Acyltransferase involved in GPI anchor remodelling (homologue of yeast GUP1)
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: 30 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S7WSP5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 16 |
GO:0006793 | phosphorus metabolic process | 3 | 16 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016310 | phosphorylation | 5 | 16 |
GO:0019538 | protein metabolic process | 3 | 16 |
GO:0036211 | protein modification process | 4 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043412 | macromolecule modification | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004672 | protein kinase activity | 3 | 16 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 15 |
GO:0004707 | MAP kinase activity | 5 | 10 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016301 | kinase activity | 4 | 16 |
GO:0016740 | transferase activity | 2 | 16 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.273 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.204 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.495 |
CLV_PCSK_FUR_1 | 97 | 101 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.683 |
CLV_Separin_Metazoa | 497 | 501 | PF03568 | 0.428 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.285 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.323 |
DOC_CDC14_PxL_1 | 342 | 350 | PF14671 | 0.251 |
DOC_CKS1_1 | 390 | 395 | PF01111 | 0.337 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.299 |
DOC_CYCLIN_RxL_1 | 371 | 378 | PF00134 | 0.314 |
DOC_CYCLIN_RxL_1 | 464 | 472 | PF00134 | 0.320 |
DOC_CYCLIN_RxL_1 | 546 | 555 | PF00134 | 0.298 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.273 |
DOC_MAPK_gen_1 | 341 | 350 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 425 | 436 | PF00069 | 0.222 |
DOC_MAPK_HePTP_8 | 338 | 350 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 341 | 350 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 521 | 528 | PF00069 | 0.400 |
DOC_PP1_RVXF_1 | 465 | 472 | PF00149 | 0.299 |
DOC_PP4_FxxP_1 | 487 | 490 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.357 |
DOC_USP7_UBL2_3 | 150 | 154 | PF12436 | 0.291 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.362 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 500 | 506 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 541 | 548 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.344 |
LIG_Actin_WH2_2 | 152 | 169 | PF00022 | 0.284 |
LIG_Actin_WH2_2 | 205 | 223 | PF00022 | 0.372 |
LIG_Actin_WH2_2 | 382 | 398 | PF00022 | 0.337 |
LIG_AP2alpha_2 | 485 | 487 | PF02296 | 0.337 |
LIG_APCC_ABBA_1 | 48 | 53 | PF00400 | 0.294 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.314 |
LIG_BRCT_BRCA1_1 | 530 | 534 | PF00533 | 0.358 |
LIG_Clathr_ClatBox_1 | 468 | 472 | PF01394 | 0.337 |
LIG_CtBP_PxDLS_1 | 458 | 462 | PF00389 | 0.348 |
LIG_deltaCOP1_diTrp_1 | 304 | 311 | PF00928 | 0.474 |
LIG_EH1_1 | 205 | 213 | PF00400 | 0.285 |
LIG_EH1_1 | 416 | 424 | PF00400 | 0.337 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.227 |
LIG_eIF4E_1 | 343 | 349 | PF01652 | 0.298 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.529 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.308 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.258 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.419 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.486 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.332 |
LIG_GBD_Chelix_1 | 234 | 242 | PF00786 | 0.337 |
LIG_LIR_Apic_2 | 340 | 346 | PF02991 | 0.273 |
LIG_LIR_Apic_2 | 485 | 490 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 144 | 152 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 153 | 160 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 199 | 208 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.371 |
LIG_NRBOX | 215 | 221 | PF00104 | 0.337 |
LIG_NRP_CendR_1 | 571 | 573 | PF00754 | 0.483 |
LIG_Pex14_2 | 534 | 538 | PF04695 | 0.382 |
LIG_REV1ctd_RIR_1 | 485 | 489 | PF16727 | 0.283 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.350 |
LIG_SH2_GRB2like | 80 | 83 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 129 | 133 | PF00017 | 0.531 |
LIG_SH2_SRC | 244 | 247 | PF00017 | 0.278 |
LIG_SH2_STAT3 | 382 | 385 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.288 |
LIG_SH3_1 | 396 | 402 | PF00018 | 0.342 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.487 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.354 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.405 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.288 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.286 |
LIG_SUMO_SIM_anti_2 | 347 | 352 | PF11976 | 0.332 |
LIG_SUMO_SIM_anti_2 | 384 | 392 | PF11976 | 0.337 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.391 |
LIG_TRAF2_1 | 509 | 512 | PF00917 | 0.496 |
LIG_UBA3_1 | 165 | 170 | PF00899 | 0.384 |
LIG_WRC_WIRS_1 | 468 | 473 | PF05994 | 0.351 |
LIG_WW_1 | 329 | 332 | PF00397 | 0.251 |
MOD_CDK_SPxxK_3 | 389 | 396 | PF00069 | 0.337 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.587 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.596 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.319 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.662 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.464 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.297 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.309 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.435 |
MOD_Cter_Amidation | 161 | 164 | PF01082 | 0.273 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.297 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.334 |
MOD_GlcNHglycan | 297 | 301 | PF01048 | 0.670 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.583 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.555 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.452 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.326 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.251 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.545 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.301 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.491 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.620 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.337 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.337 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.572 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.251 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.228 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.337 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.424 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.338 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.275 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.289 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.246 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.284 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.379 |
MOD_PKA_1 | 475 | 481 | PF00069 | 0.316 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.382 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.204 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.298 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.455 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.521 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.402 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.361 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.341 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.354 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.318 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.332 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.355 |
MOD_SUMO_rev_2 | 248 | 257 | PF00179 | 0.274 |
MOD_SUMO_rev_2 | 410 | 418 | PF00179 | 0.337 |
TRG_DiLeu_BaEn_3 | 413 | 419 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_3 | 89 | 95 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.647 |
TRG_NLS_MonoExtN_4 | 132 | 138 | PF00514 | 0.492 |
TRG_NLS_MonoExtN_4 | 473 | 478 | PF00514 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 549 | 553 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E2 | Leptomonas seymouri | 30% | 100% |
A0A0N1I304 | Leptomonas seymouri | 68% | 99% |
A0A0N1II59 | Leptomonas seymouri | 28% | 100% |
A0A0S4ILC2 | Bodo saltans | 33% | 100% |
A0A0S4IUF2 | Bodo saltans | 25% | 100% |
A0A0S4IXW3 | Bodo saltans | 30% | 100% |
A0A0S4J343 | Bodo saltans | 24% | 100% |
A0A0S4J8M8 | Bodo saltans | 23% | 71% |
A0A0S4JCX8 | Bodo saltans | 26% | 100% |
A0A0S4JXW9 | Bodo saltans | 35% | 100% |
A0A0S4KIN4 | Bodo saltans | 37% | 84% |
A0A1X0NQM7 | Trypanosomatidae | 29% | 100% |
A0A1X0P018 | Trypanosomatidae | 28% | 100% |
A0A1X0P3B9 | Trypanosomatidae | 32% | 100% |
A0A3Q8IH39 | Leishmania donovani | 29% | 100% |
A0A3Q8ITZ9 | Leishmania donovani | 33% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 31% | 100% |
A0A3R7KBU3 | Trypanosoma rangeli | 26% | 100% |
A0A3R7M0A0 | Trypanosoma rangeli | 31% | 100% |
A0A3R7NAU1 | Trypanosoma rangeli | 25% | 100% |
A0A3S5H528 | Leishmania donovani | 30% | 100% |
A0A3S5H7N7 | Leishmania donovani | 34% | 100% |
A0A3S7WR45 | Leishmania donovani | 32% | 100% |
A0A3S7XA45 | Leishmania donovani | 30% | 100% |
A0A422N878 | Trypanosoma rangeli | 25% | 100% |
A0A451EJH2 | Leishmania donovani | 27% | 99% |
A4H601 | Leishmania braziliensis | 30% | 100% |
A4H641 | Leishmania braziliensis | 31% | 96% |
A4H7F4 | Leishmania braziliensis | 82% | 100% |
A4HFF3 | Leishmania braziliensis | 25% | 100% |
A4HIM5 | Leishmania braziliensis | 36% | 100% |
A4HLJ9 | Leishmania braziliensis | 33% | 100% |
A4HNG3 | Leishmania braziliensis | 32% | 100% |
A4HNT2 | Leishmania braziliensis | 31% | 100% |
A4HRN3 | Leishmania infantum | 27% | 99% |
A4HRT2 | Leishmania infantum | 30% | 100% |
A4HUC8 | Leishmania infantum | 29% | 100% |
A4HUG1 | Leishmania infantum | 32% | 100% |
A4HVU2 | Leishmania infantum | 100% | 100% |
A4I5X0 | Leishmania infantum | 34% | 100% |
A4I910 | Leishmania infantum | 33% | 100% |
A4IC54 | Leishmania infantum | 30% | 100% |
A4ICR2 | Leishmania infantum | 31% | 100% |
B5X564 | Arabidopsis thaliana | 31% | 89% |
B6DTC0 | Bodo saltans | 33% | 100% |
C9ZJF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 74% |
D0A105 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9ACB1 | Leishmania major | 27% | 95% |
E9ACG8 | Leishmania major | 29% | 100% |
E9AFX4 | Leishmania major | 30% | 100% |
E9AJJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 99% |
E9AN28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AN59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9API8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9ASJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B164 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B3X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B727 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F4ICB6 | Arabidopsis thaliana | 30% | 81% |
G4N374 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 33% | 100% |
O13352 | Magnaporthe oryzae | 33% | 100% |
O23145 | Arabidopsis thaliana | 27% | 100% |
O60145 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P27704 | Rattus norvegicus | 29% | 80% |
P43068 | Candida albicans | 28% | 100% |
P46551 | Caenorhabditis elegans | 29% | 78% |
P49185 | Rattus norvegicus | 27% | 100% |
Q00536 | Homo sapiens | 26% | 100% |
Q04735 | Mus musculus | 26% | 100% |
Q16659 | Homo sapiens | 29% | 79% |
Q336M2 | Oryza sativa subsp. japonica | 28% | 100% |
Q4Q204 | Leishmania major | 31% | 100% |
Q4Q449 | Leishmania major | 33% | 100% |
Q4Q701 | Leishmania major | 34% | 100% |
Q4Q7S2 | Leishmania major | 31% | 100% |
Q4QFZ0 | Leishmania major | 94% | 100% |
Q4QHG6 | Leishmania major | 32% | 100% |
Q4QHJ8 | Leishmania major | 31% | 100% |
Q5AAG6 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 100% |
Q5F3W3 | Gallus gallus | 30% | 79% |
Q5R7U1 | Pongo abelii | 29% | 79% |
Q60EZ2 | Oryza sativa subsp. japonica | 28% | 100% |
Q61532 | Mus musculus | 29% | 80% |
Q6Z8C8 | Oryza sativa subsp. japonica | 26% | 100% |
Q80Y86 | Mus musculus | 33% | 100% |
Q8I7M8 | Caenorhabditis elegans | 27% | 86% |
Q8QHK8 | Xenopus laevis | 27% | 100% |
Q9DGD9 | Danio rerio | 27% | 100% |
Q9LWN0 | Oryza sativa subsp. japonica | 28% | 100% |
Q9SJG9 | Arabidopsis thaliana | 32% | 95% |
Q9TVL3 | Caenorhabditis elegans | 31% | 100% |
V5BCX5 | Trypanosoma cruzi | 26% | 100% |
V5BI43 | Trypanosoma cruzi | 25% | 100% |
V5BSG8 | Trypanosoma cruzi | 32% | 100% |
V5DCN7 | Trypanosoma cruzi | 27% | 96% |
V5DIC3 | Trypanosoma cruzi | 24% | 95% |