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- PDB-7lj1: Human Prx1-Srx Decameric Complex -

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ID or keywords:

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Basic information

Entry
Database: PDB / ID: 7lj1
TitleHuman Prx1-Srx Decameric Complex
Components
  • Peroxiredoxin-1
  • Sulfiredoxin-1
KeywordsOXIDOREDUCTASE / PRX / SRX
Function / homology
Function and homology information


sulfiredoxin / oxidoreductase activity, acting on a sulfur group of donors / sulfiredoxin activity / leukocyte activation / regulation of non-canonical NF-kappaB signal transduction / thioredoxin-dependent peroxiredoxin / natural killer cell mediated cytotoxicity / thioredoxin peroxidase activity / natural killer cell activation / erythrocyte homeostasis ...sulfiredoxin / oxidoreductase activity, acting on a sulfur group of donors / sulfiredoxin activity / leukocyte activation / regulation of non-canonical NF-kappaB signal transduction / thioredoxin-dependent peroxiredoxin / natural killer cell mediated cytotoxicity / thioredoxin peroxidase activity / natural killer cell activation / erythrocyte homeostasis / NFE2L2 regulating anti-oxidant/detoxification enzymes / regulation of stress-activated MAPK cascade / Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models / Detoxification of Reactive Oxygen Species / canonical NF-kappaB signal transduction / removal of superoxide radicals / cell redox homeostasis / skeletal system development / hydrogen peroxide catabolic process / TP53 Regulates Metabolic Genes / peroxidase activity / melanosome / cellular response to oxidative stress / fibroblast proliferation / response to oxidative stress / cell population proliferation / cadherin binding / endoplasmic reticulum membrane / RNA binding / extracellular space / extracellular exosome / ATP binding / identical protein binding / nucleus / cytoplasm / cytosol
Similarity search - Function
Sulfiredoxin / ParB/Sulfiredoxin / ParB-like nuclease domain / ParB/Sulfiredoxin superfamily / Peroxiredoxin, AhpC-type / Peroxiredoxin, C-terminal / C-terminal domain of 1-Cys peroxiredoxin / Alkyl hydroperoxide reductase subunit C/ Thiol specific antioxidant / AhpC/TSA family / Thioredoxin domain profile. ...Sulfiredoxin / ParB/Sulfiredoxin / ParB-like nuclease domain / ParB/Sulfiredoxin superfamily / Peroxiredoxin, AhpC-type / Peroxiredoxin, C-terminal / C-terminal domain of 1-Cys peroxiredoxin / Alkyl hydroperoxide reductase subunit C/ Thiol specific antioxidant / AhpC/TSA family / Thioredoxin domain profile. / Thioredoxin domain / Thioredoxin-like superfamily
Similarity search - Domain/homology
ADENOSINE-5'-TRIPHOSPHATE / DI(HYDROXYETHYL)ETHER / PHOSPHATE ION / Peroxiredoxin-1 / Sulfiredoxin-1
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.97 Å
AuthorsForshaw, T.E. / Reisz, J.A. / Nelson, K.J. / Gumpena, R. / Lawson, J.R. / Jonsson, T. / Wu, H. / Clodfelter, J.E. / Johnson, L. / Furdui, C.M. / Lowther, W.T.
Funding support United States, 1items
OrganizationGrant numberCountry
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)GM072866 United States
CitationJournal: Antioxidants (Basel) / Year: 2021
Title: Specificity of Human Sulfiredoxin for Reductant and Peroxiredoxin Oligomeric State.
Authors: Forshaw, T.E. / Reisz, J.A. / Nelson, K.J. / Gumpena, R. / Lawson, J.R. / Jonsson, T.J. / Wu, H. / Clodfelter, J.E. / Johnson, L.C. / Furdui, C.M. / Lowther, W.T.
History
DepositionJan 28, 2021Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jul 14, 2021Provider: repository / Type: Initial release
Revision 1.1Sep 1, 2021Group: Database references / Structure summary / Category: audit_author / citation / database_2
Item: _audit_author.name / _citation.country ..._audit_author.name / _citation.country / _database_2.pdbx_DOI / _database_2.pdbx_database_accession
Revision 1.2Oct 18, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model / struct_ncs_dom_lim
Item: _struct_ncs_dom_lim.beg_auth_comp_id / _struct_ncs_dom_lim.beg_label_asym_id ..._struct_ncs_dom_lim.beg_auth_comp_id / _struct_ncs_dom_lim.beg_label_asym_id / _struct_ncs_dom_lim.beg_label_comp_id / _struct_ncs_dom_lim.beg_label_seq_id / _struct_ncs_dom_lim.end_auth_comp_id / _struct_ncs_dom_lim.end_label_asym_id / _struct_ncs_dom_lim.end_label_comp_id / _struct_ncs_dom_lim.end_label_seq_id

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Peroxiredoxin-1
a: Sulfiredoxin-1
B: Peroxiredoxin-1
C: Peroxiredoxin-1
D: Peroxiredoxin-1
E: Peroxiredoxin-1
F: Peroxiredoxin-1
G: Peroxiredoxin-1
H: Peroxiredoxin-1
I: Peroxiredoxin-1
J: Peroxiredoxin-1
K: Peroxiredoxin-1
L: Peroxiredoxin-1
M: Peroxiredoxin-1
N: Peroxiredoxin-1
O: Peroxiredoxin-1
P: Peroxiredoxin-1
Q: Peroxiredoxin-1
R: Peroxiredoxin-1
S: Peroxiredoxin-1
T: Peroxiredoxin-1
b: Sulfiredoxin-1
c: Sulfiredoxin-1
d: Sulfiredoxin-1
e: Sulfiredoxin-1
f: Sulfiredoxin-1
g: Sulfiredoxin-1
h: Sulfiredoxin-1
i: Sulfiredoxin-1
j: Sulfiredoxin-1
k: Sulfiredoxin-1
l: Sulfiredoxin-1
m: Sulfiredoxin-1
n: Sulfiredoxin-1
o: Sulfiredoxin-1
p: Sulfiredoxin-1
q: Sulfiredoxin-1
r: Sulfiredoxin-1
s: Sulfiredoxin-1
t: Sulfiredoxin-1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)684,84087
Polymers679,99540
Non-polymers4,84547
Water3,603200
1
A: Peroxiredoxin-1
a: Sulfiredoxin-1
B: Peroxiredoxin-1
C: Peroxiredoxin-1
D: Peroxiredoxin-1
E: Peroxiredoxin-1
F: Peroxiredoxin-1
G: Peroxiredoxin-1
H: Peroxiredoxin-1
I: Peroxiredoxin-1
J: Peroxiredoxin-1
b: Sulfiredoxin-1
c: Sulfiredoxin-1
d: Sulfiredoxin-1
e: Sulfiredoxin-1
f: Sulfiredoxin-1
g: Sulfiredoxin-1
h: Sulfiredoxin-1
i: Sulfiredoxin-1
j: Sulfiredoxin-1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)342,72943
Polymers339,99720
Non-polymers2,73223
Water32418
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area65560 Å2
ΔGint-453 kcal/mol
Surface area106300 Å2
MethodPISA
2
K: Peroxiredoxin-1
L: Peroxiredoxin-1
M: Peroxiredoxin-1
N: Peroxiredoxin-1
O: Peroxiredoxin-1
P: Peroxiredoxin-1
Q: Peroxiredoxin-1
R: Peroxiredoxin-1
S: Peroxiredoxin-1
T: Peroxiredoxin-1
k: Sulfiredoxin-1
l: Sulfiredoxin-1
m: Sulfiredoxin-1
n: Sulfiredoxin-1
o: Sulfiredoxin-1
p: Sulfiredoxin-1
q: Sulfiredoxin-1
r: Sulfiredoxin-1
s: Sulfiredoxin-1
t: Sulfiredoxin-1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)342,11044
Polymers339,99720
Non-polymers2,11324
Water32418
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area63610 Å2
ΔGint-441 kcal/mol
Surface area105220 Å2
MethodPISA
Unit cell
Length a, b, c (Å)330.834, 109.937, 260.143
Angle α, β, γ (deg.)90.00, 122.34, 90.00
Int Tables number5
Space group name H-MC121
Noncrystallographic symmetry (NCS)NCS domain:
IDEns-IDDetails
11A
21B
12A
22C
13A
23D
14A
24E
15A
25F
16A
26G
17A
27H
18A
28I
19A
29J
110A
210K
111A
211L
112A
212M
113A
213N
114A
214O
115A
215P
116A
216Q
117A
217R
118A
218S
119A
219T
120a
220b
121a
221c
122a
222d
123a
223e
124a
224f
125a
225g
126a
226h
127a
227i
128a
228j
129a
229k
130a
230l
131a
231m
132a
232n
133a
233o
134a
234p
135a
235q
136a
236r
137a
237s
138a
238t
139B
239C
140B
240D
141B
241E
142B
242F
143B
243G
144B
244H
145B
245I
146B
246J
147B
247K
148B
248L
149B
249M
150B
250N
151B
251O
152B
252P
153B
253Q
154B
254R
155B
255S
156B
256T
157C
257D
158C
258E
159C
259F
160C
260G
161C
261H
162C
262I
163C
263J
164C
264K
165C
265L
166C
266M
167C
267N
168C
268O
169C
269P
170C
270Q
171C
271R
172C
272S
173C
273T
174D
274E
175D
275F
176D
276G
177D
277H
178D
278I
179D
279J
180D
280K
181D
281L
182D
282M
183D
283N
184D
284O
185D
285P
186D
286Q
187D
287R
188D
288S
189D
289T
190E
290F
191E
291G
192E
292H
193E
293I
194E
294J
195E
295K
196E
296L
197E
297M
198E
298N
199E
299O
1100E
2100P
1101E
2101Q
1102E
2102R
1103E
2103S
1104E
2104T
1105F
2105G
1106F
2106H
1107F
2107I
1108F
2108J
1109F
2109K
1110F
2110L
1111F
2111M
1112F
2112N
1113F
2113O
1114F
2114P
1115F
2115Q
1116F
2116R
1117F
2117S
1118F
2118T
1119G
2119H
1120G
2120I
1121G
2121J
1122G
2122K
1123G
2123L
1124G
2124M
1125G
2125N
1126G
2126O
1127G
2127P
1128G
2128Q
1129G
2129R
1130G
2130S
1131G
2131T
1132H
2132I
1133H
2133J
1134H
2134K
1135H
2135L
1136H
2136M
1137H
2137N
1138H
2138O
1139H
2139P
1140H
2140Q
1141H
2141R
1142H
2142S
1143H
2143T
1144I
2144J
1145I
2145K
1146I
2146L
1147I
2147M
1148I
2148N
1149I
2149O
1150I
2150P
1151I
2151Q
1152I
2152R
1153I
2153S
1154I
2154T
1155J
2155K
1156J
2156L
1157J
2157M
1158J
2158N
1159J
2159O
1160J
2160P
1161J
2161Q
1162J
2162R
1163J
2163S
1164J
2164T
1165K
2165L
1166K
2166M
1167K
2167N
1168K
2168O
1169K
2169P
1170K
2170Q
1171K
2171R
1172K
2172S
1173K
2173T
1174L
2174M
1175L
2175N
1176L
2176O
1177L
2177P
1178L
2178Q
1179L
2179R
1180L
2180S
1181L
2181T
1182M
2182N
1183M
2183O
1184M
2184P
1185M
2185Q
1186M
2186R
1187M
2187S
1188M
2188T
1189N
2189O
1190N
2190P
1191N
2191Q
1192N
2192R
1193N
2193S
1194N
2194T
1195O
2195P
1196O
2196Q
1197O
2197R
1198O
2198S
1199O
2199T
1200P
2200Q
1201P
2201R
1202P
2202S
1203P
2203T
1204Q
2204R
1205Q
2205S
1206Q
2206T
1207R
2207S
1208R
2208T
1209S
2209T
1210b
2210c
1211b
2211d
1212b
2212e
1213b
2213f
1214b
2214g
1215b
2215h
1216b
2216i
1217b
2217j
1218b
2218k
1219b
2219l
1220b
2220m
1221b
2221n
1222b
2222o
1223b
2223p
1224b
2224q
1225b
2225r
1226b
2226s
1227b
2227t
1228c
2228d
1229c
2229e
1230c
2230f
1231c
2231g
1232c
2232h
1233c
2233i
1234c
2234j
1235c
2235k
1236c
2236l
1237c
2237m
1238c
2238n
1239c
2239o
1240c
2240p
1241c
2241q
1242c
2242r
1243c
2243s
1244c
2244t
1245d
2245e
1246d
2246f
1247d
2247g
1248d
2248h
1249d
2249i
1250d
2250j
1251d
2251k
1252d
2252l
1253d
2253m
1254d
2254n
1255d
2255o
1256d
2256p
1257d
2257q
1258d
2258r
1259d
2259s
1260d
2260t
1261e
2261f
1262e
2262g
1263e
2263h
1264e
2264i
1265e
2265j
1266e
2266k
1267e
2267l
1268e
2268m
1269e
2269n
1270e
2270o
1271e
2271p
1272e
2272q
1273e
2273r
1274e
2274s
1275e
2275t
1276f
2276g
1277f
2277h
1278f
2278i
1279f
2279j
1280f
2280k
1281f
2281l
1282f
2282m
1283f
2283n
1284f
2284o
1285f
2285p
1286f
2286q
1287f
2287r
1288f
2288s
1289f
2289t
1290g
2290h
1291g
2291i
1292g
2292j
1293g
2293k
1294g
2294l
1295g
2295m
1296g
2296n
1297g
2297o
1298g
2298p
1299g
2299q
1300g
2300r
1301g
2301s
1302g
2302t
1303h
2303i
1304h
2304j
1305h
2305k
1306h
2306l
1307h
2307m
1308h
2308n
1309h
2309o
1310h
2310p
1311h
2311q
1312h
2312r
1313h
2313s
1314h
2314t
1315i
2315j
1316i
2316k
1317i
2317l
1318i
2318m
1319i
2319n
1320i
2320o
1321i
2321p
1322i
2322q
1323i
2323r
1324i
2324s
1325i
2325t
1326j
2326k
1327j
2327l
1328j
2328m
1329j
2329n
1330j
2330o
1331j
2331p
1332j
2332q
1333j
2333r
1334j
2334s
1335j
2335t
1336k
2336l
1337k
2337m
1338k
2338n
1339k
2339o
1340k
2340p
1341k
2341q
1342k
2342r
1343k
2343s
1344k
2344t
1345l
2345m
1346l
2346n
1347l
2347o
1348l
2348p
1349l
2349q
1350l
2350r
1351l
2351s
1352l
2352t
1353m
2353n
1354m
2354o
1355m
2355p
1356m
2356q
1357m
2357r
1358m
2358s
1359m
2359t
1360n
2360o
1361n
2361p
1362n
2362q
1363n
2363r
1364n
2364s
1365n
2365t
1366o
2366p
1367o
2367q
1368o
2368r
1369o
2369s
1370o
2370t
1371p
2371q
1372p
2372r
1373p
2373s
1374p
2374t
1375q
2375r
1376q
2376s
1377q
2377t
1378r
2378s
1379r
2379t
1380s
2380t

NCS domain segments:

Component-ID: _ / Refine code: _

Dom-IDEns-IDBeg auth comp-IDBeg label comp-IDEnd auth comp-IDEnd label comp-IDAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
11SERSERPROPROAA2 - 1862 - 186
21SERSERPROPROBC2 - 1862 - 186
12SERSERLYSLYSAA2 - 1852 - 185
22SERSERLYSLYSCD2 - 1852 - 185
13SERSERGLYGLYAA2 - 1802 - 180
23SERSERGLYGLYDE2 - 1802 - 180
14SERSERPROPROAA2 - 1862 - 186
24SERSERPROPROEF2 - 1862 - 186
15SERSERPROPROAA2 - 1862 - 186
25SERSERPROPROFG2 - 1862 - 186
16SERSERASPASPAA2 - 1822 - 182
26SERSERASPASPGH2 - 1822 - 182
17SERSERTHRTHRAA2 - 1832 - 183
27SERSERTHRTHRHI2 - 1832 - 183
18SERSERLYSLYSAA2 - 1852 - 185
28SERSERLYSLYSIJ2 - 1852 - 185
19SERSERPROPROAA2 - 1862 - 186
29SERSERPROPROJK2 - 1862 - 186
110SERSERTHRTHRAA2 - 1832 - 183
210SERSERTHRTHRKL2 - 1832 - 183
111SERSERILEILEAA2 - 1842 - 184
211SERSERILEILELM2 - 1842 - 184
112SERSERLYSLYSAA2 - 1782 - 178
212SERSERLYSLYSMN2 - 1782 - 178
113SERSERPROPROAA2 - 1862 - 186
213SERSERPROPRONO2 - 1862 - 186
114SERSERLYSLYSAA2 - 1852 - 185
214SERSERLYSLYSOP2 - 1852 - 185
115SERSERTHRTHRAA2 - 1832 - 183
215SERSERTHRTHRPQ2 - 1832 - 183
116SERSERILEILEAA2 - 1842 - 184
216SERSERILEILEQR2 - 1842 - 184
117SERSERLYSLYSAA2 - 1852 - 185
217SERSERLYSLYSRS2 - 1852 - 185
118SERSERPROPROAA2 - 1862 - 186
218SERSERPROPROST2 - 1862 - 186
119SERSERPROPROAA2 - 1862 - 186
219SERSERPROPROTU2 - 1862 - 186
120METMETGLNGLNaB31 - 1373 - 109
220METMETGLNGLNbV31 - 1373 - 109
121METMETGLNGLNaB31 - 1373 - 109
221METMETGLNGLNcW31 - 1373 - 109
122PROPROGLNGLNaB30 - 1372 - 109
222PROPROGLNGLNdX30 - 1372 - 109
123METMETGLNGLNaB31 - 1373 - 109
223METMETGLNGLNeY31 - 1373 - 109
124SERSERGLNGLNaB32 - 1374 - 109
224SERSERGLNGLNfZ32 - 1374 - 109
125GLYGLYLEULEUaB36 - 1368 - 108
225ILEILELEULEUgAA38 - 13610 - 108
126PROPROGLNGLNaB30 - 1372 - 109
226PROPROGLNGLNhBA30 - 1372 - 109
127SERSERLEULEUaB32 - 1364 - 108
227SERSERLEULEUiCA32 - 1364 - 108
128METMETGLNGLNaB31 - 1373 - 109
228METMETGLNGLNjDA31 - 1373 - 109
129VALVALLEULEUaB41 - 13613 - 108
229VALVALLEULEUkEA41 - 13613 - 108
130SERSERLEULEUaB32 - 1364 - 108
230SERSERLEULEUlFA32 - 1364 - 108
131METMETGLNGLNaB31 - 1373 - 109
231METMETGLNGLNmGA31 - 1373 - 109
132ALAALALEULEUaB40 - 13612 - 108
232ALAALALEULEUnHA40 - 13612 - 108
133METMETGLNGLNaB31 - 1373 - 109
233METMETGLNGLNoIA31 - 1373 - 109
134PROPROGLNGLNaB30 - 1372 - 109
234PROPROGLNGLNpJA30 - 1372 - 109
135METMETGLNGLNaB31 - 1373 - 109
235METMETGLNGLNqKA31 - 1373 - 109
136ALAALALEULEUaB39 - 13611 - 108
236ALAALALEULEUrLA39 - 13611 - 108
137METMETGLNGLNaB31 - 1373 - 109
237METMETGLNGLNsMA31 - 1373 - 109
138METMETGLNGLNaB31 - 1373 - 109
238METMETGLNGLNtNA31 - 1373 - 109
139SERSERLYSLYSBC2 - 1852 - 185
239SERSERLYSLYSCD2 - 1852 - 185
140SERSERGLYGLYBC2 - 1802 - 180
240SERSERGLYGLYDE2 - 1802 - 180
141SERSERPROPROBC2 - 1862 - 186
241SERSERPROPROEF2 - 1862 - 186
142SERSERPROPROBC2 - 1862 - 186
242SERSERPROPROFG2 - 1862 - 186
143SERSERASPASPBC2 - 1822 - 182
243SERSERASPASPGH2 - 1822 - 182
144SERSERTHRTHRBC2 - 1832 - 183
244SERSERTHRTHRHI2 - 1832 - 183
145SERSERLYSLYSBC2 - 1852 - 185
245SERSERLYSLYSIJ2 - 1852 - 185
146SERSERPROPROBC2 - 1862 - 186
246SERSERPROPROJK2 - 1862 - 186
147SERSERTHRTHRBC2 - 1832 - 183
247SERSERTHRTHRKL2 - 1832 - 183
148SERSERILEILEBC2 - 1842 - 184
248SERSERILEILELM2 - 1842 - 184
149SERSERLYSLYSBC2 - 1782 - 178
249SERSERLYSLYSMN2 - 1782 - 178
150SERSERPROPROBC2 - 1862 - 186
250SERSERPROPRONO2 - 1862 - 186
151SERSERLYSLYSBC2 - 1852 - 185
251SERSERLYSLYSOP2 - 1852 - 185
152SERSERTHRTHRBC2 - 1832 - 183
252SERSERTHRTHRPQ2 - 1832 - 183
153SERSERILEILEBC2 - 1842 - 184
253SERSERILEILEQR2 - 1842 - 184
154SERSERLYSLYSBC2 - 1852 - 185
254SERSERLYSLYSRS2 - 1852 - 185
155SERSERPROPROBC2 - 1862 - 186
255SERSERPROPROST2 - 1862 - 186
156SERSERPROPROBC2 - 1862 - 186
256SERSERPROPROTU2 - 1862 - 186
157SERSERGLYGLYCD2 - 1802 - 180
257SERSERGLYGLYDE2 - 1802 - 180
158SERSERLYSLYSCD2 - 1852 - 185
258SERSERLYSLYSEF2 - 1852 - 185
159SERSERASPASPCD2 - 1872 - 187
259SERSERASPASPFG2 - 1872 - 187
160SERSERASPASPCD2 - 1822 - 182
260SERSERASPASPGH2 - 1822 - 182
161SERSERTHRTHRCD2 - 1832 - 183
261SERSERTHRTHRHI2 - 1832 - 183
162SERSERASPASPCD2 - 1872 - 187
262SERSERASPASPIJ2 - 1872 - 187
163SERSERLYSLYSCD2 - 1852 - 185
263SERSERLYSLYSJK2 - 1852 - 185
164SERSERTHRTHRCD2 - 1832 - 183
264SERSERTHRTHRKL2 - 1832 - 183
165SERSERTHRTHRCD2 - 1832 - 183
265SERSERTHRTHRLM2 - 1832 - 183
166SERSERLYSLYSCD2 - 1782 - 178
266SERSERLYSLYSMN2 - 1782 - 178
167SERSERLYSLYSCD2 - 1852 - 185
267SERSERLYSLYSNO2 - 1852 - 185
168SERSERVALVALCD2 - 1882 - 188
268SERSERVALVALOP2 - 1882 - 188
169SERSERTHRTHRCD2 - 1832 - 183
269SERSERTHRTHRPQ2 - 1832 - 183
170SERSERILEILECD2 - 1842 - 184
270SERSERILEILEQR2 - 1842 - 184
171SERSERPROPROCD2 - 1862 - 186
271SERSERPROPRORS2 - 1862 - 186
172SERSERLYSLYSCD2 - 1852 - 185
272SERSERLYSLYSST2 - 1852 - 185
173SERSERLYSLYSCD2 - 1852 - 185
273SERSERLYSLYSTU2 - 1852 - 185
174SERSERGLYGLYDE2 - 1802 - 180
274SERSERGLYGLYEF2 - 1802 - 180
175SERSERGLYGLYDE2 - 1802 - 180
275SERSERGLYGLYFG2 - 1802 - 180
176SERSERGLYGLYDE2 - 1802 - 180
276SERSERGLYGLYGH2 - 1802 - 180
177SERSERGLYGLYDE2 - 1802 - 180
277SERSERGLYGLYHI2 - 1802 - 180
178SERSERGLYGLYDE2 - 1802 - 180
278SERSERGLYGLYIJ2 - 1802 - 180
179SERSERGLYGLYDE2 - 1802 - 180
279SERSERSERSERJK2 - 1812 - 181
180SERSERGLYGLYDE2 - 1802 - 180
280SERSERGLYGLYKL2 - 1802 - 180
181SERSERGLYGLYDE2 - 1802 - 180
281SERSERASPASPLM2 - 1822 - 182
182SERSERLYSLYSDE2 - 1782 - 178
282SERSERLYSLYSMN2 - 1782 - 178
183SERSERGLYGLYDE2 - 1802 - 180
283SERSERGLYGLYNO2 - 1802 - 180
184SERSERGLYGLYDE2 - 1802 - 180
284SERSERGLYGLYOP2 - 1802 - 180
185SERSERGLYGLYDE2 - 1802 - 180
285SERSERGLYGLYPQ2 - 1802 - 180
186SERSERGLYGLYDE2 - 1802 - 180
286SERSERGLYGLYQR2 - 1802 - 180
187SERSERGLYGLYDE2 - 1802 - 180
287SERSERGLYGLYRS2 - 1802 - 180
188SERSERGLYGLYDE2 - 1802 - 180
288SERSERGLYGLYST2 - 1802 - 180
189SERSERGLYGLYDE2 - 1802 - 180
289SERSERGLYGLYTU2 - 1802 - 180
190SERSERPROPROEF2 - 1862 - 186
290SERSERPROPROFG2 - 1862 - 186
191SERSERASPASPEF2 - 1822 - 182
291SERSERASPASPGH2 - 1822 - 182
192SERSERTHRTHREF2 - 1832 - 183
292SERSERTHRTHRHI2 - 1832 - 183
193SERSERLYSLYSEF2 - 1852 - 185
293SERSERLYSLYSIJ2 - 1852 - 185
194SERSERPROPROEF2 - 1862 - 186
294SERSERPROPROJK2 - 1862 - 186
195SERSERTHRTHREF2 - 1832 - 183
295SERSERTHRTHRKL2 - 1832 - 183
196SERSERILEILEEF2 - 1842 - 184
296SERSERILEILELM2 - 1842 - 184
197SERSERLYSLYSEF2 - 1782 - 178
297SERSERLYSLYSMN2 - 1782 - 178
198SERSERPROPROEF2 - 1862 - 186
298SERSERPROPRONO2 - 1862 - 186
199SERSERLYSLYSEF2 - 1852 - 185
299SERSERLYSLYSOP2 - 1852 - 185
1100SERSERTHRTHREF2 - 1832 - 183
2100SERSERTHRTHRPQ2 - 1832 - 183
1101SERSERILEILEEF2 - 1842 - 184
2101SERSERILEILEQR2 - 1842 - 184
1102SERSERLYSLYSEF2 - 1852 - 185
2102SERSERLYSLYSRS2 - 1852 - 185
1103SERSERPROPROEF2 - 1862 - 186
2103SERSERPROPROST2 - 1862 - 186
1104SERSERPROPROEF2 - 1862 - 186
2104SERSERPROPROTU2 - 1862 - 186
1105SERSERASPASPFG2 - 1822 - 182
2105SERSERASPASPGH2 - 1822 - 182
1106SERSERTHRTHRFG2 - 1832 - 183
2106SERSERTHRTHRHI2 - 1832 - 183
1107SERSERPROPROFG2 - 1862 - 186
2107SERSERPROPROIJ2 - 1862 - 186
1108SERSERPROPROFG2 - 1862 - 186
2108SERSERPROPROJK2 - 1862 - 186
1109SERSERTHRTHRFG2 - 1832 - 183
2109SERSERTHRTHRKL2 - 1832 - 183
1110SERSERILEILEFG2 - 1842 - 184
2110SERSERILEILELM2 - 1842 - 184
1111SERSERLYSLYSFG2 - 1782 - 178
2111SERSERLYSLYSMN2 - 1782 - 178
1112SERSERPROPROFG2 - 1862 - 186
2112SERSERPROPRONO2 - 1862 - 186
1113SERSERASPASPFG2 - 1872 - 187
2113SERSERASPASPOP2 - 1872 - 187
1114SERSERTHRTHRFG2 - 1832 - 183
2114SERSERTHRTHRPQ2 - 1832 - 183
1115SERSERILEILEFG2 - 1842 - 184
2115SERSERILEILEQR2 - 1842 - 184
1116SERSERASPASPFG2 - 1872 - 187
2116SERSERASPASPRS2 - 1872 - 187
1117SERSERPROPROFG2 - 1862 - 186
2117SERSERPROPROST2 - 1862 - 186
1118SERSERPROPROFG2 - 1862 - 186
2118SERSERPROPROTU2 - 1862 - 186
1119SERSERASPASPGH2 - 1822 - 182
2119SERSERASPASPHI2 - 1822 - 182
1120SERSERASPASPGH2 - 1822 - 182
2120SERSERASPASPIJ2 - 1822 - 182
1121SERSERASPASPGH2 - 1822 - 182
2121SERSERASPASPJK2 - 1822 - 182
1122SERSERASPASPGH2 - 1822 - 182
2122SERSERASPASPKL2 - 1822 - 182
1123SERSERSERSERGH2 - 1812 - 181
2123SERSERTHRTHRLM2 - 1832 - 183
1124SERSERLYSLYSGH2 - 1782 - 178
2124SERSERLYSLYSMN2 - 1782 - 178
1125SERSERASPASPGH2 - 1822 - 182
2125SERSERASPASPNO2 - 1822 - 182
1126SERSERASPASPGH2 - 1822 - 182
2126SERSERASPASPOP2 - 1822 - 182
1127SERSERASPASPGH2 - 1822 - 182
2127SERSERASPASPPQ2 - 1822 - 182
1128SERSERASPASPGH2 - 1822 - 182
2128SERSERASPASPQR2 - 1822 - 182
1129SERSERASPASPGH2 - 1822 - 182
2129SERSERASPASPRS2 - 1822 - 182
1130SERSERASPASPGH2 - 1822 - 182
2130SERSERASPASPST2 - 1822 - 182
1131SERSERASPASPGH2 - 1822 - 182
2131SERSERASPASPTU2 - 1822 - 182
1132SERSERTHRTHRHI2 - 1832 - 183
2132SERSERTHRTHRIJ2 - 1832 - 183
1133SERSERTHRTHRHI2 - 1832 - 183
2133SERSERTHRTHRJK2 - 1832 - 183
1134SERSERILEILEHI2 - 1842 - 184
2134SERSERILEILEKL2 - 1842 - 184
1135SERSERILEILEHI2 - 1842 - 184
2135SERSERILEILELM2 - 1842 - 184
1136SERSERLYSLYSHI2 - 1782 - 178
2136SERSERLYSLYSMN2 - 1782 - 178
1137SERSERTHRTHRHI2 - 1832 - 183
2137SERSERTHRTHRNO2 - 1832 - 183
1138SERSERTHRTHRHI2 - 1832 - 183
2138SERSERTHRTHROP2 - 1832 - 183
1139SERSERILEILEHI2 - 1842 - 184
2139SERSERILEILEPQ2 - 1842 - 184
1140SERSERTHRTHRHI2 - 1832 - 183
2140SERSERTHRTHRQR2 - 1832 - 183
1141SERSERTHRTHRHI2 - 1832 - 183
2141SERSERTHRTHRRS2 - 1832 - 183
1142SERSERTHRTHRHI2 - 1832 - 183
2142SERSERTHRTHRST2 - 1832 - 183
1143SERSERTHRTHRHI2 - 1832 - 183
2143SERSERTHRTHRTU2 - 1832 - 183
1144SERSERLYSLYSIJ2 - 1852 - 185
2144SERSERLYSLYSJK2 - 1852 - 185
1145SERSERTHRTHRIJ2 - 1832 - 183
2145SERSERTHRTHRKL2 - 1832 - 183
1146SERSERTHRTHRIJ2 - 1832 - 183
2146SERSERTHRTHRLM2 - 1832 - 183
1147SERSERLYSLYSIJ2 - 1782 - 178
2147SERSERLYSLYSMN2 - 1782 - 178
1148SERSERLYSLYSIJ2 - 1852 - 185
2148SERSERLYSLYSNO2 - 1852 - 185
1149SERSERASPASPIJ2 - 1872 - 187
2149SERSERASPASPOP2 - 1872 - 187
1150SERSERTHRTHRIJ2 - 1832 - 183
2150SERSERTHRTHRPQ2 - 1832 - 183
1151SERSERILEILEIJ2 - 1842 - 184
2151SERSERILEILEQR2 - 1842 - 184
1152SERSERPROPROIJ2 - 1862 - 186
2152SERSERPROPRORS2 - 1862 - 186
1153SERSERLYSLYSIJ2 - 1852 - 185
2153SERSERLYSLYSST2 - 1852 - 185
1154SERSERLYSLYSIJ2 - 1852 - 185
2154SERSERLYSLYSTU2 - 1852 - 185
1155SERSERTHRTHRJK2 - 1832 - 183
2155SERSERTHRTHRKL2 - 1832 - 183
1156SERSERTHRTHRJK2 - 1832 - 183
2156SERSERTHRTHRLM2 - 1832 - 183
1157SERSERLYSLYSJK2 - 1782 - 178
2157SERSERLYSLYSMN2 - 1782 - 178
1158SERSERPROPROJK2 - 1862 - 186
2158SERSERPROPRONO2 - 1862 - 186
1159SERSERLYSLYSJK2 - 1852 - 185
2159SERSERLYSLYSOP2 - 1852 - 185
1160SERSERTHRTHRJK2 - 1832 - 183
2160SERSERTHRTHRPQ2 - 1832 - 183
1161SERSERLYSLYSJK2 - 1852 - 185
2161SERSERLYSLYSQR2 - 1852 - 185
1162SERSERPROPROJK2 - 1862 - 186
2162SERSERPROPRORS2 - 1862 - 186
1163SERSERPROPROJK2 - 1862 - 186
2163SERSERPROPROST2 - 1862 - 186
1164SERSERPROPROJK2 - 1862 - 186
2164SERSERPROPROTU2 - 1862 - 186
1165SERSERILEILEKL2 - 1842 - 184
2165SERSERILEILELM2 - 1842 - 184
1166SERSERLYSLYSKL2 - 1782 - 178
2166SERSERLYSLYSMN2 - 1782 - 178
1167SERSERTHRTHRKL2 - 1832 - 183
2167SERSERTHRTHRNO2 - 1832 - 183
1168SERSERTHRTHRKL2 - 1832 - 183
2168SERSERTHRTHROP2 - 1832 - 183
1169SERSERILEILEKL2 - 1842 - 184
2169SERSERILEILEPQ2 - 1842 - 184
1170SERSERTHRTHRKL2 - 1832 - 183
2170SERSERTHRTHRQR2 - 1832 - 183
1171SERSERTHRTHRKL2 - 1832 - 183
2171SERSERTHRTHRRS2 - 1832 - 183
1172SERSERTHRTHRKL2 - 1832 - 183
2172SERSERTHRTHRST2 - 1832 - 183
1173SERSERTHRTHRKL2 - 1832 - 183
2173SERSERTHRTHRTU2 - 1832 - 183
1174SERSERLYSLYSLM2 - 1782 - 178
2174SERSERLYSLYSMN2 - 1782 - 178
1175SERSERILEILELM2 - 1842 - 184
2175SERSERILEILENO2 - 1842 - 184
1176SERSERTHRTHRLM2 - 1832 - 183
2176SERSERTHRTHROP2 - 1832 - 183
1177SERSERILEILELM2 - 1842 - 184
2177SERSERILEILEPQ2 - 1842 - 184
1178SERSERILEILELM2 - 1842 - 184
2178SERSERILEILEQR2 - 1842 - 184
1179SERSERTHRTHRLM2 - 1832 - 183
2179SERSERTHRTHRRS2 - 1832 - 183
1180SERSERILEILELM2 - 1842 - 184
2180SERSERILEILEST2 - 1842 - 184
1181SERSERILEILELM2 - 1842 - 184
2181SERSERILEILETU2 - 1842 - 184
1182SERSERLYSLYSMN2 - 1782 - 178
2182SERSERLYSLYSNO2 - 1782 - 178
1183SERSERLYSLYSMN2 - 1782 - 178
2183SERSERLYSLYSOP2 - 1782 - 178
1184SERSERLYSLYSMN2 - 1782 - 178
2184SERSERLYSLYSPQ2 - 1782 - 178
1185SERSERLYSLYSMN2 - 1782 - 178
2185SERSERLYSLYSQR2 - 1782 - 178
1186SERSERLYSLYSMN2 - 1782 - 178
2186SERSERLYSLYSRS2 - 1782 - 178
1187SERSERLYSLYSMN2 - 1782 - 178
2187SERSERLYSLYSST2 - 1782 - 178
1188SERSERLYSLYSMN2 - 1782 - 178
2188SERSERLYSLYSTU2 - 1782 - 178
1189SERSERLYSLYSNO2 - 1852 - 185
2189SERSERLYSLYSOP2 - 1852 - 185
1190SERSERTHRTHRNO2 - 1832 - 183
2190SERSERTHRTHRPQ2 - 1832 - 183
1191SERSERILEILENO2 - 1842 - 184
2191SERSERILEILEQR2 - 1842 - 184
1192SERSERLYSLYSNO2 - 1852 - 185
2192SERSERLYSLYSRS2 - 1852 - 185
1193SERSERPROPRONO2 - 1862 - 186
2193SERSERPROPROST2 - 1862 - 186
1194SERSERPROPRONO2 - 1862 - 186
2194SERSERPROPROTU2 - 1862 - 186
1195SERSERTHRTHROP2 - 1832 - 183
2195SERSERTHRTHRPQ2 - 1832 - 183
1196SERSERILEILEOP2 - 1842 - 184
2196SERSERILEILEQR2 - 1842 - 184
1197SERSERPROPROOP2 - 1862 - 186
2197SERSERPROPRORS2 - 1862 - 186
1198SERSERLYSLYSOP2 - 1852 - 185
2198SERSERLYSLYSST2 - 1852 - 185
1199SERSERLYSLYSOP2 - 1852 - 185
2199SERSERLYSLYSTU2 - 1852 - 185
1200SERSERTHRTHRPQ2 - 1832 - 183
2200SERSERTHRTHRQR2 - 1832 - 183
1201SERSERTHRTHRPQ2 - 1832 - 183
2201SERSERTHRTHRRS2 - 1832 - 183
1202SERSERTHRTHRPQ2 - 1832 - 183
2202SERSERTHRTHRST2 - 1832 - 183
1203SERSERTHRTHRPQ2 - 1832 - 183
2203SERSERTHRTHRTU2 - 1832 - 183
1204SERSERILEILEQR2 - 1842 - 184
2204SERSERILEILERS2 - 1842 - 184
1205SERSERILEILEQR2 - 1842 - 184
2205SERSERILEILEST2 - 1842 - 184
1206SERSERILEILEQR2 - 1842 - 184
2206SERSERILEILETU2 - 1842 - 184
1207SERSERLYSLYSRS2 - 1852 - 185
2207SERSERLYSLYSST2 - 1852 - 185
1208SERSERLYSLYSRS2 - 1852 - 185
2208SERSERLYSLYSTU2 - 1852 - 185
1209SERSERPROPROST2 - 1862 - 186
2209SERSERPROPROTU2 - 1862 - 186
1210METMETGLNGLNbV31 - 1373 - 109
2210METMETGLNGLNcW31 - 1373 - 109
1211METMETLEULEUbV31 - 1363 - 108
2211METMETLEULEUdX31 - 1363 - 108
1212METMETGLNGLNbV31 - 1373 - 109
2212METMETGLNGLNeY31 - 1373 - 109
1213SERSERLEULEUbV32 - 1364 - 108
2213SERSERLEULEUfZ32 - 1364 - 108
1214ILEILEGLNGLNbV38 - 13710 - 109
2214ILEILEGLNGLNgAA38 - 13710 - 109
1215METMETLEULEUbV31 - 1363 - 108
2215METMETLEULEUhBA31 - 1363 - 108
1216SERSERGLNGLNbV32 - 1374 - 109
2216SERSERGLNGLNiCA32 - 1374 - 109
1217METMETGLNGLNbV31 - 1373 - 109
2217METMETGLNGLNjDA31 - 1373 - 109
1218VALVALLEULEUbV41 - 13613 - 108
2218VALVALLEULEUkEA41 - 13613 - 108
1219SERSERGLNGLNbV32 - 1374 - 109
2219SERSERGLNGLNlFA32 - 1374 - 109
1220METMETGLNGLNbV31 - 1373 - 109
2220METMETGLNGLNmGA31 - 1373 - 109
1221ALAALALEULEUbV40 - 13612 - 108
2221ALAALALEULEUnHA40 - 13612 - 108
1222METMETGLNGLNbV31 - 1373 - 109
2222METMETGLNGLNoIA31 - 1373 - 109
1223METMETLEULEUbV31 - 1363 - 108
2223METMETLEULEUpJA31 - 1363 - 108
1224METMETGLNGLNbV31 - 1373 - 109
2224METMETGLNGLNqKA31 - 1373 - 109
1225ALAALALEULEUbV39 - 13611 - 108
2225ALAALALEULEUrLA39 - 13611 - 108
1226METMETGLNGLNbV31 - 1373 - 109
2226METMETGLNGLNsMA31 - 1373 - 109
1227METMETGLNGLNbV31 - 1373 - 109
2227METMETGLNGLNtNA31 - 1373 - 109
1228METMETLEULEUcW31 - 1363 - 108
2228METMETLEULEUdX31 - 1363 - 108
1229METMETGLNGLNcW31 - 1373 - 109
2229METMETGLNGLNeY31 - 1373 - 109
1230SERSERLEULEUcW32 - 1364 - 108
2230SERSERLEULEUfZ32 - 1364 - 108
1231ILEILEGLNGLNcW38 - 13710 - 109
2231ILEILEGLNGLNgAA38 - 13710 - 109
1232METMETLEULEUcW31 - 1363 - 108
2232METMETLEULEUhBA31 - 1363 - 108
1233SERSERGLNGLNcW32 - 1374 - 109
2233SERSERGLNGLNiCA32 - 1374 - 109
1234METMETGLNGLNcW31 - 1373 - 109
2234METMETGLNGLNjDA31 - 1373 - 109
1235VALVALLEULEUcW41 - 13613 - 108
2235VALVALLEULEUkEA41 - 13613 - 108
1236SERSERGLNGLNcW32 - 1374 - 109
2236SERSERGLNGLNlFA32 - 1374 - 109
1237METMETGLNGLNcW31 - 1373 - 109
2237METMETGLNGLNmGA31 - 1373 - 109
1238ALAALALEULEUcW40 - 13612 - 108
2238ALAALALEULEUnHA40 - 13612 - 108
1239METMETGLNGLNcW31 - 1373 - 109
2239METMETGLNGLNoIA31 - 1373 - 109
1240METMETLEULEUcW31 - 1363 - 108
2240METMETLEULEUpJA31 - 1363 - 108
1241METMETGLNGLNcW31 - 1373 - 109
2241METMETGLNGLNqKA31 - 1373 - 109
1242ALAALALEULEUcW39 - 13611 - 108
2242ALAALALEULEUrLA39 - 13611 - 108
1243METMETGLNGLNcW31 - 1373 - 109
2243METMETGLNGLNsMA31 - 1373 - 109
1244METMETGLNGLNcW31 - 1373 - 109
2244METMETGLNGLNtNA31 - 1373 - 109
1245METMETLEULEUdX31 - 1363 - 108
2245METMETLEULEUeY31 - 1363 - 108
1246SERSERLEULEUdX32 - 1364 - 108
2246SERSERLEULEUfZ32 - 1364 - 108
1247ILEILEGLNGLNdX38 - 13710 - 109
2247ILEILEGLNGLNgAA38 - 13710 - 109
1248PROPROGLNGLNdX30 - 1372 - 109
2248PROPROGLNGLNhBA30 - 1372 - 109
1249SERSERGLNGLNdX32 - 1374 - 109
2249SERSERGLNGLNiCA32 - 1374 - 109
1250METMETLEULEUdX31 - 1363 - 108
2250METMETLEULEUjDA31 - 1363 - 108
1251VALVALLEULEUdX41 - 13613 - 108
2251VALVALLEULEUkEA41 - 13613 - 108
1252SERSERGLNGLNdX32 - 1374 - 109
2252SERSERGLNGLNlFA32 - 1374 - 109
1253METMETLEULEUdX31 - 1363 - 108
2253METMETLEULEUmGA31 - 1363 - 108
1254ALAALALEULEUdX40 - 13612 - 108
2254ALAALALEULEUnHA40 - 13612 - 108
1255METMETLEULEUdX31 - 1363 - 108
2255METMETLEULEUoIA31 - 1363 - 108
1256PROPROGLNGLNdX30 - 1372 - 109
2256PROPROGLNGLNpJA30 - 1372 - 109
1257METMETLEULEUdX31 - 1363 - 108
2257METMETLEULEUqKA31 - 1363 - 108
1258ALAALALEULEUdX39 - 13611 - 108
2258ALAALALEULEUrLA39 - 13611 - 108
1259METMETLEULEUdX31 - 1363 - 108
2259METMETLEULEUsMA31 - 1363 - 108
1260METMETLEULEUdX31 - 1363 - 108
2260METMETLEULEUtNA31 - 1363 - 108
1261SERSERLEULEUeY32 - 1364 - 108
2261SERSERLEULEUfZ32 - 1364 - 108
1262ILEILEGLNGLNeY38 - 13710 - 109
2262ILEILEGLNGLNgAA38 - 13710 - 109
1263METMETLEULEUeY31 - 1363 - 108
2263METMETLEULEUhBA31 - 1363 - 108
1264SERSERGLNGLNeY32 - 1374 - 109
2264SERSERGLNGLNiCA32 - 1374 - 109
1265METMETGLNGLNeY31 - 1373 - 109
2265METMETGLNGLNjDA31 - 1373 - 109
1266VALVALLEULEUeY41 - 13613 - 108
2266VALVALLEULEUkEA41 - 13613 - 108
1267SERSERGLNGLNeY32 - 1374 - 109
2267SERSERGLNGLNlFA32 - 1374 - 109
1268METMETGLNGLNeY31 - 1373 - 109
2268METMETGLNGLNmGA31 - 1373 - 109
1269ALAALALEULEUeY40 - 13612 - 108
2269ALAALALEULEUnHA40 - 13612 - 108
1270METMETGLNGLNeY31 - 1373 - 109
2270METMETGLNGLNoIA31 - 1373 - 109
1271METMETLEULEUeY31 - 1363 - 108
2271METMETLEULEUpJA31 - 1363 - 108
1272METMETGLNGLNeY31 - 1373 - 109
2272METMETGLNGLNqKA31 - 1373 - 109
1273ALAALALEULEUeY39 - 13611 - 108
2273ALAALALEULEUrLA39 - 13611 - 108
1274METMETGLNGLNeY31 - 1373 - 109
2274METMETGLNGLNsMA31 - 1373 - 109
1275METMETGLNGLNeY31 - 1373 - 109
2275METMETGLNGLNtNA31 - 1373 - 109
1276ILEILELEULEUfZ38 - 13610 - 108
2276ILEILELEULEUgAA38 - 13610 - 108
1277SERSERLEULEUfZ32 - 1364 - 108
2277SERSERLEULEUhBA32 - 1364 - 108
1278SERSERGLNGLNfZ32 - 1374 - 109
2278SERSERGLNGLNiCA32 - 1374 - 109
1279SERSERLEULEUfZ32 - 1364 - 108
2279SERSERLEULEUjDA32 - 1364 - 108
1280VALVALLEULEUfZ41 - 13613 - 108
2280VALVALLEULEUkEA41 - 13613 - 108
1281SERSERGLNGLNfZ32 - 1374 - 109
2281SERSERGLNGLNlFA32 - 1374 - 109
1282SERSERLEULEUfZ32 - 1364 - 108
2282SERSERLEULEUmGA32 - 1364 - 108
1283ALAALALEULEUfZ40 - 13612 - 108
2283ALAALALEULEUnHA40 - 13612 - 108
1284SERSERLEULEUfZ32 - 1364 - 108
2284SERSERLEULEUoIA32 - 1364 - 108
1285SERSERLEULEUfZ32 - 1364 - 108
2285SERSERLEULEUpJA32 - 1364 - 108
1286SERSERLEULEUfZ32 - 1364 - 108
2286SERSERLEULEUqKA32 - 1364 - 108
1287ALAALALEULEUfZ39 - 13611 - 108
2287ALAALALEULEUrLA39 - 13611 - 108
1288SERSERLEULEUfZ32 - 1364 - 108
2288SERSERLEULEUsMA32 - 1364 - 108
1289SERSERLEULEUfZ32 - 1364 - 108
2289SERSERLEULEUtNA32 - 1364 - 108
1290ILEILEGLNGLNgAA38 - 13710 - 109
2290ILEILEGLNGLNhBA38 - 13710 - 109
1291ILEILELEULEUgAA33 - 1365 - 108
2291ILEILELEULEUiCA33 - 1365 - 108
1292ILEILEGLNGLNgAA38 - 13710 - 109
2292ILEILEGLNGLNjDA38 - 13710 - 109
1293VALVALLEULEUgAA41 - 13613 - 108
2293VALVALLEULEUkEA41 - 13613 - 108
1294ILEILELEULEUgAA33 - 1365 - 108
2294ILEILELEULEUlFA33 - 1365 - 108
1295ILEILEGLNGLNgAA38 - 13710 - 109
2295ILEILEGLNGLNmGA38 - 13710 - 109
1296ALAALAGLNGLNgAA40 - 13712 - 109
2296ALAALAGLNGLNnHA40 - 13712 - 109
1297ILEILEGLNGLNgAA38 - 13710 - 109
2297ILEILEGLNGLNoIA38 - 13710 - 109
1298ILEILEGLNGLNgAA38 - 13710 - 109
2298ILEILEGLNGLNpJA38 - 13710 - 109
1299ILEILEGLNGLNgAA38 - 13710 - 109
2299ILEILEGLNGLNqKA38 - 13710 - 109
1300ALAALALEULEUgAA39 - 13611 - 108
2300ALAALALEULEUrLA39 - 13611 - 108
1301ILEILEGLNGLNgAA38 - 13710 - 109
2301ILEILEGLNGLNsMA38 - 13710 - 109
1302ILEILEGLNGLNgAA38 - 13710 - 109
2302ILEILEGLNGLNtNA38 - 13710 - 109
1303SERSERGLNGLNhBA32 - 1374 - 109
2303SERSERGLNGLNiCA32 - 1374 - 109
1304METMETLEULEUhBA31 - 1363 - 108
2304METMETLEULEUjDA31 - 1363 - 108
1305VALVALLEULEUhBA41 - 13613 - 108
2305VALVALLEULEUkEA41 - 13613 - 108
1306SERSERGLNGLNhBA32 - 1374 - 109
2306SERSERGLNGLNlFA32 - 1374 - 109
1307METMETLEULEUhBA31 - 1363 - 108
2307METMETLEULEUmGA31 - 1363 - 108
1308ALAALALEULEUhBA40 - 13612 - 108
2308ALAALALEULEUnHA40 - 13612 - 108
1309METMETLEULEUhBA31 - 1363 - 108
2309METMETLEULEUoIA31 - 1363 - 108
1310PROPROGLNGLNhBA30 - 1372 - 109
2310PROPROGLNGLNpJA30 - 1372 - 109
1311METMETLEULEUhBA31 - 1363 - 108
2311METMETLEULEUqKA31 - 1363 - 108
1312ALAALALEULEUhBA39 - 13611 - 108
2312ALAALALEULEUrLA39 - 13611 - 108
1313METMETLEULEUhBA31 - 1363 - 108
2313METMETLEULEUsMA31 - 1363 - 108
1314METMETLEULEUhBA31 - 1363 - 108
2314METMETLEULEUtNA31 - 1363 - 108
1315SERSERGLNGLNiCA32 - 1374 - 109
2315SERSERGLNGLNjDA32 - 1374 - 109
1316VALVALLEULEUiCA41 - 13613 - 108
2316VALVALLEULEUkEA41 - 13613 - 108
1317SERSERGLNGLNiCA32 - 1374 - 109
2317SERSERGLNGLNlFA32 - 1374 - 109
1318SERSERGLNGLNiCA32 - 1374 - 109
2318SERSERGLNGLNmGA32 - 1374 - 109
1319ALAALALEULEUiCA40 - 13612 - 108
2319ALAALALEULEUnHA40 - 13612 - 108
1320SERSERGLNGLNiCA32 - 1374 - 109
2320SERSERGLNGLNoIA32 - 1374 - 109
1321SERSERGLNGLNiCA32 - 1374 - 109
2321SERSERGLNGLNpJA32 - 1374 - 109
1322SERSERGLNGLNiCA32 - 1374 - 109
2322SERSERGLNGLNqKA32 - 1374 - 109
1323ALAALALEULEUiCA39 - 13611 - 108
2323ALAALALEULEUrLA39 - 13611 - 108
1324SERSERGLNGLNiCA32 - 1374 - 109
2324SERSERGLNGLNsMA32 - 1374 - 109
1325SERSERGLNGLNiCA32 - 1374 - 109
2325SERSERGLNGLNtNA32 - 1374 - 109
1326VALVALLEULEUjDA41 - 13613 - 108
2326VALVALLEULEUkEA41 - 13613 - 108
1327SERSERGLNGLNjDA32 - 1374 - 109
2327SERSERGLNGLNlFA32 - 1374 - 109
1328METMETGLNGLNjDA31 - 1373 - 109
2328METMETGLNGLNmGA31 - 1373 - 109
1329ALAALALEULEUjDA40 - 13612 - 108
2329ALAALALEULEUnHA40 - 13612 - 108
1330METMETGLNGLNjDA31 - 1373 - 109
2330METMETGLNGLNoIA31 - 1373 - 109
1331METMETLEULEUjDA31 - 1363 - 108
2331METMETLEULEUpJA31 - 1363 - 108
1332METMETGLNGLNjDA31 - 1373 - 109
2332METMETGLNGLNqKA31 - 1373 - 109
1333ALAALALEULEUjDA39 - 13611 - 108
2333ALAALALEULEUrLA39 - 13611 - 108
1334METMETGLNGLNjDA31 - 1373 - 109
2334METMETGLNGLNsMA31 - 1373 - 109
1335METMETGLNGLNjDA31 - 1373 - 109
2335METMETGLNGLNtNA31 - 1373 - 109
1336VALVALLEULEUkEA41 - 13613 - 108
2336VALVALLEULEUlFA41 - 13613 - 108
1337VALVALLEULEUkEA41 - 13613 - 108
2337VALVALLEULEUmGA41 - 13613 - 108
1338VALVALGLNGLNkEA41 - 13713 - 109
2338VALVALGLNGLNnHA41 - 13713 - 109
1339VALVALLEULEUkEA41 - 13613 - 108
2339VALVALLEULEUoIA41 - 13613 - 108
1340VALVALLEULEUkEA41 - 13613 - 108
2340VALVALLEULEUpJA41 - 13613 - 108
1341VALVALLEULEUkEA41 - 13613 - 108
2341VALVALLEULEUqKA41 - 13613 - 108
1342VALVALLEULEUkEA41 - 13613 - 108
2342VALVALLEULEUrLA41 - 13613 - 108
1343VALVALLEULEUkEA41 - 13613 - 108
2343VALVALLEULEUsMA41 - 13613 - 108
1344VALVALLEULEUkEA41 - 13613 - 108
2344VALVALLEULEUtNA41 - 13613 - 108
1345SERSERGLNGLNlFA32 - 1374 - 109
2345SERSERGLNGLNmGA32 - 1374 - 109
1346ALAALALEULEUlFA40 - 13612 - 108
2346ALAALALEULEUnHA40 - 13612 - 108
1347SERSERGLNGLNlFA32 - 1374 - 109
2347SERSERGLNGLNoIA32 - 1374 - 109
1348SERSERGLNGLNlFA32 - 1374 - 109
2348SERSERGLNGLNpJA32 - 1374 - 109
1349SERSERGLNGLNlFA32 - 1374 - 109
2349SERSERGLNGLNqKA32 - 1374 - 109
1350ALAALALEULEUlFA39 - 13611 - 108
2350ALAALALEULEUrLA39 - 13611 - 108
1351SERSERGLNGLNlFA32 - 1374 - 109
2351SERSERGLNGLNsMA32 - 1374 - 109
1352SERSERGLNGLNlFA32 - 1374 - 109
2352SERSERGLNGLNtNA32 - 1374 - 109
1353ALAALALEULEUmGA40 - 13612 - 108
2353ALAALALEULEUnHA40 - 13612 - 108
1354METMETGLNGLNmGA31 - 1373 - 109
2354METMETGLNGLNoIA31 - 1373 - 109
1355METMETLEULEUmGA31 - 1363 - 108
2355METMETLEULEUpJA31 - 1363 - 108
1356METMETGLNGLNmGA31 - 1373 - 109
2356METMETGLNGLNqKA31 - 1373 - 109
1357ALAALALEULEUmGA39 - 13611 - 108
2357ALAALALEULEUrLA39 - 13611 - 108
1358METMETGLNGLNmGA31 - 1373 - 109
2358METMETGLNGLNsMA31 - 1373 - 109
1359METMETGLNGLNmGA31 - 1373 - 109
2359METMETGLNGLNtNA31 - 1373 - 109
1360ALAALALEULEUnHA40 - 13612 - 108
2360ALAALALEULEUoIA40 - 13612 - 108
1361ALAALALEULEUnHA40 - 13612 - 108
2361ALAALALEULEUpJA40 - 13612 - 108
1362ALAALALEULEUnHA40 - 13612 - 108
2362ALAALALEULEUqKA40 - 13612 - 108
1363ALAALAGLNGLNnHA40 - 13712 - 109
2363ALAALAGLNGLNrLA40 - 13712 - 109
1364ALAALALEULEUnHA40 - 13612 - 108
2364ALAALALEULEUsMA40 - 13612 - 108
1365ALAALALEULEUnHA40 - 13612 - 108
2365ALAALALEULEUtNA40 - 13612 - 108
1366METMETLEULEUoIA31 - 1363 - 108
2366METMETLEULEUpJA31 - 1363 - 108
1367METMETGLNGLNoIA31 - 1373 - 109
2367METMETGLNGLNqKA31 - 1373 - 109
1368ALAALALEULEUoIA39 - 13611 - 108
2368ALAALALEULEUrLA39 - 13611 - 108
1369METMETGLNGLNoIA31 - 1373 - 109
2369METMETGLNGLNsMA31 - 1373 - 109
1370METMETGLNGLNoIA31 - 1373 - 109
2370METMETGLNGLNtNA31 - 1373 - 109
1371METMETLEULEUpJA31 - 1363 - 108
2371METMETLEULEUqKA31 - 1363 - 108
1372ALAALALEULEUpJA39 - 13611 - 108
2372ALAALALEULEUrLA39 - 13611 - 108
1373METMETLEULEUpJA31 - 1363 - 108
2373METMETLEULEUsMA31 - 1363 - 108
1374METMETLEULEUpJA31 - 1363 - 108
2374METMETLEULEUtNA31 - 1363 - 108
1375ALAALALEULEUqKA39 - 13611 - 108
2375ALAALALEULEUrLA39 - 13611 - 108
1376METMETGLNGLNqKA31 - 1373 - 109
2376METMETGLNGLNsMA31 - 1373 - 109
1377METMETGLNGLNqKA31 - 1373 - 109
2377METMETGLNGLNtNA31 - 1373 - 109
1378ALAALALEULEUrLA39 - 13611 - 108
2378ALAALALEULEUsMA39 - 13611 - 108
1379ALAALALEULEUrLA39 - 13611 - 108
2379ALAALALEULEUtNA39 - 13611 - 108
1380METMETGLNGLNsMA31 - 1373 - 109
2380METMETGLNGLNtNA31 - 1373 - 109

NCS ensembles :
ID
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
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
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282
283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326
327
328
329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364
365
366
367
368
369
370
371
372
373
374
375
376
377
378
379
380

-
Components

-
Protein , 2 types, 40 molecules ABCDEFGHIJKLMNOPQRSTabcdefghij...

#1: Protein
Peroxiredoxin-1 / Natural killer cell-enhancing factor A / NKEF-A / Proliferation-associated gene protein / PAG / ...Natural killer cell-enhancing factor A / NKEF-A / Proliferation-associated gene protein / PAG / Thioredoxin peroxidase 2 / Thioredoxin-dependent peroxide reductase 2 / Thioredoxin-dependent peroxiredoxin 1


Mass: 22103.205 Da / Num. of mol.: 20 / Mutation: C71S,C83V,C173S
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: PRDX1, PAGA, PAGB, TDPX2 / Production host: Escherichia coli (E. coli)
References: UniProt: Q06830, thioredoxin-dependent peroxiredoxin
#2: Protein
Sulfiredoxin-1


Mass: 11896.539 Da / Num. of mol.: 20
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: SRXN1, C20orf139, SRX, SRX1 / Production host: Escherichia coli (E. coli) / References: UniProt: Q9BYN0, sulfiredoxin

-
Non-polymers , 6 types, 247 molecules

#3: Chemical
ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 16 / Source method: obtained synthetically / Formula: C2H6O2
#4: Chemical
ChemComp-PO4 / PHOSPHATE ION


Mass: 94.971 Da / Num. of mol.: 19 / Source method: obtained synthetically / Formula: PO4
#5: Chemical
ChemComp-PEG / DI(HYDROXYETHYL)ETHER


Mass: 106.120 Da / Num. of mol.: 8 / Source method: obtained synthetically / Formula: C4H10O3
#6: Chemical ChemComp-GOL / GLYCEROL / GLYCERIN / PROPANE-1,2,3-TRIOL


Mass: 92.094 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C3H8O3
#7: Chemical ChemComp-ATP / ADENOSINE-5'-TRIPHOSPHATE


Mass: 507.181 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C10H16N5O13P3 / Feature type: SUBJECT OF INVESTIGATION / Comment: ATP, energy-carrying molecule*YM
#8: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 200 / Source method: isolated from a natural source / Formula: H2O

-
Details

Has ligand of interestY

-
Experimental details

-
Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

-
Sample preparation

CrystalDensity Matthews: 2.93 Å3/Da / Density % sol: 57.98 %
Crystal growTemperature: 291 K / Method: vapor diffusion, hanging drop / pH: 4.5 / Details: 100 mM Citric acid pH 4.5 100 mM CsCl 26% PEG 400

-
Data collection

DiffractionMean temperature: 103 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: NSLS / Beamline: X29A / Wavelength: 1.1 Å
DetectorType: ADSC QUANTUM 315 / Detector: CCD / Date: Dec 1, 2006
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.1 Å / Relative weight: 1
ReflectionResolution: 2.97→50 Å / Num. obs: 160698 / % possible obs: 99.8 % / Redundancy: 5.4 % / CC1/2: 0.976 / Net I/σ(I): 9.05
Reflection shellResolution: 2.97→3.05 Å / Num. unique obs: 8051 / CC1/2: 0.661

-
Processing

Software
NameVersionClassification
REFMAC5.8.0257refinement
HKL-3000data reduction
HKL-3000data scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 2RII, 1QMV
Resolution: 2.97→38.97 Å / Cor.coef. Fo:Fc: 0.935 / Cor.coef. Fo:Fc free: 0.906 / SU B: 18.4 / SU ML: 0.313 / Cross valid method: THROUGHOUT / ESU R Free: 0.403 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.23006 7475 5 %RANDOM
Rwork0.19225 ---
obs0.19413 141655 91.77 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK
Displacement parametersBiso mean: 62.247 Å2
Baniso -1Baniso -2Baniso -3
1-0.33 Å2-0 Å20.98 Å2
2---2.43 Å2-0 Å2
3---0.48 Å2
Refinement stepCycle: 1 / Resolution: 2.97→38.97 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms44487 0 255 200 44942
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0080.01345858
X-RAY DIFFRACTIONr_bond_other_d0.0010.01742304
X-RAY DIFFRACTIONr_angle_refined_deg1.4841.64262416
X-RAY DIFFRACTIONr_angle_other_deg1.2071.57798269
X-RAY DIFFRACTIONr_dihedral_angle_1_deg7.29655733
X-RAY DIFFRACTIONr_dihedral_angle_2_deg37.58722.7282152
X-RAY DIFFRACTIONr_dihedral_angle_3_deg19.129157119
X-RAY DIFFRACTIONr_dihedral_angle_4_deg19.27715217
X-RAY DIFFRACTIONr_chiral_restr0.0570.25975
X-RAY DIFFRACTIONr_gen_planes_refined0.0060.0251211
X-RAY DIFFRACTIONr_gen_planes_other0.0010.029340
X-RAY DIFFRACTIONr_nbd_refined
X-RAY DIFFRACTIONr_nbd_other
X-RAY DIFFRACTIONr_nbtor_refined
X-RAY DIFFRACTIONr_nbtor_other
X-RAY DIFFRACTIONr_xyhbond_nbd_refined
X-RAY DIFFRACTIONr_xyhbond_nbd_other
X-RAY DIFFRACTIONr_metal_ion_refined
X-RAY DIFFRACTIONr_metal_ion_other
X-RAY DIFFRACTIONr_symmetry_vdw_refined
X-RAY DIFFRACTIONr_symmetry_vdw_other
X-RAY DIFFRACTIONr_symmetry_hbond_refined
X-RAY DIFFRACTIONr_symmetry_hbond_other
X-RAY DIFFRACTIONr_symmetry_metal_ion_refined
X-RAY DIFFRACTIONr_symmetry_metal_ion_other
X-RAY DIFFRACTIONr_mcbond_it5.7956.58523079
X-RAY DIFFRACTIONr_mcbond_other5.7956.58523078
X-RAY DIFFRACTIONr_mcangle_it8.8389.86828763
X-RAY DIFFRACTIONr_mcangle_other8.8389.86828764
X-RAY DIFFRACTIONr_scbond_it6.2056.85722779
X-RAY DIFFRACTIONr_scbond_other6.1966.85622772
X-RAY DIFFRACTIONr_scangle_it
X-RAY DIFFRACTIONr_scangle_other9.35210.12133646
X-RAY DIFFRACTIONr_long_range_B_refined12.48574.82847262
X-RAY DIFFRACTIONr_long_range_B_other12.48574.82947263
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
Refine LS restraints NCS

Refine-ID: X-RAY DIFFRACTION / Type: interatomic distance / Weight position: 0.05

Ens-IDDom-IDAuth asym-IDNumberRms dev position (Å)
11A58100.03
12B58100.03
21A57820.05
22C57820.05
31A56510.03
32D56510.03
41A58210.03
42E58210.03
51A57880.03
52F57880.03
61A56770.05
62G56770.05
71A56960.05
72H56960.05
81A57940.04
82I57940.04
91A57290.05
92J57290.05
101A56940.06
102K56940.06
111A56910.05
112L56910.05
121A56100.05
122M56100.05
131A57670.05
132N57670.05
141A57640.05
142O57640.05
151A56880.06
152P56880.06
161A57680.04
162Q57680.04
171A57900.05
172R57900.05
181A57930.04
182S57930.04
191A58160.04
192T58160.04
201a29370.06
202b29370.06
211a29040.08
212c29040.08
221a29160.08
222d29160.08
231a28730.08
232e28730.08
241a28830.08
242f28830.08
251a27070.08
252g27070.08
261a29390.07
262h29390.07
271a27480.07
272i27480.07
281a28910.09
282j28910.09
291a26610.07
292k26610.07
301a27150.07
302l27150.07
311a29100.07
312m29100.07
321a24800.08
322n24800.08
331a28970.07
332o28970.07
341a28940.08
342p28940.08
351a28920.09
352q28920.09
361a27200.07
362r27200.07
371a28670.08
372s28670.08
381a28980.07
382t28980.07
391B57600.04
392C57600.04
401B56480.04
402D56480.04
411B58150.03
412E58150.03
421B57610.04
422F57610.04
431B56610.04
432G56610.04
441B56860.05
442H56860.05
451B57780.04
452I57780.04
461B57240.04
462J57240.04
471B56800.05
472K56800.05
481B56860.04
482L56860.04
491B56060.04
492M56060.04
501B57450.04
502N57450.04
511B57450.04
512O57450.04
521B56710.05
522P56710.05
531B57480.04
532Q57480.04
541B57790.04
542R57790.04
551B57810.04
552S57810.04
561B57970.03
562T57970.03
571C56710.05
572D56710.05
581C57940.04
582E57940.04
591C58080.05
592F58080.05
601C56920.05
602G56920.05
611C57170.05
612H57170.05
621C58550.04
622I58550.04
631C57560.04
632J57560.04
641C56980.05
642K56980.05
651C56500.06
652L56500.06
661C55910.06
662M55910.06
671C57550.04
672N57550.04
681C58820.05
682O58820.05
691C57220.05
692P57220.05
701C57670.04
702Q57670.04
711C58590.04
712R58590.04
721C57640.05
722S57640.05
731C57800.04
732T57800.04
741D56700.03
742E56700.03
751D56320.03
752F56320.03
761D56330.05
762G56330.05
771D56040.06
772H56040.06
781D56730.05
782I56730.05
791D56520.04
792J56520.04
801D56150.05
802K56150.05
811D56210.05
812L56210.05
821D55950.05
822M55950.05
831D55950.05
832N55950.05
841D56570.04
842O56570.04
851D56360.05
852P56360.05
861D56630.04
862Q56630.04
871D56660.04
872R56660.04
881D56190.04
882S56190.04
891D56410.04
892T56410.04
901E57770.03
902F57770.03
911E56810.04
912G56810.04
921E57040.05
922H57040.05
931E58130.04
932I58130.04
941E57580.04
942J57580.04
951E57060.05
952K57060.05
961E56970.04
962L56970.04
971E55940.05
972M55940.05
981E57590.04
982N57590.04
991E57790.04
992O57790.04
1001E57040.05
1002P57040.05
1011E57850.03
1012Q57850.03
1021E58160.04
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3721p27280.09
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3792t27340.09
3801s29900.04
3802t29900.04
LS refinement shellResolution: 2.973→3.05 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.396 233 -
Rwork0.32 4416 -
obs--38.97 %

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