GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysN in Halomonas desiderata SP1

Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate WP_086509188.1 BZY95_RS06660 PLP-dependent aminotransferase family protein

Query= BRENDA::Q72LL6
         (397 letters)



>NCBI__GCF_002151265.1:WP_086509188.1
          Length = 476

 Score =  139 bits (349), Expect = 2e-37
 Identities = 100/334 (29%), Positives = 160/334 (47%), Gaps = 11/334 (3%)

Query: 68  LQYSPTEGYAPLRAFVAEWIG-----VRPEEVLITTGSQQALDLVGKVFLDEGSPVLLEA 122
           L Y   +G   LR  V          + P++VLITTG Q+AL L  +   + G  V +++
Sbjct: 141 LNYDSLQGSLALRRQVVRLAAKSGCLLHPDDVLITTGCQEALSLALRTLTEPGDVVAVDS 200

Query: 123 PSYMGAIQAFRLQGPRFLTVPAGEE-GPDLDALEEVLKRERPRFLYLIPSFQNPTGGLTP 181
           PS+ G +Q  + Q  + L +P     G  L+ALE  L++   + + + P+  NP G   P
Sbjct: 201 PSFYGTMQILKAQKLKALEIPTDPRTGISLEALELALEQWPIKAIQITPTCNNPLGYTMP 260

Query: 182 LPARKRLLQMVMERGLVVVEDDAYRELYFGEARLPSLFELAREAGYPGVIYLGSFSKVLS 241
              ++ L+ +     + +VEDD Y +L F EA  P   +   + G   V+   +FSK L 
Sbjct: 261 EARKRALVALAQRFDVAIVEDDIYGDLSF-EAPRPRTLKSFDDDGR--VLLCSAFSKTLV 317

Query: 242 PGLRVAFAVAHPEALQKLVQAKQGADLHTPMLNQMLVHELLKEGFSER-LERVRRVYREK 300
           PGLRV + +A      + +  K  +   +  L Q+ V E ++ G  ER L  + R YR  
Sbjct: 318 PGLRVGW-MAPGRYRDQALHMKYVSTGASATLPQLAVAEFVEHGHYERHLREMLRQYRRH 376

Query: 301 AQAMLHALDREVPKEVRYTRPKGGMFVWMELPKGLSAEGLFRRALEENVAFVPGGPFFAN 360
              M+  + R  P     + P+GG  +W+ELP  +    L  +   E +   PG  F A+
Sbjct: 377 RDIMIDWVTRYFPAGTGVSFPQGGFLLWLELPGDIDCVRLKEQLANEGLHITPGSLFSAS 436

Query: 361 GGGENTLRLSYATLDREGIAEGVRRLGRALKGLL 394
           G   + LRL+YA      +  G++R+G A+  LL
Sbjct: 437 GKFRHCLRLNYAAAMTPTVEAGIKRVGEAVAALL 470


Lambda     K      H
   0.320    0.139    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: 478
Number of extensions: 31
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 397
Length of database: 476
Length adjustment: 32
Effective length of query: 365
Effective length of database: 444
Effective search space:   162060
Effective search space used:   162060
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: 51 (24.3 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