Gram domain containing 1b


GRAM domain containing 1B, also known as GRAMD1B, Aster-B and KIAA1201, is a protein that is encoded by the GRAMD1B gene. It contains a transmembrane region and two domains of known function; the GRAM domain and a VASt domain. It is predicted to localize in the nucleus, supported by several nuclear transport signals and nuclearly associated motifs. This highly conserved gene is found in a variety of vertebrates and invertebrates, however is not found in bacteria or fungi.

Gene

GRAMD1B, also known as KIAA1201, is located in the human genome at 11q24.1. It is located on the + strand and is flanked by a variety of other genes. It spans 269,347 bases.

mRNA

The most verified isoform, isoform 1, contains 21 exons. There are four validated isoform variants of human GRAMD1B. These consist of truncated 5’ and 3’ regions, resulting in the loss of an exon.
IsoformmRNA length ExonsProtein length Status
1792721745Validated
2790620738Validated
3763620698Validated
4756120694Validated

Protein

GRAMD1B contains several domains, motifs and signals.

Domains

There are two confirmed domains within GRAMD1B. The protein gets its name from the GRAM domain, located approximately 100 amino acids from the start codon. The GRAM domain is commonly found in myotubularin family phosphatases and predominantly involved in membrane coupled processes. GRAMD1B also contains the VASt domain. The VASt domain is predominantly associated with lipid binding domains, such as GRAM. It is most likely to function in binding large hydrophobic ligands and may be specific for sterol.

Composition Features

There are two negative charge clusters, located from amino acids 232-267 and 348-377. The first cluster is not highly conserved, nor is it located in a motif or domain. The second cluster is located directly before the VASt domain and is conserved.
There are three repeat sequence regions, all fairly conserved in orthologs.
Repeat #Sets of RepeatsLength LocationSimilarity Score
1318Within first 100 amino acids83.44
2221GRAM domain77.22
3222VASt domain67.94

Molecular weight and isoelectric point are conserved in orthologs.
RegionAmino AcidsIsoelectric pointMolecular Weight
Human GRAMD1B745pH of 6.0286.5
GRAM domain94pH of 8.2711.3
VASt domain144pH of 9.4117.3
Transmembrane region21pH of 5.182.3

Structure

The mature protein contains two nuclear localization signals, pat4 and pat7. There are four dileucine motifs, three located within or close to the GRAM domain. A leucine zipper pattern extends through a majority the transmembrane region. A SUMOylation site is located directly after the VASt domain. The proteins secondary structure consists of alpha-helices, beta-strands and coils. Beta-strands are mainly located within the two domains, while the alpha-helixes are concentrated near the transmembrane region. Three disulfide bonds are predicted throughout the protein.

Subcellular location

GRAMD1B is predicted to localize in the nucleus and contains a transmembrane domain, most likely placing it in the membrane of the nucleus.

Expression

GRAMD1B is expressed in a variety of tissues. It is most highly expressed in the gonadal tissue, adrenal gland, brain and placenta. It has raised expression rates in adrenal tumors, lung tumors. Developmentally, it is most highly expressed during infancy. The EST profile is supported with experimental data from multiple sources

Homology

Orthologs

The ortholog space for GRAMD1B spans a large portion of evolutionary time. GRAMD1B can be found in mammals, bird, fish and invertebrates. It is not present in bacteria, archaea or fungi.
Genus speciesCommon NameAccession NumberDate of Divergence Identity
Homo sapiensHumanNP_001273492.10100.00%
Aotus nancymaaeNancy Ma's Night MonkeyXP_012325676.13.299.00%
Papio anubisOlive BaboonXP_017804515.129.4497.00%
Castor canadensisBeaverXP_020037170.19098.00%
Octodon degusDenguXP_004636450.19097.00%
Pantholops hodgsoniiTibetan AntelopeXP_005958036.19699.00%
Bos mutusDomestic YakXP_005896826.19698.00%
Tursiops truncatusDolphinXP_0197975439683.00%
Elephantulus edwardiiCape Elephant ShrewXP_006895663.110598.00%
Gallus gallusChickenXP_015153638.131293.00%
Calypte annaAnna's Humming BirdXP_008490701.131291.00%
Pygoscelis adeliaeAdelie PenguinXP_009331694.131291.00%
Coturnix japonicaJapanese QuailXP_015739426.131290.00%
Anolis carolinensisCarolina AnoleXP_008111963.131287.00%
Danio rerioZebra FishXP_009303888.143573.00%
Callorhinchus miliiAustralian Ghost SharkXP_007894251.147377.00%
Branchiostoma belcheriLanceletXP_019624725.168440.00%
Octopus bimaculoidesCalifornia Two-Spot OctopusXP_014769036.179740.00%
Lingula anatinaBrachiopodXP_01341557879738.00%
Zootermopsis nevadensisTermiteKDR17240.179737.00%
Trachymyrmex cornetziAntXP_018362289.179734.00%

Paralogs

There are four paralogs of GRAMD1B. The most closely related is GRAMD1A while the most distant ortholog is GRAMD2A/GRAMD2.
ParalogSequence LengthSequence IdentityDate of Divergence
GRAMD1A724 aa46.60%421.0
GRAMD1C662 aa37.90%934.7
GRAMD2B/GRAMD3491 aa18.50%1625.6
GRAMD2A353 aa16.70%1724.2

Phylogeny

GRAMD2 diverged earliest in history while the most recent split is GRAMD1A. The GRAMD1B gene’s rate of divergence significantly faster than Fibrinogen but is not as high as Cytochrome C.

Function

Currently, the function of GRAMD1B has not been characterized.

Protein interactions

Several different proteins have been experimentally confirmed or predicted to interact with GRAMD1B.
ProteinInteraction identified viaFunctionLocation
COPAExperimentalBinds dilysine motifs. Required for budding from the Golgi and retrograde Golgi to ER transportsystolic
SPICE1Data MiningSpindle and centriole associated. Regulates centriole duplication, proper bipolar spindle formation and chromosome congregation in mitosisnuclear
GTPBP8Data MiningGTP binding proteinunconfirmed
YwhaeCo-sedimentationAdapter protein associated with regulating nuclear transport to the cytoplasmnuclear

Clinical significance

A study tagging SNPs from chronic lymphocytic leukemia found GRAMD1B to be the second strongest risk allele region. This association is supported through a number of studies The aberrant tri-methylation of histone H3 lysine 27 induces inflammation and has been shown to increase GRAMD1B levels in colon tumors.