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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HKJ6
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 | 9 |
GO:0005215 | transporter activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0022804 | active transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140359 | ABC-type transporter activity | 3 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.514 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.283 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.197 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 414 | 422 | PF00400 | 0.651 |
DEG_APCC_DBOX_1 | 654 | 662 | PF00400 | 0.539 |
DOC_CYCLIN_RxL_1 | 207 | 216 | PF00134 | 0.397 |
DOC_MAPK_DCC_7 | 130 | 140 | PF00069 | 0.326 |
DOC_MAPK_FxFP_2 | 469 | 472 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 130 | 140 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 130 | 138 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 366 | 375 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 682 | 689 | PF00069 | 0.613 |
DOC_PP1_SILK_1 | 425 | 430 | PF00149 | 0.451 |
DOC_PP4_FxxP_1 | 469 | 472 | PF00568 | 0.596 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.402 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 301 | 309 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 319 | 324 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 345 | 351 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 415 | 419 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.402 |
LIG_Actin_WH2_2 | 400 | 417 | PF00022 | 0.472 |
LIG_Actin_WH2_2 | 681 | 698 | PF00022 | 0.610 |
LIG_APCC_ABBA_1 | 215 | 220 | PF00400 | 0.397 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.762 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.418 |
LIG_Clathr_ClatBox_1 | 670 | 674 | PF01394 | 0.505 |
LIG_deltaCOP1_diTrp_1 | 30 | 37 | PF00928 | 0.503 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.418 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.604 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.397 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.511 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.374 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.650 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.489 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.535 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.231 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.505 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.541 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.558 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.538 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.513 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.493 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.345 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.511 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.539 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.720 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.463 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.505 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.591 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.552 |
LIG_LIR_Apic_2 | 468 | 472 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 514 | 522 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 634 | 643 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 665 | 676 | PF02991 | 0.523 |
LIG_LIR_LC3C_4 | 432 | 437 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 634 | 639 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 665 | 671 | PF02991 | 0.523 |
LIG_LYPXL_yS_3 | 471 | 474 | PF13949 | 0.587 |
LIG_MLH1_MIPbox_1 | 51 | 55 | PF16413 | 0.219 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.380 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.418 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 357 | 361 | PF00017 | 0.418 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 668 | 672 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 378 | 381 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.338 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.471 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.578 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.577 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.483 |
LIG_SH3_3 | 640 | 646 | PF00018 | 0.577 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.728 |
LIG_SUMO_SIM_anti_2 | 220 | 226 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 274 | 279 | PF11976 | 0.418 |
LIG_SUMO_SIM_anti_2 | 365 | 371 | PF11976 | 0.418 |
LIG_SUMO_SIM_anti_2 | 669 | 675 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 432 | 439 | PF11976 | 0.655 |
LIG_SUMO_SIM_par_1 | 449 | 457 | PF11976 | 0.644 |
LIG_SUMO_SIM_par_1 | 47 | 53 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 556 | 561 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 669 | 675 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 701 | 707 | PF11976 | 0.553 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.590 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.539 |
LIG_WRC_WIRS_1 | 397 | 402 | PF05994 | 0.374 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.577 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.786 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.548 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.545 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.336 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.367 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.673 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.539 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.473 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.569 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.407 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.539 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.539 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.724 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.477 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.539 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.584 |
MOD_CK2_1 | 722 | 728 | PF00069 | 0.693 |
MOD_DYRK1A_RPxSP_1 | 96 | 100 | PF00069 | 0.389 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.606 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.367 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.288 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.320 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.407 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.387 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.567 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.281 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.339 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.263 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.480 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.795 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.527 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.141 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.467 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.503 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.427 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.403 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.740 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.521 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.749 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.426 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.524 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.535 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.575 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.655 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.436 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.511 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.319 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.294 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.486 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.517 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.360 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.370 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.535 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.411 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.511 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.355 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.402 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.179 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.577 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.737 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.316 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.505 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.505 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.682 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.426 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.527 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.532 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.653 |
MOD_OFUCOSY | 531 | 536 | PF10250 | 0.377 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.472 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.577 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.547 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.741 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.477 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.539 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.459 |
MOD_PKA_1 | 617 | 623 | PF00069 | 0.539 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.418 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.515 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.539 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.287 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.615 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.539 |
MOD_PKA_2 | 695 | 701 | PF00069 | 0.650 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.401 |
MOD_PKB_1 | 545 | 553 | PF00069 | 0.397 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.523 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.508 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.392 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.456 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.371 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.549 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.513 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.311 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.374 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.512 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.397 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.359 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.449 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.507 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.503 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.560 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.734 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.429 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.637 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.425 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.528 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.764 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 535 | 540 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.667 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 544 | 547 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 617 | 619 | PF00400 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 693 | 697 | PF00026 | 0.261 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7P4 | Leptomonas seymouri | 63% | 100% |
A0A0S4J6G3 | Bodo saltans | 29% | 100% |
A0A1X0NU80 | Trypanosomatidae | 35% | 100% |
A0A3S5H7S2 | Leishmania donovani | 78% | 99% |
A4I828 | Leishmania infantum | 78% | 99% |
E9B2Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
G7CBF6 | Mycolicibacterium thermoresistibile (strain ATCC 19527 / DSM 44167 / CIP 105390 / JCM 6362 / NCTC 10409 / 316) | 23% | 100% |
P0C529 | Brucella abortus biovar 1 (strain 9-941) | 23% | 100% |
P23702 | Aggregatibacter actinomycetemcomitans | 21% | 100% |
P26760 | Actinobacillus pleuropneumoniae | 22% | 100% |
P44407 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 22% | 100% |
P63359 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 22% | 100% |
P63360 | Salmonella typhi | 22% | 100% |
Q04473 | Actinobacillus pleuropneumoniae | 22% | 100% |
Q2SIN5 | Hahella chejuensis (strain KCTC 2396) | 21% | 100% |
Q2YQ73 | Brucella abortus (strain 2308) | 23% | 100% |
Q4Q570 | Leishmania major | 78% | 99% |
Q57R14 | Salmonella choleraesuis (strain SC-B67) | 22% | 100% |
Q5PGH0 | Salmonella paratyphi A (strain ATCC 9150 / SARB42) | 22% | 100% |
Q7NZU6 | Chromobacterium violaceum (strain ATCC 12472 / DSM 30191 / JCM 1249 / NBRC 12614 / NCIMB 9131 / NCTC 9757) | 22% | 100% |
Q8G0T8 | Brucella suis biovar 1 (strain 1330) | 23% | 100% |
Q8YH20 | Brucella melitensis biotype 1 (strain 16M / ATCC 23456 / NCTC 10094) | 23% | 100% |
Q9NRK6 | Homo sapiens | 26% | 99% |
Q9RCG7 | Pasteurella aerogenes | 21% | 100% |