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5GV7

Structure of NADH-cytochrome b5 reductase refined with the multipolar atomic model at 0.80 A

Functional Information from GO Data
ChainGOidnamespacecontents
A0004128molecular_functioncytochrome-b5 reductase activity, acting on NAD(P)H
A0005739cellular_componentmitochondrion
A0005741cellular_componentmitochondrial outer membrane
A0005783cellular_componentendoplasmic reticulum
A0005789cellular_componentendoplasmic reticulum membrane
A0006695biological_processcholesterol biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0050660molecular_functionflavin adenine dinucleotide binding
A0071949molecular_functionFAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues32
Detailsbinding site for residue FAD A 1301
ChainResidue
AARG1063
ATHR1088
AHIS1089
APHE1092
AGLY1095
AGLY1096
ALYS1097
AMET1098
ASER1099
ATHR1153
ATHR1156
APRO1064
AGOL1304
AGOL1305
AHOH1404
AHOH1417
AHOH1451
AHOH1481
AHOH1528
AHOH1562
AHOH1582
AHOH1596
ATYR1065
AHOH1603
AHOH1620
AHOH1740
ATHR1066
AVAL1080
AILE1081
ALYS1082
ATYR1084
APHE1085

site_idAC2
Number of Residues8
Detailsbinding site for residue GOL A 1302
ChainResidue
AGLY1075
APHE1076
AASP1170
AHOH1448
AHOH1453
AHOH1555
AHOH1643
AHOH1882

site_idAC3
Number of Residues11
Detailsbinding site for residue GOL A 1303
ChainResidue
AGLY1151
AGLY1152
AALA1180
AASN1181
AASP1211
APHE1223
APRO1247
AMET1250
AHOH1473
AHOH1675
AHOH1728

site_idAC4
Number of Residues12
Detailsbinding site for residue GOL A 1304
ChainResidue
AGLY1151
ATHR1153
AGLY1154
AGLY1246
APRO1247
AFAD1301
AHOH1417
AHOH1562
AHOH1620
AHOH1668
AHOH1695
AHOH1761

site_idAC5
Number of Residues8
Detailsbinding site for residue GOL A 1305
ChainResidue
AALA1094
AGLY1095
ALYS1097
AFAD1301
AHOH1432
AHOH1604
AHOH1921
AHOH1935

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:7893687, ECO:0007744|PDB:1NDH
ChainResidueDetails
AARG1063
APRO1064
ATYR1065
ALYS1097
AMET1098
ASER1099

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P00387
ChainResidueDetails
AVAL1080
ALYS1082
ATYR1084
ATHR1156

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P00387
ChainResidueDetails
ALYS1013

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:P00387
ChainResidueDetails
ATYR1014

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:Q9DCN2
ChainResidueDetails
ALYS1021
ALYS1091

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 862
ChainResidueDetails
AHIS1049proton shuttle (general acid/base), single electron shuttle
ATYR1065electrostatic stabiliser
ATHR1066proton shuttle (general acid/base), single electron shuttle
ACYS1245alter redox potential

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PDB entries from 2024-11-13

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