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234,136 Structures from the PDB

1,068,577 Computed Structure Models (CSM)

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QUERY: Citation Author = "Millet, O."

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Search Summary

This query matches 33 Structures.

Refinements

Structure Determination Methodology

experimental (33)

Scientific Name of Source Organism

	Homo sapiens (23)
	Human immunodeficiency virus 1 (8)
	Mus musculus (2)
	Tequatrovirus T4 (2)
	Human immunodeficiency virus 2 (1)
	Human immunodeficiency virus type 2 (ISOLATE ROD) (1)
	Lama glama (1)

Taxonomy

	Eukaryota (23)
	Riboviria (10)
	Duplodnaviria (2)

Experimental Method

	X-RAY DIFFRACTION (31)
	ELECTRON MICROSCOPY (2)

Polymer Entity Type

Protein (33)

Refinement Resolution (Å)

	1.0 - 1.5 (1)
	1.5 - 2.0 (7)
	2.0 - 2.5 (7)
	2.5 - 3.0 (12)
	3.0 - 3.5 (6)

Release Date

	1995 - 1999 (8)
	2000 - 2004 (4)
	2005 - 2009 (5)
	2010 - 2014 (4)
	2015 - 2019 (10)
	2020 - 2024 (2)

Enzyme Classification Name

	Hydrolases (19)
	Transferases (12)

Membrane Protein Annotation

	MemProtMD (4)
	PDBTM (4)
	OPM (3)
	mpstruc (2)

Symmetry Type

	Cyclic (18)
	Asymmetric (16)

SCOP Classification

	All beta proteins (13)
	Alpha and beta proteins (a+b) (7)
	Artifacts (5)
	Alpha and beta proteins (a/b) (3)
	All alpha proteins (1)
	Membrane and cell surface proteins and peptides (1)

AllSelected

1 to 25 of 33 Structures

Page 1 of 2

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1C6X \| pdb_00001c6x	Download File View File

ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP.

Munshi, S.

(2000) Acta Crystallogr D Biol Crystallogr 56: 381-388

Released	2000-12-28
Method	X-RAY DIFFRACTION 2.5 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	PROTEIN (PROTEASE) (protein)
Unique Ligands	3IN

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1C6Y \| pdb_00001c6y	Download File View File

ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP.

Munshi, S.

(2000) Acta Crystallogr D Biol Crystallogr 56: 381-388

Released	2000-12-28
Method	X-RAY DIFFRACTION 2.5 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	PROTEIN (PROTEASE) (protein)
Unique Ligands	MK1

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1HSG \| pdb_00001hsg	Download File View File

CRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES

Chen, Z.

(1994) J Biological Chem 269: 26344-26348

Released	1996-04-03
Method	X-RAY DIFFRACTION 2 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	HIV-1 PROTEASE (protein)
Unique Ligands	MK1

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1HSH \| pdb_00001hsh	Download File View File

CRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES

Chen, Z.

(1994) J Biological Chem 269: 26344-26348

Released	1996-04-03
Method	X-RAY DIFFRACTION 1.9 Å
Organisms	Human immunodeficiency virus type 2 (ISOLATE ROD)
Macromolecule	HIV-II PROTEASE (protein)
Unique Ligands	MK1

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1HSI \| pdb_00001hsi	Download File View File

CRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES

Chen, Z.

(1994) J Biological Chem 269: 26344-26348

Released	1996-04-03
Method	X-RAY DIFFRACTION 2.5 Å
Organisms	Human immunodeficiency virus 2
Macromolecule	HIV-2 PROTEASE (protein)

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1M7N \| pdb_00001m7n	Download File View File

Crystal Structure of Unactivated APO Insulin-like Growth Factor-1 Receptor Kinase Domain

Munshi, S., Kuo, L.

(2002) J Biological Chem 277: 38797-38802

Released	2003-01-07
Method	X-RAY DIFFRACTION 2.7 Å
Organisms	Homo sapiens
Macromolecule	Insulin-like growth factor I receptor (protein)

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1P4O \| pdb_00001p4o	Download File View File

Structure of Apo unactivated IGF-1R KInase domain at 1.5A resolution.

Munshi, S., Kornienko, M., Hall, D.L., Darke, P.L., Waxman, L., Kuo, L.C.

(2003) Acta Crystallogr D Biol Crystallogr 59: 1725-1730

Released	2003-04-29
Method	X-RAY DIFFRACTION 1.5 Å
Organisms	Homo sapiens
Macromolecule	Insulin-like growth factor I receptor protein (protein)

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2BPV \| pdb_00002bpv	Download File View File

HIV-1 protease-inhibitor complex

Munshi, S., Chen, Z.

(1998) Acta Crystallogr D Biol Crystallogr 54: 1053-1060

Released	1999-02-23
Method	X-RAY DIFFRACTION 1.9 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	HIV-1 PROTEASE (protein)
Unique Ligands	1IN

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2BPW \| pdb_00002bpw	Download File View File

HIV-1 protease-inhibitor complex

Munshi, S., Chen, Z.

(1998) Acta Crystallogr D Biol Crystallogr 54: 1053-1060

Released	1999-02-23
Method	X-RAY DIFFRACTION 2.8 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	HIV-1 PROTEASE (protein)
Unique Ligands	1IN

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2BPX \| pdb_00002bpx	Download File View File

HIV-1 protease-inhibitor complex

Munshi, S., Chen, Z.

(1998) Acta Crystallogr D Biol Crystallogr 54: 1053-1060

Released	1999-02-23
Method	X-RAY DIFFRACTION 2.8 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	HIV-1 PROTEASE (protein)
Unique Ligands	MK1

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2BPY \| pdb_00002bpy	Download File View File

HIV-1 protease-inhibitor complex

Munshi, S., Chen, Z.

(1998) Acta Crystallogr D Biol Crystallogr 54: 1053-1060

Released	1999-02-23
Method	X-RAY DIFFRACTION 1.9 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	HIV-1 PROTEASE (protein)
Unique Ligands	3IN

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2BPZ \| pdb_00002bpz	Download File View File

HIV-1 protease-inhibitor complex

Munshi, S., Chen, Z.

(1998) Acta Crystallogr D Biol Crystallogr 54: 1053-1060

Released	1999-02-23
Method	X-RAY DIFFRACTION 2.5 Å
Organisms	Human immunodeficiency virus 1
Macromolecule	HIV-1 PROTEASE (protein)
Unique Ligands	3IN

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3A60 \| pdb_00003a60	Download File View File

Crystal structure of unphosphorylated p70S6K1 (Form I)

Sunami, T., Byrne, N., Diehl, R.E., Funabashi, K., Hall, D.L., Ikuta, M., Patel, S.B., Shipman, J.M., Smith, R.F., Takahashi, I., Zugay-Murphy, J., Iwasawa, Y., Lumb, K.J., Munshi, S.K., Sharma, S.

(2010) J Biological Chem 285: 4587-4594

Released	2009-10-27
Method	X-RAY DIFFRACTION 2.8 Å
Organisms	Homo sapiens
Macromolecule	Ribosomal protein S6 kinase beta-1 (protein)
Unique Ligands	STU

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3A61 \| pdb_00003a61	Download File View File

Crystal structure of unphosphorylated p70S6K1 (Form II)

Sunami, T., Byrne, N., Diehl, R.E., Funabashi, K., Hall, D.L., Ikuta, M., Patel, S.B., Shipman, J.M., Smith, R.F., Takahashi, I., Zugay-Murphy, J., Iwasawa, Y., Lumb, K.J., Munshi, S.K., Sharma, S.

(2010) J Biological Chem 285: 4587-4594

Released	2009-10-27
Method	X-RAY DIFFRACTION 3.43 Å
Organisms	Homo sapiens
Macromolecule	Ribosomal protein S6 kinase beta-1 (protein)
Unique Ligands	STU

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3A62 \| pdb_00003a62	Download File View File

Crystal structure of phosphorylated p70S6K1

Sunami, T., Byrne, N., Diehl, R.E., Funabashi, K., Hall, D.L., Ikuta, M., Patel, S.B., Shipman, J.M., Smith, R.F., Takahashi, I., Zugay-Murphy, J., Iwasawa, Y., Lumb, K.J., Munshi, S.K., Sharma, S.

(2010) J Biological Chem 285: 4587-4594

Released	2009-10-27
Method	X-RAY DIFFRACTION 2.35 Å
Organisms	Homo sapiens
Macromolecule	Ribosomal protein S6 kinase beta-1 (protein)
Unique Ligands	MN, STU

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3DFJ \| pdb_00003dfj	Download File View File

Crystal structure of human Prostasin

Su, H.P., Rickert, K.W., Darke, P.L., Munshi, S.K.

(2008) J Biological Chem 283: 34864-34872

Released	2008-10-14
Method	X-RAY DIFFRACTION 1.45 Å
Organisms	Homo sapiens
Macromolecule	Prostasin (protein)
Unique Ligands	CL

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3DFL \| pdb_00003dfl	Download File View File

Crystal structure of human Prostasin complexed to 4-guanidinobenzoic acid

Su, H.P., Rickert, K.W., Darke, P.L., Munshi, S.K.

(2008) J Biological Chem 283: 34864-34872

Released	2008-10-14
Method	X-RAY DIFFRACTION 2 Å
Organisms	Homo sapiens
Macromolecule	Prostasin (protein)
Unique Ligands	GBS

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3N2Z \| pdb_00003n2z	Download File View File

The Structure of Human Prolylcarboxypeptidase at 2.80 Angstroms Resolution

Soisson, S.M., Patel, S.B., Lumb, K.J., Sharma, S.

(2010) BMC Struct Biol 10: 16-16

Released	2010-07-07
Method	X-RAY DIFFRACTION 2.79 Å
Organisms	Homo sapiens
Macromolecule	Lysosomal Pro-X carboxypeptidase (protein)
Unique Ligands	NAG, SO4
Unique branched monosaccharides	NAG

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3Q6U \| pdb_00003q6u	Download File View File

Structure of the apo MET receptor kinase in the dually-phosphorylated, activated state

Soisson, S.M., Rickert, K.W., Patel, S.B., Allison, T., Lumb, K.J.

(2011) J Biological Chem 286: 11218-11225

Released	2011-01-19
Method	X-RAY DIFFRACTION 1.6 Å
Organisms	Homo sapiens
Macromolecule	Hepatocyte growth factor receptor (protein)

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3Q6W \| pdb_00003q6w	Download File View File

Structure of dually-phosphorylated MET receptor kinase in complex with an MK-2461 analog with specificity for the activated receptor

Soisson, S.M., Rickert, K.W., Patel, S.B., Lumb, K.J.

(2011) J Biological Chem 286: 11218-11225

Released	2011-01-19
Method	X-RAY DIFFRACTION 1.75 Å
Organisms	Homo sapiens
Macromolecule	Hepatocyte growth factor receptor (protein)
Unique Ligands	Q6W

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3R7O \| pdb_00003r7o	Download File View File

Structure of dually phosphorylated c-MET receptor kinase in complex with an MK-2461 analog

Soisson, S.M., Rickert, K., Patel, S.B., Munshi, S., Lumb, K.J.

(2011) J Biological Chem 286: 11218-11225

Released	2012-02-01
Method	X-RAY DIFFRACTION 2.3 Å
Organisms	Homo sapiens
Macromolecule	Hepatocyte growth factor receptor (protein)
Unique Ligands	M61

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4XUC \| pdb_00004xuc	Download File View File

Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of catechol-O-methyltransferase (COMT): Structure with Cmpd18 (1-(biphenyl-3-yl)-3-hydroxypyridin-4(1H)-one)

Allison, T., Wolkenberg, S., Sanders, J.M., Soisson, S.M.

(2015) ACS Med Chem Lett 6: 318-323

Released	2015-04-15
Method	X-RAY DIFFRACTION 1.8 Å
Organisms	Homo sapiens
Macromolecule	Catechol O-methyltransferase (protein)
Unique Ligands	43G, MES, MG, SAM

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4XUD \| pdb_00004xud	Download File View File

Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of catechol-O-methyltransferase (COMT): Structure with Cmpd32 ([1-(biphenyl-3-yl)-5-hydroxy-4-oxo-1,4-dihydropyridin-3-yl]boronic acid)

Allison, T., Wolkenberg, S., Sanders, J.M., Soisson, S.M.

(2015) ACS Med Chem Lett 6: 318-323

Released	2015-04-15
Method	X-RAY DIFFRACTION 2.4 Å
Organisms	Homo sapiens
Macromolecule	Catechol O-methyltransferase (protein)
Unique Ligands	43H, MES, MG, SAM