Sterol metabolism/biosynthesis, Squalene monooxygenase-like
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HVU0
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006694 | steroid biosynthetic process | 5 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008202 | steroid metabolic process | 4 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0016125 | sterol metabolic process | 4 | 12 |
GO:0016126 | sterol biosynthetic process | 5 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 12 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004497 | monooxygenase activity | 3 | 12 |
GO:0004506 | squalene monooxygenase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 12 |
GO:0016709 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0071949 | FAD binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.275 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.273 |
DEG_MDM2_SWIB_1 | 501 | 508 | PF02201 | 0.221 |
DEG_MDM2_SWIB_1 | 530 | 537 | PF02201 | 0.342 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.421 |
DOC_CYCLIN_RxL_1 | 60 | 73 | PF00134 | 0.302 |
DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 252 | 260 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 517 | 525 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 562 | 569 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 206 | 215 | PF00069 | 0.226 |
DOC_MAPK_MEF2A_6 | 517 | 525 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 22 | 28 | PF00149 | 0.295 |
DOC_PP4_FxxP_1 | 536 | 539 | PF00568 | 0.360 |
DOC_PP4_FxxP_1 | 69 | 72 | PF00568 | 0.281 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.365 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 31 | 35 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 368 | 374 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 403 | 412 | PF00244 | 0.279 |
LIG_Actin_WH2_2 | 11 | 28 | PF00022 | 0.400 |
LIG_Actin_WH2_2 | 366 | 382 | PF00022 | 0.309 |
LIG_Actin_WH2_2 | 415 | 431 | PF00022 | 0.226 |
LIG_Actin_WH2_2 | 73 | 91 | PF00022 | 0.364 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.245 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.248 |
LIG_BRCT_BRCA1_2 | 140 | 146 | PF00533 | 0.403 |
LIG_CtBP_PxDLS_1 | 306 | 310 | PF00389 | 0.325 |
LIG_EH_1 | 187 | 191 | PF12763 | 0.323 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.296 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.239 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.325 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.168 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.245 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.129 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.274 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.273 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.386 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.318 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.351 |
LIG_G3BP_FGDF_1 | 130 | 135 | PF02136 | 0.285 |
LIG_HP1_1 | 211 | 215 | PF01393 | 0.304 |
LIG_LIR_Apic_2 | 181 | 186 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 281 | 285 | PF02991 | 0.226 |
LIG_LIR_Apic_2 | 67 | 72 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 504 | 513 | PF02991 | 0.358 |
LIG_LIR_LC3C_4 | 209 | 214 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.090 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 532 | 537 | PF02991 | 0.316 |
LIG_LYPXL_SIV_4 | 481 | 489 | PF13949 | 0.245 |
LIG_MAD2 | 74 | 82 | PF02301 | 0.272 |
LIG_MYND_3 | 287 | 291 | PF01753 | 0.270 |
LIG_NBox_RRM_1 | 363 | 373 | PF00076 | 0.356 |
LIG_PDZ_Class_2 | 564 | 569 | PF00595 | 0.422 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.356 |
LIG_Pex14_2 | 501 | 505 | PF04695 | 0.351 |
LIG_Pex14_2 | 530 | 534 | PF04695 | 0.298 |
LIG_PTB_Apo_2 | 456 | 463 | PF02174 | 0.155 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.226 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.228 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.155 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 177 | 181 | PF00017 | 0.369 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 230 | 234 | PF00017 | 0.245 |
LIG_SH2_NCK_1 | 482 | 486 | PF00017 | 0.256 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.288 |
LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.226 |
LIG_SH2_SRC | 234 | 237 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.240 |
LIG_SH2_STAP1 | 555 | 559 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 555 | 558 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.226 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.211 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.486 |
LIG_SH3_1 | 183 | 189 | PF00018 | 0.342 |
LIG_SH3_1 | 282 | 288 | PF00018 | 0.226 |
LIG_SH3_1 | 330 | 336 | PF00018 | 0.282 |
LIG_SH3_2 | 186 | 191 | PF14604 | 0.424 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.373 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.377 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.296 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.224 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.151 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.335 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.211 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.385 |
LIG_SH3_5 | 232 | 236 | PF00018 | 0.239 |
LIG_Sin3_3 | 14 | 21 | PF02671 | 0.236 |
LIG_SUMO_SIM_anti_2 | 13 | 19 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.249 |
LIG_UBA3_1 | 286 | 292 | PF00899 | 0.155 |
LIG_WRC_WIRS_1 | 498 | 503 | PF05994 | 0.367 |
MOD_CDC14_SPxK_1 | 28 | 31 | PF00782 | 0.425 |
MOD_CDK_SPxK_1 | 25 | 31 | PF00069 | 0.435 |
MOD_CDK_SPxxK_3 | 422 | 429 | PF00069 | 0.294 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.417 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.398 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.287 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.311 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.356 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.353 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.272 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.406 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.282 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.510 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.363 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.408 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.401 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.399 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.304 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.451 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.356 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.207 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.293 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.477 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.313 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.350 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.338 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.253 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.282 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.226 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.333 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.484 |
MOD_NEK2_2 | 375 | 380 | PF00069 | 0.210 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.328 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.365 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.275 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.322 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.328 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.111 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.282 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.402 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.302 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.356 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.331 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.300 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.200 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.309 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.435 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.294 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.393 |
MOD_SUMO_for_1 | 526 | 529 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 317 | 323 | PF00179 | 0.275 |
MOD_SUMO_rev_2 | 385 | 394 | PF00179 | 0.272 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.211 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.210 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.218 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.230 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.193 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.211 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.406 |
TRG_NES_CRM1_1 | 493 | 506 | PF08389 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.211 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5K9 | Leptomonas seymouri | 78% | 100% |
A0A0S4IT90 | Bodo saltans | 54% | 87% |
A0A1X0NLC9 | Trypanosomatidae | 61% | 100% |
A0A3S7WSP8 | Leishmania donovani | 99% | 100% |
A0A422P4A3 | Trypanosoma rangeli | 59% | 100% |
A4H7F2 | Leishmania braziliensis | 84% | 100% |
B7TWW5 | Panax ginseng | 33% | 100% |
D0A6E5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 98% |
E9API6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9R5G2 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 34% | 100% |
I1RQ76 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 31% | 100% |
O13306 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 31% | 100% |
O48651 | Panax ginseng | 32% | 100% |
O65402 | Arabidopsis thaliana | 27% | 100% |
O65403 | Arabidopsis thaliana | 26% | 100% |
O65404 | Arabidopsis thaliana | 26% | 100% |
O65726 | Brassica napus | 25% | 100% |
O65727 | Brassica napus | 26% | 100% |
O81000 | Arabidopsis thaliana | 34% | 97% |
P32476 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P52019 | Mus musculus | 34% | 99% |
P52020 | Rattus norvegicus | 33% | 99% |
Q14534 | Homo sapiens | 34% | 99% |
Q4QFZ2 | Leishmania major | 94% | 100% |
Q75F69 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 29% | 100% |
Q8VYH2 | Arabidopsis thaliana | 34% | 100% |
Q92206 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 100% |
Q9C1W3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
Q9SM02 | Arabidopsis thaliana | 33% | 100% |
V5BRL1 | Trypanosoma cruzi | 58% | 99% |