Sequence information
Variant position: 73 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:
HAAPFSAFLTDSFGRQHSYL
R ISLTEKCNLRCQYCMPEEGV
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 HAAPFSAFLTDSFGRQHSYLR ISLTEKCNLRCQYCMPEEGV
Mouse HAAPFSAFLTDSFGRQHSYLR ISLTEKCNLRCQYCMPEEGV
Bovine HAAPFSAFLTDSFGRHHSYLR ISLTERCNLRCQYCMPEEGV
Caenorhabditis elegans TKGQPPFF--DMFMREHTYLR ISLTEKCNFRCLYCMPAEGV
Drosophila NSP-----LTDSFGRHHTYLR ISLTERCNLRCDYCMPAEGV
Slime mold KK----YILTDRFNRHHTYLR ISLTERCNLRCKYCMPEEGV
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
Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A.
Reiss J.P.; Christensen E.; Kurlemann G.; Zabot M.-T.; Dorche C.;
Hum. Genet. 103:639-644(1998)
Cited for: VARIANTS MOCODA TRP-73; ASP-126; ASP-127; GLN-319 AND GLU-324;
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.