GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Methylomonas methanica MC09

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate WP_013819317.1 METME_RS13600 aminotransferase class V-fold PLP-dependent enzyme

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000214665.1:WP_013819317.1
          Length = 388

 Score =  251 bits (641), Expect = 2e-71
 Identities = 139/380 (36%), Positives = 215/380 (56%), Gaps = 4/380 (1%)

Query: 1   MDNKQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTE-NDVLML 59
           M  +  L IPGPT  P +VL AM      HRS  F  +   L  +LK + +TE     + 
Sbjct: 1   MAGRNHLFIPGPTNTPHEVLSAMHVPMEDHRSPIFPNLFKPLLEDLKKVFRTEAGQCFVF 60

Query: 60  TTSGTGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPND 119
             +GT   E ++ N L+PGD+VL+   G+F   W+  A+  G  VE  + EWGK +  + 
Sbjct: 61  PATGTAGWEVALTNCLNPGDKVLIYRFGQFAHLWMDAARKLGFDVEAHEVEWGKGIPLDA 120

Query: 120 FKTLLEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGG-ALMIVDAVTSLGATPV 178
            +  L+ D +  IKA++ TH+ETSTGV +D+A +  A  A G  AL+ VD V+S+ +   
Sbjct: 121 MEARLKEDKNHEIKAVLATHNETSTGVTSDIAGVRKAMDAAGHPALLFVDGVSSIASLEF 180

Query: 179 AIDDLGLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDS 238
            +DD G+D   SGSQKG+M+P G   ++ S KA  A ET+T PR +  LK    +  +  
Sbjct: 181 RMDDWGVDGAISGSQKGFMLPAGAAILAFSQKALAAVETSTFPRSFFSLKDQMNANKDGY 240

Query: 239 SPFTPPINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNAASNA 298
           +P+TP   +++GL+ +L ++  EG+D ++ RH R     R A+ A  L + A     S+ 
Sbjct: 241 TPYTPSTPMLHGLRKALDLLLEEGMDNVYARHHRLGEGVRRAVAAWGLQICAQPGFESDT 300

Query: 299 ITA-VAPLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALE 357
           +TA V P   +A  + ST   K++I++  G   + GK+FRIGH+G + D  +L  I  +E
Sbjct: 301 VTAIVVPADKDARHVISTAYNKYNISLGAGLTEVAGKVFRIGHIGDMNDVSLLGAIAGVE 360

Query: 358 ATLIELGYEGVTPGSGVAAA 377
             +++ G++ + PGSGVAAA
Sbjct: 361 MAMLDNGFD-IKPGSGVAAA 379


Lambda     K      H
   0.317    0.134    0.386 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 359
Number of extensions: 19
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 384
Length of database: 388
Length adjustment: 30
Effective length of query: 354
Effective length of database: 358
Effective search space:   126732
Effective search space used:   126732
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory