Peptide record

TPDB42950

Soybean lunasin anti-inflammatory peptide Anti-inflammatory Anticancer Antifungal standard
43 amino acids
Basic Information
3D PDB MODEL
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TPDB42950
Soybean lunasin anti-inflammatory peptide
Anti-inflammatory Anticancer Antifungal
Anti-infective peptides Cancer-related peptides Immunity and inflammation peptides
Peptipedia SATPdb dbACP Antifungipept
standard
No
A 43-aa standard natural multi-activity (Anti-inflammatory, Anticancer, and Antifungal) peptide sequence curated from Peptipedia, SATPdb, dbACP, and other sources, with an available 3D structural model.
Sequence
SKWQHQQDSCRKQLQGVNLTPCEKHIMEKIQGRGDDDDDDDDD
Physicochemical Analysis
C204H321N65O78S3
AFY
D
5028.36
4.23
8
12
7
-6
24.39
-1.763
43.02
Mammalian: 1.9 hour Yeast: >20 hour E.coli: >10 hour
5625
111.87
12
Residue Composition
number
0
A
2
R
1
N
10
D
2
C
2
E
6
Q
3
G
2
H
2
I
2
L
4
K
1
M
0
F
1
P
2
S
1
T
1
W
0
Y
1
V
Amino Acid Distribution
A: 0 R: 2 N: 1 D: 10 C: 2 E: 2 Q: 6 G: 3 H: 2 I: 2 L: 2 K: 4 M: 1 F: 0 P: 1 S: 2 T: 1 W: 1 Y: 0 V: 1
Chemical Descriptors
43
C204H321N65O78S3
5028.36
4.23
-6
24.39
-1.763
5028.3057
5025.2238
Evidence Records 2 records
Evidence 1 Activity

Activity

EC50
Anti-inflammatory
0.00 µM
Anti-inflammatory
anti inflammatory
ai

Source & Reference

NA
Gonzalez de Mejia E., Dia V. P.
Lunasin and lunasin-like peptides inhibit inflammation through suppression of NF-κB pathway in the macrophage. Peptides, 30, 2388-2398, 2009
2009
Journal

Other

43
BIOPEP-UWM database of bioactive peptides SMILES: N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=C[N]([H])C2=CC=CC=C12)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC3=C[N]([H])C=N3)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)N)C(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@H](O)C)C(=O)N4[C@@H](CCC4)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC5=C[N]([H])C=N5)C(=O)N[C@@H]([C@H](CC)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@H](CC)C)C(=O)N[C@@H](CCC(=O)N)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)O InChI=1S/C204H321N65O78S3/c1-13-93(9)160(199(343)245-109(38-46-138(211)274)166(310)227-81-144(280)231-102(34-25-58-223-203(217)218)164(308)226-82-145(281)232-123(68-149(287)288)183(327)253-124(69-150(289)290)184(328)254-125(70-151(291)292)185(329)255-126(71-152(293)294)186(330)256-127(72-153(295)296)187(331)257-128(73-154(297)298)188(332)258-129(74-155(299)300)189(333)259-130(75-156(301)302)190(334)261-132(202(346)347)77-158(305)306)266-178(322)106(33-20-24-57-208)236-172(316)114(43-51-147(283)284)241-177(321)116(53-61-350-12)246-200(344)161(94(10)14-2)267-193(337)121(66-98-80-222-89-230-98)251-170(314)105(32-19-23-56-207)235-173(317)115(44-52-148(285)286)244-196(340)135(87-349)264-197(341)136-36-27-60-269(136)201(345)162(95(11)272)268-192(336)118(63-91(5)6)248-182(326)122(67-143(216)279)260-198(342)159(92(7)8)265-146(282)83-228-165(309)108(37-45-137(210)273)238-179(323)117(62-90(3)4)247-174(318)111(40-48-140(213)276)239-167(311)104(31-18-22-55-206)234-168(312)107(35-26-59-224-204(219)220)237-195(339)134(86-348)263-194(338)133(85-271)262-191(335)131(76-157(303)304)252-176(320)112(41-49-141(214)277)240-171(315)110(39-47-139(212)275)243-181(325)120(65-97-79-221-88-229-97)250-175(319)113(42-50-142(215)278)242-180(324)119(64-96-78-225-101-29-16-15-28-99(96)101)249-169(313)103(30-17-21-54-205)233-163(307)100(209)84-270/h15-16,28-29,78-80,88-95,100,102-136,159-162,225,270-272,348-349H,13-14,17-27,30-77,81-87,205-209H2,1-12H3,(H2,210,273)(H2,211,274)(H2,212,275)(H2,213,276)(H2,214,277)(H2,215,278)(H2,216,279)(H,221,229)(H,222,230)(H,226,308)(H,227,310)(H,228,309)(H,231,280)(H,232,281)(H,233,307)(H,234,312)(H,235,317)(H,236,316)(H,237,339)(H,238,323)(H,239,311)(H,240,315)(H,241,321)(H,242,324)(H,243,325)(H,244,340)(H,245,343)(H,246,344)(H,247,318)(H,248,326)(H,249,313)(H,250,319)(H,251,314)(H,252,320)(H,253,327)(H,254,328)(H,255,329)(H,256,330)(H,257,331)(H,258,332)(H,259,333)(H,260,342)(H,261,334)(H,262,335)(H,263,338)(H,264,341)(H,265,282)(H,266,322)(H,267,337)(H,268,336)(H,283,284)(H,285,286)(H,287,288)(H,289,290)(H,291,292)(H,293,294)(H,295,296)(H,297,298)(H,299,300)(H,301,302)(H,303,304)(H,305,306)(H,346,347)(H4,217,218,223)(H4,219,220,224)/t93-,94-,95+,100-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,159-,160-,161-,162-/m0/s1 InChIKey=GXMLUULMDUFVAH-ASPFZTNWSA-N Review concerning Lunasin: Hsieh C.-C., Martínez-Villaluenga C., de Lumen B. O., Hernández-Ledesma B., 2018, Updating the research on the chemopreventive and therapeutic role of the peptide lunasin. J. Sci. Food Agric., 98, 2070–2079 Anticancer peptide according to the APD database the BIOPEP-UWM database of bioactive peptides (ID 9525) the EROP-Moscow database Immunomodulating peptide according to the BIOPEP-UWM database of bioactive peptides (ID 10124)
Evidence 2 Activity

Activity

Antifungal

Source & Reference

Antifungipept

Other

Also showed anti-oxidant and anti-inflammatory activity ( Ren et al., 2018 ). Found also in barley and wheat. Found in multiple species. Updated 11/2023
Additional Detail Fields 1 fields
43