Proteins belonging to the subfamily G of Eukaryotic ABC transporters. Probably functional as dimers, with broad substrate specificity.. Expanded in Kinetoplastids (also in free-living forms)
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AT67
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 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:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140359 | ABC-type transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.730 |
CLV_MEL_PAP_1 | 158 | 164 | PF00089 | 0.358 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.339 |
CLV_PCSK_FUR_1 | 414 | 418 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.302 |
CLV_Separin_Metazoa | 139 | 143 | PF03568 | 0.502 |
DOC_CDC14_PxL_1 | 201 | 209 | PF14671 | 0.530 |
DOC_CYCLIN_RxL_1 | 528 | 538 | PF00134 | 0.339 |
DOC_CYCLIN_RxL_1 | 99 | 111 | PF00134 | 0.349 |
DOC_MAPK_gen_1 | 452 | 460 | PF00069 | 0.264 |
DOC_MAPK_gen_1 | 594 | 604 | PF00069 | 0.149 |
DOC_MAPK_gen_1 | 647 | 656 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 234 | 241 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 452 | 459 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 650 | 658 | PF00069 | 0.334 |
DOC_PP1_RVXF_1 | 530 | 537 | PF00149 | 0.293 |
DOC_PP1_RVXF_1 | 595 | 602 | PF00149 | 0.249 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.394 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 399 | 408 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 603 | 609 | PF00244 | 0.301 |
LIG_Actin_WH2_2 | 133 | 150 | PF00022 | 0.502 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.775 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.474 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.461 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.477 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.413 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.502 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.629 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.434 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.309 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.539 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.275 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.512 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.453 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.506 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.512 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.701 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.562 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.452 |
LIG_IRF3_LxIS_1 | 458 | 465 | PF10401 | 0.160 |
LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 133 | 141 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 340 | 351 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 41 | 49 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 465 | 475 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 600 | 609 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.746 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 600 | 604 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 613 | 617 | PF02991 | 0.277 |
LIG_NRBOX | 224 | 230 | PF00104 | 0.597 |
LIG_NRBOX | 566 | 572 | PF00104 | 0.423 |
LIG_PCNA_PIPBox_1 | 527 | 536 | PF02747 | 0.293 |
LIG_PTB_Apo_2 | 510 | 517 | PF02174 | 0.169 |
LIG_SH2_GRB2like | 288 | 291 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.497 |
LIG_SH2_PTP2 | 134 | 137 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 645 | 649 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.478 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.750 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.486 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.764 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.453 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.390 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 235 | 242 | PF11976 | 0.566 |
LIG_SUMO_SIM_anti_2 | 255 | 261 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 298 | 304 | PF11976 | 0.611 |
LIG_SUMO_SIM_anti_2 | 568 | 575 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 651 | 657 | PF11976 | 0.160 |
LIG_SUMO_SIM_anti_2 | 72 | 78 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 85 | 92 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 200 | 206 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 301 | 306 | PF11976 | 0.689 |
LIG_SUMO_SIM_par_1 | 460 | 466 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 541 | 547 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 582 | 588 | PF11976 | 0.389 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.539 |
LIG_TRAF2_2 | 351 | 356 | PF00917 | 0.645 |
LIG_TYR_ITIM | 519 | 524 | PF00017 | 0.317 |
LIG_TYR_ITIM | 666 | 671 | PF00017 | 0.321 |
LIG_TYR_ITSM | 437 | 444 | PF00017 | 0.425 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.464 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.536 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.425 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.493 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.502 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.606 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.724 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.484 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.419 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.297 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.369 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.447 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.330 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.453 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.484 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.735 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.554 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.276 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.333 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.262 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.222 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.400 |
MOD_GlcNHglycan | 25 | 29 | PF01048 | 0.477 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.490 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.405 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.427 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.325 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.604 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.175 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.228 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.522 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.486 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.739 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.532 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.490 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.621 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.691 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.652 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.656 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.601 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.300 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.526 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.555 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.498 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.606 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.311 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.312 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.524 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.297 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.305 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.392 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.370 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.599 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.510 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.652 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.631 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.460 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.339 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.388 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.500 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.322 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.502 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.605 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.672 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.558 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.517 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.500 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.461 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.533 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.609 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.341 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.338 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.425 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.173 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.411 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.452 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.455 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.764 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.718 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.288 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.264 |
TRG_NES_CRM1_1 | 294 | 309 | PF08389 | 0.589 |
TRG_NES_CRM1_1 | 356 | 368 | PF08389 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 371 | 375 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 27% | 92% |
A0A0N1HZC7 | Leptomonas seymouri | 67% | 100% |
A0A0S4IJ55 | Bodo saltans | 26% | 89% |
A0A0S4IQG2 | Bodo saltans | 27% | 100% |
A0A0S4IUG8 | Bodo saltans | 27% | 100% |
A0A0S4IUY5 | Bodo saltans | 46% | 100% |
A0A0S4IZ09 | Bodo saltans | 22% | 100% |
A0A0S4J724 | Bodo saltans | 28% | 100% |
A0A0S4J7U2 | Bodo saltans | 29% | 97% |
A0A0S4JPA7 | Bodo saltans | 28% | 91% |
A0A0S4KMF6 | Bodo saltans | 23% | 84% |
A0A1X0NKI4 | Trypanosomatidae | 48% | 100% |
A0A1X0NM50 | Trypanosomatidae | 27% | 100% |
A0A1X0NTW9 | Trypanosomatidae | 28% | 100% |
A0A1X0NXY3 | Trypanosomatidae | 21% | 100% |
A0A1X0P4K0 | Trypanosomatidae | 22% | 100% |
A0A3Q8IA65 | Leishmania donovani | 27% | 92% |
A0A3Q8IHD8 | Leishmania donovani | 89% | 100% |
A0A3R7KEQ6 | Trypanosoma rangeli | 46% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H5N0 | Leishmania donovani | 28% | 100% |
A0A3S7WPB9 | Leishmania donovani | 28% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 28% | 98% |
A4H4G9 | Leishmania braziliensis | 28% | 100% |
A4H4H6 | Leishmania braziliensis | 28% | 100% |
A4H862 | Leishmania braziliensis | 27% | 100% |
A4HPF5 | Leishmania braziliensis | 78% | 100% |
A4HSQ0 | Leishmania infantum | 29% | 100% |
A4HSQ1 | Leishmania infantum | 28% | 100% |
A4HWI7 | Leishmania infantum | 27% | 92% |
A4ID77 | Leishmania infantum | 89% | 100% |
B8ALI0 | Oryza sativa subsp. indica | 28% | 86% |
B9G5Y5 | Oryza sativa subsp. japonica | 27% | 68% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D3ZCM3 | Rattus norvegicus | 28% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
H9BZ66 | Petunia hybrida | 29% | 100% |
O80946 | Arabidopsis thaliana | 27% | 92% |
P10090 | Drosophila melanogaster | 28% | 99% |
P45843 | Drosophila melanogaster | 26% | 100% |
P45844 | Homo sapiens | 30% | 100% |
P58428 | Rattus norvegicus | 27% | 98% |
Q05360 | Lucilia cuprina | 29% | 100% |
Q09466 | Caenorhabditis elegans | 25% | 100% |
Q11180 | Caenorhabditis elegans | 28% | 100% |
Q16928 | Anopheles albimanus | 28% | 96% |
Q17320 | Ceratitis capitata | 28% | 100% |
Q27256 | Anopheles gambiae | 28% | 98% |
Q3E9B8 | Arabidopsis thaliana | 26% | 100% |
Q4GZT4 | Bos taurus | 30% | 100% |
Q4Q1D0 | Leishmania major | 89% | 98% |
Q4QF95 | Leishmania major | 27% | 100% |
Q4QJ70 | Leishmania major | 29% | 100% |
Q4QJ71 | Leishmania major | 28% | 100% |
Q55DA0 | Dictyostelium discoideum | 28% | 100% |
Q5MB13 | Macaca mulatta | 29% | 100% |
Q64343 | Mus musculus | 30% | 100% |
Q7TMS5 | Mus musculus | 30% | 100% |
Q7XA72 | Arabidopsis thaliana | 29% | 100% |
Q80W57 | Rattus norvegicus | 29% | 100% |
Q84TH5 | Arabidopsis thaliana | 29% | 100% |
Q86HQ2 | Dictyostelium discoideum | 29% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 28% | 86% |
Q8MIB3 | Sus scrofa | 30% | 100% |
Q8RWI9 | Arabidopsis thaliana | 31% | 98% |
Q8RXN0 | Arabidopsis thaliana | 30% | 97% |
Q8T685 | Dictyostelium discoideum | 28% | 100% |
Q8T686 | Dictyostelium discoideum | 26% | 83% |
Q8T689 | Dictyostelium discoideum | 29% | 85% |
Q91WA9 | Mus musculus | 28% | 100% |
Q93YS4 | Arabidopsis thaliana | 28% | 91% |
Q99P81 | Mus musculus | 26% | 100% |
Q99PE7 | Rattus norvegicus | 24% | 100% |
Q99PE8 | Mus musculus | 25% | 100% |
Q9C6W5 | Arabidopsis thaliana | 28% | 100% |
Q9C8J8 | Arabidopsis thaliana | 28% | 100% |
Q9C8K2 | Arabidopsis thaliana | 31% | 99% |
Q9DBM0 | Mus musculus | 27% | 100% |
Q9FLX5 | Arabidopsis thaliana | 28% | 100% |
Q9FNB5 | Arabidopsis thaliana | 26% | 94% |
Q9FT51 | Arabidopsis thaliana | 29% | 92% |
Q9H221 | Homo sapiens | 27% | 100% |
Q9H222 | Homo sapiens | 25% | 100% |
Q9LFG8 | Arabidopsis thaliana | 27% | 92% |
Q9LK50 | Arabidopsis thaliana | 29% | 99% |
Q9M2V5 | Arabidopsis thaliana | 27% | 96% |
Q9M2V6 | Arabidopsis thaliana | 27% | 100% |
Q9M2V7 | Arabidopsis thaliana | 26% | 92% |
Q9M3D6 | Arabidopsis thaliana | 27% | 94% |
Q9SIT6 | Arabidopsis thaliana | 30% | 100% |
Q9SZR9 | Arabidopsis thaliana | 29% | 100% |
Q9UNQ0 | Homo sapiens | 28% | 100% |
Q9ZU35 | Arabidopsis thaliana | 29% | 94% |
Q9ZUT0 | Arabidopsis thaliana | 27% | 90% |
Q9ZUU9 | Arabidopsis thaliana | 23% | 93% |
V5BCE1 | Trypanosoma cruzi | 29% | 67% |
V5BPQ0 | Trypanosoma cruzi | 27% | 97% |
V5D8T8 | Trypanosoma cruzi | 27% | 100% |
V5DGN9 | Trypanosoma cruzi | 46% | 100% |