3S5L: CD4 mutant
Crystal structure of CD4 mutant bound to HLA-DR1. Determined by X-ray diffraction at 2.1 Å resolution. Released 21 Sept 2011.
- Method
- X-ray diffraction
- Resolution
- 2.1 Å
- Organisms
- Homo sapiens, Homo Sapiens
- Chains
- 8
- Atoms
- 9,272
- Mol. weight
- 133.88 kDa
- Released
- 21 Sept 2011
Explore 3S5L in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
3S5L contains 31 α-helices and 104 β-strands across 8 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, 16 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-15 | 11 | 1 |
| β-strand | 19-26 | 8 | 1 |
| β-strand | 29-35 | 7 | 1 |
| β-strand | 40-43 | 4 | 1 |
| α-helix | 46-50 | 5 | |
| β-strand | 53 | 1 | 2 |
| α-helix | 57-76 | 20 | |
| α-helix | 80-84 | 5 | |
| β-strand | 85 | 1 | 3 |
| α-helix | 86-87 | 2 | |
| β-strand | 88-93 | 6 | 4 |
| β-strand | 103-112 | 10 | 4 |
| β-strand | 113 | 1 | 3 |
| β-strand | 118-123 | 6 | 5 |
| β-strand | 126-128 | 3 | 5 |
| β-strand | 133-134 | 2 | 4 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 4 |
| β-strand | 145-153 | 9 | 4 |
| β-strand | 160-166 | 7 | 5 |
| β-strand | 174-179 | 6 | 5 |
Chain B: 6 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 7-18 | 12 | 1 |
| β-strand | 23-32 | 10 | 1 |
| β-strand | 35-41 | 7 | 1 |
| β-strand | 47-49 | 3 | 1 |
| α-helix | 52-54 | 3 | |
| α-helix | 55-62 | 8 | |
| α-helix | 65-74 | 10 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-86 | 6 | |
| β-strand | 95 | 1 | 11 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-103 | 6 | 12 |
| β-strand | 114-122 | 9 | 12 |
| β-strand | 123 | 1 | 11 |
| β-strand | 128-133 | 6 | 13 |
| β-strand | 136-138 | 3 | 13 |
| β-strand | 142-144 | 3 | 12 |
| β-strand | 148-149 | 2 | 12 |
| β-strand | 155-162 | 8 | 12 |
| β-strand | 170-176 | 7 | 13 |
| β-strand | 184-189 | 6 | 13 |
Chains C and F: 1 helix, 1 β-strand
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4 | 1 | 2 |
| α-helix | 8-14 | 7 | |
Chain D: 5 helices, 16 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-15 | 11 | 6 |
| β-strand | 19-26 | 8 | 6 |
| β-strand | 29-35 | 7 | 6 |
| β-strand | 40-43 | 4 | 6 |
| α-helix | 48-51 | 4 | |
| β-strand | 53 | 1 | 7 |
| α-helix | 56-76 | 21 | |
| α-helix | 80-84 | 5 | |
| β-strand | 85 | 1 | 8 |
| α-helix | 86-87 | 2 | |
| β-strand | 88-93 | 6 | 9 |
| β-strand | 103-112 | 10 | 9 |
| β-strand | 113 | 1 | 8 |
| β-strand | 118-123 | 6 | 10 |
| β-strand | 126-127 | 2 | 10 |
| β-strand | 133-134 | 2 | 9 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 9 |
| β-strand | 145-153 | 9 | 9 |
| β-strand | 160-166 | 7 | 10 |
| β-strand | 174-179 | 6 | 10 |
Chain E: 7 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 7-18 | 12 | 6 |
| β-strand | 23-32 | 10 | 6 |
| β-strand | 35-41 | 7 | 6 |
| β-strand | 47-49 | 3 | 6 |
| α-helix | 52-54 | 3 | |
| α-helix | 55-63 | 9 | |
| α-helix | 65-74 | 10 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-86 | 6 | |
| α-helix | 87-89 | 3 | |
| β-strand | 95 | 1 | 14 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-103 | 6 | 15 |
| β-strand | 114-122 | 9 | 15 |
| β-strand | 123 | 1 | 14 |
| β-strand | 128-133 | 6 | 16 |
| β-strand | 136-138 | 3 | 16 |
| β-strand | 142-144 | 3 | 15 |
| β-strand | 148-149 | 2 | 15 |
| β-strand | 155-162 | 8 | 15 |
| β-strand | 170-176 | 7 | 16 |
| β-strand | 184-189 | 6 | 16 |
Chain G: 3 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 12 |
| β-strand | 12-14 | 3 | 17 |
| β-strand | 17 | 1 | 18 |
| β-strand | 26-29 | 4 | 12 |
| β-strand | 35-40 | 6 | 12 |
| β-strand | 43-46 | 4 | 12 |
| β-strand | 55-56 | 2 | 17 |
| α-helix | 59-62 | 4 | |
| β-strand | 66 | 1 | 18 |
| β-strand | 69-71 | 3 | 17 |
| α-helix | 76-78 | 3 | |
| β-strand | 80-86 | 7 | 12 |
| β-strand | 89-98 | 10 | 12 |
| β-strand | 99-102 | 4 | 19 |
| β-strand | 108 | 1 | 20 |
| β-strand | 114-119 | 6 | 19 |
| β-strand | 127-131 | 5 | 21 |
| β-strand | 137 | 1 | 21 |
| β-strand | 140 | 1 | 21 |
| β-strand | 143-146 | 4 | 19 |
| α-helix | 151-153 | 3 | |
| β-strand | 155-163 | 9 | 21 |
| β-strand | 166-174 | 9 | 21 |
| β-strand | 176 | 1 | 20 |
Chain H: 3 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 1-7 | 7 | 15 |
| β-strand | 12-14 | 3 | 22 |
| β-strand | 17 | 1 | 23 |
| β-strand | 26-29 | 4 | 15 |
| β-strand | 35-40 | 6 | 15 |
| β-strand | 43-46 | 4 | 15 |
| β-strand | 55-56 | 2 | 22 |
| α-helix | 59-62 | 4 | |
| β-strand | 66 | 1 | 23 |
| β-strand | 69-71 | 3 | 22 |
| α-helix | 76-78 | 3 | |
| β-strand | 80-86 | 7 | 15 |
| β-strand | 89-98 | 10 | 15 |
| β-strand | 99-101 | 3 | 24 |
| β-strand | 114 | 1 | 25 |
| β-strand | 117-119 | 3 | 24 |
| β-strand | 127-131 | 5 | 26 |
| β-strand | 137-140 | 4 | 26 |
| β-strand | 146 | 1 | 25 |
| α-helix | 151-153 | 3 | |
| β-strand | 155-163 | 9 | 26 |
| β-strand | 166-174 | 9 | 26 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| HLA class II histocompatibility antigen, DR alpha chain | A, D | protein | 182 | Homo sapiens | P01903 (AlphaFold model) |
| HLA class II histocompatibility antigen DR beta chain | B, E | protein | 193 | Homo sapiens | P01911 (AlphaFold model) |
| HA peptide | C, F | protein | 13 | Homo Sapiens | P03437 |
| T-cell surface glycoprotein CD4 | G, H | protein | 191 | Homo sapiens | P01730 (AlphaFold model) |
Sequence of entity 1 (A, D), FASTA
>3S5L_1 HLA class II histocompatibility antigen, DR alpha chain (chains A, D)
IKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGAL
ANIAVDKANLEIMTKRSNYTPITNVPPEVTVLTNSPVELREPNVLICFIDKFTPPVVNVT
WLRNGKPVTTGVSETVFLPREDHLFRKFHYLPFLPSTEDVYDCRVEHWGLDEPLLKQWEF
DA
Sequence of entity 2 (B, E), FASTA
>3S5L_2 HLA class II histocompatibility antigen DR beta chain (chains B, E)
MGDTRPRFLWQLKFECHFFNGTERVRLLERCIYNQEESVRFDSDVGEYRAVTELGRPDAE
YWNSQKDLLEQRRAAVDTYCRHNYGVGESFTVQRRVEPKVTVYPSKTQPLQHHNLLVCSV
SGFYPGSIEVRWFRNGQEEKAGVVSTGLIQNGDWTFQTLVMLETVPRSGEVYTCQVEHPS
VTSPLTVEWRARS
Sequence of entity 3 (C, F), FASTA
>3S5L_3 HA peptide (chains C, F)
PKYVKQNTLKLAT
Sequence of entity 4 (G, H), FASTA
>3S5L_4 T-cell surface glycoprotein CD4 (chains G, H)
DLGSKKVVLGKKGDTVELTCTASQKKSIQFHWKNSNQIKILGNYGSFLWKGPSKLNDRAD
SRRRLWRQGNFPLIIKNLKIEDSDTYICEVEDQKEEVQLLVFGLTANSDTHLLQGQSLTL
TLESPPGSSPSVQCRSPRGKNIQGGKTLSVSQLELQDSGTWTCTVLQNQKKVEFKIDIVV
LAAAAHHHHHH
Primary citation
Affinity maturation of human CD4 by yeast surface display and crystal structure of a CD4-HLA-DR1 complex. Wang, X.X., Li, Y., Yin, Y. et al. Proc Natl Acad Sci U S A (2011) 108:15960-15965. DOI 10.1073/pnas.1109438108 · PubMed
Other PDB entries of the same protein (UniProt P01903 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 5NI9 1.33 Å, Crystal structure of HLA-DRB1*04:01 with the alpha-enolase peptide 326-340
- 4X5W 1.34 Å, HLA-DR1 with CLIP102-120(M107W)
- 5NIG 1.35 Å, Crystal structure of HLA-DRB1*04:01 with modified alpha-enolase peptide 326-340…
- 8CMC 1.42 Å, Human Leukocyte Antigen class II allotype DR1 presenting SARS-CoV-2 Spike peptide S511-530
- 8PJF 1.48 Å, Human Leukocyte Antigen class II allotype DR1 presenting P11T->R modified influenza A…
- 6QZC 1.64 Å, HLA-DR1 with the QAR Peptide
- 8CMG 1.64 Å, Human Leukocyte Antigen class II allotype DR1 presenting SARS-CoV-2 nsp14 peptide…
- 8CMH 1.64 Å, Human Leukocyte Antigen class II allotype DR1 presenting SARS-CoV-2 Omicron (BA.1) Spike…
- 4MD5 1.65 Å, Immune Receptor
- 4MDJ 1.7 Å, Immune Receptor
- 8PJE 1.7 Å, Human Leukocyte Antigen class II allotype DR1 presenting influenza A virus…
- 7YX9 1.76 Å, MHC-II dynamics are maintained in HLA-DR allotypes to ensure catalyzed peptide exchange
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