[English] 日本語
Yorodumi
- PDB-7q3a: Crystal structure of MAB_4324 a tandem repeat GNAT from Mycobacte... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 7q3a
TitleCrystal structure of MAB_4324 a tandem repeat GNAT from Mycobacterium abscessus
ComponentsPutative acetyltransferase, GNAT
KeywordsTRANSFERASE / N-acetyltransferase / acetyl-CoA
Function / homology
Function and homology information


acyltransferase activity, transferring groups other than amino-acyl groups / nucleotide binding
Similarity search - Function
: / Acetyltransferase (GNAT) family / Gcn5-related N-acetyltransferase (GNAT) domain profile. / GNAT domain / Acyl-CoA N-acyltransferase
Similarity search - Domain/homology
ACETYL COENZYME *A / ACETATE ION / COENZYME A / 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE / Chem-NDP / Acetyltransferase, GNAT
Similarity search - Component
Biological speciesMycobacteroides abscessus (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / SAD / Resolution: 2 Å
AuthorsBlaise, M. / Alsarraf, M.A.B.
Funding support France, 1items
OrganizationGrant numberCountry
Centre National de la Recherche Scientifique (CNRS) France
CitationJournal: Febs Lett. / Year: 2022
Title: Biochemical, structural, and functional studies reveal that MAB_4324c from Mycobacterium abscessus is an active tandem repeat N-acetyltransferase.
Authors: Alsarraf, H.M.A.B. / Ung, K.L. / Johansen, M.D. / Dimon, J. / Olieric, V. / Kremer, L. / Blaise, M.
History
DepositionOct 27, 2021Deposition site: PDBE / Processing site: PDBE
Revision 1.0May 4, 2022Provider: repository / Type: Initial release
Revision 1.1Jul 6, 2022Group: Database references / Category: citation / citation_author
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _citation_author.identifier_ORCID / _citation_author.name
Revision 1.2Jun 19, 2024Group: Data collection / Category: chem_comp_atom / chem_comp_bond

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Putative acetyltransferase, GNAT
B: Putative acetyltransferase, GNAT
hetero molecules


Theoretical massNumber of molelcules
Total (without water)83,45413
Polymers78,3402
Non-polymers5,11411
Water15,493860
1
A: Putative acetyltransferase, GNAT
hetero molecules


Theoretical massNumber of molelcules
Total (without water)41,6486
Polymers39,1701
Non-polymers2,4785
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
B: Putative acetyltransferase, GNAT
hetero molecules


Theoretical massNumber of molelcules
Total (without water)41,8067
Polymers39,1701
Non-polymers2,6366
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)149.960, 149.960, 183.380
Angle α, β, γ (deg.)90.000, 90.000, 120.000
Int Tables number179
Space group name H-MP6522
Space group name HallP652(x,y,z+1/12)
Symmetry operation#1: x,y,z
#2: x-y,x,z+5/6
#3: y,-x+y,z+1/6
#4: -y,x-y,z+2/3
#5: -x+y,-x,z+1/3
#6: x-y,-y,-z
#7: -x,-x+y,-z+1/3
#8: -x,-y,z+1/2
#9: y,x,-z+2/3
#10: -y,-x,-z+1/6
#11: -x+y,y,-z+1/2
#12: x,x-y,-z+5/6

-
Components

-
Protein , 1 types, 2 molecules AB

#1: Protein Putative acetyltransferase, GNAT


Mass: 39170.125 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mycobacteroides abscessus (strain ATCC 19977 / DSM 44196 / CIP 104536 / JCM 13569 / NCTC 13031 / TMC 1543) (bacteria)
Strain: ATCC 19977 / DSM 44196 / CIP 104536 / JCM 13569 / NCTC 13031 / TMC 1543
Gene: MAB_4324c / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: B1MJN9

-
Non-polymers , 8 types, 871 molecules

#2: Chemical ChemComp-NDP / NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE


Mass: 745.421 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C21H30N7O17P3 / Feature type: SUBJECT OF INVESTIGATION
#3: Chemical ChemComp-COA / COENZYME A


Mass: 767.534 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C21H36N7O16P3S / Feature type: SUBJECT OF INVESTIGATION
#4: Chemical ChemComp-ACO / ACETYL COENZYME *A


Mass: 809.571 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C23H38N7O17P3S / Feature type: SUBJECT OF INVESTIGATION
#5: Chemical ChemComp-ACT / ACETATE ION


Mass: 59.044 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C2H3O2 / Feature type: SUBJECT OF INVESTIGATION
#6: Chemical ChemComp-SO4 / SULFATE ION


Mass: 96.063 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: SO4
#7: Chemical ChemComp-NAI / 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE / NADH


Mass: 665.441 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C21H29N7O14P2 / Feature type: SUBJECT OF INVESTIGATION
#8: Chemical ChemComp-EPE / 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID / HEPES


Mass: 238.305 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C8H18N2O4S / Comment: pH buffer*YM
#9: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 860 / Source method: isolated from a natural source / Formula: H2O

-
Details

Has ligand of interestY

-
Experimental details

-
Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

-
Sample preparation

CrystalDensity Matthews: 3.8 Å3/Da / Density % sol: 67.62 %
Crystal growTemperature: 291 K / Method: vapor diffusion, sitting drop / pH: 7.5
Details: 2 M Ammonium sulphate, 0.1 M HEPES pH 7.5 and 2% w/v polyethylene glycol (PEG) 400.

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: SLS / Beamline: X06DA / Wavelength: 1 Å
DetectorType: DECTRIS PILATUS 2M-F / Detector: PIXEL / Date: Jan 31, 2019
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 2→50 Å / Num. obs: 80802 / % possible obs: 98.3 % / Redundancy: 38.3 % / Biso Wilson estimate: 26.2 Å2 / CC1/2: 1 / Rrim(I) all: 0.1 / Net I/σ(I): 37.4
Reflection shellResolution: 2→2.1 Å / Num. unique obs: 8058 / CC1/2: 0.95 / Rrim(I) all: 0.87 / % possible all: 100

-
Processing

Software
NameVersionClassification
PHENIX1.19_4092refinement
XDSdata reduction
XSCALEdata scaling
CRANKphasing
RefinementMethod to determine structure: SAD / Resolution: 2→49.09 Å / SU ML: 0.1773 / Cross valid method: FREE R-VALUE / σ(F): 1.36 / Phase error: 21.02
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.2257 1969 2.47 %
Rwork0.1862 77651 -
obs0.1871 79620 96.85 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 31.62 Å2
Refinement stepCycle: LAST / Resolution: 2→49.09 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms5378 0 323 867 6568
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00845916
X-RAY DIFFRACTIONf_angle_d0.99388119
X-RAY DIFFRACTIONf_chiral_restr0.0838851
X-RAY DIFFRACTIONf_plane_restr0.00891038
X-RAY DIFFRACTIONf_dihedral_angle_d14.2632062
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2-2.050.24821420.18325615X-RAY DIFFRACTION99.97
2.05-2.110.21511440.1815642X-RAY DIFFRACTION99.98
2.11-2.170.21311420.18055639X-RAY DIFFRACTION100
2.17-2.240.24611260.23154955X-RAY DIFFRACTION87.47
2.24-2.320.323970.26963897X-RAY DIFFRACTION69.1
2.32-2.410.22941450.17685664X-RAY DIFFRACTION100
2.41-2.520.22261430.17415666X-RAY DIFFRACTION99.98
2.52-2.650.23071440.18075688X-RAY DIFFRACTION100
2.65-2.820.21711450.18825709X-RAY DIFFRACTION99.98
2.82-3.040.22341450.19555723X-RAY DIFFRACTION99.98
3.04-3.340.23641470.18335743X-RAY DIFFRACTION100
3.34-3.830.21961460.1875753X-RAY DIFFRACTION99.38
3.83-4.820.20531470.15985823X-RAY DIFFRACTION99.58
4.82-49.090.22651560.19556134X-RAY DIFFRACTION99.92
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
11.93047638920.205462797577-0.1558005539031.52863441585-0.1018622955451.573141605910.0220981567817-0.0409215686206-0.108241067010.178926133874-0.003862516807870.14791622230.0407515001842-0.137194090013-0.03490749598010.1900304867510.002652594677560.006988981996340.2384969226070.01268123091320.169337040586-11.541117205266.127714335411.7204753073
22.28854681828-0.4768252697970.5840995233651.96987450333-0.6649430115872.2396385669-0.0223481543558-0.0578619624009-0.1175893721160.1488390777440.008698434732020.01332611600880.0589315164277-0.04747489874440.01144850237550.178367907637-0.003945460753710.02366192255340.192903431981-0.006414643090280.143089862947-10.4836323868.31899598317.92937367
32.06032421472-0.828692620642-0.6195034637340.8284141658980.11558190360.460645360274-0.094402234328-0.0174851256384-0.1445762164530.1287582357560.006986899095980.02508573727190.0541497004311-0.008766548573770.09073565316820.166299992918-0.0216338544433-0.02012304743220.2178478140430.006192562034230.188452527919.7864544744857.067546155815.4618877175
42.07996019724-0.7948633803570.2095639109913.54837181221-1.576135194663.07184614003-0.0643997614669-0.136640785331-0.2928517490520.1564599767160.1307103126340.1110951156980.100419743667-0.0472667471121-0.08365753063450.1114207202070.009219751222750.02011911707480.1919614116670.02363129172750.20052767067714.932090738655.007966321912.5602873742
52.3202650677-0.821172624057-0.8327981239320.7121348172040.3437575035641.09411728701-0.0634646298457-0.117162819380.1902031399680.1216854068760.0566766714563-0.2156506904580.07847903718590.131130525-0.01493468385580.195420662842-0.000372389115051-0.03792052906980.2208418015280.002641451512380.22539725936616.204702673663.637997160215.2803104174
62.25183768937-0.3494880189840.03103007709791.146858726580.339380048431.41356574821-0.0707627130890.10873121472-0.178335250328-0.1030331901710.0750351858008-0.2798321181510.0626474110930.3806411818610.0002794175406830.159404219040.01500700092540.03015101383720.300632192655-0.01414540032530.20940437380218.258209219964.646078766-18.5684071341
73.228476882290.0432267521138-0.5014688447454.647191527972.059272751563.29187157594-0.1259052164470.440920439149-0.323403872504-0.09174623610720.096513999252-0.177757105410.2494855958850.232807550228-0.008195639952930.2040321375580.01011629122080.0334893114710.2802988613590.001587573051170.15225698730114.559534172164.9927456086-28.7399383194
82.795982740670.58538843934-0.5894186185530.838134497829-0.1791745312420.803845031158-0.1500129067560.0869813052894-0.274254861101-0.1556755832570.074213854632-0.1666232855310.06499595565260.1049777703270.06990969788780.1898848735430.003021614085390.008847018443680.208384517104-0.02989881632680.183629574312-4.828117180558.2648666702-23.6564070349
91.732706968821.708418355330.05614237830398.379337428872.117617490052.22375956256-0.146520522988-0.00380318376687-0.890569418067-0.1995063541050.1216676074570.1251337452010.1677695400660.07409798695780.02231583694070.1524792272920.028330793460.03918897982580.2075730166560.01959943266730.39943926661-10.627468377547.5492715798-16.1127247218
102.271118219020.533419449952-0.07146691009560.831431042441-0.2581996788840.783807005859-0.06089830585910.0787262357187-0.159143012148-0.1124507191340.0405781605694-0.003117867224240.06962386051960.01518359738970.0270095543140.1579527075310.006665611104270.006966451714480.169272810685-0.009896455519550.164789145527-10.416352017261.4783982217-20.8893020842
Refinement TLS group

Refine-ID: X-RAY DIFFRACTION

IDRefine TLS-IDSelection detailsAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
11chain 'A' and (resid 11 through 77 )AA11 - 771 - 67
22chain 'A' and (resid 78 through 160 )AA78 - 16068 - 150
33chain 'A' and (resid 161 through 252 )AA161 - 252151 - 242
44chain 'A' and (resid 253 through 297 )AA253 - 297243 - 284
55chain 'A' and (resid 298 through 352 )AA298 - 352285 - 339
66chain 'B' and (resid 12 through 100 )BE12 - 1001 - 89
77chain 'B' and (resid 101 through 160 )BE101 - 16090 - 149
88chain 'B' and (resid 161 through 238 )BE161 - 238150 - 227
99chain 'B' and (resid 239 through 258 )BE239 - 258228 - 246
1010chain 'B' and (resid 259 through 352 )BE259 - 352247 - 340

+
About Yorodumi

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi

Thousand views of thousand structures

  • Yorodumi is a browser for structure data from EMDB, PDB, SASBDB, etc.
  • This page is also the successor to EM Navigator detail page, and also detail information page/front-end page for Omokage search.
  • The word "yorodu" (or yorozu) is an old Japanese word meaning "ten thousand". "mi" (miru) is to see.

Related info.:EMDB / PDB / SASBDB / Comparison of 3 databanks / Yorodumi Search / Aug 31, 2016. New EM Navigator & Yorodumi / Yorodumi Papers / Jmol/JSmol / Function and homology information / Changes in new EM Navigator and Yorodumi

Read more