GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdhA in Halomonas desiderata SP1

Align Cryptic catabolic NAD-specific glutamate dehydrogenase GudB; NAD-GDH; EC 1.4.1.2 (characterized)
to candidate WP_086511351.1 BZY95_RS18440 Glu/Leu/Phe/Val dehydrogenase

Query= SwissProt::P50735
         (427 letters)



>NCBI__GCF_002151265.1:WP_086511351.1
          Length = 345

 Score =  111 bits (277), Expect = 4e-29
 Identities = 92/295 (31%), Positives = 141/295 (47%), Gaps = 40/295 (13%)

Query: 70  AQHNDSVGPTKGGIRFHPNVTEKEVKA-VKALSIWMSLKCGIIDLPYGGGKGGIVCDPR- 127
           A H+   GP  GG+R +P  +E +    V  LS  M+ K  + DLP GGGK  I+ DPR 
Sbjct: 30  AIHDTRRGPALGGLRIYPYASEADALTDVLRLSRGMTYKSALADLPLGGGKAVIIADPRR 89

Query: 128 DMSFRELERLSRGYVRAISQIVGPTKDVPAPDVFTNSQIMAWMMDEYSRIDEFNSPGFIT 187
           D +   L  + R     +  + G  + + A D  +  + M  +  E S +      G  +
Sbjct: 90  DKTPAMLYAMGR----LVESLGG--RYITAEDSGSGEEDMRLIRQETSHVSGLGHDGN-S 142

Query: 188 GKPLVLGGSHGRESATAKGVTICIKEAAKKR--GIDIKGARVVVQGFGNAGSYLAKFMHD 245
           G P            TA GV   +K A + R    D++G RV +QG G+ G++LA+ +H+
Sbjct: 143 GDP---------SPFTAHGVFCALKSAVRHRLGRSDLQGLRVAIQGVGHVGAHLARELHE 193

Query: 246 AGAKVVGISDAYGGLYDPEGLDIDYLLDRRDSFG-TVTKLFNDTITNQELLELDCDILVP 304
           AGAK+V               D+D     RDS G  V++L  +++    + + D D+  P
Sbjct: 194 AGAKLV-------------LTDVD-----RDSLGMLVSELSAESVAPDAIFDADVDVFAP 235

Query: 305 AAIENQITEENAHNIRAKIVVEAANGP-TTLEGTKILSDRDILLVPDVLASAGGV 358
            A+   +T+E A  ++AK++  AAN    T      L  R IL  PD +A+AGGV
Sbjct: 236 CALGAVLTDEVAERLKAKVICGAANNQLATAAVAGRLQARGILYTPDYVANAGGV 290


Lambda     K      H
   0.318    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: 301
Number of extensions: 15
Number of successful extensions: 5
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: 427
Length of database: 345
Length adjustment: 30
Effective length of query: 397
Effective length of database: 315
Effective search space:   125055
Effective search space used:   125055
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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