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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P07320: Variant p.Arg37Ser

Gamma-crystallin D
Gene: CRYGD
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Variant information Variant position: help 37 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance
Residue change: help From Arginine (R) to Serine (S) at position 37 (R37S, p.Arg37Ser). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from large size and basic (R) to small size and polar (S) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page
Variant description: help In CTRCT4; very low solubility; crystallizes spontaneously. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 37 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 174 The length of the canonical sequence.
Location on the sequence: help YECSSDHPNLQPYLSRCNSA R VDSGCWMLYEQPNYSGLQYF The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         YECSSDHPNLQPYLSRCNSARVDSGCWMLYEQPNYSGLQYF

Mouse                         YECSTDHSNLQPYFSRCNSVRVDSGCWMLYEQPNFTGCQYF

Rat                           YECSTDHSNLQPYFSRCNSVRVDSGCWMLYEQPNFTGCQYF

Bovine                        YECSSDHSNLQPYLGRCNSVRVDSGCWMIYEQPNYLGPQYF
Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Chain 2 – 174 Gamma-crystallin D
Domain 2 – 40 Beta/gamma crystallin 'Greek key' 1
Mutagenesis 24 – 24 P -> TP. No effect on solubility.
Mutagenesis 24 – 24 P -> V. Slightly reduces solubility.
Beta strand 34 – 48



Literature citations
Link between a novel human gamma-D-crystallin allele and a unique cataract phenotype explained by protein crystallography.
Kmoch S.; Brynda J.; Asfaw B.; Bezouska K.; Novak P.; Rezacova P.; Ondrova L.; Filipec M.; Sedlacek J.; Elleder M.;
Hum. Mol. Genet. 9:1779-1786(2000)
Cited for: VARIANT CTRCT4 SER-37; Crystal cataracts: human genetic cataract caused by protein crystallization.
Pande A.; Pande J.; Asherie N.; Lomakin A.; Ogun O.; King J.; Benedek G.B.;
Proc. Natl. Acad. Sci. U.S.A. 98:6116-6120(2001)
Cited for: CHARACTERIZATION OF VARIANTS CTRCT4 SER-37 AND HIS-59;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.