Domains within Homo sapiens protein FMR1_HUMAN (Q06787)

Synaptic functional regulator FMR1

Alternative representations: 1 /

Protein length632 aa
Source databaseUniProt
Identifiers FMR1_HUMAN, Q06787, ENSP00000359506.4, ENSP00000359506, D3DWT2, G8JL90, A6NNH4, D3DWT0, D3DWT1, Q16578, Q5PQZ6, Q99054
Source gene ENSG00000102081
Alternative splicing Q06787-8, A0A087WWU4_HUMAN, A8MQB8_HUMAN, Q8IXW7_HUMAN, G3V0J0_HUMAN, FMR1_HUMAN, A0A087X1M7_HUMAN, A0A087WY29_HUMAN, Q06787-6, A0A087WWR6_HUMAN, A0A087WXC0_HUMAN, Q06787-9, Q06787-10, R9WNI0_HUMAN, A0A087WXI3_HUMAN

Domain architecture analysis

Display all proteins with similar:

Domain organisationProteins having all the domains as the query in the same order. Additional domains are allowed.
Domain compositionProteins with the same domain composition have at least one copy of each of the domains of the query.

This domain architecture was probably invented with the emergence of cellular organisms

Predicted functional partners

FMR1_HUMAN is shown as FMR1 in the network

Click and drag to pan the network, and zoom by using your mouse wheel. Click the protein nodes for additional options.

The network on the left comes from STRING, a database of known and predicted protein interactions. Displayed here is the evidence view, where different line colors represent the types of evidence for the association.

Open the STRING annotation page for FMR1

Protein FMR1_HUMAN is possibly involved in these pathways, based on its similarity to the listed KEGG orthologous groups:

KEGG pathways

PathwayDescription
map04216Ferroptosis

KEGG orthologous groups

KONameDescription
K15516FMRfragile X mental retardation protein

Post-translational modifications

PTM annotation is taken from PTMcode, a resource of known and predicted functional associations between protein post-translational modifications (PTMs). There are 24 PTMs annotated in this protein:

PTMCount
Phosphorylation16
Methylation6
Acetylation2

To see the full details, including possible functional associations between the PTMs, please visit the PTMcode annotation page for protein FMR1.

Orthologous groups

Orthology information is taken from eggNOG, a database of orthologous groups of genes. Orthologous groups containing this protein are listed below. This protein is named 9606.ENSP00000359506 in eggNOG.

OGTaxonomic classDescription
7222SAll organisms (root)fragile X mental retardation protein,diamine N-acetyltransferase [EC:2.3.1.57]
5E83DEukaryota (superkingdom)fragile X mental retardation protein,diamine N-acetyltransferase [EC:2.3.1.57]
HVM6MMetazoa (kingdom)fragile X mental retardation protein,diamine N-acetyltransferase [EC:2.3.1.57]
94A68Chordata (phylum)fragile X mental retardation protein,diamine N-acetyltransferase [EC:2.3.1.57]
5R4XVSarcopterygii (superclass)fragile X mental retardation protein
8ZD7KMammalia (class)fragile X mental retardation protein
4RBTNEuarchontoglires (superorder)fragile X mental retardation protein
50355Primates (order)fragile X mental retardation protein
98FNVHaplorrhini (suborder)fragile X mental retardation protein
BUYI7Simiiformes (infraorder)fragile X mental retardation protein
9EYNICatarrhini (parvorder)fragile X mental retardation protein
7MXAGOpisthokonta (clade)fragile X mental retardation protein,diamine N-acetyltransferase [EC:2.3.1.57]
9G039Vertebrata (clade)fragile X mental retardation protein
H49YUBilateria (clade)fragile X mental retardation protein,diamine N-acetyltransferase [EC:2.3.1.57]
FX14THominoidea (superfamily)fragile X mental retardation protein
5N5NNHominidae (family)fragile X mental retardation protein
5XSJ4Homininae (subfamily)fragile X mental retardation protein

The SMART diagram above represents a summary of the results shown below. Domains with scores less significant than established cutoffs are not shown in the diagram. Features are also not shown when two or more occupy the same piece of sequence; the priority for display is given by SMART > PFAM > PROSPERO repeats > Signal peptide > Transmembrane > Coiled coil > Low complexity. In either case, features not shown in the above diagram are listed in the right side table below, and the reason for their omission is shown in the 'Reason' column.

Confidently predicted domains, repeats, motifs and features:

Outlier homologues and homologues of known structure:

Features NOT shown in the diagram: