2ECL,6V9I


Conserved Protein Domain Family
RING-H2_RBX2

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cd16466: RING-H2_RBX2 
Click on image for an interactive view with Cn3D
RING finger, H2 subclass, found in RING-box protein 2 (RBX2) and similar proteins
RBX2, also known as CKII beta-binding protein 1 (CKBBP1), RING finger protein 7 (RNF7), regulator of cullins 2 (ROC2), or sensitive to apoptosis gene protein (SAG), is an E3 ubiquitin-protein ligase that protects cells from apoptosis, confers radioresistance, and plays an essential and non-redundant role in embryogenesis and vasculogenesis. It promotes ubiquitination and degradation of a number of protein substrates, including c-JUN, DEPTOR, HIF-1alpha, IkappaBalpha, NF1, NOXA, p27, and procaspase-3, thus regulating various signaling pathways and biological processes. RBX2 is necessary for ubiquitin ligation activity of the multimeric cullin (Cul)-RING E3 ligases (CRLs). RBX2-containing CRLs are involved in the NEDD8 pathway and RBX2 specifically regulates NEDD8ylation of Cul5. It can bind and activate the HIV-1 Vif-Cullin5 E3 ligase complex in vitro. It is also a substrate of NEDD4-1 E3 ubiquitin ligase and mediates NEDD4-1 induced chemosensitization. The inactivation of RBX2 E3 ubiquitin ligase activity triggers senescence and inhibits Kras-induced immortalization. Endothelial deletion of RBX2 causes embryonic lethality and blocks tumor angiogenesis, and may have potential use in anti-angiogenesis therapy of human cancers. Moreover, as a component of the Cullin 5-RING E3 ubiquitin ligase (CRL5) complex, RBX2 regulates neuronal migration through different CRL5 adaptors, such as SOCS7. RBX2 also functions as a redox inducible antioxidant protein that scavenges oxygen radicals by forming inter- and intra-molecular disulfide bonds when acting alone. It contains a C-terminal C3H2C3-type RING-H2 finger that is essential for its ligase activity.
Statistics
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PSSM-Id: 438129
Aligned: 17 rows
Threshold Bit Score: 92.2215
Created: 2-May-2013
Updated: 17-Oct-2022
Structure
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Program:
Drawing:
Aligned Rows:
 
Zn binding siteZn binding site
Conserved site includes 8 residues -Click on image for an interactive view with Cn3D
Feature 1: Zn binding site [ion binding site], 8 residue positions
Conserved feature residue pattern:C C C H H C C CClick to see conserved feature residue pattern help
Evidence:
  • Structure:2ECL; Homo sapiens Ring-box protein 2 binds two Zn2+ ions through its RING-H2 finger.
    View structure with Cn3D
  • Comment:C3H2C3-type RING-H2 finger consensus motif: C-X2-C-X(9-39)-C-X(1-3)-H-X(2-3)-H-X2-C-X(4-48)-C-X2-C, where X is any amino acid and the number of X residues varies in different fingers
  • Comment:A RING finger typically binds two zinc atoms, with its Cys and/or His side chains in a unique "cross-brace" arrangement.

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1           #  #                               # #  #  #          #  #    
2ECL_A        15 CDTCAICRvqVMDACLRCQAENKq-----eDCVVVWGECNHSFHNCCMSLWVKqNNRCPLCQQDW 74  human
NP_610691     42 CDICAICRvqVMDSCLRCQADNKrdvmgrqDCVVVWGECNHSFHHCCMSLWVKqNNRCPLCQQEW 106 fruit fly
CBY25103     168 CDICAICRvvVTEPCLKCQSSGKga----aDCAVVWGECNHSYHNCCMSRWVAtTPRCPLCQQDW 228 Oikopleura dioica
P91404        47 CDTCAICRvhLMEECLRCQSEPSa------ECYVVWGDCNHSFHHCCMTQWIRqNNRCPLCQKDW 105 Caenorhabditis elegans
XP_002737179  45 CDTCAICRvqVMDACLRCQAENKq-----eDCVVVWGECNHSFHNCCMSLWVKqNNRCPLCQQEW 104 Saccoglossus kowalevskii
ADF87937      44 CDTCAICRvqVMDACLRCQGENKq-----dDCVVIWGECNHSFHNCCMSLWVKqNNRCPLCQQEW 103 Chinese mitten crab
ELU03891      19 CDTCAICRvqVMDACLRCQSENKq-----eECVVVWGDCNHSFHNCCMSLWVKqNNRCPLCQQEW 78  Capitella sp. I Grassle & Gras...
Q9UBF6        47 CDTCAICRvqVMDACLRCQAENKq-----eDCVVVWGECNHSFHNCCMSLWVKqNNRCPLCQQDW 106 human
XP_006002827  47 CDTCAICRvqVMDACLRCQAENKq-----eDCVVVWGECNHSFHNCCMSLWVKqNNRCPLCQQDW 106 coelacanth
XP_013081006  35 CDTCAICRvqVMDACLRCQSENKq-----dDCVVVWGECNHSFHNCCMSLWVKqNNRCPLCQQEW 94  Biomphalaria glabrata

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