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: 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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 |
Related structures:
AlphaFold database: A4H7F4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004672 | protein kinase activity | 3 | 8 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 8 |
GO:0004707 | MAP kinase activity | 5 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.387 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.351 |
CLV_PCSK_FUR_1 | 107 | 111 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.275 |
CLV_PCSK_PC7_1 | 103 | 109 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.361 |
CLV_Separin_Metazoa | 507 | 511 | PF03568 | 0.446 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.334 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.444 |
DEG_SCF_FBW7_1 | 124 | 131 | PF00400 | 0.430 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.444 |
DOC_CDC14_PxL_1 | 352 | 360 | PF14671 | 0.351 |
DOC_CKS1_1 | 400 | 405 | PF01111 | 0.310 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.281 |
DOC_CYCLIN_RxL_1 | 474 | 482 | PF00134 | 0.324 |
DOC_CYCLIN_yClb1_LxF_4 | 238 | 244 | PF00134 | 0.194 |
DOC_CYCLIN_yCln2_LP_2 | 382 | 388 | PF00134 | 0.206 |
DOC_MAPK_gen_1 | 173 | 181 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 351 | 360 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 530 | 538 | PF00069 | 0.384 |
DOC_MAPK_HePTP_8 | 348 | 360 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 351 | 360 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 530 | 538 | PF00069 | 0.555 |
DOC_PP1_RVXF_1 | 475 | 482 | PF00149 | 0.324 |
DOC_PP2B_LxvP_1 | 583 | 586 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.415 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.522 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.275 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.243 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 510 | 518 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.609 |
LIG_Actin_WH2_2 | 162 | 179 | PF00022 | 0.275 |
LIG_Actin_WH2_2 | 215 | 233 | PF00022 | 0.334 |
LIG_Actin_WH2_2 | 392 | 408 | PF00022 | 0.334 |
LIG_AP2alpha_2 | 495 | 497 | PF02296 | 0.334 |
LIG_APCC_ABBA_1 | 58 | 63 | PF00400 | 0.423 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.582 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.351 |
LIG_Clathr_ClatBox_1 | 478 | 482 | PF01394 | 0.334 |
LIG_CtBP_PxDLS_1 | 468 | 472 | PF00389 | 0.335 |
LIG_deltaCOP1_diTrp_1 | 314 | 321 | PF00928 | 0.553 |
LIG_EH1_1 | 215 | 223 | PF00400 | 0.275 |
LIG_EH1_1 | 426 | 434 | PF00400 | 0.334 |
LIG_eIF4E_1 | 216 | 222 | PF01652 | 0.275 |
LIG_eIF4E_1 | 353 | 359 | PF01652 | 0.275 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.605 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.323 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.293 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.390 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.221 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.327 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.346 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.367 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.530 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.478 |
LIG_GBD_Chelix_1 | 244 | 252 | PF00786 | 0.334 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.275 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 154 | 163 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.483 |
LIG_NRBOX | 225 | 231 | PF00104 | 0.334 |
LIG_Pex14_2 | 544 | 548 | PF04695 | 0.499 |
LIG_PTB_Apo_2 | 538 | 545 | PF02174 | 0.363 |
LIG_Rb_LxCxE_1 | 6 | 25 | PF01857 | 0.365 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.354 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.503 |
LIG_SH2_NCK_1 | 139 | 143 | PF00017 | 0.566 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 392 | 395 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.275 |
LIG_SH3_1 | 406 | 412 | PF00018 | 0.334 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.536 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.334 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.275 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 357 | 362 | PF11976 | 0.275 |
LIG_SUMO_SIM_anti_2 | 394 | 402 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.194 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.348 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.530 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.492 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.471 |
LIG_WRC_WIRS_1 | 478 | 483 | PF05994 | 0.334 |
LIG_WW_1 | 339 | 342 | PF00397 | 0.351 |
MOD_CDC14_SPxK_1 | 131 | 134 | PF00782 | 0.457 |
MOD_CDK_SPxK_1 | 128 | 134 | PF00069 | 0.445 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.334 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.260 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.543 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.650 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.274 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.302 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.521 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.313 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.351 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.568 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.338 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.344 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.418 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.386 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.456 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.275 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.502 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.403 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.275 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.578 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.369 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.268 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.691 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.446 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.502 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.506 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.674 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.362 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.532 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.530 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.442 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.532 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.430 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.442 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.445 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.330 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.442 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.308 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.513 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.517 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.423 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.334 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.446 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.334 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.298 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.334 |
MOD_PKA_1 | 485 | 491 | PF00069 | 0.275 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.450 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.275 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.353 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.470 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.548 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.445 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.578 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.221 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.146 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.445 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.530 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.484 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.608 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.376 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.299 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.336 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.405 |
MOD_SUMO_rev_2 | 258 | 267 | PF00179 | 0.275 |
MOD_SUMO_rev_2 | 420 | 428 | PF00179 | 0.334 |
TRG_DiLeu_BaEn_2 | 151 | 157 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_3 | 423 | 429 | PF01217 | 0.334 |
TRG_DiLeu_BaEn_3 | 99 | 105 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.351 |
TRG_NLS_MonoExtN_4 | 142 | 148 | PF00514 | 0.539 |
TRG_NLS_MonoExtN_4 | 483 | 488 | PF00514 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 444 | 449 | PF00026 | 0.194 |
TRG_Pf-PMV_PEXEL_1 | 559 | 563 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I304 | Leptomonas seymouri | 65% | 100% |
A0A0S4J343 | Bodo saltans | 24% | 100% |
A0A0S4JCX8 | Bodo saltans | 24% | 100% |
A0A0S4JTP3 | Bodo saltans | 24% | 73% |
A0A0S4KIN4 | Bodo saltans | 39% | 87% |
A0A3Q8IB74 | Leishmania donovani | 25% | 100% |
A0A3Q8IH39 | Leishmania donovani | 32% | 100% |
A0A3Q8ITZ9 | Leishmania donovani | 32% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 32% | 100% |
A0A3R7M0A0 | Trypanosoma rangeli | 31% | 100% |
A0A3R7MSS9 | Trypanosoma rangeli | 24% | 100% |
A0A3R7NBN7 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WSP5 | Leishmania donovani | 82% | 100% |
A0A3S7X2Z6 | Leishmania donovani | 31% | 100% |
A0A3S7X9D1 | Leishmania donovani | 25% | 100% |
A0A3S7XA45 | Leishmania donovani | 31% | 100% |
A0A422N878 | Trypanosoma rangeli | 24% | 100% |
A2QN07 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 34% | 100% |
A4H601 | Leishmania braziliensis | 32% | 100% |
A4HFF3 | Leishmania braziliensis | 24% | 100% |
A4HLJ9 | Leishmania braziliensis | 33% | 100% |
A4HMK7 | Leishmania braziliensis | 26% | 100% |
A4HNT2 | Leishmania braziliensis | 32% | 100% |
A4HUC8 | Leishmania infantum | 32% | 100% |
A4HVU2 | Leishmania infantum | 82% | 100% |
A4I564 | Leishmania infantum | 31% | 100% |
A4I910 | Leishmania infantum | 32% | 100% |
A4IB86 | Leishmania infantum | 25% | 100% |
A4IC54 | Leishmania infantum | 31% | 100% |
A4ICR2 | Leishmania infantum | 32% | 100% |
B1H3E1 | Xenopus tropicalis | 30% | 100% |
E9AF07 | Leishmania major | 25% | 100% |
E9AFX4 | Leishmania major | 31% | 100% |
E9AGS0 | Leishmania infantum | 25% | 100% |
E9AN28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9API8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AQQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ARW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B0G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B3X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B663 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B727 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
O04160 | Brassica napus | 28% | 100% |
O23145 | Arabidopsis thaliana | 28% | 100% |
P27704 | Rattus norvegicus | 29% | 82% |
P46551 | Caenorhabditis elegans | 29% | 81% |
Q0CQK1 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 100% |
Q16659 | Homo sapiens | 29% | 82% |
Q336M2 | Oryza sativa subsp. japonica | 26% | 100% |
Q4Q204 | Leishmania major | 32% | 100% |
Q4Q449 | Leishmania major | 31% | 100% |
Q4Q7S2 | Leishmania major | 31% | 100% |
Q4QDK3 | Leishmania major | 25% | 100% |
Q4QFZ0 | Leishmania major | 80% | 100% |
Q4QHJ8 | Leishmania major | 32% | 100% |
Q5F3W3 | Gallus gallus | 30% | 82% |
Q5R7U1 | Pongo abelii | 29% | 82% |
Q61532 | Mus musculus | 29% | 82% |
Q6FQ83 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 89% |
Q6P5G0 | Mus musculus | 29% | 100% |
Q8QGV6 | Xenopus laevis | 30% | 100% |
Q96287 | Arabidopsis thaliana | 28% | 100% |
Q96Q40 | Homo sapiens | 27% | 100% |
Q96WV9 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
V5BCX5 | Trypanosoma cruzi | 26% | 100% |
V5DIC3 | Trypanosoma cruzi | 25% | 98% |