| P50 | author | Carl F. Nathan | Q1037710 |
| | K Heran Darwin | Q95968250 |
| P2093 | author name string | Tao Wang | |
| | Hua Li | |
| | Huilin Li | |
| | Gang Lin | |
| | Dongyang Li | |
| | Chunyan Tang | |
| P2860 | cites work | Docking of the proteasomal ATPases' carboxyl termini in the 20S proteasome's alpha ring opens the gate for substrate entry | Q24674433 |
| | The solution structure and DNA-binding properties of the cold-shock domain of the human Y-box protein YB-1 | Q27637878 |
| | X-ray crystal structure and functional analysis of vaccinia virus K3L reveals molecular determinants for PKR subversion and substrate recognition | Q27639516 |
| | Structure and activity of the N-terminal substrate recognition domains in proteasomal ATPases | Q27655687 |
| | Structural Insights into the Regulatory Particle of the Proteasome from Methanocaldococcus jannaschii | Q27655690 |
| | NMR Structure of a Stable “OB-fold” Sub-domain Isolated from Staphylococcal Nuclease | Q27729763 |
| | Structure of 20S proteasome from yeast at 2.4 A resolution | Q27735081 |
| | The ubiquitin system | Q27860803 |
| | Central pore residues mediate the p97/VCP activity required for ERAD | Q28241412 |
| | Mycobacterium tuberculosis prcBA genes encode a gated proteasome with broad oligopeptide specificity | Q28486412 |
| | Bacterial ubiquitin-like modifier Pup is deamidated and conjugated to substrates by distinct but homologous enzymes | Q28486639 |
| | Characterization of the proteasome accessory factor (paf) operon in Mycobacterium tuberculosis | Q28486680 |
| | Identification of substrates of the Mycobacterium tuberculosis proteasome | Q28487088 |
| | Ubiquitin-like protein involved in the proteasome pathway of Mycobacterium tuberculosis | Q28487196 |
| | The proteasome of Mycobacterium tuberculosis is required for resistance to nitric oxide | Q28487442 |
| | Characterization of a Mycobacterium tuberculosis proteasomal ATPase homologue | Q28487523 |
| | In vivo gene silencing identifies the Mycobacterium tuberculosis proteasome as essential for the bacteria to persist in mice | Q28909142 |
| | The 26S proteasome: a molecular machine designed for controlled proteolysis | Q29619692 |
| | OB(oligonucleotide/oligosaccharide binding)-fold: common structural and functional solution for non-homologous sequences | Q29620102 |
| | A comprehensive analysis of the Greek key motifs in protein beta-barrels and beta-sandwiches | Q30168943 |
| | NMR hydrogen exchange of the OB-fold protein LysN as a function of denaturant: the most conserved elements of structure are the most stable to unfolding | Q30175424 |
| | A philosophy of anti-infectives as a guide in the search for new drugs for tuberculosis. | Q30371769 |
| | Architecture and molecular mechanism of PAN, the archaeal proteasome regulatory ATPase | Q30490705 |
| | Microscopic stability of cold shock protein A examined by NMR native state hydrogen exchange as a function of urea and trimethylamine N-oxide | Q30587207 |
| | Distinct specificities of Mycobacterium tuberculosis and mammalian proteasomes for N-acetyl tripeptide substrates | Q33373239 |
| | ATP binding to PAN or the 26S ATPases causes association with the 20S proteasome, gate opening, and translocation of unfolded proteins. | Q33991996 |
| | Proteasomes and their associated ATPases: a destructive combination | Q33998676 |
| | The pore of activated 20S proteasomes has an ordered 7-fold symmetric conformation | Q36065854 |
| | Proteasome-associated proteins: regulation of a proteolytic machine | Q36275413 |
| | Self-compartmentalized bacterial proteases and pathogenesis | Q36455856 |
| | ATP-dependent proteases of bacteria: recognition logic and operating principles | Q36639201 |
| | Functions of the proteasome: from protein degradation and immune surveillance to cancer therapy | Q36703005 |
| | 20S proteasome and its inhibitors: crystallographic knowledge for drug development | Q36742369 |
| | The 20S proteasome of Streptomyces coelicolor. | Q39568209 |
| | Structure of the Mycobacterium tuberculosis proteasome and mechanism of inhibition by a peptidyl boronate | Q41626376 |
| | Diverse pore loops of the AAA+ ClpX machine mediate unassisted and adaptor-dependent recognition of ssrA-tagged substrates. | Q43151994 |
| | Pore loops of the AAA+ ClpX machine grip substrates to drive translocation and unfolding | Q43218186 |
| | ATP hydrolysis by the proteasome regulatory complex PAN serves multiple functions in protein degradation | Q44283109 |
| | The N-terminal coiled coil of the Rhodococcus erythropolis ARC AAA ATPase is neither necessary for oligomerization nor nucleotide hydrolysis | Q47904859 |
| | Characterization of ARC, a divergent member of the AAA ATPase family from Rhodococcus erythropolis | Q48038753 |
| | A versatile and general prokaryotic expression vector, pLACT7 | Q72443424 |
| P433 | issue | 10 | |
| P921 | main subject | Mycobacterium tuberculosis | Q130971 |
| | structural biology | Q908902 |
| P304 | page(s) | 1377-85 | |
| P577 | publication date | 2009-10-14 | |
| P1433 | published in | Structure | Q15709970 |
| P1476 | title | Structural Insights on the Mycobacterium tuberculosis Proteasomal ATPase Mpa | |
| P478 | volume | 17 | |