GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Methanosarcina mazei Go1

Align [amino group carrier protein]-gamma-(L-lysyl)-L-glutamate aminotransferase (EC 2.6.1.118) (characterized)
to candidate WP_011033352.1 MM_RS07280 aspartate aminotransferase family protein

Query= BRENDA::Q93R93
         (395 letters)



>NCBI__GCF_000007065.1:WP_011033352.1
          Length = 395

 Score =  323 bits (828), Expect = 5e-93
 Identities = 171/368 (46%), Positives = 239/368 (64%), Gaps = 6/368 (1%)

Query: 24  YNKHDLLIVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMAMPQT 83
           Y +  L++ +G+GA V D  G EYIDCV G  V N+GH +P VV+A++ QAE L+ +   
Sbjct: 30  YGRQPLVLSKGKGAVVQDIYGKEYIDCVAGIAVNNVGHCHPTVVKAIQAQAEKLIHVSNL 89

Query: 84  LPTPMRGEFYRTLTAILPPELNRVFPVNSGTEANEAALKFARAHTGRKKFVAAMRGFSGR 143
             T ++ EF  TL +I   E   VF  NSG EA EAA+K AR  TG+  FVAA   F GR
Sbjct: 90  YYTEIQAEFAETLASITGMEC--VFFCNSGAEAVEAAMKLARVATGKSAFVAAEHSFHGR 147

Query: 144 TMGSLSVTWEPKYREPFLPLVEP-VEFIPYNDVEALKRAVDEETAAVILEPVQGEGGVRP 202
           T+G+LSVT +  YR+PF+P V     F+PY+D +A+++A+ E+TAAV+LEP+QGEGGV  
Sbjct: 148 TIGALSVTHKSMYRDPFMPPVSSKTSFVPYSDADAIRKAISEDTAAVVLEPIQGEGGVNV 207

Query: 203 ATPEFLRAAREITQEKGALLILDEIQTGMGRTGKRFAFEHFGIVPDILTLAKALGGGVPL 262
             P +L+  REI  E G LLI DE+QTG GRTG  F  E FG+ PDI+++AKA+GGG P+
Sbjct: 208 PDPGYLKEVREICDETGTLLIFDEVQTGFGRTGTWFCKEQFGVEPDIMSMAKAIGGGFPM 267

Query: 263 GVAVMREEVARSMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAELGPWFMEKLR 322
           G    R  +  S  +G H +TFGG PLA AA +A+I+ ++  +L ER+ E+G +F +KL 
Sbjct: 268 GAIAARSGL--SFGRGQHASTFGGGPLACAAALASIQAIKEEKLLERSKEMGAYFTKKLS 325

Query: 323 AIPSPKIREVRGMGLMVGLELKEKAAPYIARLEKEHRVLALQAGPTVIRFLPPLVIEKED 382
            +    I EVRG GLM+G+E+K     ++    +EH VL      +V+R +PPLVI KE 
Sbjct: 326 GMARDDIVEVRGKGLMIGVEIKYPCGKFV-DFAREHGVLVNCTSDSVLRLVPPLVITKEQ 384

Query: 383 LERVVEAV 390
           ++ VV+ +
Sbjct: 385 IDSVVDVL 392


Lambda     K      H
   0.319    0.137    0.403 

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: 404
Number of extensions: 24
Number of successful extensions: 5
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: 395
Length of database: 395
Length adjustment: 31
Effective length of query: 364
Effective length of database: 364
Effective search space:   132496
Effective search space used:   132496
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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