GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Stenotrophomonas chelatiphaga DSM 21508

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_042613067.1 ABB28_RS07920 branched-chain amino acid aminotransferase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_001431535.1:WP_042613067.1
          Length = 364

 Score =  101 bits (252), Expect = 2e-26
 Identities = 94/311 (30%), Positives = 148/311 (47%), Gaps = 29/311 (9%)

Query: 16  PFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAKFLHY--- 72
           P+    +  A   LHYG   F G++     +  G++  FR D +G RL +SA+ L     
Sbjct: 57  PYGPLLLDPAAAVLHYGQEIFEGIKAYRHAD--GSVWTFRPDANGRRLQRSAQRLALPEL 114

Query: 73  --DISAEKIKEVIV---DFVKKNQPDKSFYIRPLVYSSGLGIAPRLHNLEKDFLVYGLEM 127
             DI  E +K+++    D+V  +  + S Y RP +      +  R  + +  + V     
Sbjct: 115 PVDIFVESLKQLVALDKDWVP-SADESSLYFRPFMIGDEAFLGVRGAH-KAGYYVIASPA 172

Query: 128 GDYLAAD--GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAILMN-S 184
           G Y A     VS  +S+ Y +  +      K    Y  S L + +A   G  + + ++ +
Sbjct: 173 GPYFAKGVAPVSIWLSTEYARAAKGGTGAAKCGGNYAASLLPQQKAQAQGCSQVLFLDPT 232

Query: 185 QGKVCEATG-MNVFMV-RNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQR--PIDK 240
           +GK  E  G MNVF+V ++G +VTP     ILEGITR+SIL +A D G+   +R   ID+
Sbjct: 233 EGKYLEELGGMNVFLVYKDGTLVTPQLSGSILEGITRESILQLARDRGMKVEERKVSIDE 292

Query: 241 SELMIAD----EVFLSGTAAKITPVKRI--ENFTLGGDR----PITEKLRSVLTAVTENR 290
            +  +A     EVF  GTAA +TP+ ++  E F +G        +T  LR  LT +   R
Sbjct: 293 WKQGVASGEITEVFACGTAAVVTPIGQLKGEGFEVGDINAPAGEVTLSLRKELTDIQYGR 352

Query: 291 EPKYQDWVFKI 301
            P    W+ K+
Sbjct: 353 LPDRHGWLVKL 363


Lambda     K      H
   0.320    0.138    0.406 

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: 282
Number of extensions: 20
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: 305
Length of database: 364
Length adjustment: 28
Effective length of query: 277
Effective length of database: 336
Effective search space:    93072
Effective search space used:    93072
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 Jul 25 2024. The underlying query database was built on Jul 25 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