Statistics Summary Report for ISPC Center
Last updated: Mar 11 2010
Target Status Statistics
Total number of targets deposited by ISPC to TargetDB: 136
View ISPC Target ListTable 1: Status Statistics for ISPC
| Status | Total Number of Targets | (%) Relative to "Cloned" Targets | (%) Relative to "Expressed" Targets | (%) Relative to "Purified" Targets | (%) Relative to "Crystallized" Targets |
| Cloned | 132 | 100.0 | - | - | - |
| Expressed | 107 | 81.1 | 100.0 | - | - |
| Soluble | 89 | 67.4 | 83.2 | - | - |
| Purified | 82 | 62.1 | 76.6 | 100.0 | - |
| Crystallized | 46 | 34.8 | 43.0 | 56.1 | 100.0 |
| Diffraction-quality Crystals | 34 | 25.8 | 31.8 | 41.5 | 73.9 |
| Diffraction | 0 | 0.0 | 0.0 | 0.0 | 0.0 |
| NMR Assigned | 0 | 0.0 | 0.0 | 0.0 | - |
| HSQC | 0 | 0.0 | 0.0 | 0.0 | - |
| Crystal Structure | 26 | 19.7 | 24.3 | 31.7 | 56.5 |
| NMR Structure | 0 | 0.0 | 0.0 | 0.0 | - |
| In PDB1 | 14 | 10.6 | 13.1 | 17.1 | 30 |
| Work Stopped | 16 | - | - | - | - |
| Test Target | 0 | - | - | - | - |
| Other | 0 | - | - | - | - |
Table 2: Status Statistics for ISPC by Organism
These statistics are derived from mapping of target sequences to GenBank using
>=98% sequence identity cut off
| Organism | Total Number1 | Work Stopped | Cloned | Expressed | Purified | Crystallized | Crystal Structure | NMR Structure | In PDB2 |
| Viruses | 6 | 0 | 5 | 3 | 1 | 0 | 0 | 0 | 0 |
| Bacteria | 70 | 10 | 70 | 54 | 39 | 25 | 12 | 0 | 5 |
| Prokaryota | 70 | 10 | 70 | 54 | 39 | 25 | 12 | 0 | 5 |
| Arabidopsis | 1 | 0 | 1 | 1 | 1 | 0 | 0 | 0 | 0 |
| Drosophila | 4 | 0 | 3 | 3 | 1 | 1 | 0 | 0 | 0 |
| Mouse | 15 | 2 | 15 | 12 | 10 | 2 | 1 | 0 | 1 |
| Human | 31 | 5 | 30 | 23 | 19 | 6 | 5 | 0 | 3 |
| Eukaryota | 60 | 5 | 57 | 49 | 42 | 20 | 14 | 0 | 9 |
Last updated: Mar 11 2010
back to topDeposited Structure Statistics for ISPC Center
Number of Released X-Ray Structures: 13
Number of Released NMR Structures: 0
Total number of released structures from ISPC center in the PDB: 13
Table 3: PDB Status Statistics for Structures from ISPC
| PDB Status | Number of Structures |
| Total Deposited | 13 |
| Released | 13 |
| Release on Publication | 0 |
| Release on Certain Date | 0 |
| In Process | 0 |
| Last updated: Mar 11 2010 |
| Note 1: "Total Deposited" are all structures in the PDB including structures released to the public and structures that are in the process to be released("Released on Publication" , "Released on Certain Date", etc.). |
Table 4: List of Structures Deposited in the PDB by ISPC
Total number of structures: 14
Structures of distinct targets: 141
1
A target may reference several PDB IDs
(example: structure of the same polypeptides with different ligands).
In this case only one structure is counted to compute number of structures of
distinct targets
Related PDB_ID(s): PDB_ID(s) associated with the same target in targetDB
| PDB_ID | Title | Target_id | Deposition Date | Released Date | PDB Status | Related PDB_ID in TargetDB |
| 2NVB | contribution of pro275 to the thermostability of the alcohol dehydrogenases (adhs) | W00208 | 2006-11-12 | 2007-11-13 | REL | none |
| 1ZGB | crystal structure of torpedo californica acetylcholinesterase in complex with an (r)-tacrine(10)-hupyridone inhibitor. | W00568 | 2005-04-21 | 2005-08-16 | REL | none |
| 1ZGC | crystal structure of torpedo californica acetylcholinesterase in complex with an (rs)-tacrine(10)-hupyridone inhibitor. | W00567 | 2005-04-21 | 2005-08-16 | REL | none |
| 1V04 | serum paraoxonase by directed evolution | W00066 | 2004-03-22 | 2004-04-23 | REL | none |
| 2F1O | crystal structure of nqo1 with dicoumarol | W00027 | 2005-11-15 | 2006-05-16 | REL | none |
| 1OGS | human acid-beta-glucosidase | W00186 | 2003-05-13 | 2003-07-03 | REL | none |
| 1Y7V | x-ray structure of human acid-beta-glucosidase covalently bound to conduritol b epoxide | W00572 | 2004-12-10 | 2005-04-12 | REL | none |
| 2B5R | 1b lactamase / b lactamase inhibitor | W00364 | 2005-09-29 | 2006-04-11 | REL | none |
| 1S0W | 1b lactamse/ b lactamase inhibitor | W00187 | 2004-01-05 | 2004-02-10 | REL | none |
| 2B83 | a single amino acid substitution in the clostridium beijerinckii alcohol dehydrogenase is critical for thermostabilization | W00283 | 2005-10-06 | 2006-09-19 | REL | none |
| 1Y7W | crystal structure of a halotolerant carbonic anhydrase from dunaliella salina | W00565 | 2004-12-10 | 2005-05-03 | REL | none |
| 1U65 | ache w. cpt-11 | W00566 | 2004-07-29 | 2005-07-19 | REL | none |
| 1XXM | the modular architecture of protein-protein binding site | W00178 | 2004-11-07 | 2005-01-18 | REL | none |
| 2OET | crystal structure of antizyme inhibitor | W00007 | 2007-01-01 | 0000-00-00 | WDRN | none |
Note 1: Last updated: Mar 11 2010
back to topSequence Redundancy Statistics
Table 5: Sequence Redundancy Statistics for ISPC by Experimental Status
| Sequence Identity(%) | Novel Targets
Status: Selected |
Novel Targets Status: Cloned |
Novel Targets Status: Expressed |
Novel Targets Status: Purified |
Novel Targets Status: Crystallized |
Novel Targets Status: Crystal Structure | Novel Targets Status: in PDB |
| <100 | 110 | 106 | 84 | 59 | 31 | 17 | 10 |
| <90 | 104 | 100 | 78 | 55 | 28 | 16 | 9 |
| <70 | 97 | 93 | 72 | 50 | 23 | 11 | 8 |
| <50 | 93 | 90 | 69 | 47 | 22 | 11 | 8 |
| <30 | 77 | 77 | 67 | 47 | 22 | 11 | 8 |
| Last updated: 10-03-08 |
| Sequence redundancy is calculated by clustering analysis using BLASTClust program with similarity threshold set to percent of sequence identity. Please view detailed explanation of sequence redundancy calculations and BLASTClust threshold settings. Sequence redundancy calculations are based on comparison to all protein sequences in TargetDB which are in the same experimental status category and at least 20 amino acids long |
Table 6:Sequence Redundancy Statistics for Structures Released by ISPC by Year
| Year | Released Structures | Number of Released Structures <30% Identity at Time of Release | Percent(%) of Released Structures <30% Identity(%) at Time of Release |
| 2003 | 1 | 1 | 100 |
| 2004 | 2 | 1 | 50 |
| 2005 | 6 | 0 | 0 |
| 2006 | 3 | 0 | 0 |
| 2007 | 1 | 0 | 0 |
| Total | 13 | 2 | 15 |
| Last updated:10-03-11 |
| Sequence redundancy is calculated by clustering analysis using BLASTClust program with similarity threshold set to percent of sequence identity. Please view detailed explanation of sequence redundancy calculations and BLASTClust threshold settings. Sequence redundancy calculations are based on comparison to all protein sequences in the PDB which are at least 20 amino acids long |
