An L2 SUMO interacting motif is important for PML localization and infection of human papillomavirus type 16

The Evolving Field of Human Papillomavirus Receptor Research: a Review of Binding and Entry

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Tetraspanin CD151 Mediates Papillomavirus Type 16 Endocytosis

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Identification of a Role for the trans-Golgi Network in Human Papillomavirus 16 Pseudovirus Infection

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Human Papillomavirus Types 16, 18, and 31 Share Similar Endocytic Requirements for Entry

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HPV virions hitchhike a ride on retromer complexes

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Genome-wide siRNA screen identifies the retromer as a cellular entry factor for human papillomavirus

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Sp100 Provides Intrinsic Immunity against Human Papillomavirus Infection

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Cyclophilins Facilitate Dissociation of the Human Papillomavirus Type 16 Capsid Protein L1 from the L2/DNA Complex following Virus Entry

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Principles of polyoma- and papillomavirus uncoating

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Host-cell factors involved in papillomavirus entry

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The S100A10 Subunit of the Annexin A2 Heterotetramer Facilitates L2-Mediated Human Papillomavirus Infection

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Entry of Human Papillomavirus Type 16 by Actin-Dependent, Clathrin- and Lipid Raft-Independent Endocytosis

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Essential Roles for Soluble Virion-Associated Heparan Sulfonated Proteoglycans and Growth Factors in Human Papillomavirus Infections

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The story so far: post-translational regulation of peroxisome proliferator-activated receptors by ubiquitination and SUMOylation

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Polyethylenimine Is a Strong Inhibitor of Human Papillomavirus and Cytomegalovirus Infection

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Crosstalk between viruses and PML nuclear bodies: a network-based approach

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Regulation of Vaccinia Virus E3 Protein by Small Ubiquitin-Like Modifier Proteins

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The high risk HPV16 L2 minor capsid protein has multiple transport signals that mediate its nucleocytoplasmic traffic

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Disruption of PML Nuclear Bodies Is Mediated by ORF61 SUMO-Interacting Motifs and Required for Varicella-Zoster Virus Pathogenesis in Skin

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A Viral Ubiquitin Ligase Has Substrate Preferential SUMO Targeted Ubiquitin Ligase Activity that Counteracts Intrinsic Antiviral Defence

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SUMO chains: polymeric signals: Figure 1

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Identification of the dynein light chains required for human papillomavirus infection

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Structural Basis of Oligosaccharide Receptor Recognition by Human Papillomavirus

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Modification of Human Papillomavirus Minor Capsid Protein L2 by Sumoylation

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Role of Noncovalent SUMO Binding by the Human Cytomegalovirus IE2 Transactivator in Lytic Growth

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The SUMO E3 Ligase Activity of Pc2 Is Coordinated through a SUMO Interaction Motif

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Jalview Version 2--a multiple sequence alignment editor and analysis workbench

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Sumo-2/3-ylation following in vitro modeled ischemia is reduced in delayed ischemic tolerance

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Direct Binding of CoREST1 to SUMO-2/3 Contributes to Gene-Specific Repression by the LSD1/CoREST1/HDAC Complex

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Phospho-Regulated SUMO Interaction Modules Connect the SUMO System to CK2 Signaling

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Structure, attachment and entry of polyoma- and papillomaviruses

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Interplay between Herpesvirus Infection and Host Defense by PML Nuclear Bodies

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Target Cell Cyclophilins Facilitate Human Papillomavirus Type 16 Infection

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New insights into the role of the subnuclear structure ND10 for viral infection

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Papillomavirus 3' UTR regulatory elements

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HPV-16 RNA processing

(2008) Stefan Schwartz   Frontiers in Bioscience-Landmark

Structure of the Small Ubiquitin-like Modifier (SUMO)-interacting Motif of MBD1-containing Chromatin-associated Factor 1 Bound to SUMO-3

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Arrangement of L2 within the Papillomavirus Capsid

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Mechanism and Consequences for Paralog-Specific Sumoylation of Ubiquitin-Specific Protease 25

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RNF4 is a poly-SUMO-specific E3 ubiquitin ligase required for arsenic-induced PML degradation

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Clathrin- and Caveolin-Independent Entry of Human Papillomavirus Type 16—Involvement of Tetraspanin-Enriched Microdomains (TEMs)

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