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)
Transporters, ATP-binding cassette G, member 6 ABCG6
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: A4ID77
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 | 0.732 |
CLV_MEL_PAP_1 | 161 | 167 | PF00089 | 0.359 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.340 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.254 |
CLV_PCSK_PC7_1 | 398 | 404 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.359 |
CLV_Separin_Metazoa | 142 | 146 | PF03568 | 0.503 |
DOC_CDC14_PxL_1 | 204 | 212 | PF14671 | 0.531 |
DOC_CYCLIN_RxL_1 | 532 | 541 | PF00134 | 0.339 |
DOC_MAPK_gen_1 | 455 | 463 | PF00069 | 0.265 |
DOC_MAPK_gen_1 | 650 | 659 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 237 | 244 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 455 | 462 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 653 | 661 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 533 | 540 | PF00149 | 0.295 |
DOC_PP1_RVXF_1 | 598 | 605 | PF00149 | 0.254 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.721 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.580 |
DOC_USP7_UBL2_3 | 98 | 102 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 145 | 151 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 164 | 172 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 178 | 186 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 402 | 411 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 606 | 612 | PF00244 | 0.302 |
LIG_Actin_WH2_2 | 136 | 153 | PF00022 | 0.503 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.769 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.462 |
LIG_Clathr_ClatBox_1 | 210 | 214 | PF01394 | 0.479 |
LIG_eIF4E_1 | 551 | 557 | PF01652 | 0.387 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.417 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.508 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.549 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.622 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.470 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.419 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.349 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.311 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.527 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.503 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.454 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.507 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.514 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.571 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 268 | 274 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 136 | 144 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 251 | 262 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 426 | 435 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 603 | 612 | PF02991 | 0.359 |
LIG_LIR_LC3C_4 | 654 | 659 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 426 | 430 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 616 | 620 | PF02991 | 0.273 |
LIG_NRBOX | 227 | 233 | PF00104 | 0.596 |
LIG_NRBOX | 569 | 575 | PF00104 | 0.424 |
LIG_PCNA_PIPBox_1 | 530 | 539 | PF02747 | 0.295 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 427 | 430 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 648 | 652 | PF00017 | 0.421 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.454 |
LIG_SH2_STAT3 | 329 | 332 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 666 | 669 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.480 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.743 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.501 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.446 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.775 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.716 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.540 |
LIG_SUMO_SIM_anti_2 | 238 | 245 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 258 | 264 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.592 |
LIG_SUMO_SIM_anti_2 | 571 | 578 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 88 | 95 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 203 | 209 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 508 | 515 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 544 | 550 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 585 | 591 | PF11976 | 0.366 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.540 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.611 |
LIG_TRAF2_2 | 354 | 359 | PF00917 | 0.642 |
LIG_TYR_ITIM | 522 | 527 | PF00017 | 0.322 |
LIG_TYR_ITIM | 664 | 669 | PF00017 | 0.322 |
LIG_TYR_ITSM | 440 | 447 | PF00017 | 0.421 |
LIG_UBA3_1 | 556 | 562 | PF00899 | 0.414 |
LIG_UBA3_1 | 90 | 98 | PF00899 | 0.465 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.538 |
LIG_WRC_WIRS_1 | 467 | 472 | PF05994 | 0.427 |
MOD_CDC14_SPxK_1 | 395 | 398 | PF00782 | 0.677 |
MOD_CDK_SPxK_1 | 392 | 398 | PF00069 | 0.686 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.495 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.554 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.741 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.602 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.706 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.562 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.421 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.317 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.241 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.448 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.314 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.422 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.454 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.485 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.446 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.793 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.278 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.334 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.295 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.205 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.402 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.424 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.454 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.441 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.388 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.340 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.461 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.590 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.249 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.250 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.229 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.513 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.502 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.758 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.534 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.498 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.622 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.525 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.677 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.625 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.643 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.595 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.317 |
MOD_LATS_1 | 401 | 407 | PF00433 | 0.471 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.178 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.270 |
MOD_N-GLC_2 | 418 | 420 | PF02516 | 0.206 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.527 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.554 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.589 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.623 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.329 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.336 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.532 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.298 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.363 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.393 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.323 |
MOD_NEK2_2 | 363 | 368 | PF00069 | 0.605 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.533 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.622 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.450 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.340 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.385 |
MOD_PKA_1 | 402 | 408 | PF00069 | 0.463 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.515 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.515 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.548 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.612 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.619 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.668 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.578 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.501 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.462 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.532 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.601 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.339 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.227 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.427 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.407 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.451 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.456 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.772 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.762 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.695 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.623 |
TRG_DiLeu_BaEn_1 | 59 | 64 | PF01217 | 0.642 |
TRG_DiLeu_BaEn_4 | 309 | 315 | PF01217 | 0.593 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.162 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 416 | 419 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 454 | 457 | PF00400 | 0.265 |
TRG_NES_CRM1_1 | 297 | 311 | PF08389 | 0.575 |
TRG_NES_CRM1_1 | 359 | 371 | PF08389 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 27% | 93% |
A0A0N1HZC7 | Leptomonas seymouri | 68% | 100% |
A0A0S4IJ55 | Bodo saltans | 27% | 90% |
A0A0S4IQG2 | Bodo saltans | 27% | 100% |
A0A0S4IUG8 | Bodo saltans | 26% | 100% |
A0A0S4IUY5 | Bodo saltans | 46% | 100% |
A0A0S4IY23 | Bodo saltans | 29% | 100% |
A0A0S4IZ09 | Bodo saltans | 22% | 100% |
A0A0S4J724 | Bodo saltans | 28% | 100% |
A0A0S4J7U2 | Bodo saltans | 30% | 98% |
A0A0S4JPA7 | Bodo saltans | 29% | 91% |
A0A1X0NKI4 | Trypanosomatidae | 49% | 100% |
A0A1X0NM50 | Trypanosomatidae | 27% | 100% |
A0A1X0NTW9 | Trypanosomatidae | 27% | 100% |
A0A1X0P4K0 | Trypanosomatidae | 22% | 100% |
A0A3Q8IA65 | Leishmania donovani | 27% | 92% |
A0A3Q8IHD8 | Leishmania donovani | 100% | 100% |
A0A3R7KEQ6 | Trypanosoma rangeli | 45% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H5N0 | Leishmania donovani | 28% | 100% |
A0A3S7WPB9 | Leishmania donovani | 28% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 28% | 98% |
A4H4G9 | Leishmania braziliensis | 29% | 100% |
A4H4H6 | Leishmania braziliensis | 29% | 100% |
A4H862 | Leishmania braziliensis | 26% | 100% |
A4HPF5 | Leishmania braziliensis | 79% | 100% |
A4HSQ0 | Leishmania infantum | 28% | 100% |
A4HSQ1 | Leishmania infantum | 28% | 100% |
A4HWI7 | Leishmania infantum | 27% | 100% |
B8ALI0 | Oryza sativa subsp. indica | 29% | 87% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D3ZCM3 | Rattus norvegicus | 28% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
H9BZ66 | Petunia hybrida | 27% | 100% |
O80946 | Arabidopsis thaliana | 28% | 92% |
P10090 | Drosophila melanogaster | 28% | 99% |
P45843 | Drosophila melanogaster | 26% | 100% |
P45844 | Homo sapiens | 28% | 100% |
P58428 | Rattus norvegicus | 27% | 98% |
Q05360 | Lucilia cuprina | 28% | 100% |
Q09466 | Caenorhabditis elegans | 26% | 100% |
Q11180 | Caenorhabditis elegans | 27% | 100% |
Q16928 | Anopheles albimanus | 29% | 96% |
Q17320 | Ceratitis capitata | 27% | 100% |
Q27256 | Anopheles gambiae | 29% | 98% |
Q4GZT4 | Bos taurus | 29% | 100% |
Q4Q1D0 | Leishmania major | 93% | 98% |
Q4QF95 | Leishmania major | 27% | 100% |
Q4QJ70 | Leishmania major | 29% | 100% |
Q4QJ71 | Leishmania major | 29% | 100% |
Q55DA0 | Dictyostelium discoideum | 28% | 100% |
Q5MB13 | Macaca mulatta | 30% | 100% |
Q64343 | Mus musculus | 28% | 100% |
Q7TMS5 | Mus musculus | 30% | 100% |
Q7XA72 | Arabidopsis thaliana | 29% | 100% |
Q80W57 | Rattus norvegicus | 30% | 100% |
Q84TH5 | Arabidopsis thaliana | 29% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 29% | 87% |
Q8MIB3 | Sus scrofa | 30% | 100% |
Q8RWI9 | Arabidopsis thaliana | 31% | 99% |
Q8RXN0 | Arabidopsis thaliana | 30% | 97% |
Q8T686 | Dictyostelium discoideum | 26% | 84% |
Q8T689 | Dictyostelium discoideum | 29% | 86% |
Q91WA9 | Mus musculus | 28% | 100% |
Q93YS4 | Arabidopsis thaliana | 28% | 91% |
Q99P81 | Mus musculus | 26% | 100% |
Q99PE7 | Rattus norvegicus | 26% | 100% |
Q99PE8 | Mus musculus | 26% | 100% |
Q9C6W5 | Arabidopsis thaliana | 28% | 100% |
Q9C8J8 | Arabidopsis thaliana | 29% | 100% |
Q9C8K2 | Arabidopsis thaliana | 31% | 99% |
Q9DBM0 | Mus musculus | 28% | 100% |
Q9FLX5 | Arabidopsis thaliana | 27% | 100% |
Q9FNB5 | Arabidopsis thaliana | 26% | 94% |
Q9FT51 | Arabidopsis thaliana | 28% | 93% |
Q9H221 | Homo sapiens | 27% | 100% |
Q9H222 | Homo sapiens | 26% | 100% |
Q9LFG8 | Arabidopsis thaliana | 28% | 92% |
Q9LK50 | Arabidopsis thaliana | 28% | 100% |
Q9M2V5 | Arabidopsis thaliana | 27% | 96% |
Q9M2V6 | Arabidopsis thaliana | 28% | 100% |
Q9M2V7 | Arabidopsis thaliana | 26% | 93% |
Q9M3D6 | Arabidopsis thaliana | 28% | 94% |
Q9SIT6 | Arabidopsis thaliana | 27% | 100% |
Q9SW08 | Arabidopsis thaliana | 27% | 100% |
Q9SZR9 | Arabidopsis thaliana | 29% | 100% |
Q9UNQ0 | Homo sapiens | 29% | 100% |
Q9ZU35 | Arabidopsis thaliana | 30% | 94% |
Q9ZUT0 | Arabidopsis thaliana | 27% | 90% |
Q9ZUU9 | Arabidopsis thaliana | 22% | 94% |
V5B0X3 | Trypanosoma cruzi | 21% | 100% |
V5BCE1 | Trypanosoma cruzi | 29% | 67% |
V5BPQ0 | Trypanosoma cruzi | 27% | 98% |
V5D8T8 | Trypanosoma cruzi | 27% | 100% |
V5DGN9 | Trypanosoma cruzi | 46% | 100% |