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FireProt: web server for automated design of thermostable proteins

Abstract

There is a continuous interest in increasing proteins stability to enhance their usability in numerous biomedical and biotechnological applications. A number of in silico tools for the prediction of the effect of mutations on protein stability have been developed recently. However, only single-point mutations with a small effect on protein stability are typically predicted with the existing tools and have to be followed by laborious protein expression, purification, and characterization. Here, we present FireProt, a web server for the automated design of multiple-point thermostable mutant proteins that combines structural and evolutionary information in its calculation core. FireProt utilizes sixteen tools and three protein engineering strategies for making reliable protein designs. The server is complemented with interactive, easy-to-use interface that allows users to directly analyze and optionally modify designed thermostable mutants. FireProt is freely available at http://loschmidt.chemi.muni.cz/fireprot.

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FireProt: web server for automated design of thermostable proteins

Author: Musil, Miloš
Publisher: Oxford University Press
Year: 2017
DOI: 10.1093/nar/gkx285
Source: https://dspace.vsb.cz/bitstreams/ed10f5db-a965-4214-adcb-b172edafcc8d/download
Published online 26 Ap il 2017 Nucleic Acids Resea ch, 2017, Vol. 45, Web Se e issue W393–W399
doi: 10.1093/na /gkx285
Fi eP o : web se e o au oma ed design o
he mos able p o eins
Milos Musil1,2,3,†, Jan S ou ac1,3,†, Ja osla Bendl1,2,3, Jan B ezo sky1,3, Zbynek P okop1,3,
Ja osla Zendulka2,4, Tomas Ma inek1,2,4, Da id Bedna 1,3,* and Ji i Dambo sky1,3,*
1Loschmid Labo a o ies, Depa men o Expe imen al Biology, Masa yk Uni e si y, B no, Czech Republic,
2Depa men o In o ma ion Sys ems, Facul y o In o ma ion Technology, B no Uni e si y o Technology, B no, Czech
Republic, 3In e na ional Cen e o Clinical Resea ch, S . Anne’s Uni e si y Hospi al B no, B no, Czech Republic and
4Cen e o Excellence IT4Inno a ions, Technical Uni e si y Os a a, Os a a
Recei ed Feb ua y 11, 2017; Re ised Ap il 02, 2017; Edi o ial Decision Ap il 10, 2017; Accep ed Ap il 11, 2017
ABSTRACT
The e is a con inuous in e es in inc easing p o-
eins s abili y o enhance hei usabili y in nume -
ous biomedical and bio echnological applica ions. A
numbe o
in silico
ools o he p edic ion o he
e ec o mu a ions on p o ein s abili y ha e been de-
eloped ecen ly. Howe e , only single-poin mu a-
ions wi h a small e ec on p o ein s abili y a e ypi-
cally p edic ed wi h he exis ing ools and ha e o be
ollowed by labo ious p o ein exp ession, pu i ica-
ion, and cha ac e iza ion. He e, we p esen Fi eP o ,
a web se e o he au oma ed design o mul iple-
poin he mos able mu an p o eins ha combines
s uc u al and e olu iona y in o ma ion in i s calcu-
la ion co e. Fi eP o u ilizes six een ools and h ee
p o ein enginee ing s a egies o making eliable
p o ein designs. The se e is complemen ed wi h
in e ac i e, easy- o-use in e ace ha allows use s
o di ec ly analyze and op ionally modi y designed
he mos able mu an s. Fi eP o is eely a ailable a
h p://loschmid .chemi.muni.cz/ i ep o .
INTRODUCTION
P o eins a e widely used in nume ous biomedical and
bio echnological applica ions. Howe e , na u ally occu -
ing p o eins canno usually wi hs and he ha sh indus ial
en i onmen , since hey a e mos ly e ol ed o unc ion a
mild condi ions (1). P o ein enginee ing has e olu ionized
he u iliza ion o na u ally a ailable p o eins o di e en
indus ial applica ions by imp o ing a ious p o ein ea-
u es such as s abili y, ac i i y o enan ioselec i i y o su -
pass hei na u al limi a ions. P o ein s abili y is gene ally
s ongly co ela ed wi h i s exp ession yield (2), hal -li e (3),
se um su i al ime (4) and pe o mance in he p esence o
dena u ing agen s (5). Thus, s abili y is one o he key de-
e minan s o p o eins applicabili y in bio echnological p o-
cesses.
In he ideal case, he sa u a ion mu agenesis would be
applied o e alua e e e y possible mu a ion on e e y posi-
ion o he enginee ed p o ein (6). Howe e , such a sea ch
space would be eno mous and he expe imen al e alua-
ion can delay he design o uly he mos able p o ein o
mon hs o e en yea s. The e o e, he e a e demands o e -
ec i e and p ecise p edic i e compu a ion o p o ein s a-
bili y. To sa is y his goal a numbe o in silico ools ha e
been de eloped ecen ly. Some o hese ools such as EASE-
MM (7), I-Mu an (8)o mCSM(9)a ebasedonma-
chine lea ning echniques. O he s a e using so-called ene -
ge ic unc ions. These p og ams can be u he ca ego ized
in o wo g oups. The i s g oup u ilizes a physical e ec i e
ene gy unc ion o simula ing he undamen al o ces be-
ween a oms and is ep esen ed by he p og ams like Rose a
(10) and E is (11). The second g oup is based on s a is ical
po en ials o which he ene gies a e de i ed om equen-
cies o esidues o a om con ac s epo ed in he da ase s
o expe imen ally cha ac e ized p o ein mu an s, e.g. Pop-
MuSiC (12) and FoldX (13). Howe e , due o he po en-
ially an agonis ic e ec o mu a ions, only single-poin mu-
a ions a e usually p edic ed in silico andha e obe ol-
lowed by labo ious and cos ly p o ein exp ession, pu i ica-
ion and cha ac e iza ion. Single-poin mu a ions ypically
enhance he mel ing empe a u e o a ge p o eins by uni s
o deg ee (3,14). A much highe deg ee o s abiliza ion can
be achie ed by cons uc ing mul iple-poin mu an s (15).
We ha e ecen ly de eloped he Fi eP o (16), combining
ene gy- and e olu ion-based app oaches o eliable design
o s able mul iple-poin mu an s. The p o ocol includes se -
e al p eceding il e s ha accele a e he calcula ion by omi -
ing po en ially dele e ious mu a ions. Fi eP o is cu en ly
*To whom co espondence should be add essed. Tel: +420 5 4949 3467; Fax: +420 5 4949 6302; Email: [email p o ec ed]uni.cz; Websi e add ess: h p://
loschmid .chemi.muni.cz/ i ep o ( ype o web se e : compu a ional wo k low)
Co espondence may also be add essed o Da id Bedna . Email: [email p o ec ed]uni.cz
†These au ho s con ibu ed equally o he wo k as i s au ho s.
C
The Au ho (s) 2017. Published by Ox o d Uni e si y P ess on behal o Nucleic Acids Resea ch.
This is an Open Access a icle dis ibu ed unde he e ms o he C ea i e Commons A ibu ion License (h p://c ea i ecommons.o g/licenses/by-nc/4.0/), which
pe mi s non-comme cial e-use, dis ibu ion, and ep oduc ion in any medium, p o ided he o iginal wo k is p ope ly ci ed. Fo comme cial e-use, please con ac
jou nals.pe [email protected]
W394 Nucleic Acids Resea ch, 2017, Vol. 45, Web Se e issue
a ailable only in a s and-alone o ma and equi es ex en-
si e expe ience in bioin o ma ics o ca y ou all necessa y
s eps o he wo k low. Cu en ly, we a e awa e o only one
se e o design o s able mul iple-poin mu an s - PROSS
(17), u ilizing Rose a modeling and phylogene ic sequence
in o ma ion in i s compu a ion co e.
He e, we p esen a web e sion o Fi eP o o he au o-
ma ed design o he mos able p o eins. Fi eP o in eg a es
six een compu a ional ools and u ilizes bo h sequence and
s uc u al in o ma ion. Fi eP o web se e p o ides use s
wi h he mos able p o eins, cons uc ed by h ee dis inc
s a egies: (i) e olu ion-based app oach, u ilizing back- o-
consensus analysis; (ii) ene gy-based app oach, e alua ing
change in ee ene gy upon mu a ion and (iii) combina ion
o bo h e olu ion-based and ene gy-based app oaches. In
ou iew, i is e y impo an o ha e his in eg a ed ap-
p oach, since phylogene ic analysis enables iden i ica ion o
he mu a ions s abilized by en opy, which canno be p e-
dic ed by o ce ield calcula ions (Bee ens e al., unde e-
iew). The se e allows use s o include p e e ed mu a-
ions in o he he mos able p o ein, o gene a e co espond-
ing s uc u es and sequences o gene syn heses. Compa ed
o he p e iously published Fi eP o p o ocol (16), mini-
mum e o and no bioin o ma ics knowledge is equi ed
om use s o calcula e and analyze he esul s. Fu he -
mo e, all inpu pa ame e s and compu a ional p o ocols
we e op imized o minimize o he wise highly ime demand-
ing p ocedu e. The se e was complemen ed wi h a g aph-
ical in e ace allowing use s o di ec ly analyze he p o ein
o in e es and design mul iple-poin mu an s.
MATERIALS AND METHODS
The basic wo k low o Fi eP o s a egy is ou lined in Fig-
u e 1. In o de o design a highly eliable he mos able
mul iple-poin mu an , a p o ein de ined by he use is an-
no a ed using se e al p edic ion ools and da abases (Phase
1). Wi h his knowledge in hand, ene gy- and e olu ion-
based app oach is applied o assemble a lis o po en ially
s abilizing single-poin mu a ions (Phase 2). Finally, h ee
mul iple-poin mu an s a e gene a ed in an addi i e man-
ne , while emo ing po en ially an agonis ic e ec s o mu-
a ions (Phase 3).
Phase 1: Anno a ion o he p o ein
Ini ially, he use is eques ed o speci y he p o ein s uc-
u e, ei he by p o iding i s PDB ID o by uploading a use -
de ined PDB ile. The biological assembly o he a ge p o-
ein is hen au oma ically gene a ed by he MakeMul ime
ool (h p://wa cu .uwa e loo.ca/ ools/makemul ime /). Se-
quence homologs a e ob ained by pe o ming a BLAST
sea ch (18) agains he UniRe 90 da abase (19), using he
a ge p o ein sequence as an inpu que y. Iden i ied ho-
mologs a e hen aligned wi h he que y p o ein using USE-
ARCH (20), while sequences whose iden i y wi h he que y
is below o abo e he use de ined h esholds (de aul : 30
and 90%) a e excluded om he lis o homologs. The
emaining sequences a e clus e ed using UCLUST (20),
wi h a 90% iden i y h eshold o emo e close homologs.
The clus e ep esen a i es a e so ed based on he BLAST
que y co e age and by de aul , he i s 200 o hem a e used
o c ea e a mul iple sequence alignmen wi h Clus al Omega
ool (21). The mul iple sequence alignmen is used o: (i)
es ima e he conse a ion coe icien o each esidue posi-
ion in he p o ein based on he Jensen–Shannon en opy
(22); (ii) iden i y co ela ed posi ions employing a consen-
sual decision o he OMES (23), MI (24), aMIc (25), DCA
(26), SCA (27), ELSC (28), McBASC (29) and (iii) analyze
amino acid equencies a indi idual posi ions wi hin he
p o ein.
Phase 2: P edic ion o single-poin mu a ions
In acco dance wi h he o iginal Fi eP o p o ocol, po en-
ially s abilizing single-poin mu a ions a e iden i ied ia
wo sepa a e b anches: one elying on he es ima ion o he
change o ee ene gy upon mu a ion and second u ilizing
back- o-consensus app oach.
The i s , ene gy-based app oach is employing FoldX and
Rose a ools ha pe o med bes on ou es ing da ase .
P eceding il e s accele a e he calcula ion by omi ing po-
en ially dele e ious mu a ions. P io o he iden i ica ion o
he single-poin mu a ions i sel , he a ge p o ein s uc u e
is amended and minimized. FoldX p o ocol is u ilized o ill
in he missing a oms in he esidues and pa ched s uc u e
is consequen ly minimized wi h Rose a minimiza ion mod-
ule. Conse ed and co ela ed posi ions a e immedia ely ex-
cluded om u he analysis. I was obse ed ha unc-
ional and s uc u al cons ain s in p o eins gene ally lead
o he conse a ion o amino acid esidues (30–33). Simi-
la ly, co ela ed esidues o dina ily help o main ain p o-
ein unc ion, olding o s abili y (34–36). Mu a ions con-
duc ed on hese posi ions a e he e o e conside ed unsa e
by cu en Fi eP o s a egy, e en hough he e is ce ainly
a space o mo e sophis ica ed ea men o co ela ed posi-
ions, which will be u he de eloped in u u e e sions o
Fi eP o se e .
The emaining posi ions a e subjec ed o sa u a ion mu-
agenesis by using FoldX ool. Mu a ions wi h p edic ed
ddG o e gi en h eshold (de aul : –1 kcal/mol) a e s ee ed
away and es is o wa ded o Rose a calcula ions. Finally,
he mu a ions p edic ed by Rose a as s ongly s abilizing
(de aul cu -o : –1 kcal/mol) a e agged as po en ial candi-
da es o he design o he mul iple-poin mu an s.
A high ime demands o Rose a analysis we e one o
he mos exc ucia ing issues wi h he o iginal Fi eP o p o-
ocol. E en wi h he applica ion o il e s o e 100 mu a-
ions was usually le o p ecise, bu slow, Rose a calcula-
ions. Fo his eason, we ha e e alua ed se e al o ce ields
and Rose a p o ocols wi h he newly assembled da ase
con aining 1573 mu a ions om P oThe m da abase (37)
and Ho MuSiC da ase (38). Based on he esul s o he
e alua ions, he bes ade-o be ween he ime equi e-
men s and p ecision was selec ed. Wi h Rose a p o ocol 3,
we ha e achie ed mo e han en old inc ease in calcula ion
speed while p ese ing high p edic ion accu acy. De ails on
da ase cons uc ion and p o ocols e alua ion can be ound
in he Supplemen 1 (Supplemen a y Tables S1–S5).
The second app oach is based on he in o ma ion ob-
ained om mul iple sequence alignmen . The mos com-
mon amino acid in each posi ion o p o ein sequence o en
Nucleic Acids Resea ch, 2017, Vol. 45, Web Se e issue W395
Figu e 1. Wo k low o Fi eP o s a egy.
p o ides a non-negligible e ec on p o ein s abili y (39–42).
The e o e, Fi eP o implemen s majo i y and equency a-
io app oach o iden i y mu a ions a posi ions whe e he
wild- ype amino acid di e s om he mos p e alen one.
By de aul , he single ou mu a ions a e loca ed in he posi-
ions whe e he consensus esidue is p esen in a leas 50%
o all analyzed sequences (majo i y me hod) o whe e con-
sensus esidue equency is 40% and is a leas i e imes
mo e equen han he wild- ype amino acid ( equency a-
io me hod). These h esholds we e chosen in acco dance o
he p e iously published Ho Spo Wiza d me hod (43). Se-
lec ed mu a ions a e e alua ed by FoldX and he s abilizing
ones a e lis ed as candida e mu a ions o he enginee ing
o mul iple-poin mu an .
Phase 3: Design o he mos able p o ein
In o al, h ee p o ein designs a e p o ided by Fi eP o
s a egy. The i s design includes only he mu a ions om
ene gy-based app oach, he second con ains he mu a ions
sugges ed by he e olu ion-based app oach and he hi d is
he combina ion o bo h. Na u ally, because o po en ially
an agonis ic e ec s be ween indi idual mu a ions, we can-
no combine indi idual mu a ions blindly.
To a oid possible clashes, Fi eP o s a egy is ying o
minimize an agonis ic e ec s by u ilizing Rose a. In he
i s s ep, all pai s o single-poin mu a ions wi hin he ange
o 10 ˚
A a e e alua ed sepa a ely o ene gy- and e olu ion-
based app oach. Once change in ee ene gy is ob ained o
all esidue pai s, Fi eP o s a s o in oduce hem in o he
mul iple-poin mu an in he o de based on hei p edic ed
W396 Nucleic Acids Resea ch, 2017, Vol. 45, Web Se e issue
s abili y, excluding he mu a ions ha a e colliding wi h al-
eady included mu a ions. Algo i hm s ops once he e a e
no mu a ions le o he s abilizing e ec o analyzed pai
d ops below de ined h eshold.
Upon he comple ion o p e ious s ep, p ocedu e is e-
pea ed his ime conside ing only he pai s be ween he
mu a ions chosen o he cons uc ion o ene gy- and
e olu ion-based mu an s. Finally, s uc u es o all h ee mu-
an s a e modeled using he Rose a p o ocol 16.
DESCRIPTION OF THE WEB SERVER
Inpu
The only equi ed inpu o he web se e is a e ia y s uc-
u e o he p o ein o in e es , p o ided ei he as a PDB ID
o a use -de ined PDB ile. The use can hen choose a p e-
de ined biological uni gene a ed by he MakeMul ime ool
o manually selec chains o which he calcula ion should
be pe o med. The calcula ions can be con igu ed in ei he
basic o ad anced mode.
In he basic mode, use is allowed o change he se ing o
BLAST sea ch and alignmen cons uc ion. The ad anced
mode expands he lis o modi iable pa ame e s by he ones
connec ed wi h: (i) he iden i ica ion o consensus esidues
by majo i y and equency a io app oach, (ii) he h esh-
olds used by FoldX and Rose a p edic ion ools and (iii)
he decision h eshold employed in he consensual analysis
o co ela ed posi ions. Ad anced mode allows expe use s
o ine- une he pa ame e s o calcula ion acco ding o s ud-
ied sys ems. Howe e , he p esen ed de aul alues a e op-
imized o p o ide eliable esul s o mos o he sys ems
and we he e o e do no ad ice hei change in he gene al
scena ios.
Ou pu
Upon submission, a unique iden i ie is assigned o each job
o ack he calcula ion and he ‘Resul s b owse ’ in o ms
he use abou he s a us o he indi idual s eps in he Fi e-
P o wo k low (Figu e 2B). Once he job is inished, use s
can ei he di ec ly download he esul s in he .zip a chi e o
na iga e hemsel es in o he ‘Resul s page’ o u he anal-
ysis. The ‘Resul s page’ is in ui i ely o ganized in o se e al
panels as desc ibed below.
P o ein isualiza ion. The wild- ype and he mu an s uc-
u e is in e ac i ely isualized in he web b owse (Fig-
u e 2D) u ilizing he Jsmol apple (h p://wiki.jmol.o g/
index.php/JSmol). Use s can swi ch be ween di e en p o-
ein isualiza ion s yles and also highligh selec ed amino
acids in he p o ein s uc u e. Residues ha we e included
in o ene gy-based mu an a e colo ed in o ange, e olu ion-
based mu a ions a e in blue and all o he esidues a e in
g ay. Use selec ed esidues ha we e no pa o any mu-
an a e unde lined in ed.
Mu an o e iew. The ‘Mu an o e iew’ panel is o ga-
nized in o ou abs (Figu e 2A). The i s h ee abs p o-
ide in o ma ion abou mu a ions included in o combined,
ene gy-based and e olu ion-based mu an . The checkbox,
allowing use s o isualize he chosen esidues in Jsmol ap-
ple , can be ound in each ow oge he wi h all da a ele-
an o a gi en compu a ional app oach. The las ab con-
ains he lis o all esidues in he wild- ype s uc u e. While
‘wild- ype’ ab is ac i e, he wild- ype s uc u e is isualized
in Jsmol apple ins ead o he mu a ed one and he use is
allowed o in oduce use -de ined mu a ions in o mul iple-
poin mu an ia he ‘plus’ icon in he las column.
Gene al in o ma ion. The ‘Fi eP o p o ocol design’ panel
p o ides use s wi h gene al in o ma ion abou he a ge
p o ein and he designs cons uc ed by Fi eP o s a egy,
such as a numbe o mu a ions and es ima ed change in ee
ene gy (Figu e 2C).
Mu an designe . The ‘Mu an designe ’ panel allows he
use o design own mul iple-poin mu an by managing mu-
a ions di ided in o ene gy- and e olu ion-based subse . I
all mu a ions in he subse ha e hei p edic ed ene gy al-
ues assigned, a o al change in Gibbs ee ene gy is im-
media ely es ima ed assuming simple addi i i y. Use s can
also gene a e an amino acid sequence om he designed
mul iple-poin mu an ha combines mu a ions included
in o ene gy- and e olu ion-based subse s. All p epa ed de-
signs can be downloaded in one .zip a chi e (Figu e 2E).
EXPERIMENTAL VALIDATION
The o iginal Fi eP o s a egy was expe imen ally e i-
ied wi h h ee p o eins (haloalkane dehalogenase DhaA,
PDB ID 4E46; ␥-hexachlo ocyclohexane dehyd ochlo i-
nase LinA, PDB ID 3A76; and ib oblas g ow h ac o
2, PDB ID 4OEE) and p o ided espec i e s abiliza ion o
p o eins Tm=25, 21 and 15◦C(Table1). The o iginal
p o ocol was modi ied o enable ully au oma ed calcula-
ion a he easonable ime, while main aining high p e-
dic ion accu acy (Supplemen a y Table S6). P edic ion o
eigh mul iple-poin mu an s using his modi ied p o ocol
was alida ed using he da a o FRESCO (44) and iden i-
ied mu a ions we e compa ed wi h ano he online p o ein
s abiliza ion ool PROSS (17). Fi eP o and PROSS showed
simila p edic i e powe , co ec ly iden i ying 29 and 20 po-
en ially s abilizing posi ions, espec i ely (Supplemen a y
Table S7).
CONCLUSIONS AND OUTLOOK
Fi eP o is a web se e ha p o ides use s wi h a one-
s op-shop solu ion o he design o he mos able mul iple-
poin mu an p o eins. In compa ison wi h he s andalone
Fi eP o s a egy (16), all de aul pa ame e s and compu-
a ional p o ocols we e op imized o inc ease he calcula-
ion speed, while main aining he p edic ion accu acy. The
designs p oduced by he Fi eP o wo k low we e expe -
imen ally e i ied and hus use s can ob ain highly eli-
able he mos able p o eins wi h minimal expe imen al e -
o . The se e is complemen ed by an easy- o-use g aphi-
cal in e ace ha allows use s o in e ac i ely analyze indi-
idual mu a ions selec ed as a pa o ene gy- o e olu ion-
based app oach oge he wi h he abili y o design hei own
mul iple-poin mu an s on op o ou obus s a egy.
Nucleic Acids Resea ch, 2017, Vol. 45, Web Se e issue W397
Figu e 2. Fi eP o ’s g aphical use in e ace showing he esul s ob ained o he haloalkane dehalogenase DhaA (PDB ID: 4e46). (A) The ‘Mu an
o e iew’ panel p o ides a lis o mu a ions in oduced in o p o ein s uc u e. (B) The ‘Repo ’ panel shows he s a us o calcula ion in he indi idual
s eps o he compu a ional pipeline. (C) The ‘P o ocol design’ panel p o ides gene al in o ma ion abou Fi eP o designs. (D) The JSmol ´Viewe ´ allows
in e ac i e isualiza ion o he p o ein. (E) The ‘Mu an designe ’ panel enables manual adjus men o a new combined mu an .
Table 1. Expe imen al alida ion o Fi eP o s a egy
P o ein Ene gy-based mu a ions E olu ion-based mu a ions Tm[◦C]
PDB ID
4E46 8 3 +25
3A76 4 3 +21
4OEE 4 2 +15

W398 Nucleic Acids Resea ch, 2017, Vol. 45, Web Se e issue
The au oma ion o he whole p ocedu e makes he p o-
cess o he design o he mos able p o eins accessible o
use s wi hou any p io expe ise in bioin o ma ics since i
elimina es he need o selec , ins all and e alua e ools, op-
imize hei pa ame e s, and in e p e in e media e esul s.
Howe e , he ene gy-based app oach o he Fi eP o s a -
egy depends on he quali y o p o ided p o ein s uc u e
and he e o e he p edic ion accu acy migh be comp o-
mised in he case o low- esolu ion s uc u es o homology
models.
In he u u e, we plan o implemen new s a egies such as
a design based on he analysis o co ela ed posi ions ha
would con ibu e o he cons uc ion o he inal combined
mu an , elimina ion o highly lexible egions and in oduc-
ion o disul ide b idges. Also, we plan o equip Fi eP o
wi h se e al new il e s, e.g. exclusion o he amino acids lo-
ca ed in he close neighbo hoods o he ac i e si es o he
ones pa icipa ing in oligome iza ion.
SUPPLEMENTARY DATA
Supplemen a y Da a a e a ailable a NAR Online.
ACKNOWLEDGEMENTS
We would like o hank he de elope s o PROSS Adi
Goldenzweig and D Sa el Fleishman (Weizmann Ins i-
u e o Science, Is ael) o p o iding he da a se o al-
ida ion pu poses. Compu a ional esou ces we e supplied
by he Minis y o Educa ion, You h and Spo s o he
Czech Republic unde he P ojec s CESNET (P ojec No.
LM2015042) and CERIT-Scien i ic Cloud (P ojec No.
LM2015085) p o ided wi hin he p og am P ojec s o La ge
Resea ch, De elopmen and Inno a ions In as uc u es.
FUNDING
This esea ch and open access cha ge was unded by Min-
is y o Educa ion, You h and Spo s o he Czech Re-
public om he Na ional P og amme o Sus ainabili y II
[LQ1605, LO1214]; Eu opean Regional De elopmen Fund
[ELIXIR-CZ LM2015047]; G an Academy o he Czech
Republic [16-06096S]; B no Uni e si y Technology [FIT-S-
17-3964].
Con lic o in e es s a emen . None decla ed.
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