3IWE: Glycylpeptide N-tetradecanoyltransferase 1

Crystal Structure of human type-I N-myristoyltransferase with bound myristoyl-CoA and inhibitor DDD85646. Determined by X-ray diffraction at 1.79 Å resolution. Released 15 Sept 2009.

Method
X-ray diffraction
Resolution
1.79 Å
Organism
Homo sapiens
Chains
2
Atoms
7,527
Mol. weight
92.03 kDa
Ligands
MYA, 646
Released
15 Sept 2009

Explore 3IWE in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3IWE contains 35 α-helices and 46 β-strands across 2 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: 17 helices, 23 β-strands

ElementResiduesLengthSheet
α-helix120-1223
α-helix126-1272
β-strand13611
α-helix140-1423
α-helix149-1535
β-strand156-16052
α-helix166-17914
β-strand18213
β-strand188-19033
α-helix194-2018
α-helix208-2103
β-strand211-21662
β-strand222-235142
β-strand238-250132
α-helix252-2543
α-helix259-27214
β-strand279-28352
β-strand292-30092
α-helix303-3086
α-helix320-3278
β-strand338-34032
α-helix343-3453
α-helix346-35712
β-strand362-36432
α-helix368-3758
β-strand37812
β-strand382-38872
β-strand394-40292
β-strand405-40733
β-strand415-41623
β-strand418-42142
β-strand42512
α-helix431-44414
β-strand449-45352
α-helix458-4603
β-strand468-479122
β-strand48211
β-strand48612
α-helix488-4903
β-strand49112
Chain B: 18 helices, 23 β-strands
ElementResiduesLengthSheet
α-helix120-1223
α-helix126-1272
β-strand13614
α-helix140-1423
α-helix149-1524
β-strand156-16055
α-helix166-17914
β-strand18216
β-strand188-19036
α-helix194-2018
α-helix208-2103
β-strand211-21665
β-strand222-235145
β-strand238-250135
α-helix252-2543
α-helix259-27214
β-strand279-28355
β-strand292-30095
α-helix303-3086
α-helix320-3278
β-strand338-34035
α-helix343-3453
α-helix346-35712
β-strand362-36545
α-helix368-3758
β-strand37815
β-strand382-38875
β-strand394-40295
β-strand405-40736
α-helix414-4152
β-strand41616
β-strand418-42145
β-strand42515
α-helix431-44414
β-strand449-45355
α-helix458-4603
β-strand468-479125
β-strand48214
β-strand48615
α-helix488-4903
β-strand49115

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Glycylpeptide N-tetradecanoyltransferase 1A, Bprotein383Homo sapiensP30419 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>3IWE_1 Glycylpeptide N-tetradecanoyltransferase 1 (chains A, B)
GRSYQFWDTQPVPKLGEVVNTHGPVEPDKDNIRQEPYTLPQGFTWDALDLGDRGVLKELY
TLLNENYVEDDDNMFRFDYSPEFLLWALRPPGWLPQWHCGVRVVSSRKLVGFISAIPANI
HIYDTEKKMVEINFLCVHKKLRSKRVAPVLIREITRRVHLEGIFQAVYTAGVVLPKPVGT
CRYWHRSLNPRKLIEVKFSHLSRNMTMQRTMKLYRLPETPKTAGLRPMETKDIPVVHQLL
TRYLKQFHLTPVMSQEEVEHWFYPQENIIDTFVVENANGEVTDFLSFYTLPSTIMNHPTH
KSLKAAYSFYNVHTQTPLLDLMSDALVLAKMKGFDVFNALDLMENKTFLEKLKFGIGDGN
LQYYLYNWKCPSMGAEKVGLVLQ

Ligands and cofactors

IDNameFormulaCopies
MYATetradecanoyl-CoAC35 H62 N7 O17 P3 S2
6462,6-dichloro-4-(2-piperazin-1-ylpyridin-4-yl)-N-(1,3,5-trimethyl-1H-pyrazol-4-y…C21 H24 Cl2 N6 O2 S2

Primary citation

Crystal Structure of human type-I N-myristoyltransferase with bound myristoyl-CoA and inhibitor DDD85646. Qiu, W., Hutchinson, A., Wernimont, A. et al. To be published.

Other PDB entries of the same protein (UniProt P30419 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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