GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gabT in Oleispira antarctica

Align Probable 4-aminobutyrate aminotransferase; EC 2.6.1.19; (S)-3-amino-2-methylpropionate transaminase; EC 2.6.1.22; GABA aminotransferase; GABA-AT; Gamma-amino-N-butyrate transaminase; GABA transaminase; Glutamate:succinic semialdehyde transaminase; L-AIBAT (uncharacterized)
to candidate WP_046010708.1 OLEAN_RS01080 glutamate-1-semialdehyde-2,1-aminomutase

Query= curated2:P94427
         (436 letters)



>NCBI__GCF_000967895.1:WP_046010708.1
          Length = 434

 Score =  154 bits (390), Expect = 4e-42
 Identities = 107/323 (33%), Positives = 169/323 (52%), Gaps = 35/323 (10%)

Query: 23  KGVSNGNRSLAVKGEGAELYDLDGRRFIDFAGAIGTLNVGHSHPKVVEAVKRQAEELIHP 82
           KGV  G      +GEG+ L+D DG R+ID+ G+ G + +GH+   V+EAVK + ++ +  
Sbjct: 27  KGVG-GTPIFFERGEGSCLFDADGNRYIDYVGSWGPMIMGHARGDVIEAVKARLDQGLSF 85

Query: 83  GFNVMMYPTYIEL--AEKLCGIAPGSHEKKAIFLNSGAEAVENAVKIARKYTKRQGVVSF 140
           G      PT IE+  A+ +CGI PG    + +  NSG EA  +A+++AR +T R  +V F
Sbjct: 86  GA-----PTEIEIDMAQTVCGIMPGMDMVRMV--NSGTEATMSAIRLARGFTGRDKLVKF 138

Query: 141 TRGFHGRTNMTMSMTSKVKPYKFGFGPFAPEVYQAPFPYYYQKPAGMSDESYDDMVIQAF 200
              +HG  +  +         K G G     V  +P       PAG ++    D +   +
Sbjct: 139 EGCYHGHADSLL--------VKAGSGALTLGVPSSP-----GVPAGAAN----DTITLDY 181

Query: 201 NDFFIASVA----PETVACVVMEPVQGEGGFIIPSKRFVQHVASFCKEHGIVFVADEIQT 256
           ND            + +AC+++E V G    I PSK F+Q +   C ++G V + DE+ T
Sbjct: 182 NDIDDVKACFAEQGDKIACIIVEAVAGNMNCIPPSKEFLQGLRDVCDQYGAVLIFDEVMT 241

Query: 257 GFARTGTYFAIEHFDVVPDLITVSKSLAAGLPLSGVIGRAEMLDAAAP-GEL--GGTYAG 313
           GF R     A  ++DV PDL T+ K +  GLP+    G+ E+++  AP G +   GT +G
Sbjct: 242 GF-RVSLTGAQGYYDVQPDLTTLGKVIGGGLPVGAFGGKREIMEYLAPIGPVYQAGTLSG 300

Query: 314 SPLGCAAALAVLDIIEEEGLNER 336
           +PL  AA LA++  +++ GL E+
Sbjct: 301 NPLAMAAGLAMMKSVQQPGLYEQ 323


Lambda     K      H
   0.319    0.136    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: 462
Number of extensions: 25
Number of successful extensions: 6
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: 436
Length of database: 434
Length adjustment: 32
Effective length of query: 404
Effective length of database: 402
Effective search space:   162408
Effective search space used:   162408
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. 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