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. 2013 Dec 12;9(12):e1003393. doi: 10.1371/journal.pcbi.1003393

Table 1. Structures representative of the 30 most populated protein meta-folds.

Symb Fig. 3 PDB code Molecule name
a 1AGI Angiogenin-1
b 1CHN Chemotaxis protein CheY
c 1FVQ Copper-transporting ATPase
d 1GND Rab GDP dissociation inhibitor alpha
e 1KTE Glutaredoxin-1 (Thioltransferase)
f 1LIT Lithostathine-1-alpha
g 1PDO Mannose Permease – IIA domain
h 1SDF Stromal cell-derived factor-1
i 1SUR PAPS Reductase
j 2HVM Hevamine
k 1BFG Basic fibroblast growth factor
l 1BJ7 Allergen Bos D2
m 1CQY β-amylase, Starch-binding domain
n 1CSP Cold shock protein B
o 1CZT Coagulation factor V, C2 domain
p 1J5D Plastocyanin
q 1KXA Sindbis virus capsid protein
r 1NSO Protease
s 1PHT P13-kinase, SH3 domain
t 1BSN F1-ATPase, ε subunit
u 1EMR Leukemia Inhibitory Factor
v 1IL6 Interleukin-6
w 1JLI Interleukin-3
x 1K40 Focal adhesion kinase, FAT domain
y 1LKI Leukemia Inhibitory Factor
z 1OOI Odorant binding protein LUSH
α 1OPC OMPR, Dna-binding domain
β 1FAS Fasciculin-1
γ 1I6F Alpha-like toxin CsEv5
δ 1SP2 SP1F2, zinc-finger dna binding domain

all-α, all-β and α/β). The three ultra representative proteins used in the protocol validation are in bold. The list is divided according to the SCOP fold group (in order