Acyltransferase involved in GPI anchor remodelling (homologue of yeast GUP1)
Protein kinase, mitogen-activated kinase 7
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: 16 |
NetGPI | no | yes: 0, no: 16 |
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: A4HVU2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 17 |
GO:0006793 | phosphorus metabolic process | 3 | 17 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 17 |
GO:0006807 | nitrogen compound metabolic process | 2 | 17 |
GO:0008152 | metabolic process | 1 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0016310 | phosphorylation | 5 | 17 |
GO:0019538 | protein metabolic process | 3 | 17 |
GO:0036211 | protein modification process | 4 | 17 |
GO:0043170 | macromolecule metabolic process | 3 | 17 |
GO:0043412 | macromolecule modification | 4 | 17 |
GO:0044237 | cellular metabolic process | 2 | 17 |
GO:0044238 | primary metabolic process | 2 | 17 |
GO:0071704 | organic substance metabolic process | 2 | 17 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 17 |
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 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004672 | protein kinase activity | 3 | 17 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 15 |
GO:0004707 | MAP kinase activity | 5 | 10 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016301 | kinase activity | 4 | 17 |
GO:0016740 | transferase activity | 2 | 17 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 17 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.321 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.418 |
CLV_PCSK_FUR_1 | 98 | 102 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.463 |
CLV_Separin_Metazoa | 498 | 502 | PF03568 | 0.495 |
DEG_APCC_DBOX_1 | 163 | 171 | PF00400 | 0.326 |
DOC_CDC14_PxL_1 | 343 | 351 | PF14671 | 0.271 |
DOC_CKS1_1 | 391 | 396 | PF01111 | 0.383 |
DOC_CKS1_1 | 400 | 405 | PF01111 | 0.348 |
DOC_CYCLIN_RxL_1 | 372 | 379 | PF00134 | 0.362 |
DOC_CYCLIN_RxL_1 | 465 | 473 | PF00134 | 0.331 |
DOC_CYCLIN_RxL_1 | 547 | 556 | PF00134 | 0.316 |
DOC_MAPK_gen_1 | 164 | 172 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 254 | 263 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 342 | 351 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 426 | 437 | PF00069 | 0.236 |
DOC_MAPK_HePTP_8 | 339 | 351 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 522 | 529 | PF00069 | 0.440 |
DOC_PP1_RVXF_1 | 466 | 473 | PF00149 | 0.313 |
DOC_PP4_FxxP_1 | 488 | 491 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.358 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.300 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.383 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 542 | 549 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 153 | 170 | PF00022 | 0.301 |
LIG_Actin_WH2_2 | 206 | 224 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 383 | 399 | PF00022 | 0.333 |
LIG_AP2alpha_2 | 486 | 488 | PF02296 | 0.383 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.310 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.637 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.377 |
LIG_Clathr_ClatBox_1 | 469 | 473 | PF01394 | 0.383 |
LIG_CtBP_PxDLS_1 | 459 | 463 | PF00389 | 0.393 |
LIG_deltaCOP1_diTrp_1 | 305 | 312 | PF00928 | 0.482 |
LIG_EH1_1 | 206 | 214 | PF00400 | 0.309 |
LIG_EH1_1 | 417 | 425 | PF00400 | 0.383 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.250 |
LIG_eIF4E_1 | 344 | 350 | PF01652 | 0.346 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.574 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.344 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.296 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.473 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.679 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.329 |
LIG_GBD_Chelix_1 | 235 | 243 | PF00786 | 0.383 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.298 |
LIG_LIR_Apic_2 | 486 | 491 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 145 | 153 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 154 | 161 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.376 |
LIG_NRBOX | 216 | 222 | PF00104 | 0.383 |
LIG_NRP_CendR_1 | 572 | 574 | PF00754 | 0.499 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.433 |
LIG_REV1ctd_RIR_1 | 486 | 490 | PF16727 | 0.331 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.371 |
LIG_SH2_GRB2like | 81 | 84 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 130 | 134 | PF00017 | 0.587 |
LIG_SH2_SRC | 245 | 248 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 383 | 386 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.281 |
LIG_SH3_1 | 397 | 403 | PF00018 | 0.383 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.590 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.343 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.411 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.287 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.467 |
LIG_SUMO_SIM_anti_2 | 348 | 353 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 385 | 393 | PF11976 | 0.383 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.355 |
LIG_UBA3_1 | 166 | 171 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 469 | 474 | PF05994 | 0.395 |
LIG_WW_1 | 330 | 333 | PF00397 | 0.463 |
MOD_CDK_SPxxK_3 | 390 | 397 | PF00069 | 0.383 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.541 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.637 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.355 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.693 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.467 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.308 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.336 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.420 |
MOD_Cter_Amidation | 162 | 165 | PF01082 | 0.321 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.314 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.334 |
MOD_GlcNHglycan | 298 | 302 | PF01048 | 0.462 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.633 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.578 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.466 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.338 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.428 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.563 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.273 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.566 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.570 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.630 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.316 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.383 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.542 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.404 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.175 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.383 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.372 |
MOD_NEK2_2 | 548 | 553 | PF00069 | 0.327 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.383 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.268 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.383 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.368 |
MOD_PKA_1 | 476 | 482 | PF00069 | 0.340 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.367 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.195 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.327 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.481 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.506 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.382 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.369 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.523 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.375 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.364 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.348 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.375 |
MOD_SUMO_rev_2 | 249 | 258 | PF00179 | 0.323 |
MOD_SUMO_rev_2 | 411 | 419 | PF00179 | 0.383 |
TRG_DiLeu_BaEn_3 | 414 | 420 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_3 | 90 | 96 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 474 | 477 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.667 |
TRG_NLS_MonoExtN_4 | 133 | 139 | PF00514 | 0.522 |
TRG_NLS_MonoExtN_4 | 474 | 479 | PF00514 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 490 | 494 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 550 | 554 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.449 |
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% |
A0A3R7K7W6 | Trypanosoma rangeli | 32% | 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% |
A0A3S7WSP5 | Leishmania donovani | 100% | 100% |
A0A3S7XA45 | Leishmania donovani | 30% | 100% |
A0A422N878 | Trypanosoma rangeli | 26% | 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% |
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% |
D0A105 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9ACB1 | Leishmania major | 27% | 99% |
E9ACG8 | Leishmania major | 29% | 100% |
E9AFX4 | Leishmania major | 31% | 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% |
P27704 | Rattus norvegicus | 29% | 80% |
P43068 | Candida albicans | 28% | 100% |
P46551 | Caenorhabditis elegans | 29% | 79% |
P49185 | Rattus norvegicus | 27% | 100% |
Q00536 | Homo sapiens | 26% | 100% |
Q04735 | Mus musculus | 26% | 100% |
Q16659 | Homo sapiens | 29% | 80% |
Q336M2 | Oryza sativa subsp. japonica | 29% | 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% |
Q4WTN5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 99% |
Q5AAG6 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 100% |
Q5F3W3 | Gallus gallus | 30% | 80% |
Q5R7U1 | Pongo abelii | 29% | 80% |
Q60EZ2 | Oryza sativa subsp. japonica | 28% | 100% |
Q61532 | Mus musculus | 29% | 80% |
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% |
Q9TVL3 | Caenorhabditis elegans | 31% | 100% |
V5BCX5 | Trypanosoma cruzi | 26% | 100% |
V5BI43 | Trypanosoma cruzi | 25% | 100% |
V5BSG8 | Trypanosoma cruzi | 32% | 100% |
V5DA09 | Trypanosoma cruzi | 29% | 100% |
V5DCN7 | Trypanosoma cruzi | 27% | 96% |
V5DIC3 | Trypanosoma cruzi | 24% | 95% |