GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Azospirillum brasilense Sp245

Align Homoserine O-acetyltransferase; HAT; EC 2.3.1.31; Homoserine transacetylase; HTA (uncharacterized)
to candidate AZOBR_RS14580 AZOBR_RS14580 homoserine O-acetyltransferase

Query= curated2:Q3AAW2
         (379 letters)



>FitnessBrowser__azobra:AZOBR_RS14580
          Length = 398

 Score =  231 bits (590), Expect = 2e-65
 Identities = 136/371 (36%), Positives = 201/371 (54%), Gaps = 11/371 (2%)

Query: 6   GIVETKKVTFPEITLECGEKIAPVTVAYETYGELNERGDNAILILHALTGDAHVAGKHRP 65
           G+VE K    P  T   G  I  V + +E+YG+LN+  DN IL+ H  +G++H AGK++ 
Sbjct: 28  GLVEKKVFEMPSYTTVGGGTIKNVRIGWESYGKLNDARDNVILVTHFFSGNSHAAGKYKM 87

Query: 66  EDKVAGWWDPMVGPGRPFDTNKYFIVCSNVLGGC------YGTTGPSSINPATGRPWGMS 119
           ED   G+WD ++GPG+P DT+K+FI+ S+ L           TTGP+S+NP TG+P+GMS
Sbjct: 88  EDPAPGYWDSIIGPGKPLDTDKFFIISSDTLVNLSPKDPTVTTTGPASVNPDTGKPYGMS 147

Query: 120 FPIITIRDMVNLQYKLVRHLGITKILAAVGGSMGGMQALEWAYMYPEMLKSVVAIATSAR 179
           FP++TIRD VN+Q  L+  L +  + A +GGSMG +QALEW   +PEM+K VVA+   A 
Sbjct: 148 FPVVTIRDFVNVQKALLDSLNVKSLHAVMGGSMGSLQALEWGATHPEMVKRVVAVIGGAE 207

Query: 180 LSPFGIAFNAVGREAIMTDPEWRGGNYYGFEGPKRGLALARMIGIITYKSDISW-QYRFG 238
             PF I +  +    I  DP W+GG+YYG   PK GL  A  + +  +     W    FG
Sbjct: 208 ADPFLIGWLNLWAAPIRVDPNWQGGDYYGKAEPKAGLTEALKL-VTLHARHWKWADATFG 266

Query: 239 RTHTYETDQELFSHTSRFEIENYLYYQGDKLVKRFDANTYLYLLKAMDLHDISRGRGRYR 298
           R    E      S  +++ IE +L           DAN +LYL+KA     +  G G   
Sbjct: 267 RGWAEEGKDPAASMNNQYAIEAWLDKAAAARAAVSDANHFLYLVKANQTFLVG-GGGSLD 325

Query: 299 EILKELKTPLLAIGIDTDFLYPTYQ-QKEIVEAL-KEAKKEAYYWELSSPHGHDAFLIEF 356
           E L ++K P+L I    D ++P  +  + + E L K+     Y   +++  GH   +   
Sbjct: 326 EGLAKIKAPVLLIPSADDLVFPPERAMRPLKERLEKQGIAVTYTDAITTSLGHLDGIANI 385

Query: 357 SKMAPILSNFL 367
           +K    +S F+
Sbjct: 386 AKAGDAISAFM 396


Lambda     K      H
   0.321    0.139    0.426 

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: 447
Number of extensions: 20
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: 379
Length of database: 398
Length adjustment: 30
Effective length of query: 349
Effective length of database: 368
Effective search space:   128432
Effective search space used:   128432
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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