review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Nick Grishin | Q21339744 |
P2093 | author name string | Lisa N Kinch | |
P2860 | cites work | Crystal structure and mutational analysis of the human CDK2 kinase complex with cell cycle-regulatory protein CksHs1 | Q24322626 |
Structure of the EMAPII domain of human aminoacyl-tRNA synthetase complex reveals evolutionary dimer mimicry | Q24536732 | ||
X-ray structure of HPr kinase: a bacterial protein kinase with a P-loop nucleotide-binding domain | Q24550266 | ||
Sialidase-like Asp-boxes: sequence-similar structures within different protein folds | Q24644728 | ||
Evolution of a protein fold in vitro | Q27617828 | ||
Protein plasticity to the extreme: changing the topology of a 4-alpha-helical bundle with a single amino acid substitution | Q27619031 | ||
The solution structure of VAT-N reveals a 'missing link' in the evolution of complex enzymes from a simple betaalphabetabeta element | Q27620039 | ||
The small subunit of carbamoyl phosphate synthetase: snapshots along the reaction pathway | Q27620602 | ||
Peptide exosite inhibitors of factor VIIa as anticoagulants | Q27622190 | ||
Structural evidence for evolution of the beta/alpha barrel scaffold by gene duplication and fusion | Q27626847 | ||
A comparative analysis of 23 structures of the amyloidogenic protein transthyretin | Q27627061 | ||
The N-terminal domain of betaB2-crystallin resembles the putative ancestral homodimer | Q27628614 | ||
The beta-slip: a novel concept in transthyretin amyloidosis | Q27628857 | ||
Crystal structure of an intracellular protease from Pyrococcus horikoshii at 2-A resolution | Q27628891 | ||
Effect of pH and salt bridges on structural assembly: Molecular structures of the monomer and intertwined dimer of the Eps8 SH3 domain | Q27631320 | ||
Crystal structures of mitochondrial processing peptidase reveal the mode for specific cleavage of import signal sequences | Q27633600 | ||
??? | Q57266876 | ||
The factor VII zymogen structure reveals reregistration of beta strands during activation | Q27633608 | ||
Conversion of monomeric protein L to an obligate dimer by computational protein design | Q27634559 | ||
The structure of an engineered domain-swapped ribonuclease dimer and its implications for the evolution of proteins toward oligomerization | Q27635280 | ||
Structure and properties of a dimeric N-terminal fragment of human ubiquitin | Q27636584 | ||
Crystal structures at 2.2 A resolution of the catalytic domains of normal ras protein and an oncogenic mutant complexed with GDP | Q27652843 | ||
Structure of ubiquitin refined at 1.8 A resolution | Q27728512 | ||
Slow- and fast-binding inhibitors of thermolysin display different modes of binding: crystallographic analysis of extended phosphonamidate transition-state analogues | Q27728601 | ||
Crystal structure of the cell cycle-regulatory protein suc1 reveals a beta-hinge conformational switch | Q27729296 | ||
Crystal structure of Vibrio cholerae neuraminidase reveals dual lectin-like domains in addition to the catalytic domain | Q27730702 | ||
Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria | Q27730864 | ||
The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor | Q27732597 | ||
Molecular basis of sulfite oxidase deficiency from the structure of sulfite oxidase | Q27748778 | ||
The crystal structure of a 3D domain-swapped dimer of RNase A at a 2.1-A resolution | Q27748984 | ||
Adenylyl cyclase Rv1625c of Mycobacterium tuberculosis: a progenitor of mammalian adenylyl cyclases | Q28343731 | ||
Evolution of function in protein superfamilies, from a structural perspective. | Q30328084 | ||
Of barn owls and bankers: a lush variety of alpha/beta hydrolases | Q33686427 | ||
Human alpha 1-proteinase inhibitor. Crystal structure analysis of two crystal modifications, molecular model and preliminary analysis of the implications for function | Q34255957 | ||
Fold change in evolution of protein structures | Q34364834 | ||
On the evolution of protein folds: are similar motifs in different protein folds the result of convergence, insertion, or relics of an ancient peptide world? | Q34364840 | ||
Molecular structure of a new family of ribonucleases | Q36646102 | ||
The bifunctional cytochrome c reductase/processing peptidase complex from plant mitochondria | Q40966587 | ||
Structure of the complex of yeast adenylate kinase with the inhibitor P1,P5-di(adenosine-5'-)pentaphosphate at 2.6 A resolution | Q43563682 | ||
An evolutionary bridge to a new protein fold. | Q44361211 | ||
Supersites within superfolds. Binding site similarity in the absence of homology | Q47749122 | ||
Observation of signal transduction in three-dimensional domain swapping | Q57838465 | ||
The C-terminal domain of HPII catalase is a member of the type I glutamine amidotransferase superfamily | Q73303306 | ||
P433 | issue | 3 | |
P304 | page(s) | 400-408 | |
P577 | publication date | 2002-06-01 | |
P1433 | published in | Current Opinion in Structural Biology | Q15758416 |
P1476 | title | Evolution of protein structures and functions | |
P478 | volume | 12 |