GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagA in Echinicola vietnamensis KMM 6221, DSM 17526

Align N-acetylglucosamine 6-phosphate deacetylase (NagA;BSU35010) (EC 3.5.1.25) (characterized)
to candidate Echvi_4311 Echvi_4311 N-acetylglucosamine-6-phosphate deacetylase

Query= CAZy::CAB15506.1
         (396 letters)



>FitnessBrowser__Cola:Echvi_4311
          Length = 386

 Score =  129 bits (325), Expect = 1e-34
 Identities = 98/325 (30%), Positives = 152/325 (46%), Gaps = 12/325 (3%)

Query: 54  VLLPGMIDIHIHGGYGADTMDASFSTLDIMSS--RLPEEGTTSFLATTITQEHGNISQAL 111
           ++ PG++D+ ++G  G D  +   +  +++S   RL E G T+F  T IT     +S A+
Sbjct: 41  MIAPGLVDLQVNGFQGVDFNEPGLTVDEVVSCTRRLWENGVTTFFPTLITASEAALSDAI 100

Query: 112 VNAREWKAAEESSLLGAELLGIHLEGPFVSPKRA--GAQPKEWIRPSDVELFKKWQQEAG 169
              ++   A +  ++   + GIHLEGPF+S      GA P ++++  +  L  + Q+ A 
Sbjct: 101 ---KKIVQACQDPVIARTIAGIHLEGPFISKDAGPRGAHPLKYVQAPNWGLVSRLQKVAK 157

Query: 170 GLIKIVTLAPEEDQHFELIRHLKDESIIASMGHTDADSALLSDAAKAGASHMTHLYNAMS 229
           G IK+VTL+PE DQ  E+I+    E I  ++GHT A +  L  A + GA   THL NA  
Sbjct: 158 GKIKLVTLSPEHDQTNEVIKKCVAEQIHVAIGHTAAKTDQLGKAVEVGADLSTHLGNAAH 217

Query: 230 PFHHREPGVIGTALAHDGFVTELIADGIHSHPLAAKLAFLAKGSSKLILITDSMRAKGLK 289
               R P  I   LA DG  T +I+DG H  P A    F+     K  L++DS +  G  
Sbjct: 218 LSLPRHPNYIWDQLALDGLWTSMISDGFHL-PDAVMKVFMRVKPDKTFLVSDSTKFAGQP 276

Query: 290 DGVYE--FGGQSVTVRGRTALLSD--GTLAGSILKMNEGARHMREFTNCSWTDIANITSE 345
            G Y+   GG      G    + D    LAGS   +     ++      S     ++ S 
Sbjct: 277 AGSYQSPIGGTVRLSPGGRLCMQDNPNLLAGSAASLKSCLEYLARAKLASLPQAIDMASI 336

Query: 346 NAAKQLGIFDRKGSVTVGKDADLVI 370
                L    +  +   G  AD+V+
Sbjct: 337 RPLSYLAKGKKIKAFQKGSRADVVL 361


Lambda     K      H
   0.316    0.132    0.377 

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: 316
Number of extensions: 15
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: 396
Length of database: 386
Length adjustment: 31
Effective length of query: 365
Effective length of database: 355
Effective search space:   129575
Effective search space used:   129575
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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