|
140
|
558
|
3sbgA |
Crystal structure of a prp8 c-terminal fragment |
|
140
|
440
|
3s8dA |
Crystal structure of ripa from yersinia pestis |
|
140
|
557
|
5y58A |
Crystal structure of ku70/80 and tlc1 |
|
140
|
534
|
5xzrA |
The atomic structure of shp2 e76a mutant in complex with allosteric inhibitor 9b |
|
140
|
323
|
3rn9B |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/l272e double mutant |
|
140
|
745
|
6faik |
Structure of a eukaryotic cytoplasmic pre-40s ribosomal subunit |
|
140
|
431
|
3rc0A |
Human setd6 in complex with rela lys310 peptide |
|
140
|
452
|
3rg6A |
Crystal structure of a chaperone-bound assembly intermediate of form i rubisco |
|
140
|
455
|
2ivdA |
Structure of protoporphyrinogen oxidase from myxococcus xanthus with acifluorfen |
|
140
|
392
|
5xinA |
Protein engineering of xylose (glucose) isomerase from actinoplanes missouriensis. 1. crystallography and site-directed mutagenesis of metal binding sites |
|
140
|
392
|
5wv9A |
Crystal structure of a insect group iii chitinase complex with (glcnac)6 (cad1-(glcnac)6 ) from ostrinia furnacalis |
|
140
|
437
|
5wb2A |
Us28 bound to engineered chemokine cx3cl1.35 and nanobodies |
|
140
|
418
|
5w78B |
Human acyloxyacyl hydrolase (aoah), proteolytically processed |
|
140
|
381
|
5wcxA |
Streptococcus pyogenes phosphoglycerol transferase gach in complex with sn-glycerol-1-phosphate, crystal form 1 |
|
140
|
399
|
5v8sA |
Flavo di-iron protein h90d mutant from thermotoga maritima |
|
140
|
448
|
5v0uA |
Crystal structure of polymerase acid protein (pa) from influenza a virus, wilson-smith/1933 (h1n1) bound to follow on fragment ebsi-4723 4-(5-chlorothiophen-2-yl)-1h-pyrazole |
|
140
|
448
|
5v12C |
Crystal structure of carbon sulfoxide lyase, egt2 y134f with sulfenic acid intermediate |
|
140
|
352
|
5up0A |
Crystal structure of human pde1b catalytic domain in complex with inhibitor 3 (6-(4-chlorobenzyl)-8,9,10,11-tetrahydrobenzo[4,5]thieno[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6h)-one) |
|
140
|
338
|
5u7dA |
Pde2 catalytic domain complexed with inhibitors |
|
140
|
361
|
5u20A |
X-ray structure of the wlarg aminotransferase from campylobacter jejuni, internal plp-aldimine |
|
140
|
335
|
5tqbB |
Crystal structure of assembly chaperone of ribosomal protein l4 (acl4) in complex with ribosomal protein l4 (rpl4) |
|
140
|
363
|
5tlhA |
Fructose-1,6-bisphosphate aldolase from rabbit muscle in complex with the inhibitor 2-naphthol 6-bisphosphonate |
|
140
|
376
|
5thzA |
Crystal structure of curj carbon methyltransferase |
|
140
|
492
|
5ttdA |
Minor pilin fctb from s. pyogenes with engineered intramolecular isopeptide bond |
|
140
|
448
|
5tspA |
Crystal structure of the catalytic domain of clostridium perfringens neuraminidase (nani) in complex with a ches |
|
140
|
406
|
5t6bA |
X-ray structure of the kijd1 c3-methyltransfeerase, converted to monomeric form |
|
140
|
428
|
5taoA |
Haloferax volcanii malate synthase lead(ii) complex |
|
140
|
464
|
5t6kA |
Crystal structure of tgcdpk1 from toxoplasma gondii complexed with gw780159x |
|
140
|
411
|
5sunA |
Idh1 r132h in complex with idh146 |
|
140
|
472
|
5osqA |
Zp-n domain of mammalian sperm receptor zp3 (crystal form ii, processed in p21221) |
|
140
|
350
|
5ormA |
Crystal structure of designed cppr-telo1 |
|
140
|
467
|
5oexA |
Complex with iodine ion for thiocyanate dehydrogenase from thioalkalivibrio paradoxus |
|
140
|
428
|
5o66A |
Asymmetric acrabz-tolc |
|
140
|
371
|
5o1mA |
Structure of latex clearing protein lcp in the closed state |
|
140
|
413
|
5np8A |
Pgk1 in complex with crt0063465 (3-[2-(4-bromophenyl)-5,7-dimethyl-pyrazolo[1,5-a]pyrimidin-6-yl]propanoic acid) |
|
140
|
428
|
5ng5C |
Multi-drug efflux; membrane transport; rnd superfamily; drug resistance |
|
140
|
398
|
5na1A |
Nadh:quinone oxidoreductase (ndh-ii) from staphylococcus aureus - holoprotein structure - 2.32 a resolution |
|
140
|
475
|
5n8xA |
Trigonal structure of mutant v173i of 3d polymerase from foot-and-mouth disease virus |
|
140
|
330
|
5lboA |
Crystal structure of human phosphodiesterase 4d2 catalytic domain with inhibitor npd-001 |
|
140
|
389
|
5l92A |
The 2.1 a crystal structure of cyp109e1 from bacillus megaterium in complex with corticosterone |
|
140
|
373
|
5j9oA |
Trna guanine transglycosylase (tgt) in co-crystallized complex with 1-(2-(methylamino)-1h-benzo[d]imidazol-6-yl)guanidine |
|
140
|
576
|
5k1hB |
Eif3b relocated to the intersubunit face to interact with eif1 and below the eif2 ternary-complex. from the structure of a partial yeast 48s preinitiation complex in closed conformation. |
|
140
|
402
|
5kqoA |
1-deoxy-d-xylulose 5-phosphate reductoisomerase from vibrio vulnificus |
|
140
|
386
|
5i7gA |
Metal free glucose isomerase collected at room temperature using the hc1b humidity controller |
|
140
|
398
|
5hvfA |
Crystal structure of thrombin-activatable fibrinolysis inhibitor in complex with an inhibitory nanobody (vhh-i83) |
|
140
|
455
|
5hasA |
Crystal structure of the n-terminal dcb-hus domain of t. terrestris sec7 |
|
140
|
648
|
5gasN |
Thermus thermophilus v/a-atpase, conformation 2 |
|
140
|
462
|
5fysA |
Crystal structure of the catalytic domain of human jarid1b in complex with d-2-hydroxyglutarate |
|
140
|
462
|
5fzkA |
Crystal structure of the catalytic domain of human jarid1b in complex with 3d fragment n,3-dimethyl-n-(pyridin-3-ylmethyl)-1,2-oxazole-5- carboxamide (n10051a) (ligand modelled based on pandda event map, sgc - diamond i04-1 fragment screening) |
|
140
|
462
|
5fz6A |
Crystal structure of the catalytic domain of human jarid1b in complex with maybridge fragment n05859b (ligand modelled based on pandda event map, sgc - diamond i04-1 fragment screening) |
