Related to other eukaryotic steroid 5 alpha reductases. Localization: ER (by homology)
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AR82
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003865 | 3-oxo-5-alpha-steroid 4-dehydrogenase activity | 5 | 6 |
GO:0016229 | steroid dehydrogenase activity | 3 | 6 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 7 |
GO:0033765 | steroid dehydrogenase activity, acting on the CH-CH group of donors | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.537 |
CLV_MEL_PAP_1 | 135 | 141 | PF00089 | 0.500 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.225 |
CLV_PCSK_FUR_1 | 354 | 358 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.278 |
CLV_Separin_Metazoa | 456 | 460 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.337 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.318 |
DEG_SPOP_SBC_1 | 385 | 389 | PF00917 | 0.722 |
DEG_SPOP_SBC_1 | 460 | 464 | PF00917 | 0.615 |
DOC_ANK_TNKS_1 | 398 | 405 | PF00023 | 0.450 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.362 |
DOC_CYCLIN_yCln2_LP_2 | 232 | 238 | PF00134 | 0.390 |
DOC_MAPK_DCC_7 | 226 | 234 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 477 | 484 | PF00069 | 0.209 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.315 |
DOC_PP1_RVXF_1 | 479 | 485 | PF00149 | 0.358 |
DOC_PP1_RVXF_1 | 92 | 98 | PF00149 | 0.556 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.381 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.323 |
DOC_PP4_FxxP_1 | 522 | 525 | PF00568 | 0.460 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.651 |
DOC_SPAK_OSR1_1 | 115 | 119 | PF12202 | 0.398 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.566 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 206 | 216 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 459 | 469 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 510 | 518 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 98 | 102 | PF00244 | 0.423 |
LIG_Actin_WH2_2 | 8 | 25 | PF00022 | 0.358 |
LIG_Actin_WH2_2 | 99 | 117 | PF00022 | 0.398 |
LIG_APCC_ABBA_1 | 32 | 37 | PF00400 | 0.581 |
LIG_BIR_III_4 | 381 | 385 | PF00653 | 0.559 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.478 |
LIG_deltaCOP1_diTrp_1 | 59 | 64 | PF00928 | 0.667 |
LIG_EH1_1 | 102 | 110 | PF00400 | 0.209 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.321 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.398 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.253 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.537 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.366 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.601 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.537 |
LIG_GBD_Chelix_1 | 449 | 457 | PF00786 | 0.292 |
LIG_Integrin_isoDGR_2 | 256 | 258 | PF01839 | 0.485 |
LIG_Integrin_RGD_1 | 357 | 359 | PF01839 | 0.417 |
LIG_LIR_Apic_2 | 227 | 231 | PF02991 | 0.306 |
LIG_LIR_Apic_2 | 403 | 408 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 521 | 525 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 62 | 67 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 148 | 158 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 429 | 437 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 524 | 534 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.237 |
LIG_LIR_LC3C_4 | 240 | 245 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.237 |
LIG_LYPXL_yS_3 | 160 | 163 | PF13949 | 0.385 |
LIG_MYND_1 | 171 | 175 | PF01753 | 0.484 |
LIG_MYND_1 | 63 | 67 | PF01753 | 0.652 |
LIG_NRBOX | 213 | 219 | PF00104 | 0.369 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.424 |
LIG_Pex14_1 | 174 | 178 | PF04695 | 0.384 |
LIG_Pex14_1 | 320 | 324 | PF04695 | 0.248 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.345 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.358 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.478 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.537 |
LIG_SH2_PTP2 | 431 | 434 | PF00017 | 0.478 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.568 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.537 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.316 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.433 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.202 |
LIG_SUMO_SIM_anti_2 | 8 | 14 | PF11976 | 0.209 |
LIG_SUMO_SIM_par_1 | 104 | 110 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 240 | 246 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 432 | 439 | PF11976 | 0.429 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.661 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.250 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.420 |
LIG_TYR_ITSM | 427 | 434 | PF00017 | 0.398 |
MOD_CDC14_SPxK_1 | 167 | 170 | PF00782 | 0.376 |
MOD_CDK_SPxK_1 | 164 | 170 | PF00069 | 0.359 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.394 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.581 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.581 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.531 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.533 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.522 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.587 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.519 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.501 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.375 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.480 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.534 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.453 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.347 |
MOD_Cter_Amidation | 371 | 374 | PF01082 | 0.658 |
MOD_Cter_Amidation | 529 | 532 | PF01082 | 0.250 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.625 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.397 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.377 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.478 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.528 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.555 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.398 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.578 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.530 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.467 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.472 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.535 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.632 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.538 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.394 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.341 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.460 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.716 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.458 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.488 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.579 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.513 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.420 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.502 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.557 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.629 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.447 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.319 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.522 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.432 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.495 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.521 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.370 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.615 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.413 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.425 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.362 |
MOD_NEK2_2 | 97 | 102 | PF00069 | 0.209 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.390 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.464 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.525 |
MOD_PKA_1 | 373 | 379 | PF00069 | 0.414 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.476 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.390 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.502 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.466 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.228 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.453 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.572 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.254 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.362 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.339 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.398 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.573 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.455 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.348 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.340 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.524 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.258 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.359 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.555 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.597 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.587 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.564 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 318 | 323 | PF01217 | 0.290 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.316 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.209 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P837 | Leptomonas seymouri | 46% | 100% |
A0A3S7WUK3 | Leishmania donovani | 86% | 100% |
A4H965 | Leishmania braziliensis | 72% | 100% |
A4HXI7 | Leishmania infantum | 87% | 100% |
Q4QE81 | Leishmania major | 85% | 100% |