Structure of PDB 1req Chain C Binding Site BS02
Receptor Information
>1req Chain C (length=727) Species:
1752
(Propionibacterium freudenreichii subsp. shermanii) [
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STLPRFDSVDLGNAPVPADAARRFEELAAKAGTGEAWETAEQIPVGTLFN
EDVYKDMDWLDTYAGIPPFVHGPYATMYAFRPWTIRQYAGFSTAKESNAF
YRRNLAAGQKGLSVAFDLPTHRGYDSDNPRVAGDVGMAGVAIDSIYDMRE
LFAGIPLDQMSVSMTMNGAVLPILALYVVTAEEQGVKPEQLAGTIQNDIL
KEFMVRNTYIYPPQPSMRIISEIFAYTSANMPKWNSISISGYHMQEAGAT
ADIEMAYTLADGVDYIRAGESVGLNVDQFAPRLSFFWGIGMNFFMEVAKL
RAARMLWAKLVHQFGPKNPKSMSLRTHSQTSGWSLTAQDVYNNVVRTCIE
AMAATQGHTQSLHTNSLDEAIALPTDFSARIARNTQLFLQQESGTTRVID
PWSGSAYVEELTWDLARKAWGHIQEVEKVGGMAKAIEKGIPKMRIEEAAA
RTQARIDSGRQPLIGVNKYRLEHEPPLDVLKVDNSTVLAEQKAKLVKLRA
ERDPEKVKAALDKITWAAGNPDDKDPDRNLLKLCIDAGRAMATVGEMSDA
LEKVFGRYTAQIRTISGVYSKEVKNTPEVEEARELVEEFEQAEGRRPRIL
LAKMGQDGHDRGQKVIATAYADLGFDVDVGPLFQTPEETARQAVEADVHV
VGVSSLAGGHLTLVPALRKELDKLGRPDILITVGGVIPEQDFDELRKDGA
VEIYTPGTVIPESAISLVKKLRASLDA
Ligand information
Ligand ID
DCA
InChI
InChI=1S/C21H36N7O16P3/c1-4-23-12(29)5-6-24-19(32)16(31)21(2,3)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31H,4-8H2,1-3H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
ILWZMFJBPIYQKW-IBOSZNHHSA-N
SMILES
Software
SMILES
CACTVS 3.341
CCNC(=O)CCNC(=O)[CH](O)C(C)(C)CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
ACDLabs 10.04
O=C(NCC)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
OpenEye OEToolkits 1.5.0
CCNC(=O)CCNC(=O)[C@@H](C(C)(C)CO[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
CACTVS 3.341
CCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
CCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
Formula
C21 H36 N7 O16 P3
Name
DESULFO-COENZYME A
ChEMBL
DrugBank
DB01829
ZINC
ZINC000085433024
PDB chain
1req Chain C Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
1req
How coenzyme B12 radicals are generated: the crystal structure of methylmalonyl-coenzyme A mutase at 2 A resolution.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
Y75 M78 R82 T85 R87 Y89 S114 S164 T166 T195 R283 S285 H328 Q361
Binding residue
(residue number reindexed from 1)
Y74 M77 R81 T84 R86 Y88 S113 S163 T165 T194 R282 S284 H327 Q360
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
Y89 Y243 H244 K604 D608 H610
Catalytic site (residue number reindexed from 1)
Y88 Y242 H243 K603 D607 H609
Enzyme Commision number
5.4.99.2
: methylmalonyl-CoA mutase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004494
methylmalonyl-CoA mutase activity
GO:0005515
protein binding
GO:0016853
isomerase activity
GO:0016866
intramolecular transferase activity
GO:0031419
cobalamin binding
GO:0046872
metal ion binding
Biological Process
GO:0019678
propionate metabolic process, methylmalonyl pathway
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1req
,
PDBe:1req
,
PDBj:1req
PDBsum
1req
PubMed
8805541
UniProt
P11653
|MUTB_PROFR Methylmalonyl-CoA mutase large subunit (Gene Name=mutB)
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