GapMind for catabolism of small carbon sources

 

Alignments for a candidate for davT in Stenotrophomonas chelatiphaga DSM 21508

Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate WP_057507751.1 ABB28_RS05895 aspartate aminotransferase family protein

Query= BRENDA::Q9I6M4
         (426 letters)



>NCBI__GCF_001431535.1:WP_057507751.1
          Length = 450

 Score =  172 bits (436), Expect = 2e-47
 Identities = 128/363 (35%), Positives = 182/363 (50%), Gaps = 36/363 (9%)

Query: 25  PVVAERAENSTVWDVEGREYIDFAGGIAVLNTGHLHPKVIAAVQEQLGKLSHT-CFQVLA 83
           P +  RA+     DVEGR+ +D   G+   N GH   K++ A+ EQ G L     FQ+ +
Sbjct: 36  PRLLVRAQGMYYEDVEGRQILDGTAGLWCCNAGHGRKKIVQAIAEQAGTLDFAPTFQMGS 95

Query: 84  YEPYIELAEEIAKRVPGDFPKKTLLVTSGSEAVENAVKIARA---ATGRAGVIAFTG--- 137
             P++ LA+ +A   P           SGSEAV++A+KI  A   A G      F G   
Sbjct: 96  PLPFV-LAQRLAALAPAGL-NHVFFTNSGSEAVDSAMKIVLAHHRARGEGQRTRFIGREK 153

Query: 138 AYHGRTMMTLGLTGKVVPYSAGM-GLMPGGIFRALAPCEL-----------HGVSEDDSI 185
           AYHG     + + G  +P +    GL  GG        +L           HG    D++
Sbjct: 154 AYHGVGFGGMAIGG--LPNNRRQFGLQLGGSAHLPHTLDLQRNAFSQGLPRHGAELADAL 211

Query: 186 ASIERIFKNDAQPQDIAAIIIEPVQGEGGFYVNSKSFMQRLRALCDQHGILLIADEVQTG 245
             +  I  +DA    IAA+ +EP+ G  G  + +  ++QRLR +CD HGI+L+ DEV TG
Sbjct: 212 ERL--IALHDAST--IAAVFVEPIAGSAGVILPAPGYLQRLREICDHHGIVLVFDEVITG 267

Query: 246 AGRTGTFFATEQLGIVPDLTTFAKSV-GGGFPISGVAGKAEIMDAIAPGGL-------GG 297
            GR G  FA ++ G+ PDL TFAK    G  P+ GV     I  ++  G         G 
Sbjct: 268 FGRVGMPFAAQRFGVTPDLITFAKGASNGAVPLGGVLVGDAIHSSLQQGPTQAIDLFHGY 327

Query: 298 TYAGSPIACAAALAVLKVFEEEKLLERSQAVGERLKAGLREIQAKHKVIGDVRGLGSMVA 357
           TY+G P+ACAAALA L V+ EE+L ER+  +GE  +  L  +Q    V+ D+R  G + A
Sbjct: 328 TYSGHPLACAAALATLDVYAEERLFERAIELGEHWQRALHGLQGLPNVV-DIRNFGLVGA 386

Query: 358 IEL 360
           +EL
Sbjct: 387 VEL 389


Lambda     K      H
   0.319    0.137    0.393 

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: 477
Number of extensions: 22
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: 426
Length of database: 450
Length adjustment: 32
Effective length of query: 394
Effective length of database: 418
Effective search space:   164692
Effective search space used:   164692
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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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