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: 29 |
NetGPI | no | yes: 0, no: 29 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 30 |
GO:0110165 | cellular anatomical entity | 1 | 30 |
Related structures:
AlphaFold database: E9AFI7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0042908 | xenobiotic transport | 4 | 13 |
GO:0046618 | xenobiotic export from cell | 3 | 13 |
GO:0051179 | localization | 1 | 13 |
GO:0051234 | establishment of localization | 2 | 13 |
GO:0055085 | transmembrane transport | 2 | 13 |
GO:0140115 | export across plasma membrane | 3 | 13 |
GO:0140352 | export from cell | 2 | 13 |
GO:1990961 | xenobiotic detoxification by transmembrane export across the plasma membrane | 4 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 30 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 30 |
GO:0015297 | antiporter activity | 5 | 30 |
GO:0022804 | active transmembrane transporter activity | 3 | 30 |
GO:0022857 | transmembrane transporter activity | 2 | 30 |
GO:0042910 | xenobiotic transmembrane transporter activity | 3 | 30 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.326 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.747 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.258 |
DEG_COP1_1 | 591 | 601 | PF00400 | 0.585 |
DEG_SCF_FBW7_1 | 590 | 595 | PF00400 | 0.532 |
DOC_CKS1_1 | 519 | 524 | PF01111 | 0.422 |
DOC_CYCLIN_RxL_1 | 103 | 111 | PF00134 | 0.170 |
DOC_CYCLIN_yCln2_LP_2 | 252 | 258 | PF00134 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 423 | 429 | PF00134 | 0.208 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.359 |
DOC_MAPK_gen_1 | 400 | 407 | PF00069 | 0.432 |
DOC_MAPK_HePTP_8 | 397 | 409 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 187 | 194 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 446 | 453 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 476 | 484 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 187 | 195 | PF00069 | 0.423 |
DOC_PIKK_1 | 10 | 18 | PF02985 | 0.577 |
DOC_PP1_RVXF_1 | 307 | 313 | PF00149 | 0.627 |
DOC_PP1_RVXF_1 | 398 | 405 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 528 | 535 | PF00149 | 0.476 |
DOC_PP4_FxxP_1 | 232 | 235 | PF00568 | 0.308 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 502 | 506 | PF12436 | 0.362 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 165 | 171 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 245 | 252 | PF00244 | 0.480 |
LIG_Actin_WH2_2 | 287 | 305 | PF00022 | 0.341 |
LIG_AP2alpha_1 | 457 | 461 | PF02296 | 0.422 |
LIG_APCC_ABBA_1 | 537 | 542 | PF00400 | 0.578 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.752 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.456 |
LIG_CaM_IQ_9 | 237 | 252 | PF13499 | 0.332 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.212 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.503 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.428 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.310 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.212 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.276 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.714 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.698 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.660 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.495 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.516 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.521 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.586 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.234 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.672 |
LIG_GBD_Chelix_1 | 294 | 302 | PF00786 | 0.208 |
LIG_LIR_Gen_1 | 339 | 349 | PF02991 | 0.214 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 483 | 493 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 494 | 503 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 521 | 532 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 494 | 498 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.328 |
LIG_NRBOX | 419 | 425 | PF00104 | 0.324 |
LIG_PCNA_PIPBox_1 | 73 | 82 | PF02747 | 0.465 |
LIG_Pex14_1 | 509 | 513 | PF04695 | 0.341 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.389 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.328 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.281 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.312 |
LIG_Pex14_2 | 457 | 461 | PF04695 | 0.400 |
LIG_Pex14_2 | 495 | 499 | PF04695 | 0.258 |
LIG_PTB_Apo_2 | 14 | 21 | PF02174 | 0.713 |
LIG_REV1ctd_RIR_1 | 496 | 506 | PF16727 | 0.380 |
LIG_SH2_PTP2 | 524 | 527 | PF00017 | 0.264 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.363 |
LIG_SH2_SRC | 6 | 9 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.530 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.501 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.278 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.251 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.208 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.267 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.300 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.652 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.561 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.524 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.569 |
LIG_Sin3_3 | 206 | 213 | PF02671 | 0.193 |
LIG_SUMO_SIM_anti_2 | 189 | 194 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 377 | 384 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 415 | 420 | PF11976 | 0.282 |
LIG_SUMO_SIM_anti_2 | 514 | 521 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 256 | 262 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 84 | 90 | PF11976 | 0.268 |
LIG_UBA3_1 | 269 | 276 | PF00899 | 0.344 |
LIG_UBA3_1 | 528 | 533 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 428 | 433 | PF05994 | 0.315 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.735 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.726 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.721 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.514 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.521 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.232 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.707 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.724 |
MOD_CMANNOS | 226 | 229 | PF00535 | 0.422 |
MOD_CMANNOS | 312 | 315 | PF00535 | 0.295 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.404 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.371 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.369 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.394 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.280 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.393 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.736 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.723 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.254 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.750 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.694 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.655 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.569 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.253 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.508 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.399 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.356 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.318 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.332 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.281 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.492 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.411 |
MOD_PKB_1 | 556 | 564 | PF00069 | 0.563 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.698 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.682 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.521 |
MOD_Plk_2-3 | 69 | 75 | PF00069 | 0.547 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.263 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.468 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.540 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.503 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.251 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.257 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.250 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.320 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.242 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.739 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.422 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.703 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 532 | 535 | PF00179 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.170 |
TRG_DiLeu_LyEn_5 | 393 | 398 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.267 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 583 | 585 | PF00400 | 0.756 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I213 | Leptomonas seymouri | 68% | 98% |
A0A0N1I703 | Leptomonas seymouri | 23% | 67% |
A0A0N1IJ56 | Leptomonas seymouri | 41% | 86% |
A0A0N1ILQ1 | Leptomonas seymouri | 22% | 100% |
A0A0S4IHH9 | Bodo saltans | 34% | 100% |
A0A0S4INI5 | Bodo saltans | 38% | 100% |
A0A0S4JEP9 | Bodo saltans | 22% | 100% |
A0A0S4JTQ3 | Bodo saltans | 25% | 100% |
A0A0S4JV01 | Bodo saltans | 22% | 100% |
A0A0S4JV08 | Bodo saltans | 23% | 100% |
A0A0S4JVA6 | Bodo saltans | 24% | 83% |
A0A0S4JZ61 | Bodo saltans | 22% | 90% |
A0A1X0NM81 | Trypanosomatidae | 21% | 100% |
A0A1X0NU76 | Trypanosomatidae | 43% | 100% |
A0A1X0P579 | Trypanosomatidae | 52% | 100% |
A0A1X0P5F0 | Trypanosomatidae | 38% | 100% |
A0A1X0P8J4 | Trypanosomatidae | 20% | 100% |
A0A3Q8ID83 | Leishmania donovani | 23% | 69% |
A0A3Q8IGH9 | Leishmania donovani | 41% | 87% |
A0A3Q8II95 | Leishmania donovani | 93% | 98% |
A0A3R7M3E2 | Trypanosoma rangeli | 43% | 100% |
A0A3R7NUJ8 | Trypanosoma rangeli | 50% | 100% |
A0A422NN08 | Trypanosoma rangeli | 21% | 73% |
A0A422NR58 | Trypanosoma rangeli | 37% | 100% |
A1L1P9 | Danio rerio | 27% | 100% |
A4HN33 | Leishmania braziliensis | 73% | 98% |
A4HN34 | Leishmania braziliensis | 76% | 100% |
A4IBQ2 | Leishmania infantum | 93% | 98% |
A4IIS8 | Xenopus tropicalis | 26% | 100% |
A7KAU2 | Oryctolagus cuniculus | 27% | 100% |
A7KAU3 | Oryctolagus cuniculus | 27% | 100% |
C9ZP79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZP80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZQ36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZYX8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZYX9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZYY0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZYY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AD56 | Leishmania major | 23% | 68% |
E9AFI2 | Leishmania major | 40% | 100% |
E9AHF1 | Leishmania infantum | 23% | 69% |
E9AHW7 | Leishmania infantum | 41% | 87% |
E9AYY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 69% |
E9B6N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 94% |
E9B6P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 98% |
F4HPH2 | Arabidopsis thaliana | 23% | 100% |
F4HQ05 | Arabidopsis thaliana | 24% | 100% |
F4HZH9 | Arabidopsis thaliana | 24% | 100% |
F4I4Q3 | Arabidopsis thaliana | 24% | 100% |
F4IHU9 | Arabidopsis thaliana | 26% | 100% |
F4JH46 | Arabidopsis thaliana | 23% | 100% |
F4JTB3 | Arabidopsis thaliana | 21% | 100% |
O49660 | Arabidopsis thaliana | 21% | 100% |
O82752 | Arabidopsis thaliana | 24% | 100% |
P38767 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P45272 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 23% | 100% |
Q05497 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 88% |
Q10085 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q1PDX9 | Arabidopsis thaliana | 23% | 100% |
Q1PFG9 | Arabidopsis thaliana | 26% | 100% |
Q38956 | Arabidopsis thaliana | 24% | 100% |
Q3V050 | Mus musculus | 27% | 100% |
Q5I0E9 | Rattus norvegicus | 26% | 100% |
Q5R7E4 | Pongo abelii | 25% | 100% |
Q5RFD2 | Pongo abelii | 27% | 100% |
Q65SY9 | Mannheimia succiniciproducens (strain MBEL55E) | 25% | 100% |
Q6NB79 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 25% | 100% |
Q86VL8 | Homo sapiens | 26% | 100% |
Q89W72 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 25% | 100% |
Q8GXM8 | Arabidopsis thaliana | 26% | 100% |
Q8K0H1 | Mus musculus | 25% | 100% |
Q8L731 | Arabidopsis thaliana | 25% | 100% |
Q8RWF5 | Arabidopsis thaliana | 24% | 100% |
Q8VYL8 | Arabidopsis thaliana | 23% | 100% |
Q8W488 | Arabidopsis thaliana | 23% | 100% |
Q940N9 | Arabidopsis thaliana | 22% | 100% |
Q94AL1 | Arabidopsis thaliana | 23% | 100% |
Q96FL8 | Homo sapiens | 26% | 100% |
Q98D15 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 24% | 100% |
Q9C994 | Arabidopsis thaliana | 23% | 100% |
Q9C9M8 | Arabidopsis thaliana | 24% | 100% |
Q9C9U1 | Arabidopsis thaliana | 25% | 100% |
Q9FH21 | Arabidopsis thaliana | 22% | 100% |
Q9FHB6 | Arabidopsis thaliana | 26% | 100% |
Q9FJ87 | Arabidopsis thaliana | 24% | 100% |
Q9FKQ1 | Arabidopsis thaliana | 24% | 100% |
Q9FNC1 | Arabidopsis thaliana | 22% | 100% |
Q9LE20 | Arabidopsis thaliana | 24% | 100% |
Q9LPV4 | Arabidopsis thaliana | 24% | 100% |
Q9LS19 | Arabidopsis thaliana | 25% | 100% |
Q9LUH2 | Arabidopsis thaliana | 23% | 100% |
Q9LUH3 | Arabidopsis thaliana | 24% | 100% |
Q9LVD9 | Arabidopsis thaliana | 22% | 100% |
Q9LYT3 | Arabidopsis thaliana | 24% | 100% |
Q9SIA1 | Arabidopsis thaliana | 25% | 100% |
Q9SIA3 | Arabidopsis thaliana | 25% | 100% |
Q9SIA4 | Arabidopsis thaliana | 25% | 100% |
Q9SIA5 | Arabidopsis thaliana | 24% | 100% |
Q9SLV0 | Arabidopsis thaliana | 24% | 100% |
Q9SX83 | Arabidopsis thaliana | 23% | 100% |
Q9SZE2 | Arabidopsis thaliana | 23% | 100% |
Q9USK3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q9UT92 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q9ZVH5 | Arabidopsis thaliana | 22% | 100% |
V5BE59 | Trypanosoma cruzi | 22% | 75% |
V5BJE3 | Trypanosoma cruzi | 40% | 100% |
V5C2T9 | Trypanosoma cruzi | 51% | 100% |