Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 10 |
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: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AX52
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0006098 | pentose-phosphate shunt | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006739 | NADP metabolic process | 7 | 1 |
GO:0006740 | NADPH regeneration | 4 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009052 | pentose-phosphate shunt, non-oxidative branch | 4 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019362 | pyridine nucleotide metabolic process | 5 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046496 | nicotinamide nucleotide metabolic process | 6 | 1 |
GO:0051156 | glucose 6-phosphate metabolic process | 4 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072524 | pyridine-containing compound metabolic process | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004802 | transketolase activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016744 | transketolase or transaldolase activity | 3 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.265 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 654 | 656 | PF00082 | 0.384 |
CLV_PCSK_PC7_1 | 650 | 656 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.364 |
CLV_Separin_Metazoa | 644 | 648 | PF03568 | 0.430 |
DEG_SCF_FBW7_2 | 105 | 110 | PF00400 | 0.320 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.364 |
DOC_CDC14_PxL_1 | 364 | 372 | PF14671 | 0.496 |
DOC_CKS1_1 | 104 | 109 | PF01111 | 0.413 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.378 |
DOC_CKS1_1 | 508 | 513 | PF01111 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 382 | 388 | PF00134 | 0.560 |
DOC_MAPK_gen_1 | 233 | 243 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 636 | 642 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 103 | 111 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 399 | 406 | PF00149 | 0.488 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.413 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.433 |
DOC_SPAK_OSR1_1 | 404 | 408 | PF12202 | 0.478 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.300 |
LIG_14-3-3_CanoR_1 | 353 | 362 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 384 | 393 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 573 | 578 | PF00244 | 0.526 |
LIG_APCC_ABBA_1 | 295 | 300 | PF00400 | 0.266 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.412 |
LIG_BIR_III_2 | 584 | 588 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.200 |
LIG_CtBP_PxDLS_1 | 473 | 477 | PF00389 | 0.560 |
LIG_deltaCOP1_diTrp_1 | 51 | 60 | PF00928 | 0.300 |
LIG_EH1_1 | 409 | 417 | PF00400 | 0.478 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.300 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.300 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.407 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.244 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.511 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.428 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.355 |
LIG_FHA_2 | 639 | 645 | PF00498 | 0.511 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.546 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 102 | 107 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 136 | 140 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 146 | 152 | PF02991 | 0.204 |
LIG_LIR_Gen_1 | 183 | 190 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 399 | 407 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 431 | 440 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 605 | 615 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 666 | 671 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 605 | 610 | PF02991 | 0.503 |
LIG_Pex14_2 | 428 | 432 | PF04695 | 0.478 |
LIG_PTB_Apo_2 | 662 | 669 | PF02174 | 0.480 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.326 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.343 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.211 |
LIG_SH2_NCK_1 | 316 | 320 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 537 | 541 | PF00017 | 0.321 |
LIG_SH2_PTP2 | 186 | 189 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.296 |
LIG_SH2_STAT3 | 47 | 50 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.540 |
LIG_SH3_2 | 98 | 103 | PF14604 | 0.300 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.300 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.506 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.465 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.347 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.465 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.346 |
LIG_SUMO_SIM_anti_2 | 176 | 184 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 176 | 184 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 538 | 544 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 546 | 552 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 600 | 605 | PF11976 | 0.465 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.419 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.465 |
LIG_TRAF2_1 | 641 | 644 | PF00917 | 0.480 |
LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.300 |
LIG_WRC_WIRS_1 | 607 | 612 | PF05994 | 0.565 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.487 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.494 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.478 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.478 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.424 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.475 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.433 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.298 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.370 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.480 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.397 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.467 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.480 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.527 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.307 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.457 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.474 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.601 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.316 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.297 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.314 |
MOD_GlcNHglycan | 496 | 500 | PF01048 | 0.272 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.469 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.272 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.265 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.300 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.231 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.224 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.246 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.364 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.531 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.493 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.493 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.502 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.438 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.544 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.265 |
MOD_N-GLC_1 | 664 | 669 | PF02516 | 0.500 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.262 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.286 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.350 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.546 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.498 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.506 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.300 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.465 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.557 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.394 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.354 |
MOD_PKA_1 | 353 | 359 | PF00069 | 0.478 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.479 |
MOD_PKB_1 | 571 | 579 | PF00069 | 0.394 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.463 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.474 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.497 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.318 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.373 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.494 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.465 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.270 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.300 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.392 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.495 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.577 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.300 |
MOD_SUMO_rev_2 | 300 | 308 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 334 | 344 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 85 | 90 | PF00179 | 0.327 |
TRG_DiLeu_BaEn_2 | 322 | 328 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.433 |
TRG_PTS1 | 668 | 671 | PF00515 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0I9QGZ2 | Geobacillus stearothermophilus | 49% | 100% |
A0A0N1HR26 | Leptomonas seymouri | 78% | 100% |
A0A1X0NVW8 | Trypanosomatidae | 68% | 100% |
A0A3R7M6C6 | Trypanosoma rangeli | 68% | 100% |
A0A3S5H7D7 | Leishmania donovani | 92% | 100% |
A4HDR8 | Leishmania braziliensis | 85% | 100% |
A4I115 | Leishmania infantum | 92% | 100% |
A6YB01 | Physarum polycephalum | 43% | 100% |
C9ZW96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
D5AV94 | Rhodobacter capsulatus (strain ATCC BAA-309 / NBRC 16581 / SB1003) | 45% | 100% |
F4IW47 | Arabidopsis thaliana | 51% | 91% |
O20250 | Spinacia oleracea | 49% | 91% |
O67642 | Aquifex aeolicus (strain VF5) | 44% | 97% |
O83571 | Treponema pallidum (strain Nichols) | 42% | 100% |
O93884 | Candida boidinii | 42% | 95% |
O94039 | Candida albicans | 49% | 99% |
P06834 | Pichia angusta | 42% | 95% |
P0CZ16 | Rhodobacter capsulatus | 45% | 100% |
P21725 | Cupriavidus necator (strain ATCC 17699 / DSM 428 / KCTC 22496 / NCIMB 10442 / H16 / Stanier 337) | 49% | 100% |
P21726 | Cupriavidus necator (strain ATCC 17699 / DSM 428 / KCTC 22496 / NCIMB 10442 / H16 / Stanier 337) | 49% | 100% |
P22976 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 47% | 100% |
P23254 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 52% | 99% |
P27302 | Escherichia coli (strain K12) | 48% | 100% |
P29277 | Cereibacter sphaeroides | 45% | 100% |
P29401 | Homo sapiens | 28% | 100% |
P33315 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 48% | 99% |
P33570 | Escherichia coli (strain K12) | 48% | 100% |
P34736 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 50% | 99% |
P40142 | Mus musculus | 28% | 100% |
P43757 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 48% | 100% |
P45694 | Bacillus subtilis (strain 168) | 46% | 100% |
P46708 | Mycobacterium leprae (strain TN) | 42% | 96% |
P47312 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 31% | 100% |
P50137 | Rattus norvegicus | 28% | 100% |
P51010 | Xanthobacter flavus | 47% | 100% |
P51854 | Homo sapiens | 22% | 100% |
P56900 | Sinorhizobium medicae (strain WSM419) | 44% | 97% |
P57195 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 46% | 100% |
P57927 | Pasteurella multocida (strain Pm70) | 46% | 100% |
P57958 | Pasteurella multocida (strain Pm70) | 46% | 100% |
P58333 | Rhizobium meliloti (strain 1021) | 44% | 97% |
P59956 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 42% | 96% |
P66962 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 46% | 100% |
P66963 | Staphylococcus aureus (strain MW2) | 46% | 100% |
P75611 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 33% | 100% |
P99161 | Staphylococcus aureus (strain N315) | 46% | 100% |
P9WG24 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 42% | 96% |
P9WG25 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 42% | 96% |
Q0TPD8 | Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A) | 21% | 100% |
Q12630 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 51% | 99% |
Q2NKZ4 | Bos taurus | 27% | 100% |
Q2NL26 | Bos taurus | 24% | 100% |
Q42675 | Craterostigma plantagineum | 48% | 99% |
Q42676 | Craterostigma plantagineum | 46% | 100% |
Q42677 | Craterostigma plantagineum | 49% | 99% |
Q43848 | Solanum tuberosum | 51% | 91% |
Q4QAC4 | Leishmania major | 92% | 100% |
Q4R6M8 | Macaca fascicularis | 23% | 100% |
Q556J0 | Dictyostelium discoideum | 41% | 100% |
Q5DZP0 | Aliivibrio fischeri (strain ATCC 700601 / ES114) | 47% | 100% |
Q5E7R1 | Aliivibrio fischeri (strain ATCC 700601 / ES114) | 47% | 100% |
Q5HG77 | Staphylococcus aureus (strain COL) | 46% | 100% |
Q5HPJ9 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 45% | 100% |
Q5R1W6 | Pan troglodytes | 28% | 100% |
Q5R4C1 | Pongo abelii | 28% | 100% |
Q5XAK5 | Streptococcus pyogenes serotype M6 (strain ATCC BAA-946 / MGAS10394) | 47% | 92% |
Q60103 | Xanthobacter flavus | 49% | 98% |
Q60HC7 | Macaca fascicularis | 28% | 100% |
Q6B855 | Bos taurus | 28% | 100% |
Q6G9L6 | Staphylococcus aureus (strain MSSA476) | 46% | 100% |
Q6GH64 | Staphylococcus aureus (strain MRSA252) | 45% | 100% |
Q7MDD4 | Vibrio vulnificus (strain YJ016) | 47% | 100% |
Q7MHK7 | Vibrio vulnificus (strain YJ016) | 47% | 100% |
Q7SIC9 | Zea mays | 50% | 99% |
Q87GY4 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 48% | 100% |
Q87LK8 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 47% | 100% |
Q89AY2 | Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) | 44% | 100% |
Q8CPC7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 45% | 100% |
Q8D6H8 | Vibrio vulnificus (strain CMCP6) | 47% | 100% |
Q8DCA2 | Vibrio vulnificus (strain CMCP6) | 47% | 100% |
Q8KA26 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 45% | 100% |
Q8NZX4 | Streptococcus pyogenes serotype M18 (strain MGAS8232) | 46% | 92% |
Q8RWV0 | Arabidopsis thaliana | 50% | 91% |
Q8XJE1 | Clostridium perfringens (strain 13 / Type A) | 21% | 100% |
Q8YRU9 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 51% | 100% |
Q99MX0 | Mus musculus | 23% | 100% |
Q9D4D4 | Mus musculus | 26% | 100% |
Q9H0I9 | Homo sapiens | 26% | 100% |
Q9KAD7 | Halalkalibacterium halodurans (strain ATCC BAA-125 / DSM 18197 / FERM 7344 / JCM 9153 / C-125) | 47% | 100% |
Q9KLW7 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 48% | 100% |
Q9KUP2 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 48% | 100% |
Q9URM2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 48% | 98% |
V5BF33 | Trypanosoma cruzi | 68% | 100% |