Phospholipid biosynthesis, Alkyldihydroxyacetonephosphate synthase ADS1
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 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: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: A4I507
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006662 | glycerol ether metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008611 | ether lipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018904 | ether metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046485 | ether lipid metabolic process | 4 | 1 |
GO:0046504 | glycerol ether biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0097384 | cellular lipid biosynthetic process | 4 | 1 |
GO:1901503 | ether biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008609 | alkylglycerone-phosphate synthase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 8 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 12 |
GO:0071949 | FAD binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.372 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.297 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.259 |
DEG_APCC_DBOX_1 | 391 | 399 | PF00400 | 0.414 |
DEG_SCF_FBW7_1 | 276 | 283 | PF00400 | 0.378 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.369 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.259 |
DOC_CKS1_1 | 277 | 282 | PF01111 | 0.362 |
DOC_CYCLIN_RxL_1 | 46 | 53 | PF00134 | 0.454 |
DOC_CYCLIN_RxL_1 | 599 | 609 | PF00134 | 0.491 |
DOC_CYCLIN_yClb1_LxF_4 | 49 | 55 | PF00134 | 0.451 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 49 | 55 | PF00134 | 0.463 |
DOC_MAPK_gen_1 | 183 | 190 | PF00069 | 0.265 |
DOC_MAPK_gen_1 | 193 | 201 | PF00069 | 0.251 |
DOC_MAPK_gen_1 | 391 | 398 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 46 | 54 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 599 | 608 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.261 |
DOC_MAPK_MEF2A_6 | 183 | 192 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 391 | 400 | PF00069 | 0.241 |
DOC_MAPK_MEF2A_6 | 514 | 523 | PF00069 | 0.366 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 404 | 410 | PF00149 | 0.369 |
DOC_PP1_RVXF_1 | 602 | 609 | PF00149 | 0.488 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.467 |
DOC_USP7_MATH_2 | 589 | 595 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 572 | 576 | PF12436 | 0.381 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 185 | 191 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 357 | 361 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 372 | 381 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 386 | 391 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 392 | 396 | PF00244 | 0.175 |
LIG_14-3-3_CanoR_1 | 528 | 534 | PF00244 | 0.343 |
LIG_Actin_WH2_2 | 375 | 393 | PF00022 | 0.291 |
LIG_AP2alpha_2 | 179 | 181 | PF02296 | 0.376 |
LIG_APCC_ABBA_1 | 348 | 353 | PF00400 | 0.261 |
LIG_EVH1_1 | 585 | 589 | PF00568 | 0.456 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.261 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.373 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.340 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.438 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.311 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.283 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.328 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.264 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.283 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.475 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.369 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.261 |
LIG_LIR_Apic_2 | 436 | 442 | PF02991 | 0.237 |
LIG_LIR_Apic_2 | 555 | 560 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 236 | 246 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 605 | 616 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.455 |
LIG_MYND_1 | 69 | 73 | PF01753 | 0.541 |
LIG_PDZ_Class_1 | 616 | 621 | PF00595 | 0.505 |
LIG_Pex14_1 | 454 | 458 | PF04695 | 0.261 |
LIG_Pex14_1 | 553 | 557 | PF04695 | 0.261 |
LIG_Pex14_2 | 224 | 228 | PF04695 | 0.408 |
LIG_Pex14_2 | 328 | 332 | PF04695 | 0.277 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.400 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.295 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.383 |
LIG_SH2_CRK | 439 | 443 | PF00017 | 0.117 |
LIG_SH2_CRK | 557 | 561 | PF00017 | 0.310 |
LIG_SH2_NCK_1 | 439 | 443 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 548 | 552 | PF00017 | 0.277 |
LIG_SH2_SRC | 548 | 551 | PF00017 | 0.277 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.247 |
LIG_SH3_1 | 583 | 589 | PF00018 | 0.422 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.277 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.277 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.277 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.401 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.463 |
LIG_SUMO_SIM_anti_2 | 394 | 399 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 186 | 191 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 197 | 202 | PF11976 | 0.261 |
LIG_TYR_ITIM | 546 | 551 | PF00017 | 0.277 |
LIG_UBA3_1 | 152 | 158 | PF00899 | 0.273 |
LIG_UBA3_1 | 521 | 527 | PF00899 | 0.346 |
LIG_WRC_WIRS_1 | 207 | 212 | PF05994 | 0.346 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.261 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.398 |
LIG_WRC_WIRS_1 | 506 | 511 | PF05994 | 0.261 |
LIG_WW_3 | 587 | 591 | PF00397 | 0.552 |
MOD_CDC14_SPxK_1 | 587 | 590 | PF00782 | 0.541 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.272 |
MOD_CDK_SPxK_1 | 584 | 590 | PF00069 | 0.523 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.477 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.338 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.564 |
MOD_CMANNOS | 20 | 23 | PF00535 | 0.312 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.261 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.277 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.376 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.465 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.542 |
MOD_GlcNHglycan | 96 | 100 | PF01048 | 0.453 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.333 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.256 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.195 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.369 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.274 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.271 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.304 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.295 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.295 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.277 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.262 |
MOD_N-GLC_1 | 591 | 596 | PF02516 | 0.540 |
MOD_N-GLC_2 | 577 | 579 | PF02516 | 0.253 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.436 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.342 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.344 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.300 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.175 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.271 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.211 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.250 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.295 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.425 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.381 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.447 |
MOD_PK_1 | 197 | 203 | PF00069 | 0.273 |
MOD_PKA_1 | 391 | 397 | PF00069 | 0.328 |
MOD_PKA_1 | 527 | 533 | PF00069 | 0.328 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.361 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.259 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.261 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.330 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.346 |
MOD_PKB_1 | 384 | 392 | PF00069 | 0.194 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.334 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.261 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.452 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.326 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.297 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.238 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.275 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.259 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.361 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.375 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.433 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.415 |
MOD_SUMO_for_1 | 309 | 312 | PF00179 | 0.313 |
MOD_SUMO_rev_2 | 104 | 112 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 312 | 319 | PF00179 | 0.354 |
MOD_SUMO_rev_2 | 515 | 522 | PF00179 | 0.278 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.223 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.330 |
TRG_NLS_MonoExtC_3 | 525 | 531 | PF00514 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 604 | 609 | PF00026 | 0.493 |
TRG_PTS1 | 618 | 621 | PF00515 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Q0 | Leptomonas seymouri | 23% | 100% |
A0A0N1PE88 | Leptomonas seymouri | 23% | 100% |
A0A0N1PEY1 | Leptomonas seymouri | 81% | 100% |
A0A0S4JD99 | Bodo saltans | 25% | 100% |
A0A0S4JV88 | Bodo saltans | 63% | 98% |
A0A1X0P026 | Trypanosomatidae | 22% | 100% |
A0A1X0P2J0 | Trypanosomatidae | 60% | 100% |
A0A3Q8IDH3 | Leishmania donovani | 24% | 100% |
A0A3Q8IDH5 | Leishmania donovani | 23% | 100% |
A0A3Q8IEJ5 | Leishmania donovani | 23% | 100% |
A0A3Q8IRN9 | Leishmania donovani | 99% | 100% |
A0A422N649 | Trypanosoma rangeli | 64% | 100% |
A4HFX9 | Leishmania braziliensis | 23% | 98% |
A4HHV7 | Leishmania braziliensis | 88% | 100% |
A4I0D2 | Leishmania infantum | 23% | 100% |
A4I309 | Leishmania infantum | 22% | 91% |
A4I481 | Leishmania infantum | 24% | 100% |
A4VGK4 | Pseudomonas stutzeri (strain A1501) | 23% | 100% |
C9ZQF7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
D4MUV9 | Anaerostipes hadrus | 24% | 100% |
E9ADI2 | Leishmania major | 22% | 90% |
E9ADN0 | Leishmania major | 23% | 100% |
E9AM50 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AZA6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 94% |
E9B0D7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
F1QXM5 | Danio rerio | 24% | 100% |
H6LBS1 | Acetobacterium woodii (strain ATCC 29683 / DSM 1030 / JCM 2381 / KCTC 1655 / WB1) | 23% | 100% |
O00116 | Homo sapiens | 31% | 94% |
O23240 | Arabidopsis thaliana | 24% | 100% |
O29853 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 23% | 100% |
O45218 | Caenorhabditis elegans | 30% | 100% |
O96759 | Dictyostelium discoideum | 38% | 100% |
O97157 | Trypanosoma brucei brucei | 60% | 100% |
P32891 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P39976 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
P94535 | Bacillus subtilis (strain 168) | 25% | 100% |
P97275 | Cavia porcellus | 31% | 94% |
Q12627 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 100% |
Q46911 | Escherichia coli (strain K12) | 25% | 100% |
Q7TNG8 | Mus musculus | 24% | 100% |
Q7YWB6 | Leishmania major | 96% | 100% |
Q86WU2 | Homo sapiens | 23% | 100% |
Q8C0I1 | Mus musculus | 31% | 96% |
Q8X7S0 | Escherichia coli O157:H7 | 25% | 100% |
Q94AX4 | Arabidopsis thaliana | 24% | 100% |
Q9EQR2 | Rattus norvegicus | 31% | 96% |
Q9V778 | Drosophila melanogaster | 31% | 98% |
V5BCB2 | Trypanosoma cruzi | 64% | 100% |