Tricarboxylic acid cycle, Aconitate hydratase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005829 | cytosol | 2 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HXS6
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006099 | tricarboxylic acid cycle | 3 | 1 |
GO:0006101 | citrate metabolic process | 7 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072350 | tricarboxylic acid metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003994 | aconitate hydratase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016829 | lyase activity | 2 | 12 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 12 |
GO:0016836 | hydro-lyase activity | 4 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0047780 | citrate dehydratase activity | 5 | 12 |
GO:0051536 | iron-sulfur cluster binding | 3 | 12 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 12 |
GO:0051540 | metal cluster binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0030350 | iron-responsive element binding | 6 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.262 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.252 |
CLV_PCSK_PC7_1 | 114 | 120 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 864 | 868 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.262 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.473 |
DEG_APCC_DBOX_1 | 811 | 819 | PF00400 | 0.462 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.587 |
DOC_ANK_TNKS_1 | 736 | 743 | PF00023 | 0.462 |
DOC_CKS1_1 | 608 | 613 | PF01111 | 0.429 |
DOC_MAPK_DCC_7 | 767 | 776 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 384 | 392 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 717 | 725 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 767 | 776 | PF00069 | 0.544 |
DOC_PP1_RVXF_1 | 287 | 294 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.457 |
DOC_PP2B_LxvP_1 | 659 | 662 | PF13499 | 0.591 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.473 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.414 |
DOC_USP7_UBL2_3 | 259 | 263 | PF12436 | 0.523 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.331 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.448 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 640 | 644 | PF12436 | 0.509 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 683 | 688 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.401 |
LIG_14-3-3_CanoR_1 | 306 | 310 | PF00244 | 0.473 |
LIG_APCC_ABBA_1 | 673 | 678 | PF00400 | 0.362 |
LIG_BRCT_BRCA1_1 | 173 | 177 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 842 | 846 | PF00533 | 0.383 |
LIG_CtBP_PxDLS_1 | 132 | 136 | PF00389 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 788 | 795 | PF00928 | 0.487 |
LIG_DLG_GKlike_1 | 345 | 353 | PF00625 | 0.512 |
LIG_EH_1 | 15 | 19 | PF12763 | 0.396 |
LIG_EH1_1 | 49 | 57 | PF00400 | 0.329 |
LIG_eIF4E_1 | 608 | 614 | PF01652 | 0.379 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.449 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.462 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.462 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.567 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.462 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.376 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.373 |
LIG_FHA_1 | 771 | 777 | PF00498 | 0.491 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.544 |
LIG_FHA_1 | 865 | 871 | PF00498 | 0.477 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.462 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.462 |
LIG_FHA_2 | 835 | 841 | PF00498 | 0.401 |
LIG_FHA_2 | 872 | 878 | PF00498 | 0.380 |
LIG_LIR_Apic_2 | 292 | 296 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 174 | 185 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 616 | 624 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 805 | 815 | PF02991 | 0.462 |
LIG_LIR_LC3C_4 | 134 | 137 | PF02991 | 0.487 |
LIG_LIR_LC3C_4 | 563 | 568 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 612 | 617 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 710 | 714 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 744 | 750 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 805 | 810 | PF02991 | 0.462 |
LIG_PCNA_yPIPBox_3 | 592 | 605 | PF02747 | 0.397 |
LIG_PCNA_yPIPBox_3 | 879 | 890 | PF02747 | 0.392 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.527 |
LIG_Pex14_2 | 842 | 846 | PF04695 | 0.383 |
LIG_PTB_Apo_2 | 44 | 51 | PF02174 | 0.421 |
LIG_PTB_Apo_2 | 584 | 591 | PF02174 | 0.396 |
LIG_PTB_Apo_2 | 632 | 639 | PF02174 | 0.559 |
LIG_PTB_Phospho_1 | 584 | 590 | PF10480 | 0.441 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.461 |
LIG_SH2_CRK | 618 | 622 | PF00017 | 0.416 |
LIG_SH2_GRB2like | 618 | 621 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 618 | 622 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 608 | 611 | PF00017 | 0.405 |
LIG_SH2_SRC | 647 | 650 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 747 | 750 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 880 | 883 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 889 | 892 | PF00017 | 0.316 |
LIG_SH3_1 | 126 | 132 | PF00018 | 0.457 |
LIG_SH3_2 | 90 | 95 | PF14604 | 0.462 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.462 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.467 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.462 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 599 | 606 | PF11976 | 0.455 |
LIG_TRAF2_1 | 597 | 600 | PF00917 | 0.437 |
LIG_TRAF2_2 | 822 | 827 | PF00917 | 0.442 |
LIG_TYR_ITSM | 318 | 325 | PF00017 | 0.435 |
MOD_CDK_SPxxK_3 | 692 | 699 | PF00069 | 0.415 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.314 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.452 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.452 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.314 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.414 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.372 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.314 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.314 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.403 |
MOD_CK2_1 | 834 | 840 | PF00069 | 0.399 |
MOD_CK2_1 | 871 | 877 | PF00069 | 0.385 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.314 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.513 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.423 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.480 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.382 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.330 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.314 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.222 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.314 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.418 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.314 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.307 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.314 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.349 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.412 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.372 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.314 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.314 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.407 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.385 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.450 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.426 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.373 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.303 |
MOD_N-GLC_1 | 506 | 511 | PF02516 | 0.309 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.536 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.430 |
MOD_N-GLC_1 | 829 | 834 | PF02516 | 0.565 |
MOD_N-GLC_1 | 844 | 849 | PF02516 | 0.363 |
MOD_N-GLC_2 | 81 | 83 | PF02516 | 0.376 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.582 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.539 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.314 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.314 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.314 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.357 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.225 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.353 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.330 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.397 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.374 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.317 |
MOD_NEK2_1 | 834 | 839 | PF00069 | 0.405 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.399 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.371 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.314 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.314 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.314 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.409 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.330 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.411 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.532 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.486 |
MOD_Plk_1 | 829 | 835 | PF00069 | 0.378 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.330 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.384 |
MOD_Plk_2-3 | 655 | 661 | PF00069 | 0.473 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.314 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.314 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.314 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.339 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.384 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.419 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.314 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.314 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.362 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.438 |
MOD_Plk_4 | 745 | 751 | PF00069 | 0.435 |
MOD_Plk_4 | 770 | 776 | PF00069 | 0.435 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.520 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.314 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.314 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.393 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.434 |
MOD_ProDKin_1 | 683 | 689 | PF00069 | 0.392 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.395 |
MOD_SUMO_rev_2 | 394 | 401 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 637 | 646 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 703 | 711 | PF00179 | 0.313 |
MOD_SUMO_rev_2 | 873 | 881 | PF00179 | 0.378 |
TRG_DiLeu_BaEn_2 | 164 | 170 | PF01217 | 0.314 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.394 |
TRG_NLS_MonoExtC_3 | 419 | 424 | PF00514 | 0.248 |
TRG_NLS_MonoExtN_4 | 420 | 425 | PF00514 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 699 | 703 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 851 | 855 | PF00026 | 0.393 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5H1 | Leptomonas seymouri | 87% | 100% |
A0A0S4IZ58 | Bodo saltans | 74% | 100% |
A0A0S4J7M0 | Bodo saltans | 61% | 100% |
A0A1X0P887 | Trypanosomatidae | 78% | 100% |
A0A3Q8IAZ4 | Leishmania donovani | 100% | 100% |
A0A3R7RJL9 | Trypanosoma rangeli | 76% | 100% |
A0JMA0 | Xenopus tropicalis | 51% | 94% |
A0QX20 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 50% | 95% |
A4H9F9 | Leishmania braziliensis | 89% | 100% |
B3VKQ2 | Sus scrofa | 45% | 93% |
C8VG90 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 100% |
D0A059 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 75% | 100% |
D4AT77 | Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) | 27% | 100% |
E9ARI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O04916 | Solanum tuberosum | 61% | 100% |
O08451 | Mycobacterium avium | 49% | 93% |
O13966 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
O53166 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 50% | 95% |
P09339 | Bacillus subtilis (strain 168) | 53% | 99% |
P16276 | Sus scrofa | 26% | 100% |
P19414 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P20004 | Bos taurus | 26% | 100% |
P21399 | Homo sapiens | 59% | 100% |
P25516 | Escherichia coli (strain K12) | 52% | 100% |
P28271 | Mus musculus | 59% | 100% |
P34455 | Caenorhabditis elegans | 27% | 100% |
P37032 | Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) | 55% | 100% |
P39533 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P48200 | Homo sapiens | 45% | 93% |
P49601 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 100% |
P49608 | Cucurbita maxima | 64% | 100% |
P49609 | Gracilaria gracilis | 29% | 100% |
P63433 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 53% | 99% |
P63434 | Staphylococcus aureus (strain MW2) | 53% | 99% |
P70920 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 53% | 99% |
P82611 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 26% | 100% |
P99148 | Staphylococcus aureus (strain N315) | 53% | 99% |
Q01059 | Oryctolagus cuniculus | 59% | 100% |
Q0VCU1 | Bos taurus | 59% | 100% |
Q1RKD5 | Rickettsia bellii (strain RML369-C) | 54% | 100% |
Q23500 | Caenorhabditis elegans | 60% | 100% |
Q2A1K3 | Francisella tularensis subsp. holarctica (strain LVS) | 52% | 96% |
Q42560 | Arabidopsis thaliana | 63% | 100% |
Q42669 | Cucumis melo var. conomon | 61% | 100% |
Q4JVM4 | Corynebacterium jeikeium (strain K411) | 50% | 96% |
Q4QDZ1 | Leishmania major | 97% | 100% |
Q4UK20 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 54% | 100% |
Q4WJ90 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q4WLN1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 100% |
Q54X73 | Dictyostelium discoideum | 60% | 100% |
Q54XS2 | Dictyostelium discoideum | 27% | 100% |
Q59938 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 54% | 100% |
Q5B6D6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 100% |
Q5HG69 | Staphylococcus aureus (strain COL) | 53% | 99% |
Q5HPJ0 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 53% | 99% |
Q5SMF6 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 57% | 99% |
Q5ZLQ4 | Gallus gallus | 50% | 93% |
Q62751 | Rattus norvegicus | 45% | 93% |
Q63270 | Rattus norvegicus | 59% | 100% |
Q68VV0 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 53% | 100% |
Q6G9K9 | Staphylococcus aureus (strain MSSA476) | 53% | 99% |
Q6GH55 | Staphylococcus aureus (strain MRSA252) | 53% | 99% |
Q6NH63 | Corynebacterium diphtheriae (strain ATCC 700971 / NCTC 13129 / Biotype gravis) | 50% | 96% |
Q6NTP2 | Xenopus laevis | 51% | 94% |
Q6YZX6 | Oryza sativa subsp. japonica | 63% | 100% |
Q811J3 | Mus musculus | 45% | 93% |
Q8CPC2 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 53% | 99% |
Q8EJW3 | Shewanella oneidensis (strain MR-1) | 43% | 100% |
Q8FTA8 | Corynebacterium efficiens (strain DSM 44549 / YS-314 / AJ 12310 / JCM 11189 / NBRC 100395) | 50% | 96% |
Q8NQ98 | Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / BCRC 11384 / JCM 1318 / LMG 3730 / NCIMB 10025) | 50% | 95% |
Q8ZP52 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 53% | 100% |
Q90875 | Gallus gallus | 60% | 100% |
Q92G90 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 54% | 100% |
Q937N8 | Cupriavidus necator | 43% | 100% |
Q94A28 | Arabidopsis thaliana | 62% | 90% |
Q99798 | Homo sapiens | 27% | 100% |
Q99KI0 | Mus musculus | 26% | 100% |
Q9ER34 | Rattus norvegicus | 26% | 100% |
Q9I3F5 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 53% | 98% |
Q9P7D4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 98% |
Q9RTN7 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 55% | 99% |
Q9SIB9 | Arabidopsis thaliana | 64% | 91% |
Q9ZCF4 | Rickettsia prowazekii (strain Madrid E) | 52% | 100% |
V5B6G9 | Trypanosoma cruzi | 78% | 94% |