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3W2G

Crystal structure of fully reduced form of NADH-cytochrome b5 reductase from pig liver

Functional Information from GO Data
ChainGOidnamespacecontents
A0004128molecular_functioncytochrome-b5 reductase activity, acting on NAD(P)H
A0005575cellular_componentcellular_component
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 Residues33
DetailsBINDING SITE FOR RESIDUE FAD A 301
ChainResidue
AHIS49
APHE85
AHIS89
APHE92
AGLY95
AGLY96
ALYS97
AMET98
ASER99
ATHR153
ATHR156
AARG63
ANAD302
AHOH401
AHOH403
AHOH406
AHOH419
AHOH421
AHOH429
AHOH450
AHOH505
AHOH519
APRO64
AHOH579
AHOH584
AHOH617
AHOH620
ATYR65
ATHR66
AVAL80
AILE81
ALYS82
ATYR84

site_idAC2
Number of Residues32
DetailsBINDING SITE FOR RESIDUE NAD A 302
ChainResidue
ALYS82
ATYR84
AGLY152
ATHR153
AGLY154
AALA180
AASN181
AGLN182
AASP211
APHE223
ACYS245
AGLY246
APRO247
APRO248
APRO249
AMET250
APHE272
AFAD301
AHOH404
AHOH407
AHOH418
AHOH421
AHOH432
AHOH439
AHOH474
AHOH476
AHOH547
AHOH571
AHOH616
AHOH670
AHOH672
AHOH741

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:7893687, ECO:0007744|PDB:1NDH
ChainResidueDetails
AARG63
APRO64
ATYR65
ALYS97
AMET98
ASER99

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P00387
ChainResidueDetails
AVAL80
ALYS82
ATYR84
ATHR156

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P00387
ChainResidueDetails
ALYS13

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:P00387
ChainResidueDetails
ATYR14

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:Q9DCN2
ChainResidueDetails
ALYS21
ALYS91

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 862
ChainResidueDetails
AHIS49proton shuttle (general acid/base), single electron shuttle
ATYR65electrostatic stabiliser
ATHR66proton shuttle (general acid/base), single electron shuttle
ACYS245alter redox potential

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PDB entries from 2024-10-09

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