Statistics Summary Report for ISFI Center
Last updated: Mar 11 2010
Target Status Statistics
Total number of targets deposited by ISFI to TargetDB: 378
View ISFI Target ListTable 1: Status Statistics for ISFI
| Status | Total Number of Targets | (%) Relative to "Cloned" Targets | (%) Relative to "Expressed" Targets | (%) Relative to "Purified" Targets | (%) Relative to "Crystallized" Targets |
| Cloned | 293 | 100.0 | - | - | - |
| Expressed | 200 | 68.3 | 100.0 | - | - |
| Soluble | 150 | 51.2 | 75.0 | - | - |
| Purified | 137 | 46.8 | 68.5 | 100.0 | - |
| Crystallized | 95 | 32.4 | 47.5 | 69.3 | 100.0 |
| Diffraction-quality Crystals | 76 | 25.9 | 38.0 | 55.5 | 80.0 |
| Diffraction | 68 | 23.2 | 34.0 | 49.6 | 71.6 |
| NMR Assigned | 0 | 0.0 | 0.0 | 0.0 | - |
| HSQC | 0 | 0.0 | 0.0 | 0.0 | - |
| Crystal Structure | 60 | 20.5 | 30.0 | 43.8 | 63.2 |
| NMR Structure | 0 | 0.0 | 0.0 | 0.0 | - |
| In PDB1 | 35 | 11.9 | 17.5 | 25.5 | 37 |
| Work Stopped | 11 | - | - | - | - |
| Test Target | 3 | - | - | - | - |
| Other | 0 | - | - | - | - |
Table 2: Status Statistics for ISFI 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 |
| Archaea | 2 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 0 |
| Bacteria | 364 | 11 | 282 | 196 | 135 | 95 | 60 | 0 | 35 |
| Prokaryota | 366 | 11 | 284 | 196 | 135 | 95 | 60 | 0 | 35 |
| Yeast | 9 | 0 | 9 | 4 | 2 | 0 | 0 | 0 | 0 |
| Human | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Eukaryota | 12 | 0 | 9 | 4 | 2 | 0 | 0 | 0 | 0 |
Last updated: Mar 11 2010
back to topDeposited Structure Statistics for ISFI Center
Number of Released X-Ray Structures: 12
Number of Released NMR Structures: 1
Total number of released structures from ISFI center in the PDB: 13
Table 3: PDB Status Statistics for Structures from ISFI
| PDB Status | Number of Structures |
| Total Deposited | 31 |
| Released | 13 |
| In Process | 18 |
| 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 ISFI
Total number of structures: 31
Structures of distinct targets: 311
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 |
| ND_148 | Experimental status "in PDB", PDB ID is not provided | ISFI425 | - | - | - | none |
| ND_140 | Experimental status "in PDB", PDB ID is not provided | ISFI490 | - | - | - | none |
| ND_151 | Experimental status "in PDB", PDB ID is not provided | ISFI704 | - | - | - | none |
| ND_152 | Experimental status "in PDB", PDB ID is not provided | ISFI734 | - | - | - | none |
| ND_139 | Experimental status "in PDB", PDB ID is not provided | ISFI397 | - | - | - | none |
| ND_145 | Experimental status "in PDB", PDB ID is not provided | ISFI508 | - | - | - | none |
| ND_153 | Experimental status "in PDB", PDB ID is not provided | ISFI735 | - | - | - | none |
| ND_146 | Experimental status "in PDB", PDB ID is not provided | ISFI516 | - | - | - | none |
| ND_136 | Experimental status "in PDB", PDB ID is not provided | ISFI107 | - | - | - | none |
| ND_149 | Experimental status "in PDB", PDB ID is not provided | ISFI426 | - | - | - | none |
| ND_143 | Experimental status "in PDB", PDB ID is not provided | ISFI493 | - | - | - | none |
| ND_144 | Experimental status "in PDB", PDB ID is not provided | ISFI502 | - | - | - | none |
| ND_141 | Experimental status "in PDB", PDB ID is not provided | ISFI491 | - | - | - | none |
| ND_138 | Experimental status "in PDB", PDB ID is not provided | ISFI394 | - | - | - | none |
| ND_147 | Experimental status "in PDB", PDB ID is not provided | ISFI422 | - | - | - | none |
| ND_142 | Experimental status "in PDB", PDB ID is not provided | ISFI492 | - | - | - | none |
| ND_137 | Experimental status "in PDB", PDB ID is not provided | ISFI418 | - | - | - | none |
| ND_150 | Experimental status "in PDB", PDB ID is not provided | ISFI430 | - | - | - | none |
| 3G5O | the crystal structure of the toxin-antitoxin complex relbe2 (rv2865-2866) from mycobacterium tuberculosis | ISFI120 ISFI:ISFI121 | 2009-02-05 | 2009-04-14 | REL | none |
| 3E57 | crystal structure of tm1382, a putative nudix hydrolase | ISFI338 | 2008-08-13 | 2008-09-30 | REL | none |
| 2NYX | crystal structure of rv1404 from mycobacterium tuberculosis | ISFI155 TB:Rv1404 | 2006-11-21 | 2006-12-05 | REL | none |
| 3FHK | crystal structure of apc1446, b.subtilis yphp disulfide isomerase | ISFI308 | 2008-12-09 | 2009-09-01 | REL | none |
| 2IB0 | crystal structure of a conserved hypothetical protein, rv2844, from mycobacterium tuberculosis | ISFI195 TB:Rv2844 | 2006-09-08 | 2006-09-26 | REL | none |
| 3H87 | rv0301 rv0300 toxin antitoxin complex from mycobacterium tuberculosis | ISFI521 ISFI:ISFI522 | 2009-04-28 | 2009-05-05 | REL | none |
| 3FMS | crystal structure of tm0439, a gntr transcriptional regulator | ISFI332 | 2008-06-02 | 2008-07-01 | REL | none |
| 2G38 | a pe/ppe protein complex from mycobacterium tuberculosis | ISFI142 TB:Rv2430c TB:Rv2431c ISFI:ISFI141 | 2006-02-17 | 2006-03-14 | REL | none |
| 2JPB | solution structure of ompr-c dna binding protein | ISFI333 | 2007-05-03 | 2007-06-12 | REL | none |
| 3DBO | crystal structure of a member of the vapbc family of toxin-antitoxin systems, vapbc-5, from mycobacterium tuberculosis | ISFI449 ISFI:ISFI450 | 2008-06-02 | 2008-07-15 | REL | none |
| 2G2D | crystal structure of a putative pduo-type atp:cobalamin adenosyltransferase from mycobacterium tuberculosis | ISFI15 TB:Rv1314c | 2006-02-15 | 2006-03-28 | REL | none |
| 3H3E | crystal structure of tm1679, a metal-dependent hydrolase of the beta-lactamase superfamily | ISFI337 | 2009-04-16 | 2009-07-14 | REL | none |
| 3E4X | crystal structure of putative metal-dependent hydrolases apc36150 | ISFI154 | 2008-08-12 | 2008-10-14 | Replaced by:3GOR | none |
Note 1: Last updated: Mar 11 2010
back to topSequence Redundancy Statistics
Table 5: Sequence Redundancy Statistics for ISFI 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 | 314 | 239 | 146 | 111 | 81 | 49 | 26 |
| <90 | 310 | 235 | 142 | 108 | 78 | 49 | 26 |
| <70 | 307 | 234 | 141 | 107 | 78 | 49 | 26 |
| <50 | 301 | 229 | 139 | 105 | 77 | 49 | 26 |
| <30 | 245 | 198 | 124 | 99 | 73 | 48 | 26 |
| 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 ISFI 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 |
| 2006 | 4 | 3 | 75 |
| 2007 | 1 | 0 | 0 |
| 2008 | 4 | 3 | 75 |
| 2009 | 4 | 4 | 100 |
| Total | 13 | 10 | 77 |
| 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 |
