Solute carrier family
The solute carrier group of membrane transport proteins include over 400 members organized into 65 families. Most members of the SLC group are located in the cell membrane. The SLC gene nomenclature system was originally proposed by the HUGO Gene Nomenclature Committee and is the basis for the official HGNC names of the genes that encode these transporters. A more general transmembrane transporter classification can be found in TCDB database.
Solutes that are transported by the various SLC group members are extremely diverse and include both charged and uncharged organic molecules as well as inorganic ions and the gas ammonia.
As is typical of integral membrane proteins, SLCs contain a number of hydrophobic transmembrane alpha helices connected to each other by hydrophilic intra- and extra-cellular loops. Depending on the SLC, these transporters are functional as either monomers or obligate homo- or hetero-oligomers. Many SLC families are members of the major facilitator superfamily.
Scope
By convention of the nomenclature system, members within an individual SLC family have greater than 20-25% sequence identity to each other. In contrast, the homology between SLC families is very low to non-existent. Hence, the criteria for inclusion of a family into the SLC group is not evolutionary relatedness to other SLC families but rather functional.The SLC group include examples of transport proteins that are:
- facilitative transporters
- secondary active transporters
- primary active transporters such as ABC transporters by coupling transport to an energy releasing event such as ATP hydrolysis
- ion channels
- aquaporins
Subcellular distribution
Nomenclature system
Names of individual SLC members have the following format:- SLCnXm
- SLC is the root name
- n = an integer representing a family
- X = a single letter denoting a subfamily
- m = an integer representing an individual family member.
An exception occurs with SLC family 21, which for historical reasons have names in the format SLCOnXm where n = family number, X = subfamily letter, and m = member number.
While the HGNC only assign nomenclature to human genes, by convention vertebrate orthologs of these genes adopt the same nomenclature. For rodents, the case of the symbols differs from other vertebrates by using title case, i.e. Slc1a1 denotes the rodent ortholog of the human SLC1A1 gene.
Families
- high-affinity glutamate and neutral amino acid transporter
- *
- facilitative GLUT transporter
- *
- heavy subunits of heterodimeric amino acid transporters
- *
- bicarbonate transporter
- *
- sodium glucose cotransporter
- *
- sodium- and chloride-dependent
- *
- cationic amino acid transporter/glycoprotein-associated
- * cationic amino acid transporters
- * glycoprotein-associated/light or catalytic subunits of heterodimeric amino acid transporters
- Na+/Ca2+ exchanger
- *
- Na+/H+ exchanger
- *
- sodium bile salt cotransport
- *
- proton coupled metal ion transporter
- *
- electroneutral cation-Cl cotransporter
- *
- Na+-sulfate/carboxylate cotransporter
- *
- urea transporter
- *
- proton oligopeptide cotransporter
- *
- monocarboxylate transporter
- *
- vesicular glutamate transporter
- *
- vesicular amine transporter
- *
- folate/thiamine transporter
- *
- type III Na+-phosphate cotransporter
- *
- organic anion transporting
- * subfamily 1
- * subfamily 2
- * subfamily 3
- * subfamily 4
- * subfamily 5
- * subfamily 6
- organic cation/anion/zwitterion transporter
- *
- Na+-dependent ascorbic acid transporter
- *
- Na+/ exchanger
- *
- mitochondrial carrier
- *
- multifunctional anion exchanger
- *
- fatty acid transport proteins
- *
- Na+-coupled nucleoside transport
- *
- facilitative nucleoside transporter
- *
- zinc transporter
- *
- copper transporter
- *
- vesicular inhibitory amino acid transporter
- *
- Acetyl-CoA transporter
- *
- type II Na+-phosphate cotransporter
- *
- nucleotide-sugar transporter
- * subfamily A
- * subfamily B
- * subfamily C
- * subfamily D
- * subfamily E
- * subfamily F
- * subfamily G
- proton-coupled amino acid transporter
- *
- sugar-phosphate/phosphate exchanger
- *
- System A & N, sodium-coupled neutral amino acid transporter
- *
- metal ion transporter
- *
- basolateral iron transporter
- *
- MgtE-like magnesium transporter
- *
- Ammonia transporter
- *
- Na+-independent, system-L like amino acid transporter
- *
- Choline-like transporter
- *
- Putative sugar transporter
- *
- Folate transporter
- *
- multidrug and toxin extrusion
- *
- Heme transporter family
- *
- Heme transporter
- *
- Sugar efflux transporters of the SWEET family
- *
- Transporters of steroid-derived molecules
- *
- Riboflavin transporter family RFVT/SLC52
- *
- Phosphate carriers
- *
- Mitochondrial pyruvate carriers
- *
- Mitochondrial cation/proton exchangers
- *
- Sideroflexins
- *
- NiPA-like magnesium transporter family
- *
- MagT-like magnesium transporter family
- *
- Sodium-dependent lysophosphatidylcholine symporter family
- *
- Glucose transporters
- *
- Molybdate transporter family
- *
- Pyrophosphate transporters
- *
- Sphingosine-phosphate transporters
- *
- Golgi Ca2+/H+ exchangers
- *
- NPC-type cholesterol transporters
- *
Putative SLCs
All the putative SLCs are plausible SLC transporters. They are only "atypical" when it comes to their names; the genes are not called according to the SLC root system.
Here are some Putative SLCs listed: OCA2, CLN3, TMEM104, SPNS1, SPNS2, SPNS3, SV2A, SV2B, SV2C, SVOP, SVOPL, MFSD1, MFSD2A, MFSD2B, MFSD3, MFSD4A, MFSD4B, MFSD5, MFSD6, MFSD6L, MFSD8, MFSD9, MFSD10, MFSD11, MFSD12, MFSD13A, MFSD14A, MFSD14B, UNC93A and UNC93B1.