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: A4HXI7
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 | 401 | 405 | PF00656 | 0.299 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.589 |
CLV_MEL_PAP_1 | 135 | 141 | PF00089 | 0.491 |
CLV_MEL_PAP_1 | 316 | 322 | PF00089 | 0.278 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.488 |
CLV_PCSK_FUR_1 | 356 | 360 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.274 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.327 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.621 |
DEG_SCF_FBW7_1 | 281 | 288 | PF00400 | 0.577 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.468 |
DEG_SPOP_SBC_1 | 386 | 390 | PF00917 | 0.501 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.384 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.338 |
DOC_CYCLIN_yCln2_LP_2 | 232 | 238 | PF00134 | 0.373 |
DOC_MAPK_DCC_7 | 226 | 234 | PF00069 | 0.290 |
DOC_MAPK_HePTP_8 | 316 | 328 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.512 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.349 |
DOC_PP1_RVXF_1 | 317 | 323 | PF00149 | 0.523 |
DOC_PP1_RVXF_1 | 480 | 486 | PF00149 | 0.353 |
DOC_PP1_RVXF_1 | 92 | 98 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.366 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.307 |
DOC_PP4_FxxP_1 | 523 | 526 | PF00568 | 0.454 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.619 |
DOC_SPAK_OSR1_1 | 115 | 119 | PF12202 | 0.383 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.551 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.639 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 206 | 216 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.499 |
LIG_Actin_WH2_2 | 8 | 25 | PF00022 | 0.345 |
LIG_Actin_WH2_2 | 99 | 117 | PF00022 | 0.383 |
LIG_APCC_ABBA_1 | 32 | 37 | PF00400 | 0.560 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.349 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 57 | 64 | PF00928 | 0.666 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.331 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.405 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.379 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.429 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.349 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.402 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.543 |
LIG_Integrin_isoDGR_2 | 256 | 258 | PF01839 | 0.279 |
LIG_Integrin_RGD_1 | 359 | 361 | PF01839 | 0.600 |
LIG_LIR_Apic_2 | 227 | 231 | PF02991 | 0.300 |
LIG_LIR_Apic_2 | 404 | 409 | PF02991 | 0.299 |
LIG_LIR_Apic_2 | 522 | 526 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 62 | 67 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 148 | 158 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 430 | 438 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 465 | 475 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 525 | 535 | PF02991 | 0.526 |
LIG_LIR_LC3C_4 | 240 | 245 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.633 |
LIG_LYPXL_yS_3 | 160 | 163 | PF13949 | 0.354 |
LIG_MYND_1 | 171 | 175 | PF01753 | 0.479 |
LIG_MYND_1 | 63 | 67 | PF01753 | 0.616 |
LIG_NRBOX | 213 | 219 | PF00104 | 0.355 |
LIG_PCNA_PIPBox_1 | 248 | 257 | PF02747 | 0.358 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.387 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.532 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.345 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.274 |
LIG_SH2_CRK | 527 | 531 | PF00017 | 0.526 |
LIG_SH2_PTP2 | 432 | 435 | PF00017 | 0.274 |
LIG_SH2_SRC | 432 | 435 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.551 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.526 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.310 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.407 |
LIG_SUMO_SIM_par_1 | 104 | 110 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 240 | 246 | PF11976 | 0.309 |
LIG_TRAF2_1 | 453 | 456 | PF00917 | 0.338 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.649 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.414 |
LIG_TYR_ITSM | 428 | 435 | PF00017 | 0.383 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.365 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.588 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.605 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.480 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.553 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.567 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.439 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.392 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.537 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.440 |
MOD_CMANNOS | 58 | 61 | PF00535 | 0.574 |
MOD_Cter_Amidation | 373 | 376 | PF01082 | 0.706 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.538 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.651 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.616 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.521 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.439 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.648 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.410 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.412 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.515 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.439 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.626 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.584 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.412 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.289 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.546 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.697 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.543 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.610 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.648 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.513 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.510 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.436 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.563 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.555 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.408 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.310 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.418 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.639 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.455 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.512 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.310 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.371 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.520 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.498 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.285 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.320 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.500 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.310 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.381 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.392 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.383 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.580 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.430 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.321 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.502 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.365 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.482 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.547 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.466 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.540 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.345 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P837 | Leptomonas seymouri | 47% | 100% |
A0A3S7WUK3 | Leishmania donovani | 99% | 100% |
A4H965 | Leishmania braziliensis | 72% | 100% |
E9AR82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QE81 | Leishmania major | 92% | 100% |