UniProtKB/SwissProt variant VAR

Variant information

Variant position:

67

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:

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:

From Arginine (R) to Tryptophan (W) at position 67 (R67W, p.Arg67Trp).

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:

Change from large size and basic (R) to large size and aromatic (W)

The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:

-3

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:

In MOCODA.

Any additional useful information about the variant.

Other resources:

Links to websites of interest for the variant.

Variant rs754441164 [ dbSNP | Ensembl ]

Sequence information

Variant position:

67

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:

636

The length of the canonical sequence.

Location on the sequence:

RQFLREHAAPFSAFLTDSFG R QHSYLRISLTEKCNLRCQYC

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:

The multiple alignment of the region surrounding the variant against various orthologous sequences.

Human                         RQFLREHAAPFSAFLTDSFGRQHSYLRISLTEKCNLRCQYC

Mouse                         LQFLQEHAAPFSAFLTDSFGRQHSYLRISLTEKCNLRCQYC

Bovine                        RPFLGEHAAPFSAFLTDSFGRHHSYLRISLTERCNLRCQYC

Caenorhabditis elegans        IQEIEHTKGQPPFF--DMFMREHTYLRISLTEKCNFRCLYC

Drosophila                    KQVLRKNSP-----LTDSFGRHHTYLRISLTERCNLRCDYC

Slime mold                    IQNVDDKK----YILTDRFNRHHTYLRISLTERCNLRCKYC

Sequence annotation in neighborhood:

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.

Type	Positions	Description
Chain	1 – 636	Molybdenum cofactor biosynthesis protein 1
Domain	64 – 277	Radical SAM core
Region	1 – 383	Molybdenum cofactor biosynthesis protein A
Metal binding	80 – 80	Iron-sulfur (4Fe-4S) 1; 4Fe-4S-S-AdoMet
Metal binding	84 – 84	Iron-sulfur (4Fe-4S) 1; 4Fe-4S-S-AdoMet
Metal binding	87 – 87	Iron-sulfur (4Fe-4S) 1; 4Fe-4S-S-AdoMet
Binding site	73 – 73	GTP
Binding site	86 – 86	S-adenosyl-L-methionine
Modified residue	64 – 64	Phosphoserine
Alternative sequence	1 – 87	Missing. In isoform 4 and isoform 7.
Mutagenesis	80 – 80	C -> S. Impairs precursor Z synthesis.
Mutagenesis	84 – 84	C -> S. Impairs precursor Z synthesis.
Mutagenesis	87 – 87	C -> S. Impairs precursor Z synthesis.

Literature citations

Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase.
Leimkuehler S.; Charcosset M.; Latour P.; Dorche C.; Kleppe S.; Scaglia F.; Szymczak I.; Schupp P.; Hahnewald R.; Reiss J.;
Hum. Genet. 117:565-570(2005)
Cited for: VARIANTS MOCODA TRP-67; GLY-80 AND PHE-84;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9NZB8: Variant p.Arg67Trp