GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Thioalkalivibrio halophilus HL17

Align phosphoserine aminotransferase monomer (EC 2.6.1.1; EC 2.6.1.52) (characterized)
to candidate WP_077244352.1 B1A74_RS08315 alanine--glyoxylate aminotransferase family protein

Query= metacyc::MONOMER-15919
         (385 letters)



>NCBI__GCF_001995255.1:WP_077244352.1
          Length = 400

 Score =  229 bits (584), Expect = 1e-64
 Identities = 132/366 (36%), Positives = 210/366 (57%), Gaps = 5/366 (1%)

Query: 7   KKLLMIPGPTMVPPEVLNAMALPVIGHRTKDYSNLLEDTIEKLKKVFITEND-TFLITGS 65
           ++ LM PGP+ V P VL+AM+ P+IGH    +  ++E+    L+  F TEN  T  ++  
Sbjct: 10  QRTLMGPGPSDVNPRVLSAMSRPIIGHLDPVFVGMMEEMKGLLQYAFQTENALTLPVSAP 69

Query: 66  GTAAMDMAISNIIKRGDKVLNIVTGNFGERFANIVKAYKGEAIRLDVEWGDMAEPEAVKE 125
           G+A M+    N+++ GDKV+  + G FG R    V+   G A+ ++ +WG+   P+ V +
Sbjct: 70  GSAGMETCFVNLVEPGDKVIVCINGVFGTRMKENVERCGGTAVVVEDDWGNPVSPDKVAD 129

Query: 126 ILDKYDDIKAVTVVHNETSTGARNPIKEIGEVVKDYDALYIVDTVSSLGGDYVNVDKFHI 185
            L    D K +  VH ETSTGAR+ ++ +  + +++D L IVD+V+ L G  + VD + +
Sbjct: 130 ALKGNPDAKILAFVHAETSTGARSDVETLCRLAREHDCLTIVDSVTGLAGSPLYVDDWGV 189

Query: 186 DICVTGSQKCLAAPPGLAAITVSEKAWEVIKKNDDKV-GFYLDLLAYKKYY--EEKKQTP 242
           D   +G+QKCL+  PGL+ ++ S++A + I+    KV  ++LDL     Y+    K+   
Sbjct: 190 DAIYSGTQKCLSCTPGLSPVSFSQRAVDRIQARSHKVQSWFLDLNLVMGYWGGGSKRAYH 249

Query: 243 YTPSVNLTYALNVALDLVLEEGIENRVKRHERLAKATRAGLEAMGIELFAKERARSVTVT 302
           +T  +N  YAL+ +L ++ EEG+EN   RH R   A RAGLEAMG+E    E  R   + 
Sbjct: 250 HTAPINALYALHESLVILQEEGLENSWARHCRHHDALRAGLEAMGLEFLVAEEHRLPQLN 309

Query: 303 SAKYPEGIEDSKFRGILSNKYNIVVAGGQKHLAGKIFRIGHMGI-CGEKEVLATLACVEL 361
           S   PEG++++  RG L  +Y + +  G    AGK++RIG MG    E+ VL  L+ +E 
Sbjct: 310 SVYVPEGVDEAAVRGELLERYGLEIGAGLGPYAGKVWRIGLMGYGANERNVLTCLSALEA 369

Query: 362 ALKELG 367
            L + G
Sbjct: 370 VLADRG 375


Lambda     K      H
   0.316    0.135    0.379 

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: 356
Number of extensions: 19
Number of successful extensions: 3
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: 385
Length of database: 400
Length adjustment: 31
Effective length of query: 354
Effective length of database: 369
Effective search space:   130626
Effective search space used:   130626
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 (21.6 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