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Conserved domains on  [gi|6322561|ref|NP_012635|]
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mitochondrial 37S ribosomal protein RSM26 [Saccharomyces cerevisiae S288C]

Protein Classification

Graphical summary

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List of domain hits

Name Accession Description Interval E-value
Sod_Fe_C super family cl29408
Iron/manganese superoxide dismutases, C-terminal domain; superoxide dismutases (SODs) catalyze ...
115-259 5.81e-13

Iron/manganese superoxide dismutases, C-terminal domain; superoxide dismutases (SODs) catalyze the conversion of superoxide radicals to hydrogen peroxide and molecular oxygen. Three evolutionarily distinct families of SODs are known, of which the Mn/Fe-binding family is one. In humans, there is a cytoplasmic Cu/Zn SOD, and a mitochondrial Mn/Fe SOD. C-terminal domain is a mixed alpha/beta fold.


The actual alignment was detected with superfamily member pfam02777:

Pssm-ID: 460691  Cd Length: 102  Bit Score: 63.21  E-value: 5.81e-13
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561    115 PSRLFLSKIKDSFnGSdWEVVKEEMIyRAENEVLGQGWLFLVENNEKKLFILTSNNNGTPYyfprnqsfdlnsaisidef 194
Cdd:pfam02777   1 PTGALAEAIEKDF-GS-FDAFKEEFN-AAAAGVFGSGWAWLVYDPDGKLEIVTTPNQDNPL------------------- 58
                          90       100       110       120       130       140
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 6322561    195 atlkqMKELIgkstklngkvqdwtmPIICVNLWDHAYLHDYGvGNRSKYVKNVLDNLNWSVVNNR 259
Cdd:pfam02777  59 -----TDGLT---------------PLLGLDVWEHAYYLDYQ-NRRADYVKAFWNVVNWDEVEKR 102
 
Name Accession Description Interval E-value
Sod_Fe_C pfam02777
Iron/manganese superoxide dismutases, C-terminal domain; superoxide dismutases (SODs) catalyze ...
115-259 5.81e-13

Iron/manganese superoxide dismutases, C-terminal domain; superoxide dismutases (SODs) catalyze the conversion of superoxide radicals to hydrogen peroxide and molecular oxygen. Three evolutionarily distinct families of SODs are known, of which the Mn/Fe-binding family is one. In humans, there is a cytoplasmic Cu/Zn SOD, and a mitochondrial Mn/Fe SOD. C-terminal domain is a mixed alpha/beta fold.


Pssm-ID: 460691  Cd Length: 102  Bit Score: 63.21  E-value: 5.81e-13
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561    115 PSRLFLSKIKDSFnGSdWEVVKEEMIyRAENEVLGQGWLFLVENNEKKLFILTSNNNGTPYyfprnqsfdlnsaisidef 194
Cdd:pfam02777   1 PTGALAEAIEKDF-GS-FDAFKEEFN-AAAAGVFGSGWAWLVYDPDGKLEIVTTPNQDNPL------------------- 58
                          90       100       110       120       130       140
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 6322561    195 atlkqMKELIgkstklngkvqdwtmPIICVNLWDHAYLHDYGvGNRSKYVKNVLDNLNWSVVNNR 259
Cdd:pfam02777  59 -----TDGLT---------------PLLGLDVWEHAYYLDYQ-NRRADYVKAFWNVVNWDEVEKR 102
PLN02622 PLN02622
iron superoxide dismutase
38-260 1.11e-07

iron superoxide dismutase


Pssm-ID: 166263 [Multi-domain]  Cd Length: 261  Bit Score: 51.55  E-value: 1.11e-07
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561    38 WFDYQRYLCDKLTLATAGQSLESYYPFHILLKTA---GNPLQSniFNLASSIHNNHLFVENILPSAVEHgtnsnavvkte 114
Cdd:PLN02622  73 WGEHHRGYVEGLNKQLAKDDILYGYTMDELVKVTynnGNPLPE--FNNAAQVWNHDFFWESMQPGGGDM----------- 139
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561   115 PSRLFLSKIKDSFnGSdWEVVKEEMIYRAENeVLGQGWLFLV-ENNEKKLFILTSNNNGTPyyfprnqsfdlnsaISIDE 193
Cdd:PLN02622 140 PELGVLEQIEKDF-GS-FTNFREKFTEAALT-LFGSGWVWLVlKREERRLEVVKTSNAINP--------------LVWDD 202
                        170       180       190       200       210       220
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 6322561   194 fatlkqmkeligkstklngkvqdwtMPIICVNLWDHAYLHDYGvGNRSKYVKNVLDNL-NWSVVNNRI 260
Cdd:PLN02622 203 -------------------------IPIICLDVWEHAYYLDYK-NDRGKYVNAFMNHLvSWNAAMARM 244
 
Name Accession Description Interval E-value
Sod_Fe_C pfam02777
Iron/manganese superoxide dismutases, C-terminal domain; superoxide dismutases (SODs) catalyze ...
115-259 5.81e-13

Iron/manganese superoxide dismutases, C-terminal domain; superoxide dismutases (SODs) catalyze the conversion of superoxide radicals to hydrogen peroxide and molecular oxygen. Three evolutionarily distinct families of SODs are known, of which the Mn/Fe-binding family is one. In humans, there is a cytoplasmic Cu/Zn SOD, and a mitochondrial Mn/Fe SOD. C-terminal domain is a mixed alpha/beta fold.


Pssm-ID: 460691  Cd Length: 102  Bit Score: 63.21  E-value: 5.81e-13
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561    115 PSRLFLSKIKDSFnGSdWEVVKEEMIyRAENEVLGQGWLFLVENNEKKLFILTSNNNGTPYyfprnqsfdlnsaisidef 194
Cdd:pfam02777   1 PTGALAEAIEKDF-GS-FDAFKEEFN-AAAAGVFGSGWAWLVYDPDGKLEIVTTPNQDNPL------------------- 58
                          90       100       110       120       130       140
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 6322561    195 atlkqMKELIgkstklngkvqdwtmPIICVNLWDHAYLHDYGvGNRSKYVKNVLDNLNWSVVNNR 259
Cdd:pfam02777  59 -----TDGLT---------------PLLGLDVWEHAYYLDYQ-NRRADYVKAFWNVVNWDEVEKR 102
PLN02622 PLN02622
iron superoxide dismutase
38-260 1.11e-07

iron superoxide dismutase


Pssm-ID: 166263 [Multi-domain]  Cd Length: 261  Bit Score: 51.55  E-value: 1.11e-07
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561    38 WFDYQRYLCDKLTLATAGQSLESYYPFHILLKTA---GNPLQSniFNLASSIHNNHLFVENILPSAVEHgtnsnavvkte 114
Cdd:PLN02622  73 WGEHHRGYVEGLNKQLAKDDILYGYTMDELVKVTynnGNPLPE--FNNAAQVWNHDFFWESMQPGGGDM----------- 139
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561   115 PSRLFLSKIKDSFnGSdWEVVKEEMIYRAENeVLGQGWLFLV-ENNEKKLFILTSNNNGTPyyfprnqsfdlnsaISIDE 193
Cdd:PLN02622 140 PELGVLEQIEKDF-GS-FTNFREKFTEAALT-LFGSGWVWLVlKREERRLEVVKTSNAINP--------------LVWDD 202
                        170       180       190       200       210       220
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 6322561   194 fatlkqmkeligkstklngkvqdwtMPIICVNLWDHAYLHDYGvGNRSKYVKNVLDNL-NWSVVNNRI 260
Cdd:PLN02622 203 -------------------------IPIICLDVWEHAYYLDYK-NDRGKYVNAFMNHLvSWNAAMARM 244
PTZ00078 PTZ00078
Superoxide dismutase [Fe]; Provisional
79-257 6.27e-06

Superoxide dismutase [Fe]; Provisional


Pssm-ID: 185432 [Multi-domain]  Cd Length: 193  Bit Score: 45.55  E-value: 6.27e-06
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561    79 IFNLASSIHNNHLFVENILPSAvehgtnsnavvKTEPSRLFLSKIKDSFNgsDWEVVKEEMIYRAENEvLGQGWLFLVEN 158
Cdd:PTZ00078  59 VFNNAAQIWNHNFYWLSMGPNG-----------GGEPTGEIKEKIDEKFG--SFDNFKNEFSNVLSGH-FGSGWGWLVLK 124
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 6322561   159 NEKKLFILTSNNNGTPyyfprnqsfdlnsaisidefatlkqMKELIGKstklngkvqdwtmPIICVNLWDHAYLHDYGvG 238
Cdd:PTZ00078 125 NDGKLEIVQTHDAGNP-------------------------IKDNTGK-------------PLLTCDIWEHAYYIDYR-N 165
                        170
                 ....*....|....*....
gi 6322561   239 NRSKYVKNVLDNLNWSVVN 257
Cdd:PTZ00078 166 DRASYVNSWWNKVNWDFAN 184
 
Blast search parameters
Data Source: Precalculated data, version = cdd.v.3.21
Preset Options:Database: CDSEARCH/cdd   Low complexity filter: no  Composition Based Adjustment: yes   E-value threshold: 0.01

References:

  • Wang J et al. (2023), "The conserved domain database in 2023", Nucleic Acids Res.51(D)384-8.
  • Lu S et al. (2020), "The conserved domain database in 2020", Nucleic Acids Res.48(D)265-8.
  • Marchler-Bauer A et al. (2017), "CDD/SPARCLE: functional classification of proteins via subfamily domain architectures.", Nucleic Acids Res.45(D)200-3.
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