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Conserved domains on  [gi|592747176|gb|AHL43606|]
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Marf, partial [Drosophila pseudotalamancana]

Protein Classification

P-loop NTPase family protein( domain architecture ID 1562424)

P-loop NTPase (nucleoside triphosphate hydrolase) family protein contains two conserved sequence signatures, the Walker A motif (the P-loop proper) and Walker B motif which bind, respectively, the beta and gamma phosphate moieties of the bound nucleotide (typically ATP or GTP), and a Mg(2+) cation

Graphical summary

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List of domain hits

Name Accession Description Interval E-value
P-loop_NTPase super family cl38936
P-loop containing Nucleoside Triphosphate Hydrolases; Members of the P-loop NTPase domain ...
1-130 4.54e-24

P-loop containing Nucleoside Triphosphate Hydrolases; Members of the P-loop NTPase domain superfamily are characterized by a conserved nucleotide phosphate-binding motif, also referred to as the Walker A motif (GxxxxGK[S/T], where x is any residue), and the Walker B motif (hhhh[D/E], where h is a hydrophobic residue). The Walker A and B motifs bind the beta-gamma phosphate moiety of the bound nucleotide (typically ATP or GTP) and the Mg2+ cation, respectively. The P-loop NTPases are involved in diverse cellular functions, and they can be divided into two major structural classes: the KG (kinase-GTPase) class which includes Ras-like GTPases and its circularly permutated YlqF-like; and the ASCE (additional strand catalytic E) class which includes ATPase Binding Cassette (ABC), DExD/H-like helicases, 4Fe-4S iron sulfur cluster binding proteins of NifH family, RecA-like F1-ATPases, and ATPases Associated with a wide variety of Activities (AAA). Also included are a diverse set of nucleotide/nucleoside kinase families.


The actual alignment was detected with superfamily member cd09912:

Pssm-ID: 476819 [Multi-domain]  Cd Length: 180  Bit Score: 91.07  E-value: 4.54e-24
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 592747176   1 DNHCLNADVFVLVLNAESTMTRAEKQFFHTVSQKlSKPNIFILNNRWDASANEPEFQESVKSQHtercvdfltkELKVSN 80
Cdd:cd09912   68 ESFLPRADAVIFVLSADQPLTESEREFLKEILKW-SGKKIFFVLNKIDLLSEEELEEVLEYSRE----------ELGVLE 136
                         90       100       110       120       130
                 ....*....|....*....|....*....|....*....|....*....|
gi 592747176  81 EKEAGERVFFVSARETLQARIEESKGNpphlgaiaegfqIRYFEFQDFER 130
Cdd:cd09912  137 LGGGEPRIFPVSAKEALEARLQGDEEL------------LEQSGFEELEE 174
 
Name Accession Description Interval E-value
DLP_2 cd09912
Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins; The ...
1-130 4.54e-24

Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins; The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.


Pssm-ID: 206739 [Multi-domain]  Cd Length: 180  Bit Score: 91.07  E-value: 4.54e-24
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 592747176   1 DNHCLNADVFVLVLNAESTMTRAEKQFFHTVSQKlSKPNIFILNNRWDASANEPEFQESVKSQHtercvdfltkELKVSN 80
Cdd:cd09912   68 ESFLPRADAVIFVLSADQPLTESEREFLKEILKW-SGKKIFFVLNKIDLLSEEELEEVLEYSRE----------ELGVLE 136
                         90       100       110       120       130
                 ....*....|....*....|....*....|....*....|....*....|
gi 592747176  81 EKEAGERVFFVSARETLQARIEESKGNpphlgaiaegfqIRYFEFQDFER 130
Cdd:cd09912  137 LGGGEPRIFPVSAKEALEARLQGDEEL------------LEQSGFEELEE 174
 
Name Accession Description Interval E-value
DLP_2 cd09912
Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins; The ...
1-130 4.54e-24

Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins; The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.


Pssm-ID: 206739 [Multi-domain]  Cd Length: 180  Bit Score: 91.07  E-value: 4.54e-24
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 592747176   1 DNHCLNADVFVLVLNAESTMTRAEKQFFHTVSQKlSKPNIFILNNRWDASANEPEFQESVKSQHtercvdfltkELKVSN 80
Cdd:cd09912   68 ESFLPRADAVIFVLSADQPLTESEREFLKEILKW-SGKKIFFVLNKIDLLSEEELEEVLEYSRE----------ELGVLE 136
                         90       100       110       120       130
                 ....*....|....*....|....*....|....*....|....*....|
gi 592747176  81 EKEAGERVFFVSARETLQARIEESKGNpphlgaiaegfqIRYFEFQDFER 130
Cdd:cd09912  137 LGGGEPRIFPVSAKEALEARLQGDEEL------------LEQSGFEELEE 174
 
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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