Structure of PDB 5ync Chain A

Receptor sequence
>5yncA (length=1052) Species: 573 (Klebsiella pneumoniae) [Search protein sequence]
DVVVRLPDVAVPGEAVQASARQAVIHLVDIAGITSSTPADYATKNLYLWN
NETCDALSAPVADWNDVSTTPTGSDKYGPYWVIPLTKESGCINVIVRDGT
NKLIDSDLRVSFSDFTDRTVSVIAGNSAVYDSRADAFRAAFGVALADAHW
VDKTTLLWPGGENKPIVRLYYSHSSKVAADSNGEFSDKYVKLTPTTVNQQ
VSMRFPHLASYPAFKLPDDVNVDELLQGETVAIAAESDGILSSATQVQTA
GVLDDTYAAAAEALSYGAQLTDSGVTFRVWAPTAQQVELVIYSADKKVIA
SHPMTRDSASGAWSWQGGSDLKGAFYRYAMTVYHPQSRKVEQYEVTDPYA
HSLSTNSEYSQVVDLNDSALKPEGWDGLTMPHAQKTKADLAKMTIHESHI
RDLSAWDQTVPAELRGKYLALTAQESNMVQHLKQLSASGVTHIELLPVFD
LATVNEFSDKVADIQQPFSRLCEVNSAVKSSEFAGYCDSGSTVEEVLTQL
KQNDSKDNPQVQALNTLVAQTDSYNWGYDPFHYTVPEGSYATDPEGTARI
KEFRTMIQAIKQDLGMNVIMDVVYNHTNAAGPTDRTSVLDKIVPWYYQRL
NETTGSVESATCCSDSAPEHRMFAKLIADSLAVWTTDYKIDGFRFDLMLY
HPKAQILSAWERIKALNPDIYFFGEGWDSNQSDRFEIASQINLKGTGIGT
FSDRLRDAVRGGGPFDSGDALRQNQGVGSGAGVLPNELTTLSDDQARHLA
DLTRLGMAGNLADFVLIDKDGAVKRGSEIDYNGAPGGYAADPTEVVNYVS
KHDNQTLWDMISYKAAQEADLDTRVRMQAVSLATVMLGQGIAFDQQGSEL
LRSKSFTRDSYDSGDWFNRVDYSLQDNNYNVGMPRSSDDGSNYDIIARVK
DAVATPGETELKQMTAFYQELTALRKSSPLFTLGDGATVMKRVDFRNTGA
DQQTGLLVMTIDDGMQAGASLDSRVDGIVVAINAAPESRTLQDFAGTSLQ
LSAIQQAAGDRSLASGVQVAADGSVTLPAWSVAVLELPQGESQGAGLPVS
SK
3D structure
PDB5ync Elucidation of the mechanism of interaction between Klebsiella pneumoniae pullulanase and cyclodextrin
ChainA
Resolution2.32 Å
3D
structure
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Enzymatic activity
Enzyme Commision number 3.2.1.41: pullulanase.
Interaction with ligand
Site
#		 Ligand Ligand
chain		 Binding residues on receptor
(original residue number in PDB)		 Binding residues on receptor
(residue number reindexed from 1)		 Binding affinity
BS01 GLC A W95 K133 W64 K102
BS02 GLC A Y78 I126 D138 Y47 I95 D107
BS03 GLC A W708 D734 R737 W677 D703 R706
BS04 GLC A W708 N835 W677 N804
BS05 CA A A550 D553 Y555 D893 A519 D522 Y524 D862
BS06 CA A D148 T150 D162 D117 T119 D131
BS07 CA A D994 S1001 D1003 V1006 Q1070 D963 S970 D972 V975 Q1039
BS08 CA A D481 L482 E487 E568 D450 L451 E456 E537
Gene Ontology
Molecular Function
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0016798 hydrolase activity, acting on glycosyl bonds
GO:0030246 carbohydrate binding
GO:0051060 pullulanase activity
Biological Process
GO:0005975 carbohydrate metabolic process

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Molecular Function
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Biological Process
External links
PDB RCSB:5ync, PDBe:5ync, PDBj:5ync
PDBsum5ync
PubMed30387770
UniProtW9BQ28

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