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Protein data for UVRB_RICCN:

Description:
UvrABC system protein B (Protein uvrB) (Excinuclease ABC subunit B).

Molecular weight: 75333

View which proteins in this organism that is involved with DNA Repair;
classified after biological processes (using data from the GOA project):

DNA repair( GO:0006281 ) base-excision repair( GO:0006284 ) nucleotide-excision repair (and GO:0045001, a synonym)( GO:0006289 )


Important dates:
20-JUN-2002, integrated into UniProtKB/Swiss-Prot.
01-DEC-2001, sequence version 1.
07-MAR-2006, entry version 23.

Phylogenetic order:
Bacteria Proteobacteria Alphaproteobacteria Rickettsiales Rickettsiaceae Rickettsieae Rickettsia spotted fever group.

To calculate the pI (Isoelectric point - the pH where a protein has a neutral charge),
go to this page and enter the protein ID (e.g 3MG_ECOLI): http://us.expasy.org/tools/pi_tool.html

Links to references in other databases for protein UVRB_RICCN:

DatabasePointerAdd. info#1Add. info#2
EMBLAE008592AAL02804.1-
PIRB97733B97733.
HSSPP569811D9Z
GenomeReviewsAE006914_GRRC0266.1
BioCycRCON781:RC0266-MONOMER-.1
HAMAPMF_00204-1.
InterProIPR001410DEAD.
InterProIPR011545DEAD/DEAH_N.
InterProIPR001650Helicase_C.
InterProIPR006935ResIII.
InterProIPR001943UvrB/C.
InterProIPR004807UvrB_ABC.
PfamPF00271Helicase_C1.
PfamPF04851ResIII1.
PfamPF02151UVR1.
SMARTSM00487DEXDc1.
SMARTSM00490HELICc1.
TIGRFAMsTIGR00631uvrb1.
PROSITEPS50151UVR1.

General information about the databases mentioned above

Keywords:
ATP-binding; Complete proteome; DNA damage; DNA excision; DNA repair; Excision nuclease; Nucleotide-binding; SOS response.

References:
RN [1]
RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC STRAIN=Malish 7;
RX MEDLINE=21442074; PubMed=11557893; DOI=10.1126/science.1061471;
RA Ogata H., Audic S., Renesto-Audiffren P., Fournier P.-E., Barbe V.,
RA Samson D., Roux V., Cossart P., Weissenbach J., Claverie J.-M.,
RA Raoult D.;
RT "Mechanisms of evolution in Rickettsia conorii and R. prowazekii.";
RL Science 293:2093-2098(2001).

Feature:
CHAIN 1 661 UvrABC system protein B.
/FTId=PRO_0000138420.
DOMAIN 621 656 UVR.
NP_BIND 38 45 ATP (Potential).
MOTIF 91 114 Beta-hairpin.

Comments:
-!- FUNCTION: The UvrABC repair system catalyzes the recognition and
processing of DNA lesions. A damage recognition complex composed
of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. Upon
binding of the uvrA(2)B(2) complex to a putative damaged site, the
DNA wraps around one uvrB monomer. DNA wrap is dependent on ATP
binding by uvrB and probably causes local melting of the DNA
helix, facilitating insertion of uvrB beta-hairpin between the DNA
strands. Then uvrB probes one DNA strand for the presence of a
lesion. If a lesion is found the uvrA subunits dissociate and the
uvrB-DNA preincision complex is formed. This complex is
subsequently bound by uvrC and the second uvrB is released. If no
lesion is found, the DNA wraps around the other uvrB subunit that
will check the other stand for damage (By similarity).
-!- SUBUNIT: Forms a heterotetramer with uvrA during the search for
lesions. Interacts with uvrC in an incision complex (By
similarity).
-!- SUBCELLULAR LOCATION: Cytoplasm (By similarity).
-!- DOMAIN: The beta-hairpin motif is involved in DNA binding (By
similarity).
-!- SIMILARITY: Belongs to the uvrB family.
-!- SIMILARITY: Contains 1 UVR domain.
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Sequence length: 661

     MNNFSIISEY KPAGDQPKAI DEIIAGLSSK KRSQMLLGIT GSGKTFTMAN IIERTNRPTL
     IMAHNKTLAA QIYSEMKSLF PKNAVEYFVS YYDYYQPEAY IARTDTFIEK DSSINEQIDL
     MRHAATRSLL ERRDVIVVSS VSCIYGLGSP DLYYQMMVNL EPGQSYPRDQ LLNDLINLQY
     ERNDIGFERG CFRVKGDNID IFPSHYSDKA WRLSFFGNEL EYIHEFDPLT GEKLAKLDKA
     MVFGNSHFVM PQETVNNAIS GIEEELQKRL EFLKSQDKPL ETQRLNQRTQ YDLEMLTETG
     SCKGVENYSR FFTGRNAGEP PPTLFEYLPE DALLFVDESH VSVPQIRAMY NGDRARKKVL
     VEHGFRLPSA LDNRPLKFEE WDKFRPQTVF VSATPGPFEL EETGGTVVEL IIRPTGLLDP
     ECIIKPATNQ VEDLISEIQT TIAQGFRVLV TTLTKKMAED LTAYLQELKY KTSYLHSNVH
     TLERIEILRD LRQGTIDVLV GINLLREGLD IPECGLVAIL DADKEGFLRS EVSLIQTIGR
     AARNSAGRVI LYADKMTKSI DKAVSETLRR RQIQQEYNEK HGIIPKTINR AIHALAEFEK
     IDSKLDKKQA HTLFDNPAKL KTHIDKLKKE MLKAASNLEF EQAVKLRDQL KTLEEAALEL
     S

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