<p>This section provides information about the protein and gene name(s) and synonym(s) and about the organism that is the source of the protein sequence.<p><a href='/help/names_and_taxonomy_section' target='_top'>More...</a></p>Detailed information on MDP05711

Description Mediator of RNA polymerase II transcription subunit 4
SequenceMCAGVPTKQKLFSQLEDLDYLLKELLDKVNRRSRYDDIEHTIFSLLDKDKELKATLQTVSEQMEVQLKIEKLRADCENSDAQINACQHHLKKCELLLCTALFYSRQKLDSMVKAVKNPTDIDELIKYAHRISCTYGAVAPDNWTPSDPRRPYPNKEEIRRGYLGHLDDSGKFLPTLKDAVAQFQPNINTPAASSIEVSLSQQQMSLTSSTQLPNPTSVSSESLENSSVYSPSVGMSGINITPSPGGMVPSNGSGSGWIEPRHPTSSLNAILSGGGSSGNSNRPSGYPSESPSPNMWHQQQQLRQTLPGVHSSTPPQQQIKQPHPDDMRTYSDNSDDDGGLGF
Length342
PositionMiddle
OrganismHymenolepis diminuta (Rat tapeworm)
KingdomMetazoa
LineageEukaryota> Metazoa> Spiralia> Lophotrochozoa> Platyhelminthes> Cestoda> Eucestoda> Cyclophyllidea> Hymenolepididae> Hymenolepis.
Aromaticity0.06
Grand average of hydropathy-0.688
Instability index65.32
Isoelectric point5.73
Molecular weight37701.66
Publications

Function

Annotated function Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene- specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors.
ECO:0000256	RuleBase:RU364141
GO - Cellular Component
mediator complex	GO:0016592	IEA:InterPro
GO - Biological Function
transcription coregulator activity	GO:0003712	IEA:InterPro
GO - Biological Process
regulation of transcription by RNA polymerase II	GO:0006357	IEA:InterPro

Interaction

Binary Interactions

Repeat regions

Repeats

>MDP05711
---------------------------------------------------------------------------
No. of Repeats|Total Score|Length  |Diagonal| BW-From|   BW-To|   Level
             2|      69.12|      18|      60|     244|     263|       2
---------------------------------------------------------------------------
  244-  263 (32.48/22.59)	PGgmVPSNGSGSGWIEPRHP
  307-  324 (36.64/19.02)	PG..VHSSTPPQQQIKQPHP
---------------------------------------------------------------------------
---------------------------------------------------------------------------
No. of Repeats|Total Score|Length  |Diagonal| BW-From|   BW-To|   Level
             2|      54.25|      16|      18|      13|      28|       3
---------------------------------------------------------------------------
   13-   28 (26.15/18.48)	SQLEDLDYLLKELLDK
   33-   48 (28.10/20.35)	SRYDDIEHTIFSLLDK
---------------------------------------------------------------------------




Explaination for Stockholm format The "Stockholm" format is a system for marking up features in a multiple alignment. These mark-up annotations are preceded by a 'magic' label, of which there are four types. The Stockholm format is used by HMMER, Pfam, and Belvu. Mark-up lines include any characters except whitespace. Underscore ("_") is used instead of space.

#=GR (seqname) PP (Generic per-Sequence AND per-Column markup, exactly 1 char per column) where PP is Posterior Probability [0-9*], (0=0.00-0.05; 1=0.05-0.15; *=0.95-1.00)

#=GC PP_cons line is Stockholm-format consensus posterior probability annotation for the entire column. It’s calculated simply as the arithmetic mean of the per-residue posterior probabilities in that column. This should prove useful in phylogenetic inference applications, for example, where it’s common to mask away non confidently aligned columns of a multiple alignment. The PP_cons line provides an objective measure of the confidence assigned to each column.

#=GC RF line is Stockholm-format reference coordinate annotation, with an x marking each column that the profile considered to be consensus.

Alignment of MDP05711 with Med4 domain of Kingdom Metazoa

Intrinsically Disordered Regions

IDR SequenceStartStop
1) AASSIEVSLSQQQMSLTSSTQLPNPTSVSSESLENSSVYSPSVGMSGINITPSPGGMVPSNGSGSGWIEPRHPTSSLNAILSGGGSSGNSNRPSGYPSESPSPNMWHQQQQLRQTLPGVHSSTPPQQQIKQPHPDDMRTYSDNSDDDGGLGF
191
342

Molecular Recognition Features

MoRF SequenceStartStop
1) IRRGYL
2) QIKQPHPDDMRT
158
318
163
329