7NKU: Diazaborine bound Drg1(AFG2)

diazaborine bound Drg1(AFG2). Determined by electron microscopy at 3.4 Å resolution. Released 23 Jun 2021.

Method
Electron microscopy
Resolution
3.4 Å
Organism
Saccharomyces cerevisiae (strain ATCC 204508 / S288c)
Chains
6
Atoms
25,332
Mol. weight
517.02 kDa
Ligands
TDB, AGS
Released
23 Jun 2021

Explore 7NKU in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7NKU contains 197 α-helices and 91 β-strands across 6 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 31 helices, 13 β-strands

ElementResiduesLengthSheet
α-helix251-26212
α-helix269-2746
β-strand282-28431
α-helix292-30211
β-strand306-31051
α-helix312-3143
α-helix320-33617
β-strand340-34561
α-helix347-3493
α-helix363-37412
β-strand383-38861
β-strand407-40931
α-helix416-42914
β-strand43512
α-helix439-4479
α-helix455-47521
β-strand48612
α-helix488-49811
α-helix522-5287
α-helix529-5335
α-helix534-5363
α-helix539-5446
α-helix548-5503
β-strand552-55653
α-helix564-5729
β-strand577-58263
α-helix584-5874
α-helix593-60715
β-strand611-61663
α-helix618-6203
α-helix628-64417
α-helix647-6493
β-strand653-65973
α-helix662-6643
α-helix667-6693
β-strand675-68063
α-helix684-6852
α-helix686-69611
α-helix703-7053
α-helix709-7157
α-helix721-73818
α-helix747-75610
α-helix763-77513
β-strand77813
Chain B: 34 helices, 18 β-strands
ElementResiduesLengthSheet
α-helix240-2423
α-helix251-26212
α-helix269-2724
α-helix277-2782
β-strand282-28434
α-helix292-30211
β-strand306-31054
α-helix312-3143
α-helix320-33617
β-strand340-34564
α-helix347-3493
α-helix363-37412
β-strand383-38864
β-strand407-40934
α-helix416-42914
β-strand43515
α-helix439-4479
α-helix455-47521
β-strand48615
α-helix488-49811
α-helix5061
β-strand50816
α-helix509-5102
α-helix522-5287
α-helix529-5335
α-helix534-5374
α-helix539-5457
α-helix548-5503
β-strand552-55656
β-strand55917
β-strand56117
α-helix564-5729
β-strand57716
β-strand580-58236
α-helix584-5874
α-helix591-60717
β-strand611-61666
α-helix618-6203
α-helix629-64416
α-helix647-6493
β-strand653-65976
α-helix662-6643
α-helix667-6693
β-strand675-68066
α-helix686-69611
α-helix703-7053
α-helix709-7157
α-helix721-73818
α-helix747-7559
β-strand75718
α-helix763-77513
β-strand77816
Chain C: 33 helices, 14 β-strands
ElementResiduesLengthSheet
α-helix240-2423
α-helix251-26212
α-helix269-2724
α-helix277-2793
β-strand281-28449
α-helix292-30211
β-strand306-31059
α-helix312-3143
α-helix320-33617
β-strand340-34569
α-helix347-3493
α-helix363-37412
β-strand383-38869
β-strand405-40959
α-helix416-42914
β-strand435110
α-helix439-4479
α-helix455-47521
β-strand486110
α-helix488-49811
α-helix5061
β-strand50818
α-helix522-5287
α-helix529-5335
α-helix539-5457
α-helix548-5503
β-strand552-55658
α-helix564-5729
β-strand577-58268
α-helix583-5853
α-helix591-60717
β-strand611-61668
α-helix618-6203
α-helix629-64416
α-helix647-6493
β-strand653-65978
α-helix662-6643
α-helix667-6693
β-strand675-68068
α-helix686-69611
α-helix703-7053
α-helix709-7157
α-helix721-73818
α-helix747-75610
α-helix757-7593
α-helix763-77513
β-strand77818
Chain D: 35 helices, 14 β-strands
ElementResiduesLengthSheet
α-helix240-2423
α-helix251-26212
α-helix268-2725
α-helix277-2782
β-strand282-284311
α-helix292-30211
β-strand306-310511
α-helix312-3143
α-helix320-33617
β-strand340-345611
α-helix347-3493
α-helix363-37412
β-strand383-388611
β-strand407-409311
α-helix416-42914
β-strand435112
α-helix439-4479
α-helix455-47521
α-helix484-4852
β-strand486112
α-helix488-49811
α-helix5061
β-strand508113
α-helix522-5287
α-helix529-5335
α-helix534-5374
α-helix539-5457
α-helix548-5503
β-strand552-556513
α-helix564-5729
β-strand577-581513
α-helix583-5864
α-helix591-60717
β-strand611-616613
α-helix618-6203
α-helix627-6304
α-helix633-64412
α-helix647-6493
β-strand653-659713
α-helix662-6643
α-helix667-6693
β-strand675-680613
α-helix686-69611
α-helix703-7053
α-helix709-7157
α-helix721-73818
α-helix747-75610
α-helix763-77412
β-strand778113
Chain E: 34 helices, 18 β-strands
ElementResiduesLengthSheet
α-helix240-2423
α-helix251-26212
α-helix268-2736
α-helix276-2783
β-strand282-284314
α-helix292-30211
β-strand306-310514
α-helix312-3143
α-helix320-33617
β-strand340-345614
α-helix347-3493
α-helix363-37412
β-strand383-388614
β-strand407-409314
α-helix416-42914
β-strand435115
α-helix439-4479
α-helix455-47521
α-helix484-4852
β-strand486115
α-helix488-49811
α-helix5061
β-strand508116
α-helix509-5102
α-helix522-5287
α-helix529-5335
α-helix534-5374
α-helix539-5457
α-helix548-5503
β-strand552-556516
β-strand559117
β-strand561117
α-helix564-5729
β-strand577116
β-strand580-582316
α-helix583-5864
α-helix591-60717
β-strand611-616616
α-helix618-6203
α-helix628-64518
α-helix647-6493
β-strand653-659716
α-helix662-6643
α-helix667-6693
β-strand677-680416
α-helix686-69611
α-helix709-7157
α-helix721-73818
α-helix747-7559
β-strand757118
α-helix763-77513
β-strand778116
Chain F: 30 helices, 14 β-strands
ElementResiduesLengthSheet
α-helix240-2423
α-helix251-26212
α-helix269-2724
β-strand282-284319
α-helix292-30211
β-strand306-310519
α-helix312-3143
α-helix320-33617
β-strand340-345619
α-helix347-3493
α-helix363-37412
β-strand383-388619
β-strand407-409319
α-helix416-42914
β-strand435120
α-helix439-4479
α-helix455-47521
β-strand486120
α-helix488-49811
α-helix5061
β-strand508118
α-helix522-5287
α-helix529-5335
α-helix539-5446
α-helix548-5503
β-strand552-556518
α-helix564-5729
β-strand577-582618
α-helix583-5853
α-helix591-60717
β-strand611-616618
α-helix618-6203
α-helix627-64519
α-helix647-6493
β-strand653-659718
α-helix662-6643
β-strand677-680418
α-helix686-69611
α-helix703-7053
α-helix709-7157
α-helix721-73818
α-helix747-75610
α-helix763-77513
β-strand778118

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
ATPase family gene 2 proteinA, B, C, D, E, Fprotein780Saccharomyces cerevisiae (strain ATCC 204508 / S288c)P32794 (AlphaFold model)
Sequence of entity 1 (A, B, C, D, E, F), FASTA
>7NKU_1 ATPase family gene 2 protein (chains A, B, C, D, E, F)
MAPKSSSSGSKKKSSASSNSADAKASKFKLPAEFITRPHPSKDHGKETCTAYIHPNVLSS
LEINPGSFCTVGKIGENGILVIARAGDEEVHPVNVITLSTTIRSVGNLILGDRLELKKAQ
VQPPYATKVTVGSLQGYNILECMEEKVIQKLLDDSGVIMPGMIFQNLKTKAGDESIDVVI
TDASDDSLPDVSQLDLNMDDMYGGLDNLFYLSPPFIFRKGSTHITFSKETQANRKYNLPE
PLSYAAVGGLDKEIESLKSAIEIPLHQPTLFSSFGVSPPRGILLHGPPGTGKTMLLRVVA
NTSNAHVLTINGPSIVSKYLGETEAALRDIFNEARKYQPSIIFIDEIDSIAPNRANDDSG
EVESRVVATLLTLMDGMGAAGKVVVIAATNRPNSVDPALRRPGRFDQEVEIGIPDVDARF
DILTKQFSRMSSDRHVLDSEAIKYIASKTHGYVGADLTALCRESVMKTIQRGLGTDANID
KFSLKVTLKDVESAMVDIRPSAMREIFLEMPKVYWSDIGGQEELKTKMKEMIQLPLEASE
TFARLGISAPKGVLLYGPPGCSKTLTAKALATESGINFLAVKGPEIFNKYVGESERAIRE
IFRKARSAAPSIIFFDEIDALSPDRDGSSTSAANHVLTSLLNEIDGVEELKGVVIVAATN
RPDEIDAALLRPGRLDRHIYVGPPDVNARLEILKKCTKKFNTEESGVDLHELADRTEGYS
GAEVVLLCQEAGLAAIMEDLDVAKVELRHFEKAFKGIARGITPEMLSYYEEFALRSGSSS

Ligands and cofactors

IDNameFormulaCopies
TDB6-methyl-2(PROPANE-1-sulfonyl)-2H-THIENO[3,2-D][1,2,3]DIAZABORININ-1-olC9 H13 B N2 O3 S26
AGSPhosphothiophosphoric acid-adenylate esterC10 H16 N5 O12 P3 S12

Primary citation

Structural basis for inhibition of the AAA-ATPase Drg1 by diazaborine. Prattes, M., Grishkovskaya, I., Hodirnau, V.V. et al. Nat Commun (2021) 12:3483-3483. DOI 10.1038/s41467-021-23854-x · PubMed

Other PDB entries of the same protein (UniProt P32794 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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