SitesBLAST

SitesBLAST – Find functional sites

SitesBLAST

Comparing WP_068331067.1 NCBI__GCF_001650345.1:WP_068331067.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.

Or try Sites on a Tree, PaperBLAST, Conserved Domains, or compare to all protein structures

Found 13 hits to proteins with known functional sites (download)

P0A6L0 Deoxyribose-phosphate aldolase; DERA; 2-deoxy-D-ribose 5-phosphate aldolase; Phosphodeoxyriboaldolase; Deoxyriboaldolase; EC 4.1.2.4 from Escherichia coli (strain K12) (see 2 papers)
75% identity, 100% coverage: 1:257/257 of query aligns to 1:259/259 of P0A6L0

query
sites
P0A6L0

M

M

S

T

E

D

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

D

L

L

T

T

L

L

N

N

D

D

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

A

V

I

C
|
C

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

K

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

A

T

T

V

V

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

Y

G

G

A

A

D

D

E

E

V

V

D
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D

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K
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K

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

F

I

I

K
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K

T

T

S

S

T

T

G

G

K

K

V

V

P

A

V

V

N

N

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K
|
K

P

P

A

A

G

G

V

V

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

R

F

F

G

G

A

A

S

S

L

L

A

A

N

S

L

L

H

K

T

A

L

L

G

G

E

H

G

G

E

D

K

G

A

K

A

S

E

A

G

S

Y
|
Y

C47 (= C47) mutation C->A,S: 3-fold decrease in catalytic efficiency.
D102 (= D102) mutation to E: 44-fold decrease in catalytic efficiency.; mutation to L: 2000-fold decrease in catalytic efficiency.; mutation to N: 1500-fold decrease in catalytic efficiency.
K137 (= K135) mutation to L: 20-fold decrease in catalytic efficiency.
K167 (= K165) active site, Schiff-base intermediate with acetaldehyde; modified: N6-acetyllysine; mutation to L: 1000-fold decrease in catalytic efficiency.; mutation to R: 20-fold decrease in catalytic efficiency.
K201 (= K199) mutation to L: 1500-fold decrease in catalytic efficiency.; mutation to R: 1000-fold decrease in catalytic efficiency.
Y259 (= Y257) mutation to F: 200-fold decrease in catalytic efficiency.

1jcjA Observation of covalent intermediates in an enzyme mechanism at atomic resolution (see paper)
77% identity, 97% coverage: 1:249/257 of query aligns to 2:252/252 of 1jcjA

query
sites
1jcjA

M

M

S

T

E

D

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

D

L

L

T

T

L

L

N

N

D

D

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

A

V

I

C

C

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

K

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

A

T

T

V

V

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

Y

G

G

A

A

D

D

E

E

V

V

D
|
D

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K

K

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

F

I

I

K
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K

T

T

S

S

T
|
T

G

G

K

K

V

V

P

A

V

V

N

N

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K
x
L

P

P

A

A

G
|
G

G

G

V

V

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

R

F

F

G
|
G

A
|
A

S
|
S

S

S

L

L

A

A

N

S

L

L

H

K

T

A

L

L

G

G

E

H

G

G

active site: D103 (= D102), K168 (= K165), L202 (≠ K199)
binding 1-hydroxy-pentane-3,4-diol-5-phosphate: K168 (= K165), T171 (= T168), G205 (= G202), G237 (= G234), A238 (= A235), S239 (= S236)

6z9iB Escherichia coli d-2-deoxyribose-5-phosphate aldolase - n21k mutant complex with reaction products (see paper)
77% identity, 90% coverage: 3:234/257 of query aligns to 1:234/248 of 6z9iB

query
sites
6z9iB

E

D

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

D

L

L

T

T

L

L

N

K

D

D

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

A

V

I

C

C

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

K

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

A

T

T

V

V

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

Y

G

G

A

A

D

D

E

E

V

V

D

D

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K

K

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

F

I

I

K

K

T

T

S

S

T
|
T

G

G

K

K

V

V

P

A

V

V

N

N

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K

K

P

P

A

A

G
|
G

V

V

R
|
R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

R

F

F

G
|
G

binding glyceraldehyde-3-phosphate: T168 (= T168), G202 (= G202), G203 (= G203), R205 (= R205), G234 (= G234)

Sites not aligning to the query:

binding glyceraldehyde-3-phosphate: 235, 236

5el1A Crystal structure of deoxyribose-phosphate aldolase from escherichia coli (k58e-y96w mutant) after acetaldehyde treatment (see paper)
77% identity, 90% coverage: 3:234/257 of query aligns to 1:234/248 of 5el1A

query
sites
5el1A

E

D

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

D

L

L

T
|
T

T

T

L

L

N

N

D

D

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

A

V

I

C
|
C

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

E

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

A

T

T

V

V

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

W

G

G

A

A

D

D

E

E

V

V

D
|
D

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K

K

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

F

I

I

K
|
K

T

T

S

S

T

T

G

G

K

K

V

V

P

A

V

V

N

N

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K
|
K

P

P

A

A

G

G

V

V

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

R

F

F

G

G

active site: D100 (= D102), K165 (= K165), K199 (= K199)
binding 1-butanol: T16 (= T18), C45 (= C47), K165 (= K165), K199 (= K199)

Sites not aligning to the query:

binding 1-butanol: 248

5ekyA Crystal structure of deoxyribose-phosphate aldolase from escherichia coli (k58e-y96w mutant) (see paper)
77% identity, 90% coverage: 3:234/257 of query aligns to 1:234/248 of 5ekyA

query
sites
5ekyA

E

D

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

D

L

L

T

T

L

L

N

N

D

D

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

A

V

I

C

C

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

E

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

A

T

T

V

V

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

W

G

G

A

A

D

D

E

E

V

V

D
|
D

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K

K

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

F

I

I

K
|
K

T

T

S

S

T
|
T

G
|
G

K

K

V

V

P

A

V

V

N

N

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K
|
K

P

P

A
|
A

G

G

V

V

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

R

F

F

G

G

active site: D100 (= D102), K165 (= K165), K199 (= K199)
binding 1,3-butanediol: K165 (= K165), T168 (= T168), G169 (= G169), A201 (= A201)

Sites not aligning to the query:

binding 1,3-butanediol: 248

7p76A Re-engineered 2-deoxy-d-ribose-5-phosphate aldolase catalysing asymmetric michael addition reactions, schiff base complex with cinnamaldehyde (see paper)
74% identity, 95% coverage: 4:248/257 of query aligns to 1:247/247 of 7p76A

query
sites
7p76A

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

D

L

L

T

S

T

T

L

L

N

N

D

G

D

D

D

Y

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

A

V

I

C
x
S

I
|
I

Y
|
Y

P

P

R

R

F

S

I

I

P

P

V

I

A

A

K

R

K

K

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

A

T

T

V
|
V

T

T

N

N

F
|
F

P

P

H

H

G

G

N

N

D

D

I

I

E

E

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

Y

G

G

A

A

D

D

E

E

V

V

D

D

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K

K

V

V

I

I

E

E

T

S

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

F

I

I

K
|
K

T

T

S

S

T

T

G

G

K

L

V

V

P

A

V

V

N

N

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

S

V

V

G

G

F

F

K

K

P

V

A

T

G

G

V

A

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

R

F

F

G

G

A

A

S

S

S

G

L

L

A

A

N

S

L

L

H

K

T

A

L

L

G

G

E

H

binding (2E)-3-phenylprop-2-enal: S44 (≠ C47), I45 (= I48), Y46 (= Y49), V70 (= V73), F73 (= F76), K164 (= K165)

8forA Crystal structure of kemp eliminase ke70-core with bound transition state analogue
71% identity, 90% coverage: 4:234/257 of query aligns to 1:234/249 of 8forA

query
sites
8forA

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D

H

L

L

-

A

T

T

T

S

L

A

N

N

D

D

T

T

D

D

A

E

K

K

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

T

T

T

A

D

A

A

V

I

C
x
F

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

K

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A

C

T

T

V

S

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

Y

G

G

A

A

D

D

E

S

V

V

D
x
A

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K

A

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

N

I

I

K

V

T

T

S

S

T

T

G

G

K

K

V

V

P

A

V

V

N

G

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K

I

P

P

A
x
V

G

G

V

V

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

A

F

F

G
|
G

binding 6-nitrobenzotriazole: F45 (≠ C47), A100 (≠ D102), V201 (≠ A201), G234 (= G234)

3q2dA Optimization of the in silico designed kemp eliminase ke70 by computational design and directed evolution (see paper)
69% identity, 91% coverage: 2:234/257 of query aligns to 1:232/246 of 3q2dA

query
sites
3q2dA

S

T

E

D

L

L

K

K

A

A

A

S

L

L

R

R

A

A

L

L

K

K

L

L

M

M

D
x
H

L

L

T

A

T

T

L

-

N

-

D

-

D

S

D

D

T

T

D

D

A

E

K

N

V

V

I

I

E

A

L

L

C

C

K

H

N

Q

A

A

K

K

T

T

A

P

V

V

G

G

N

N

T

T

A

D

A

A

V

I

C
x
F

I

I

Y

Y

P

P

R

R

F

F

I

I

P

P

V

I

A

A

K

R

K

K

Q

T

L

L

R

K

E

E

Q

Q

G

G

T

T

P

P

E

E

V

I

R

R

I

I

A
x
C

T

T

V

S

T

T

N

N

F

F

P

P

H

H

G

G

N

N

D

D

I

I

E

D

I

I

A

A

V

L

A

A

E

E

T

T

K

R

A

A

V

I

A

A

Y

Y

G

G

A

A

D

D

E
x
S

V

V

D
x
A

V

V

F

F

P

P

Y

Y

R

R

A

A

L

L

I

M

A

A

G

G

N

N

E

E

E

Q

V

V

G

G

F

F

E

D

L

L

V

V

-

K

-

A

K

C

Q

K

C

E

K

A

A

C

A

A

C

A

G

A

D

N

I

V

L

L

K
x
A

V

V

I

I

E

E

T

T

G

G

E

E

L

L

K

K

E

D

E

E

A

A

L

L

I

I

K

R

K

K

A

A

S

S

E

E

I

I

S

S

I

I

N

K

A

A

G

G

A

A

D

D

F

N

I

I

K

V

T

T

S

S

T

T

G

G

K

K

V

V

P

A

V

V

N

G

A

A

T

T

P

P

E

E

S

S

A

A

E

R

I

I

M

M

L

M

N

E

V

V

I

I

K

R

A

D

M

M

G

G

V

V

A

E

E

K

K

T

V

V

G

G

F

F

K
x
I

P

P

A

V

G

G

V

V

R

R

T

T

A

A

E

E

D

D

A

A

Q

Q

T

K

Y

Y

L

L

A

A

M

I

A

A

D

D

R

E

I

L

L

F

G

G

A

A

E

D

W

W

A

A

D

D

N

A

M

R

H

H

Y

Y

R

A

F

F

G

G

binding 5-nitro-1H-benzotriazole: H15 (≠ D16), F43 (≠ C47), C67 (≠ A71), S96 (≠ E100), A98 (≠ D102), A133 (≠ K135), I197 (≠ K199)

Q9Y315 Deoxyribose-phosphate aldolase; DERA; 2-deoxy-D-ribose 5-phosphate aldolase; Phosphodeoxyriboaldolase; Deoxyriboaldolase; EC 4.1.2.4 from Homo sapiens (Human) (see paper)
39% identity, 92% coverage: 6:242/257 of query aligns to 45:297/318 of Q9Y315

query
sites
Q9Y315

A

A

A

W

A

L

L

L

R

K

A

A

L

V

K

T

L

F

M

I

D

D

L

L

T

T

L

L

N

S

D

G

D

D

T

T

D

S

A

S

K

N

V

I

I

Q

E

R

L

L

C

C

K

Y

N

K

A

A

K

K

T

Y

A

P

V

I

G

R

-

E

-

D

-

L

-

K

-

A

-

L

-

N

-

M

-

H

-

D

-

K

-

G

-

I

N

T

T

T

A

A

V

V

C

C

I

V

Y

Y

P

P

R

A

F

R

I

V

P

C

V

D

A

A

K

V

K

K

Q

A

L

L

R

K

E

A

Q

A

G

G

T

C

P

-

E

N

V

I

R

P

I

V

A

A

T

S

V

V

T

A

-

A

N

G

F

F

P

P

H

A

G

G

N

Q

D

T

D

H

I

L

E

K

I

T

A

R

V

L

A

E

E

E

T

I

K

R

A

L

A

A

V

V

A

E

Y

D

G

G

A

A

D

T

E

E

V

I

D

D

V

V

F

I

P

N

Y

R

R

S

A

L

L

V

I

L

A

T

G

G

N

Q

E

W

E

E

V

A

G

L

F

Y

E

D

L

E

V

I

K

R

Q

Q

C

F

K

R

A

K

A

A

C

C

G

G

D

E

I

A

L

H

L

L

K

K

V

T

I

I

I

L

E

A

T

T

G

G

E

E

L

L

K

G

E

T

E

L

A

T

L

N

I

V

K

Y

K

K

A

A

S

S

E

M

I

I

S

A

I

M

N

M

A

A

G

G

A

S

D

D

F

F

I

I

K
|
K

T

T

S

S

T

T

G

G

K

K

V

E

P

T

V

V

N

N

A

A

T

T

P

F

E

P

S

V

A

A

E

I

I

V

M

M

L

L

N

R

V

A

I

I

K

R

-

D

-

F

A

F

M

W

G

K

V

T

A

G

E

N

K

K

V

I

G

G

F

F

K
|
K

P

P

A

A

G

G

V

I

R

R

T

S

A

A

E

K

D

D

A

S

Q

L

T

A

Y

W

L

L

A

S

M

L

A

V

D

K

R

E

I

E

L

L

G

G

A

D

E

E

W

W

A

L

D

K

N

P

M

E

H

L

Y

F

R

R

F

I

G

G

A

A

S

S

S

T

L

L

A

S

N

D

L

I

K218 (= K165) active site, Schiff-base intermediate with acetaldehyde; mutation to A: Abolishes deoxyribose-phosphate aldolase activity.
K254 (= K199) active site, Proton donor/acceptor; mutation to A: Abolishes deoxyribose-phosphate aldolase activity.

3ngjD Crystal structure of a putative deoxyribose-phosphate aldolase from entamoeba histolytica
34% identity, 89% coverage: 13:242/257 of query aligns to 12:218/222 of 3ngjD

query
sites
3ngjD

K

K

L

Y

M

I

D

D

L

H

T

T

T

L

L

L

N

K

D

A

D

D

D

A

T

T

D

E

A

E

K

Q

V

I

I

R

E

K

L

L

C

C

K

S

N

E

A

A

K

-

T

-

A

A

V

E

G

Y

N

K

T

F

A

A

A

S

V

V

C
|
C

I

V

Y

N

P

P

R

T

F

W

I

V

P

P

V

L

A

C

K

A

K

E

Q

L

L

L

R

K

E

G

Q

T

G

G

T

-

P

-

E

-

V

V

R

K

I

V

A
x
C

T

T

V

V

T

I

N

G

F

F

P

P

H

L

G

G

N

A

D

T

D

P

I

S

E

E

I

V

A

K

V

A

A

Y

E

E

T

T

K

K

A

V

A

A

V

V

A

E

Y

Q

G

G

A

A

D

E

E

E

V

V

D
|
D

V

M

V

V

F

I

P

N

Y

I

R

G

A

M

L

V

I

K

A

A

G

K

N

K

E

Y

E

D

V

D

G

V

F

E

E

K

L

D

V

V

K

K

Q

A

C

V

K

V

A

D

A

A

C

S

G

G

D

K

I

A

L

L

L

T

K

K

V

V

I

I

E

E

T

C

G

C

E

Y

L

L

K

T

E

N

E

E

A

E

L

K

I

V

K

-

K

E

A

V

S

C

E

K

I

R

S

C

I

V

N

A

A

A

G

G

A

A

D

E

F

Y

I

V

K
|
K

T

T

S

S

T

T

G

G

K

F

V

G

P

T

V

H

N

G

A

A

T

T

P

P

E

E

S

D

A

V

E

K

I

L

M

M

L

K

N

D

V

T

I

-

K

-

A

-

M

-

G

-

V

V

A

G

E

D

K

K

V

A

G

L

F

V

K
|
K

P

A

A

A

G

G

V

I

R

R

T

T

A

F

E
x
D

D

D

A

A

Q

M

T

K

Y

M

L

I

A

-

M

-

A

-

D

-

R

-

I

-

L

-

G

-

A

-

E

-

W

-

A

-

D

N

N

N

M

G

H

A

Y

S

R

R

F

I

G

G

A

A

S

S

S

A

L

G

L

I

A

A

N

I

L

L

active site: D96 (= D102), K158 (= K165), K187 (= K199)
binding zinc ion: C44 (= C47), C65 (≠ A71), D96 (= D102), D196 (≠ E208)

Sites not aligning to the query:

binding zinc ion: 222

1ub3A Crystal structure of tetrameric structure of aldolase from thermus thermophilus hb8 (see paper)
37% identity, 69% coverage: 46:222/257 of query aligns to 35:202/211 of 1ub3A

query
sites
1ub3A

V

L

C

C

I

I

Y

P

P

P

R

S

F

Y

I

-

P

-

V

V

A

A

K

W

K

V

Q

R

L

A

R

R

E

Y

Q

P

G

H

T

A

P

P

E

-

V

F

R

R

I

L

A

V

T

T

V

V

T

V

N

G

F

F

P

P

H

L

G

G

N

Y

D

Q

D

E

I

K

E

E

I

V

A

K

V

A

A

L

E

E

T

A

K

A

A

L

A

A

V

C

A

A

Y

R

G

G

A

A

D

D

E

E

V

V

D
|
D

V

M

V

V

F

L

P

H

Y

L

R

G

A

R

L

A

I

K

A

A

G

G

N

D

E

L

E

D

V

Y

G

L

F

E

E

A

L

E

V

V

K

R

Q

A

C

V

K

R

A

E

A

A

C

V

G

P

D

Q

I

A

L

V

L

L

K

K

V

V

I

I

I

L

E

E

T

T

G

G

E

Y

L

F

K

S

E

P

E

E

A

E

L

-

I

I

K

A

K

R

A

L

S

A

E

E

I

A

S

A

I

I

N

R

A

G

G

G

A

A

D

D

F

F

I

L

K
|
K

T

T

S

S

T
|
T

G

G

K

F

V

G

P

P

V

R

N

G

A

A

T

S

P

L

E

E

S

D

A

V

E

A

I

L

M

L

L

V

N

R

V

V

I

-

K

-

A

A

M

Q

G

G

V

R

A

A

E

Q

K

-

V

-

G

-

F

V

K
|
K

P

A

A

A

G
|
G

G

G

V

I

R
|
R

T

D

A

R

E

E

D

T

A

A

Q

L

T

R

Y

M

L

L

A

K

M

A

A

G

D

A

R

S

I

R

L

L

G
|
G

active site: D88 (= D102), K150 (= K165), K179 (= K199)
binding 1-hydroxy-pentane-3,4-diol-5-phosphate: K150 (= K165), T153 (= T168), G182 (= G202), R185 (= R205), G202 (= G222)

Sites not aligning to the query:

binding 1-hydroxy-pentane-3,4-diol-5-phosphate: 203, 204

Q4ZMV1 Deoxyribose-phosphate aldolase; DERA; 2-deoxy-D-ribose 5-phosphate aldolase; Phosphodeoxyriboaldolase; Deoxyriboaldolase; EC 4.1.2.4 from Pseudomonas syringae pv. syringae (strain B728a) (see paper)
31% identity, 83% coverage: 1:214/257 of query aligns to 1:201/226 of Q4ZMV1

query
sites
Q4ZMV1

M

M

S

N

E

S

L

L

K

E

A

P

A

A

L

L

R

A

A

-

L

-

K

Q

L

A

M

I

D

D

L

H

T
|
T

T

L

L

L

N

A

D

A

D

D

D

A

T

S

D

R

A

E

K

Q

V

I

I

A

E

T

L

L

C

C

K

A

N

E

A

A

K

R

T

E

A

H

V

-

G

-

N

G

T

F

A

Y

A

S

V

V

C

C

I

V

Y

N

P

S

R

S

F

Q

I

V

P

P

V

F

A

A

K

A

K

R

Q

Q

L

L

R

-

E

-

Q

-

G

A

T

G

P

S

E

A

V

V

R

K

I

V

A

C

T

A

V
|
V

T

V

N

G

F
|
F

P

P

H

L

G

G

N

A

D

G

D

L

I

S

E

A

I

S

A

K

V

A

A

S

E

E

T

A

K

A

A

L

A

T

V

I

A

A

Y

A

G

G

A

A

D

Q

E

E

V

I

D

D

V

M

V

V

F

L

P

N

Y

I

R

G

A

W

L

L

I

K

A

D

G

G

N

L

E

F

E

D

V

E

G

V

F

R

E

D

L

D

V

I

K

A

Q

A

C

V

K

L

A

Q

A

A

C

C

G

G

D

K

I

V

L

P

L

L

K

K

V

V

I

I

I

L

E

E

T

T

G

C

E

-

L

L

K

L

E

D

E

E

A

A

L

Q

I

K

K

V

K

R

A

A

S

C

E

E

I

I

S

C

I

R

N

E

A

L

G

G

A

V

D

A

F

F

I

V

K

K

T

T

S

S

T

T

G

G

K

F

V

S

P

R

V

S

N

G

A

A

T

T

P

L

E

E

S

D

A

V

E

A

I

L

M

M

L

R

N

R

V

V

I

-

K

-

A

-

M

-

G

-

V

V

A

G

E

P

K

D

V

I

G

G

F

V

K

K

P

A

A
x
S

G
|
G

G

G

V

V

R

R

T

D

A

V

E

A

D

T

A

A

Q

R

T

A

Y

M

L

I

T16 (= T18) mutation to L: Decreases synthesis of CTeHP.
V66 (= V73) mutation to K: Exhibits 12% higher activity for synthesis of CTeHP.
F69 (= F76) mutation to R: Decreases synthesis of CTeHP.
S188 (≠ A201) mutation to V: Decreases synthesis of CTeHP.
G189 (= G202) mutation to R: Exhibits higher activity toward DR5P. Decreases synthesis of CTeHP.

3qyqA 1.8 angstrom resolution crystal structure of a putative deoxyribose- phosphate aldolase from toxoplasma gondii me49 (see paper)
27% identity, 80% coverage: 12:216/257 of query aligns to 17:236/273 of 3qyqA

query
sites
3qyqA

L

L

K

N

L

F

M

F

D

E

L

V

T

A

L

L

N

T

D

D

D
x
G

D
x
E

T

T

D

N

A

E

K
x
S

V

V

I

A

E

A

L
x
V

C

C

K

K

N

I

A

A

K

A

T

K

A

D

V

P

G

A

N

-

T

I

A

V

A

G

V

V

C

S

I

V

Y

R

P

P

R

A

F

F

I

V

P

R

V

F

A

I

K

R

K

Q

Q

E

L

L

R

-

E

V

Q

K

G

S

T

A

P

P

E

E

V

V

-

A

-

G

-

I

R

K

I

V

A

C

T

A

V

A

T

V

N

N

F

F

P

P

H
x
E

G

G

N

T

D

G

D

T

I

P

E

D

I

T

A

V

V

S

A

L

E

E

T

A

K

V

A

G

A

A

V

L

A

K

Y

D

G

G

A

A

D

D

E

E

V

I

D
x
E

V

C

V

L

F

I

P

D

Y

W

R

R

A

R

L

M

-

N

-

E

-

N

I

V

A

A

G

D

N

G

E

E

E

S

V

R

G

I

F

R

E

L

L

L

V

V

K

S

Q

E

C

V

K

K

A

K

A

V

C

V

G

G

D

P

I

K

L

T

L

L

K

K

V

V

I

V

I

L

E

S

T

G

G

G

E
|
E

L

L

K

Q

E

G

A

D

L

I

I

I

K

S

K

R

A

A

S

A

E

V

I

A

S

A

I

L

N

E

A

G

G

G

A

A

D

D

F

F

I

L

K
x
Q

T

T

S

S

T

S

G

G

K

L

V

G

P

A

V

T

N

H

A

A

T

T

P

M

E

F

S

T

A

V

E

H

I

L

M

I

L

S

N

I

V

A

I

L

K

R

A

E

M

Y

G

M

V

V

A

R

E

E

K

N

-

E

-

R

-

I

-

R

-

V

-

E

-

G

-

V

-

R

-

C

V

I

G

G

F

I

K
|
K

-

I

P

E

A

V

G

G

G

D

V

V

R

H

T

M

A

A

E

E

D

T

A

A

Q

D

T

F

Y

L

L

M

A

Q

M

M

active site: E108 (≠ D102), Q174 (≠ K165), K218 (= K199)
binding beta-D-fructofuranose: E29 (≠ D24), S33 (≠ K28), V37 (≠ L32)
binding alpha-D-glucopyranose: G28 (≠ D23), S33 (≠ K28), E84 (≠ H78), E151 (= E142)

Sites not aligning to the query:

binding beta-D-fructofuranose: 256

Query Sequence

>WP_068331067.1 NCBI__GCF_001650345.1:WP_068331067.1
MSELKAAALRALKLMDLTTLNDDDTDAKVIELCKNAKTAVGNTAAVCIYPRFIPVAKKQL
REQGTPEVRIATVTNFPHGNDDIEIAVAETKAAVAYGADEVDVVFPYRALIAGNEEVGFE
LVKQCKAACGDILLKVIIETGELKEEALIKKASEISINAGADFIKTSTGKVPVNATPESA
EIMLNVIKAMGVAEKVGFKPAGGVRTAEDAQTYLAMADRILGAEWADNMHYRFGASSLLA
NLLHTLGEGEKAAEGGY

Or try a new SitesBLAST search

SitesBLAST's Database

SitesBLAST's database includes (1) SwissProt entries with experimentally-supported functional features; and (2) protein structures with bound ligands, from the BioLip database.

by Morgan Price, Arkin group
Lawrence Berkeley National Laboratory