Homologous to bacterial FtsH and Eukaryotic AFG3 proteins. Probably involved in mitochondrial protein processing.. Localization: Mitochondrial (by homology)
Proteases, ATP-dependent zinc metallopeptidase
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: 31 |
NetGPI | no | yes: 0, no: 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 23 |
GO:0110165 | cellular anatomical entity | 1 | 24 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005745 | m-AAA complex | 4 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
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:0098796 | membrane protein complex | 2 | 3 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 3 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:1905368 | peptidase complex | 3 | 3 |
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: A4I809
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 32 |
GO:0006807 | nitrogen compound metabolic process | 2 | 32 |
GO:0008152 | metabolic process | 1 | 32 |
GO:0019538 | protein metabolic process | 3 | 32 |
GO:0043170 | macromolecule metabolic process | 3 | 32 |
GO:0044238 | primary metabolic process | 2 | 32 |
GO:0071704 | organic substance metabolic process | 2 | 32 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 32 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0016485 | protein processing | 5 | 3 |
GO:0022607 | cellular component assembly | 4 | 3 |
GO:0034982 | mitochondrial protein processing | 6 | 3 |
GO:0043933 | protein-containing complex organization | 4 | 3 |
GO:0051604 | protein maturation | 4 | 3 |
GO:0065003 | protein-containing complex assembly | 5 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 32 |
GO:0003824 | catalytic activity | 1 | 32 |
GO:0004175 | endopeptidase activity | 4 | 32 |
GO:0004176 | ATP-dependent peptidase activity | 2 | 32 |
GO:0004222 | metalloendopeptidase activity | 5 | 32 |
GO:0005488 | binding | 1 | 32 |
GO:0005524 | ATP binding | 5 | 32 |
GO:0008233 | peptidase activity | 3 | 32 |
GO:0008237 | metallopeptidase activity | 4 | 32 |
GO:0016462 | pyrophosphatase activity | 5 | 32 |
GO:0016787 | hydrolase activity | 2 | 32 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 32 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 32 |
GO:0016887 | ATP hydrolysis activity | 7 | 32 |
GO:0017076 | purine nucleotide binding | 4 | 32 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 32 |
GO:0030554 | adenyl nucleotide binding | 5 | 32 |
GO:0032553 | ribonucleotide binding | 3 | 32 |
GO:0032555 | purine ribonucleotide binding | 4 | 32 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 32 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 32 |
GO:0036094 | small molecule binding | 2 | 32 |
GO:0043167 | ion binding | 2 | 32 |
GO:0043168 | anion binding | 3 | 32 |
GO:0097159 | organic cyclic compound binding | 2 | 32 |
GO:0097367 | carbohydrate derivative binding | 2 | 32 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 32 |
GO:0140657 | ATP-dependent activity | 1 | 32 |
GO:1901265 | nucleoside phosphate binding | 3 | 32 |
GO:1901363 | heterocyclic compound binding | 2 | 32 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.364 |
CLV_C14_Caspase3-7 | 642 | 646 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.214 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.214 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.323 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.457 |
DOC_CYCLIN_RxL_1 | 288 | 296 | PF00134 | 0.431 |
DOC_CYCLIN_RxL_1 | 674 | 684 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 38 | 44 | PF00134 | 0.317 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 369 | 379 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 685 | 694 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 372 | 381 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 500 | 507 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 551 | 558 | PF00069 | 0.366 |
DOC_MAPK_NFAT4_5 | 551 | 559 | PF00069 | 0.501 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.373 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.213 |
DOC_PP4_MxPP_1 | 26 | 29 | PF00568 | 0.350 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.353 |
DOC_USP7_UBL2_3 | 218 | 222 | PF12436 | 0.475 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 551 | 555 | PF12436 | 0.380 |
DOC_USP7_UBL2_3 | 639 | 643 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 697 | 701 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 647 | 653 | PF00244 | 0.454 |
LIG_BIR_III_2 | 451 | 455 | PF00653 | 0.660 |
LIG_BIR_III_2 | 5 | 9 | PF00653 | 0.345 |
LIG_BIR_III_4 | 311 | 315 | PF00653 | 0.414 |
LIG_CaM_IQ_9 | 610 | 625 | PF13499 | 0.404 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.701 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.478 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.471 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.387 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.467 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.439 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.591 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.457 |
LIG_IBAR_NPY_1 | 58 | 60 | PF08397 | 0.355 |
LIG_LIR_Apic_2 | 134 | 138 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 11 | 19 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 277 | 282 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 467 | 472 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 533 | 543 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 582 | 592 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.332 |
LIG_NRBOX | 688 | 694 | PF00104 | 0.406 |
LIG_PCNA_yPIPBox_3 | 509 | 522 | PF02747 | 0.490 |
LIG_PDZ_Class_2 | 711 | 716 | PF00595 | 0.604 |
LIG_Pex14_2 | 278 | 282 | PF04695 | 0.404 |
LIG_PTB_Apo_2 | 139 | 146 | PF02174 | 0.383 |
LIG_PTB_Apo_2 | 462 | 469 | PF02174 | 0.486 |
LIG_PTB_Phospho_1 | 462 | 468 | PF10480 | 0.490 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.429 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.430 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.506 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.344 |
LIG_SH2_GRB2like | 394 | 397 | PF00017 | 0.479 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 468 | 472 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 567 | 571 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 17 | 20 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 32 | 35 | PF00017 | 0.317 |
LIG_SH2_STAT3 | 567 | 570 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 79 | 82 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 91 | 94 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.423 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.438 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.313 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.596 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.407 |
LIG_SH3_4 | 406 | 413 | PF00018 | 0.561 |
LIG_SH3_4 | 639 | 646 | PF00018 | 0.501 |
LIG_Sin3_3 | 664 | 671 | PF02671 | 0.367 |
LIG_SUMO_SIM_anti_2 | 349 | 355 | PF11976 | 0.418 |
LIG_SxIP_EBH_1 | 555 | 565 | PF03271 | 0.396 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.446 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.427 |
LIG_TRAF2_2 | 107 | 112 | PF00917 | 0.390 |
LIG_TYR_ITSM | 531 | 538 | PF00017 | 0.263 |
LIG_UBA3_1 | 187 | 195 | PF00899 | 0.458 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.383 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.400 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.272 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.278 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.227 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.518 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.400 |
MOD_CK2_1 | 648 | 654 | PF00069 | 0.317 |
MOD_CMANNOS | 649 | 652 | PF00535 | 0.383 |
MOD_Cter_Amidation | 517 | 520 | PF01082 | 0.402 |
MOD_Cter_Amidation | 694 | 697 | PF01082 | 0.424 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.458 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.408 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.535 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.581 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.630 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.521 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.249 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.293 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.690 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.687 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.287 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.541 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.535 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.250 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.462 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.350 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.263 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.265 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.177 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.187 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.216 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.248 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.291 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.242 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.277 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.226 |
MOD_NEK2_2 | 8 | 13 | PF00069 | 0.566 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.478 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.261 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.261 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.503 |
MOD_PK_1 | 453 | 459 | PF00069 | 0.374 |
MOD_PK_1 | 603 | 609 | PF00069 | 0.383 |
MOD_PKA_1 | 375 | 381 | PF00069 | 0.177 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.479 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.279 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.265 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.261 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.251 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.287 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.339 |
MOD_Plk_2-3 | 577 | 583 | PF00069 | 0.383 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.250 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.261 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.337 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.275 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.290 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.300 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.518 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.302 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.683 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.654 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.354 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.410 |
MOD_SUMO_for_1 | 452 | 455 | PF00179 | 0.588 |
MOD_SUMO_for_1 | 658 | 661 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 292 | 300 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 370 | 378 | PF00179 | 0.261 |
MOD_SUMO_rev_2 | 437 | 447 | PF00179 | 0.689 |
MOD_SUMO_rev_2 | 450 | 454 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_1 | 443 | 448 | PF01217 | 0.672 |
TRG_DiLeu_BaEn_1 | 663 | 668 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.263 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 522 | 525 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.247 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.260 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.286 |
TRG_Pf-PMV_PEXEL_1 | 665 | 669 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8A5 | Leptomonas seymouri | 47% | 100% |
A0A0N1HUW7 | Leptomonas seymouri | 32% | 100% |
A0A0N1I6C1 | Leptomonas seymouri | 34% | 92% |
A0A0N1IMN9 | Leptomonas seymouri | 80% | 100% |
A0A0N1PBB9 | Leptomonas seymouri | 49% | 100% |
A0A0N1PGD9 | Leptomonas seymouri | 32% | 72% |
A0A0S4J3N2 | Bodo saltans | 71% | 100% |
A0A0S4J9Q2 | Bodo saltans | 35% | 100% |
A0A0S4JAH0 | Bodo saltans | 49% | 100% |
A0A0S4JGG9 | Bodo saltans | 50% | 100% |
A0A0S4JTL4 | Bodo saltans | 33% | 85% |
A0A0S4KHE9 | Bodo saltans | 35% | 89% |
A0A1X0NKD8 | Trypanosomatidae | 33% | 100% |
A0A1X0NW32 | Trypanosomatidae | 76% | 100% |
A0A1X0P749 | Trypanosomatidae | 51% | 100% |
A0A1X0P7E6 | Trypanosomatidae | 51% | 100% |
A0A1X0P9F5 | Trypanosomatidae | 34% | 99% |
A0A3Q8IFG3 | Leishmania donovani | 100% | 100% |
A0A3Q8IHD0 | Leishmania donovani | 34% | 100% |
A0A3Q8IJP7 | Leishmania donovani | 48% | 100% |
A0A3R7KKD0 | Trypanosoma rangeli | 47% | 100% |
A0A3R7L0P7 | Trypanosoma rangeli | 75% | 100% |
A0A3S5H775 | Leishmania donovani | 47% | 100% |
A0A3S5H828 | Leishmania donovani | 32% | 100% |
A0A422N673 | Trypanosoma rangeli | 36% | 100% |
A0A422NJ44 | Trypanosoma rangeli | 51% | 100% |
A0LN68 | Syntrophobacter fumaroxidans (strain DSM 10017 / MPOB) | 35% | 100% |
A0LR74 | Acidothermus cellulolyticus (strain ATCC 43068 / DSM 8971 / 11B) | 34% | 100% |
A0PXM8 | Clostridium novyi (strain NT) | 39% | 100% |
A1URA3 | Bartonella bacilliformis (strain ATCC 35685 / NCTC 12138 / KC583) | 33% | 94% |
A2ZVG7 | Oryza sativa subsp. japonica | 35% | 91% |
A4H9H1 | Leishmania braziliensis | 53% | 100% |
A4HAA8 | Leishmania braziliensis | 47% | 98% |
A4HAL9 | Leishmania braziliensis | 35% | 91% |
A4HJ48 | Leishmania braziliensis | 31% | 70% |
A4HKD8 | Leishmania braziliensis | 85% | 99% |
A4HPD5 | Leishmania braziliensis | 33% | 100% |
A4HXT7 | Leishmania infantum | 52% | 100% |
A4HYI8 | Leishmania infantum | 47% | 99% |
A4I9Q6 | Leishmania infantum | 34% | 100% |
A4ICH8 | Leishmania infantum | 32% | 100% |
A5U8T5 | Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) | 34% | 94% |
A5W382 | Pseudomonas putida (strain ATCC 700007 / DSM 6899 / BCRC 17059 / F1) | 36% | 100% |
A6LD25 | Parabacteroides distasonis (strain ATCC 8503 / DSM 20701 / CIP 104284 / JCM 5825 / NCTC 11152) | 32% | 100% |
A6QBN8 | Sulfurovum sp. (strain NBC37-1) | 33% | 100% |
A6TSZ1 | Alkaliphilus metalliredigens (strain QYMF) | 33% | 100% |
A6TWP7 | Alkaliphilus metalliredigens (strain QYMF) | 37% | 100% |
A8F7F7 | Pseudothermotoga lettingae (strain ATCC BAA-301 / DSM 14385 / NBRC 107922 / TMO) | 39% | 100% |
A8ZNZ4 | Acaryochloris marina (strain MBIC 11017) | 36% | 100% |
A9BFL9 | Petrotoga mobilis (strain DSM 10674 / SJ95) | 32% | 100% |
A9BHD3 | Petrotoga mobilis (strain DSM 10674 / SJ95) | 32% | 100% |
A9EXK6 | Sorangium cellulosum (strain So ce56) | 32% | 100% |
A9NE17 | Acholeplasma laidlawii (strain PG-8A) | 36% | 100% |
B0B970 | Chlamydia trachomatis serovar L2 (strain 434/Bu / ATCC VR-902B) | 36% | 78% |
B0K5A3 | Thermoanaerobacter sp. (strain X514) | 36% | 100% |
B0K657 | Thermoanaerobacter sp. (strain X514) | 34% | 100% |
B1AI94 | Ureaplasma parvum serovar 3 (strain ATCC 27815 / 27 / NCTC 11736) | 32% | 99% |
B1ZMG6 | Opitutus terrae (strain DSM 11246 / JCM 15787 / PB90-1) | 34% | 100% |
B2JVU2 | Paraburkholderia phymatum (strain DSM 17167 / CIP 108236 / LMG 21445 / STM815) | 36% | 100% |
B2UE66 | Ralstonia pickettii (strain 12J) | 36% | 100% |
B2UMY1 | Akkermansia muciniphila (strain ATCC BAA-835 / DSM 22959 / JCM 33894 / BCRC 81048 / CCUG 64013 / CIP 107961 / Muc) | 34% | 88% |
B3DY14 | Methylacidiphilum infernorum (isolate V4) | 35% | 100% |
B3PNH3 | Metamycoplasma arthritidis (strain 158L3-1) | 35% | 96% |
B3QZS3 | Phytoplasma mali (strain AT) | 32% | 100% |
B3R057 | Phytoplasma mali (strain AT) | 34% | 100% |
B3R0R7 | Phytoplasma mali (strain AT) | 33% | 100% |
B4SCV5 | Pelodictyon phaeoclathratiforme (strain DSM 5477 / BU-1) | 35% | 100% |
B4U7U4 | Hydrogenobaculum sp. (strain Y04AAS1) | 34% | 100% |
B7J0N5 | Borreliella burgdorferi (strain ZS7) | 34% | 100% |
B7T1V0 | Vaucheria litorea | 33% | 100% |
B8D065 | Halothermothrix orenii (strain H 168 / OCM 544 / DSM 9562) | 35% | 100% |
B8G4Q6 | Chloroflexus aggregans (strain MD-66 / DSM 9485) | 32% | 100% |
B8H444 | Caulobacter vibrioides (strain NA1000 / CB15N) | 34% | 100% |
B8I4B9 | Ruminiclostridium cellulolyticum (strain ATCC 35319 / DSM 5812 / JCM 6584 / H10) | 35% | 100% |
B8J992 | Anaeromyxobacter dehalogenans (strain 2CP-1 / ATCC BAA-258) | 35% | 100% |
B9L3S8 | Thermomicrobium roseum (strain ATCC 27502 / DSM 5159 / P-2) | 37% | 100% |
B9MPK5 | Caldicellulosiruptor bescii (strain ATCC BAA-1888 / DSM 6725 / Z-1320) | 36% | 100% |
C0ZPK5 | Rhodococcus erythropolis (strain PR4 / NBRC 100887) | 35% | 84% |
C1F8X6 | Acidobacterium capsulatum (strain ATCC 51196 / DSM 11244 / BCRC 80197 / JCM 7670 / NBRC 15755 / NCIMB 13165 / 161) | 37% | 100% |
C5CES8 | Kosmotoga olearia (strain ATCC BAA-1733 / DSM 21960 / TBF 19.5.1) | 34% | 100% |
C5J6A7 | Mesomycoplasma conjunctivae (strain ATCC 25834 / NCTC 10147 / HRC/581) | 33% | 95% |
C6V4R9 | Neorickettsia risticii (strain Illinois) | 33% | 100% |
C6VKW6 | Lactiplantibacillus plantarum (strain JDM1) | 38% | 96% |
C7M0M0 | Acidimicrobium ferrooxidans (strain DSM 10331 / JCM 15462 / NBRC 103882 / ICP) | 35% | 100% |
C7MC16 | Brachybacterium faecium (strain ATCC 43885 / DSM 4810 / JCM 11609 / LMG 19847 / NBRC 14762 / NCIMB 9860 / 6-10) | 33% | 100% |
C7N1I1 | Slackia heliotrinireducens (strain ATCC 29202 / DSM 20476 / NCTC 11029 / RHS 1) | 35% | 91% |
C7N914 | Leptotrichia buccalis (strain ATCC 14201 / DSM 1135 / JCM 12969 / NCTC 10249 / C-1013-b) | 35% | 93% |
C8W731 | Lancefieldella parvula (strain ATCC 33793 / DSM 20469 / CCUG 32760 / JCM 10300 / KCTC 3663 / VPI 0546 / 1246) | 32% | 100% |
C8WEG0 | Zymomonas mobilis subsp. mobilis (strain NCIMB 11163 / B70) | 36% | 100% |
C9ZMX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZZX3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
D0A3J7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0AA32 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
D0LWB8 | Haliangium ochraceum (strain DSM 14365 / JCM 11303 / SMP-2) | 36% | 100% |
D0MGU8 | Rhodothermus marinus (strain ATCC 43812 / DSM 4252 / R-10) | 36% | 100% |
D1AXT4 | Streptobacillus moniliformis (strain ATCC 14647 / DSM 12112 / NCTC 10651 / 9901) | 37% | 100% |
D1BLD0 | Veillonella parvula (strain ATCC 10790 / DSM 2008 / CCUG 5123 / JCM 12972 / NCTC 11810 / Te3) | 38% | 100% |
D1C2C6 | Sphaerobacter thermophilus (strain DSM 20745 / S 6022) | 36% | 100% |
D1CDT8 | Thermobaculum terrenum (strain ATCC BAA-798 / YNP1) | 37% | 100% |
D2NQQ7 | Rothia mucilaginosa (strain DY-18) | 37% | 95% |
D2QZ34 | Pirellula staleyi (strain ATCC 27377 / DSM 6068 / ICPB 4128) | 35% | 100% |
D3EZK2 | Conexibacter woesei (strain DSM 14684 / CIP 108061 / JCM 11494 / NBRC 100937 / ID131577) | 38% | 96% |
D3FFN2 | Mycoplasma gallisepticum (strain R(high / passage 156)) | 33% | 94% |
D4HA34 | Cutibacterium acnes (strain SK137) | 37% | 100% |
D5D8E3 | Sulcia muelleri (strain DMIN) | 35% | 100% |
D5H7Z5 | Salinibacter ruber (strain M8) | 35% | 100% |
D5HA94 | Salinibacter ruber (strain M8) | 33% | 100% |
E9ARJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9ASB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 99% |
E9B1M1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 81% |
E9B2S6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B4S8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
O19922 | Cyanidium caldarium | 34% | 100% |
O32617 | Helicobacter felis (strain ATCC 49179 / NCTC 12436 / CS1) | 34% | 100% |
O69076 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 37% | 100% |
O78516 | Guillardia theta | 33% | 100% |
O80983 | Arabidopsis thaliana | 36% | 100% |
O82150 | Nicotiana tabacum | 37% | 100% |
P0A4V9 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 34% | 94% |
P0AAI3 | Escherichia coli (strain K12) | 33% | 100% |
P0AAI4 | Shigella flexneri | 33% | 100% |
P32795 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 96% |
P37476 | Bacillus subtilis (strain 168) | 34% | 100% |
P39925 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 94% |
P40341 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 87% |
P46469 | Lactococcus lactis subsp. lactis (strain IL1403) | 34% | 100% |
P47695 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 33% | 100% |
P49825 | Trieres chinensis | 31% | 100% |
P51327 | Porphyra purpurea | 34% | 100% |
P57462 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 32% | 100% |
P59652 | Streptococcus pneumoniae (strain ATCC BAA-255 / R6) | 37% | 100% |
P63343 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 33% | 100% |
P63344 | Salmonella typhi | 33% | 100% |
P71377 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 33% | 100% |
P71408 | Helicobacter pylori (strain ATCC 700392 / 26695) | 33% | 100% |
P73179 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 36% | 100% |
P73437 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 34% | 100% |
P75120 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 34% | 100% |
P94304 | Alkalihalophilus pseudofirmus (strain ATCC BAA-2126 / JCM 17055 / OF4) | 35% | 100% |
P9WQN2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 34% | 94% |
P9WQN3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 34% | 94% |
Q03Z46 | Leuconostoc mesenteroides subsp. mesenteroides (strain ATCC 8293 / DSM 20343 / BCRC 11652 / CCM 1803 / JCM 6124 / NCDO 523 / NBRC 100496 / NCIMB 8023 / NCTC 12954 / NRRL B-1118 / 37Y) | 36% | 100% |
Q04Q03 | Leptospira borgpetersenii serovar Hardjo-bovis (strain JB197) | 35% | 100% |
Q0DHL4 | Oryza sativa subsp. japonica | 38% | 87% |
Q0TTK8 | Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A) | 33% | 100% |
Q10ZF7 | Trichodesmium erythraeum (strain IMS101) | 37% | 100% |
Q1AV13 | Rubrobacter xylanophilus (strain DSM 9941 / NBRC 16129 / PRD-1) | 36% | 100% |
Q1D491 | Myxococcus xanthus (strain DK1622) | 36% | 100% |
Q1LLA9 | Cupriavidus metallidurans (strain ATCC 43123 / DSM 2839 / NBRC 102507 / CH34) | 34% | 100% |
Q1RGP0 | Rickettsia bellii (strain RML369-C) | 31% | 100% |
Q1XDF9 | Neopyropia yezoensis | 35% | 100% |
Q2JNP0 | Synechococcus sp. (strain JA-2-3B'a(2-13)) | 37% | 100% |
Q2KJI7 | Bos taurus | 35% | 89% |
Q2NIN5 | Aster yellows witches'-broom phytoplasma (strain AYWB) | 36% | 100% |
Q2SF13 | Hahella chejuensis (strain KCTC 2396) | 30% | 100% |
Q39102 | Arabidopsis thaliana | 36% | 100% |
Q39444 | Capsicum annuum | 36% | 100% |
Q3B6R3 | Chlorobium luteolum (strain DSM 273 / BCRC 81028 / 2530) | 36% | 100% |
Q3JEE4 | Nitrosococcus oceani (strain ATCC 19707 / BCRC 17464 / JCM 30415 / NCIMB 11848 / C-107) | 36% | 100% |
Q3JMH0 | Burkholderia pseudomallei (strain 1710b) | 36% | 100% |
Q3ULF4 | Mus musculus | 36% | 92% |
Q4A5F0 | Mycoplasmopsis synoviae (strain 53) | 34% | 100% |
Q4Q399 | Leishmania major | 34% | 100% |
Q4Q5D1 | Leishmania major | 97% | 100% |
Q4Q6J3 | Leishmania major | 32% | 81% |
Q4QD50 | Leishmania major | 46% | 99% |
Q4QDY0 | Leishmania major | 52% | 100% |
Q4UN68 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 34% | 100% |
Q55700 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 34% | 100% |
Q5SI82 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 36% | 100% |
Q5Z974 | Oryza sativa subsp. japonica | 36% | 100% |
Q60AK1 | Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) | 33% | 100% |
Q655S1 | Oryza sativa subsp. japonica | 35% | 100% |
Q67JH0 | Symbiobacterium thermophilum (strain T / IAM 14863) | 39% | 100% |
Q67LC0 | Symbiobacterium thermophilum (strain T / IAM 14863) | 35% | 100% |
Q67T82 | Symbiobacterium thermophilum (strain T / IAM 14863) | 37% | 100% |
Q67WJ2 | Oryza sativa subsp. japonica | 35% | 100% |
Q68XR9 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 34% | 100% |
Q6KHA4 | Mycoplasma mobile (strain ATCC 43663 / 163K / NCTC 11711) | 32% | 100% |
Q6LUJ8 | Photobacterium profundum (strain SS9) | 35% | 100% |
Q6M2F0 | Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / BCRC 11384 / JCM 1318 / LMG 3730 / NCIMB 10025) | 35% | 84% |
Q6MDI5 | Protochlamydia amoebophila (strain UWE25) | 38% | 78% |
Q6MJV1 | Bdellovibrio bacteriovorus (strain ATCC 15356 / DSM 50701 / NCIMB 9529 / HD100) | 35% | 100% |
Q6MLS7 | Bdellovibrio bacteriovorus (strain ATCC 15356 / DSM 50701 / NCIMB 9529 / HD100) | 34% | 100% |
Q7TT47 | Rattus norvegicus | 37% | 92% |
Q7URM7 | Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) | 33% | 98% |
Q7UUZ7 | Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) | 36% | 100% |
Q83FV7 | Tropheryma whipplei (strain Twist) | 35% | 100% |
Q83XX3 | Oenococcus oeni | 35% | 100% |
Q84WU8 | Arabidopsis thaliana | 39% | 89% |
Q88Z31 | Lactiplantibacillus plantarum (strain ATCC BAA-793 / NCIMB 8826 / WCFS1) | 38% | 96% |
Q89AF2 | Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) | 32% | 100% |
Q8EUA6 | Malacoplasma penetrans (strain HF-2) | 34% | 87% |
Q8JZQ2 | Mus musculus | 35% | 89% |
Q8K9G8 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 32% | 100% |
Q8LQJ8 | Oryza sativa subsp. japonica | 36% | 100% |
Q8LQJ9 | Oryza sativa subsp. japonica | 37% | 100% |
Q8S2A7 | Oryza sativa subsp. japonica | 37% | 89% |
Q8VZI8 | Arabidopsis thaliana | 38% | 88% |
Q8W585 | Arabidopsis thaliana | 34% | 100% |
Q8X9L0 | Escherichia coli O157:H7 | 33% | 100% |
Q8YMZ8 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 35% | 100% |
Q920A7 | Mus musculus | 37% | 91% |
Q92JJ9 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 34% | 100% |
Q98PE4 | Mycoplasmopsis pulmonis (strain UAB CTIP) | 32% | 99% |
Q9BAE0 | Medicago sativa | 36% | 100% |
Q9CD58 | Mycobacterium leprae (strain TN) | 34% | 91% |
Q9FH02 | Arabidopsis thaliana | 37% | 100% |
Q9HGM3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 93% |
Q9N3T5 | Caenorhabditis elegans | 36% | 92% |
Q9TJ83 | Cyanidioschyzon merolae (strain NIES-3377 / 10D) | 33% | 100% |
Q9UQ90 | Homo sapiens | 36% | 90% |
Q9WZ49 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 36% | 100% |
Q9Y4W6 | Homo sapiens | 35% | 90% |
Q9ZEA2 | Rickettsia prowazekii (strain Madrid E) | 34% | 100% |
Q9ZM66 | Helicobacter pylori (strain J99 / ATCC 700824) | 33% | 100% |
V5B092 | Trypanosoma cruzi | 35% | 100% |
V5B4C8 | Trypanosoma cruzi | 48% | 100% |
V5BEV9 | Trypanosoma cruzi | 35% | 100% |
V5BP04 | Trypanosoma cruzi | 73% | 100% |