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: A4HPF5
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 | 323 | 327 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.543 |
CLV_MEL_PAP_1 | 158 | 164 | PF00089 | 0.359 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.174 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.340 |
CLV_PCSK_FUR_1 | 414 | 418 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.174 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.465 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.374 |
DOC_CYCLIN_RxL_1 | 528 | 540 | PF00134 | 0.341 |
DOC_CYCLIN_yCln2_LP_2 | 289 | 295 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 161 | 171 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 192 | 199 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 378 | 387 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 452 | 460 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 192 | 201 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 234 | 241 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 452 | 459 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 501 | 510 | PF00069 | 0.195 |
DOC_PP1_RVXF_1 | 530 | 537 | PF00149 | 0.295 |
DOC_PP1_RVXF_1 | 595 | 602 | PF00149 | 0.254 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.742 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.595 |
DOC_PP4_MxPP_1 | 28 | 31 | PF00568 | 0.591 |
DOC_SPAK_OSR1_1 | 247 | 251 | PF12202 | 0.429 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.399 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 17 | 24 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.572 |
LIG_Actin_WH2_2 | 357 | 373 | PF00022 | 0.436 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.770 |
LIG_BIR_III_4 | 274 | 278 | PF00653 | 0.427 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.551 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.479 |
LIG_eIF4E_1 | 548 | 554 | PF01652 | 0.387 |
LIG_EVH1_1 | 332 | 336 | PF00568 | 0.586 |
LIG_EVH1_2 | 205 | 209 | PF00568 | 0.475 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.417 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.411 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.513 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.419 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.349 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.527 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.503 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.454 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.516 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.559 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.705 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.571 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 26 | 30 | PF02991 | 0.775 |
LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 133 | 141 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 252 | 260 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 41 | 49 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 465 | 475 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 513 | 524 | PF02991 | 0.201 |
LIG_LIR_Gen_1 | 600 | 609 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 600 | 604 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 613 | 617 | PF02991 | 0.277 |
LIG_NRBOX | 224 | 230 | PF00104 | 0.598 |
LIG_NRBOX | 566 | 572 | PF00104 | 0.424 |
LIG_PCNA_PIPBox_1 | 527 | 536 | PF02747 | 0.295 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 134 | 137 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 645 | 649 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.174 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.342 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.743 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.446 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.766 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.379 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.540 |
LIG_SUMO_SIM_anti_2 | 235 | 242 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 255 | 261 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 298 | 304 | PF11976 | 0.595 |
LIG_SUMO_SIM_anti_2 | 568 | 575 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 615 | 622 | PF11976 | 0.336 |
LIG_SUMO_SIM_anti_2 | 72 | 78 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 85 | 92 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 654 | 659 | PF11976 | 0.437 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.540 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.379 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.622 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.546 |
LIG_TYR_ITIM | 519 | 524 | PF00017 | 0.322 |
LIG_TYR_ITIM | 661 | 666 | PF00017 | 0.322 |
LIG_TYR_ITSM | 437 | 444 | PF00017 | 0.421 |
LIG_UBA3_1 | 553 | 559 | PF00899 | 0.415 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.465 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.537 |
LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.412 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.427 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.201 |
LIG_WRC_WIRS_1 | 598 | 603 | PF05994 | 0.170 |
MOD_CDC14_SPxK_1 | 392 | 395 | PF00782 | 0.674 |
MOD_CDK_SPK_2 | 20 | 25 | PF00069 | 0.592 |
MOD_CDK_SPxK_1 | 389 | 395 | PF00069 | 0.684 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.495 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.716 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.733 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.495 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.619 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.486 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.421 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.317 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.241 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.454 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.476 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.446 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.649 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.560 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.639 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.278 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.335 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.295 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.205 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.408 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.404 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.388 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.340 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.201 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.379 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.595 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.250 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.250 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.229 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.732 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.537 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.499 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.713 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.656 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.622 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.646 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.602 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.317 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.379 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.408 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.527 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.461 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.683 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.555 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.591 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.641 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.329 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.336 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.532 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.299 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.363 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.393 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.313 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.323 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.604 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.562 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.575 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.608 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.450 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.340 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.394 |
MOD_PKA_1 | 119 | 125 | PF00069 | 0.382 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.382 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.515 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.515 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.626 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.619 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.675 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.508 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.581 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.381 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.501 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.534 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.672 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.610 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.605 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.515 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.477 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.227 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.427 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.411 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.452 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.452 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.748 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.408 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.579 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.620 |
TRG_DiLeu_BaEn_1 | 615 | 620 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_4 | 306 | 312 | PF01217 | 0.610 |
TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.178 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.174 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.265 |
TRG_NES_CRM1_1 | 294 | 309 | PF08389 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.218 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 27% | 92% |
A0A0N1HZC7 | Leptomonas seymouri | 70% | 100% |
A0A0S4IJ55 | Bodo saltans | 27% | 89% |
A0A0S4IQG2 | Bodo saltans | 26% | 100% |
A0A0S4IUG8 | Bodo saltans | 28% | 100% |
A0A0S4IUY5 | Bodo saltans | 46% | 100% |
A0A0S4IZ09 | Bodo saltans | 22% | 100% |
A0A0S4J724 | Bodo saltans | 29% | 100% |
A0A0S4J7U2 | Bodo saltans | 29% | 97% |
A0A0S4JPA7 | Bodo saltans | 28% | 91% |
A0A0S4KMF6 | Bodo saltans | 22% | 84% |
A0A1X0NKI4 | Trypanosomatidae | 49% | 100% |
A0A1X0NM50 | Trypanosomatidae | 27% | 100% |
A0A1X0NTW9 | Trypanosomatidae | 27% | 100% |
A0A1X0P4K0 | Trypanosomatidae | 22% | 100% |
A0A3Q8IA65 | Leishmania donovani | 27% | 92% |
A0A3Q8IHD8 | Leishmania donovani | 79% | 100% |
A0A3R7KEQ6 | Trypanosoma rangeli | 47% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 28% | 100% |
A0A3S5H5N0 | Leishmania donovani | 29% | 100% |
A0A3S7WPB9 | Leishmania donovani | 29% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 28% | 98% |
A4H4G9 | Leishmania braziliensis | 28% | 100% |
A4H4H6 | Leishmania braziliensis | 29% | 100% |
A4H862 | Leishmania braziliensis | 28% | 100% |
A4HSQ0 | Leishmania infantum | 29% | 100% |
A4HSQ1 | Leishmania infantum | 29% | 100% |
A4HWI7 | Leishmania infantum | 27% | 92% |
A4ID77 | Leishmania infantum | 79% | 100% |
B8ALI0 | Oryza sativa subsp. indica | 29% | 86% |
B9G5Y5 | Oryza sativa subsp. japonica | 27% | 68% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D3ZCM3 | Rattus norvegicus | 29% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 92% |
E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
H9BZ66 | Petunia hybrida | 30% | 100% |
O80946 | Arabidopsis thaliana | 29% | 92% |
P10090 | Drosophila melanogaster | 29% | 99% |
P45843 | Drosophila melanogaster | 28% | 100% |
P45844 | Homo sapiens | 29% | 100% |
P58428 | Rattus norvegicus | 27% | 98% |
Q05360 | Lucilia cuprina | 31% | 100% |
Q09466 | Caenorhabditis elegans | 26% | 100% |
Q11180 | Caenorhabditis elegans | 28% | 100% |
Q16928 | Anopheles albimanus | 32% | 96% |
Q17320 | Ceratitis capitata | 29% | 100% |
Q27256 | Anopheles gambiae | 31% | 98% |
Q4GZT4 | Bos taurus | 32% | 100% |
Q4Q1D0 | Leishmania major | 78% | 98% |
Q4QF95 | Leishmania major | 27% | 100% |
Q4QJ70 | Leishmania major | 29% | 100% |
Q4QJ71 | Leishmania major | 29% | 100% |
Q55DA0 | Dictyostelium discoideum | 29% | 100% |
Q5MB13 | Macaca mulatta | 32% | 100% |
Q64343 | Mus musculus | 29% | 100% |
Q7TMS5 | Mus musculus | 33% | 100% |
Q7XA72 | Arabidopsis thaliana | 31% | 100% |
Q80W57 | Rattus norvegicus | 31% | 100% |
Q84TH5 | Arabidopsis thaliana | 30% | 100% |
Q86HQ2 | Dictyostelium discoideum | 27% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 29% | 86% |
Q8MIB3 | Sus scrofa | 31% | 100% |
Q8RWI9 | Arabidopsis thaliana | 30% | 98% |
Q8RXN0 | Arabidopsis thaliana | 29% | 97% |
Q8T685 | Dictyostelium discoideum | 27% | 100% |
Q8T686 | Dictyostelium discoideum | 26% | 83% |
Q8T689 | Dictyostelium discoideum | 28% | 85% |
Q93YS4 | Arabidopsis thaliana | 29% | 91% |
Q99P81 | Mus musculus | 28% | 100% |
Q99PE7 | Rattus norvegicus | 26% | 100% |
Q99PE8 | Mus musculus | 27% | 100% |
Q9C6W5 | Arabidopsis thaliana | 29% | 100% |
Q9C8J8 | Arabidopsis thaliana | 28% | 100% |
Q9C8K2 | Arabidopsis thaliana | 29% | 99% |
Q9DBM0 | Mus musculus | 28% | 100% |
Q9FLX5 | Arabidopsis thaliana | 28% | 100% |
Q9FNB5 | Arabidopsis thaliana | 28% | 94% |
Q9FT51 | Arabidopsis thaliana | 30% | 92% |
Q9H221 | Homo sapiens | 27% | 100% |
Q9H222 | Homo sapiens | 26% | 100% |
Q9LFG8 | Arabidopsis thaliana | 29% | 92% |
Q9LK50 | Arabidopsis thaliana | 30% | 99% |
Q9M2V5 | Arabidopsis thaliana | 28% | 96% |
Q9M2V6 | Arabidopsis thaliana | 28% | 100% |
Q9M2V7 | Arabidopsis thaliana | 29% | 92% |
Q9M3D6 | Arabidopsis thaliana | 28% | 94% |
Q9SIT6 | Arabidopsis thaliana | 27% | 100% |
Q9SW08 | Arabidopsis thaliana | 28% | 100% |
Q9SZR9 | Arabidopsis thaliana | 31% | 100% |
Q9UNQ0 | Homo sapiens | 32% | 100% |
Q9ZU35 | Arabidopsis thaliana | 32% | 94% |
Q9ZUT0 | Arabidopsis thaliana | 27% | 90% |
Q9ZUU9 | Arabidopsis thaliana | 22% | 93% |
V5B0X3 | Trypanosoma cruzi | 23% | 100% |
V5BPQ0 | Trypanosoma cruzi | 27% | 97% |
V5D8T8 | Trypanosoma cruzi | 27% | 100% |
V5DGN9 | Trypanosoma cruzi | 45% | 100% |