GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Teredinibacter turnerae T7901

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_015818205.1 TERTU_RS17580 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_000023025.1:WP_015818205.1
          Length = 309

 Score =  267 bits (683), Expect = 2e-76
 Identities = 137/301 (45%), Positives = 193/301 (64%), Gaps = 3/301 (0%)

Query: 9   IWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDS-HKGPVVFRHREHMQRLHDSAKI 67
           IWF+GE+V W DAKVHV++H LHYG  VFEG+R Y +   G  +FR +EH  RL  SA I
Sbjct: 10  IWFDGELVPWRDAKVHVLTHTLHYGMGVFEGVRAYHAGENGTSIFRLQEHTDRLFRSAHI 69

Query: 68  YRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGVNPPAGYSTDVIIAAFPW 127
               +  S DE+ EA R V+R+NNL  AY+RP+ F+G  GMG+         +I+AA+ W
Sbjct: 70  MNMKMPWSKDEVNEAQRLVVRENNLNEAYLRPMAFLGSEGMGLRAD-NLKVHLIVAAWDW 128

Query: 128 GAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQEGIALD 187
            +Y+  EA E GI   VSS+ R   N     AKA G+Y++S+L   EA   G +E + LD
Sbjct: 129 PSYMSPEAKEIGIKVRVSSYTRHHVNISMCKAKANGHYINSMLALKEALDCGCEEALLLD 188

Query: 188 VNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVREQVLSRESL 247
             GY++EG+GEN+F V++GV++TP  TS  L GITR+ I +LA E G ++ E+ +SR+ +
Sbjct: 189 AEGYVAEGSGENVFIVRNGVIYTPELTS-CLDGITRNTIFQLADECGYKIVEKRISRDEV 247

Query: 248 YLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLFTGETEDKWGWLDQV 307
           Y+ADE F +GTAAE+ P+R +DG Q+G G  GP+T+++Q  +F    GE      WL  V
Sbjct: 248 YVADEAFFTGTAAEVLPIRELDGRQIGPGHRGPITEKLQSLYFAAVRGELPQHREWLAPV 307

Query: 308 N 308
           +
Sbjct: 308 S 308


Lambda     K      H
   0.319    0.136    0.413 

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: 309
Number of extensions: 13
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: 309
Length of database: 309
Length adjustment: 27
Effective length of query: 282
Effective length of database: 282
Effective search space:    79524
Effective search space used:    79524
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 (21.8 bits)
S2: 48 (23.1 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