Anpl-UAA*01 binding "MVMELIRMI" at 1.71Å resolution
Data provenance
Information sections
- Publication
- Peptide details
- Peptide neighbours
- Binding cleft pockets
- Chain sequences
- Downloadable data
- Data license
- Footnotes
Complex type
Anpl-UAA*01
MVMELIRMI
Species
Locus / Allele group
Structural Definition Of Duck MHC Class I Explains the Resistance to Influenza A virus
Structure deposition and release
Data provenance
Publication data retrieved from PDBe REST API8 and PMCe REST API9
Other structures from this publication
![](https://images.histo.fyi/cleft/side/combined/5gjy_1_combined_medium.png)
![](https://images.histo.fyi/cleft/yrb/5gjy_1_yrb_medium.png)
![](https://images.histo.fyi/cleft/top/combined/5gjy_1_combined_medium.png)
Data provenance
MHC:peptide complexes are visualised using PyMol. The peptide is superimposed on a consistent cutaway slice of the MHC binding cleft (displayed as a grey mesh) which best indicates the binding pockets for the P1/P5/PC positions (side view - pockets A, E, F) and for the P2/P3/PC-2 positions (top view - pockets B, C, D). In some cases peptides will use a different pocket for a specific peptide position (atypical anchoring). On some structures the peptide may appear to sterically clash with a pocket. This is an artefact of picking a standardised slice of the cleft and overlaying the peptide.
Peptide neighbours
P1
MET
TYR159
TYR10
TYR61
GLU65
LEU8
TYR171
TRP167
ARG64
|
P2
VAL
ASN72
THR68
TYR159
SER69
TYR10
MET46
HIS100
TYR12
GLU65
THR27
|
P5
LEU
GLN155
TYR159
GLN113
TRP156
|
P6
ILE
TYR12
TRP156
HIS100
ASN72
ILE75
PHE76
|
P7
ARG
THR151
ASN79
ILE75
GLU149
VAL152
GLN155
TRP146
|
P8
MET
LYS145
VAL78
ASN79
TRP146
ILE75
|
P9
ILE
LYS145
ARG86
ASN79
THR82
TRP96
THR142
TRP146
ALA83
PHE122
|
Colour key
Data provenance
Neighbours are calculated by finding residues with atoms within 5Å of each other using BioPython Neighboursearch module. The list of neighbours is then sorted and filtered to inlcude only neighbours where between the peptide and the MHC Class I alpha chain.
Colours selected to match the YRB scheme. [https://www.frontiersin.org/articles/10.3389/fmolb.2015.00056/full]
1. Beta 2 microglobulin
Beta 2 microglobulin
|
10 20 30 40 50 60
MEFGQAKAAPKVQVYSRHPATAGTENILNCYVEGFHPPKIDIALLKNGEPMKDVKYNDMS 70 80 90 100 FGDDWTFQRLVYAPFTPTKSDVYTCRVDHEAFTEPQSFRWEPDF |
2. Class I alpha
Anpl-UAA*01
|
10 20 30 40 50 60
MEFEPHSLRYFYTAVSDPSPGVPQFVTVGSVDGEVFVRYDSETRKMEPRVDWIVANVDQQ 70 80 90 100 110 120 YWDRETETSRGNEQIFRVNLDTARERYNQSRGSHTWQCMHGCDLEDGSIRGFQQCGYDGK 130 140 150 160 170 180 DFIALDKDTLTYTAADAAAQITKRKWEQEGTVAEQWKNYLENTCIEWLRKYVSYGKDVLE 190 200 210 220 230 240 RRERPKVRVSGMESNKILTLSCRAHGFYPPPISISWLKDGVVQEQETKRGSTVPNSDGTY 250 260 270 HAWATIDVLPGNRDKYQCRVEHASLPQPGLFSW |
3. Peptide
|
MVMELIRMI
|
Data provenance
Sequences are retrieved via the Uniprot method of the RSCB REST API. Sequences are then compared to those derived from the PDB file and matched against sequences retrieved from the IPD-IMGT/HLA database for human sequences, or the IPD-MHC database for other species. Mouse sequences are matched against FASTA files from Uniprot. Sequences for the mature extracellular protein (signal petide and cytoplasmic tail removed) are compared to identical length sequences from the datasources mentioned before using either exact matching or Levenshtein distance based matching.
Downloadable data
Components
Data license
Footnotes
- Protein Data Bank Europe - Coordinate Server
- 1HHK - HLA-A*02:01 binding LLFGYPVYV at 2.5Å resolution - PDB entry for 1HHK
- Protein structure alignment by incremental combinatorial extension (CE) of the optimal path. - PyMol CEALIGN Method - Publication
- PyMol - PyMol.org/pymol
- Levenshtein distance - Wikipedia entry
- Protein Data Bank Europe REST API - Molecules endpoint
- 3Dmol.js: molecular visualization with WebGL - 3DMol.js - Publication
- Protein Data Bank Europe REST API - Publication endpoint
- PubMed Central Europe REST API - Articles endpoint
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This work is licensed under a Creative Commons Attribution 4.0 International License.