36  structures 1041  species 4  interactions 19516  sequences 83  architectures

Family: Trans_reg_C (PF00486)

Summary

Transcriptional regulatory protein, C terminal Add an annotation

No Pfam abstract.


Literature references

  1. Martinez-Hackert E, Stock AM; , Structure 1997;5:109-124.: The DNA-binding domain of OmpR: crystal structures of a winged helix transcription factor. PUBMED:9016718

  2. Wietzorrek A, Bibb M; , Mol Microbiol 1997;25:1181-1184.: A novel family of proteins that regulates antibiotic production in streptomycetes appears to contain an OmpR-like DNA-binding fold. PUBMED:9350875


InterPro entry IPR001867

Two-component signal transduction systems enable bacteria to sense, respond, and adapt to a wide range of environments, stressors, and growth conditions PUBMED:16176121. Some bacteria can contain up to as many as 200 two-component systems that need tight regulation to prevent unwanted cross-talk PUBMED:18076326. These pathways have been adapted to response to a wide variety of stimuli, including nutrients, cellular redox state, changes in osmolarity, quorum signals, antibiotics, and more PUBMED:12372152. Two-component systems are comprised of a sensor histidine kinase (HK) and its cognate response regulator (RR) PUBMED:10966457. The HK catalyses its own auto-phosphorylation followed by the transfer of the phosphoryl group to the receiver domain on RR; phosphorylation of the RR usually activates an attached output domain, which can then effect changes in cellular physiology, often by regulating gene expression. Some HK are bifunctional, catalysing both the phosphorylation and dephosphorylation of their cognate RR. The input stimuli can regulate either the kinase or phosphatase activity of the bifunctional HK.

A variant of the two-component system is the phospho-relay system. Here a hybrid HK auto-phosphorylates and then transfers the phosphoryl group to an internal receiver domain, rather than to a separate RR protein. The phosphoryl group is then shuttled to histidine phosphotransferase (HPT) and subsequently to a terminal RR, which can evoke the desired response PUBMED:11934609, PUBMED:11489844.

This entry represents a domain that is almost always found associated with the response regulator receiver domain (see ). It may play a role in DNA binding PUBMED:9016718.

Clan

This family is a member of clan HTH (CL0123), which contains the following 141 members:

Arg_repressor B-block_TFIIIC Bac_DnaA_C BetR BrkDBD CENP-B_N Coprinus_mating Cro Crp DDRGK Dimerisation DUF1133 DUF1153 DUF1323 DUF134 DUF1441 DUF1492 DUF1495 DUF1670 DUF1804 DUF1836 DUF2089 DUF2250 DUF2316 DUF293 DUF3116 DUF387 DUF739 DUF742 DUF977 E2F_TDP ELK Ets Exc F-112 FaeA Fe_dep_repr_C Fe_dep_repress FeoC Ftsk_gamma FUR GcrA GerE GntR Homeobox Homez HSF_DNA-bind HTH_1 HTH_10 HTH_11 HTH_12 HTH_13 HTH_14 HTH_15 HTH_3 HTH_5 HTH_6 HTH_7 HTH_8 HTH_9 HTH_AraC HTH_CodY HTH_DeoR HTH_IclR HTH_Mga HTH_psq HTH_WhiA HxlR IF2_N Ins_element1 KorB LacI LexA_DNA_bind MarR Med9 MerR MerR-DNA-bind Mga Mnd1 Mor MotA_activ Mu_DNA_bind Myb_DNA-bind_2 Myb_DNA-binding NUMOD1 PaaX PadR PAX PCI PCI_Csn8 Pencillinase_R Phage_AlpA Phage_antitermQ Phage_CI_repr Phage_CII Phage_rep_org_N Phage_terminase Pou Pox_D5 PuR_N Put_DNA-bind_N Rap1-DNA-bind Rep_3 RepA_C RepA_N RepC RepL RFX_DNA_binding Rio2_N RNA_pol_Rpc34 RP-C RPA RPA_C RQC Rrf2 RTP SAC3_GANP Sigma54_CBD Sigma54_DBD Sigma70_ECF Sigma70_r2 Sigma70_r3 Sigma70_r4 Sigma70_r4_2 SpoIIID Sulfolobus_pRN TBPIP Tc3_transposase Terminase_5 TetR_N TFIIE_alpha Trans_reg_C Transposase_14 Transposase_5 Transposase_8 Transposase_Tc5 TrfA TrmB Trp_repressor UPF0122 z-alpha

Gene Ontology

External database links

Domain organisation

Below is a listing of the unique domain organisations or architectures in which this domain is found. More...

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Alignments

There are various ways to view or download the sequence alignments that we store. You can use a sequence viewer to look at either the seed or full alignment for the family, or you can look at a plain text version of the sequence in a variety of different formats. More...

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Very large alignments can often cause problems for the formatting tool above. If you find that downloading or viewing a large alignment is problematic, you can also download a gzip-compressed, Stockholm-format file containing the seed or full alignment for this family.

You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.

The main seed and full alignments are generated using sequences from the UniProt sequence database. However, we also generate alignments using sequences from the NCBI sequence database and the "metaseq" metagenomics dataset.

You can view alignments from these two additional datasets using the form above, or you can download alignments of NCBI or metagenomics sequences, as gzip-compressed files.

Pfam alignments:
Full length sequences

External links

MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER2.

Pfam alignments:

HMM logo

HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...

Trees

This page displays the phylogenetic tree for this family. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed or full alignments.

Note: You can also download the data files for the seed, full, NCBI or metagenomics trees.

Curation and family details

This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.

Curation View help on the curation process

Seed source: Pfam-B_94 (release 1.0)
Previous IDs: trans_reg_C;
Type: Domain
Author: Finn RD
Number in seed: 362
Number in full: 19516
Average length of the domain: 75.80 aa
Average identity of full alignment: 31 %
Average coverage of the sequence by the domain: 29.61 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 9421015 -E 1000 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 20.8 20.8
Trusted cut-off 20.8 20.8
Noise cut-off 20.7 20.7
Model length: 77
Family (HMM) version: 21
Download: download the raw HMM for this family

Species distribution

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Interactions

There are 4 interactions for this family. More...

Trans_reg_C BTAD Response_reg FHA

Structures

For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the Trans_reg_C domain has been found.

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