Summary: Nup93/Nic96
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Nup93/Nic96 Provide feedback
Nup93/Nic96 is a component of the nuclear pore complex. It is required for the correct assembly of the nuclear pore complex [1]. In Saccharomyces cerevisiae, Nic96 has been shown to be involved in the distribution and cellular concentration of the GTPase Gsp1 [3]. The structure of Nic96 has revealed a mostly alpha helical structure [4].
Literature references
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Grandi P, Dang T, Pane N, Shevchenko A, Mann M, Forbes D, Hurt E; , Mol Biol Cell. 1997;8:2017-2038.: Nup93, a vertebrate homologue of yeast Nic96p, forms a complex with a novel 205-kDa protein and is required for correct nuclear pore assembly. PUBMED:9348540 EPMC:9348540
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Yoon JH, Whalen WA, Bharathi A, Shen R, Dhar R; , Mol Cell Biol 1997;17:7047-7060.: Npp106p, a Schizosaccharomyces pombe nucleoporin similar to Saccharomyces cerevisiae Nic96p, functionally interacts with Rae1p in mRNA export. PUBMED:9372936 EPMC:9372936
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Gao H, Sumanaweera N, Bailer SM, Stochaj U; , J Biol Chem. 2003;278:25331-25340.: Nuclear accumulation of the small GTPase Gsp1p depends on nucleoporins Nup133p, Rat2p/Nup120p, Nup85p, Nic96p, and the acetyl-CoA carboxylase Acc1p. PUBMED:12730220 EPMC:12730220
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Jeudy S, Schwartz TU; , J Biol Chem. 2007; [Epub ahead of print]: Crystal structure of nucleoporin Nic96 reveals a novel, intricate helical domain architecture. PUBMED:17897938 EPMC:17897938
External database links
| PANDIT: | PF04097 |
| Pseudofam: | PF04097 |
| SYSTERS: | Nic96 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR007231
Nup93/Nic96 is a component of the nuclear pore complex. It is required for the correct assembly of the nuclear pore complex [PUBMED:17897938]. In Saccharomyces cerevisiae, Nic96 has been shown to be involved in the distribution and cellular concentration of the GTPase Gsp1 [PUBMED:9372936]. The structure of Nic96 has revealed a mostly alpha helical structure [PUBMED:9348540].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | nuclear pore (GO:0005643) |
| Biological process | transport (GO:0006810) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Alignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database using the family HMM. We also generate alignments using four representative proteomes (RP) sets, the NCBI sequence database, and our metagenomics sequence database. More...
View options
We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
| Seed (40) |
Full (382) |
Representative proteomes | NCBI (382) |
Meta (2) |
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| RP15 (88) |
RP35 (139) |
RP55 (216) |
RP75 (256) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
not generated,
— not available.
Format an alignment
Download options
We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.
| Seed (40) |
Full (382) |
Representative proteomes | NCBI (382) |
Meta (2) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (88) |
RP35 (139) |
RP55 (216) |
RP75 (256) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
HMM logo
HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...
Trees
This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.
Note: You can also download the data file for the tree.
Curation and family details
This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.
Curation
| Seed source: | Pfam-B_5541 (release 7.3); |
| Previous IDs: | NIC; |
| Type: | Family |
| Author: | Wood V, Finn RD |
| Number in seed: | 40 |
| Number in full: | 382 |
| Average length of the domain: | 536.10 aa |
| Average identity of full alignment: | 25 % |
| Average coverage of the sequence by the domain: | 67.14 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 613 | ||||||||||||
| Family (HMM) version: | 9 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Sunburst controls
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Interactions
There is 1 interaction for this family. More...
Nic96Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the Nic96 domain has been found. There are 4 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence