana | 31% | 99% |
F4JMJ1 | Arabidopsis thaliana | 24% | 95% |
O59838 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
O74225 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 32% | 100% |
O88600 | Rattus norvegicus | 29% | 98% |
O93866 | Trichophyton rubrum | 27% | 100% |
O97125 | Drosophila melanogaster | 26% | 100% |
P08108 | Oncorhynchus mykiss | 26% | 100% |
P09435 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P09446 | Caenorhabditis elegans | 26% | 100% |
P11147 | Drosophila melanogaster | 25% | 100% |
P17066 | Homo sapiens | 27% | 100% |
P17804 | Leishmania donovani | 25% | 100% |
P27541 | Brugia malayi | 25% | 100% |
P29844 | Drosophila melanogaster | 24% | 100% |
P29845 | Drosophila melanogaster | 25% | 100% |
P32589 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P32590 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P36604 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P41825 | Anopheles albimanus | 27% | 100% |
P41826 | Anopheles albimanus | 27% | 100% |
P41827 | Anopheles albimanus | 26% | 100% |
P48722 | Mus musculus | 29% | 98% |
P49118 | Solanum lycopersicum | 25% | 100% |
P78695 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% |
Q01233 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 100% |
Q02028 | Pisum sativum | 26% | 100% |
Q05036 | Caenorhabditis elegans | 31% | 100% |
Q05944 | Hydra vulgaris | 27% | 100% |
Q39043 | Arabidopsis thaliana | 25% | 100% |
Q4Q7Y0 | Leishmania major | 25% | 100% |
Q4Q7Y4 | Leishmania major | 25% | 97% |
Q4QDQ2 | Leishmania major | 96% | 100% |
Q557E0 | Dictyostelium discoideum | 24% | 100% |
Q5B0C0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 100% |
Q5B2V1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 28% | 100% |
Q61699 | Mus musculus | 29% | 96% |
Q6FJI3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 31% | 100% |
Q6TMK3 | Dictyostelium discoideum | 32% | 100% |
Q74ZJ0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 31% | 100% |
Q75C78 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q875P5 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 29% | 100% |
Q875V0 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 30% | 100% |
Q91233 | Oncorhynchus tshawytscha | 27% | 100% |
Q91291 | Pleurodeles waltl | 25% | 100% |
Q96VB9 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 100% |
Q96W30 | Paracoccidioides lutzii (strain ATCC MYA-826 / Pb01) | 28% | 100% |
Q99170 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 25% | 100% |
Q9LKR3 | Arabidopsis thaliana | 25% | 100% |
Q9S7C0 | Arabidopsis thaliana | 31% | 99% |
Q9SAB1 | Arabidopsis thaliana | 28% | 100% |
V5DFF3 | Trypanosoma cruzi | 58% | 99% |