Reaction center protein L chain
Details
- Name
- Reaction center protein L chain
- Synonyms
- Photosynthetic reaction center L subunit
- Gene Name
- pufL
- Organism
- Blastochloris viridis
- Amino acid sequence
>lcl|BSEQ0017249|Reaction center protein L chain MALLSFERKYRVRGGTLIGGDLFDFWVGPYFVGFFGVSAIFFIFLGVSLIGYAASQGPTW DPFAISINPPDLKYGLGAAPLLEGGFWQAITVCALGAFISWMLREVEISRKLGIGWHVPL AFCVPIFMFCVLQVFRPLLLGSWGHAFPYGILSHLDWVNNFGYQYLNWHYNPGHMSSVSF LFVNAMALGLHGGLILSVANPGDGDKVKTAEHENQYFRDVVGYSIGALSIHRLGLFLASN IFLTGAFGTIASGPFWTRGWPEWWGWWLDIPFWS
- Number of residues
- 274
- Molecular Weight
- 30578.225
- Theoretical pI
- 6.95
- GO Classification
- Functionsbacteriochlorophyll binding / electron transporter, transferring electrons within the cyclic electron transport pathway of photosynthesis activity / metal ion bindingProcessesphotosynthetic electron transport in photosystem II / protein-chromophore linkageComponentsintegral component of membrane / plasma membrane light-harvesting complex / plasma membrane-derived chromatophore membrane
- General Function
- Metal ion binding
- Specific Function
- The reaction center is a membrane-bound complex that mediates the initial photochemical event in the electron transfer process of photosynthesis.
- Pfam Domain Function
- Photo_RC (PF00124)
- Transmembrane Regions
- 33-53 84-111 116-139 171-198 226-249
- Cellular Location
- Cellular chromatophore membrane
- Gene sequence
>lcl|BSEQ0007379|825 bp ATGGCACTGCTCAGCTTTGAGAGAAAGTATCGCGTCCGCGGGGGGACGCTGATCGGTGGA GACTTGTTCGATTTCTGGGTGGGGCCGTACTTTGTCGGCTTCTTCGGAGTTTCGGCAATC TTCTTCATTTTCCTCGGCGTTAGTTTGATCGGCTACGCGGCGTCTCAAGGGCCCACCTGG GATCCCTTCGCCATTAGCATCAATCCGCCCGACCTGAAGTACGGGCTCGGAGCGGCGCCG CTGCTCGAGGGCGGCTTCTGGCAGGCGATCACCGTCTGCGCTCTTGGTGCATTCATTTCG TGGATGCTCCGTGAGGTCGAAATTTCCCGCAAGCTCGGAATTGGTTGGCACGTCCCGCTG GCCTTCTGCGTTCCGATCTTCATGTTCTGCGTCCTGCAGGTTTTTCGCCCGCTGCTTCTT GGGTCGTGGGGTCATGCTTTCCCCTACGGCATCCTGAGCCATCTCGATTGGGTGAACAAC TTCGGGTATCAGTACCTTAACTGGCACTATAACCCGGGACACATGTCGTCCGTTTCGTTC CTGTTCGTGAACGCAATGGCGCTGGGTCTGCACGGTGGTCTGATTCTGTCGGTCGCTAAC CCGGGCGATGGCGACAAGGTCAAGACGGCAGAGCACGAGAACCAGTACTTCCGTGATGTC GTTGGCTATTCGATCGGCGCGCTCAGCATTCACCGCCTGGGCCTCTTCCTCGCCTCGAAT ATCTTCCTGACAGGCGCCTTTGGCACCATCGCTAGCGGTCCGTTCTGGACTCGCGGCTGG CCGGAATGGTGGGGCTGGTGGCTCGACATTCCGTTCTGGAGCTAA
- Chromosome Location
- Not Available
- Locus
- Not Available
- External Identifiers
Resource Link UniProtKB ID P06009 UniProtKB Entry Name RCEL_BLAVI GenBank Protein ID 46480 GenBank Gene ID X03915 - General References
- Michel H, Weyer KA, Gruenberg H, Dunger I, Oesterhelt D, Lottspeich F: The 'light' and 'medium' subunits of the photosynthetic reaction centre from Rhodopseudomonas viridis: isolation of the genes, nucleotide and amino acid sequence. EMBO J. 1986 Jun;5(6):1149-58. [Article]
- Deisenhofer J, Epp O, Miki K, Huber R, Michel H: X-ray structure analysis of a membrane protein complex. Electron density map at 3 A resolution and a model of the chromophores of the photosynthetic reaction center from Rhodopseudomonas viridis. J Mol Biol. 1984 Dec 5;180(2):385-98. [Article]
- Lancaster CR, Michel H: The coupling of light-induced electron transfer and proton uptake as derived from crystal structures of reaction centres from Rhodopseudomonas viridis modified at the binding site of the secondary quinone, QB. Structure. 1997 Oct 15;5(10):1339-59. [Article]
- Lancaster CR, Michel H: Refined crystal structures of reaction centres from Rhodopseudomonas viridis in complexes with the herbicide atrazine and two chiral atrazine derivatives also lead to a new model of the bound carotenoid. J Mol Biol. 1999 Feb 26;286(3):883-98. [Article]
- Deisenhofer J, Michel H: Nobel lecture. The photosynthetic reaction centre from the purple bacterium Rhodopseudomonas viridis. EMBO J. 1989 Aug;8(8):2149-70. [Article]
Drug Relations
- Drug Relations
DrugBank ID Name Drug group Pharmacological action? Actions Details DB07392 Atrazine experimental unknown Details DB07551 (2S)-2-{[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino}-2-methylbutanenitrile experimental unknown Details DB07552 (2R)-2-{[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino}-2-methylbutanenitrile experimental unknown Details DB04464 N-Formylmethionine experimental unknown Details DB04147 Dodecyldimethylamine N-oxide experimental unknown Details DB08215 Terbutryn experimental unknown Details DB08689 Ubiquinone Q1 experimental unknown Details DB08690 Ubiquinone Q2 experimental unknown Details