GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Hydrogenophaga taeniospiralis NBRC 102512

Align threonine ammonia-lyase (EC 4.3.1.19) (characterized)
to candidate WP_068176041.1 HTA01S_RS23390 hypothetical protein

Query= BRENDA::Q74FW6
         (402 letters)



>NCBI__GCF_001592305.1:WP_068176041.1
          Length = 323

 Score =  147 bits (370), Expect = 6e-40
 Identities = 106/314 (33%), Positives = 160/314 (50%), Gaps = 11/314 (3%)

Query: 2   LPYTLIQEADDRLRKRVRRTELIHSHHF-----SEKLGIPIYFKCENLQRTGAFKIRGAL 56
           +P+TL   AD     RV   E   +  +     S++LG   + K EN    GAFKIRG L
Sbjct: 1   MPHTLPTLADIEAATRVVYREFPATPQYRWATLSQRLGADCWIKHENHTPVGAFKIRGGL 60

Query: 57  NFMTS-QPREALAKGVITASAGNHAQGVAFSADLLGVPSTVFMPESTPPQKVFATRDYGA 115
            +    + R  L + V++A+ GNH Q + ++A   GV  ++ +P     +K  A R  G 
Sbjct: 61  TYFDQLRQRGELPREVVSATRGNHGQSIGWAARTHGVACSIVVPRGNSLEKNAAMRALGV 120

Query: 116 EVVLTGRNFDEAYAAAVQAQEERGALFVHPFDDPLVMAGQGTIGLEVLQELPDVANILVP 175
            ++  G +F E+   A++   ERGA  V  F   L + G  T   E  + +P +  + VP
Sbjct: 121 NLIEHGADFQESREHAMRLAAERGAHMVPSFHKDL-LRGVSTYWWEFFKAVPQLDVVYVP 179

Query: 176 IG-GGGLIAGIATAIRETHPHVRIIGVETAAAPSAHYSLQKGKIVQVPVTVTLADGIAVK 234
           IG G G  + IA  +   H   RI+GV +A A +   S+  G++V+ PVT  LADG+A +
Sbjct: 180 IGQGSGACSAIAAKLALGH-QARIVGVVSAHATTYADSIAAGRVVEAPVTTELADGMACR 238

Query: 235 KPGVNTFPIIRDLVDEVVLVEEEEIALAIVALLERTKLLVEGAGAVPLAALLNRRVTDLS 294
               +   ++   +D +V V ++E+A A+  L   T  L EGAGA   AA    + T L 
Sbjct: 239 VADADALAVLAPHLDHIVRVTDDEVAAAMRTLFADTHNLAEGAGAAAFAAAWQEKET-LQ 297

Query: 295 GKTVCV-LSGGNID 307
           G +V V LSGGN+D
Sbjct: 298 GLSVGVSLSGGNVD 311


Lambda     K      H
   0.319    0.137    0.383 

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: 246
Number of extensions: 14
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: 402
Length of database: 323
Length adjustment: 29
Effective length of query: 373
Effective length of database: 294
Effective search space:   109662
Effective search space used:   109662
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: 49 (23.5 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