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Results for Proteins associated with the Gene: MTFMT
MTFMT
123263


Known Diseases associated with this Protein:
  COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15
  COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15 (COXPD15)
  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY, INCLUDED
6
1
4
1
2
Tips:
 The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model.
 Clicking a check box on the left will display or hide the corresponding domain(s).
 To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic.


Default View:

Fmt - COG0223
Formyl_trans_N - pfam00551
PurN - COG0299
Formyl_trans_C - pfam02911


Swiss-Prot Protein: Q96DP5
Identical to: NP_640335
   Default View:





Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
Q96DP5FmtCOG0223473551.4e-47
Q96DP5PurNCOG0299772370.0008
Q96DP5Formyl_trans_Npfam00551482202e-24
Q96DP5Formyl_trans_Cpfam029112433508.5e-16



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