3GVC


Conserved Protein Domain Family
SDR_c12

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cd08944: SDR_c12 
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classical (c) SDR, subgroup 12
These are classical SDRs, with the canonical active site tetrad and glycine-rich NAD-binding motif. 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 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-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: 187648
Aligned: 6 rows
Threshold Bit Score: 289.776
Created: 8-Jan-2010
Updated: 2-Oct-2020
Structure
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Program:
Drawing:
Aligned Rows:
 
Conserved site includes 4 residues -Click on image for an interactive view with Cn3D
Feature 1:active site [active site]
Evidence:

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                                                                                        
3GVC_A        27 LAGKVAIVTGAGAGIGLAVARRLADEGcHVLCADIDGDAADAAATKIg---cGAAACRVDVSDEQQIIAMVDACVaaFGG 103 Mycobacterium t...
CAD31474     103 FEGKVAVVTGAGAGIGKACALAIAREGgRVVVADIDGSAAVACTAQIaaeagHALALAMDIADAQAVAALFETAErhFGG 182 Mesorhizobium loti
ZP_04383372    5 LANKVAIVTGAGAGIGAAIARAFGAEGaRVVVSDINGGAAQAVADSId----GAIAVTTDVTDEQQVKDLVARAVeeFGG 80  Rhodococcus ery...
BAC47411       4 FEGKVAVVTGAGAGIGKACALAIAREGgRVVVADIDGSAAIACTAQIaaeagHALALAIDIADAQAVAALFETAErhFGG 83  Bradyrhizobium ...
YP_001774481   4 VKGKIAIVTGAASGIGAACAARLAHEGaSVVVADLNLEGAQEQVRHIadsggHAVAARVDIGDECSIEALFDLTLktWGG 83  Burkholderia ce...
YP_702630      5 LEGKVVIVTGSGGGIGAVIAARFAKEGaRVVVSDRHRGAAEAVVSRIp----GASAIPADVTREQDVSALIERTVeeHGA 80  Rhodococcus sp....
Feature 1                                           #                           #            #   
3GVC_A       104 VDKLVANAGVVHLAs-----LIDTTVEDFDRVIAINLRGAWLCTKHAAPRMIERGGGAIVNLSSLAGqvavggtGAYGMS 178 Mycobacterium t...
CAD31474     183 VDLLVNNASAMHLTprd-rtILDLDLAVWDQTMATNLRGTLLCCRQAIPRMIARGGGAIVNMSSCQGlsgdtaqTSYAAS 261 Mesorhizobium loti
ZP_04383372   81 LNVVVPNAGIATTTp-----LIETSFEDWRKVMSVNLDGVFLTVRHSLPALVASGGGSIVNISSISSttgspliGSYAAA 155 Rhodococcus ery...
BAC47411      84 VDLLVNNASAMHLTprd-raILELELAVWDQTMATNLRGTLLCCRQAIPRMIARGGGAIVNMSSCQGlsgdtalTSYAAS 162 Bradyrhizobium ...
YP_001774481  84 LDILHNNAAATSLSstadaaIEAIDVAVWDDTMRINLRGTMLASRRALPLMRSRGGGSIINTSSGAAqagalgySAYGVC 163 Burkholderia ce...
YP_702630     81 LHHVVANAGIISASh----pIAQTPLDVWRSTMSVNLDGVFLTIKHSAAAIANSGGGSILTLSSISGtggtplaAAYGAS 156 Rhodococcus sp....
Feature 1        #                                                                               
3GVC_A       179 KAGIIQLSRITAAELrssGIRSNTLLPAFVDTPMqqtamamfdgalg--aggarsmiarlqgRMAAPEEMAGIVVFLLSD 256 Mycobacterium t...
CAD31474     262 KAAMNMLSASLATQYghaQIRCNAVAPGLIMTERllakldecmq--------rhlsrhqllqRVGRPEDVAALVAFLLSD 333 Mesorhizobium loti
ZP_04383372  156 KAAVRNLTETLSAELrfhGIRANALLPGFIDTDLvkshqqdfenalglesggfddlmvtkqtRYGRTEEVAAAAVFFASD 235 Rhodococcus ery...
BAC47411     163 KAAMNMLSSSLATQYghaQIRCNAVAPGLIMTERllakldacmq--------thlrrhqllpRVGRPEDVAALVAFLLSD 234 Bradyrhizobium ...
YP_001774481 164 KAGIENLTRYIAAQYgkeGIRCNAIAPGLIVTPVtrayyagelg--------emmlshhltpRLGVPEDIAHAVVYLASD 235 Burkholderia ce...
YP_702630    157 KAAVRNLTATAAGELraqNVRVNALVPGYVDTPLidsevpvwestmglapggfaqvidqkqgRLISPEDIADAALFLTSD 236 Rhodococcus sp....
Feature 1                       
3GVC_A       257 DASMITGTTQIADGG 271 Mycobacterium tuberculosis H37Rv
CAD31474     334 DAAFITGQVLCIDGG 348 Mesorhizobium loti
ZP_04383372  236 QSSWCNGSSLVLDGG 250 Rhodococcus erythropolis SK121
BAC47411     235 DAAFITGQVVCIDGG 249 Bradyrhizobium japonicum USDA 110
YP_001774481 236 EAAFVTGQVFNVDGG 250 Burkholderia cenocepacia MC0-3
YP_702630    237 QASMITGSALTVDGG 251 Rhodococcus sp. RHA1

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