trans-2,3-enoyl-CoA reductase-like isoform 2 [Homo sapiens]
steroid 5-alpha reductase family protein( domain architecture ID 708466)
steroid 5-alpha reductase family protein similar to Homo sapiens very-long-chain enoyl-CoA reductase and trans-2,3-enoyl-CoA reductase-like
List of domain hits
Name | Accession | Description | Interval | E-value | |||||
PLN02560 super family | cl28409 | enoyl-CoA reductase |
79-322 | 1.26e-55 | |||||
enoyl-CoA reductase The actual alignment was detected with superfamily member PLN02560: Pssm-ID: 178174 [Multi-domain] Cd Length: 308 Bit Score: 183.00 E-value: 1.26e-55
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Name | Accession | Description | Interval | E-value | |||||
PLN02560 | PLN02560 | enoyl-CoA reductase |
79-322 | 1.26e-55 | |||||
enoyl-CoA reductase Pssm-ID: 178174 [Multi-domain] Cd Length: 308 Bit Score: 183.00 E-value: 1.26e-55
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Ubl_TECRL | cd17125 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase-like (TECRL); TECRL, also ... |
60-137 | 2.60e-47 | |||||
ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase-like (TECRL); TECRL, also termed steroid 5-alpha-reductase 2-like 2 protein (SRD5A2L2), is associated with life?threatening inherited arrhythmias displaying features of both long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). TECRL contains an N-terminal ubiquitin-like (Ubl) domain with a beta-grasp Ubl fold, a common structure involved in protein-protein interactions, as well as a C-terminal catalytic domain. Pssm-ID: 340645 Cd Length: 78 Bit Score: 153.87 E-value: 2.60e-47
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Steroid_dh | pfam02544 | 3-oxo-5-alpha-steroid 4-dehydrogenase; This family consists of 3-oxo-5-alpha-steroid ... |
212-322 | 1.19e-05 | |||||
3-oxo-5-alpha-steroid 4-dehydrogenase; This family consists of 3-oxo-5-alpha-steroid 4-dehydrogenases, EC:1.3.99.5 Also known as Steroid 5-alpha-reductase, the reaction catalyzed by this enzyme is: 3-oxo-5-alpha-steroid + acceptor <=> 3-oxo-delta(4)-steroid + reduced acceptor. The Steroid 5-alpha-reductase enzyme is responsible for the formation of dihydrotestosterone, this hormone promotes the differentiation of male external genitalia and the prostate during fetal development. In humans mutations in this enzyme can cause a form of male pseudohermaphorditism in which the external genitalia and prostate fail to develop normally. A related enzyme is also found in plants is DET2, a steroid reductase from Arabidopsis. Mutations in this enzyme cause defects in light-regulated development. Pssm-ID: 460585 [Multi-domain] Cd Length: 150 Bit Score: 44.70 E-value: 1.19e-05
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Name | Accession | Description | Interval | E-value | |||||
PLN02560 | PLN02560 | enoyl-CoA reductase |
79-322 | 1.26e-55 | |||||
enoyl-CoA reductase Pssm-ID: 178174 [Multi-domain] Cd Length: 308 Bit Score: 183.00 E-value: 1.26e-55
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Ubl_TECRL | cd17125 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase-like (TECRL); TECRL, also ... |
60-137 | 2.60e-47 | |||||
ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase-like (TECRL); TECRL, also termed steroid 5-alpha-reductase 2-like 2 protein (SRD5A2L2), is associated with life?threatening inherited arrhythmias displaying features of both long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). TECRL contains an N-terminal ubiquitin-like (Ubl) domain with a beta-grasp Ubl fold, a common structure involved in protein-protein interactions, as well as a C-terminal catalytic domain. Pssm-ID: 340645 Cd Length: 78 Bit Score: 153.87 E-value: 2.60e-47
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Ubl_TECR | cd17124 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR); TECR, also termed ... |
59-137 | 4.28e-23 | |||||
ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR); TECR, also termed very-long-chain enoyl-CoA reductase, or synaptic glycoprotein SC2, or TER, or GPSN2, is a synaptic glycoprotein that catalyzes the fourth reaction in the synthesis of very long-chain fatty acids (VLCFA) which is the reduction step of the microsomal fatty acyl-elongation process. Diseases involving perturbations to normal synthesis and degradation of VLCFA (e.g. adrenoleukodystrophy and Zellweger syndrome) have significant neurological consequences. The mammalian TECR P182L mutation causes nonsyndromic mental retardation. Deletion of the yeast TECR homolog (TSC13p) is lethal. TECR contains an N-terminal ubiquitin-like (Ubl) domain with a beta-grasp Ubl fold, a common structure involved in protein-protein interactions, as well as a C-terminal catalytic domain. Pssm-ID: 340644 [Multi-domain] Cd Length: 79 Bit Score: 90.78 E-value: 4.28e-23
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Ubl_TECR_like | cd01801 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR) and similar proteins; ... |
61-137 | 4.62e-23 | |||||
ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR) and similar proteins; This family includes TECR and many TECR-like proteins, such as TECRL. TECR, also termed very-long-chain enoyl-CoA reductase, or synaptic glycoprotein SC2, or TER, or GPSN2, is a synaptic glycoprotein that catalyzes the fourth reaction in the synthesis of very long-chain fatty acids (VLCFA) which is the reduction step of the microsomal fatty acyl-elongation process. Diseases involving perturbations to normal synthesis and degradation of VLCFA (e.g. adrenoleukodystrophy and Zellweger syndrome) have significant neurological consequences. The mammalian TECR P182L mutation causes nonsyndromic mental retardation. Deletion of the yeast TECR (TSC13) homolog is lethal. TECR contains an N-terminal ubiquitin-like (Ubl) domain with a beta-grasp Ubl fold, a common structure involved in protein-protein interactions, as well as a C-terminal catalytic domain. TECRL, also termed steroid 5-alpha-reductase 2-like 2 protein (SRD5A2L2), is associated with life-threatening inherited arrhythmias displaying features of both long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). Both TECR and TECRL contain an N-terminal Ubl domain with a beta-grasp Ubl fold, and a C-terminal catalytic domain. Pssm-ID: 340499 [Multi-domain] Cd Length: 77 Bit Score: 90.81 E-value: 4.62e-23
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Steroid_dh | pfam02544 | 3-oxo-5-alpha-steroid 4-dehydrogenase; This family consists of 3-oxo-5-alpha-steroid ... |
212-322 | 1.19e-05 | |||||
3-oxo-5-alpha-steroid 4-dehydrogenase; This family consists of 3-oxo-5-alpha-steroid 4-dehydrogenases, EC:1.3.99.5 Also known as Steroid 5-alpha-reductase, the reaction catalyzed by this enzyme is: 3-oxo-5-alpha-steroid + acceptor <=> 3-oxo-delta(4)-steroid + reduced acceptor. The Steroid 5-alpha-reductase enzyme is responsible for the formation of dihydrotestosterone, this hormone promotes the differentiation of male external genitalia and the prostate during fetal development. In humans mutations in this enzyme can cause a form of male pseudohermaphorditism in which the external genitalia and prostate fail to develop normally. A related enzyme is also found in plants is DET2, a steroid reductase from Arabidopsis. Mutations in this enzyme cause defects in light-regulated development. Pssm-ID: 460585 [Multi-domain] Cd Length: 150 Bit Score: 44.70 E-value: 1.19e-05
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Blast search parameters | ||||
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