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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 28 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0017101 | aminoacyl-tRNA synthetase multienzyme complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:0016020 | membrane | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 16 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 16 |
GO:0006399 | tRNA metabolic process | 7 | 16 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 16 |
GO:0006433 | prolyl-tRNA aminoacylation | 7 | 16 |
GO:0006520 | amino acid metabolic process | 3 | 16 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016070 | RNA metabolic process | 5 | 16 |
GO:0019752 | carboxylic acid metabolic process | 5 | 16 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 16 |
GO:0034660 | ncRNA metabolic process | 6 | 16 |
GO:0043038 | amino acid activation | 4 | 16 |
GO:0043039 | tRNA aminoacylation | 5 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043436 | oxoacid metabolic process | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0044281 | small molecule metabolic process | 2 | 16 |
GO:0046483 | heterocycle metabolic process | 3 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0090304 | nucleic acid metabolic process | 4 | 16 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0002161 | aminoacyl-tRNA editing activity | 5 | 15 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 16 |
GO:0004827 | proline-tRNA ligase activity | 5 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 15 |
GO:0016874 | ligase activity | 2 | 16 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 16 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 16 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.490 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.182 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.310 |
DOC_CYCLIN_yCln2_LP_2 | 21 | 27 | PF00134 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.318 |
DOC_MAPK_gen_1 | 337 | 347 | PF00069 | 0.479 |
DOC_MAPK_HePTP_8 | 113 | 125 | PF00069 | 0.394 |
DOC_MAPK_JIP1_4 | 119 | 125 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 116 | 125 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 340 | 349 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 483 | 491 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 566 | 574 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 84 | 91 | PF00149 | 0.504 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 406 | 409 | PF13499 | 0.479 |
DOC_PP2B_LxvP_1 | 693 | 696 | PF13499 | 0.479 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 697 | 700 | PF00568 | 0.479 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.463 |
DOC_USP7_UBL2_3 | 711 | 715 | PF12436 | 0.535 |
DOC_USP7_UBL2_3 | 77 | 81 | PF12436 | 0.436 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 119 | 124 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 324 | 333 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 503 | 513 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 594 | 598 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 630 | 640 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 62 | 79 | PF00022 | 0.522 |
LIG_APCC_ABBA_1 | 489 | 494 | PF00400 | 0.400 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.522 |
LIG_BIR_III_4 | 47 | 51 | PF00653 | 0.394 |
LIG_deltaCOP1_diTrp_1 | 371 | 381 | PF00928 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 635 | 639 | PF00928 | 0.352 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.511 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.509 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.479 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.479 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.507 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.456 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.429 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.522 |
LIG_FHA_1 | 716 | 722 | PF00498 | 0.580 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.535 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.522 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.344 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.490 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.484 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.483 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.485 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.479 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.511 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.580 |
LIG_LIR_Apic_2 | 359 | 363 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 144 | 151 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 396 | 406 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 634 | 643 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 718 | 727 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 144 | 148 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 634 | 639 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 718 | 723 | PF02991 | 0.547 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.479 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.616 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 398 | 402 | PF00017 | 0.490 |
LIG_SH2_PTP2 | 233 | 236 | PF00017 | 0.415 |
LIG_SH2_SRC | 233 | 236 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.497 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.490 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.378 |
LIG_SUMO_SIM_anti_2 | 35 | 42 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 390 | 396 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 506 | 513 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 98 | 104 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 390 | 396 | PF11976 | 0.546 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.443 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.520 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.524 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.483 |
LIG_TYR_ITIM | 243 | 248 | PF00017 | 0.387 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.443 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.540 |
LIG_WW_3 | 500 | 504 | PF00397 | 0.377 |
MOD_CDK_SPxxK_3 | 361 | 368 | PF00069 | 0.490 |
MOD_CDK_SPxxK_3 | 552 | 559 | PF00069 | 0.479 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.654 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.490 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.546 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.533 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.357 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.483 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.497 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.480 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.578 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.428 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.485 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.479 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.479 |
MOD_Cter_Amidation | 412 | 415 | PF01082 | 0.290 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.314 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.566 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.659 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.295 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.270 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.370 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.279 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.582 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.395 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.514 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.479 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.504 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.496 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.479 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.580 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.462 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.279 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.467 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.463 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.605 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.495 |
MOD_NEK2_2 | 397 | 402 | PF00069 | 0.510 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.461 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.505 |
MOD_PKA_1 | 664 | 670 | PF00069 | 0.479 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.479 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.580 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.504 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.531 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.521 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.483 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.465 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.522 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.540 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.504 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.490 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.510 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.504 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.492 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.461 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.505 |
MOD_Plk_4 | 716 | 722 | PF00069 | 0.585 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.490 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.490 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.479 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.552 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.443 |
MOD_SUMO_for_1 | 223 | 226 | PF00179 | 0.403 |
MOD_SUMO_for_1 | 382 | 385 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 211 | 219 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 5 | 15 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 666 | 674 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 71 | 79 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_2 | 10 | 16 | PF01217 | 0.267 |
TRG_DiLeu_BaEn_2 | 634 | 640 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_3 | 35 | 41 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 108 | 113 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 630 | 633 | PF00400 | 0.492 |
TRG_NES_CRM1_1 | 36 | 47 | PF08389 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 533 | 538 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 577 | 581 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY85 | Leptomonas seymouri | 84% | 100% |
A0A0S4JN58 | Bodo saltans | 57% | 89% |
A0A1X0P793 | Trypanosomatidae | 63% | 90% |
A0A3R7KPX0 | Trypanosoma rangeli | 64% | 85% |
A0A3S7WV15 | Leishmania donovani | 85% | 100% |
A0A3S7WV32 | Leishmania donovani | 94% | 100% |
A0M4Z3 | Gramella forsetii (strain KT0803) | 35% | 100% |
A1RSR6 | Pyrobaculum islandicum (strain DSM 4184 / JCM 9189 / GEO3) | 29% | 100% |
A3MV50 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 30% | 100% |
A4H9N1 | Leishmania braziliensis | 89% | 99% |
A4HXZ5 | Leishmania infantum | 94% | 90% |
A4HY00 | Leishmania infantum | 85% | 100% |
A4WJ22 | Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321 / PZ6) | 28% | 100% |
A5FA31 | Flavobacterium johnsoniae (strain ATCC 17061 / DSM 2064 / JCM 8514 / NBRC 14942 / NCIMB 11054 / UW101) | 35% | 100% |
A6L5I2 | Phocaeicola vulgatus (strain ATCC 8482 / DSM 1447 / JCM 5826 / CCUG 4940 / NBRC 14291 / NCTC 11154) | 37% | 100% |
A6LAP3 | Parabacteroides distasonis (strain ATCC 8503 / DSM 20701 / CIP 104284 / JCM 5825 / NCTC 11152) | 36% | 100% |
B0R3A3 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 39% | 100% |
B1Y963 | Pyrobaculum neutrophilum (strain DSM 2338 / JCM 9278 / NBRC 100436 / V24Sta) | 28% | 100% |
B2RJG1 | Porphyromonas gingivalis (strain ATCC 33277 / DSM 20709 / CIP 103683 / JCM 12257 / NCTC 11834 / 2561) | 38% | 100% |
B2UL92 | Akkermansia muciniphila (strain ATCC BAA-835 / DSM 22959 / JCM 33894 / BCRC 81048 / CCUG 64013 / CIP 107961 / Muc) | 35% | 100% |
B3ER64 | Amoebophilus asiaticus (strain 5a2) | 37% | 100% |
B7J1X2 | Borreliella burgdorferi (strain ZS7) | 37% | 100% |
B9LUM0 | Halorubrum lacusprofundi (strain ATCC 49239 / DSM 5036 / JCM 8891 / ACAM 34) | 41% | 100% |
D0A5B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 90% |
E9ARQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
O51363 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 37% | 100% |
O60155 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 44% | 100% |
P38708 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
Q0SNA5 | Borreliella afzelii (strain PKo) | 36% | 100% |
Q11Q45 | Cytophaga hutchinsonii (strain ATCC 33406 / DSM 1761 / CIP 103989 / NBRC 15051 / NCIMB 9469 / D465) | 34% | 100% |
Q18JG3 | Haloquadratum walsbyi (strain DSM 16790 / HBSQ001) | 39% | 100% |
Q1J0W2 | Deinococcus geothermalis (strain DSM 11300 / AG-3a) | 35% | 100% |
Q2ILX2 | Anaeromyxobacter dehalogenans (strain 2CP-C) | 39% | 100% |
Q2RZJ2 | Salinibacter ruber (strain DSM 13855 / M31) | 36% | 100% |
Q2W136 | Magnetospirillum magneticum (strain AMB-1 / ATCC 700264) | 37% | 100% |
Q4QDS0 | Leishmania major | 84% | 100% |
Q4QDS1 | Leishmania major | 93% | 100% |
Q5LCF0 | Bacteroides fragilis (strain ATCC 25285 / DSM 2151 / CCUG 4856 / JCM 11019 / NCTC 9343 / Onslow) | 36% | 100% |
Q64TJ6 | Bacteroides fragilis (strain YCH46) | 36% | 100% |
Q661L6 | Borrelia garinii subsp. bavariensis (strain ATCC BAA-2496 / DSM 23469 / PBi) | 37% | 100% |
Q67PA6 | Symbiobacterium thermophilum (strain T / IAM 14863) | 41% | 100% |
Q6MIW2 | Bdellovibrio bacteriovorus (strain ATCC 15356 / DSM 50701 / NCIMB 9529 / HD100) | 36% | 100% |
Q7MVS7 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 38% | 100% |
Q7X2P1 | Sphingomonas elodea | 36% | 100% |
Q81Z76 | Bacillus anthracis | 41% | 100% |
Q8A988 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 37% | 100% |
Q8I5R7 | Plasmodium falciparum (isolate 3D7) | 39% | 97% |
Q8SSD7 | Encephalitozoon cuniculi (strain GB-M1) | 48% | 100% |
Q8ZVQ9 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 28% | 100% |
Q9FYR6 | Arabidopsis thaliana | 37% | 100% |
Q9HS52 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 39% | 100% |
Q9M1R2 | Arabidopsis thaliana | 53% | 100% |
Q9RUW4 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 36% | 100% |
Q9Y9G0 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 32% | 100% |
V5AZ66 | Trypanosoma cruzi | 65% | 90% |