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.
Explore 3IWE in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 120-122 | 3 | |
| α-helix | 126-127 | 2 | |
| β-strand | 136 | 1 | 1 |
| α-helix | 140-142 | 3 | |
| α-helix | 149-153 | 5 | |
| β-strand | 156-160 | 5 | 2 |
| α-helix | 166-179 | 14 | |
| β-strand | 182 | 1 | 3 |
| β-strand | 188-190 | 3 | 3 |
| α-helix | 194-201 | 8 | |
| α-helix | 208-210 | 3 | |
| β-strand | 211-216 | 6 | 2 |
| β-strand | 222-235 | 14 | 2 |
| β-strand | 238-250 | 13 | 2 |
| α-helix | 252-254 | 3 | |
| α-helix | 259-272 | 14 | |
| β-strand | 279-283 | 5 | 2 |
| β-strand | 292-300 | 9 | 2 |
| α-helix | 303-308 | 6 | |
| α-helix | 320-327 | 8 | |
| β-strand | 338-340 | 3 | 2 |
| α-helix | 343-345 | 3 | |
| α-helix | 346-357 | 12 | |
| β-strand | 362-364 | 3 | 2 |
| α-helix | 368-375 | 8 | |
| β-strand | 378 | 1 | 2 |
| β-strand | 382-388 | 7 | 2 |
| β-strand | 394-402 | 9 | 2 |
| β-strand | 405-407 | 3 | 3 |
| β-strand | 415-416 | 2 | 3 |
| β-strand | 418-421 | 4 | 2 |
| β-strand | 425 | 1 | 2 |
| α-helix | 431-444 | 14 | |
| β-strand | 449-453 | 5 | 2 |
| α-helix | 458-460 | 3 | |
| β-strand | 468-479 | 12 | 2 |
| β-strand | 482 | 1 | 1 |
| β-strand | 486 | 1 | 2 |
| α-helix | 488-490 | 3 | |
| β-strand | 491 | 1 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 120-122 | 3 | |
| α-helix | 126-127 | 2 | |
| β-strand | 136 | 1 | 4 |
| α-helix | 140-142 | 3 | |
| α-helix | 149-152 | 4 | |
| β-strand | 156-160 | 5 | 5 |
| α-helix | 166-179 | 14 | |
| β-strand | 182 | 1 | 6 |
| β-strand | 188-190 | 3 | 6 |
| α-helix | 194-201 | 8 | |
| α-helix | 208-210 | 3 | |
| β-strand | 211-216 | 6 | 5 |
| β-strand | 222-235 | 14 | 5 |
| β-strand | 238-250 | 13 | 5 |
| α-helix | 252-254 | 3 | |
| α-helix | 259-272 | 14 | |
| β-strand | 279-283 | 5 | 5 |
| β-strand | 292-300 | 9 | 5 |
| α-helix | 303-308 | 6 | |
| α-helix | 320-327 | 8 | |
| β-strand | 338-340 | 3 | 5 |
| α-helix | 343-345 | 3 | |
| α-helix | 346-357 | 12 | |
| β-strand | 362-365 | 4 | 5 |
| α-helix | 368-375 | 8 | |
| β-strand | 378 | 1 | 5 |
| β-strand | 382-388 | 7 | 5 |
| β-strand | 394-402 | 9 | 5 |
| β-strand | 405-407 | 3 | 6 |
| α-helix | 414-415 | 2 | |
| β-strand | 416 | 1 | 6 |
| β-strand | 418-421 | 4 | 5 |
| β-strand | 425 | 1 | 5 |
| α-helix | 431-444 | 14 | |
| β-strand | 449-453 | 5 | 5 |
| α-helix | 458-460 | 3 | |
| β-strand | 468-479 | 12 | 5 |
| β-strand | 482 | 1 | 4 |
| β-strand | 486 | 1 | 5 |
| α-helix | 488-490 | 3 | |
| β-strand | 491 | 1 | 5 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Glycylpeptide N-tetradecanoyltransferase 1 | A, B | protein | 383 | Homo sapiens | P30419 (AlphaFold model) |
>3IWE_1 Glycylpeptide N-tetradecanoyltransferase 1 (chains A, B) GRSYQFWDTQPVPKLGEVVNTHGPVEPDKDNIRQEPYTLPQGFTWDALDLGDRGVLKELY TLLNENYVEDDDNMFRFDYSPEFLLWALRPPGWLPQWHCGVRVVSSRKLVGFISAIPANI HIYDTEKKMVEINFLCVHKKLRSKRVAPVLIREITRRVHLEGIFQAVYTAGVVLPKPVGT CRYWHRSLNPRKLIEVKFSHLSRNMTMQRTMKLYRLPETPKTAGLRPMETKDIPVVHQLL TRYLKQFHLTPVMSQEEVEHWFYPQENIIDTFVVENANGEVTDFLSFYTLPSTIMNHPTH KSLKAAYSFYNVHTQTPLLDLMSDALVLAKMKGFDVFNALDLMENKTFLEKLKFGIGDGN LQYYLYNWKCPSMGAEKVGLVLQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| MYA | Tetradecanoyl-CoA | C35 H62 N7 O17 P3 S | 2 |
| 646 | 2,6-dichloro-4-(2-piperazin-1-ylpyridin-4-yl)-N-(1,3,5-trimethyl-1H-pyrazol-4-y… | C21 H24 Cl2 N6 O2 S | 2 |
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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