2e6q
Solution structure of the Ig-like domain (615-713) from human Obscurin-like protein 1Solution structure of the Ig-like domain (615-713) from human Obscurin-like protein 1
Structural highlights
Disease[OBSL1_HUMAN] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:612921]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.[1] FunctionEvolutionary Conservation![]() Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. See AlsoReferences
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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Homo sapiens
- Hayashi, F.
- Qin, X R.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Suetake, T.
- Yokoyama, S.
- Ig-like domain
- National project on protein structural and functional analyse
- Nppsfa
- Obscurin-like protein 1
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomic
- Structural protein