Protein Export

Proteins On the Cell Surface

First, we should briefly consider proteins that reside in cell membrane. Like all other organisms, Halophile proteins begin with a signal sequence (20 - 30 residues long) that has many positive charges on it. We do not know enough to search for these in a reliable way. See five examples in the figure below from a review paper by Jerry Eichler, 2000. Archaeal protein translocation: Crossing membranes in the third domain of life. Eur. J. Biochem. 267: 3402-3412.

Three-domain comparison from Albert Bolhuis. 2004. The archaeal Sec-dependent protein translocation pathway. Phil. Trans. R. Soc. Lond. B. Vol. 359: 919–927.

Proteins Exported Completely

There are three main systems for protein export.

http://www.membranetransport.org/

1. Sec pathway using SecA, SecD, SecE, SecY, SecC, SecF proteins.

• Our genome does not have any SecA annotations.
• Our genome has 2500587981 HutaDRAFT_03460 Preprotein translocase subunit SecD
• Our genome has 2500589223 HutaDRAFT_15880 protein translocase subunit secE/sec61 gamma
• Our genome has >2500590667 HutaDRAFT_30320 protein translocase subunit secY/sec61 alpha
• Our genome does not have SecC annotations
• Our genome has >2500587980 HutaDRAFT_03450 protein translocase subunit secF

SPaseI and II cleave peptides off for export. Sec11a and sec11b have been found in halophiles.

YidC Oxa 1p

2. Tat pathway using TatA, TatCo, TatCt, TatAo TatAt, TatB, TorD and TorA are chaperones that bind to signal sequences bound for Tat protein export. Our Organism has these genes:

• ORF01012 sec-independent protein translocase component TatA 1
• No TatCo in annotations
• No TatCt in annotations
• No TatAo in annotations
• No TatAt in annotations
• No TatB in annotations
• No TorD in annotations
• No TorA in annotations

Tat proteins use protein domain of SRRXFLK can we find this? They transport fully folded proteins. Many halophiles have a lot of K+ in cytoplasm to counter balance extracellular salt. Their proteins have many negative amino acids that help keep the proteins and bacteria from “salting out” and may lead to rapid protein folding. Therefore, the Tet system may be more important than the Sec system. Figure from Sonja-Verena Albers, Zalán Szabó and Arnold J. M. Driessen. 2006. Nature Reviews: Microbiology. VOLUME 4.

3. lipobox pathway for lipid-modified proteins, lipobox = [I/L/G/A][A/G/S]"cut_here"C is the target for SPaseII enzymes.

Type I – V secretion systems possible. I is ABC protein transporter Our genome has:

• ORF00738 type II-IV secretion system proteins VirB11-TadA

Flagella and pilus or pili proteins. PibD trims off cytoplasmic parts of flagellar proteins