human | Q5 |
P8179 | Canadiana Name Authority ID | ncf11610423 |
P2456 | DBLP author ID | 49/5583 |
P1960 | Google Scholar author ID | AtclWv4AAAAJ |
P269 | IdRef ID | 154778524 |
P213 | ISNI | 0000000122674821 |
P244 | Library of Congress authority ID | no2011112810 |
P8189 | National Library of Israel J9U ID | 987007332718905171 |
P1006 | Nationale Thesaurus voor Auteursnamen ID | 334422434 |
P1315 | NLA Trove people ID | 1709564 |
P1207 | NUKAT ID | n2011055928 |
P856 | official website | https://research.monash.edu/en/persons/d2afe85c-0d13-4da3-aaa1-8a53a054a118 |
P496 | ORCID iD | 0000-0003-4200-5611 |
P3065 | RERO ID (obsolete) | 02-A019083483 |
P1153 | Scopus author ID | 56247908700 |
P214 | VIAF ID | 172544423 |
P10832 | WorldCat Entities ID | E39PCjvmyMRrBjqp8Cc4K739fy |
P166 | award received | Gottschalk Medal | Q5588086 |
P69 | educated at | University of Cambridge | Q35794 |
P108 | employer | Monash University | Q598841 |
P734 | family name | Whisstock | Q121437845 |
Whisstock | Q121437845 | ||
Whisstock | Q121437845 | ||
P735 | given name | James | Q677191 |
James | Q677191 | ||
P106 | occupation | structural biologist | Q84505215 |
P21 | sex or gender | male | Q6581097 |
Q27677421 | A Molecular Switch Governs the Interaction between the Human Complement Protease C1s and Its Substrate, Complement C4 |
Q27647495 | A common fold mediates vertebrate defense and bacterial attack |
Q27321259 | A new model for pore formation by cholesterol-dependent cytolysins |
Q34785379 | A serpin in the cellulosome of the anaerobic fungus Piromyces sp. strain E2. |
Q27649735 | A structural basis for loop C-sheet polymerization in serpins |
Q27640322 | A structural basis for the selection of dominant alphabeta T cell receptors in antiviral immunity |
Q38149466 | A tale of two specificities: bispecific antibodies for therapeutic and diagnostic applications |
Q36351013 | A versatile monoclonal antibody specific to human SERPINB5 |
Q53595113 | AB5 subtilase cytotoxin inactivates the endoplasmic reticulum chaperone BiP. |
Q34652212 | Aeropin from the extremophile Pyrobaculum aerophilum bypasses the serpin misfolding trap |
Q50212903 | An Essential Role of Maspin in Embryogenesis and Tumor Suppression-Letter. |
Q41736938 | An atlas of serpin conformations. |
Q24684030 | An overview of the serpin superfamily |
Q49235374 | An ultrastructural investigation of tumors undergoing regression mediated by immunotherapy |
Q36407319 | Analysis of Perforin Assembly by Quartz Crystal Microbalance Reveals a Role for Cholesterol and Calcium-independent Membrane Binding |
Q101575486 | Ancient but Not Forgotten: New Insights Into MPEG1, a Macrophage Perforin-Like Immune Effector |
Q36249909 | Antibodies: From novel repertoires to defining and refining the structure of biologically important targets. |
Q35612476 | Antithrombin: in control of coagulation |
Q57079380 | Assembling the machinery of coagulation |
Q30408074 | Automatic generation of protein structure cartoons with Pro-origami |
Q27671783 | Bestatin-based chemical biology strategy reveals distinct roles for malaria M1- and M17-family aminopeptidases |
Q37844034 | Bioinformatic approaches for predicting substrates of proteases |
Q53504215 | Bone morphogenetic protein/retinoic acid inducible neural-specific protein (brinp) expression during Danio rerio development. |
Q27322895 | Brinp1(-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density |
Q57079437 | CLIMS: Crystallography Laboratory Information Management System |
Q57079408 | COOH-Terminal Clustering of Autoantibody and T-Cell Determinants on the Structure of GAD65 Provide Insights Into the Molecular Basis of Autoreactivity |
Q57079378 | Capturing embryonic development from metamorphosis: how did the terminal patterning signalling pathway of Drosophila evolve? |
Q47837736 | Cascleave 2.0, a new approach for predicting caspase and granzyme cleavage targets |
Q43174713 | Cascleave: towards more accurate prediction of caspase substrate cleavage sites |
Q33925076 | Cationic sites on granzyme B contribute to cytotoxicity by promoting its uptake into target cells |
Q30042214 | Cell Traversal Activity Is Important for Plasmodium falciparum Liver Infection in Humanized Mice |
Q33932541 | Characterization of an adapter subunit to a phosphatidylinositol (3)P 3-phosphatase: identification of a myotubularin-related protein lacking catalytic activity |
Q57079453 | Characterization of epitope regions of thyrotropin β-subunit recognized by the monoclonal antibodies mAb279 and mAb299: a chimeric peptide approach |
Q44608196 | Characterization of the specificity of arginine-specific gingipains from Porphyromonas gingivalis reveals active site differences between different forms of the enzymes |
Q24672272 | Cleaved antitrypsin polymers at atomic resolution |
Q34943452 | Cloning and expression of the major secreted cathepsin B-like protein from juvenile Fasciola hepatica and analysis of immunogenicity following liver fluke infection. |
Q48213232 | Computational analysis of evolution and conservation in a protein superfamily |
Q33415482 | Conformational change in the chromatin remodelling protein MENT |
Q27313232 | Conformational changes during pore formation by the perforin-related protein pleurotolysin |
Q57079448 | Conformational changes in serpins: I. the native and cleaved conformations of α 1 -antitrypsin 1 1Edited by J. M. Thornton |
Q33916072 | Conformational changes in serpins: II. The mechanism of activation of antithrombin by heparin. |
Q57079460 | Conservation within the myosin motor domain: implications for structure and function |
Q36824107 | Corrigendum: N-terminal domain of Bothrops asper Myotoxin II Enhances the Activity of Endothelin Converting Enzyme-1 and Neprilysin. |
Q58028932 | Crystal structure of TcpK in complex with oriT DNA of the antibiotic resistance plasmid pCW3 |
Q33707312 | Crystallization of the virulent and benign subtilisin-like proteases from the ovine footrot pathogen Dichelobacter nodosus |
Q51763918 | Crystallography of serpins and serpin complexes. |
Q34007408 | DNA accelerates the inhibition of human cathepsin V by serpins |
Q27686809 | Defining the interaction of perforin with calcium and the phospholipid membrane |
Q30874190 | Determination of the P1', P2' and P3' subsite-specificity of factor Xa. |
Q39479462 | Development of the Cellular Immune System of Drosophila Requires the Membrane Attack Complex/Perforin-Like Protein Torso-Like |
Q48199620 | EGM: encapsulated gene-by-gene matching to identify gene orthologs and homologous segments in genomes |
Q35860618 | Efficient large-scale protein sequence comparison and gene matching to identify orthologs and co-orthologs |
Q33223538 | Elucidation of the substrate specificity of the C1s protease of the classical complement pathway |
Q33294670 | Elucidation of the substrate specificity of the MASP-2 protease of the lectin complement pathway and identification of the enzyme as a major physiological target of the serpin, C1-inhibitor |
Q33958456 | Evidence that serpin architecture intrinsically supports papain-like cysteine protease inhibition: engineering alpha(1)-antitrypsin to inhibit cathepsin proteases |
Q33345190 | Federated repositories of X-ray diffraction images |
Q34168471 | Fingerprinting the substrate specificity of M1 and M17 aminopeptidases of human malaria, Plasmodium falciparum |
Q35046397 | Functional analysis of the Listeria monocytogenes secretion chaperone PrsA2 and its multiple contributions to bacterial virulence |
Q33736258 | Functional insights from the distribution and role of homopeptide repeat-containing proteins |
Q27644229 | GABA production by glutamic acid decarboxylase is regulated by a dynamic catalytic loop |
Q49832688 | Genome-Wide Screen for New Components of the Drosophila melanogaster Torso Receptor Tyrosine Kinase Pathway |
Q38647638 | Giant MACPF/CDC pore forming toxins: A class of their own. |
Q35539708 | GlycoMine: a machine learning-based approach for predicting N-, C- and O-linked glycosylation in the human proteome |
Q35131686 | Glycoprotein Ib-IX-V. |
Q27683525 | High resolution structure of cleaved Serpin 42 Da from Drosophila melanogaster |
Q57079396 | Highlight: The Biology of Proteolytic Systems |
Q56917400 | Hijacking of a Substrate-binding Protein Scaffold for use in Mycobacterial Cell Wall Biosynthesis |
Q57079372 | Homodimerization attenuates the anti-inflammatory activity of interleukin-37 |
Q35652972 | Human clade B serpins (ov-serpins) belong to a cohort of evolutionarily dispersed intracellular proteinase inhibitor clades that protect cells from promiscuous proteolysis. |
Q24305291 | Hurpin is a selective inhibitor of lysosomal cathepsin L and protects keratinocytes from ultraviolet-induced apoptosis |
Q31967214 | IFI60/ISG60/IFIT4, a new member of the human IFI54/IFIT2 family of interferon-stimulated genes. |
Q28258076 | IL-37 requires the receptors IL-18Rα and IL-1R8 (SIGIRR) to carry out its multifaceted anti-inflammatory program upon innate signal transduction |
Q24292896 | Identification of a novel domain in two mammalian inositol-polyphosphate 5-phosphatases that mediates membrane ruffle localization. The inositol 5-phosphatase skip localizes to the endoplasmic reticulum and translocates to membrane ruffles ... |
Q43559280 | Importance of the P4' residue in human granzyme B inhibitors and substrates revealed by scanning mutagenesis of the proteinase inhibitor 9 reactive center loop |
Q33195942 | Importance of the prime subsites of the C1s protease of the classical complement pathway for recognition of substrates |
Q30804202 | Inhibitory activity of a heterochromatin-associated serpin (MENT) against papain-like cysteine proteinases affects chromatin structure and blocks cell proliferation |
Q44561956 | Introduction of a mutation in the shutter region of antithrombin (Phe77 --> Leu) increases affinity for heparin and decreases thermal stability |
Q51806809 | Leucine-rich repeats 2-4 (Leu60-Glu128) of platelet glycoprotein Ibalpha regulate shear-dependent cell adhesion to von Willebrand factor. |
Q33553223 | MUSTANG-MR structural sieving server: applications in protein structural analysis and crystallography |
Q51190031 | MUSTANG: a multiple structural alignment algorithm. |
Q31018502 | Managing and mining protein crystallization data. |
Q24634632 | Maspin (SERPINB5) is an obligate intracellular serpin |
Q24612315 | Maspin is not required for embryonic development or tumour suppression |
Q38790905 | Maternal Torso-Like Coordinates Tissue Folding During Drosophila Gastrulation |
Q34589048 | Mechanisms of serpin dysfunction in disease. |
Q27680739 | Mechanistic characterization and crystal structure of a small molecule inactivator bound to plasminogen activator inhibitor-1 |
Q30370262 | Mice Lacking Brinp2 or Brinp3, or Both, Exhibit Behaviors Consistent with Neurodevelopmental Disorders. |
Q71856538 | Modeling of serpin-protease complexes: antithrombin-thrombin, alpha 1-antitrypsin (358Met-->Arg)-thrombin, alpha 1-antitrypsin (358Met-->Arg)-trypsin, and antitrypsin-elastase |
Q45971313 | Modulation of the proteolytic activity of the complement protease C1s by polyanions: implications for polyanion-mediated acceleration of interaction between C1s and SERPING1. |
Q24337646 | Molecular basis of α1-antitrypsin deficiency revealed by the structure of a domain-swapped trimer |
Q42929194 | Molecular contortionism - on the physical limits of serpin 'loop-sheet' polymers |
Q40749760 | Molecular determinants of the mechanism underlying acceleration of the interaction between antithrombin and factor Xa by heparin pentasaccharide |
Q34000643 | Molecular gymnastics: serpin structure, folding and misfolding |
Q33553231 | MrGrid: a portable grid based molecular replacement pipeline |
Q30785263 | Multiple alignment and sorting of peptides derived from phage-displayed random peptide libraries with polyclonal sera allows discrimination of relevant phagotopes |
Q38711306 | N-terminal domain of Bothrops asper Myotoxin II Enhances the Activity of Endothelin Converting Enzyme-1 and Neprilysin |
Q38164155 | New insights into the structure and function of the plasminogen/plasmin system. |
Q34500105 | PROSPER: an integrated feature-based tool for predicting protease substrate cleavage sites |
Q38496608 | Perforin and granzymes: function, dysfunction and human pathology |
Q34253572 | Perforin evolved from a gene duplication of MPEG1, followed by a complex pattern of gene gain and loss within Euteleostomi |
Q44770736 | Perforin forms transient pores on the target cell plasma membrane to facilitate rapid access of granzymes during killer cell attack |
Q50129807 | Perforin proteostasis is regulated through its C2 domain: supra-physiological cell death mediated by T431D-perforin. |
Q38652776 | Perforin-A key (shaped) weapon in the immunological arsenal. |
Q34620426 | Perforin: structure, function, and role in human immunopathology |
Q54977796 | PhosContext2vec: a distributed representation of residue-level sequence contexts and its application to general and kinase-specific phosphorylation site prediction. |
Q33928073 | Phylogeny of the serpin superfamily: implications of patterns of amino acid conservation for structure and function. |
Q37606793 | Plasmodium falciparum neutral aminopeptidases: new targets for anti-malarials |
Q51369996 | PoPS: a computational tool for modeling and predicting protease specificity. |
Q30155348 | Predicting giant transmembrane β-barrel architecture |
Q34073203 | Predicting serpin/protease interactions |
Q33976748 | Prediction of protein function from protein sequence and structure |
Q40883950 | Preferential Acquisition and Activation of Plasminogen Glycoform II by PAM Positive Group A Streptococcal Isolates. |
Q43942603 | Probing the role of the F-helix in serpin stability through a single tryptophan substitution |
Q52534363 | Probing the unfolding pathway of alpha1-antitrypsin. |
Q21142748 | Prodepth: predict residue depth by support vector regression approach from protein sequences only |
Q51562730 | Progressive multiple alignment using sequence triplet optimizations and three-residue exchange costs. |
Q38011488 | Protecting a serial killer: pathways for perforin trafficking and self-defence ensure sequential target cell death |
Q39527555 | Protection from endogenous perforin: glycans and the C terminus regulate exocytic trafficking in cytotoxic lymphocytes |
Q27331221 | RAB-like 2 has an essential role in male fertility, sperm intra-flagellar transport, and tail assembly |
Q35854840 | RCPdb: An evolutionary classification and codon usage database for repeat-containing proteins |
Q42667386 | REFOLD: an analytical database of protein refolding methods |
Q40343450 | Real-time visualization of perforin nanopore assembly. |
Q27683425 | Reconciling the Structural Attributes of Avian Antibodies |
Q47952775 | Regulation of perforin activation and pre-synaptic toxicity through C-terminal glycosylation |
Q54519784 | Role of the M-loop and reactive center loop domains in the folding and bridging of nucleosome arrays by MENT. |
Q27674974 | S1 Pocket of a Bacterially Derived Subtilisin-like Protease Underpins Effective Tissue Destruction |
Q34636554 | SERPINB11 is a new noninhibitory intracellular serpin. Common single nucleotide polymorphisms in the scaffold impair conformational change |
Q30175759 | SH3 domains in prokaryotes |
Q24338773 | SerpinB6 is an inhibitor of kallikrein-8 in keratinocytes |
Q46714514 | Serpins 2005 - fun between the beta-sheets. Meeting report based upon presentations made at the 4th International Symposium on Serpin Structure, Function and Biology (Cairns, Australia). |
Q24597270 | Serpins flex their muscle: I. Putting the clamps on proteolysis in diverse biological systems |
Q24597208 | Serpins flex their muscle: II. Structural insights into target peptidase recognition, polymerization, and transport functions |
Q57079410 | Serpins' mystery solved |
Q34974665 | Serpins: finely balanced conformational traps |
Q37282499 | Smoothing a rugged protein folding landscape by sequence-based redesign |
Q35586527 | Stability of the octameric structure affects plasminogen-binding capacity of streptococcal enolase |
Q36394195 | Stonefish toxin defines an ancient branch of the perforin-like superfamily. |
Q28266624 | Structural Basis for Ca2+-mediated Interaction of the Perforin C2 Domain with Lipid Membranes |
Q27676177 | Structural and Functional Analysis of the Pore-Forming Toxin NetB from Clostridium perfringens |
Q57079439 | Structural and functional analysis of the Josephin domain of the polyglutamine protein ataxin-3 |
Q27653672 | Structural basis for the inhibition of the essential Plasmodium falciparum M1 neutral aminopeptidase |
Q54714680 | Structural biology: Torqueing about pores. |
Q27674978 | Structural characterization of the mechanism through which human glutamic acid decarboxylase auto-activates |
Q39943963 | Structural determinants of GAD antigenicity |
Q47575939 | Structural insights into multi-protein communication systems |
Q27655427 | Structural mechanisms of inactivation in scabies mite serine protease paralogues |
Q27654213 | Structure of granzyme C reveals an unusual mechanism of protease autoinhibition |
Q27659580 | Structure of the Plasmodium falciparum M17 aminopeptidase and significance for the design of drugs targeting the neutral exopeptidases |
Q28115911 | Structure of the poly-C9 component of the complement membrane attack complex |
Q44203934 | Subunit gamma-green fluorescent protein fusions are functionally incorporated into mitochondrial F1F0-ATP synthase, arguing against a rigid cap structure at the top of F1. |
Q27667128 | Synthesis of New (−)-Bestatin-Based Inhibitor Libraries Reveals a Novel Binding Mode in the S1 Pocket of the Essential Malaria M1 Metalloaminopeptidase |
Q40368484 | T cell receptor recognition of a 'super-bulged' major histocompatibility complex class I-bound peptide |
Q40913192 | TcpM: a novel relaxase that mediates transfer of large conjugative plasmids from Clostridium perfringens |
Q37239059 | Temperature sensitivity of human perforin mutants unmasks subtotal loss of cytotoxicity, delayed FHL, and a predisposition to cancer |
Q27640892 | The 1.5 A crystal structure of a prokaryote serpin: controlling conformational change in a heated environment |
Q27643380 | The 1.6 A crystal structure of the catalytic domain of PlyB, a bacteriophage lysin active against Bacillus anthracis |
Q27734997 | The 2.6 A structure of antithrombin indicates a conformational change at the heparin binding site |
Q34462442 | The AprV5 subtilase is required for the optimal processing of all three extracellular serine proteases from Dichelobacter nodosus. |
Q27673121 | The Extracellular Protein Factor Epf from Streptococcus pyogenes Is a Cell Surface Adhesin That Binds to Cells through an N-terminal Domain Containing a Carbohydrate-binding Module |
Q30736622 | The FxRxHrS motif: a conserved region essential for DNA binding of the VirR response regulator from Clostridium perfringens |
Q30157659 | The MACPF/CDC family of pore-forming toxins |
Q24681654 | The N terminus of the serpin, tengpin, functions to trap the metastable native state |
Q35978229 | The Phosphatidylinositol (3,4,5)-Trisphosphate-dependent Rac Exchanger 1·Ras-related C3 Botulinum Toxin Substrate 1 (P-Rex1·Rac1) Complex Reveals the Basis of Rac1 Activation in Breast Cancer Cells |
Q25255516 | The REFOLD database: a tool for the optimization of protein expression and refolding |
Q47614108 | The Structural Basis for Complement Inhibition by Gigastasin, a Protease Inhibitor from the Giant Amazon Leech. |
Q27666157 | The Subtilisin-Like Protease AprV2 Is Required for Virulence and Uses a Novel Disulphide-Tethered Exosite to Bind Substrates |
Q27681123 | The Three-dimensional Structure of the Extracellular Adhesion Domain of the Sialic Acid-binding Adhesin SabA fromHelicobacter pylori |
Q27659983 | The X-Ray Crystal Structure of Escherichia coli Succinic Semialdehyde Dehydrogenase; Structural Insights into NADP+/Enzyme Interactions |
Q27678744 | The X-ray Crystal Structure of Mannose-binding Lectin-associated Serine Proteinase-3 Reveals the Structural Basis for Enzyme Inactivity Associated with the Carnevale, Mingarelli, Malpuech, and Michels (3MC) Syndrome |
Q27681852 | The X-ray crystal structure of full-length human plasminogen |
Q27676030 | The conjugation protein TcpC from Clostridium perfringens is structurally related to the type IV secretion system protein VirB8 from Gram-negative bacteria |
Q27650111 | The crystal structure of DehI reveals a new alpha-haloacid dehalogenase fold and active-site mechanism |
Q50079513 | The crystal structure of the transthyretin-like protein from Salmonella dublin, a prokaryote 5-hydroxyisourate hydrolase. |
Q44577217 | The evolution of enzyme specificity in Fasciola spp. |
Q57651515 | The first transmembrane region of complement component-9 acts as a brake on its self-assembly |
Q34375148 | The high resolution crystal structure of a native thermostable serpin reveals the complex mechanism underpinning the stressed to relaxed transition |
Q42650519 | The high resolution crystal structure of the human tumor suppressor maspin reveals a novel conformational switch in the G-helix |
Q36519309 | The human serpin proteinase inhibitor-9 self-associates at physiological temperatures |
Q24682724 | The major human and mouse granzymes are structurally and functionally divergent |
Q57079434 | The matrix refolded |
Q39850780 | The molecular basis for perforin oligomerization and transmembrane pore assembly |
Q34448263 | The murine orthologue of human antichymotrypsin: a structural paradigm for clade A3 serpins |
Q37691703 | The perforin pore facilitates the delivery of cationic cargos |
Q28364511 | The role of strand 1 of the C beta-sheet in the structure and function of alpha(1)-antitrypsin |
Q43894620 | The serpin SQN-5 is a dual mechanistic-class inhibitor of serine and cysteine proteinases |
Q29618777 | The serpins are an expanding superfamily of structurally similar but functionally diverse proteins. Evolution, mechanism of inhibition, novel functions, and a revised nomenclature |
Q27665482 | The structural basis for membrane binding and pore formation by lymphocyte perforin |
Q34644375 | The structure and function of catalytic domains within inositol polyphosphate 5-phosphatases. |
Q37791183 | The structure and function of mammalian membrane-attack complex/perforin-like proteins. |
Q27644771 | The structure of chagasin in complex with a cysteine protease clarifies the binding mode and evolution of an inhibitor family |
Q33582255 | The type III effectors NleE and NleB from enteropathogenic E. coli and OspZ from Shigella block nuclear translocation of NF-kappaB p65. |
Q24523405 | The type Ialpha inositol polyphosphate 4-phosphatase generates and terminates phosphoinositide 3-kinase signals on endosomes and the plasma membrane |
Q50324222 | The x-ray crystal structure of mannose-binding lectin-associated serine proteinase-3 reveals the structural basis for enzyme inactivity associated with the Carnevale, Mingarelli, Malpuech, and Michels (3MC) syndrome. |
Q27940135 | The yeast inositol polyphosphate 5-phosphatase Inp54p localizes to the endoplasmic reticulum via a C-terminal hydrophobic anchoring tail: regulation of secretion from the endoplasmic reticulum. |
Q57079444 | Thermal Unfolding of Proteins Studied by Coupled Reversed-Phase HPLC−Electrospray Ionization Mass Spectrometry Techniques Based on Isotope Exchange Effects |
Q50422650 | Torso-Like Is a Component of the Hemolymph and Regulates the Insulin Signalling Pathway in Drosophila |
Q37157370 | Torso-like functions independently of Torso to regulate Drosophila growth and developmental timing |
Q36266903 | Torso-like mediates extracellular accumulation of Furin-cleaved Trunk to pattern the Drosophila embryo termini |
Q62472376 | Tranexamic acid is an active site inhibitor of urokinase plasminogen activator |
Q52766958 | Trunk cleavage is essential for Drosophila terminal patterning and can occur independently of Torso-like. |
Q27681227 | X-ray crystal structure and specificity of the Plasmodium falciparum malaria aminopeptidase PfM18AAP |
Q24550849 | X-ray crystal structure of MENT: evidence for functional loop-sheet polymers in chromatin condensation |
Q57079373 | X-ray crystal structure of plasmin with tranexamic acid-derived active site inhibitors |
Q27649233 | X-ray crystal structure of the fibrinolysis inhibitor alpha2-antiplasmin |
Q24623471 | X-ray crystal structure of the streptococcal specific phage lysin PlyC. |
Q49046548 | alpha 1-Antitrypsin Mmalton (Phe52-deleted) forms loop-sheet polymers in vivo. Evidence for the C sheet mechanism of polymerization |
Q57079459 | α1-Antitrypsin Polymerisation Can Occur by both Loop A and C Sheet Mechanisms |
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