GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Desulfobacter vibrioformis DSM 8776

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_035237517.1 Q366_RS06780 acyl-CoA dehydrogenase family protein

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_000745975.1:WP_035237517.1
          Length = 382

 Score =  212 bits (539), Expect = 2e-59
 Identities = 123/367 (33%), Positives = 194/367 (52%), Gaps = 4/367 (1%)

Query: 23  RMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQYGGPGLDYVSY 82
           ++VR     +A+ ++ P      R       I  +MG +   G  +P   GG GLD +SY
Sbjct: 10  QVVRKTVREFAENEIGPHAASLDREGRFPTEIIEKMGPLNYFGLQVPPSLGGAGLDTISY 69

Query: 83  GLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEWIGCFGLTEPN 142
            ++  E+ RV +     +SV +S+ + PI  FG+D Q  +++P +A G+ IG F LTE N
Sbjct: 70  AIVIEELSRVCAALGLCVSVHNSVGLYPILRFGTDEQIARFVPDMAAGKHIGAFCLTEAN 129

Query: 143 HGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIADVFVVWAKLDEDGRDEIRG--FILEK 200
            GSD G + T A K   GY+++G+K+++TN  + DV +V+A +D  G+++ R   FI+EK
Sbjct: 130 AGSDAGGVETTAAKTEEGYTINGTKIFVTNGGVCDVVLVFA-VDAGGKEQSRPNVFIVEK 188

Query: 201 GCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEENILPHV-KGLRGPFTCLNSARYGIAW 259
            C G S   I    G+RA+    +  ++  +PE N+L    +GL+   T L++ R GIA 
Sbjct: 189 TCPGFSVGEIEDLCGMRANPVSSLFFEDCRIPETNLLGKPGQGLKIGLTALDTGRIGIAA 248

Query: 260 GALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQGVLRLGRMKDE 319
            ALG A++ +  A  Y  +R+QF  PL   Q IQ  LADM T I      + R    KD+
Sbjct: 249 QALGIAQAAFEAALSYAKERQQFNSPLTKFQTIQNYLADMATSIESSRMLLYRAAAAKDK 308

Query: 320 GTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVVNTYEGTHDI 379
           G       ++ K +    A  +  LA  + GG G S E+ V R+    +V   YEGT ++
Sbjct: 309 GGDFGAQAAMAKLSCSATARTVTDLAVQIHGGYGYSREYDVERYFREAKVTQIYEGTSEV 368

Query: 380 HALILGR 386
             +++ R
Sbjct: 369 QKMVIAR 375


Lambda     K      H
   0.320    0.138    0.414 

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: 368
Number of extensions: 16
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: 395
Length of database: 382
Length adjustment: 30
Effective length of query: 365
Effective length of database: 352
Effective search space:   128480
Effective search space used:   128480
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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