1D5M: HLA-DR4

X-ray crystal structure of HLA-DR4 complexed with peptide and seb. Determined by X-ray diffraction at 2.0 Å resolution. Released 28 Jun 2000.

Method
X-ray diffraction
Resolution
2.0 Å
Organisms
Homo sapiens, Staphylococcus aureus, synthetic construct
Chains
4
Atoms
5,076
Mol. weight
73.15 kDa
Ligands
NAG
Released
28 Jun 2000

Explore 1D5M in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1D5M contains 23 α-helices and 47 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 5 helices, 15 β-strands

ElementResiduesLengthSheet
β-strand5-15111
β-strand19-2681
β-strand29-3571
β-strand40-4341
α-helix46-516
α-helix56-583
α-helix59-7618
α-helix80-845
β-strand8512
β-strand88-9363
β-strand103-112103
β-strand11312
β-strand118-12364
β-strand126-12834
β-strand133-13423
α-helix1371
β-strand138-13923
β-strand145-15393
β-strand161-16664
β-strand174-17854
Chain B: 8 helices, 15 β-strands
ElementResiduesLengthSheet
β-strand7-18121
β-strand23-32101
β-strand35-4171
β-strand47-4931
α-helix52-543
α-helix55-628
α-helix65-728
α-helix741
α-helix75-806
α-helix81-866
α-helix87-893
β-strand9515
α-helix96-972
β-strand98-10366
β-strand114-12296
β-strand12315
β-strand128-13367
β-strand136-13727
β-strand142-14436
β-strand148-14926
β-strand155-16286
β-strand170-17677
β-strand184-18967
Chain C: 9 helices, 17 β-strands
ElementResiduesLengthSheet
α-helix3-53
α-helix12-132
α-helix14-163
β-strand1718
α-helix22-287
β-strand33-3869
β-strand42110
β-strand48-52510
β-strand61-67710
α-helix71-788
β-strand82-8659
β-strand89110
β-strand110-115610
β-strand118-12039
β-strand125-1381411
β-strand141-1521211
β-strand154-156312
α-helix157-17216
β-strand182-1911011
β-strand194-199611
α-helix202-2032
β-strand20518
α-helix210-2145
α-helix215-2173
β-strand222-224312
β-strand228-236911
Chain D: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix806-8094

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
HLA class II histocompatibility antigenAprotein181Homo sapiensP01903 (AlphaFold model)
HLA class II histocompatibility antigenBprotein192Homo sapiensP01911 (AlphaFold model)
Enterotoxin type BCprotein239Staphylococcus aureusP01552 (AlphaFold model)
InhibitorDprotein9synthetic construct
Sequence of entity 1 (A), FASTA
>1D5M_1 HLA CLASS II HISTOCOMPATIBILITY ANTIGEN (chains A)
IKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGAL
ANIAVDKANLEIMTKRSNYTPITNVPPEVTVLTNSPVELREPNVLICFIDKFTPPVVNVT
WLRNGKPVTTGVSETVFLPREDHLFRKFHYLPFLPSTEDVYDCRVEHWGLDEPLLKHWEF
D
Sequence of entity 2 (B), FASTA
>1D5M_2 HLA CLASS II HISTOCOMPATIBILITY ANTIGEN (chains B)
GDTRPRFLEQVKHECHFFNGTERVRFLDRYFYHQEEYVRFDSDVGEYRAVTELGRPDAEY
WNSQKDLLEQKRAAVDTYCRHNYGVGESFTVQRRVYPEVTVYPAKTQPLQHHNLLVCSVN
GFYPGSIEVRWFRNGQEEKTGVVSTGLIQNGDWTFQTLVMLETVPRSGEVYTCQVEHPSV
TSPLTVEWRARS
Sequence of entity 3 (C), FASTA
>1D5M_3 ENTEROTOXIN TYPE B (chains C)
ESQPDPKPDELHKSSKFTGLMENMKVLYDDNHVSAINVKSIDQFLYFDLIYSIKDTKLGN
YDNVRVEFKNKDLADKYKDKYVDVFGANYYYQCYFSKKTNDINSHQTDKRKTCMYGGVTE
HNGNQLDKYRSITVRVFEDGKNLLSFDVQTNKKKVTAQELDYLTRHYLVKNKKLYEFNNS
PYETGYIKFIENENSFWYDMMPAPGDKFDQSKYLMMYNDNKMVDSKDVKIEVYLTTKKK
Sequence of entity 4 (D), FASTA
>1D5M_4 INHIBITOR (chains D)
XARAMCSLX

Ligands and cofactors

IDNameFormulaCopies
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O61

Primary citation

Peptide and peptide mimetic inhibitors of antigen presentation by HLA-DR class II MHC molecules. Design, structure-activity relationships, and X-ray crystal structures. Bolin, D.R., Swain, A.L., Sarabu, R. et al. J Med Chem (2000) 43:2135-2148. DOI 10.1021/jm000034h · PubMed

Other PDB entries of the same protein (UniProt P01903 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

About this viewer

MolViewer shows 1D5M directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.