PubMed:22128166
Annnotations
GlyCosmos6-Glycan-Motif-Image
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 64-67 | Glycan_Motif | denotes | Gm1 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G48558GR|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46613JI |
| T3 | 107-112 | Glycan_Motif | denotes | G(M1) | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G48558GR|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46613JI |
| T5 | 438-443 | Glycan_Motif | denotes | G(M1) | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G48558GR|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46613JI |
| T7 | 461-476 | Glycan_Motif | denotes | keratan sulfate | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G82109MW |
| T8 | 556-565 | Glycan_Motif | denotes | galactose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G68158BT|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G65889KE |
| T10 | 669-678 | Glycan_Motif | denotes | galactose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G68158BT|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G65889KE |
Glycosmos6-GlycoEpitope
| Id | Subject | Object | Predicate | Lexical cue | glyco_epitope_db_id |
|---|---|---|---|---|---|
| T1 | 461-476 | GlycoEpitope | denotes | keratan sulfate | http://www.glycoepitope.jp/epitopes/EP0085 |
GlyCosmos6-Glycan-Motif-Structure
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 64-67 | https://glytoucan.org/Structures/Glycans/G46613JI | denotes | Gm1 |
| T2 | 64-67 | https://glytoucan.org/Structures/Glycans/G48558GR | denotes | Gm1 |
| T3 | 107-112 | https://glytoucan.org/Structures/Glycans/G46613JI | denotes | G(M1) |
| T4 | 107-112 | https://glytoucan.org/Structures/Glycans/G48558GR | denotes | G(M1) |
| T5 | 438-443 | https://glytoucan.org/Structures/Glycans/G46613JI | denotes | G(M1) |
| T6 | 438-443 | https://glytoucan.org/Structures/Glycans/G48558GR | denotes | G(M1) |
| T7 | 461-476 | https://glytoucan.org/Structures/Glycans/G82109MW | denotes | keratan sulfate |
| T8 | 556-565 | https://glytoucan.org/Structures/Glycans/G65889KE | denotes | galactose |
| T9 | 556-565 | https://glytoucan.org/Structures/Glycans/G68158BT | denotes | galactose |
| T10 | 669-678 | https://glytoucan.org/Structures/Glycans/G65889KE | denotes | galactose |
| T11 | 669-678 | https://glytoucan.org/Structures/Glycans/G68158BT | denotes | galactose |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-106 | Sentence | denotes | Crystal structure of human β-galactosidase: structural basis of Gm1 gangliosidosis and morquio B diseases. |
| T2 | 107-291 | Sentence | denotes | G(M1) gangliosidosis and Morquio B are autosomal recessive lysosomal storage diseases associated with a neurodegenerative disorder or dwarfism and skeletal abnormalities, respectively. |
| T3 | 292-575 | Sentence | denotes | These diseases are caused by deficiencies in the lysosomal enzyme β-d-galactosidase (β-Gal), which lead to accumulations of the β-Gal substrates, G(M1) ganglioside, and keratan sulfate. β-Gal is an exoglycosidase that catalyzes the hydrolysis of terminal β-linked galactose residues. |
| T4 | 576-727 | Sentence | denotes | This study shows the crystal structures of human β-Gal in complex with its catalytic product galactose or with its inhibitor 1-deoxygalactonojirimycin. |
| T5 | 728-823 | Sentence | denotes | Human β-Gal is composed of a catalytic TIM barrel domain followed by β-domain 1 and β-domain 2. |
| T6 | 824-989 | Sentence | denotes | To gain structural insight into the molecular defects of β-Gal in the above diseases, the disease-causing mutations were mapped onto the three-dimensional structure. |
| T7 | 990-1049 | Sentence | denotes | Finally, the possible causes of the diseases are discussed. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 27-42 | gene:2720 | denotes | β-galactosidase |
| T1 | 64-82 | disease:C0085131 | denotes | Gm1 gangliosidosis |
| R1 | T0 | T1 | associated_with | β-galactosidase,Gm1 gangliosidosis |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 146-165 | HP_0000007 | denotes | autosomal recessive |
| T2 | 241-249 | HP_0003510 | denotes | dwarfism |
| T3 | 254-276 | HP_0000924 | denotes | skeletal abnormalities |
Allie
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| SS1_22128166_2_0 | 358-375 | expanded | denotes | β-d-galactosidase |
| SS2_22128166_2_0 | 377-382 | abbr | denotes | β-Gal |
| AE1_22128166_2_0 | SS1_22128166_2_0 | SS2_22128166_2_0 | abbreviatedTo | β-d-galactosidase,β-Gal |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 22128166-0#27#42#gene2720 | 27-42 | gene2720 | denotes | β-galactosidase |
| 22128166-0#64#82#diseaseC0085131 | 64-82 | diseaseC0085131 | denotes | Gm1 gangliosidosis |
| 27#42#gene272064#82#diseaseC0085131 | 22128166-0#27#42#gene2720 | 22128166-0#64#82#diseaseC0085131 | associated_with | β-galactosidase,Gm1 gangliosidosis |
GlyCosmos15-Glycan
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 64-67 | Glycan | denotes | Gm1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR |
| T2 | 107-112 | Glycan | denotes | G(M1) | https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR |
| T3 | 438-443 | Glycan | denotes | G(M1) | https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR |
| T4 | 461-476 | Glycan | denotes | keratan sulfate | https://api.glycosmos.org/wurcs2image/latest/png/binary/G82109MW |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 241-249 | Phenotype | denotes | dwarfism | HP:0003510 |
| T2 | 254-276 | Phenotype | denotes | skeletal abnormalities | HP:0000924 |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 64-82 | Disease | denotes | Gm1 gangliosidosis | http://purl.obolibrary.org/obo/MONDO_0018149 |
| T2 | 107-127 | Disease | denotes | G(M1) gangliosidosis | http://purl.obolibrary.org/obo/MONDO_0018149 |
| T3 | 166-192 | Disease | denotes | lysosomal storage diseases | http://purl.obolibrary.org/obo/MONDO_0002561 |
Glycan-GlyCosmos
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 461-476 | Glycan | denotes | keratan sulfate | https://api.glycosmos.org/wurcs2image/latest/png/binary/G82109MW |
GlyCosmos-GlycoEpitope
| Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
|---|---|---|---|---|---|
| T1 | 461-476 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | keratan sulfate | http://www.glycoepitope.jp/epitopes/EP0085 |
GlyCosmos15-HP
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 241-249 | Phenotype | denotes | dwarfism | HP:0003510 |
| T2 | 254-276 | Phenotype | denotes | skeletal abnormalities | HP:0000924 |
GlyCosmos15-MONDO
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 64-82 | Disease | denotes | Gm1 gangliosidosis | MONDO:0018149 |
| T2 | 107-127 | Disease | denotes | G(M1) gangliosidosis | MONDO:0018149 |
| T3 | 166-192 | Disease | denotes | lysosomal storage diseases | MONDO:0002561 |
GlyCosmos15-Taxon
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 21-26 | Organism | denotes | human | 9606 |
| T2 | 619-624 | Organism | denotes | human | 9606 |
| T3 | 728-733 | Organism | denotes | Human | 9606 |
GlyCosmos15-Sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-106 | Sentence | denotes | Crystal structure of human β-galactosidase: structural basis of Gm1 gangliosidosis and morquio B diseases. |
| T2 | 107-291 | Sentence | denotes | G(M1) gangliosidosis and Morquio B are autosomal recessive lysosomal storage diseases associated with a neurodegenerative disorder or dwarfism and skeletal abnormalities, respectively. |
| T3 | 292-575 | Sentence | denotes | These diseases are caused by deficiencies in the lysosomal enzyme β-d-galactosidase (β-Gal), which lead to accumulations of the β-Gal substrates, G(M1) ganglioside, and keratan sulfate. β-Gal is an exoglycosidase that catalyzes the hydrolysis of terminal β-linked galactose residues. |
| T4 | 576-727 | Sentence | denotes | This study shows the crystal structures of human β-Gal in complex with its catalytic product galactose or with its inhibitor 1-deoxygalactonojirimycin. |
| T5 | 728-823 | Sentence | denotes | Human β-Gal is composed of a catalytic TIM barrel domain followed by β-domain 1 and β-domain 2. |
| T6 | 824-989 | Sentence | denotes | To gain structural insight into the molecular defects of β-Gal in the above diseases, the disease-causing mutations were mapped onto the three-dimensional structure. |
| T7 | 990-1049 | Sentence | denotes | Finally, the possible causes of the diseases are discussed. |
GlyCosmos15-GlycoEpitope
| Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
|---|---|---|---|---|---|
| T1 | 461-476 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | keratan sulfate | http://www.glycoepitope.jp/epitopes/EP0085 |
GlyCosmos15-FMA
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 146-155 | Body_part | denotes | autosomal | FMA:74406 |
| T2 | 166-175 | Body_part | denotes | lysosomal | FMA:63836 |
| T3 | 341-350 | Body_part | denotes | lysosomal | FMA:63836 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 21-26 | OrganismTaxon | denotes | human | 9606 |
| T2 | 619-624 | OrganismTaxon | denotes | human | 9606 |
| T3 | 728-733 | OrganismTaxon | denotes | Human | 9606 |