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: Q4QE81
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 | 404 | 408 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.682 |
CLV_MEL_PAP_1 | 135 | 141 | PF00089 | 0.576 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 359 | 363 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.346 |
CLV_Separin_Metazoa | 460 | 464 | PF03568 | 0.590 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.403 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.478 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 389 | 393 | PF00917 | 0.793 |
DEG_SPOP_SBC_1 | 464 | 468 | PF00917 | 0.671 |
DOC_ANK_TNKS_1 | 402 | 409 | PF00023 | 0.486 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 232 | 238 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 60 | 66 | PF00134 | 0.574 |
DOC_MAPK_DCC_7 | 226 | 234 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.409 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.422 |
DOC_PP1_RVXF_1 | 320 | 326 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 483 | 489 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 92 | 98 | PF00149 | 0.635 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.385 |
DOC_PP2B_LxvP_1 | 60 | 63 | PF13499 | 0.580 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.687 |
DOC_SPAK_OSR1_1 | 115 | 119 | PF12202 | 0.512 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.641 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.437 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 206 | 216 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 279 | 287 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 463 | 473 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 8 | 25 | PF00022 | 0.450 |
LIG_Actin_WH2_2 | 99 | 117 | PF00022 | 0.512 |
LIG_APCC_ABBA_1 | 32 | 37 | PF00400 | 0.673 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.627 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.459 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.546 |
LIG_CSL_BTD_1 | 60 | 63 | PF09270 | 0.580 |
LIG_deltaCOP1_diTrp_1 | 57 | 64 | PF00928 | 0.751 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.431 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.459 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.618 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.601 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.429 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.671 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.618 |
LIG_Integrin_isoDGR_2 | 256 | 258 | PF01839 | 0.564 |
LIG_Integrin_RGD_1 | 362 | 364 | PF01839 | 0.469 |
LIG_LIR_Apic_2 | 227 | 231 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 407 | 412 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 148 | 158 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 433 | 441 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 528 | 538 | PF02991 | 0.618 |
LIG_LIR_LC3C_4 | 240 | 245 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 525 | 529 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.705 |
LIG_LYPXL_yS_3 | 160 | 163 | PF13949 | 0.482 |
LIG_MYND_1 | 171 | 175 | PF01753 | 0.531 |
LIG_MYND_1 | 63 | 67 | PF01753 | 0.690 |
LIG_NRBOX | 213 | 219 | PF00104 | 0.449 |
LIG_PCNA_PIPBox_1 | 248 | 257 | PF02747 | 0.419 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.492 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.450 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.546 |
LIG_SH2_CRK | 530 | 534 | PF00017 | 0.618 |
LIG_SH2_PTP2 | 435 | 438 | PF00017 | 0.546 |
LIG_SH2_SRC | 435 | 438 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 522 | 526 | PF00017 | 0.618 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.577 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.411 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.479 |
LIG_SUMO_SIM_par_1 | 104 | 110 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 240 | 246 | PF11976 | 0.391 |
LIG_TRAF2_1 | 456 | 459 | PF00917 | 0.593 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.736 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.579 |
LIG_TYR_ITSM | 431 | 438 | PF00017 | 0.512 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.469 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.637 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.661 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.520 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.584 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.628 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.585 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.599 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.434 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.396 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.562 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.651 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.550 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.486 |
MOD_CMANNOS | 58 | 61 | PF00535 | 0.667 |
MOD_Cter_Amidation | 376 | 379 | PF01082 | 0.736 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.577 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.707 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.403 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.573 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.652 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.638 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.685 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.512 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.478 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.555 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.513 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.661 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.249 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.684 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.570 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.488 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.448 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.695 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.641 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.618 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.732 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.443 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.645 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.614 |
MOD_N-GLC_1 | 446 | 451 | PF02516 | 0.510 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.460 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.600 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.610 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.507 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.482 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.482 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.723 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.513 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.539 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.469 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.447 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.494 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.591 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.586 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.385 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.584 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.409 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.645 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.336 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.469 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.448 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.512 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.659 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.525 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.453 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.573 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.380 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.603 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.698 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.535 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P837 | Leptomonas seymouri | 46% | 100% |
A0A3S7WUK3 | Leishmania donovani | 91% | 100% |
A4H965 | Leishmania braziliensis | 72% | 100% |
A4HXI7 | Leishmania infantum | 92% | 100% |
E9AR82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |