Related to both fungal ergosterol C-24 reductases and to a lesser extent, animal delta-14 lanosterol reductases (all preferentially ER-localized).. The highly changed Ser/Arg rich N-terminus might point to a mitochondrial transit signal (ergosterols are essential for Kinetoplastid mitochondria).. Localization: ER (by homology) / Mitochondrial (by feature)
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4HLA8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006694 | steroid biosynthetic process | 5 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008202 | steroid metabolic process | 4 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0016125 | sterol metabolic process | 4 | 9 |
GO:0016126 | sterol biosynthetic process | 5 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 9 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 9 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006696 | ergosterol biosynthetic process | 5 | 1 |
GO:0008204 | ergosterol metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016128 | phytosteroid metabolic process | 4 | 1 |
GO:0016129 | phytosteroid biosynthetic process | 5 | 1 |
GO:0044107 | obsolete cellular alcohol metabolic process | 3 | 1 |
GO:0044108 | obsolete cellular alcohol biosynthetic process | 4 | 1 |
GO:0044237 | cellular 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:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046165 | alcohol biosynthetic process | 4 | 1 |
GO:0097384 | cellular lipid biosynthetic process | 4 | 1 |
GO:1902652 | secondary alcohol metabolic process | 4 | 1 |
GO:1902653 | secondary alcohol biosynthetic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000246 | delta24(24-1) sterol reductase activity | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016491 | oxidoreductase activity | 2 | 9 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 9 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.349 |
CLV_PCSK_FUR_1 | 382 | 386 | PF00082 | 0.234 |
CLV_PCSK_FUR_1 | 468 | 472 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.281 |
DEG_APCC_DBOX_1 | 353 | 361 | PF00400 | 0.349 |
DOC_AGCK_PIF_1 | 455 | 460 | PF00069 | 0.186 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.643 |
DOC_CYCLIN_RxL_1 | 150 | 160 | PF00134 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 145 | 151 | PF00134 | 0.333 |
DOC_MAPK_gen_1 | 109 | 116 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 382 | 392 | PF00069 | 0.498 |
DOC_MAPK_HePTP_8 | 243 | 255 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 128 | 136 | PF00069 | 0.249 |
DOC_MAPK_MEF2A_6 | 246 | 255 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 260 | 268 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 354 | 363 | PF00069 | 0.225 |
DOC_MAPK_NFAT4_5 | 354 | 362 | PF00069 | 0.212 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.345 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.372 |
DOC_PP2B_PxIxI_1 | 147 | 153 | PF00149 | 0.186 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.431 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.172 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 164 | 168 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 260 | 264 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 410 | 420 | PF00244 | 0.478 |
LIG_AP2alpha_1 | 420 | 424 | PF02296 | 0.477 |
LIG_APCC_ABBA_1 | 253 | 258 | PF00400 | 0.431 |
LIG_BH_BH3_1 | 423 | 439 | PF00452 | 0.372 |
LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.372 |
LIG_deltaCOP1_diTrp_1 | 59 | 67 | PF00928 | 0.424 |
LIG_EH1_1 | 175 | 183 | PF00400 | 0.269 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.224 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.186 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.438 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.269 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.527 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.551 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.351 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.245 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.466 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.551 |
LIG_LIR_Apic_2 | 64 | 70 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.207 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 173 | 184 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 215 | 223 | PF02991 | 0.192 |
LIG_LIR_Gen_1 | 262 | 271 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 276 | 284 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 314 | 325 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 44 | 54 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 485 | 495 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 451 | 455 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.436 |
LIG_NRBOX | 133 | 139 | PF00104 | 0.362 |
LIG_NRBOX | 264 | 270 | PF00104 | 0.186 |
LIG_Pex14_1 | 313 | 317 | PF04695 | 0.457 |
LIG_Pex14_1 | 322 | 326 | PF04695 | 0.305 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.551 |
LIG_Pex14_2 | 420 | 424 | PF04695 | 0.412 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.269 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.306 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 298 | 301 | PF00017 | 0.269 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.269 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.565 |
LIG_SH2_PTP2 | 487 | 490 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 88 | 91 | PF00017 | 0.362 |
LIG_SH2_SRC | 298 | 301 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 433 | 437 | PF00017 | 0.269 |
LIG_SH2_STAT3 | 336 | 339 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.269 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.660 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.431 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.256 |
LIG_Sin3_3 | 142 | 149 | PF02671 | 0.212 |
LIG_SUMO_SIM_anti_2 | 262 | 268 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 264 | 270 | PF11976 | 0.263 |
LIG_SxIP_EBH_1 | 450 | 459 | PF03271 | 0.172 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.545 |
LIG_TYR_ITIM | 185 | 190 | PF00017 | 0.303 |
LIG_TYR_ITIM | 491 | 496 | PF00017 | 0.431 |
LIG_TYR_ITIM | 84 | 89 | PF00017 | 0.269 |
LIG_WRC_WIRS_1 | 115 | 120 | PF05994 | 0.288 |
LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.197 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.231 |
LIG_WRC_WIRS_1 | 457 | 462 | PF05994 | 0.269 |
MOD_CDK_SPK_2 | 30 | 35 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.663 |
MOD_CDK_SPxK_1 | 52 | 58 | PF00069 | 0.496 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.420 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.560 |
MOD_Cter_Amidation | 107 | 110 | PF01082 | 0.372 |
MOD_Cter_Amidation | 427 | 430 | PF01082 | 0.231 |
MOD_DYRK1A_RPxSP_1 | 30 | 34 | PF00069 | 0.664 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.402 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.231 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.247 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.365 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.172 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.671 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.704 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.660 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.186 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.403 |
MOD_N-GLC_2 | 328 | 330 | PF02516 | 0.269 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.443 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.337 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.299 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.421 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.263 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.294 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.180 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.362 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.431 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.722 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.517 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.431 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.269 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.641 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.444 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.390 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.602 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.686 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.231 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.275 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.276 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.301 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.248 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.642 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.560 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.467 |
MOD_SUMO_for_1 | 104 | 107 | PF00179 | 0.232 |
MOD_SUMO_for_1 | 303 | 306 | PF00179 | 0.372 |
TRG_DiLeu_BaEn_1 | 486 | 491 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.270 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.262 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.517 |
TRG_NLS_MonoExtC_3 | 223 | 228 | PF00514 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C6 | Leptomonas seymouri | 75% | 99% |
A0A0N1PBH8 | Leptomonas seymouri | 29% | 100% |
A0A0S4IS37 | Bodo saltans | 27% | 100% |
A0A0S4KLN5 | Bodo saltans | 29% | 100% |
A0A1D8PIC7 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 29% | 100% |
A0A1D8PJ25 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 38% | 100% |
A0A1X0NRH6 | Trypanosomatidae | 28% | 100% |
A0A1X0P0Q6 | Trypanosomatidae | 64% | 100% |
A0A3Q8IM20 | Leishmania donovani | 86% | 100% |
A0A3R7KUI7 | Trypanosoma rangeli | 64% | 100% |
A0A3R7N804 | Trypanosoma rangeli | 29% | 100% |
A0A3S7X5R0 | Leishmania donovani | 26% | 100% |
A4HKM3 | Leishmania braziliensis | 27% | 100% |
A4I855 | Leishmania infantum | 26% | 100% |
A4I8T4 | Leishmania infantum | 86% | 100% |
D0AAC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9B312 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B3Q0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
G4SW86 | Methylotuvimicrobium alcaliphilum (strain DSM 19304 / NCIMB 14124 / VKM B-2133 / 20Z) | 32% | 100% |
I1RF79 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 27% | 100% |
I1RR90 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 26% | 100% |
I1RZZ3 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 40% | 84% |
O08984 | Rattus norvegicus | 31% | 81% |
O13597 | Septoria lycopersici | 26% | 98% |
O76062 | Homo sapiens | 33% | 100% |
O88455 | Mus musculus | 26% | 100% |
P23913 | Gallus gallus | 29% | 78% |
P25340 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 39% | 100% |
P32462 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P36209 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P38670 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 27% | 100% |
P78575 | Ascobolus immersus | 28% | 100% |
Q01447 | Fusarium vanettenii | 27% | 100% |
Q09195 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q14739 | Homo sapiens | 31% | 81% |
Q3U9G9 | Mus musculus | 31% | 80% |
Q4Q4D7 | Leishmania major | 85% | 100% |
Q4Q543 | Leishmania major | 26% | 95% |
Q4WJ59 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 36% | 88% |
Q4WJJ9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 97% |
Q4WKA5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 100% |
Q4WW43 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 42% | 100% |
Q54PP1 | Dictyostelium discoideum | 30% | 100% |
Q5E9J5 | Bos taurus | 26% | 100% |
Q5R7H4 | Pongo abelii | 31% | 81% |
Q5UQI4 | Acanthamoeba polyphaga mimivirus | 31% | 100% |
Q6P4M0 | Xenopus tropicalis | 27% | 100% |
Q71KT5 | Mus musculus | 33% | 100% |
Q7SXF1 | Danio rerio | 27% | 100% |
Q7ZXH1 | Xenopus laevis | 27% | 100% |
Q8WMV1 | Bos taurus | 33% | 100% |
Q9LDR4 | Arabidopsis thaliana | 29% | 100% |
Q9LDU6 | Arabidopsis thaliana | 25% | 100% |
Q9UBM7 | Homo sapiens | 26% | 100% |
Q9Z2Z8 | Rattus norvegicus | 27% | 100% |
V5BKN3 | Trypanosoma cruzi | 26% | 100% |