GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruG in Halomonas xinjiangensis TRM 0175

Align arginine N-succinyltransferase (EC 2.3.1.109) (characterized)
to candidate WP_043529622.1 JH15_RS09235 arginine N-succinyltransferase

Query= BRENDA::P80358
         (340 letters)



>NCBI__GCF_000759345.1:WP_043529622.1
          Length = 354

 Score =  235 bits (600), Expect = 1e-66
 Identities = 134/340 (39%), Positives = 200/340 (58%), Gaps = 5/340 (1%)

Query: 1   MIVRPVTSADLPALIELARSTGTGLTTLPANEQRLQHRVSWAEKAFRGEAE-RGDADYLF 59
           ++VRP   ADLPAL  LA S    LT LPA+  RL+ R++ +++AF  + +  G+ +Y F
Sbjct: 2   LVVRPARPADLPALERLASSATPRLTNLPAHRDRLEERIARSQRAFSHDIDFPGEENYTF 61

Query: 60  VLED-DAGKVVGISAIAGAVGLREPWYNYRVGLTVSASQELNIHREIPTLFLANDLTGNS 118
           V+ED +  +VVG + I    G  E +Y YR    + ASQ+LN+ RE+ TL L+++++  S
Sbjct: 62  VIEDRERDEVVGTATIRALAGAHEAYYTYRQETLIHASQQLNVRREVQTLALSHEVSDAS 121

Query: 119 ELCSLFLHADHRSGLNGKLLSRARFLFIAEFRHLFGDKLIAEMRGMSDEEGRSPFWESLG 178
            LC+L LH  ++      LL R+R +FIA++   F   L     G  D +G SPFW S+G
Sbjct: 122 LLCALSLHPRYKDTSAESLLRRSRLMFIAQYPERFSQILAVAFPGYLDNDGESPFWNSVG 181

Query: 179 RHFFKMEFSQADYLTGVGNKAFIAELMPKFPLYTCFLSEEARGVIGRVHPNTEPALAMLK 238
           RHFF   + + +++ GV +K+FIAE+MP+FPLY   L+ +AR  IGR HP  E AL  + 
Sbjct: 182 RHFFVRGYQEMNHVAGVRSKSFIAEVMPQFPLYLPLLTPQARAAIGREHPAHERALEEML 241

Query: 239 AEGFSYQGYVDIFDAGPAIEAETDKIRAIAESQNLVLAVGTPG--DDAEPYLIHNRKRED 296
           AEGF    +VDIFDAGP ++ E D++     +    + +       DAEP +I N+K  D
Sbjct: 242 AEGFLRSRHVDIFDAGPVVKGERDRLATFRNAAWHPVRIRPQHTLPDAEPAMIANQKLGD 301

Query: 297 CR-ITAAPARAAAGTLVVDPLTAKRLRLSAGASVRAVPLS 335
            R + A  A +  G L++ P  A+ L +  G +V A PL+
Sbjct: 302 FRCVVARYALSPTGQLMLSPEHAEVLGVEEGRAVLAAPLA 341


Lambda     K      H
   0.320    0.136    0.398 

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: 285
Number of extensions: 14
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: 340
Length of database: 354
Length adjustment: 29
Effective length of query: 311
Effective length of database: 325
Effective search space:   101075
Effective search space used:   101075
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 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