Protein Family Models for Protein (Select 2054967001) - Protein Family Models

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Select item 4030091.

methyltransferase domain-containing protein

This family appears to be a methyltransferase domain. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF025033.4
Method:: HMM

Select item 4028282.

methyltransferase domain-containing protein

This family appears to have methyltransferase activity. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF025217.4
Method:: HMM

Select item 3996943.

methyltransferase domain-containing protein

This family appears to be a methyltransferase domain. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF024880.4
Method:: HMM

Select item 3971944.

methyltransferase

Members of this family are SAM dependent methyltransferases. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF019847.4
Method:: HMM

Select item 3963065.

methyltransferase domain-containing protein

Members of this family are SAM dependent methyltransferases. (from Pfam)

GO Terms:

Molecular Function:: methyltransferase activity (GO:0008168)

Molecular Function:: S-adenosylmethionine-dependent methyltransferase activity (GO:0008757)

Date:: 2024-07-08

Family Accession:: NF019846.4
Method:: HMM

Select item 3938786.

methionine biosynthesis protein MetW

This family consists of several bacterial and one archaeal methionine biosynthesis MetW proteins. Biosynthesis of methionine from homoserine in Pseudomonas putida takes place in three steps. The first step is the acylation of homoserine to yield an acyl-L-homoserine. This reaction is catalysed by the products of the metXW genes and is equivalent to the first step in enterobacteria, gram-positive bacteria and fungi, except that in these microorganisms the reaction is catalysed by a single polypeptide (the product of the metA gene in Escherichia coli and the met5 gene product in Neurospora crassa). In Pseudomonas putida, as in gram-positive bacteria and certain fungi, the second and third steps are a direct sulfhydrylation that converts the O-acyl-L-homoserine into homocysteine and further methylation to yield methionine. The latter reaction can be mediated by either of the two methionine synthetases present in the cells [1]. [1]. 11479715. The methionine biosynthetic pathway from homoserine in. Pseudomonas putida involves the metW, metX, metZ, metH and metE. gene products.. Alaminos M, Ramos JL;. Arch Microbiol 2001;176:151-154. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF018696.4
Method:: HMM

Select item 3927127.

50S ribosomal protein L11 methyltransferase

This family consists of several Ribosomal protein L11 methyltransferase (EC:2.1.1.-) sequences. [1]. 8226664. Cotranscription of two genes necessary for ribosomal protein L11. methylation (prmA) and pantothenate transport (panF) in. Escherichia coli K-12.. Vanet A, Plumbridge JA, Alix JH;. J Bacteriol 1993;175:7178-7188. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF018076.4
Method:: HMM

Select item 3925778.

methyltransferase

This domain is found in ribosomal RNA small subunit methyltransferase C (eg Swiss:P44453) as well as other methyltransferases (eg Swiss:Q53742). (from Pfam)

GO Terms:

Molecular Function:: methyltransferase activity (GO:0008168)

Date:: 2024-07-08

Family Accession:: NF017026.4
Method:: HMM

Select item 3902059.

class I SAM-dependent methyltransferase

GO Terms:

Molecular Function:: methyltransferase activity (GO:0008168)

Date:: 2024-07-08

Family Accession:: NF013382.4
Method:: HMM

Select item 38974710.

class I SAM-dependent methyltransferase

This family consist of Cyclopropane-fatty-acyl-phospholipid synthase or CFA synthase EC:2.1.1.79 this enzyme catalyse the reaction: S-adenosyl-L-methionine + phospholipid olefinic fatty acid <=> S-adenosyl-L-homocysteine + phospholipid cyclopropane fatty acid. [1]. 8917504. A common mechanism for the biosynthesis of methoxy and. cyclopropyl mycolic acids in Mycobacterium tuberculosis.. Yuan Y, Barry CE 3rd;. Proc Natl Acad Sci U S A 1996;93:12828-12833.. [2]. 7592990. The biosynthesis of cyclopropanated mycolic acids in. Mycobacterium tuberculosis. Identification and functional. analysis of CMAS-2.. George KM, Yuan Y, Sherman DR, Barry CE 3d;. J Biol Chem 1995;270:27292-27298.. [3]. 10882107. A novel mycolic acid cyclopropane synthetase is required for. cording, persistence, and virulence of Mycobacterium. tuberculosis.. Glickman MS, Cox JS, Jacobs WR Jr;. Mol Cell. 2000;5:717-727. (from Pfam)

Date:: 2024-07-08

Family Accession:: NF014414.4
Method:: HMM

Select item 36391511.