GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Luteimonas huabeiensis HB2

Align branched-chain-amino-acid transaminase (EC 2.6.1.42) (characterized)
to candidate WP_024891497.1 Z164_RS0114980 branched-chain amino acid transaminase

Query= BRENDA::P0AB80
         (309 letters)



>NCBI__GCF_000559025.1:WP_024891497.1
          Length = 303

 Score =  358 bits (918), Expect = e-103
 Identities = 181/301 (60%), Positives = 221/301 (73%), Gaps = 2/301 (0%)

Query: 7   DYIWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGPVVFRHREHMQRLHDSAK 66
           ++IW NGE+  W +A  HVM+HALHYG+SVFEGIRCY +  GP +FR  +H +RLH SAK
Sbjct: 5   EWIWHNGEIKPWAEATTHVMAHALHYGSSVFEGIRCYRTPDGPAIFRLSDHNRRLHASAK 64

Query: 67  IYRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGVNPPAGYSTDVIIAAFP 126
           I+ F +  S+DEL  A R+V+R+N L +AYIRP+ F G  G G+   A    +V I A+P
Sbjct: 65  IHDFAIPYSLDELNAATREVLRRNRLDAAYIRPVAFRGLGGFGLT--AETPIEVSIGAWP 122

Query: 127 WGAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQEGIAL 186
           WG YLG   LE GIDA VSSW R APNTIP  AKAGGNYLS  LV  EARR G+ EGIAL
Sbjct: 123 WGTYLGEGVLESGIDACVSSWQRFAPNTIPAGAKAGGNYLSGQLVAREARRLGFGEGIAL 182

Query: 187 DVNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVREQVLSRES 246
              G +SEGAGENLF V DGVL TPP +++ L GITR ++I LA++ G+EV E+ + RE 
Sbjct: 183 ASTGLLSEGAGENLFLVFDGVLHTPPVSAALLNGITRHSLIVLARQAGLEVVERDMPREY 242

Query: 247 LYLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLFTGETEDKWGWLDQ 306
           LYL DE+FM GTAAEITP+RSVDG QVGEGR GPVT+R+Q+ FFGLF G T D  GWL++
Sbjct: 243 LYLCDELFMCGTAAEITPIRSVDGRQVGEGRAGPVTRRLQELFFGLFDGRTPDVHGWLER 302

Query: 307 V 307
           V
Sbjct: 303 V 303


Lambda     K      H
   0.319    0.136    0.413 

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: 339
Number of extensions: 9
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: 309
Length of database: 303
Length adjustment: 27
Effective length of query: 282
Effective length of database: 276
Effective search space:    77832
Effective search space used:    77832
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: 48 (23.1 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