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PID | QueryLength | Homolgous Sequence in PDB | UniProt Query | TITLE |
56766 | 306 | 213 | YP_009725301.1() | |
QUERYSEQ |
SGFRKMAFPSGKVEGCMVQVTCGTTTLNGLWLDDVVYCPRHVICTSEDMLNPNYEDLLIRKSNHNFLVQAGNVQLRVIGHSMQNCVLKLKVDTANPKTPKYKFVRIQPGQTFSVLACYNGSPSGVYQCAMRPNFTIKGSFLNGSCGSVGF NIDYDCVSFCYMHHMELPTGVHAGTDLEGNFYGPFVDRQTAQAAGTDTTITVNVLAWLYAAVINGDRWFLNRFTTTLNDFNLVAMKYNYEPLTQDHVDILGPLSAQTGIAVLDMCASLKELLQNGMNGRTILGSALLEDEFTPFDVVRQC SGVTFQ |
306 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
region | name | description |
![]() ![]() ![]() ![]() |
1-8 | DISORDER | predicted by DISOPRED (1-6,8-8) |
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306 | |||||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
pdb_id | a1 | identity[%]2 | description | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 main protease | |||
1.a1:asym_id for the homologue. 2.identity[%]2:sequence identity between the query and the homologue. |
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306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | inhibitor UAW241[4 aa] | A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | inhibitor UAW247[3 aa] | A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C | inhibitor UAW248[5 aa] | A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | Z-VAD(OMe)-FMK[5 aa] | A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | UAW243[4 aa] | A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-.. | A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 main protease |
![]() ![]() |
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B | N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-.. | A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 main protease |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
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306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B |
T8M
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T8J
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JFM
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
HU5
|
B | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
T8D
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T8A
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T71
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
T8Y
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T8V
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
V7G
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T8S
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T8P
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
UJ4
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T0J
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
NNA
|
B | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
AWP
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T0V
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T0S
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SV6
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T0Y
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Q5T
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 Main Protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U1M
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
JJG
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7A
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7G
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7D
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
SFY
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7J
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
QYS
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UGV
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7S
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7P
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7V
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
T84
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T81
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
RZG
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
GWS
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
TG3
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
TG3
|
A | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UH7
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UH4
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UH1
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T2J
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UGM
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UGG
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
B |
UGG
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T2G
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UGD
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T2Y
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
SZY
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UGS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UGP
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UPD
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T2V
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T9M
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
UPJ
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
6SU
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T9J
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
PK8
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
JGG
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
JGY
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
JGY
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
FHR
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
JGP
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
T9P
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
GKF
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NOL
|
A | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UHG
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T7Y
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UHA
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T1M
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
UHM
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
S7D
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T1J
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T4D
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T1V
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
NTG
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T1S
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T1Y
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
UHY
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
NEN
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NEN
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T4Y
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
FJC
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T4V
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
UJ1
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T4J
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
USD
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T4M
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
HV2
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
G65
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U0M
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
HWH
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UED
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
K0G
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U0V
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U0S
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U0P
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
E |
U0P
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X77
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U0Y
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
O6K
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() |
![]() |
D |
O6K
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
LPZ
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
V2M
|
B | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
C |
V2M
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T3J
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
3WL
|
A | 100.0 /100.0 |
13 /13 |
SARS-CoV-2 3CL protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U1A
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T3G
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
K1Y
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T47
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U1D
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
U1G
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
K1G
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
K1G
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T3V
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JRY
|
A | 100.0 /100.0 |
8 /8 |
SARS-CoV-2 virus Main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
U1V
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
U1V
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
K36
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
K36
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T6Y
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
USA
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T6V
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T6M
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T6J
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
LWA
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
P6N
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
P6N
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UHV
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
N |
UCS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
UCS
|
C | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T54
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
FK3
|
B | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
UHS
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A82
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T5Y
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
O0S
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
RZJ
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T5V
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
RZS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
NZD
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T5D
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T5D
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T5G
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
K3S
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
T67
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
US7
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
S7V
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
![]() |
|||||||
306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
NA
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
NA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Main Protease |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() |
![]() |
G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() |
![]() |
L |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
MG
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
MG
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Main Protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Main Protease |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() |
![]() |
O |
CL
|
C | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
![]() |
|||||||
306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[304 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 Replicase polyprotein 1ab[298 aa] | A | 100.0 /100.0 |
26 /26 |
R1AB_SARS2 Replicase polyprotein 1ab |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
![]() |
|||||||
306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
GOL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
GOL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
GOL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
GOL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
GOL
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
GOL
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
GOL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
GOL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 main protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
GOL
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
IMD
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Main Protease |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
FMT
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
FMT
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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F |
FMT
|
A | 85.7 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
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G |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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E |
HVB
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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B |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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D |
EDO
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
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B |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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D |
EDO
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
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C |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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C |
EDO
|
A | 80.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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E |
1PE
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
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C |
GLY
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
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C |
GLY
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
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E |
PG4
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
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B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 main protease |
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D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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B |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 Replicase polyprotein 1ab |
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C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
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H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
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E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
SARS-CoV-2 virus Main protease |
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E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
SARS-CoV-2 virus Main protease |
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C |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Main Protease |
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D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
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I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
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K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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H |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 main protease |
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H |
ACT
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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K |
PEG
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
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E |
PEG
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
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J |
PEG
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
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I |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Replicase polyprotein 1ab |
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E |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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F |
PEG
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 Replicase polyprotein 1ab |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. |