2JAP,2JAH


Conserved Protein Domain Family
CAD_SDR_c

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cd08934: CAD_SDR_c 
Click on image for an interactive view with Cn3D
clavulanic acid dehydrogenase (CAD), classical (c) SDR
CAD catalyzes the NADP-dependent reduction of clavulanate-9-aldehyde to clavulanic acid, a beta-lactamase inhibitor. 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: 187639
Aligned: 8 rows
Threshold Bit Score: 347.218
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                                                                                                 
2JAP_A                  5 LQGKVALITGASSGIGEATARALAAEGAAVAIAARRVEKLRALGDELTAAGAKVHVLELDVADRQGVDAAVASTVEALGG 84  Strept...
2JAH_A                  5 LQGKVALITGASSGIGEATARALAAEGAAVAIAARRVEKLRALGDELTAAGAKVHVLELDVADRQGVDAAVASTVEALGG 84  Strept...
ZP_05804874             5 LEGHVALVTGAGSGIGRATARALASAGASVAVAGRRVDRLEELRDELEAEGGTVLVLELDVTDEQAVGAAVRAAVETLGR 84  Strept...
CAA04227                5 LQGKVALITGRELGHRRATARALAPEGAAVAIAARRVEKLRALGDELTAAGAKVHVLELDVADRQGVDAAVASTVEALGG 84  Strept...
EEW71481                5 LEGHVALVTGAGSGIGRATARALASAGASVAVAGRRVDRLEELRDELEAEGGTVLVLELDVTDEQAVGAAVRAAVETLGR 84  Strept...
DeideDB:Deide_3p00660   8 LAGKVAVVTGASSGIGAATALALAAQGASVVLVARREDRLQDLARQVQSSGGHAEVVVADLADEAQARLTVERAVSAFGR 87  Deinoc...
EFA72770                5 LDGKVAIITGASSGIGEATAFALAAEGAKVAIAARRAELLHALAKRIEASGGQALPIVTDITDESQVNHLVQKTKVELGH 84  Raphid...
CAJ63380                1 MTGTVAFVTGASSGIGAATGRELARRGAAVALVARRKDRLEQLAAEIQGEGGRALVVGTDITDQRQAIDAVERTVAELGR 80  Franki...
Feature 1                                               #                                 #            #  
2JAP_A                 85 LDILVNNAGIMLLGPVEDADTTDWTRMIDTNLLGLMYMTRAALP-------HLLRSKGTVVQMSSIAGRVNVRNAAVYQA 157 Strept...
2JAH_A                 85 LDILVNNAGIXLLGPVEDADTTDWTRXIDTNLLGLXYXTRAALP-------HLLRSKGTVVQXSSIAGRVNVRNAAVYQA 157 Strept...
ZP_05804874            85 LDILVNNAGLMLLGPVENADTTDWTRMMDTNVMGLMYTTHAALP-------ELIRNQGTIVQISSIAARVVGRGSAVYNA 157 Strept...
CAA04227               85 LDILVNNAGIMLLGPVEDADTTDWTRMIDTNLLGLMYMTRAALP-------HLLRSKGTVVQMSSIAGRVTVRNAAVYQA 157 Strept...
EEW71481               85 LDILVNNAGLMLLGPVENADTTDWTRMMDTNVMGLMYTTHAALP-------ELIRNQGTIVQISSIAARVVGRGSAVYNA 157 Strept...
DeideDB:Deide_3p00660  88 VDILVNNAGLMLLGPVTGADTTDWRRMIDVNLLGLMYTTHAALPh------MRTQGGGHIVNISSVSGRGASPTSAGYSA 161 Deinoc...
EFA72770               85 VDILVNNAGIGVFGAIDTGNPADWRRAFDVNVLGVLYAIHAVLPl------LKAQKSGHIVNISSVDGRIAQSGAVVYSA 158 Raphid...
CAJ63380               81 LDTVVNNAGVMLLGPIVDAPTAEWDRMVALNLQGLLYVAHAALPhlltaadSGPRNVADLVNISSVAGRRATPNSGVYNL 160 Franki...
Feature 1                  #                                                                              
2JAP_A                158 TKFGVNAFSETLRQEVTERGVRVVVIEPGTTDTELRGHITHTATKemyeQRISQIRKLQAQDIAEAVRYAVTAPHHATVH 237 Strept...
2JAH_A                158 TKFGVNAFSETLRQEVTERGVRVVVIEPGTTDTELRGHITHTATKexyeQRISQIRKLQAQDIAEAVRYAVTAPHHATVH 237 Strept...
ZP_05804874           158 TKFAVNGFSEGLRQEVTERGVRVVVIEPGTVETELREHITHAPSKaaiaERVAKIRQLQSEDIAAAVLYAVTAPPHATVN 237 Strept...
CAA04227              158 TKFGVNAFSETVRQEVTERGVRVVVIEPGTTDTELRGHITHTATKemyeQRISQIRKLQAQDIAEAVRYAVTAPHHATVH 237 Strept...
EEW71481              158 TKFAVNGFSEGLRQEVTERGVRVVVIEPGTVETELREHITHAPSKaaiaERVAKIRQLQSEDIAAAVLYAVTAPPHATVN 237 Strept...
DeideDB:Deide_3p00660 162 SKWGVGGFSEGLRQEVRLDRIRVTVIEPGVVATELTDHITHQDTKvayeGRIQTMIPLEAEDIAAAVVYAVTQPERVNVN 241 Deinoc...
EFA72770              159 AKSGVNALSEALRQEVSLDNIRVTIIEPGLVDTPFNDLISDPITKqlskEQLSTITPLQSEDIARAIIYAVTQPDHVNVN 238 Raphid...
CAJ63380              161 TKFGVNAFTESLRQEVTERRVRVSVVEPGAVVTELADHLREEIREta-mRVFADVEKLQADDIADAIAYIVTRPRRVAVN 239 Franki...
Feature 1                          
2JAP_A                238 EIFIRPTDQ 246 Streptomyces clavuligerus
2JAH_A                238 EIFIRPTDQ 246 Streptomyces clavuligerus
ZP_05804874           238 EIFIRPTDQ 246 Streptomyces flavogriseus ATCC 33331
CAA04227              238 EIFIRPTDQ 246 Streptomyces clavuligerus ATCC 27064
EEW71481              238 EIFIRPTDQ 246 Streptomyces flavogriseus ATCC 33331
DeideDB:Deide_3p00660 242 EILIRPLDQ 250 Deinococcus deserti VCD115
EFA72770              239 EILIRPTAE 247 Raphidiopsis brookii D9
CAJ63380              240 EMLIRPTEQ 248 Frankia alni ACN14a

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