GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Stenotrophomonas chelatiphaga DSM 21508

Align threonine deaminase (EC 4.3.1.19) (characterized)
to candidate WP_057508536.1 ABB28_RS10275 serine dehydratase

Query= reanno::Korea:Ga0059261_3694
         (420 letters)



>NCBI__GCF_001431535.1:WP_057508536.1
          Length = 320

 Score =  167 bits (424), Expect = 3e-46
 Identities = 109/310 (35%), Positives = 158/310 (50%), Gaps = 3/310 (0%)

Query: 16  QPLPVTLADVQAAAARIMGAVVHTPTLHSKTLSDLTGATVYLKFENLQFTAAYKERGALN 75
           + LP     V  AAARI      TP L S+TL  L GA +  K E+LQ + A+K RGA N
Sbjct: 3   EALPPPAQAVLEAAARIAPHAAVTPVLRSQTLDALAGAQLAFKAEHLQRSGAFKFRGACN 62

Query: 76  TLLQLDDAARAKGVIAASAGNHAQGLAYHGNRLGIPVTIVMPKSTPTVKVMQTESHGATI 135
            +  L       GV+  S+GNH   LA      GI   +V+P      K+     HGAT+
Sbjct: 63  AVWSLSADRAPAGVVTHSSGNHGAALALAARTRGIACHVVVPDGAVAAKLANIARHGATL 122

Query: 136 ILEGETFDEAYAHARQLEASNGYTFVHPFDDPRIIAGQGTVFLEMLADAPAIDTLIVPIG 195
                T     A   Q++A  G T VHP+ D  +IAGQGT  LE+L      D ++VP+G
Sbjct: 123 WRCAPTIAAREAVCAQVQADTGATLVHPYADAAVIAGQGTAVLELLQAEGPFDVVVVPVG 182

Query: 196 GGGLISG-ALTVAKAADKPIEVVGVQAELFPSMFNRFTGAHE-PIGGDTLAEGIAVKEPG 253
           GGGL +G AL + + +     V+   A    +  +   G        DT+ +G+     G
Sbjct: 183 GGGLAAGTALALQQVSPHTRLVLAEPAGAADTARSLQAGERRIDFVPDTVCDGLR-GTLG 241

Query: 254 GLTAQIVEALVDEIMLVSERSLEEAVSLLLQIEKTVVEGAGAAGLAALMTQPERFRGKTV 313
               Q+++A   E+++V + +   A+ LL Q+ K  VE + A  LAA++ QP+RF G  V
Sbjct: 242 APNFQLLQAAGAEVIVVDDAATVAAMRLLWQVLKQTVEPSSAIALAAVLAQPQRFAGLRV 301

Query: 314 GVILTGGNID 323
           G++L+GGN+D
Sbjct: 302 GLVLSGGNVD 311


Lambda     K      H
   0.319    0.135    0.374 

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: 279
Number of extensions: 13
Number of successful extensions: 2
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: 420
Length of database: 320
Length adjustment: 30
Effective length of query: 390
Effective length of database: 290
Effective search space:   113100
Effective search space used:   113100
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: 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