ABCD proteins
The ABC protein family
ATP-binding cassette (ABC) proteins are the largest family of transmembrane proteins. They are pumps that move substrates into (influx) or out of (efflux) cells. ABC transporters have important physiological functions in all living organisms. They are found in all prokaryotes, plants, fungi, yeast and animals. There are 49 ABC genes in the human genome. In mammals, ABC transporters are expressed primarily in the liver, intestine, blood-brain barrier, blood-testis barrier, placenta and kidney. ABC transporters bind and hydrolyze ATP and use the energy of this reaction to drive the transport of various molecules across cellular membranes, often against steep concentration gradients.
The typical structure of an ABC transporter consists of two transmembrane domains (TMD) and two nucleotide-binding domains (NBD). There are several different arrangements of TMD and NBD domains found among human ABC proteins (Figure). In general, however, a fully functional transporter is built according to the TMD-NBD-TMD-NBD composition. The four domains can be present in one polypeptide (as in the MDR P-glycoproteins) or they can be formed by dimerization of two ABC half-transporters, TAP1 (ABCB2) and TAP2 (ABCB3). The two NBD domains bind and hydrolyze ATP, which provides the driving force for transport. The two TMDs are involved in substrate recognition and translocation across the membrane.
The adrenoleukodystrophy protein (ALDP) is a half-transporter that must dimerize with another half-transporter to form a full transporter.

Figure: Schematic structure of the ABC half-transporters and full-transporters.
The peroxisomal ABC transporters (ABCD)
The peroxisomal ABC half-transporters ALDP (ABCD1), adrenoleukodystrophy-related protein (ALDRP, ABCD2) and the 70 kDa peroxisomal membrane protein (PMP70, ABCD3) form a distinct subclass of ABC proteins (subclass D). PMP69 (or P70R, ABCD4) is the fourth member of the ABCD family. While ABCD4 was originally identified as a peroxisomal protein, subsequent studies have shown that it is a lysosomal membrane protein. While ABCD1, ABCD2 and ABCD3 have a peptide signal that is necessary for their localization to the peroxisome, ABCD4 lacks this peptide signal. At the lysosomal membrane, the ABCD4 protein interacts with another protein called LMBD1. Together, these two proteins play an important role in vitamin B12 metabolism.
| protein | gene name | Cellular localization | chromosomal location |
|---|---|---|---|
| ALDP | ABCD1 | peroxisomal | Xq28 |
| ALDRP | ABCD2 | peroxisomal | 12q11 |
| PMP70 | ABCD3 | peroxisomal | 1p21-22 |
| PMP69 or P70R | ABCD4 | lysosome | 14q24.3 |
Alignment peroxisomal ABCD proteins
ABCD1 ----MPVLSRPRPWRGNTLKRTAVLLALAAYGAHKVYPLVRQCLAP-ARGLQAPAGEPTQ 55
ABCD2 MTHMLNAAADRVKWTRSSAAKRAACLVAAAYALKTLYPIIGKRLKQSGHGKKKAAAYPAA 60
ABCD3 ----MAAFSKYLTARNSSLAGAAFLLLCLLHKRRRALGLHGK-----------KSGKPPL 45
: . : .: * * : : : : :. *.
ABCD1 EASGVAAAKA--------GMNRVFLQRLLWLLRLLFPRVLCRETGLLALHSAALVSRTFL 107
ABCD2 ENTEILHCTETICEKPSPGVNADFFKQLLELRKILFPKLVTTETGWLCLHSVALISRTFL 120
ABCD3 QNNEKEGKKER------AVVDKVFFSRLIQILKIMVPRTFCKETGYLVLIAVMLVSRTYC 99
: . . :: *:.:*: : :::.*: . *** * * :. *:***:
ABCD1 SVYVARLDGRLARCIVRKDPRAFGWQLLQWLLIALPATFVNSAIRYLEGQLALSFRSRLV 167
ABCD2 SIYVAGLDGKIVKSIVEKKPRTFIIKLIKWLMIAIPATFVNSAIRYLECKLALAFRTRLV 180
ABCD3 DVWMIQNGTLIESGIIGRSRKDFKRYLLNFIAAMPLISLVNNFLKYGLNELKLCFRVRLT 159
.::: . : *: :. : * *:::: ::**. ::* :* *.** **.
ABCD1 AHAYRLYFSQQTYYRVSNMDGRLRNPDQSLTEDVVAFAASVAHLYSNLTKPLLDVAVTSY 227
ABCD2 DHAYETYFTNQTYYKVINMDGRLANPDQSLTEDIMMFSQSVAHLYSNLTKPILDVMLTSY 240
ABCD3 KYLYEEYLQAFTYYKMGNLDNRIANPDQLLTQDVEKFCNSVVDLYSNLSKPFLDIVLYIF 219
: *. *: ***:: *:*.*: **** **:*: *. **..*****:**:**: : :
ABCD1 TLLRAARSRGAGTAWPSAIAGLVVFLTANVLRAFSPKFGELVAEEARRKGELRYMHSRVV 287
ABCD2 TLIQTATSRGASPIGPTLLAGLVVYATAKVLKACSPKFGKLVAEEAHRKGYLRYVHSRII 300
ABCD3 KLTSAIGAQGP----ASMMAYLVVSG--LFLTRLRRPIGKMTITEQKYEGEYRYVNSRLI 273
.* : ::*. .: :* *** .* :*::. * : :* **::**::
ABCD1 ANSEEIAFYGGHEVELALLQRSYQDLASQINLILLERLWYVMLEQFLMKYVWSASGLLMV 347
ABCD2 ANVEEIAFYRGHKVEMKQLQKSYKALADQMNLILSKRLWYIMIEQFLMKYVWSSSGLIMV 360
ABCD3 TNSEEIAFYNGNKREKQTVHSVFRKLVEHLHNFILFRFSMGFIDSIIAKYLATVVGYLVV 333
:* ****** *:: * :: :: *..::: :: *: :::.:: **: : * ::*
ABCD1 AVPIITATGYSESDAEAVKKAALEKKEEELVSERTEAFTIARNLLTAAADAIERIMSSYK 407
ABCD2 AIPIITATGFADGE---------DGQKQVMVSERTEAFTTARNLLASGADAIERIMSSYK 411
ABCD3 SRPFLDLS--------------HPRHLKSTHSELLEDYYQSGRMLLRMSQALGRIVLAGR 379
: *:: : : : ** * : : .:* ::*: **: : :
ABCD1 EVTELAGYTARVHEMFQVFEDVQRCHFKRPRELEDAQAGSGTIGRSGVRVEGPLKIRGQV 467
ABCD2 EVTELAGYTARVYNMFWVFDEVKRGIYKRTAVIQESESHSKNGAKVELPLSDTLAIKGKV 471
ABCD3 EMTRLAGFTARITELMQVLKDLNHGKYERTMVSQQEK------GIEGVQVIPLIPGAGEI 433
*:*.***:***: ::: *:.:::: ::*. :: : . : : : *::
ABCD1 VDVEQGIICENIPIVTPSGEVVVASLNIRVEEGMHLLITGPNGCGKSSLFRILGGLWPTY 527
ABCD2 IDVDHGIICENVPIITPAGEVVASRLNFKVEEGMHLLITGPNGCGKSSLFRILSGLWPVY 531
ABCD3 IIADNIIKFDHVPLATPNGDVLIRDLNFEVRSGANVLICGPNGCGKSSLFRVLGELWPLF 493
: .:: * :::*: ** *:*: **:.*..* ::** ************:*. *** :
ABCD1 GGVLYKPPPQRMFYIPQRPYMSVGSLRDQVIYPDSVEDMQRKGYSEQDLEAILDVVHLHH 587
ABCD2 EGVLYKPPPQHMFYIPQRPYMSLGSLRDQVIYPDSVDDMHDKGYTDQDLERILHNVHLYH 591
ABCD3 GGRLTKPERGKLFYVPQRPYMTLGTLRDQVIYPDGREDQKRKGISDLVLKEYLDNVQLGH 553
* * ** ::**:******::*:*********. :* : ** :: *: *. *:* *
ABCD1 ILQREGGWEAMCDWKDVLSGGEKQRIGMARMFYHRPKYALLDECTSAVSIDVEGKIFQAA 647
ABCD2 IVQREGGWDAVMDWKDVLSGGEKQRMGMARMFYHKPKYALLDECTSAVSIDVEGKIFQAA 651
ABCD3 ILEREGGWDSVQDWMDVLSGGEKQRMAMARLFYHKPQFAILDECTSAVSVDVEGYIYSHC 613
*::*****::: ** **********:.***:***:*::*:*********:**** *:. .
ABCD1 KDAGIALLSITHRPSLWKYHTHLLQFDGEGGWKFEKLDSAARLSLTEEKQRLEQQLAGIP 707
ABCD2 KGAGISLLSITHRPSLWKYHTHLLQFDGEGGWRFEQLDTAIRLTLSEEKQKLESQLAGIP 711
ABCD3 RKVGITLFTVSHRKSLWKHHEYYLHMDGRGNYEFKQIT--------EDTVEFGS------ 659
: .**:*::::** ****:* : *::**.*.:.*::: *:. .: .
ABCD1 KMQRRLQELCQILGEAVAPAHVPAPSPQGPGGLQGAST 745
ABCD2 KMQQRLNELCKILGEDSVLKTIKNEDETS--------- 740
ABCD3 --------------------------------------
Last modified | 2024-06-25