Describing the hexapeptide identity platform between the influenza A H5N1 and Homo sapiens proteomes

Figures & data

Figure 1 Identity platform shared by influenza A polyprotein and the human proteome at the hexapeptide level. A) Location of the 10 viral proteins along the primary sequence of the influenza A polyprotein. Viral protein abbreviations as detailed in Methods section. B) Similarity profile of influenza A H5N1 polyprotein vs the human proteome at the hexapeptide level. The columns indicate the number of viral hexapeptide occurrences in the human proteome. Hexapeptide amino acid sequences in one-letter code.

Table 1 Numerical description of the hexapeptide overlap between influenza A polyprotein and Homo sapiens proteome

Unique viral hexamers	4,416
Viral hexamers occurring in the human proteins (including multiple occurrences)a	1,905
Expected number of viral hexamer occurrences in the human proteome	569

a Human protein sequences corresponding to fragments, duplicates, and obsolete entries were filtered out.

Table 2 Examples of human proteins sharing hexapeptide sequence(s) with influenza A H5N1 polyprotein

Influenza A hexapeptide			Human protein descriptiona
Protein	Aa pos	Sequence
NSP1	2	DSNTITb	ALMS1: Alstrom syndrome protein 1. Involved in sensory transduction of extracellular signals, such as light, taste, sound, touch, or smell, into electric signals. Expressed in the pancreas β-cells of the islets in fetal aorta and the brain. Defects in ALMS1 are the cause of Alstrom syndrome, characterized by cone-rod retinal dystrophy, neurosensory hearing loss, early childhood obesity, and type 2 diabetes mellitus.
	42	ALKGRG	EPMIP: EPM2A interacting protein 1. Laforin-interacting protein. The first recognized Laforin binding partner that may play a critical role in discovering the underlying pathogenesis of progressive myoclonic epilepsy type 2 (Lafora disease), characterized by grand mal seizures and/or myoclonus at about 15 years of age. Mental deterioration follows, often with psychotic features. Q96A48: Paroxysmal nonkinesiogenic dyskinesia (PNKD) protein. Myofibrillogenesis regulator 1. PNKD plays a role in the development of cardiac hypertrophy. Isoform 1 is only expressed in the brain. Isoform 2 is ubiquitous. Defects in PNKD cause dystonia type 8, a paroxysmal nonkinesigenic dystonia/dyskinesia.
	47	GSTLGL	GRIP2: Glutamate receptor-interacting protein 2. Glutamate receptors mediate neurotransmission in the brain and play an important role in neural plasticity, neural development, and neurodegeneration. GRIP1 and GRIP2 are widely expressed in brain, with the highest levels in the cerebral cortex, hippocampus, and olfactory bulb. GRIP1 is expressed in early development, specifically postnatal days 8–10, while GRIP2 is expressed during later developmental stages.
	50	LGLDLR	DHE3: Glutamate dehydrogenase 1, mitochondrial. Involved in learning and memory. Defects in DHE3 are the cause of hyperinsulinism–hyperammonemia Syndrome. DHE4: Glutamate dehydrogenase 2, mitochondrial. Important for recycling the chief excitatory neurotransmitter, glutamate, in neurotransmission. Expressed in retina, testis, and brain. NPCL1: Niemann–Pick C1-like protein 1. Plays a major role in cholesterol homeostasis. Niemann–Pick C disease is characterized by a disruption of sphingolipid and cholesterol trafficking that produces cognitive impairment, ataxia, and death, often in childhood.
	77	LKIAIA	P04114: Apolipoprotein B (APOB)-100. The APOB is a major protein constituent of chylomicrons. Defects in APOB are a cause of familial hypobetalipoproteinemia. Subjects have low plasma low-density lipoprotein (LDL) cholesterol and APOB-100 concentrations. Clinical presentation varies from no symptoms to severe gastrointestinal and neurological dysfunction similar to abetalipoproteinemia.
	82	ASSPAP	CTRO: Citron. Rho-interacting, serine/threonine-protein kinase 21. Required for KIF14 localization to the central spindle and midbody. Regulates the development of the CNS. NCOR1: Nuclear receptor corepressor 1. Mediates transcription repression of thyroid hormone and retinoic acid receptors. The corresponding gene is located between the CMT and Smith–Magenis syndrome critical regions on chromosome 17. Forms a large corepressor complex that contains SIN3A/B and histone deacetylases HDAC1 and HDAC2.
	83	SSPAPR	ITPR1: Inositol 1,4,5-trisphosphate receptor (IP3R) type 1. The IP3R mediates calcium release following stimulation by inositol 1,4,5-trisphosphate. Interacts with RYR1, RYR2, ITPR1, SHANK1, and SHANK3. Defects in ITPR1 are the cause of spinocerebellum ataxia type 15, with incoordination of gait, poor coordination of hands, speech, and eye movements, due to cerebellar degeneration.
	107	PRQKIT	PMM2: Phosphomannomutase 2. Involved in the synthesis of GDP-mannose and dolichol-phosphate-mannose. Defects in PMM2 are the cause of Jaeken syndrome, characterized by severe encephalopathy with axial hypotonia, abnormal eye movement, psychomotor retardation, peripheral neuropathy, cerebellar hypoplasia, and retinitis pigmentosa.
	141	LETLVS	MLL3: Myeloid/lymphoid or mixed-lineage leukemia protein 3. Histone-lysine N-methyltransferase MLL3. Methylates ‘Lys-4’ of histone H3. H3 ‘Lys-4’ methylation represents a specific tag for epigenetic transcriptional activation. Highly expressed in testis and ovary, followed by brain and liver. Within brain, expression is highest in the hippocampus, caudate nucleus, and substantia nigra.
	178	IGILIG	IRAK3: Interleukin-1 receptor-associated kinase 3. Expressed in peripheral blood lymphocytes. Defects in IRAK3 are associated with susceptibility to asthma-related traits type 5, which include clinical symptoms such as coughing, wheezing, dyspnea, serum IgE levels, atopy, and atopic dermatitis.
	205	IHDENG	Q9HC59: The α-synuclein-interacting protein (SNCAIP). Synphilin-1c protein. Widely expressed, with highest levels in the brain, heart, and placenta. Defects in SNCAIP are a cause of Parkinson disease, characterized by bradykinesia, resting tremor, muscular rigidity, loss of dopaminergic neurons in the substantia nigra, and intraneuronal accumulations of aggregated proteins (ie, Lewy bodies) in surviving neurons.
NEP	18	KMQLES	GLRB: Glycine receptor subunit β. A neurotransmitter-gated ion channel. Binding of glycine to its receptor produces hyperpolarization (inhibition of neuronal firing). Defects in GLRB are a cause of startle disease characterized by muscular rigidity of CNS origin, particularly in the neonatal period, and by an exaggerated startle response to unexpected acoustic or tactile stimuli.
	22	ESSSVD	AHI1: Abelson helper integration site 1 protein homolog. Jouberin. Highly expressed in primitive normal hematopoietic cells. Expressed in the brain, particularly in neurons that give rise to the crossing axons of the corticospinal tract and superior cerebellum peduncles. Upregulated in leukemic cells at all stages of differentiation from patients with chronic myeloid leukemia. Defects in AHI1 are the cause of Joubert syndrome type 3. Joubert syndrome is characterized by cerebellum ataxia, oculomotor apraxia, hypotonia, neonatal breathing abnormalities, and psychomotor delay. Neuroradiologically, it is characterized by cerebellum vermian hypoplasia/aplasia, thickened and reoriented superior cerebellum peduncles, and abnormally large interpeduncular fossa (molar tooth sign). Additional variable features include retinal dystrophy and renal disease. Joubert syndrome type 3 shows minimal extra CNS involvement and appears not to be associated with renal dysfunction.
	24	SSVDLN	VLDLR: Very low density lipoprotein (VLDL) receptor. Binds VLDL and transports it to cells by endocytosis. Binding to reelin induces tyrosine phosphorylation of Dab1. Deletions involving VLDLR may be the cause of cerebellum hypoplasia, with mental retardation, delayed ambulation, predominantly truncal ataxia, strabismus and pesplanus, seizures (in 40% of patients), and short stature (in 15% of patients).
	36	ERLKIY	NARG1: NMDA receptor-regulated protein 1. Important for vascular and neuronal development. Controls retinal neovascularization. Found in brain (corpus callosum).
	101	QALQLL	SYT9: Synaptotagmin-9. Integral membrane protein involved in norepinephrine secretion.
	104	QLLLEV	ABCA1: Adenosine 5’-triphosphate (ATP)-binding cassette subfamily A member 1. Widely expressed. Defects in ABCA1 cause Tangier disease, a high density lipoprotein deficiency characterized by premature coronary artery disease, hepatosplenomegaly, recurrent peripheral neuropathy, and progressive muscle wasting and Weakness. MESD1: Mesoderm development candidate 1.
MP1	15	VPSGPL	SALL1: Sal-like protein 1. Zinc finger protein SALL1. Involved in organogenesis. Interacts with HDAC1, HDAC2, RBBP4, RBPP7, MTA1, and MTA2. Highest levels expressed in the kidney. Lower levels in adult brain (enriched in corpus callosum, lower expression in substantia nigra) and liver. In fetal brain, expressed exclusively in neurons of the subependymal region of hypothalamus lateral to the third ventricle.
	16	PSGPLK	MYLK: Myosin light chain kinase (MLCK). Smooth muscle. Telokin. Implicated in smooth muscle contraction. Implicated in the regulation of endothelial as well as vascular permeability. In the nervous system, it has been shown to control the growth initiation of astrocytic processes in culture and to participate in transmitter release at synapses formed between cultured sympathetic ganglion cells.
	20	LKAEIA	CNGA3: Cyclic nucleotide-gated cation channel α-3. Essential for the generation of light-evoked electrical responses in the red-, green- and blue-sensitive cones. Prominently expressed in retina. Defects in CNGA3 are the cause of achromatopsia type 2 (or total color blindness or rod monochromacy).
	38	DLEALM	USH1G: Usher syndrome type-1G protein. Required for normal hearing. Expressed in vestibule of the inner ear, eye, and small intestine. Defects in USH1G are the cause of Usher syndrome type 1G, characterized by the association of retinitis pigmentosa and sensorineural deafness. Usher syndrome type 1 is characterized by prepubertal onset of progressive retinitis pigmentosa leading to blindness. Q86U74: Phosphoglucomutase-1. This enzyme participates in both the breakdown and synthesis of glucose.
	54	PLTKGI	Q6RJU1: Rho GTPase-activating protein 20. Expressed predominantly in the brain.
	72	RGLQRR	LAP4: Protein scribble homolog. Scribble. Involved in different aspects of epithelial and neuronal morphogenesis. Localizes to neuronal post- and presynaptic regions.
MP2	59	LKRGPS	CLCN2: Chloride channel protein 2. Functions include the regulation of cell volume. Defects in CLCN2 may be the cause of (1) epilepsy with grand mal seizures on awakening; (2) childhood absence epilepsy type 3, with onset at age 6–7 y, frequent absence seizures, and bilateral, synchronous, and symmetric 3-Hz spike waves on electroencephalogram (EEG); and (3) juvenile absence epilepsy characterized by tonic–clonic seizures on awakening.
HA	143	ASSGVS	DOCK3: Dedicator of cytokinesis protein 3. Presenilin-binding protein. May be involved in Alzheimer disease. In normal brains, it is localized in the neuropil, while in brains affected by Alzheimer disease it is associated with neurofibrillary tangles. A chromosomal aberration involving DOCK3 may be a cause of early onset of behavioral/developmental disorder with features of attention deficit–hyperactivity disorder. HD: Huntingtin. Huntington disease protein.
	157	SSFFRN	TBEc: Tubulin, epsilon 1.
	158	SFFRNV	TBEc: Tubulin, epsilon 1. See previous.
	330	ATGLRN	UBP3: Ubiquitin carboxyl-terminal hydrolase 3. Ubiquitous, with strongest expression in pancreas.
	419	LERRIE	DESM: Desmin. Intermediate filament found in muscle cells. Defects in desmin cause (1) desmin-related cardioskeletal myopathy, with skeletal muscle weakness, cardiac conduction blocks, arrhythmias, and restrictive heart failure; (2) cardiomyopathy dilated type 1I, resulting in congestive heart failure and arrhythmia, with risk of premature death; (3) neurogenic scapuloperoneal syndrome Kaeser type.
	534	SIYSTV	TMEM1: Trafficking protein particle complex subunit 10. Epilepsy holoprosencephaly candidate 1.
NA	17	VGIISL	RYR1: Ryanodine receptor 1. Present in skeletal muscle, cerebellum, and hippocampus. Defects in RYR1 are the cause of (1) malignant hyperthermia susceptibility type 1, one of the main causes of death due to anesthesia, with accelerated muscle metabolism, contractures, metabolic acidosis, tachycardia, and even death; (2) central core disease, one of the conditions that produces the “floppy” infant, with neonatal hypotonia, delayed motor development, muscle weakness, and amyotrophy.
	23	MLQIGN	SC10Ac: Sodium channel protein type 10, subunit α. Expressed in the dorsal root ganglia and sciatic nerve. Plays a role in neuropathic pain mechanisms.
	24	LQIGNI	SC10Ac: sodium channel protein type 10 subunit α. See previous entry.
	28	NIISIW	TOP2B: Deoxyribonucleic acid (DNA) topoisomerase II, β. Reduced activity of this enzyme may also play a role in ataxia–telangiectasia, a neurodegenerative disease that causes poor coordination and dilation of small blood vessels.
	78	KAVASAV	GEMI4: Component of gems 4. Gemin-4. P97. Component of the SMN protein complex. SMN is the product of the neurodegenerative disease spinal muscular atrophy gene.
	102	KDNGIR	ECHB: Trifunctional enzyme subunit β, mitochondrial. HADHB. Defects in HADHB are a cause of trifunctional protein deficiency. Manifestations include hypoglycemia, cardiomyopathy, and sudden death.
	440	GSSISF	CSMD2: CUB and sushi domain-containing protein 2. Expressed at intermediate levels in the brain, including cerebellum, substantia nigra, hippocampus, and fetal brain.
	463	LPFTID	TAAR5: Trace amine-associated receptor 5. Mediates aspects of movement control. Expressed exclusively in skeletal muscle and selected areas of the brain (amygdala, hippocampus, caudate nucleus, hypothalamus, and thalamus).
NC	63	IERMVL	HS70L: Heat shock 70 kDa protein (Hsp70) 1-Hom. Hsp70s stabilize proteins against aggregation.
	127	EDATAG	DPYS: Dihydropyrimidinase (DHP) protein. Defects in DPYS are the cause of DHP deficiency. DHP deficiency is characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features, developmental delay, and congenital microvillous atrophy.
	375	DSSTLE	ATMd: Ataxia–telangiectasia mutated protein. Defects in ATM cause ataxia–telangiectasia, characterized by cerebellum ataxia, blood vessel dilation in the conjunctiva, growth retardation, and sexual immaturity.
	453	PEDVSF	TBCD: Tubulin-specific chaperone D. Tubulin-folding protein. Involved in the first step of the tubulin-folding pathway. Modulates microtubule dynamics by capturing guanosine triphosphate (GTP)-bound β-tubulin.
PA	13	IVELAE	RYR2: Ryanodine receptor 2. RYR-2. Cardiac muscle-type ryanodine receptor. Expressed in heart muscle, brain (cerebellum and hippocampus), and placenta. Expressed in myometrium during pregnancy. Defects in RYR2 cause (1) arrhythmogenic right ventricular cardiomyopathy 2 and (2) catecholaminergic polymorphic ventricular tachycardia type that may degenerate into cardiac arrest and cause sudden death. ZDH17: Zinc finger palmitoyltransferase specific for a subset of neuronal proteins. Huntingtin-interacting protein 3. Highest expression in the brain cortex, cerebellum, occipital lobe, and caudate.
	118	IEIGVT	Q9H0B0e: Neuralized-like protein 4. Widely expressed at high levels (including brain).
	343	AELQDI	Q4VY19: Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, β polypeptide.
	351	EEKIPK	Q2NKJ7: Neuronal-specific septin-3. Filament-forming cytoskeletal GTPase. GTPase activity is required for brain-specific filament formation. Up-regulated during neuronal differentiation.
	378	KVDFED	CABP2: Caveolin-3. CAV3. Involved in repair mechanism of both skeletal muscle and cardiomyocytes. Defects in CAV3 cause (1) limb-girdle muscular dystrophy type 1C; (2) hyperCKmia (ie, elevated levels of serum creatine kinase); (3) rippling muscle disease; (4) cardiomyopathy familial hypertrophy, with dyspnea, syncope, collapse, palpitations, and chest pain; and (5) long QT syndrome type 9 (long QT syndromes cause syncope and sudden death in response to stress; they can present with a sentinel event of sudden cardiac death in infancy); (6) Sudden infant death syndrome (SIDS), the sudden death of an infant younger than 1yr that remains unexplained after a thorough case investigation, including a complete autopsy, examination of the death scene, and review of clinical history.
	626	KGVEEG	ATMd: Serine-protein kinase ATM. Ataxia–telangiectasia mutated. See earlier entry.
	627	GVEEGS	MINT: Msx2-interacting protein. SMART/HDAC1-associated repressor protein. Regulates different key pathways such as the Notch pathway. Expressed at high level in brain, testis, spleen, and thymus.
	671	ALRDNL	NBEAL: NBEA L1 protein. Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 17 protein. Neurobeachin-like protein 1. Highly expressed in brain, kidney, prostate, and testis.
	684	GGLYEA	DOCK6: Dedicator of cytokinesis protein 6 guanine nucleotide exchange factor. Widely expressed. Expressed at low level in spleen, cerebellum, hippocampus, and substantia nigra.
RDRP	202	QRTIGK	AFF2: Fragile X mental retardation 2 protein. Expressed in hippocampus and amygdala.
	276	NEKKAK	DCX: Neuronal migration protein doublecortin. Lissencephalin-X. Involved in cortex lamination during cerebral cortex development. Highly expressed in neuronal cells of fetal brain (in the majority of cells of the cortical plate, intermediate zone, and ventricular zone). Not expressed in other fetal tissues. In adults, highly expressed in the brain frontal lobe. Defects in DCX cause lissencephaly X-linked type 1, with mental retardation and seizures that are more severe in male patients. Affected boys show a thick cortex with absent or reduced gyri, feeding problems, abnormal muscular tone, seizures, and psychomotor retardation. Females display a less severe phenotype (“doublecortex”).
	401	ASLSPG	CAD22: Cadherin-22. Pituitary and brain cadherin. SALL3: Sal-like protein 3. Expressed in fetal brain of the 24th gestational week (in hippocampus, cortex, mediodorsal and ventrolateral thalamic nuclei, putamen, cerebellum, and brainstem).
	510	PSFGVS	Q8IVF2f: Protein AHNAK2. Is a component of the dysferlin protein complex. In dysferlinopathies, reduction or absence of dysferlin correlates with a secondary muscle-specific loss of AHNAK.
	616	MDEDYQ	VP13A: Vacuolar protein sorting-associated protein 13A. Chorein. Higher expression is found in brain, heart, skeletal muscle, and kidney. Defects in VPS13A are the cause of chorea-acanthocytosis, characterized by hyperkinetic movements, abnormal erythrocyte morphology, psychiatric features, epilepsy, peripheral neuropathy, myopathy, oral self-mutilation, and basal ganglia atrophy in the brain.
	702	SSSYRR	VIME: Vimentin. Vimentins are class-III intermediate filaments found especially in mesenchymal cells.
PB2	4	IKELRD	A0MZ66: Shootin-1. Localized in axons. Acts upstream of phosphoinositide 3-kinase (PI3K). Involved in the generation of internal asymmetric signals required for neuronal polarization.
	128	GTEGPV	HEXA: β-hexosaminidase subunit α. Defects in HEXA are the cause of GM2-gangliosidosis type 1 also known as “Tay–Sachs disease,” with accumulation of GM2 gangliosides in the neuronal cells.
	156	AKEAQD	EZRI: Ezrin. Expressed in cerebral cortex, basal ganglia, hippocampus, hypophysis, and optic nerve. Stronger expression in gray matter of frontal lobe compared to white matter. Preferentially expressed in astrocytes of hippocampus, frontal cortex, thalamus, parahippocampal cortex, amygdala, insula, and corpus callosum. Very strong staining of the Purkinje cell layer and in part of the molecular layer of the infant brain compared to adult brain.
	187	KEKKEE	RS14: 40S ribosomal protein S14. SFR11: Splicing factor, Arg/Ser-rich 11 that localizes with spliceosome components.
	207	LERELV	SPTN5: Spectrin β chain, brain 4. Spectrin, nonerythroid β chain 4. Detected prominently in the outer segments of photoreceptor rods and cones, and in the basolateral membrane and gastric epithelial cells. Expressed in cerebellum, spinal cord, pituitary gland, stomach, liver, pancreas, kidney, bladder, and heart.
	227	VYIEVL	PCDBD: Protocadherin β-13. Involved in the establishment of neuronal connections in the brain. Q5VY39: Protocadherin-15. Essential for normal retinal and cochlear function. Found in the inner and outer synaptic layers, and the nerve fiber layer in adult and fetal retinas. Found in the supporting cells, outer sulcus cells, and spiral ganglion of fetal cochlea. Defects in PCDH15 cause (1) Usher syndrome type 1F, characterized by the association of retinitis pigmentosa and sensorineural deafness, (2) Usher syndrome type 1D/F, and (3) nonsyndromic sensorineural deafness autosomal recessive type 23.
	274	ADPLAS	TECT2: Tectonic-2. Participates in hedgehog-mediated patterning of the neural tube. During neural tube development, mouse tectonic is required for formation of most of the ventral cell types.
	275	DPLASL	CNTP5: Contactin-associated protein-like 5. Caspr5. CNTNAP5. May play a role in the correct development and proper functioning of the peripheral and CNS and may be involved in cell adhesion and intercellular communication. Belongs to the neurexin family.
	277	LASLLE	FA38A: Protein FAM38A. In normal brain, expressed exclusively in neurons, not in astrocytes. In Alzheimer disease, expressed in approximately half of the activated astrocytes located around classical senile plaques.
	316	GLRISS	MASS1: G-protein coupled receptor 98. GPR98. Involved in the development of the CNS. Defects in GPR98 may be a cause of (1) Usher syndrome type 2C, characterized by the association of retinitis pigmentosa with sensorineural deafness; and (2) familial febrile convulsions type 4. Febrile convulsions are seizures in childhood without any evidence of intracranial infection or defined pathologic or traumatic cause. Affects 2%–5% of children aged 3 m to 5 yr.
	317	LRISSS	LEPR: Leptin receptor. Receptor for obesity factor (leptin). Involved in the regulation of fat metabolism.
	339	KKEEEV	Q52LR0: Cingulin-like protein 1. Paracingulin. Localizes to the apical junction complex composed of tight and adherens junctions. Present in smooth muscle, spleen, testis, fetal brain, amygdala, corpus callosum, cerebellum, thalamus, and the subthalamic nucleus of adult brain. A chromosomal aberration involving CGNL1 is a cause of aromatase excess syndrome, characterized by estrogen excess.

	341	EEEVLT	TTBK2: Tau-tubulin kinase 2. Serine/threonine kinase, which is able to phosphorylate tau on serines. Defects in TTBK2 cause spinocerebellum ataxia type 11. Patients show incoordination of gait and often poor coordination of hands, speech, and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord.
	347	GNLQTL	NEB2: Neurabin-2. Modulates synaptic transmission and dendritic spine morphology. Involved in G-protein coupled receptor signaling, including dopamine D2 receptors and α-adrenergic receptors.
	476	RGVRVS	ANK2: Ankyrin-2. Brain ankyrin. Required for the regulation of neonatal cardiomyocyte contraction rate. Expressed in fetal brain and the temporal cortex of adult brain. Defects in ANK2 cause long QT syndrome type 4. Long QT syndromes cause syncope and sudden death in response to stress.
	565	SQDPTM	PSD5: 26S proteasome non-ATPase regulatory subunit 5. 26S proteasome subunit S5B.
	678	DPDEGT	CELR2: Cadherin EGF LAG G-type receptor. Flamingo 1. Receptor that may have an important role in cell–cell signaling during nervous system formation. Highest expression in brain and testis. PCD19: Protocadherin-19. Expressed in developing cortical plate, amygdala, and subcortical regions and in the ganglionic eminence. Defects in PCDH19 cause epilepsy (female-restricted), with mental retardation, and convulsive disorder, characterized by seizure onset in infancy and cognitive impairment. PCDGM: Protocadherin γ-c5. Involved in the establishment of neuronal connections in the brain.

a UniProt/Swissprot accession numbers are given in bold. Brain and/or peripheral nervous system localization are given in boldface. For references and potential disease involvement, refer to www.uniprot.org;

b DSNTIT is present in the viral NEP too;

c Tubulin and sodium channel protein type 10, subunit α, have 2 consecutive overlapping viral hexapeptides;

d The ATM has 2 viral hexapeptides: NC375–380DSSTLE and PA626–631KGVEEG;

e The viral hexapeptide IEIGVT occurs 3 times in the human neuralized-like protein 4;

f The viral PSFGVS hexapeptide occurs 17 times in the human AHNAK2 protein.

Table 3 Hexapeptide sharing between influenza A polyprotein and human proteins potentially associated with autism, Williams–Beuren syndrome, Bardet–Biedl syndrome, and schizophrenia

Influenza A hexapeptide			Human protein descriptiona
Protein	Aa pos	Sequence
NSP1	145	VSLRAF	Q6ZN28: Metastasis-associated in colon cancer protein 1 (MACC1). Acts as a transcription activator for MET and as a key regulator of HGF-MET signaling. Alterations in MET and HGF-MET signaling have been associated with autism.^Citation20
	162	PIPSVP	VASH: Vasohibin-1. Angiogenesis inhibitor. Highly expressed in fetal organs. Expressed in brain and placenta. Associated with autism.^Citation21
NEP	25	SVDLNG	NRX1Ab: Neurexin I-α. Neuronal cell surface protein that may be involved in cell recognition and adhesion. Tissue specificity: heart and brain. Associated with autism. 22
	42	RDSLGE	Q9H8T5c: Myosin-IXa. Unconventional myosin-9a. Regulates Rho activity in neurons, and has a role in the regulation of neuronal morphology and function. Candidate gene for the Bardet–Biedl syndrome, which may be characterized by retinal dystrophy, obesity, mental retardation, repetitive behavior, and some autistic-like features.^Citation23
	43	DSLGES	Q9H8T5c: Myosin-IXa see previous entry.^Citation23
	247	SNGQAS	CSMD1: CUB and sushi domain-containing protein 1. Expressed at intermediate level in brain, including cerebellum, substantia nigra, hippocampus, and fetal brain. Disruption of the CSMD1 gene is associated with speech delay, autism, and learning difficulties. 24
HA	64	KPLILR	BBS10b: Bardet–Biedl syndrome 10 protein. Probable molecular chaperone. Defects in BBS10 are the cause of Bardet–Biedl syndrome type 10, characterized by severe retinopathy, early onset of obesity, polydactyly, hypogenitalism, renal malformation, mental retardation, repetitive behavior, and some autistic-like features.
NC	25	IRASVG	C1TC: C-1-tetrahydrofolatesynthase. Includes methylenetetrahydrofolate dehydrogenase, methenyltetrahydrofolate cyclohydrolase, and formyltetrahydrofolate synthetase. Defects in this trifunctional enzyme may cause susceptibility to folate-sensitive neural tube defects, such as open spina bifida and anencephaly. Aberrations in folate metabolic pathway might have a role in the altered susceptibility to schizophrenia, autism, and depression.^Citation25,Citation26
	335	SAAFED	BAZ1B: Williams syndrome transcription factor. Tyrosine-protein kinase BAZ1B. Involved in chromatin remodeling and acts as a transcription regulator. Ubiquitous. Expressed at equal levels in 19–23 week-old fetal tissues. Chromosomal aberrations involving BAZ1B may be the cause of certain cardiovascular and musculoskeletal abnormalities observed in Williams–Beuren syndrome.
	390	TRSGGN	NRX1Ab: Neurexin I-α. Associated with autism. See earlier entry.^Citation22 NRX1B: Neurexin-1-β. Involved in cell adhesion by forming intracellular junctions through binding to neuroligins. May play a role in formation or maintenance of synaptic junctions. Disruption of NRX1B has been associated with autism spectrum disorder.^Citation27
	401	ASAGQI	DISC1: Disrupted in schizophrenia 1 protein. Expressed in the dentate gyrus of the hippocampus, and temporal and parahippocampal cortices and cells of the white matter. Expression rises within the dentate gyrus and temporal cortex from the neonatal period to infancy, declines markedly in adolescence, and declines further with aging. Defects in DISC1 may be associated with (1) susceptibility to schizophrenia, and psychosis; (2) susceptibility to schizoaffective disorder characterized by the co-occurrence of symptoms of both mood disorder and psychosis; (3) autism and Asperger syndrome.^Citation28
PA	2	EDFVRQ	MAGG1: Melanoma-associated antigen G1. Ubiquitous. Associated with autism.^Citation29
	131	YLEKAN	DMDc: Dystrophin. May play a role in anchoring the cytoskeleton to the plasma membrane. Defects in dystrophin are the cause of the following: (1) Duchenne muscular dystrophy, with proximal muscle weakness causing waddling gait, toe-walking, lordosis, frequent falls, and difficulty in standing up and climbing up stairs (most patients are confined to a wheelchair by the age of 10 or 12 y; contractures and scoliosis ultimately occur); (2) Becker muscular dystrophy, later in onset and more benign; and (3) cardiomyopathy dilated X-linked type 3B. Associated with autism spectrum disorder.^Citation30,Citation31
	132	LEKANK	DMDc: Dystrophin. Associated with autism spectrum disorder. See previous entry.^Citation30,Citation31
	377	EKVDFE	O75129: Astrotactin-2. A neuronal cell surface protein expressed on postmitotic neuronal precursors in the cerebellum, hippocampus, cerebrum, and olfactory bulb. Astrotactin mediates neuronastroglial interactions and is also implicated in synaptic development as well as many other neuronal activities. Mutations in the astrotactin gene are linked to neuronal migration. Involved in autism and schizophrenia.^Citation32,Citation33
	389	DLRQYD	SBP1: Selenium-binding protein 1. Highly expressed in liver, lung, colon, prostate, kidney, and pancreas. Present in neurons and glia. Upregulated in brain and blood from schizophrenia patients.^Citation34
	400	PRSLAS	RELN: Reelin. Plays a role in layering of neurons in the cerebral cortex and cerebellum. Abundantly produced during brain ontogenesis by the Cajal–Retzius cells and other pioneer neurons located in the telencephalic marginal zone and by granule cells of the granular layer of the cerebellum. In adult brain, preferentially expressed in GABAergic interneurons of prefrontal cortices, temporal cortex, hippocampus, and glutamatergic granule cells of cerebellum. Expression in postnatal human brain is high in the cerebellum. Defects in RELN are the cause of lissencephaly type 2 (Norman–Roberts syndrome). Individuals are ataxic and mentally retarded, and suffer from epilepsy. Defects in RELN may contribute to susceptibility to schizophrenia. Expression of the protein is reduced to about 50% in patients with schizophrenia. Defects in RELN may predispose to autistic disorder.^Citation35,Citation36
	513	NDTDVV	DPP10: Inactive dipeptidyl peptidase 10. May modulate activity of the K+ channels KCND1 and KCND2. Defects in DPP10 may be a cause of susceptibility to asthma. Associated with autism.^Citation37
RDRP	271	LPVGGN	BBS10b :Bardet–Biedl syndrome 10 protein. See earlier entry.
	299	SFTITG	L1CAM: Neural cell adhesion molecule L1. Involved in the development of the nervous system. Involved in neuron–neuron adhesion, neurite fasciculation, outgrowth of neurites, etc. Defects in L1CAM are the cause of (1) hydrocephalus due to stenosis of the aqueduct of Sylvius, with abnormal accumulation of cerebrospinal fluid in the brain; (2) CRASH syndrome (Corpus callosum hypoplasia, psychomotor Retardation, Adducted thumbs, Spastic paraparesis, and Hydrocephalus), with spasticity and hyperreflexia of lower limbs, shuffling gait, mental retardation, aphasia, and adducted thumbs; and (3) spastic paraplegia X-linked type 1, characterized by progressive weakness and spasticity of the lower limbs. Associated with neurological disorders such as autism, 3p syndrome, and schizophrenia.^Citation38
PB2	295	VDILRQ	BAZ1A: Bromodomain adjacent to zinc finger domain protein 1A. Williams syndrome transcription factor-related chromatin-remodeling factor 180. Involved in the formation or maintenance of heterochromatin playing a critical role in developmental control. Expressed in the testis. Williams syndrome patients are diagnosed by their unique profile of physical and mental abnormalities. Some degree of mental retardation, visual–spatial processing defects, as well as characteristic “elfin” features are obvious traits of most patients.^Citation39
	314	AMGLRI	CECR1: Adenosine deaminase CECR1. Cat eye syndrome critical region protein 1. In embryo, expressed in the outflow tract and atrium of the developing heart, the VII/VIII cranial nerve ganglion, and the notochord. Candidate gene for the cat eye syndrome, a developmental disorder characterized by coloboma of the iris, anal atresia with fistula, downslanting palpebral fissures, heart and renal malformations, and normal or near-normal mental development. Has been associated with autism.^Citation40
	319	ISSSFS	WBS23: Williams–Beuren syndrome chromosomal region 23 protein. PAX6: Paired box protein Pax-6. Oculorhombin. Aniridia type II protein. Required for the differentiation of pancreatic islet α cells. Regulates specification of the ventral neuron subtypes. Present in fetal eye, brain, spinal cord, and olfactory epithelium. Defects in PAX6 are the cause of (1) aniridia type II, characterized by absence of the iris, absence of the fovea, malformations of the lens and anterior chamber; (2) Peters anomaly, consisting of a central corneal leukoma; (3) ectopia pupilla; (4) autosomal dominant keratitis, with corneal opacification and vascularization, and by foveal hypoplasia; (5) ocular coloboma (may cause as much as 10% of the childhood blindness); and (6) Gillespie syndrome, with aniridia cerebellum ataxia and mental deficiency. Has been associated with autism.^Citation41
	346	TGNLQT	Q8N2F4: Cell adhesion molecule 1. CADM1. May act in synapse assembly. May be involved in neuronal migration, axon growth, path finding, and fasciculation on the axons of differentiating neurons. Mutations in the gene encoding CADM1 are associated with autism spectrum disorder.^Citation42
	371	TAILRK	NBEA: Neurobeachin. Lysosomal-trafficking regulator 2. Protein BCL8B. LYST2. Expressed predominantly in the brain. Neurobeachin has been associated with idiopathic autism and is disrupted in patients with multiple myeloma.^Citation43
	388	GRDEQS	MYH9: Myosin-9. Nonmuscle myosin heavy chain Iia. Defects in MYH9 are a cause of Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, Alport syndrome, nonsyndromic sensorineural deafness, and macrothrombocy-topenia with progressive sensorineural deafness. May be related to many neurological disorders such as depression and autism with only a subclinical platelet defect.^Citation44

a UniProt/Swissprot accession numbers are given in bold. For additional references and potential disease involvement, refer to www.uniprot.org;

b Neurexin I-α and Bardet–Biedl syndrome-10 protein have 2 viral hexamers;

c Myosin-IXa and dystrophin have a viral heptamer.

Table 4 Influenza A hexapeptide occurrences in human proteins related to myelination

Influenza A hexapeptide			Human protein descriptiona
Protein	Aa pos	sequence
HA	116	ELKHLL	Q5VUM2: Laminin subunit α-2. Merosin heavy chain. LAMA2. Involved in the attachment, migration, and organization of cells into tissues during embryonic development. Defects in LAMA2 are the cause of merosin-deficient congenital muscular dystrophy type 1A, characterized by difficulty in walking, hypotonia, hyporeflexia, and white matter hypodensity on MRI. A single point mutation in the LN domain of LAMA2 may cause muscular dystrophy and peripheral amyelination.^Citation47
	442	AELLVL	NFL: Neurofilament light polypeptide. NEFL. Involved in the maintenance of neuronal caliber. Defects in NEFL are the cause of CMT disease type 1F (CMT1F), characterized by severely reduced nerve conduction velocities (less than 38 m/s), segmental demyelination and remyelination with onion bulb formations on nerve biopsy, slowly progressive distal muscle atrophy and weakness, absence of deep tendon reflexes, and hollow feet. The CMT1F condition is characterized by onset in infancy or childhood (range 1–13 yr). Defects in NEFL are the cause of CMT disease type 2E, characterized by signs of axonal regeneration in the absence of obvious myelin alterations and progressive distal muscle weakness and atrophy.^Citation48
NA	26	IGNIIS	CH60: 60 kDa heat shock protein, mitochondrial. HSP-60. CPN60. Mitochondrial matrix protein P1. HSPD1. Defects in HSPD1 are a cause of (1) spastic paraplegia, a degenerative spinal cord disorder characterized by a progressive weakness and spasticity of the lower limbs and (2) leukodystrophy hypomyelinating type 4, a severe hypomyelinating leukodystrophy, characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, and mental retardation.^Citation49,Citation50
	107	RIGSKG	MYEF2: Myelin expression factor 2. Transcriptional repressor of the myelin basic protein gene.
	201	GAVAVL	Q4KMR1: Synaptojanin-1. Synaptic inositol-1,4,5-trisphosphate 5-phosphatase 1. Isoform 1 is more enriched than isoform 2 in developing brain. Isoform 2 is abundant in nerve terminals. Possibly involved in the development of chromosome 21q22-linked bipolar disorders and schizophrenia. May contribute to brain dysfunction and cognitive disabilities in Down’s syndrome. Involved in the interaction of myelin basic protein with the plasma membrane in oligodendroglial cells.^Citation51^–^Citation53
	202	AVAVLK	ARHGA: Rho guanine nucleotide exchange factor 10. ARHGEF10. Defects in ARHGEF10 cause slow nerve conduction, without any clinical signs of peripheral or CNS dysfunction. Involved in developmental myelination of peripheral nerves.^Citation54
NP	178	AAGAAV	CTDP1: RNA polymerase II subunit A C-terminal domain phosphatase. TFIIF-associating CTD phosphatase. Processively dephosphorylates “Ser-2” and “Ser-5” of the heptad repeats YSPTSPS in the COOH domain of the largest RNA polymerase II subunit. This promotes the activity of RNA polymerase II. The phosphorylation is required for the physical interaction with GTF2F1. Defects in CTDP1 may cause congenital cataracts facial dysmorphism neuropathy syndrome, with hypogonadism, hypomyelination of the peripheral nervous system, and delayed motor and intellectual development. Central nervous system involvement, with cerebral and spinal cord atrophy, may be the result of disrupted development. Affected individuals are prone to severe rhabdomyolysis after viral infections and to serious complications related to general anesthesia as pulmonary edema and epileptic seizures.^Citation55
	282	GLAVAS	ATRN: Attractin. Mahogany homolog. Involved in the initial immune cell clustering during inflammatory response. Involved in melanocortin signaling pathways that regulate energy homeostasis and hair color. Has a critical role in normal myelination in the CNS.^Citation56,Citation57
	283	LAVASG	SOX10: Transcription factor SOX-10. Could confer cell specificity to the function of other transcription factors in developing and mature glia. Expressed in fetal brain and in adult brain, heart, small intestine, and colon. Defects in SOX10 are the cause of (1) Waardenburg syndrome type 2E, with sensorineural deafness, pigmentary disturbances, and absence of dystopia canthorum; (2) Waardenburg syndrome type 4, with association of Waardenburg features (depigmentation and deafness) and the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease); (3) Yemenite deaf–blind hypopigmentation syndrome, with cutaneous hypopigmented or hyperpigmented spots and patches, microcornea, coloboma, and severe hearing loss; and (4) PCWH, with features of Peripheral demyelinating neuropathy, Central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease.^Citation58,Citation59
	372	ETMDSS	Q16301: Replication initiation-like protein. Myelin transcription factor 2. MyT2. Cerebrin-50. Binds to the promoter of the myelin proteolipid protein. Strongly detected in cerebrospinal fluid. Expressed in oligodendrocyte progenitor cells, pyramidal and Purkinje neurons, neurons of the hypothalamus, hippocampus, ventromedial thalamus, cells of the choroid plexus, and ciliated ependymal cells.^Citation60
	389	RTRSGG	Q9P0W5: Schwannomin-interacting protein 1. SCHIP-1. Component of both axon initial segments and nodes of Ranvier, essential regions for saltatory conduction of the action potential along the axon, in the central and peripheral nervous systems. Isoforms 5 and 6 are highly expressed in the brain.^Citation61
RDRP	363	KLRTQI	MYT1L: Myelin transcription factor 1-like protein. MyT1L protein. May function as a panneural transcription factor associated with neuronal differentiation with a role in the development of neurons and oligodendrogalia in the CNS. Involved in schizophrenia.^Citation33
	513	GVSGIN	PRAX: Periaxin. PRX. Involved in the early phases of myelin deposition, in the maintenance of peripheral nerve myelin sheath, and in axon–glial interactions, by interacting with the cytoplasmic domains of integral membrane proteins such as myelin-associated glycoprotein in the periaxonal regions of the Schwann cell plasma membrane. Isoforms 1 and 2 are found in sciatic nerve and Schwann cells. Defects in PRX are a cause of Dejerine–Sottas syndrome, a neuropathy of the demyelinating CMT disease category, with onset by age 2 yr, characterized by motor and sensory neuropathy with slow nerve conduction velocities, increased cerebrospinal fluid protein concentrations, hypertrophic nerve changes, and delayed age of walking as well as areflexia.^Citation62,Citation63
PB2	113	KVYKTY	TSN3: Tetraspanin-3. Tspan-3. Regulates the proliferation and migration of oligodendrocytes, a process essential for normal myelination and repair.^Citation64
	185	ITKEKK	MTMRD: Myotubularin-related protein 13. SBF2. Expressed in spinal cord. Defects in SBF2 are the cause of CMT4B2, a recessive form of CMT disease, the most common inherited disorder of the peripheral nervous system, characterized by abnormal folding of myelin sheaths with pathological hallmarks on nerve biopsies including concentric sheaths (onion bulbs).^Citation65,Citation66
	190	KEELQD	SYYC: Tyrosyl-tRNA synthetase, cytoplasmic. TyrRS. YARS. Defects in YARS are the cause of CMT disease dominant intermediate type C, a form of CMT disease characterized by clinical and pathologic features intermediate between demyelinating and axonal peripheral neuropathies, and motor median nerve conduction velocities ranging from 25 to 45 m/s.^Citation67
	746	DSQTAT	IKAP: IκB kinase complex-associated protein. IKBKAP. May play a role in chromatin remodeling and is involved in acetylation of histones H3 and probably H4. Defects in IKBKAP are the cause of familial dysautonomia or Riley–Day syndrome or hereditary sensory and autonomic neuropathy type III due to progressive degeneration of the sensory, sympathetic and parasympathetic neurons. FD individuals are affected with a variety of symptoms such as decreased sensitivity to pain and temperature, cardiovascular instability, recurrent pneumonias, vomiting crises, and gastrointestinal dysfunction. IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination.^Citation68

a UniProt/Swissprot accession numbers are given in bold. For additional references and potential disease involvement, refer to www.uniprot.org

Table 5 Description in numbers of the hexapeptide overlap between TMV coat protein and the human proteome

Unique viral hexamers	154
Viral hexamers occurring in the human proteins	75
Expected number of viral hexamer occurrences in the human proteome	19.84

Table 6 Human proteins sharing hexapeptide sequence(s) with TMV coat protein

Sequence	Matches	Human protein(s) descriptiona
TTPSQF	2	BIN1: Myc box-dependent-interacting protein 1. NIPBL: Nipped-B-like protein.
VFLSSA	2	FRAS1: Extracellular matrix protein FRAS1. Highest levels found in kidneys, pancreas, and thalamus. R3HC1: R3H and coiled-coil domain-containing protein 1.
LSSAWA	1	SC6A3: Sodium-dependent dopamine transporter. Terminates the action of dopamine by its high affinity sodium-dependent reuptake into presynaptic terminals.
SAWADP	1	NACAD: NAC-alpha domain-containing protein 1.
WADPIE	1	HNRPQ: Heterogeneous nuclear ribonucleoprotein Q. Detected in the heart, brain, pancreas, and placenta.
LINLCT	1	GP112: Probable G-protein coupled receptor 112. Detected in fetal retina. Highly expressed in normal enterochromaffin cells and in neuroendocrine carcinoma.
CTNALG	1	EMR1b: EGF-like module-containing mucin-like hormone receptor-like 1.
NALGNQ	1	TACC2: Transforming acidic coiled-coil-containing protein 2. Acts in the nuclear migration of neural progenitors.
FQTQQA	2	TM40L: Mitochondrial import receptor subunit TOM40B. ZN687: Zinc finger protein 687.
QARTVV	1	FND3A: Fibronectin type-III domain-containing protein 3A expressed in odontoblasts.
TVVQRQ	1	RBM22: Pre-mRNA-splicing factor RBM22.
RQFSEV	1	Q96CH6: MGC20647 protein.
PSPQVT	1	NBAS: Neuroblastoma-amplified gene protein.
SPQVTR	2	NPHP1: Juvenile nephronophthisis 1 protein. VRK3: Serine/threonine-protein kinase VRK3.
PQVTRF	1	Q6ZR66: The cDNA FLJ46600 fis, clone THYMU3047144.
TVRFPD	1	ACHA7: Neuronal acetylcholine receptor subunit α-7.
DSDFKV	1	PHF14: Putative uncharacterized protein PHF14.
FKVYRY	1	TRIM2: Tripartite motif-containing protein 2.
YNAVLD	1	QSOX2: Neuroblastoma-derived sulfhydryl oxidase 2. Expressed in pancreas, brain, placenta, and fetal tissues.
VLDPLV	1	LPAR5: Lysophosphatidic acid receptor 5.
LDPLVT	2	LZTS1: Leucine zipper putative tumor suppressor 1. Involved in the regulation of cell growth. Highly expressed in testis, prostate, spleen, thymus, ovary, and brain. Q08E86: KIAA0100 protein.
LVTALL	2	KLRAQ: KLRAQ motif-containing protein 1. TENS4: C-terminal tensin-like protein.
VTALLG	3	KDM5C: Lysine-specific demethylase 5C. Defects in KDM5C are the cause of mental retardation. Syndromic X-linked JARID1C-related. O52B4: Olfactory receptor, family 52, subfamily B, member 4. MSLNL: Mesothelin-like protein.
TALLGA	1	STRA6: Stimulated by retinoic acid gene 6 protein homolog.
ALLGAF	1	TRUA: The tRNA pseudouridine synthase A.
TRNRII	1	A6NIH1: Putative uncharacterized protein ENSP00000350479.
NRIIEV	1	TIF1A: Transcription intermediary factor 1-alpha.
RIIEVE	1	B7Z872: cDNA FLJ56895, highly similar to Echinoderm microtubule-associated protein-like.
IIEVEN	3	SEP12: Septin-12. Widely expressed. CC110: Coiled-coil domain-containing protein 110. SEPT3: Neuronal-specific septin-3. Upregulated during neuronal differentiation.
EVENQA	2	COG5: Conserved oligomeric golgi complex subunit 5.
PTTAET	1	SFRS8: SFRS8 protein.
TTAETL	2	REEP2: Receptor expression-enhancing protein 2. Detected in the brain, heart, and skeletal muscle. BPIc: Bactericidal permeability-increasing protein.
TAETLD	2	KLD8B: Kelch domain-containing protein 8B. BPIc: Bactericidal permeability-increasing protein.
ETLDAT	1	SYFA: Phenylalanyl-tRNA synthetase α chain.
DDATVA	1	FBXW8: F-box/WD repeat-containing protein 8.
DATVAI	1	S13A5: Solute carrier family 13 member 5.
AIRSAI	1	B4DVQ1: The cDNA FLJ59288. Highly similar to roundabout homolog 2.
IRSAIN	1	RAD17: Cell cycle checkpoint protein RAD17.
NNLIVE	1	D3DXA2: Brain expressed X-linked 2 protein, isoform CRA_a.
NLIVEL	1	CS051: UPF0470 protein c19orf51.
LIRGTG	1	SRPRc: Signal recognition particle receptor subunit α.
IRGTGS	2	SRPRc: Signal recognition particle receptor subunit α. PSTK: Putative uncharacterized protein.
RSSFES	2	PRUN2: BNIP2 motif-containing molecule at the C-terminal region 1. Q5JUB6: Prune homolog 2.
SSFESS	4	ARMC2: Armadillo repeat-containing protein 2. ANKS6: Ankyrin repeat and SAM domain-containing protein 6. Required for renal function. ZEP3: Transcription factor HIVEP3. CA031: Uncharacterized protein C1orf31.
FESSSG	2	PTN13c: Protein–tyrosine phosphatase 1E. Most abundant in the lung, kidney, and fetal brain. EMR1b : EGF-like module-containing mucin-like hormone receptor-like 1.
ESSSGL	4	PTN13c: Protein–tyrosine phosphatase 1E. Most abundant in the lung, kidney and fetal brain. NF2L1: Nuclear factor erythroid 2-related factor 1. RGS9: Regulator of G-protein signaling 9. Highly expressed in the caudate and putamen. Q9Y628: Putative uncharacterized protein.
SGLVWT	1	AL8A1: Aldehyde dehydrogenase family 8 member A1.
LVWTSG	1	EIF3L: Eukaryotic translation initiation factor 3 subunit L.
TSGPAT	5	MUC16: Ovarian carcinoma antigen CA125. K1755: Uncharacterized protein KIAA1755. SF01: Splicing factor 1. MAP2: Microtubule-associated protein 2. A2RRB4: Regulation of transcription, DNA dependent.

a UniProt/Swissprot accession numbers are given in bold. Brain and/or peripheral nervous system localization given in boldface. For references and potential disease involvement, visit www.uniprot.org;

b The EMR1, EGF-like module-containing mucin-like hormone receptor-like 1 contains 2 viral hexapeptides;

c The bactericidal permeability-increasing protein (BPI); signal recognition particle receptor (SRPR) subunit α; and protein-tyrosine phosphatase 1E (PTN13) have 2 consecutive overlapping viral hexamers.

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