BMRBj - BMREntryMaster

Found 1 Document (0.449 seconds)

BMRB: 30178

5TBQ

The Solution Structure of the Magnesium-bound Conantokin-R1B Mutant

Authors

Castellino, F.J., Yuan, Y.

Assembly

Conantokin

Entity

1. Conantokin (polymer, Thiol state: not present), 19 monomers, 2287.241 Da Detail

GEXXLAXKAX FARXLANYX

Formula weight

2287.241 Da

Source organism

Conus rolani

Exptl. method

solution NMR

Data set

assigned_chemical_shifts, spectral_peak_list

Chem. Shift Complete

Sequence coverage: 68.4 %, Completeness: 82.7 %, Completeness (bb): 93.6 % Detail

Polymer type: polypeptide(L)

	Total	¹H	¹³C	¹⁵N
All	82.7 % (124 of 150)	76.6 % (59 of 77)	88.1 % (52 of 59)	92.9 % (13 of 14)
Backbone	93.6 % (73 of 78)	88.9 % (24 of 27)	97.4 % (37 of 38)	92.3 % (12 of 13)
Sidechain	75.0 % (63 of 84)	70.0 % (35 of 50)	81.8 % (27 of 33)	100.0 % (1 of 1)
Aromatic	38.9 % (7 of 18)	33.3 % (3 of 9)	44.4 % (4 of 9)
Methyl	100.0 % (16 of 16)	100.0 % (8 of 8)	100.0 % (8 of 8)

1. entity 1

GEXXLAXKAX FARXLANYX

Show sample condition

Sample

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 7.0, Details 20 mM [U-2H] HEPES, 20 mM MgCl2, 90% H2O/10% D2O

#	Name	Isotope labeling	Concentration
1	entity_1		0.0 ~ 0.0 mM
2	HEPES	[U-2H]	20 mM
3	MgCl2	natural abundance	20 mM

Protein Blocks Logo

Calculated from 20 models in PDB: 5TBQ, Strand ID: A Detail

Release date

2016-12-08

Citation

Discerning the Role of the Hydroxyproline Residue in the Structure of Conantokin Rl-B and Its Role in GluN2B Subunit-Selective Antagonistic Activity toward N-Methyl-d-Aspartate Receptors
Yuan, Y., Balsara, R.D., Zajicek, J., Kunda, S., Castellino, F.J.
Biochemistry (2016), 55, 7112-7122, PubMed 27981829 , DOI 10.1021/acs.biochem.6b00962 , Abstract

Experiments performed 4 experiments Detail

NMR combined restraints 4 contents Detail

Properties

Input source #1: NMR data (NEF) - Assigned chemical shifts, Distance restraints, Dihedral angle restraints	combined_30178_5tbq.nef
Input source #2: Coordindates	5tbq.cif
Diamagnetism of the molecular assembly	True (excluding Oxygen atoms)
Whether the assembly has a disulfide bond	None
Whether the assembly has a other bond	True (see coodinates for details)
Whether the assembly contains a cyclic polymer	None
Overall data processing status	Warning

Disulfide bonds

None

Other bonds (neither disulfide, covalent nor hydrogen bonds, e.g. Zinc–sulphur bond)

Ptnr_site_1	Ptnr_site_2	Redox_state_prediction_1	Redox_state_prediction_2	Distance (Å)
1:2:GLU:C	1:3:CGU:N	unknown	unknown	n/a
1:3:CGU:C	1:4:CGU:N	unknown	unknown	n/a
1:4:CGU:C	1:5:LEU:N	unknown	unknown	n/a
1:6:ALA:C	1:7:CGU:N	unknown	unknown	n/a
1:7:CGU:C	1:8:LYS:N	unknown	unknown	n/a
1:9:ALA:C	1:10:CGU:N	unknown	unknown	n/a
1:10:CGU:C	1:11:PHE:N	unknown	unknown	n/a
1:13:ARG:C	1:14:CGU:N	unknown	unknown	n/a
1:14:CGU:C	1:15:LEU:N	unknown	unknown	n/a
1:18:TYR:C	1:19:NH2:N	unknown	unknown	n/a

Non-standard residues

Chain_ID	Seq_ID	Comp_ID	Chem_comp_name	Experimental evidences
A	3	CGU	GAMMA-CARBOXY-GLUTAMIC ACID	Assigned chemical shifts, Distance restraints, Torsion angle restraints, Coordinates
A	4	CGU	GAMMA-CARBOXY-GLUTAMIC ACID	Assigned chemical shifts, Distance restraints, Torsion angle restraints, Coordinates
A	7	CGU	GAMMA-CARBOXY-GLUTAMIC ACID	Assigned chemical shifts, Distance restraints, Torsion angle restraints, Coordinates
A	10	CGU	GAMMA-CARBOXY-GLUTAMIC ACID	Assigned chemical shifts, Distance restraints, Torsion angle restraints, Coordinates
A	14	CGU	GAMMA-CARBOXY-GLUTAMIC ACID	Assigned chemical shifts, Distance restraints, Torsion angle restraints, Coordinates
A	19	NH2	AMINO GROUP	Assigned chemical shifts, Coordinates

Sequence alignments

Entity_assembly_ID (NMR): A vs Auth_asym_ID (model): A

--------10---------
GEXXLAXKAXFARXLANYX
|||||||||||||||||||
GEXXLAXKAXFARXLANYX

Chain assignments

Entity_assembly_ID (NMR)	Auth_asym_ID (model)	Length	Unmapped	Conflict	Sequence coverage (%)
A	A	19	0	0	100.0

Content subtype: combined_30178_5tbq.nef

#	Content subtype	Saveframe	Status	# of rows (sets)	Experiment type	Sequence coverage (%)
1	Covalent bonds	assembly	OK	10		No information
1	Assigned chemical shifts	assigned_chemical_shifts_1	Warning	185		100.0 (chain: A, length: 19)
1	Distance restraints	CNS/XPLOR_distance_constraints_3	Warning	158 (1)	noe	89.5 (chain: A, length: 19)
1	Dihedral angle restraints	CNS/XPLOR_dihedral_2	OK	32 (32)	.	94.7 (chain: A, length: 19)

Assigned chemical shifts

Saveframe: assigned_chemical_shifts_1
- Status: Warning
- Sequence coverage of experimental data
  - Entity_assembly_ID: A, Chain length: 19, Sequence coverage: 100.0%
- Total number of assignments
  - ¹H chemical shifts: 92
  - ¹³C chemical shifts: 74
  - ¹⁵N chemical shifts: 19
- Completeness of assignments
  - Entity_assemble_ID: A
- Rotameric state of ILE , LEU, and VAL
- Histogram of normalized assigned chemical shifts
- Random coil index and derived parameters (S² and NMR RMSD)
  - Chain_ID: A

Comp_index_ID	Comp_ID
3	CGU
4	CGU
7	CGU
10	CGU
14	CGU

Comp_index_ID	Comp_ID	Atom_ID	CS value (ppm)
17	ASN	CG	113.3
18	TYR	CZ	126.43

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	79	67	84.8
¹³C chemical shifts	59	52	88.1
¹⁵N chemical shifts	16	14	87.5

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	27	26	96.3
¹³C chemical shifts	26	25	96.2
¹⁵N chemical shifts	14	13	92.9

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	52	41	78.8
¹³C chemical shifts	33	27	81.8
¹⁵N chemical shifts	2	1	50.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	8	8	100.0
¹³C chemical shifts	8	8	100.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	9	5	55.6
¹³C chemical shifts	9	4	44.4

Covalent bonds

Saveframe: assembly
- Status: OK

Distance restraints

Saveframe: CNS/XPLOR_distance_constraints_3
- Status: Warning
- Experiment type: noe
- Sequence coverage of experimental data
  - Entity_assembly_ID: A, Chain length: 19, Sequence coverage: 89.5%
- Total number of restraints: 158
- Weight of restraints: 1.0 (158)
- Potential type of restraints: square-well-parabolic (158)
- Range of distance target values: 2.4, 4.4 (Å)
- Histogram of distance target values
- Distance restraints per residue
  - Chain_ID: A
- Distance restraints on contact map

Dihedral angle restraints

Saveframe: CNS/XPLOR_dihedral_2
- Status: OK
- Experiment type: .
- Sequence coverage of experimental data
  - Entity_assembly_ID: A, Chain length: 19, Sequence coverage: 94.7%
- Total number of restraints: 32
- Total number of restraints per polymer type: 32
- Weight of restraints: 1.0 (32)
- Potential type of restraints: square-well-parabolic (32)
- Plot of Phi-Psi angle restraints
- Dihedral angle restraints per residue
  - Chain_ID: A

Keywords TOXIN, TRANSPORT PROTEIN INHIBITOR

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Found 1 Document (0.449 seconds)

BMRB: 30178

Sample

Experiments performed 4 experiments Detail

Instrument

Sample

Instrument

Sample

Instrument

Sample

Instrument

Sample

NMR combined restraints 4 contents Detail