8XL5

Structure of human propionyl-CoA carboxylase in complex with propionyl-CoA (PCC-PCO)


Experimental Data Snapshot

  • Method: ELECTRON MICROSCOPY
  • Resolution: 2.80 Å
  • Aggregation State: PARTICLE 
  • Reconstruction Method: SINGLE PARTICLE 

wwPDB Validation   3D Report Full Report


This is version 1.1 of the entry. See complete history


Literature

Structural insights into human propionyl-CoA carboxylase (PCC) and 3-methylcrotonyl-CoA carboxylase (MCC)

Zhou, F.Zhang, Y.Zhu, Y.Zhou, Q.Shi, Y.Hu, Q.

(2024) Elife 


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Propionyl-CoA carboxylase alpha chain, mitochondrial
A, C, E, G, I
A, C, E, G, I, K
728Homo sapiensMutation(s): 0 
EC: 6.4.1.3
UniProt & NIH Common Fund Data Resources
Find proteins for P05165 (Homo sapiens)
Explore P05165 
Go to UniProtKB:  P05165
PHAROS:  P05165
GTEx:  ENSG00000175198 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP05165
Sequence Annotations
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  • Reference Sequence
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 2
MoleculeChains Sequence LengthOrganismDetailsImage
Propionyl-CoA carboxylase beta chain, mitochondrial
B, D, F, H, J
B, D, F, H, J, L
539Homo sapiensMutation(s): 0 
EC: 6.4.1.3
UniProt & NIH Common Fund Data Resources
Find proteins for P05166 (Homo sapiens)
Explore P05166 
Go to UniProtKB:  P05166
PHAROS:  P05166
GTEx:  ENSG00000114054 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP05166
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 2 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
1VU (Subject of Investigation/LOI)
Query on 1VU

Download Ideal Coordinates CCD File 
N [auth B]
P [auth D]
R [auth F]
T [auth H]
V [auth J]
N [auth B],
P [auth D],
R [auth F],
T [auth H],
V [auth J],
X [auth L]
propionyl Coenzyme A
C24 H40 N7 O17 P3 S
QAQREVBBADEHPA-IEXPHMLFSA-N
BTN (Subject of Investigation/LOI)
Query on BTN

Download Ideal Coordinates CCD File 
M [auth A]
O [auth C]
Q [auth E]
S [auth G]
U [auth I]
M [auth A],
O [auth C],
Q [auth E],
S [auth G],
U [auth I],
W [auth K]
BIOTIN
C10 H16 N2 O3 S
YBJHBAHKTGYVGT-ZKWXMUAHSA-N
Experimental Data & Validation

Experimental Data

  • Method: ELECTRON MICROSCOPY
  • Resolution: 2.80 Å
  • Aggregation State: PARTICLE 
  • Reconstruction Method: SINGLE PARTICLE 

Structure Validation

View Full Validation Report



Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
Not funded--

Revision History  (Full details and data files)

  • Version 1.0: 2024-10-30
    Type: Initial release
  • Version 1.1: 2024-11-20
    Changes: Data collection