1FBV,1BOR,1CHC,1G25,1JM7,1JM7,1RMD,1UR6,1WEO,1WIM,2CS3,2CSY,2CT2,2EA5,2ECJ,2ECN,2ECY,2HDP,2MA6,2Y43,2YHO,2YSL,3FL2,3HCS,3KNV,3L11,3LRQ,3VK6,3ZTG,4A49,4AYC,4B7Y,4IC2,4KBL,4PPE,4QPL,4R8P,4R8P,4TKP,4TXA,5CAW,5DIN,5DKA,5EDV,5EYA,5JW7,5OLM,5OQJ,5TRB,5VZV,5ZI6,6I9H,6L8N,6TAX,6YXE,7L3L


Conserved Protein Domain Family
RING-HC

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cd16449: RING-HC 
Click on image for an interactive view with Cn3D
HC subclass of RING (RING-HC) finger and its variants
The RING finger is a specialized type of Zn-finger of 40 to 60 residues that binds two atoms of zinc. It is defined by the "cross-brace" motif that chelates zinc atoms by eight amino acid residues, typically Cys or His, arranged in a characteristic spacing. Canonical RING motifs have been categorized into two major subclasses, RING-HC (C3HC4-type) and RING-H2 (C3H2C3-type), according to their Cys/His content. There are also many variants of RING fingers. Some have a different Cys/His pattern. Some lack a single Cys or His residue at typical Zn ligand positions, especially, the fourth or eighth zinc ligand is prevalently exchanged for an Asp, which can chelate Zn in a RING finger as well. This family corresponds to the HC subclass of RING (RING-HC) fingers that are characterized by containing C3HC4-type canonical RING-HC fingers or noncanonical RING-HC finger variants, including C4C4-, C3HC3D-, C2H2C4-, and C3HC5-type modified RING-HC fingers. The canonical RING-HC finger has been defined as C-X2-C-X(9-39)-C-X(1-3)-H-X(2-3)-C-X2-C-X(4-48)-C-X2-C. It binds two Zn ions in a unique "cross-brace" arrangement, which distinguishes it from tandem zinc fingers and other similar motifs. RING-HC fingers can be found in a group of diverse proteins with a variety of cellular functions, including oncogenesis, development, viral replication, signal transduction, the cell cycle, and apoptosis. Many of them are ubiquitin-protein ligases (E3s) that serve as scaffolds for binding to ubiquitin-conjugating enzymes (E2s, also referred to as ubiquitin carrier proteins or UBCs) in close proximity to substrate proteins, which enables efficient transfer of ubiquitin from E2 to the substrates.
Statistics
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PSSM-Id: 438113
Aligned: 326 rows
Threshold Bit Score: 25.5241
Created: 29-Oct-2015
Updated: 17-Oct-2022
Structure
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Program:
Drawing:
Aligned Rows:
 
Zn 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 C C C CClick to see conserved feature residue pattern help
Evidence:
  • Structure:1JM7; Homo sapiens BARD1 binds two Zn2+ ions through its RING-HC finger.
  • Comment:C3HC4-type RING-HC finger consensus motif: C-X2-C-X(9-39)-C-X(1-3)-H-X(2-3)-C-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          #  #            # #   #  #                   #  #
1FBV_A       333 QLCkICAENdk-dvKIEPCgHl-MCtsCLTSwqes--------egqGCPfC 373  human
1JM7_A        22 LECpICLELik-epVSTKCdHi-FCkfCMLKllnqk------kgpsQCPlC 64   human
Q96EP1       302 LTCiICQDLlhdcvSLQPCmHt-FCaaCYSGwme---------rssLCPtC 342  human
Q8IS11        14 LTCgICQNLfkdpnTLIPCgHa-FCldCLTTnas----------ikNCIqC 53   Dictyostelium discoideum AX4
P40629       146 LTCiICLTNqv-qiLTIPCgHliMCnpCSLNlnnsvctrgvnsnyeKCPkC 195  Invertebrate iridescent virus 6
P47732       161 LTCkICFTNki-tkVLIPCgHs-SCyeCVFKl-------------qTCPiC 196  Invertebrate iridescent virus 6
XP_001307778  42 LTCkVCLTNki-nlITYPCsHacMCyeCFKAlpi----------pkQCPvC 81   Trichomonas vaginalis G3
F4I443        23 LKCpLCLKLln-rpVLLPCdHv-FCdsCVHKssq---------vesGCPvC 62   thale cress
Q92021       143 LTCpLCVELfk-dpVMVACgHn-FCrsCIDKaweg-------qssfACPeC 184  African clawed frog
Q91431       144 LTCpLCVELfk-dpVMVACgHn-FCrsCIDKvweg-------qssfACPeC 185  African clawed frog

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