trans-2,3-enoyl-CoA reductase b isoform X1 [Danio rerio]
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 |
63-345 | 1.83e-85 | |||||
enoyl-CoA reductase The actual alignment was detected with superfamily member PLN02560: Pssm-ID: 178174 [Multi-domain] Cd Length: 308 Bit Score: 260.43 E-value: 1.83e-85
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Name | Accession | Description | Interval | E-value | |||||
PLN02560 | PLN02560 | enoyl-CoA reductase |
63-345 | 1.83e-85 | |||||
enoyl-CoA reductase Pssm-ID: 178174 [Multi-domain] Cd Length: 308 Bit Score: 260.43 E-value: 1.83e-85
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Ubl_TECR | cd17124 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR); TECR, also termed ... |
43-121 | 4.18e-57 | |||||
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: 179.76 E-value: 4.18e-57
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Steroid_dh | pfam02544 | 3-oxo-5-alpha-steroid 4-dehydrogenase; This family consists of 3-oxo-5-alpha-steroid ... |
195-348 | 2.77e-28 | |||||
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: 107.49 E-value: 2.77e-28
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Name | Accession | Description | Interval | E-value | |||||
PLN02560 | PLN02560 | enoyl-CoA reductase |
63-345 | 1.83e-85 | |||||
enoyl-CoA reductase Pssm-ID: 178174 [Multi-domain] Cd Length: 308 Bit Score: 260.43 E-value: 1.83e-85
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Ubl_TECR | cd17124 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR); TECR, also termed ... |
43-121 | 4.18e-57 | |||||
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: 179.76 E-value: 4.18e-57
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Steroid_dh | pfam02544 | 3-oxo-5-alpha-steroid 4-dehydrogenase; This family consists of 3-oxo-5-alpha-steroid ... |
195-348 | 2.77e-28 | |||||
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: 107.49 E-value: 2.77e-28
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Ubl_TECR_like | cd01801 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase (TECR) and similar proteins; ... |
45-121 | 3.98e-22 | |||||
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: 88.50 E-value: 3.98e-22
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Ubl_TECRL | cd17125 | ubiquitin-like (Ubl) domain found in trans-2,3-enoyl-CoA reductase-like (TECRL); TECRL, also ... |
44-121 | 5.33e-22 | |||||
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: 88.38 E-value: 5.33e-22
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PLN02392 | PLN02392 | probable steroid reductase DET2 |
280-347 | 3.71e-06 | |||||
probable steroid reductase DET2 Pssm-ID: 178015 Cd Length: 260 Bit Score: 47.50 E-value: 3.71e-06
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PLN03164 | PLN03164 | 3-oxo-5-alpha-steroid 4-dehydrogenase, C-terminal domain containing protein; Provisional |
236-347 | 1.30e-04 | |||||
3-oxo-5-alpha-steroid 4-dehydrogenase, C-terminal domain containing protein; Provisional Pssm-ID: 215610 [Multi-domain] Cd Length: 323 Bit Score: 43.26 E-value: 1.30e-04
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Ubl_ubiquitin_like | cd17039 | ubiquitin-like (Ubl) domain found in ubiquitin and ubiquitin-like Ubl proteins; Ubiquitin-like ... |
62-117 | 5.03e-04 | |||||
ubiquitin-like (Ubl) domain found in ubiquitin and ubiquitin-like Ubl proteins; Ubiquitin-like (Ubl) proteins have a similar ubiquitin (Ub) beta-grasp fold and attach to other proteins in a Ubl manner but with biochemically distinct roles. Ub and Ubl proteins conjugate and deconjugate via ligases and peptidases to covalently modify target polypeptides. Some Ubl domains have adaptor roles in Ub-signaling by mediating protein-protein interaction. Prokaryotic sulfur carrier proteins are Ub-related proteins that can be activated in an ATP-dependent manner. Polyubiquitination signals for a diverse set of cellular events via different isopeptide linkages formed between the C terminus of one ubiquitin (Ub) and the epsilon-amine of K6, K11, K27, K29, K33, K48, or K63 of a second Ub. One of these seven lysine residues (K27, Ub numbering) is conserved in this Ubl_ubiquitin_like family. K27-linked Ub chains are versatile and can be recognized by several downstream receptor proteins. K27 has roles beyond chain linkage, such as in Ubl NEDD8 (which contains many of the same lysines (K6, K11, K27, K33, K48) as Ub) where K27 has a role (other than conjugation) in the mechanism of protein neddylation. Pssm-ID: 340559 [Multi-domain] Cd Length: 68 Bit Score: 37.96 E-value: 5.03e-04
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Blast search parameters | ||||
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