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GENERAL
TITLE
BOVINE ATP SYNTHASE F1-PERIPHERAL STALK DOMAIN, STATE 2
DATE LAST MODIFIED
30 Sept 2020
RELEASE
9 Sept 2020
OBSOLETE
CLASSIFICATION
HYDROLASE
EXPERIMENT TYPE
ELECTRON MICROSCOPY
SPACE GROUP
P 1
RESOLUTION RANGE HIGH
3.29
RESOLUTION RANGE LOW
3.29
PUBMED ID
DOI
10.1073/PNAS.2013998117
PDBe
--
Chains
| Structure Chain | Target Protein | Gene | Expression System | Organism | Synonyms | Actions | ||
|---|---|---|---|---|---|---|---|---|
| P19483 | -- | -- | CATTLE | ATP SYNTHASE F1 SUBUNIT ALPHASEQUENCE FOR THIS PROTEIN ENCODES GLU. THE ACTUAL RESIDUE IS PYROGLU.HOWEVER PYROGLU AND PYROGLN ARE THE SAME. RESIDUE 481 IN CHAINS A, B,AND C CAN BE GLY OR SER. E.G. IN THIS STRUCTURE SHOULD BE GLY. WEREFERENCE FOR THE ALPHA SUBUNIT J. E. WALKER, S. J. REMARK 999POWELL,O. VINAS AND M. J. RUNSWICK, BIOCHEMISTRY,VOL 28,PP REMARK 9994702-4708, 1989. REMARK 999 REMARK 999 SER 481 GLY IN CHAINS A, B ANDC REMARK 999 WAS IDENTIFIED AS A GLY FROM THE PROTEIN REMARK 999SEQUENCE. IN THE CDNA SEQUENCE, THE CODON FOR THIS REMARK 999 RESIDUEWAS AGC SER IN THREE CLONES WHILE IN TWO REMARK 999 OTHERS IT WAS GGCGLY. THE DIFFERENCE WAS THOUGHT TO REMARK 999 BE DUE TO A MUTATIONOCCURRING DURING EITHER PROPAGATION REMARK 999 OF THE CLONES IN THELIBRARY OR SUBCLONING INTO M13 REMARK 999 VECTORS. THE ELECTRONDENSITY SUGGESTS A GLY IN REMARK 999 THIS POSITION. | CATTLE | ATP SYNTHASE F1 SUBUNIT ALPHASEQUENCE FOR THIS PRO ... | Mutations | |
| P19483 | -- | -- | CATTLE | ATP SYNTHASE F1 SUBUNIT ALPHASEQUENCE FOR THIS PROTEIN ENCODES GLU. THE ACTUAL RESIDUE IS PYROGLU.HOWEVER PYROGLU AND PYROGLN ARE THE SAME. RESIDUE 481 IN CHAINS A, B,AND C CAN BE GLY OR SER. E.G. IN THIS STRUCTURE SHOULD BE GLY. WEREFERENCE FOR THE ALPHA SUBUNIT J. E. WALKER, S. J. REMARK 999POWELL,O. VINAS AND M. J. RUNSWICK, BIOCHEMISTRY,VOL 28,PP REMARK 9994702-4708, 1989. REMARK 999 REMARK 999 SER 481 GLY IN CHAINS A, B ANDC REMARK 999 WAS IDENTIFIED AS A GLY FROM THE PROTEIN REMARK 999SEQUENCE. IN THE CDNA SEQUENCE, THE CODON FOR THIS REMARK 999 RESIDUEWAS AGC SER IN THREE CLONES WHILE IN TWO REMARK 999 OTHERS IT WAS GGCGLY. THE DIFFERENCE WAS THOUGHT TO REMARK 999 BE DUE TO A MUTATIONOCCURRING DURING EITHER PROPAGATION REMARK 999 OF THE CLONES IN THELIBRARY OR SUBCLONING INTO M13 REMARK 999 VECTORS. THE ELECTRONDENSITY SUGGESTS A GLY IN REMARK 999 THIS POSITION. | CATTLE | ATP SYNTHASE F1 SUBUNIT ALPHASEQUENCE FOR THIS PRO ... | Mutations | |
| P19483 | -- | -- | CATTLE | ATP SYNTHASE F1 SUBUNIT ALPHASEQUENCE FOR THIS PROTEIN ENCODES GLU. THE ACTUAL RESIDUE IS PYROGLU.HOWEVER PYROGLU AND PYROGLN ARE THE SAME. RESIDUE 481 IN CHAINS A, B,AND C CAN BE GLY OR SER. E.G. IN THIS STRUCTURE SHOULD BE GLY. WEREFERENCE FOR THE ALPHA SUBUNIT J. E. WALKER, S. J. REMARK 999POWELL,O. VINAS AND M. J. RUNSWICK, BIOCHEMISTRY,VOL 28,PP REMARK 9994702-4708, 1989. REMARK 999 REMARK 999 SER 481 GLY IN CHAINS A, B ANDC REMARK 999 WAS IDENTIFIED AS A GLY FROM THE PROTEIN REMARK 999SEQUENCE. IN THE CDNA SEQUENCE, THE CODON FOR THIS REMARK 999 RESIDUEWAS AGC SER IN THREE CLONES WHILE IN TWO REMARK 999 OTHERS IT WAS GGCGLY. THE DIFFERENCE WAS THOUGHT TO REMARK 999 BE DUE TO A MUTATIONOCCURRING DURING EITHER PROPAGATION REMARK 999 OF THE CLONES IN THELIBRARY OR SUBCLONING INTO M13 REMARK 999 VECTORS. THE ELECTRONDENSITY SUGGESTS A GLY IN REMARK 999 THIS POSITION. | CATTLE | ATP SYNTHASE F1 SUBUNIT ALPHASEQUENCE FOR THIS PRO ... | Mutations | |
| P00829 | -- | -- | CATTLE | -- | CATTLE | -- | Mutations | |
| P00829 | -- | -- | CATTLE | -- | CATTLE | -- | Mutations | |
| P00829 | -- | -- | CATTLE | -- | CATTLE | -- | Mutations | |
| P05631 | -- | -- | CATTLE | F-ATPASE GAMMA SUBUNIT | CATTLE | F-ATPASE GAMMA SUBUNIT | Mutations | |
| P05630 | -- | -- | CATTLE | F-ATPASE DELTA SUBUNIT | CATTLE | F-ATPASE DELTA SUBUNIT | Mutations | |
| P05632 | -- | -- | CATTLE | ATPASE SUBUNIT EPSILON | CATTLE | ATPASE SUBUNIT EPSILON | Mutations | |
| P01096 | ATPIF1, ATPI | ESCHERICHIA COLI | CATTLE | INHIBITOR OF F(1)F(O)-ATPASE,IF16HIS AFFINITY TAG. | CATTLE | INHIBITOR OF F(1)F(O)-ATPASE,IF16HIS AFFINITY TAG. ... | Mutations |
NGL Viewer is used for the molecular visualization.
- AS Rose, AR Bradley, Y Valasatava, JM Duarte, A Prlić and PW Rose. NGL viewer: web-based molecular graphics for large complexes. Bioinformatics: bty419, 2018. doi:10.1093/bioinformatics/bty419
- AS Rose and PW Hildebrand. NGL Viewer: a web application for molecular visualization. Nucl Acids Res (1 July 2015) 43 (W1): W576-W579 first published online April 29, 2015. doi:10.1093/nar/gkv402