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: A4IBQ2
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 | 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 | 437 | 441 | PF00656 | 0.326 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.765 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.479 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.249 |
DEG_COP1_1 | 592 | 602 | PF00400 | 0.564 |
DOC_CKS1_1 | 520 | 525 | PF01111 | 0.422 |
DOC_CYCLIN_RxL_1 | 103 | 111 | PF00134 | 0.170 |
DOC_CYCLIN_yCln2_LP_2 | 253 | 259 | PF00134 | 0.460 |
DOC_MAPK_DCC_7 | 586 | 596 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 401 | 408 | PF00069 | 0.432 |
DOC_MAPK_HePTP_8 | 398 | 410 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 188 | 195 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 447 | 454 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 477 | 485 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 188 | 196 | PF00069 | 0.423 |
DOC_PIKK_1 | 10 | 18 | PF02985 | 0.581 |
DOC_PP1_RVXF_1 | 308 | 314 | PF00149 | 0.622 |
DOC_PP1_RVXF_1 | 399 | 406 | PF00149 | 0.533 |
DOC_PP1_RVXF_1 | 529 | 536 | PF00149 | 0.470 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.307 |
DOC_PP4_FxxP_1 | 424 | 427 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.701 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.242 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 246 | 253 | PF00244 | 0.479 |
LIG_Actin_WH2_2 | 288 | 306 | PF00022 | 0.341 |
LIG_AP2alpha_1 | 458 | 462 | PF02296 | 0.422 |
LIG_APCC_ABBA_1 | 538 | 543 | PF00400 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.759 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.456 |
LIG_CaM_IQ_9 | 238 | 253 | PF13499 | 0.332 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.212 |
LIG_CORNRBOX | 96 | 104 | PF00104 | 0.157 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.428 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.310 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.212 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.276 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.208 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.708 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.557 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.493 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.484 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.581 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.234 |
LIG_GBD_Chelix_1 | 295 | 303 | PF00786 | 0.207 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.214 |
LIG_LIR_Gen_1 | 448 | 459 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 484 | 494 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 495 | 504 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 522 | 533 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 495 | 499 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.328 |
LIG_PCNA_PIPBox_1 | 73 | 82 | PF02747 | 0.456 |
LIG_Pex14_1 | 510 | 514 | PF04695 | 0.341 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.389 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.335 |
LIG_Pex14_2 | 370 | 374 | PF04695 | 0.281 |
LIG_Pex14_2 | 424 | 428 | PF04695 | 0.388 |
LIG_Pex14_2 | 458 | 462 | PF04695 | 0.400 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.257 |
LIG_PTB_Apo_2 | 14 | 21 | PF02174 | 0.712 |
LIG_REV1ctd_RIR_1 | 497 | 507 | PF16727 | 0.382 |
LIG_SH2_PTP2 | 525 | 528 | PF00017 | 0.264 |
LIG_SH2_SRC | 525 | 528 | PF00017 | 0.363 |
LIG_SH2_SRC | 6 | 9 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 363 | 367 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.462 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.278 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.251 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.207 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.267 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.300 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.542 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.472 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.551 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.564 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.464 |
LIG_Sin3_3 | 207 | 214 | PF02671 | 0.193 |
LIG_SUMO_SIM_anti_2 | 190 | 195 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 378 | 385 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 416 | 421 | PF11976 | 0.282 |
LIG_SUMO_SIM_anti_2 | 515 | 522 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 592 | 598 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 190 | 197 | PF11976 | 0.202 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 84 | 90 | PF11976 | 0.268 |
LIG_TRAF2_1 | 609 | 612 | PF00917 | 0.712 |
LIG_UBA3_1 | 270 | 277 | PF00899 | 0.344 |
LIG_UBA3_1 | 529 | 534 | PF00899 | 0.485 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.314 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.731 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.731 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.683 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.492 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.487 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.232 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.692 |
MOD_CMANNOS | 227 | 230 | PF00535 | 0.422 |
MOD_CMANNOS | 313 | 316 | PF00535 | 0.286 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.404 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.365 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.369 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.280 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.731 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.728 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.704 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.720 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.571 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.253 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.506 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.399 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.264 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.349 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.318 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.332 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.714 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.281 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.739 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.491 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.404 |
MOD_PKB_1 | 557 | 565 | PF00069 | 0.565 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.696 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.518 |
MOD_Plk_2-3 | 69 | 75 | PF00069 | 0.542 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.263 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.468 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.502 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.251 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.257 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.250 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.319 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.242 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.422 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.665 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.641 |
MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.457 |
MOD_SUMO_for_1 | 533 | 536 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 152 | 157 | PF00179 | 0.525 |
TRG_DiLeu_BaEn_4 | 152 | 158 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.170 |
TRG_DiLeu_LyEn_5 | 394 | 399 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.267 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.688 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P381 | Leptomonas seymouri | 21% | 100% |
A0A0N1I213 | Leptomonas seymouri | 69% | 99% |
A0A0N1I703 | Leptomonas seymouri | 23% | 68% |
A0A0N1IJ56 | Leptomonas seymouri | 40% | 88% |
A0A0N1ILQ1 | Leptomonas seymouri | 23% | 100% |
A0A0S4IHH9 | Bodo saltans | 33% | 100% |
A0A0S4INI5 | Bodo saltans | 37% | 100% |
A0A0S4JEP9 | Bodo saltans | 22% | 100% |
A0A0S4JTQ3 | Bodo saltans | 23% | 100% |
A0A0S4JV01 | Bodo saltans | 21% | 100% |
A0A0S4JV08 | Bodo saltans | 22% | 100% |
A0A0S4JVA6 | Bodo saltans | 23% | 84% |
A0A0S4JZ61 | Bodo saltans | 23% | 91% |
A0A1X0NM81 | Trypanosomatidae | 21% | 100% |
A0A1X0NU76 | Trypanosomatidae | 44% | 100% |
A0A1X0P579 | Trypanosomatidae | 52% | 100% |
A0A1X0P5F0 | Trypanosomatidae | 38% | 100% |
A0A1X0P8J4 | Trypanosomatidae | 20% | 100% |
A0A3Q8ID83 | Leishmania donovani | 22% | 70% |
A0A3Q8IGH9 | Leishmania donovani | 38% | 89% |
A0A3Q8II95 | Leishmania donovani | 100% | 100% |
A0A3R7M3E2 | Trypanosoma rangeli | 43% | 100% |
A0A3R7NUJ8 | Trypanosoma rangeli | 52% | 100% |
A0A422NN08 | Trypanosoma rangeli | 22% | 74% |
A0A422NR58 | Trypanosoma rangeli | 37% | 100% |
A1L1P9 | Danio rerio | 26% | 100% |
A4HN33 | Leishmania braziliensis | 74% | 100% |
A4HN34 | Leishmania braziliensis | 77% | 100% |
A4IIS8 | Xenopus tropicalis | 26% | 100% |
A7KAU2 | Oryctolagus cuniculus | 26% | 100% |
A7KAU3 | Oryctolagus cuniculus | 25% | 100% |
C9ZP79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZP80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZQ36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZYX8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZYX9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZYY0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZYY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A551 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AD56 | Leishmania major | 21% | 70% |
E9AFI2 | Leishmania major | 39% | 100% |
E9AFI7 | Leishmania major | 93% | 100% |
E9AHF1 | Leishmania infantum | 22% | 70% |
E9AHW7 | Leishmania infantum | 38% | 89% |
E9AYY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 20% | 70% |
E9B6N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B6P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F4HPH2 | Arabidopsis thaliana | 24% | 100% |
F4HQ05 | Arabidopsis thaliana | 24% | 100% |
F4HZH9 | Arabidopsis thaliana | 23% | 100% |
F4I4Q3 | Arabidopsis thaliana | 23% | 100% |
F4IHU9 | Arabidopsis thaliana | 26% | 100% |
F4JH46 | Arabidopsis thaliana | 24% | 100% |
F4JTB3 | Arabidopsis thaliana | 21% | 100% |
O49660 | Arabidopsis thaliana | 21% | 100% |
O82752 | Arabidopsis thaliana | 25% | 100% |
P38767 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P45272 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 24% | 100% |
Q05497 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 89% |
Q10085 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q1PDX9 | Arabidopsis thaliana | 24% | 100% |
Q1PFG9 | Arabidopsis thaliana | 24% | 100% |
Q38956 | Arabidopsis thaliana | 25% | 100% |
Q3V050 | Mus musculus | 27% | 100% |
Q4PSF4 | Arabidopsis thaliana | 23% | 100% |
Q5I0E9 | Rattus norvegicus | 26% | 100% |
Q5R7E4 | Pongo abelii | 23% | 100% |
Q5RFD2 | Pongo abelii | 26% | 100% |
Q6NB79 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 23% | 100% |
Q86VL8 | Homo sapiens | 23% | 100% |
Q89W72 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 23% | 100% |
Q8GXM8 | Arabidopsis thaliana | 25% | 100% |
Q8K0H1 | Mus musculus | 25% | 100% |
Q8L731 | Arabidopsis thaliana | 24% | 100% |
Q8RWF5 | Arabidopsis thaliana | 25% | 100% |
Q8RXK1 | Arabidopsis thaliana | 24% | 100% |
Q8UDF5 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 22% | 100% |
Q8VYL8 | Arabidopsis thaliana | 23% | 100% |
Q8W488 | Arabidopsis thaliana | 23% | 100% |
Q94AL1 | Arabidopsis thaliana | 23% | 100% |
Q96FL8 | Homo sapiens | 26% | 100% |
Q98D15 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 23% | 100% |
Q9C994 | Arabidopsis thaliana | 24% | 100% |
Q9C9M8 | Arabidopsis thaliana | 23% | 100% |
Q9C9U1 | Arabidopsis thaliana | 26% | 100% |
Q9FH21 | Arabidopsis thaliana | 23% | 100% |
Q9FHB6 | Arabidopsis thaliana | 28% | 100% |
Q9FJ87 | Arabidopsis thaliana | 24% | 100% |
Q9FKQ1 | Arabidopsis thaliana | 26% | 100% |
Q9LE20 | Arabidopsis thaliana | 25% | 100% |
Q9LPV4 | Arabidopsis thaliana | 25% | 100% |
Q9LS19 | Arabidopsis thaliana | 25% | 100% |
Q9LUH2 | Arabidopsis thaliana | 23% | 100% |
Q9LUH3 | Arabidopsis thaliana | 23% | 100% |
Q9LYT3 | Arabidopsis thaliana | 24% | 100% |
Q9SIA1 | Arabidopsis thaliana | 24% | 100% |
Q9SIA3 | Arabidopsis thaliana | 24% | 100% |
Q9SIA4 | Arabidopsis thaliana | 25% | 100% |
Q9SIA5 | Arabidopsis thaliana | 24% | 100% |
Q9SLV0 | Arabidopsis thaliana | 24% | 100% |
Q9SX83 | Arabidopsis thaliana | 24% | 100% |
Q9SZE2 | Arabidopsis thaliana | 23% | 100% |
Q9USK3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
Q9UT92 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q9ZVH5 | Arabidopsis thaliana | 22% | 100% |
V5BE59 | Trypanosoma cruzi | 21% | 76% |
V5BJE3 | Trypanosoma cruzi | 40% | 100% |
V5C2T9 | Trypanosoma cruzi | 51% | 100% |