2YUT


Conserved Protein Domain Family
Tthb094_like_SDR_c

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cd11730: Tthb094_like_SDR_c 
Click on image for an interactive view with Cn3D
Tthb094 and related proteins, classical (c) SDRs
Tthb094 from Thermus Thermophilus is a classical SDR which binds NADP. Members of this subgroup contain the YXXXK active site characteristic of SDRs. Also, an upstream Asn residue of the canonical catalytic tetrad is partially conserved in this subgroup of proteins of undetermined function. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.
Statistics
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PSSM-Id: 212496
Aligned: 6 rows
Threshold Bit Score: 180.411
Created: 10-May-2012
Updated: 2-Oct-2020
Structure
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Program:
Drawing:
Aligned Rows:
 
putative activeNAD(P) binding
Conserved site includes 3 residues -Click on image for an interactive view with Cn3D
Feature 1:putative active site [active site]
Evidence:

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                                                                                     
2YUT_A      3 VLITGATGGLGGAFARALKG--HDLLLSGRRAgaLAELAREVGa--rALPADLADel-eAKALLEEaGPLDLLVHAVGKa 77  Thermus thermophilus
ABU58191    4 ALIWGAAGGIGRALIEILSKngWRVLGIARDAtaLSGTAAEVYsadlARDADMAAa--aLWAAQQSdGVVHLWVYAAGDm 81  Roseiflexus casten...
BAM00866    4 AFIFGASGGIGRALAEQLRKreWTVGAVSRHPqdLAHITEFRYe---ADVADEFAvqaaVYAAAQElPPVDLWIYAVGDi 80  Caldilinea aerophi...
ADI13339    3 ALIVGATGGIGSALVTALKGs-YALTLVGRDArkLQGLGGGAT----LVPTDVTSel-eVEALFEDlPPQDLLIYAAGAi 76  Truepera radiovict...
AFD24412    3 TMILGATGGIGAATARAFAAqgDTLTLSGRDEgkLAQLAAELGa--aSRVADVGFes-hVRALFEGaPALDTLVYAAGAa 79  Deinococcus gobien...
ADD28919    3 TLLLGATGGIGQALARGLAGrvGRLWLSGRNGavLAALARDLGa--lAVPTELAHel-eVQALAQEvGPLDLLIYAAGAv 79  Meiothermus ruber ...
Feature 1                         #                                      #   #                
2YUT_A     78 -GRASVREAGrdlVEEXLAAHLLTAAFVLKHARFqk--gARAVFFGAYPRYVQVPGfAAYAAAKGALEAYLEAARKEllr 154 Thermus thermophilus
ABU58191   82 lGKPLADTTPa-eWDRILSANVTGAHLAVTHSLAlvpagGHLVFIGAYVDRIMLPKlGAYAASKAALDAYVTVLGKEv-- 158 Roseiflexus casten...
BAM00866   81 lSSPVAELKPa-aWRRILDANLTGAYLATHYSLPllaeqAHLIYLGAYSEKLRLPGlSAYAAAKAGLEAFAAALAKEq-- 157 Caldilinea aerophi...
ADI13339   77 qPAPLSRTSAe-aWARVVDTNLTGLFYTLKHAEPklvtgARVYVLGARPELVNFRGfGAYAAAKAGVAALVKVAAAEw-r 154 Truepera radiovict...
AFD24412   80 wPHPLAEAKAe-qVRQVWNANYFGALWVLKHGLArlapgGRVYLIGARPELVTARGfSQYAASKAALARAAEIARLEt-- 156 Deinococcus gobien...
ADD28919   80 -QKASLREQGmgdLERLSAANLTGLARVLKYAAFnp--qARGVLLGVYPELIAVPGlSGYAATKLGAEGLLNVARKEfrr 156 Meiothermus ruber ...
Feature 1                                                          
2YUT_A    155 EGVHLVLVRLPAVATGLWa-pLGGPPKGALsPEEAARKVLEGLFrePVPALLE 206 Thermus thermophilus
ABU58191  159 RDRRITNVRVGAVDTPLWrkaPFRLPKGAHtPADVAAAVLRAHTegHRGNLDL 211 Roseiflexus castenholzii DSM 13941
BAM00866  158 RKLRITVVRPGAVDTPLWnkmPARLPRNALtPEALAERILDAHQagASGVLDL 210 Caldilinea aerophila DSM 14535
ADI13339  155 RKAHLTLVLPKAVATDFWq-sVGQPPKDALsPEDVAEAIVNSLQgePQAELRV 206 Truepera radiovictrix DSM 17093
AFD24412  157 RGLALTLVLPPAVDTGLWt-qVGRAPKGALsPDAVARAIVADRAgpVQTELRV 208 Deinococcus gobiensis I-0
ADD28919  157 EGVRFCLVRLPAVATGLWa-pLGGAPKNALhPDEAAARILEGVLsePMPEVLE 208 Meiothermus ruber DSM 1279

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