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: A4H965
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 | 85 | 89 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.278 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.293 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.346 |
CLV_Separin_Metazoa | 456 | 460 | PF03568 | 0.387 |
DEG_SCF_FBW7_1 | 286 | 293 | PF00400 | 0.580 |
DEG_SPOP_SBC_1 | 386 | 390 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 460 | 464 | PF00917 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 233 | 239 | PF00134 | 0.471 |
DOC_MAPK_MEF2A_6 | 125 | 134 | PF00069 | 0.331 |
DOC_PP1_RVXF_1 | 137 | 143 | PF00149 | 0.424 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.383 |
DOC_SPAK_OSR1_1 | 116 | 120 | PF12202 | 0.512 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.244 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.463 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.693 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 133 | 137 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 139 | 143 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 459 | 469 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 100 | 118 | PF00022 | 0.512 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 409 | 413 | PF00533 | 0.227 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.244 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 58 | 65 | PF00928 | 0.748 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.431 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.411 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.244 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.385 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.448 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.471 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.618 |
LIG_GBD_Chelix_1 | 449 | 457 | PF00786 | 0.506 |
LIG_Integrin_isoDGR_2 | 257 | 259 | PF01839 | 0.361 |
LIG_LIR_Apic_2 | 228 | 232 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 111 | 119 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 251 | 260 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 410 | 421 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 429 | 437 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 524 | 534 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 410 | 416 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.556 |
LIG_LYPXL_yS_3 | 161 | 164 | PF13949 | 0.486 |
LIG_NRBOX | 214 | 220 | PF00104 | 0.447 |
LIG_PCNA_PIPBox_1 | 249 | 258 | PF02747 | 0.471 |
LIG_Pex14_1 | 323 | 327 | PF04695 | 0.284 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.592 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.278 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.346 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.618 |
LIG_SH2_PTP2 | 112 | 115 | PF00017 | 0.244 |
LIG_SH2_PTP2 | 431 | 434 | PF00017 | 0.346 |
LIG_SH2_SRC | 353 | 356 | PF00017 | 0.274 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.618 |
LIG_SH2_STAT3 | 73 | 76 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.618 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.364 |
LIG_SH3_4 | 371 | 378 | PF00018 | 0.417 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 242 | 247 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 431 | 436 | PF11976 | 0.255 |
LIG_TRAF2_1 | 68 | 71 | PF00917 | 0.752 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.286 |
LIG_TYR_ITIM | 153 | 158 | PF00017 | 0.481 |
LIG_TYR_ITIM | 159 | 164 | PF00017 | 0.579 |
LIG_TYR_ITSM | 427 | 434 | PF00017 | 0.512 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.469 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.649 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.620 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.593 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.572 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.572 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.613 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.472 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.517 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.404 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.550 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.508 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.434 |
MOD_CMANNOS | 59 | 62 | PF00535 | 0.667 |
MOD_Cter_Amidation | 529 | 532 | PF01082 | 0.286 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.378 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.581 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.638 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.629 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.536 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.471 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.520 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.504 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.244 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.479 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.199 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.528 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.566 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.679 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.662 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.486 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.382 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.680 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.470 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.513 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.587 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.754 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.443 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.647 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.639 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.382 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.453 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.244 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.541 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.454 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.604 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.618 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.512 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.473 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.485 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.281 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.404 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.494 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.419 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.482 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.733 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.534 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.670 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.411 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.486 |
MOD_PK_1 | 192 | 198 | PF00069 | 0.453 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.516 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.469 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.300 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.289 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.453 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.460 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.469 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.512 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.525 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.439 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.366 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.285 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.597 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.342 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.439 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.514 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.615 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.460 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P837 | Leptomonas seymouri | 46% | 100% |
A0A3S7WUK3 | Leishmania donovani | 72% | 100% |
A4HXI7 | Leishmania infantum | 72% | 100% |
E9AR82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QE81 | Leishmania major | 72% | 100% |