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. | 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: 8 |
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:0032838 | plasma membrane bounded cell projection cytoplasm | 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: A4HBR7
Term | Name | Level | Count |
---|---|---|---|
GO:0000054 | ribosomal subunit export from nucleus | 3 | 1 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0006415 | translational termination | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0033750 | ribosome localization | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051656 | establishment of organelle localization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0005506 | iron ion binding | 6 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043024 | ribosomal small subunit binding | 4 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 621 | 625 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.376 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 520 | 522 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.373 |
DOC_CKS1_1 | 484 | 489 | PF01111 | 0.298 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 78 | 87 | PF00134 | 0.359 |
DOC_CYCLIN_yCln2_LP_2 | 484 | 490 | PF00134 | 0.258 |
DOC_MAPK_gen_1 | 202 | 211 | PF00069 | 0.302 |
DOC_MAPK_gen_1 | 331 | 339 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 565 | 574 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 314 | 321 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 477 | 484 | PF00069 | 0.258 |
DOC_MAPK_MEF2A_6 | 565 | 574 | PF00069 | 0.343 |
DOC_PP1_SILK_1 | 128 | 133 | PF00149 | 0.171 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.320 |
DOC_SPAK_OSR1_1 | 232 | 236 | PF12202 | 0.258 |
DOC_USP7_UBL2_3 | 132 | 136 | PF12436 | 0.231 |
DOC_USP7_UBL2_3 | 423 | 427 | PF12436 | 0.258 |
DOC_USP7_UBL2_3 | 616 | 620 | PF12436 | 0.672 |
DOC_USP7_UBL2_3 | 633 | 637 | PF12436 | 0.521 |
DOC_USP7_UBL2_3 | 654 | 658 | PF12436 | 0.715 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.399 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 268 | 278 | PF00244 | 0.396 |
LIG_AP2alpha_1 | 320 | 324 | PF02296 | 0.315 |
LIG_APCC_ABBA_1 | 245 | 250 | PF00400 | 0.258 |
LIG_APCC_ABBA_1 | 317 | 322 | PF00400 | 0.305 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.334 |
LIG_deltaCOP1_diTrp_1 | 144 | 155 | PF00928 | 0.276 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.452 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.359 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.394 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.270 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.258 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.258 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.330 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.388 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.475 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.258 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.258 |
LIG_IRF3_LxIS_1 | 412 | 418 | PF10401 | 0.258 |
LIG_LIR_Apic_2 | 442 | 447 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 206 | 214 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 252 | 261 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 273 | 284 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 291 | 301 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 394 | 404 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.298 |
LIG_LYPXL_yS_3 | 358 | 361 | PF13949 | 0.336 |
LIG_PCNA_yPIPBox_3 | 183 | 196 | PF02747 | 0.390 |
LIG_PCNA_yPIPBox_3 | 423 | 436 | PF02747 | 0.258 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.315 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.331 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.285 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.277 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.334 |
LIG_SH2_PTP2 | 276 | 279 | PF00017 | 0.282 |
LIG_SH2_SRC | 248 | 251 | PF00017 | 0.302 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.289 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.361 |
LIG_SH2_SRC | 499 | 502 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 419 | 422 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.421 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.317 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.402 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.258 |
LIG_SH3_4 | 633 | 640 | PF00018 | 0.531 |
LIG_SUMO_SIM_anti_2 | 125 | 132 | PF11976 | 0.294 |
LIG_SUMO_SIM_anti_2 | 14 | 22 | PF11976 | 0.258 |
LIG_SUMO_SIM_anti_2 | 283 | 288 | PF11976 | 0.362 |
LIG_SUMO_SIM_anti_2 | 378 | 388 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 276 | 281 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 378 | 388 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 455 | 461 | PF11976 | 0.277 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.258 |
LIG_TYR_ITSM | 272 | 279 | PF00017 | 0.447 |
LIG_UBA3_1 | 559 | 568 | PF00899 | 0.334 |
LIG_WRC_WIRS_1 | 365 | 370 | PF05994 | 0.398 |
LIG_WW_3 | 1 | 5 | PF00397 | 0.487 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.258 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.469 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.448 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.463 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.365 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.258 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.258 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.258 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.402 |
MOD_Cter_Amidation | 613 | 616 | PF01082 | 0.642 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.263 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.258 |
MOD_GlcNHglycan | 494 | 499 | PF01048 | 0.258 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.289 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.556 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.258 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.446 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.356 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.258 |
MOD_N-GLC_1 | 468 | 473 | PF02516 | 0.301 |
MOD_N-GLC_1 | 549 | 554 | PF02516 | 0.476 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.420 |
MOD_N-GLC_2 | 389 | 391 | PF02516 | 0.258 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.484 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.289 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.274 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.343 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.208 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.359 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.589 |
MOD_PK_1 | 587 | 593 | PF00069 | 0.405 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.334 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.258 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.277 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.367 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.433 |
MOD_PKB_1 | 331 | 339 | PF00069 | 0.334 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.334 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.390 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.285 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.389 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.343 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.560 |
MOD_Plk_2-3 | 200 | 206 | PF00069 | 0.334 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.322 |
MOD_Plk_2-3 | 627 | 633 | PF00069 | 0.516 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.294 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.361 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.363 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.258 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.299 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.287 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.401 |
MOD_SUMO_rev_2 | 210 | 217 | PF00179 | 0.390 |
MOD_SUMO_rev_2 | 589 | 599 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 625 | 635 | PF00179 | 0.749 |
MOD_SUMO_rev_2 | 646 | 653 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.258 |
TRG_DiLeu_BaEn_4 | 8 | 14 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.277 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 574 | 576 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 581 | 584 | PF00400 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 433 | 437 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7M4 | Leptomonas seymouri | 90% | 99% |
A0A1X0NXL9 | Trypanosomatidae | 82% | 100% |
A0A3S7WWG1 | Leishmania donovani | 93% | 100% |
A0A422NHA0 | Trypanosoma rangeli | 82% | 100% |
A4HZ70 | Leishmania infantum | 93% | 100% |
D0A1G9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 80% | 100% |
E9AV37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
G0SEV9 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 63% | 100% |
O60102 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 61% | 100% |
P0AAF3 | Escherichia coli (strain K12) | 25% | 100% |
P0AAF4 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 25% | 100% |
P0AAF5 | Escherichia coli O157:H7 | 25% | 100% |
P33916 | Escherichia coli (strain K12) | 24% | 100% |
P61221 | Homo sapiens | 64% | 100% |
P61222 | Mus musculus | 64% | 100% |
P9WQK2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 22% | 100% |
P9WQK3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 22% | 100% |
Q03195 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 64% | 100% |
Q03CA4 | Lacticaseibacillus paracasei (strain ATCC 334 / BCRC 17002 / CCUG 31169 / CIP 107868 / KCTC 3260 / NRRL B-441) | 24% | 100% |
Q0TGT7 | Escherichia coli O6:K15:H31 (strain 536 / UPEC) | 25% | 100% |
Q1JUP7 | Azospirillum brasilense | 24% | 100% |
Q1RAN8 | Escherichia coli (strain UTI89 / UPEC) | 25% | 100% |
Q322L1 | Shigella boydii serotype 4 (strain Sb227) | 25% | 100% |
Q32HC7 | Shigella dysenteriae serotype 1 (strain Sd197) | 25% | 100% |
Q3K3R2 | Streptococcus agalactiae serotype Ia (strain ATCC 27591 / A909 / CDC SS700) | 23% | 100% |
Q3Z2S7 | Shigella sonnei (strain Ss046) | 25% | 100% |
Q4QCE4 | Leishmania major | 92% | 100% |
Q58129 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 47% | 100% |
Q6HI76 | Bacillus thuringiensis subsp. konkukian (strain 97-27) | 24% | 100% |
Q73P93 | Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) | 24% | 100% |
Q73R11 | Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) | 24% | 100% |
Q83KP2 | Shigella flexneri | 25% | 100% |
Q87FK7 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 24% | 100% |
Q8D3Z9 | Vibrio vulnificus (strain CMCP6) | 21% | 100% |
Q8E7N9 | Streptococcus agalactiae serotype III (strain NEM316) | 23% | 100% |
Q8LPJ4 | Arabidopsis thaliana | 65% | 100% |
Q8PUE7 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 20% | 100% |
Q97WT4 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 24% | 100% |
Q97X60 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 23% | 100% |
Q9LID6 | Arabidopsis thaliana | 62% | 100% |
Q9LV93 | Arabidopsis thaliana | 23% | 95% |
Q9VSS1 | Drosophila melanogaster | 65% | 100% |
Q9WXX0 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 22% | 100% |
V5BDT2 | Trypanosoma cruzi | 82% | 100% |