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hybrid · semantic + lexical · 1000 datasets ranked · 1.60s

Structurestructure150
Depthcataloged850measured150
Licenseopen1000
Accessopen1000
Formatchemical/x-cif850mmcif150
Sourcercsb-pdb1000
clear
1-20 of 1000sortrelevancemeasured firstqualitysize
declared

Cbf1-CCAN-CEN complex

0.00

Mengqiu, J. · Sue, B.

28,461 rows · 3.0 MB · mmcif

Native yeast kinetochore structures identify an essential inner kinetochore interaction

open
·
CC0-1.0
·
rcsb-pdb
·complete
Source
declared

apo CCAN purified from budding yeast

0.00

Mengqiu, J. · Sue, B.

18,830 rows · 2.0 MB · mmcif

Native yeast kinetochore structures identify an essential inner kinetochore interaction

open·CC0-1.0·rcsb-pdb·completeSource
declared

CCAN dimer purified from budding yeast

0.00

Mengqiu, J. · Sue, B.

94,342 rows · 8.9 MB · mmcif

Native yeast kinetochore structures identify an essential inner kinetochore interaction

open·CC0-1.0·rcsb-pdb·completeSource
declared

Structure of hNSP4-S218A bound to MCP3 at 2.09 A resolution

0.00

Tang, W. · Martinez, O.E. · Ultsch, M.H. · et al.

7,965 rows · 1.4 MB · mmcif

Novel macrocyclic peptides as potent and selective inhibitors of human neutrophil serine protease 4.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Structure of hNSP4 bound to MCP4 at 2.75 A resolution

0.00

Tang, W. · Ultsch, M.H. · Sudhamsu, J.

1,915 rows · 422 KB · mmcif

Novel macrocyclic peptides as potent and selective inhibitors of human neutrophil serine protease 4.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Structure of Clostridium difficile Toxin B (TcdB) glucosyltransferase in complex with UDP and isofagomine analog 2-4

0.00

Gilaj, N. · Wagner, A.G. · Paparella, A.S. · et al.

9,960 rows · 1.8 MB · mmcif

Isofagomine Derivatives as TcdB Glucosyltransferase Inhibitors.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Structure of Clostridium difficile Toxin B (TcdB) glucosyltransferase in complex with UDP linked isofagomine analog 3-5

0.00

Paparella, A.S. · Gilaj, N. · Wagner, A.G. · et al.

9,086 rows · 1.7 MB · mmcif

Isofagomine Derivatives as TcdB Glucosyltransferase Inhibitors.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Crystal Structure of NQO1 Complexed with S-Warfarin

0.00

Corrigan, M.C. · Vargas, A.L. · Moran, G.R. · et al.

9,892 rows · 1.9 MB · mmcif

Structural and Kinetic Analysis of human NQO1: Evidence for Therapeutic Inhibition by Racemic Warfarin.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Crystal structure of selective inhibitor 16 bound at the active site of CDK1

0.00

Murray, J.M. · Oh, A. · Kiefer, J.R. · et al.

5,521 rows · 1.1 MB · mmcif

Utilizing Molecular Dynamics and Mechanistic Pharmacokinetic Studies in the Design of Selective CDK2 Inhibitors.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Kindlin-3/Integrin Beta2 Cytoplasmic Tail Complex

0.00

Xu, Z. · Ma, Y.Q.

6,838 rows · 792 KB · mmcif

Structural basis of kindlin-3 in leukocyte adhesion deficiency III.

open·CC0-1.0·rcsb-pdb·completeSource
declared

Gelsolin domain G2 transitionally bound to F-actin

0.00

Saks, A.J. · Dominguez, R.

24,389 rows · 2.5 MB · mmcif

Domains G2G3 Prime the Actin Filament for Severing by Gelsolin

open·CC0-1.0·rcsb-pdb·completeSource
declared

Gelsolin domain G2G3 transitionally bound to F-actin

0.00

Saks, A.J. · Dominguez, R.

25,236 rows · 2.6 MB · mmcif

Domains G2G3 Prime the Actin Filament for Severing by Gelsolin

open·CC0-1.0·rcsb-pdb·completeSource
declared

Gelsolin domain G2G3 fully bound to F-actin

0.00

Saks, A.J. · Dominguez, R.

25,256 rows · 2.6 MB · mmcif

Domains G2G3 Prime the Actin Filament for Severing by Gelsolin

open·CC0-1.0·rcsb-pdb·completeSource
declared

Two gelsolin domains G2G3 bound to F-actin

0.00

Saks, A.J. · Dominguez, R.

27,027 rows · 2.7 MB · mmcif

Domains G2G3 Prime the Actin Filament for Severing by Gelsolin

open·CC0-1.0·rcsb-pdb·completeSource
declared

LSD1-CoREST in complex with GSK-LSD1 and peptide PRCALVKSK

0.00

Caroli, J. · Mattevi, A.

6,409 rows · 699 KB · mmcif

Covalent adduct Grob fragmentation underlies LSD1 demethylase-specific inhibitor mechanism of action and resistance.

open·CC0-1.0·rcsb-pdb·completeSource
declared

HAdV-C5 Hexon with coagulation factor II

0.00

Ma, O.X. · Reddy, V.S.

22,548 rows · 2.4 MB · mmcif

Structural requirements of blood factors binding to soluble hexon trimers with implications for adenovirus cell targeting and immune evasion

open·CC0-1.0·rcsb-pdb·completeSource
declared

HAdV-C5 hexon trimer

0.00

Ma, O.X. · Reddy, V.S.

22,005 rows · 2.0 MB · mmcif

Structural requirements of blood factors binding to soluble hexon trimers with implications for adenovirus cell targeting and immune evasion

open·CC0-1.0·rcsb-pdb·completeSource
declared

HAdV-C6 Hexon trimer

0.00

Ma, O.X. · Reddy, V.S.

21,854 rows · 2.0 MB · mmcif

Structural requirements of blood factors binding to soluble hexon trimers with implications for adenovirus cell targeting and immune evasion

open·CC0-1.0·rcsb-pdb·completeSource
declared

Cryo-EM structure of HAdV-C6 hexon trimer in complex with prothrombin (FII)

0.00

Ma, O.X. · Reddy, V.S.

22,477 rows · 2.3 MB · mmcif

Structural requirements of blood factors binding to soluble hexon trimers with implications for adenovirus cell targeting and immune evasion

open·CC0-1.0·rcsb-pdb·completeSource
declared

Cryo-EM structure of HAdV-C5 hexon trimer in complex with human coagulation factor X (FX)

0.00

Ma, O.X. · Reddy, V.S.

22,447 rows · 2.2 MB · mmcif

Structural requirements of blood factors binding to soluble hexon trimers with implications for adenovirus cell targeting and immune evasion

open·CC0-1.0·rcsb-pdb·completeSource
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