BMRBj - BMREntryMaster

Found 1 Document (1.172 seconds)

BMRB: 6966

2FWL

1H and 15N assignment of cytochrome c552 from Thermus thermophilus in the reduced state

Authors

Muresanu, L., Pristovsek, P., Loehr, F., Maneg, O., Mukrasch, M.D., Rueterjans, H., Ludwig, B., Luecke, C.

Assembly

cytochrome c552

Entity

1. cytochrome c552 (polymer, Thiol state: all other bound), 133 monomers, 14404.69 Da Detail

MAQADGAKIY AQCAGCHQQN GQGIPGAFPP LAGHVAEILA KEGGREYLIL VLLYGLQGQI EVKGMKYNGV MSSFAQLKDE EIAAVLNHIA TAWGDAKKVK GFKPFTAEEV KKLRAKKLTP QQVLTERKKL GLK

2. HEM (non-polymer), 616.487 Da

Total weight

15021.178 Da

Max. entity weight

14404.69 Da

Entity Connection

metal coordination 2, covalent 2 Detail

ID	Type	Value order	Atom ID 1	Atom ID 2
1	covalent	sing	2:HEM1:CAB	1:CYS13:SG
2	covalent	sing	2:HEM1:CAC	1:CYS16:SG
3	metal coordination	sing	2:HEM1:FE	1:HIS17:NE2
4	metal coordination	sing	2:HEM1:FE	1:MET71:SD

Source organism

Thermus thermophilus

Exptl. method

NMR

Data set

assigned_chemical_shifts

Chem. Shift Complete

Sequence coverage: 100.0 %, Completeness: 99.3 %, Completeness (bb): 99.0 % Detail

Polymer type: polypeptide(L)

	Total	¹H	¹⁵N
All	99.3 % (953 of 960)	99.3 % (812 of 818)	99.3 % (141 of 142)
Backbone	99.0 % (400 of 404)	98.9 % (273 of 276)	99.2 % (127 of 128)
Sidechain	99.5 % (553 of 556)	99.4 % (539 of 542)	100.0 % (14 of 14)
Aromatic	100.0 % (49 of 49)	100.0 % (48 of 48)	100.0 % (1 of 1)
Methyl	100.0 % (79 of 79)	100.0 % (79 of 79)

1. cytochrome c552

MAQADGAKIY AQCAGCHQQN GQGIPGAFPP LAGHVAEILA KEGGREYLIL VLLYGLQGQI EVKGMKYNGV MSSFAQLKDE EIAAVLNHIA TAWGDAKKVK GFKPFTAEEV KKLRAKKLTP QQVLTERKKL GLK

Show sample condition

Sample #1

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Type	Concentration
1	cytochrome c552	protein	2 mM
2	potassium phosphate	buffer	20 mM
3	sodium ascorbate	reducing agent	5 mM

Sample #2

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Isotope labeling	Type	Concentration
4	cytochrome c552	[U-98% 15N]	protein	2 mM
5	potassium phosphate		buffer	20 mM
6	sodium ascorbate		reducing agent	5 mM

Release date

2006-04-26

Citation

The electron transfer complex between cytochrome c552 and the CuA domain of the Thermus thermophilus ba3 oxidase. A combined NMR and computational approach
Muresanu, L., Pristovsek, P., Loehr, F., Maneg, O., Mukrasch, M.D., Rueterjans, H., Ludwig, B., Luecke, C.
J. Biol. Chem. (2006), 281, 14503-14513, PubMed 16554303 , DOI 10.1074/jbc.M601108200 , Abstract

Related entities 1. cytochrome c552, : 1 : 7 : 21 entities Detail

Experiments performed 5 experiments Detail

1 1H-1H_TOCSY

Instrument

Model Bruker DMX (600 MHz)

Sample #1

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Type	Concentration
1	cytochrome c552	protein	2 mM
2	potassium phosphate	buffer	20 mM
3	sodium ascorbate	reducing agent	5 mM

Sample #2

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Isotope labeling	Type	Concentration
4	cytochrome c552	[U-98% 15N]	protein	2 mM
5	potassium phosphate		buffer	20 mM
6	sodium ascorbate		reducing agent	5 mM

2 1H-1H_NOESY

Instrument

Model Bruker DMX (600 MHz)

Sample #1

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Type	Concentration
1	cytochrome c552	protein	2 mM
2	potassium phosphate	buffer	20 mM
3	sodium ascorbate	reducing agent	5 mM

Sample #2

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Isotope labeling	Type	Concentration
4	cytochrome c552	[U-98% 15N]	protein	2 mM
5	potassium phosphate		buffer	20 mM
6	sodium ascorbate		reducing agent	5 mM

3 15N-1H_TROSY

Instrument

Model Bruker DMX (600 MHz)

Sample #1

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Type	Concentration
1	cytochrome c552	protein	2 mM
2	potassium phosphate	buffer	20 mM
3	sodium ascorbate	reducing agent	5 mM

Sample #2

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Isotope labeling	Type	Concentration
4	cytochrome c552	[U-98% 15N]	protein	2 mM
5	potassium phosphate		buffer	20 mM
6	sodium ascorbate		reducing agent	5 mM

4 15N-1H_TOCSY-TROSY

Instrument

Model Bruker DMX (600 MHz)

Sample #1

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Type	Concentration
1	cytochrome c552	protein	2 mM
2	potassium phosphate	buffer	20 mM
3	sodium ascorbate	reducing agent	5 mM

Sample #2

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Isotope labeling	Type	Concentration
4	cytochrome c552	[U-98% 15N]	protein	2 mM
5	potassium phosphate		buffer	20 mM
6	sodium ascorbate		reducing agent	5 mM

5 15N-1H_NOESY-TROSY

Instrument

Model Bruker DMX (600 MHz)

Sample #1

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Type	Concentration
1	cytochrome c552	protein	2 mM
2	potassium phosphate	buffer	20 mM
3	sodium ascorbate	reducing agent	5 mM

Sample #2

Temperature 298 (±0.1) K, pH 6.0 (±0.1)

#	Name	Isotope labeling	Type	Concentration
4	cytochrome c552	[U-98% 15N]	protein	2 mM
5	potassium phosphate		buffer	20 mM
6	sodium ascorbate		reducing agent	5 mM

Chemical shift validation 4 contents Detail

Properties

Input source #1: Assigned chemical shifts - Assigned chemical shifts	bmr6966_3.str
Diamagnetism of the molecular assembly	False (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)
2:1:HEM:CAB	1:13:CYS:SG	unknown	unknown	n/a
2:1:HEM:CAC	1:16:CYS:SG	unknown	unknown	n/a
2:1:HEM:FE	1:17:HIS:NE2	unknown	unknown	n/a
2:1:HEM:FE	1:71:MET:SD	unknown	unknown	n/a

Non-standard residues

Chain_ID	Seq_ID	Comp_ID	Chem_comp_name	Experimental evidences
2	1	HEM	PROTOPORPHYRIN IX CONTAINING FE	Assigned chemical shifts

Content subtype: bmr6966_3.str

#	Content subtype	Saveframe	Status	# of rows	Experiment type	Sequence coverage (%)
1	Assigned chemical shifts	chem_shift_list_1	Warning	1142		100.0 (chain: 1, length: 133), 100.0 (chain: 2, length: 1)
1	Chemical shift references	chemical_shift_referencing	OK	2		No information

Assigned chemical shifts

Saveframe: chem_shift_list_1
- Status: Warning
- Sequence coverage of experimental data
  - Entity_assembly_ID: 1, Chain length: 133, Sequence coverage: 100.0%
  - Entity_assembly_ID: 2, Chain length: 1, Sequence coverage: 100.0%
- Total number of assignments
  - ¹H chemical shifts: 998
  - ¹⁵N chemical shifts: 144
- Completeness of assignments
  - Entity_assemble_ID: 1
  - Entity_assemble_ID: 2
- Tautomeric state of HIS
- Histogram of normalized assigned chemical shifts
- Random coil index and derived parameters (S² and NMR RMSD)
  - Chain_ID: 1

Comp_index_ID	Comp_ID	Atom_ID	CS value (ppm)
17	HIS	HD1	9.02
17	HIS	ND1	161.4

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	818	812	99.3
¹⁵N chemical shifts	145	143	98.6

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	276	274	99.3
¹⁵N chemical shifts	128	126	98.4

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	542	538	99.3
¹⁵N chemical shifts	17	17	100.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	82	82	100.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	48	48	100.0
¹⁵N chemical shifts	1	1	100.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	24	13	54.2
¹⁵N chemical shifts	4	0	0.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	24	13	54.2
¹⁵N chemical shifts	4	0	0.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹H chemical shifts	4	4	100.0

Atom group	# of target shifts	# of assigned shifts	Completeness (%)
¹⁵N chemical shifts	2	0	0.0

Keywords heme c, redox protein

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Found 1 Document (1.172 seconds)

BMRB: 6966

Sample #1

Sample #2

Related entities 1. cytochrome c552, : 1 : 7 : 21 entities Detail

Experiments performed 5 experiments Detail

Instrument

Sample #1

Sample #2

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Chemical shift validation 4 contents Detail