CRY2 M12-A
Protein Sequence
Sequence Variants
| ID | Name | Remain region | Mutation sites | Ref seq |
|---|---|---|---|---|
| psp04530 | CRY2 | 1-612 | - | ✓ |
| psp04448 | CRY2 M12-A | - | R557A, G558A, F559A, D560A, E561A, R562A | |
| psp03511 | CRY2 1-509 | 1-509 | - | |
| psp03535 | CRY2 510-612 | 510-612 | - | |
| psp03876 | CRY2 1-489 | 1-489 | - | |
| psp04354 | CRY2 490-612 | 490-612 | - | |
| psp04841 | CRY2 ΔN538-R557 | 1-537, 558-612 | - | |
| psp00093 | CRY2 M5-A | - | T514A, I515A, K516A, E517A, P518A, G519A | |
| psp00327 | CRY2 M18-A | - | G594A, I595A, Q596A, D597A, S598A, S599A | |
| psp00407 | CRY2 M19-A | - | D600A, Q601A, I602A, T603A, T604A, S605A | |
| psp00497 | CRY2 M6-A | - | L520A, C521A, P522A, S523A, V524A, S525A | |
| psp00639 | CRY2 M16-A | - | S582A, C583A, S584A, L585A, S587A | |
| psp00749 | CRY2 M2-A | - | G496A, P499A, D500A, E501A | |
| psp00802 | CRY2 M7-A | - | S526A, N527A, D528A, Q529A, Q530A, V531A | |
| psp01530 | CRY2 M1-A | - | E490A, Q492A, I493A, M494A, I495A | |
| psp01647 | CRY2 M11-A | - | R551A, D552A, M553A, K554A, K555A, S556A | |
| psp01914 | CRY2 M13-A | - | E563A, L564A, F565A, S566A, T567A | |
| psp02478 | CRY2 M15-A | - | V576A, F577A, F578A, V579A, S580A, Q581A | |
| psp02512 | CRY2 M9-A | - | N538A, G539A, S540A, K541A, R542A, V543A | |
| psp02629 | CRY2 M8-A | - | P532A, S533A, V535A, R536A, Y537A | |
| psp03036 | CRY2 M4-A | - | E508A, L510A, G511A, N513A | |
| psp03220 | CRY2 M14-A | - | E569A, S570A, S571A, S572A, S573A, S574A, S575A | |
| psp03849 | CRY2 M17-A | - | E588A, G589A, K590A, N591A, L592A, E593A | |
| psp04090 | CRY2 M20-A | - | L606A, G607A, K608A, N609A, G610A, C611A, K612A | |
| psp04284 | CRY2 M10-A | - | K544A, P545A, E546A, E547A, E548A, E549A, E550A | |
| psp04969 | CRY2 M3-A | - | I502A, V503A, D505A, S506A, F507A |
Orthologs and Paralogs
Biophysical Features
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IDR (Intrinsically Disordered Region) was predicted by Mobidb-lite 4.0, please refer to: MobiDB-lite 4.0: faster prediction of intrinsic protein disorder and structural compactness.
Pi-Pi interaction was predicted by PScore, please refer to: Pi-Pi contacts are an overlooked protein feature relevant to phase separation.
PLAAC and PrD. like were both predicted by PLAAC, please refer to: PLAAC: a web and command-line application to identify proteins with prion-like amino acid composition.
LCR (Low Complexity Region) was predicted by SEG, please refer to: Statistics of local complexity in amino acid sequences and sequence databases.
NCPR (Net Charge Per Residue), FCR (Fraction of Charged Residues) and hydrophobicity were both computated by CIDER, please refer to: CIDER: Resources to Analyze Sequence-Ensemble Relationships of Intrinsically Disordered Proteins.
Polarity was computated by ProtScale, please refer to: ProtScale.
SASA (Solvent-Accessible Surface Area) was computated by BioPython based on the predicted structure, please refer to: Bio.PDB.SASA module.
Protein Structure
Protein structure was predicted by Chai-1, which also produces predicted local distance difference test (pLDDT) score between 0 and 100.
For pLDDT, please refer to: pLDDT: Understanding local confidence