GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Lentibacillus jeotgali Grbi

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate WP_010531553.1 ON01_RS13295 acyl-CoA dehydrogenase

Query= metacyc::G1G01-166-MONOMER
         (393 letters)



>NCBI__GCF_000224785.1:WP_010531553.1
          Length = 379

 Score =  234 bits (598), Expect = 2e-66
 Identities = 139/375 (37%), Positives = 210/375 (56%), Gaps = 5/375 (1%)

Query: 15  LDQQLTEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAIFREMGEVGLLGATIPEQYG 74
           ++  LTEE+ M+R     FA + + P V    R E+    I R+MGE+GL+G  IPE+YG
Sbjct: 1   MNLHLTEEQEMMRKMVRDFAVNDVQPEVERMEREERFPVEIIRKMGELGLMGVPIPEKYG 60

Query: 75  GSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYLPKLASGEWI 134
           GSG++Y CY +   E+ ++ +    ++SV +S+   PI  FG E QK KYLPKLASG+++
Sbjct: 61  GSGMDYTCYIIAINELAKVSATLAVILSVHTSVGTNPILSFGNEEQKNKYLPKLASGQYL 120

Query: 135 GCFGLTEPNHGSDPGSMITRARKVDGGYRLTGSKMWITNSPIADVFVVWAK--DDAGD-- 190
           G F LTEP  GSD  ++ TRA K    Y L GSK++ITN   AD ++ +A+  D+ G   
Sbjct: 121 GAFALTEPGAGSDAANLKTRAVKDGDSYILKGSKIFITNGGQADTYITFARTSDEPGSKG 180

Query: 191 IRGFVLEKGWQGLSAPAIHGKVGLRASITGEIVMDNVFVPEENIF-PDVRGLKGPFTCLN 249
           +  FV+EK   GL       K+GL  S T ++  D+  VP+E +   +  G K     LN
Sbjct: 181 VSAFVVEKDTPGLEIGKPEKKMGLHGSNTVQLSFDHCVVPKEQLLGEEGDGFKIAMANLN 240

Query: 250 SARYGISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLALQGCL 309
             R GI+  ALG  EA    A  Y  +R+QFG+P+A NQ I  KLADM TE+  A     
Sbjct: 241 VGRIGIAAQALGIGEAALEYAVAYAKEREQFGKPIAENQGIAFKLADMATEVEAAKLLVY 300

Query: 310 RLGRMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNLEVVN 369
           +   + ++G  + +  S+ K  +   A   A  A  + GG G ++++ V R   + +V  
Sbjct: 301 QAADLVEQGVPSSKEASMAKMYASKTARKAAIEAVQVYGGYGYTEDYPVERLFRDAKVTE 360

Query: 370 TYEGTHDVHALILGR 384
            YEGT+++  +++ +
Sbjct: 361 IYEGTNEIQHIVIAK 375


Lambda     K      H
   0.320    0.137    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: 341
Number of extensions: 12
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: 393
Length of database: 379
Length adjustment: 30
Effective length of query: 363
Effective length of database: 349
Effective search space:   126687
Effective search space used:   126687
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 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