SLC47 family transporter, with potential detoxification functions
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 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 28 |
NetGPI | no | yes: 0, no: 28 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 29 |
GO:0110165 | cellular anatomical entity | 1 | 29 |
Related structures:
AlphaFold database: E9B6N7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0042908 | xenobiotic transport | 4 | 12 |
GO:0046618 | xenobiotic export from cell | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0055085 | transmembrane transport | 2 | 12 |
GO:0140115 | export across plasma membrane | 3 | 12 |
GO:0140352 | export from cell | 2 | 12 |
GO:1990961 | xenobiotic detoxification by transmembrane export across the plasma membrane | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 29 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 29 |
GO:0015297 | antiporter activity | 5 | 29 |
GO:0022804 | active transmembrane transporter activity | 3 | 29 |
GO:0022857 | transmembrane transporter activity | 2 | 29 |
GO:0042910 | xenobiotic transmembrane transporter activity | 3 | 29 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.198 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.281 |
CLV_Separin_Metazoa | 182 | 186 | PF03568 | 0.253 |
DEG_APCC_DBOX_1 | 127 | 135 | PF00400 | 0.432 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.421 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.409 |
DEG_APCC_DBOX_1 | 506 | 514 | PF00400 | 0.601 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.748 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 354 | 363 | PF00134 | 0.247 |
DOC_CYCLIN_yCln2_LP_2 | 139 | 145 | PF00134 | 0.179 |
DOC_CYCLIN_yCln2_LP_2 | 49 | 55 | PF00134 | 0.406 |
DOC_MAPK_gen_1 | 341 | 348 | PF00069 | 0.454 |
DOC_MAPK_HePTP_8 | 338 | 350 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 128 | 136 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 341 | 350 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 48 | 55 | PF00069 | 0.455 |
DOC_MAPK_NFAT4_5 | 128 | 136 | PF00069 | 0.445 |
DOC_MAPK_NFAT4_5 | 48 | 56 | PF00069 | 0.484 |
DOC_PP1_RVXF_1 | 267 | 273 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 383 | 390 | PF00149 | 0.400 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.452 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.770 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.745 |
DOC_USP7_MATH_2 | 585 | 591 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 169 | 173 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 499 | 504 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 576 | 584 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 603 | 609 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 628 | 636 | PF00244 | 0.759 |
LIG_14-3-3_CanoR_1 | 640 | 644 | PF00244 | 0.783 |
LIG_APCC_ABBA_1 | 475 | 480 | PF00400 | 0.572 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.341 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.270 |
LIG_Clathr_ClatBox_1 | 178 | 182 | PF01394 | 0.247 |
LIG_eIF4E_1 | 390 | 396 | PF01652 | 0.435 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.483 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.337 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.332 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.528 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.713 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.644 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.717 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.724 |
LIG_IRF3_LxIS_1 | 146 | 153 | PF10401 | 0.395 |
LIG_LIR_Apic_2 | 444 | 450 | PF02991 | 0.232 |
LIG_LIR_Apic_2 | 609 | 614 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 164 | 175 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 301 | 309 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 351 | 361 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 565 | 574 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.736 |
LIG_PCNA_yPIPBox_3 | 376 | 388 | PF02747 | 0.209 |
LIG_PCNA_yPIPBox_3 | 400 | 408 | PF02747 | 0.305 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.256 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.333 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.290 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.367 |
LIG_SH2_GRB2like | 469 | 472 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 294 | 298 | PF00017 | 0.209 |
LIG_SH2_NCK_1 | 424 | 428 | PF00017 | 0.292 |
LIG_SH2_NCK_1 | 593 | 597 | PF00017 | 0.559 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 593 | 597 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.487 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.620 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.298 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.330 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.604 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.542 |
LIG_SUMO_SIM_anti_2 | 177 | 182 | PF11976 | 0.247 |
LIG_SUMO_SIM_anti_2 | 360 | 365 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 419 | 425 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 509 | 519 | PF11976 | 0.643 |
LIG_SUMO_SIM_anti_2 | 64 | 69 | PF11976 | 0.262 |
LIG_SUMO_SIM_par_1 | 132 | 138 | PF11976 | 0.223 |
LIG_TYR_ITIM | 240 | 245 | PF00017 | 0.156 |
LIG_TYR_ITIM | 391 | 396 | PF00017 | 0.348 |
LIG_TYR_ITIM | 422 | 427 | PF00017 | 0.361 |
LIG_UBA3_1 | 239 | 248 | PF00899 | 0.361 |
LIG_UBA3_1 | 382 | 388 | PF00899 | 0.422 |
LIG_WRC_WIRS_1 | 396 | 401 | PF05994 | 0.283 |
LIG_WRC_WIRS_1 | 482 | 487 | PF05994 | 0.496 |
LIG_WRC_WIRS_1 | 566 | 571 | PF05994 | 0.742 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.598 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.335 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.209 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.435 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.247 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.619 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.725 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.624 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.747 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.781 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.134 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.674 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.726 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.780 |
MOD_CMANNOS | 253 | 256 | PF00535 | 0.307 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.535 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.311 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.432 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.560 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.532 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.240 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.756 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.431 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.439 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.341 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.374 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.570 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.664 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.695 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.652 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.687 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.645 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.565 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.736 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.731 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.436 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.421 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.533 |
MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.480 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.511 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.403 |
MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.372 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.429 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.288 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.442 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.366 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.308 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.378 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.274 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.228 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.366 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.270 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.296 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.224 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.458 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.711 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.699 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.652 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.770 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.305 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.251 |
MOD_NEK2_2 | 168 | 173 | PF00069 | 0.445 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.475 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.520 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.264 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.710 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.327 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.678 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.702 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.620 |
MOD_PKA_2 | 627 | 633 | PF00069 | 0.754 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.747 |
MOD_PKB_1 | 12 | 20 | PF00069 | 0.561 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.361 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.176 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.685 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.735 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.754 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.239 |
MOD_Plk_2-3 | 587 | 593 | PF00069 | 0.554 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.301 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.340 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.343 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.359 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.323 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.320 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.277 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.328 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.295 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.319 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.287 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.163 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.332 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.587 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.744 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.759 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.620 |
TRG_DiLeu_BaEn_1 | 323 | 328 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P381 | Leptomonas seymouri | 23% | 100% |
A0A0N1I213 | Leptomonas seymouri | 37% | 100% |
A0A0N1I703 | Leptomonas seymouri | 25% | 71% |
A0A0N1IJ56 | Leptomonas seymouri | 58% | 92% |
A0A0S4INI5 | Bodo saltans | 39% | 100% |
A0A0S4JEP9 | Bodo saltans | 24% | 100% |
A0A0S4JTQ3 | Bodo saltans | 26% | 100% |
A0A0S4JV08 | Bodo saltans | 24% | 100% |
A0A0S4JVA6 | Bodo saltans | 24% | 88% |
A0A0S4JZ61 | Bodo saltans | 24% | 96% |
A0A1X0NM81 | Trypanosomatidae | 25% | 100% |
A0A1X0NU76 | Trypanosomatidae | 47% | 100% |
A0A1X0P579 | Trypanosomatidae | 42% | 100% |
A0A1X0P5F0 | Trypanosomatidae | 39% | 100% |
A0A1X0P8J4 | Trypanosomatidae | 23% | 100% |
A0A3Q8IGH9 | Leishmania donovani | 85% | 93% |
A0A3Q8II95 | Leishmania donovani | 38% | 100% |
A0A3R7M3E2 | Trypanosoma rangeli | 51% | 100% |
A0A3R7NUJ8 | Trypanosoma rangeli | 43% | 100% |
A0A422NR58 | Trypanosoma rangeli | 38% | 100% |
A1L1P9 | Danio rerio | 30% | 100% |
A4HN33 | Leishmania braziliensis | 37% | 100% |
A4HN34 | Leishmania braziliensis | 38% | 100% |
A4IBQ2 | Leishmania infantum | 38% | 100% |
A7KAU3 | Oryctolagus cuniculus | 30% | 100% |
A7MFC3 | Cronobacter sakazakii (strain ATCC BAA-894) | 24% | 100% |
A9MEJ6 | Salmonella arizonae (strain ATCC BAA-731 / CDC346-86 / RSK2980) | 24% | 100% |
B4TH65 | Salmonella heidelberg (strain SL476) | 25% | 100% |
C9ZP79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZP80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZQ36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZYX8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZYX9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZYY0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZYY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A551 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9AFI2 | Leishmania major | 83% | 100% |
E9AFI7 | Leishmania major | 39% | 100% |
E9AHW7 | Leishmania infantum | 86% | 93% |
E9AYY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 73% |
E9B6P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
F4HPH2 | Arabidopsis thaliana | 25% | 100% |
F4HQ05 | Arabidopsis thaliana | 28% | 100% |
F4HZH9 | Arabidopsis thaliana | 24% | 100% |
F4I4Q3 | Arabidopsis thaliana | 22% | 100% |
F4IHU9 | Arabidopsis thaliana | 28% | 100% |
F4J158 | Arabidopsis thaliana | 25% | 100% |
F4JH46 | Arabidopsis thaliana | 24% | 100% |
F4JTB3 | Arabidopsis thaliana | 23% | 100% |
O49660 | Arabidopsis thaliana | 22% | 100% |
O82752 | Arabidopsis thaliana | 27% | 100% |
Q05497 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 93% |
Q1PDX9 | Arabidopsis thaliana | 24% | 100% |
Q1PFG9 | Arabidopsis thaliana | 26% | 100% |
Q38956 | Arabidopsis thaliana | 23% | 100% |
Q3V050 | Mus musculus | 29% | 100% |
Q5E4Y6 | Aliivibrio fischeri (strain ATCC 700601 / ES114) | 23% | 100% |
Q5QWR6 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 24% | 100% |
Q5R7E4 | Pongo abelii | 28% | 100% |
Q5RFD2 | Pongo abelii | 30% | 100% |
Q6LQ49 | Photobacterium profundum (strain SS9) | 24% | 100% |
Q6NB79 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 23% | 100% |
Q7MKP8 | Vibrio vulnificus (strain YJ016) | 24% | 100% |
Q86VL8 | Homo sapiens | 26% | 100% |
Q89W72 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 22% | 100% |
Q8D9N8 | Vibrio vulnificus (strain CMCP6) | 24% | 100% |
Q8L616 | Arabidopsis thaliana | 24% | 100% |
Q8L731 | Arabidopsis thaliana | 25% | 100% |
Q8RWF5 | Arabidopsis thaliana | 25% | 100% |
Q8UDF5 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 25% | 100% |
Q940N9 | Arabidopsis thaliana | 22% | 100% |
Q94AL1 | Arabidopsis thaliana | 25% | 100% |
Q96FL8 | Homo sapiens | 30% | 100% |
Q9C994 | Arabidopsis thaliana | 26% | 100% |
Q9C9M8 | Arabidopsis thaliana | 23% | 100% |
Q9C9U1 | Arabidopsis thaliana | 28% | 100% |
Q9F5N7 | Burkholderia vietnamiensis | 24% | 100% |
Q9FH21 | Arabidopsis thaliana | 23% | 100% |
Q9FHB6 | Arabidopsis thaliana | 27% | 100% |
Q9FJ87 | Arabidopsis thaliana | 24% | 100% |
Q9FNC1 | Arabidopsis thaliana | 23% | 100% |
Q9KRU4 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 25% | 100% |
Q9LPV4 | Arabidopsis thaliana | 23% | 100% |
Q9LUH2 | Arabidopsis thaliana | 25% | 100% |
Q9SIA4 | Arabidopsis thaliana | 25% | 100% |
Q9SIA5 | Arabidopsis thaliana | 26% | 100% |
Q9SX83 | Arabidopsis thaliana | 25% | 100% |
Q9SZE2 | Arabidopsis thaliana | 25% | 100% |
Q9UT92 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
V5BDE8 | Trypanosoma cruzi | 25% | 100% |
V5BJE3 | Trypanosoma cruzi | 52% | 100% |
V5C2T9 | Trypanosoma cruzi | 43% | 100% |