Summary: Rabaptin
Pfam includes annotations and additional family information from a range of different sources. These sources can be accessed via the tabs below.
This is the Wikipedia entry entitled "Rabaptin". More...
Rabaptin Edit Wikipedia article
| Crystallographic structure of the C-terminal Rabaptin5 domain homodimer (colored orange and magenta at the center of the figure) complexed with two independent molecules of the GTPase domain of RAB5A (rainbow colored, N-terminus = blue, C-terminus = red).[1] | |||||||||
| Identifiers | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Symbol | Rabaptin | ||||||||
| Pfam | PF03528 | ||||||||
| InterPro | IPR003914 | ||||||||
|
|||||||||
Rabaptin is a key protein involved in regeneration of injured axons.
Regeneration of injured axons at neuromuscular junctions is regulated by extra-cellular protein factors that promote neurite outgrowth. A novel neurite outgrowth factor from chick denervated skeletal muscle has been cloned and characterised. The protein, termed neurocrescin (rabaptin), has been shown to be secreted in an activity-dependent fashion.[2]
Rabaptin is a 100kDa coiled-coil protein that interacts with the GTP form of the small GTPase Rab5 (see RAB5A, RAB5B, RAB5C) a potent regulator of endocytic transport.[3] It is mainly cytosolic, but a fraction co-localises with Rab5 to early endosomes. Rab5 recruits rabaptin-5 to purified early endosomes in a GTP-dependent manner, demonstrating functional similarities with other members of the Ras family. Immunodepletion of rabaptin-5 from cytosol strongly inhibits Rab5-dependent early endosome membrane fusion. Thus, rabaptin-5 is a Rab effector required for membrane docking and fusion.
Rab5 contributes to early endosome fusion that works through the coordination of other effector proteins, as mentioned above. Rabaptin components may serve to control the SNARE activity which are vital in membrane fusion.[4]
[edit] Structure
A crystal structure of the GTPase domain of RAB5A complexed with the C-terminal domain of Rabaptin5 has been determined.[1] The two proteins form a symmetric RAB5A-Rabaptin5 ternary complex with a parallel coiled-coil Rabaptin5 homodimer in the middle complexed with two molecules of Rabaptin5, one on each side (see figure to the right).
[edit] Human proteins
[edit] References
- ^ a b PDB 1tu3; Zhu G, Zhai P, Liu J, Terzyan S, Li G, Zhang XC (October 2004). "Structural basis of Rab5-Rabaptin5 interaction in endocytosis". Nat. Struct. Mol. Biol. 11 (10): 97583. doi:10.1038/nsmb832. PMID 15378032.
- ^ Nishimune H, Uyeda A, Nogawa M, Fujimori K, Taguchi T (1997). "Neurocrescin: a novel neurite-outgrowth factor secreted by muscle after denervation". NeuroReport 8 (16): 36493654. doi:10.1097/00001756-199711100-00045. PMID 9427343.
- ^ Zerial M, Stenmark H, Vitale G, Ullrich O (1995). "Rabaptin-5 is a direct effector of the small GTPase Rab5 in endocytic membrane fusion". Cell 83 (3): 423432. doi:10.1016/0092-8674(95)90120-5. PMID 8521472.
- ^ Deneka M, Neeft M, Popa I, van Oort M, Sprong H, Oorschot V, Klumperman J, Schu P, van der Sluijs P (June 2003). "Rabaptin-5alpha/rabaptin-4 serves as a linker between rab4 and gamma(1)-adaptin in membrane recycling from endosomes". EMBO J. 22 (11): 264557. doi:10.1093/emboj/cdg257. PMC 156754. PMID 12773381. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=156754.
This article incorporates text from the public domain Pfam and InterPro IPR003914
| This membrane protein-related article is a stub. You can help Wikipedia by expanding it. |
This page is based on a Wikipedia article. The text is available under the Creative Commons Attribution/Share-Alike License.
This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
Rabaptin Provide feedback
No Pfam abstract.
Internal database links
| SCOOP: | Rapamycin_bind |
External database links
| PANDIT: | PF03528 |
| Pseudofam: | PF03528 |
| SYSTERS: | Rabaptin |
This tab holds annotation information from the InterPro database.
InterPro entry IPR018514
Regeneration of injured axons at neuromuscular junctions has been assumed to be regulated by extra-cellular factors that promote neurite outgrowth. A novel neurite outgrowth factor from chick denervated skeletal muscle has been cloned and characterised. The protein, termed neurocrescin (rabaptin), has been shown to be secreted in an activity-dependent fashion [PUBMED:9427343].
Rabaptin is a 100kDa coiled-coil protein that interacts with the GTP form of the small GTPase Rab5, a potent regulator of endocytic transport [PUBMED:8521472]. It is mainly cytosolic, but a fraction co-localises with Rab5 to early endosomes. Rab5 recruits rabaptin-5 to purified early endosomes in a GTP-dependent manner, demonstrating functional similarities with other members of the Ras superfamily. Immunodepletion of rabaptin-5 from cytosol strongly inhibits Rab5-dependent early endosome fusion. Thus, rabaptin-5 is a Rab effector required for membrane docking and fusion.Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | growth factor activity (GO:0008083) |
| GTPase activator activity (GO:0005096) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
Loading domain graphics...
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 (5) |
Full (248) |
Representative proteomes | NCBI (219) |
Meta (0) |
||||
|---|---|---|---|---|---|---|---|---|
| RP15 (9) |
RP35 (16) |
RP55 (42) |
RP75 (100) |
|||||
| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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 (5) |
Full (248) |
Representative proteomes | NCBI (219) |
Meta (0) |
||||
|---|---|---|---|---|---|---|---|---|
| RP15 (9) |
RP35 (16) |
RP55 (42) |
RP75 (100) |
|||||
| 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: | PRINTS |
| Previous IDs: | none |
| Type: | Family |
| Author: | Griffiths-Jones SR |
| Number in seed: | 5 |
| Number in full: | 248 |
| Average length of the domain: | 108.70 aa |
| Average identity of full alignment: | 41 % |
| Average coverage of the sequence by the domain: | 30.00 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
|
||||||||||||
| Model details: |
|
||||||||||||
| Model length: | 106 | ||||||||||||
| Family (HMM) version: | 10 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Sunburst controls
ShowThis visualisation provides a simple graphical representation of the distribution of this family across species. You can find the original interactive tree in the adjacent tab. More...
Tree controls
HideThe tree shows the occurrence of this domain across different species. More...
Loading...
Please note: for large trees this can take some time. While the tree is loading, you can safely switch away from this tab but if you browse away from the family page entirely, the tree will not be loaded.
Structures
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 Rabaptin domain has been found. There are 2 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.
Loading structure mapping...

Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence