1UGF

HUMAN CARBONIC ANHYDRASE II [HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY THR (A65T)

Summary for 1UGF
DescriptorCARBONIC ANHYDRASE II, MERCURY (II) ION, ZINC ION, ... (5 entities in total)
Functional Keywordslyase, acetylation, zinc, polymorphism, disease mutation
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P00918
Total number of polymer chains1
Total formula weight29408.83
Authors
Scolnick, L.R.,Christianson, D.W. (deposition date: 1996-07-24, release date: 1997-04-01, Last modification date: 2011-07-13)
Primary citationChristianson, D.W.,Scolnick, L.R.
X-ray crystallographic studies of alanine-65 variants of carbonic anhydrase II reveal the structural basis of compromised proton transfer in catalysis.
Biochemistry, 35:16429-16434, 1996
PubMed: 8987974
DOI: 110.1021/bi9617872
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation
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PDB entries from 2021-06-16