ABC transporters probably involved in multidrug resistance. A member of this family confers vinblastine resistance to Leishmania enriettii.
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: 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: Q4Q4W3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
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 | 42 | 46 | PF00656 | 0.764 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.530 |
CLV_MEL_PAP_1 | 290 | 296 | PF00089 | 0.303 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.304 |
CLV_PCSK_FUR_1 | 622 | 626 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.439 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.456 |
DEG_ODPH_VHL_1 | 134 | 146 | PF01847 | 0.256 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.503 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.681 |
DOC_CYCLIN_RxL_1 | 450 | 459 | PF00134 | 0.470 |
DOC_CYCLIN_RxL_1 | 476 | 488 | PF00134 | 0.480 |
DOC_CYCLIN_RxL_1 | 581 | 591 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 385 | 391 | PF00134 | 0.265 |
DOC_MAPK_gen_1 | 117 | 125 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 622 | 631 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 117 | 125 | PF00069 | 0.263 |
DOC_PP1_RVXF_1 | 173 | 180 | PF00149 | 0.515 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 462 | 469 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 479 | 485 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.529 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.315 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 385 | 388 | PF13499 | 0.393 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.424 |
DOC_PP4_FxxP_1 | 468 | 471 | PF00568 | 0.413 |
DOC_PP4_FxxP_1 | 486 | 489 | PF00568 | 0.413 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.742 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 223 | 229 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 438 | 443 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 454 | 459 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 548 | 553 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 634 | 639 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 106 | 122 | PF00022 | 0.272 |
LIG_Actin_WH2_2 | 159 | 177 | PF00022 | 0.243 |
LIG_Actin_WH2_2 | 603 | 619 | PF00022 | 0.616 |
LIG_APCC_ABBA_1 | 94 | 99 | PF00400 | 0.532 |
LIG_BIR_III_2 | 31 | 35 | PF00653 | 0.602 |
LIG_BIR_III_2 | 696 | 700 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 476 | 480 | PF00533 | 0.413 |
LIG_Clathr_ClatBox_1 | 332 | 336 | PF01394 | 0.480 |
LIG_Clathr_ClatBox_1 | 375 | 379 | PF01394 | 0.260 |
LIG_FAT_LD_1 | 378 | 386 | PF03623 | 0.265 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.288 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.306 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.422 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.280 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.474 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.222 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.469 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.760 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.413 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.486 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.280 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.250 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.213 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.573 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.581 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.447 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.502 |
LIG_FHA_2 | 656 | 662 | PF00498 | 0.500 |
LIG_FHA_2 | 693 | 699 | PF00498 | 0.764 |
LIG_GBD_Chelix_1 | 352 | 360 | PF00786 | 0.278 |
LIG_GBD_Chelix_1 | 377 | 385 | PF00786 | 0.265 |
LIG_LIR_Apic_2 | 465 | 471 | PF02991 | 0.424 |
LIG_LIR_Apic_2 | 92 | 96 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 227 | 238 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 285 | 294 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 666 | 677 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 285 | 290 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.441 |
LIG_Pex14_1 | 226 | 230 | PF04695 | 0.438 |
LIG_Pex14_1 | 279 | 283 | PF04695 | 0.424 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.480 |
LIG_PTB_Apo_2 | 436 | 443 | PF02174 | 0.441 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.250 |
LIG_SH2_PTP2 | 230 | 233 | PF00017 | 0.326 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 563 | 567 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.557 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.279 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.761 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.279 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.762 |
LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.280 |
LIG_SUMO_SIM_anti_2 | 374 | 379 | PF11976 | 0.256 |
LIG_SUMO_SIM_anti_2 | 627 | 632 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 262 | 268 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 331 | 336 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 374 | 379 | PF11976 | 0.213 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 591 | 599 | PF11976 | 0.426 |
LIG_SxIP_EBH_1 | 77 | 87 | PF03271 | 0.444 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.730 |
LIG_TYR_ITIM | 228 | 233 | PF00017 | 0.284 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.250 |
LIG_UBA3_1 | 643 | 650 | PF00899 | 0.355 |
LIG_Vh1_VBS_1 | 104 | 122 | PF01044 | 0.253 |
LIG_Vh1_VBS_1 | 351 | 369 | PF01044 | 0.393 |
LIG_WRC_WIRS_1 | 166 | 171 | PF05994 | 0.394 |
LIG_WW_3 | 65 | 69 | PF00397 | 0.618 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.586 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.586 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.626 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.380 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.326 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.284 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.645 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.281 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.427 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.297 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.344 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.250 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.392 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.480 |
MOD_CK2_1 | 655 | 661 | PF00069 | 0.381 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.598 |
MOD_CMANNOS | 88 | 91 | PF00535 | 0.411 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.285 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.287 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.286 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.408 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.270 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.313 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.266 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.288 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.261 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.393 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.661 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.323 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.344 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.679 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.429 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.592 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.463 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.297 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.315 |
MOD_N-GLC_1 | 523 | 528 | PF02516 | 0.265 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.496 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.403 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.409 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.277 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.272 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.258 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.325 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.276 |
MOD_NEK2_2 | 475 | 480 | PF00069 | 0.250 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.519 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.393 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.339 |
MOD_PK_1 | 505 | 511 | PF00069 | 0.393 |
MOD_PKA_1 | 624 | 630 | PF00069 | 0.338 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.275 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.257 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.265 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.350 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.386 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.308 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.361 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.346 |
MOD_PKB_1 | 320 | 328 | PF00069 | 0.376 |
MOD_PKB_1 | 622 | 630 | PF00069 | 0.444 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.280 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.354 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.315 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.754 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.267 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.393 |
MOD_Plk_2-3 | 443 | 449 | PF00069 | 0.321 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.262 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.344 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.435 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.325 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.333 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.250 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.295 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.266 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.250 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.250 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.669 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.613 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.708 |
MOD_SUMO_for_1 | 54 | 57 | PF00179 | 0.731 |
MOD_SUMO_rev_2 | 171 | 177 | PF00179 | 0.260 |
MOD_SUMO_rev_2 | 421 | 427 | PF00179 | 0.443 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.250 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.565 |
TRG_NES_CRM1_1 | 193 | 204 | PF08389 | 0.385 |
TRG_NES_CRM1_1 | 374 | 384 | PF08389 | 0.250 |
TRG_Pf-PMV_PEXEL_1 | 586 | 591 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM85 | Leptomonas seymouri | 30% | 78% |
A0A0N1PGA4 | Leptomonas seymouri | 79% | 80% |
A0A0S4IRM6 | Bodo saltans | 54% | 85% |
A0A0S4JF49 | Bodo saltans | 36% | 93% |
A0A125QXJ1 | Mesocricetus auratus | 40% | 84% |
A0A1X0NRS8 | Trypanosomatidae | 66% | 96% |
A0A3R7MZT8 | Trypanosoma rangeli | 64% | 94% |
A0A3S7X621 | Leishmania donovani | 95% | 79% |
A1USS5 | Bartonella bacilliformis (strain ATCC 35685 / NCTC 12138 / KC583) | 29% | 100% |
A4HKV4 | Leishmania braziliensis | 86% | 100% |
A4HLP7 | Leishmania braziliensis | 22% | 100% |
A4I8D3 | Leishmania infantum | 95% | 100% |
B2GUP8 | Xenopus tropicalis | 31% | 100% |
D0AAT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 98% |
E7F6F7 | Danio rerio | 42% | 95% |
E9B392 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
G5EFD4 | Caenorhabditis elegans | 38% | 88% |
H2LNR5 | Oryzias latipes | 44% | 94% |
J9VWU3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 41% | 96% |
O07549 | Bacillus subtilis (strain 168) | 28% | 100% |
O14286 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 100% |
O31707 | Bacillus subtilis (strain 168) | 27% | 100% |
O70595 | Rattus norvegicus | 40% | 84% |
O75027 | Homo sapiens | 41% | 94% |
P08716 | Escherichia coli | 31% | 100% |
P0A2V0 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 31% | 100% |
P0A2V1 | Rhizobium radiobacter | 31% | 100% |
P0C086 | Mannheimia haemolytica | 30% | 99% |
P0C087 | Mannheimia haemolytica | 30% | 99% |
P0CL92 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 42% | 96% |
P0CL93 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 42% | 96% |
P0DKX5 | Bordetella pertussis (strain Tohama I / ATCC BAA-589 / NCTC 13251) | 32% | 99% |
P0DKX6 | Bordetella pertussis (strain ATCC 9797 / DSM 5571 / NCTC 10739 / 18323) | 32% | 99% |
P10089 | Escherichia coli | 31% | 100% |
P11599 | Proteus vulgaris | 29% | 100% |
P16532 | Mannheimia haemolytica | 30% | 99% |
P18767 | Rhizobium meliloti (strain 1021) | 29% | 100% |
P22638 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 33% | 100% |
P23702 | Aggregatibacter actinomycetemcomitans | 30% | 100% |
P26760 | Actinobacillus pleuropneumoniae | 30% | 100% |
P35598 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 27% | 100% |
P36371 | Mus musculus | 29% | 100% |
P36372 | Rattus norvegicus | 29% | 100% |
P36497 | Pediococcus acidilactici | 26% | 97% |
P40416 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 100% |
P45861 | Bacillus subtilis (strain 168) | 28% | 100% |
P47260 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 25% | 100% |
P55122 | Pasteurella haemolytica-like sp. (strain 5943B) | 30% | 99% |
P59653 | Streptococcus pneumoniae (strain ATCC BAA-255 / R6) | 27% | 98% |
P59852 | Lactococcus lactis subsp. lactis | 28% | 100% |
P60752 | Escherichia coli (strain K12) | 31% | 100% |
P60753 | Escherichia coli O157:H7 | 31% | 100% |
P63359 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 30% | 100% |
P63360 | Salmonella typhi | 30% | 100% |
P63398 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P70864 | Bartonella bacilliformis | 29% | 100% |
P71082 | Bacillus subtilis (strain 168) | 32% | 100% |
P9WQJ2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WQJ3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q00564 | Lactococcus lactis subsp. lactis | 25% | 98% |
Q02592 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 85% |
Q03519 | Homo sapiens | 30% | 100% |
Q03727 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 26% | 98% |
Q04473 | Actinobacillus pleuropneumoniae | 30% | 99% |
Q07QX6 | Rhodopseudomonas palustris (strain BisA53) | 30% | 100% |
Q08D64 | Xenopus tropicalis | 40% | 83% |
Q0BKJ3 | Francisella tularensis subsp. holarctica (strain OSU18) | 28% | 100% |
Q0TJD9 | Escherichia coli O6:K15:H31 (strain 536 / UPEC) | 30% | 100% |
Q0VQP5 | Alcanivorax borkumensis (strain ATCC 700651 / DSM 11573 / NCIMB 13689 / SK2) | 30% | 100% |
Q10418 | Leuconostoc mesenteroides | 28% | 98% |
Q14JW6 | Francisella tularensis subsp. tularensis (strain FSC 198) | 28% | 100% |
Q15UY7 | Pseudoalteromonas atlantica (strain T6c / ATCC BAA-1087) | 32% | 100% |
Q1BUV6 | Burkholderia cenocepacia (strain AU 1054) | 29% | 100% |
Q1CA68 | Yersinia pestis bv. Antiqua (strain Antiqua) | 31% | 100% |
Q1CGH0 | Yersinia pestis bv. Antiqua (strain Nepal516) | 31% | 100% |
Q1GZI0 | Methylobacillus flagellatus (strain KT / ATCC 51484 / DSM 6875) | 30% | 100% |
Q1LQD3 | Cupriavidus metallidurans (strain ATCC 43123 / DSM 2839 / NBRC 102507 / CH34) | 33% | 100% |
Q1QBW0 | Psychrobacter cryohalolentis (strain ATCC BAA-1226 / DSM 17306 / VKM B-2378 / K5) | 33% | 100% |
Q1QH37 | Nitrobacter hamburgensis (strain DSM 10229 / NCIMB 13809 / X14) | 30% | 100% |
Q1QX69 | Chromohalobacter salexigens (strain ATCC BAA-138 / DSM 3043 / CIP 106854 / NCIMB 13768 / 1H11) | 31% | 100% |
Q1RDU4 | Escherichia coli (strain UTI89 / UPEC) | 30% | 100% |
Q20Z38 | Rhodopseudomonas palustris (strain BisB18) | 31% | 100% |
Q21NS8 | Saccharophagus degradans (strain 2-40 / ATCC 43961 / DSM 17024) | 32% | 100% |
Q21WN9 | Albidiferax ferrireducens (strain ATCC BAA-621 / DSM 15236 / T118) | 31% | 100% |
Q2A1U9 | Francisella tularensis subsp. holarctica (strain LVS) | 28% | 100% |
Q2G506 | Novosphingobium aromaticivorans (strain ATCC 700278 / DSM 12444 / CCUG 56034 / CIP 105152 / NBRC 16084 / F199) | 41% | 100% |
Q2HIE9 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 42% | 100% |
Q2K342 | Rhizobium etli (strain CFN 42 / ATCC 51251) | 30% | 100% |
Q2KYS6 | Bordetella avium (strain 197N) | 31% | 100% |
Q2LVL0 | Syntrophus aciditrophicus (strain SB) | 30% | 100% |
Q2SZW0 | Burkholderia thailandensis (strain ATCC 700388 / DSM 13276 / CIP 106301 / E264) | 29% | 100% |
Q2ULH4 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 39% | 98% |
Q2UPC0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 32% | 88% |
Q31YT6 | Shigella boydii serotype 4 (strain Sb227) | 31% | 100% |
Q32E34 | Shigella dysenteriae serotype 1 (strain Sd197) | 31% | 100% |
Q39E73 | Burkholderia lata (strain ATCC 17760 / DSM 23089 / LMG 22485 / NCIMB 9086 / R18194 / 383) | 29% | 100% |
Q3IGX5 | Pseudoalteromonas translucida (strain TAC 125) | 32% | 100% |
Q3JUI6 | Burkholderia pseudomallei (strain 1710b) | 29% | 100% |
Q3SFZ6 | Thiobacillus denitrificans (strain ATCC 25259) | 33% | 100% |
Q3SP57 | Nitrobacter winogradskyi (strain ATCC 25391 / DSM 10237 / CIP 104748 / NCIMB 11846 / Nb-255) | 32% | 100% |
Q3Z3K7 | Shigella sonnei (strain Ss046) | 31% | 100% |
Q46Y89 | Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) | 31% | 100% |
Q47258 | Escherichia coli | 31% | 100% |
Q47908 | Francisella novicida | 28% | 100% |
Q480N3 | Colwellia psychrerythraea (strain 34H / ATCC BAA-681) | 30% | 100% |
Q483B6 | Colwellia psychrerythraea (strain 34H / ATCC BAA-681) | 29% | 100% |
Q4FS42 | Psychrobacter arcticus (strain DSM 17307 / VKM B-2377 / 273-4) | 34% | 100% |
Q4HVU7 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 42% | 100% |
Q4PH16 | Ustilago maydis (strain 521 / FGSC 9021) | 43% | 92% |
Q4Q402 | Leishmania major | 23% | 100% |
Q4WLN7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 41% | 97% |
Q4WPP6 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 89% |
Q54BU4 | Dictyostelium discoideum | 30% | 77% |
Q54RU1 | Dictyostelium discoideum | 35% | 100% |
Q56A55 | Danio rerio | 30% | 99% |
Q57180 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 35% | 100% |
Q57R14 | Salmonella choleraesuis (strain SC-B67) | 30% | 100% |
Q59R09 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 38% | 94% |
Q5B1Q2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 43% | 98% |
Q5E0F2 | Aliivibrio fischeri (strain ATCC 700601 / ES114) | 32% | 100% |
Q5F4X8 | Neisseria gonorrhoeae (strain ATCC 700825 / FA 1090) | 32% | 100% |
Q5NIG3 | Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4) | 28% | 100% |
Q5PGH0 | Salmonella paratyphi A (strain ATCC 9150 / SARB42) | 30% | 100% |
Q5QU36 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 31% | 100% |
Q5RFQ9 | Pongo abelii | 32% | 98% |
Q5RKI8 | Rattus norvegicus | 31% | 99% |
Q60AA3 | Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) | 31% | 100% |
Q61102 | Mus musculus | 42% | 94% |
Q62IG3 | Burkholderia mallei (strain ATCC 23344) | 29% | 100% |
Q63VX7 | Burkholderia pseudomallei (strain K96243) | 29% | 100% |
Q66CI3 | Yersinia pseudotuberculosis serotype I (strain IP32953) | 31% | 100% |
Q6AJW3 | Desulfotalea psychrophila (strain LSv54 / DSM 12343) | 30% | 100% |
Q6BXD7 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 39% | 100% |
Q6C6N0 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 38% | 99% |
Q6CX96 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 39% | 98% |
Q6FIK3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 40% | 97% |
Q6FZF2 | Bartonella quintana (strain Toulouse) | 28% | 100% |
Q6G2Z5 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 28% | 100% |
Q6N1Y7 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 29% | 100% |
Q704E8 | Rattus norvegicus | 42% | 94% |
Q71ED1 | Agrobacterium vitis | 29% | 100% |
Q751N2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 38% | 100% |
Q7MJ07 | Vibrio vulnificus (strain YJ016) | 31% | 100% |
Q7NZU6 | Chromobacterium violaceum (strain ATCC 12472 / DSM 30191 / JCM 1249 / NBRC 12614 / NCIMB 9131 / NCTC 9757) | 31% | 100% |
Q7RX59 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 43% | 98% |
Q7VWD8 | Bordetella pertussis (strain Tohama I / ATCC BAA-589 / NCTC 13251) | 31% | 100% |
Q7W9N7 | Bordetella parapertussis (strain 12822 / ATCC BAA-587 / NCTC 13253) | 31% | 100% |
Q7WH20 | Bordetella bronchiseptica (strain ATCC BAA-588 / NCTC 13252 / RB50) | 31% | 100% |
Q83LP0 | Shigella flexneri | 31% | 100% |
Q89A97 | Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) | 26% | 100% |
Q89UT8 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 33% | 100% |
Q8DAV2 | Vibrio vulnificus (strain CMCP6) | 31% | 100% |
Q8FDZ8 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 31% | 100% |
Q8FJB1 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 30% | 100% |
Q8SQI5 | Encephalitozoon cuniculi (strain GB-M1) | 28% | 100% |
Q8T9W2 | Dictyostelium discoideum | 43% | 100% |
Q8XXB6 | Ralstonia solanacearum (strain GMI1000) | 30% | 100% |
Q8ZGA9 | Yersinia pestis | 31% | 100% |
Q933E0 | Bibersteinia trehalosi | 30% | 99% |
Q933I3 | Mannheimia glucosida | 30% | 99% |
Q93FG6 | Mannheimia haemolytica | 30% | 99% |
Q93FH0 | Mannheimia haemolytica | 30% | 99% |
Q93FH2 | Mannheimia haemolytica | 30% | 99% |
Q93FH3 | Mannheimia haemolytica | 30% | 99% |
Q93FH6 | Mannheimia haemolytica | 30% | 99% |
Q983H5 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 28% | 100% |
Q9CHL8 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9CJB8 | Lactococcus lactis subsp. lactis (strain IL1403) | 26% | 98% |
Q9CXJ4 | Mus musculus | 31% | 98% |
Q9DC29 | Mus musculus | 40% | 84% |
Q9FNU2 | Oryza sativa subsp. japonica | 29% | 100% |
Q9FUT3 | Arabidopsis thaliana | 41% | 100% |
Q9JI39 | Mus musculus | 33% | 98% |
Q9JJ59 | Mus musculus | 28% | 92% |
Q9JW59 | Neisseria meningitidis serogroup A / serotype 4A (strain DSM 15465 / Z2491) | 31% | 100% |
Q9JXR3 | Neisseria meningitidis serogroup B (strain MC58) | 31% | 100% |
Q9LVM1 | Arabidopsis thaliana | 44% | 97% |
Q9M0G9 | Arabidopsis thaliana | 43% | 100% |
Q9NP58 | Homo sapiens | 40% | 84% |
Q9NP78 | Homo sapiens | 28% | 92% |
Q9NRK6 | Homo sapiens | 31% | 95% |
Q9NUT2 | Homo sapiens | 32% | 96% |
Q9QYJ4 | Rattus norvegicus | 28% | 92% |
Q9RCG7 | Pasteurella aerogenes | 31% | 99% |
Q9X2W0 | Escherichia coli | 24% | 100% |
V5DM82 | Trypanosoma cruzi | 65% | 96% |