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| - | [[Image:2rkb.jpg|left|200px]] | + | {{Seed}} |
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| | {{STRUCTURE_2rkb| PDB=2rkb | SCENE= }} | | {{STRUCTURE_2rkb| PDB=2rkb | SCENE= }} |
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| - | '''Serine dehydratase like-1 from human cancer cells'''
| + | ===Serine dehydratase like-1 from human cancer cells=== |
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| - | ==Overview==
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| - | SDH (l-serine dehydratase, EC 4.3.1.17) is a pyridoxal-5'-phosphate (PLP)-dependent enzyme that catalyzes dehydration of l-Ser/Thr to yield pyruvate/ketobutyrate and ammonia. A SDH isoform (cSDH) found in human cancer cell lines has relatively low catalytic activity in comparison with the liver enzyme (hSDH). The crystal structure of cSDH has been determined at 2.8 A resolution. A PLP is covalently attached to K48 by Schiff-base linkage in the active site. The ring nitrogen of PLP is involved in a H-bonding with C309, but is apparently not protonated. Twenty-three amino residues that compose the active site surfaces were identified. The human and rat liver enzymes (hSDH and rSDH) have the same residues, while residues G72, A172, and S228 in cSDH are replaced with A66, S166, and A222, respectively, in hSDH. These residues in hSDH and cSDH were mutated to make complementary pairs of mutated enzymes, and their kinetic parameters were determined. C303 of hSDH and C309 of cSDH which are H-bonding partner of the ring nitrogen of PLP were mutated to alanine and their kinetic parameters were also determined. The crystal structures and the mutation data suggest that having a glycine at residue 72 of cSDH is the major reason for the reduction of catalytic activity of cSDH. Changing alanine to glycine at residue 72 increases the flexibility of the substrate binding-loop ((71)S(G/A)GN(74)), so that the bound substrate and PLP are not pushed deep into the active cleft. Consequently, the proton transfer rate from S(G) of C309 to N(1) of the bound PLP is decreased, which determines the rate of catalytic reaction.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_18342636}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 18342636 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_18342636}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Pyridoxal phosphate]] | | [[Category: Pyridoxal phosphate]] |
| | [[Category: Serine dehydratase]] | | [[Category: Serine dehydratase]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May 14 11:39:34 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 03:00:06 2008'' |
Revision as of 00:00, 28 July 2008
Template:STRUCTURE 2rkb
Serine dehydratase like-1 from human cancer cells
Template:ABSTRACT PUBMED 18342636
About this Structure
2RKB is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
A catalytic mechanism that explains a low catalytic activity of serine dehydratase like-1 from human cancer cells: Crystal structure and site-directed mutagenesis studies., Yamada T, Komoto J, Kasuya T, Takata Y, Ogawa H, Mori H, Takusagawa F, Biochim Biophys Acta. 2008 Feb 19;. PMID:18342636
Page seeded by OCA on Mon Jul 28 03:00:06 2008
