Target Information
Target General Information | Top | |||||
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Target ID |
T95033
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Target Name |
Oxidoreductase HTATIP2 (HTATIP2)
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Synonyms |
HIV-1 TAT-interactive protein 2; 30 kDa HIV-1 TAT-interacting protein
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Gene Name |
HTATIP2
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Target Type |
Literature-reported target
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[1] | ||||
Function |
Oxidoreductase required for tumor suppression. NAPDH-bound form inhibits nuclear import by competing with nuclear import substrates for binding to a subset of nuclear transport receptors. May act as a redox sensor linked to transcription through regulation of nuclear import. Isoform 1 is a metastasis suppressor with proapoptotic as well as antiangiogenic properties. Isoform 2 has an antiapoptotic effect.
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UniProt ID | ||||||
EC Number |
EC 1.1.1.-
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Sequence |
MAETEALSKLREDFRMQNKSVFILGASGETGRVLLKEILEQGLFSKVTLIGRRKLTFDEE
AYKNVNQEVVDFEKLDDYASAFQGHDVGFCCLGTTRGKAGAEGFVRVDRDYVLKSAELAK AGGCKHFNLLSSKGADKSSNFLYLQVKGEVEAKVEELKFDRYSVFRPGVLLCDRQESRPG EWLVRKFFGSLPDSWASGHSVPVVTVVRAMLNNVVRPRDKQMELLENKAIHDLGKAHGSL KP Click to Show/Hide
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3D Structure | Click to Show 3D Structure of This Target | PDB |
Cell-based Target Expression Variations | Top | |||||
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Cell-based Target Expression Variations |
Drug Binding Sites of Target | Top | |||||
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Ligand Name: NADPH | Ligand Info | |||||
Structure Description | CC3(TIP30)Crystal Structure | PDB:2BKA | ||||
Method | X-ray diffraction | Resolution | 1.70 Å | Mutation | No | [2] |
PDB Sequence |
EALSKLREDF
14 RMQNKSVFIL24 GASGETGRVL34 LKEILEQGLF44 SKVTLIGRRK54 LTFDEEAYKN 64 VNQEVVDFEK74 LDDYASAFQG84 HDVGFCCLGT94 TRGKAGAEGF104 VRVDRDYVLK 114 SAELAKAGGC124 KHFNLLSSKG134 ADKSSNFLYL144 QVKGEVEAKV154 EELKFDRYSV 164 FRPGVLLCDR174 QESRPGEWLV184 RKFFGSLPDS194 WASGHSVPVV204 TVVRAMLNNV 214 VRPRDKQMEL224 LENKAIHDLG234 KA
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GLY25
3.172
ALA26
4.264
SER27
2.621
GLY28
3.128
GLU29
2.823
THR30
2.899
GLY31
4.637
ARG52
2.784
ARG53
2.881
PHE72
3.789
CYS91
3.346
LEU92
2.733
GLY93
3.109
THR94
3.800
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Click to View More Binding Site Information of This Target with Different Ligands |
Different Human System Profiles of Target | Top |
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Human Similarity Proteins
of target is determined by comparing the sequence similarity of all human proteins with the target based on BLAST. The similarity proteins for a target are defined as the proteins with E-value < 0.005 and outside the protein families of the target.
A target that has fewer human similarity proteins outside its family is commonly regarded to possess a greater capacity to avoid undesired interactions and thus increase the possibility of finding successful drugs
(Brief Bioinform, 21: 649-662, 2020).
Human Tissue Distribution
of target is determined from a proteomics study that quantified more than 12,000 genes across 32 normal human tissues. Tissue Specificity (TS) score was used to define the enrichment of target across tissues.
The distribution of targets among different tissues or organs need to be taken into consideration when assessing the target druggability, as it is generally accepted that the wider the target distribution, the greater the concern over potential adverse effects
(Nat Rev Drug Discov, 20: 64-81, 2021).
Human Similarity Proteins
Human Tissue Distribution
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There is no similarity protein (E value < 0.005) for this target
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Note:
If a protein has TS (tissue specficity) scores at least in one tissue >= 2.5, this protein is called tissue-enriched (including tissue-enriched-but-not-specific and tissue-specific). In the plots, the vertical lines are at thresholds 2.5 and 4.
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References | Top | |||||
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REF 1 | Inhibition of nuclear import by the proapoptotic protein CC3. Mol Cell Biol. 2004 Aug;24(16):7091-101. | |||||
REF 2 | Crystal structure of CC3 (TIP30): implications for its role as a tumor suppressor. J Biol Chem. 2005 May 6;280(18):18229-36. |
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