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4RF5

Crystal structure of ketoreductase from Lactobacillus kefir, E145S mutant

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0008206biological_processbile acid metabolic process
A0016491molecular_functionoxidoreductase activity
A0046872molecular_functionmetal ion binding
B0000166molecular_functionnucleotide binding
B0008206biological_processbile acid metabolic process
B0016491molecular_functionoxidoreductase activity
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 301
ChainResidue
AGLN252
AHOH465
AHOH466
AHOH467
AHOH468
BGLN252

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG A 302
ChainResidue
AHOH471
AHOH472
AHOH473
AHOH474
AASP25
AASP180
AHOH470

site_idAC3
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 303
ChainResidue
AASP180
AVAL181
AARG182
ALYS236
AHOH443
AHOH519
AHOH543
BMET214

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 304
ChainResidue
AASP3
AVAL28
AGLU29
ALYS177

Functional Information from PROSITE/UniProt
site_idPS00061
Number of Residues29
DetailsADH_SHORT Short-chain dehydrogenases/reductases family signature. SisgfvgdptLgaYNASKGAVrIMSkSAA
ChainResidueDetails
ASER143-ALA171

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Proton donor/acceptor","evidences":[{"source":"PubMed","id":"26644568","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues24
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"26644568","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"4RF2","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"26644568","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"4RF4","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

238895

PDB entries from 2025-07-16

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