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- 1v7p (4,990 bytes)
24: ...ber of heterodimeric C-type lectin-like proteins (CLPs) that interact specifically with components of th... - 1r6q (4,853 bytes)
24: ... binding motif, several interfaces for binding to ClpS, and a prominent hydrophobic surface area that bi... - 1ukm (4,391 bytes)
24: ...ntral loop as observed in the structures of other CLPs. A part of the glycan was observed and identified... - 3g1b (4,697 bytes)
2: ...ture of the M53A mutant of Caulobacter crescentus clpS protease adaptor protein in complex with WLFVQRDS...
11: [https://www.uniprot.org/uniprot/CLPS_CAUVC CLPS_CAUVC] Involved in the modulation of the specific...
24: ...ns with N-terminal methionine bind very poorly to ClpS, explaining why these high-abundance proteins are...
26: ...trate selection by the N-end rule adaptor protein ClpS.,Roman-Hernandez G, Grant RA, Sauer RT, Baker TA ... - 3gpr (4,778 bytes)
22: ...ototypic molecular structure for heterotetrameric CLPs, but also a lead structure for pharmaceutical alp... - 3gq0 (4,511 bytes)
2: ==The structure of the Caulobacter crescentus clpS protease adaptor protein - apo structure with no ...
10: [https://www.uniprot.org/uniprot/CLPS_CAUVC CLPS_CAUVC] Involved in the modulation of the specific...
23: ...ns with N-terminal methionine bind very poorly to ClpS, explaining why these high-abundance proteins are...
25: ...trate selection by the N-end rule adaptor protein ClpS.,Roman-Hernandez G, Grant RA, Sauer RT, Baker TA ... - 3gw1 (4,677 bytes)
2: ==The structure of the Caulobacter crescentus CLPs protease adaptor protein in complex with FGG trip...
11: [https://www.uniprot.org/uniprot/CLPS_CAUVC CLPS_CAUVC] Involved in the modulation of the specific...
24: ...ns with N-terminal methionine bind very poorly to ClpS, explaining why these high-abundance proteins are...
26: ...trate selection by the N-end rule adaptor protein ClpS.,Roman-Hernandez G, Grant RA, Sauer RT, Baker TA ... - 4yjm (3,317 bytes)
2: ==The apo structure of Agrobacterium tumefaciens ClpS2==
10: [https://www.uniprot.org/uniprot/CLPS2_AGRFC CLPS2_AGRFC] Involved in the modulation of the specifi...
13: ...tumefaciens and conclude that the use of multiple ClpS paralogs allows fine-tuning of N-end-rule degrada... - 4yjx (3,571 bytes)
2: ==The structure of Agrobacterium tumefaciens ClpS2 bound to L-phenylalaninamide==
11: [https://www.uniprot.org/uniprot/CLPS2_AGRFC CLPS2_AGRFC] Involved in the modulation of the specifi...
14: ...tumefaciens and conclude that the use of multiple ClpS paralogs allows fine-tuning of N-end-rule degrada... - 4yka (3,568 bytes)
2: ==The structure of Agrobacterium tumefaciens ClpS2 in complex with L-tyrosinamide==
11: [https://www.uniprot.org/uniprot/CLPS2_AGRFC CLPS2_AGRFC] Involved in the modulation of the specifi...
14: ...tumefaciens and conclude that the use of multiple ClpS paralogs allows fine-tuning of N-end-rule degrada... - Proteopedia:Structure Index/num-A-C (10,899 bytes)
136: ...* [[ATP-dependent Clp protease adaptor protein]] (ClpS) - 6ygh (4,115 bytes)
13: ...g a folding-proficient extension produced regular CLPs in bacteria but failed to form stable nucleocapsi... - 6ygi (4,138 bytes)
13: ...g a folding-proficient extension produced regular CLPs in bacteria but failed to form stable nucleocapsi... - 7d34 (4,408 bytes)
2: ==AtClpS1-peptide complex==
11: [https://www.uniprot.org/uniprot/CLPS1_ARATH CLPS1_ARATH] Small adapter protein that modulate the a...
14: ...et controls the N-degron selectivity of the plant ClpS protein.
16: Structural basis for the N-degron specificity of ClpS1 from Arabidopsis thaliana.,Kim L, Heo J, Kwon DH...
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