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_010529658.1 ON01_RS03670 butyryl-CoA dehydrogenase

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



>NCBI__GCF_000224785.1:WP_010529658.1
          Length = 400

 Score =  253 bits (646), Expect = 7e-72
 Identities = 137/372 (36%), Positives = 216/372 (58%), Gaps = 5/372 (1%)

Query: 15  LDQQLTEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAIFREMGEVGLLGATIPEQYG 74
           +D   +EE+ M+R +   F   ++ P + E  R  Q DPAI + + ++GL+G  IPE+YG
Sbjct: 1   MDFNFSEEQNMLRRTVRSFVDKEIMPYIAEWDRKGQFDPAIIKRLADLGLMGVCIPEEYG 60

Query: 75  GSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYLPKLASGEWI 134
           GSG++Y    ++  E+ER D+ +R+ +SV + L  + + ++GTE QKQKYL   A G+ +
Sbjct: 61  GSGMDYNSLAIVCEELERGDTAFRTAVSVHTGLNSMTLLQWGTEEQKQKYLVPQAKGDKV 120

Query: 135 GCFGLTEPNHGSDPGSMITRARKVDGGYRLTGSKMWITNSPIADVFVVWAKDDA----GD 190
           G +GLTEP  GSD  S+ + A +    Y L GSK WI+    AD F+V+A  D       
Sbjct: 121 GAYGLTEPGAGSDVASLQSTAVEDGDHYILNGSKAWISLCDTADHFLVFAYTDKEIRHKG 180

Query: 191 IRGFVLEKGWQGLSAPAIHGKVGLRASITGEIVMDNVFVPEENIF-PDVRGLKGPFTCLN 249
           I  F++E+ W+G  + A  GK+G+R+  TGEI  DN+ VP+EN+   +  G K     L+
Sbjct: 181 ISAFIVERDWEGFDSKATKGKLGIRSGNTGEIFFDNIKVPKENLLGEEGEGFKIAMAALD 240

Query: 250 SARYGISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLALQGCL 309
           + R+ ++ GA+G   AC   +  Y  +R+ FG+P+  +QL+Q+ +A+M+  + ++     
Sbjct: 241 NGRFTVAAGAVGQIRACLEASVNYANERETFGKPIGKHQLVQQMIANMKAGLEMSSLLVY 300

Query: 310 RLGRMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNLEVVN 369
           R G +K+EG    E TS+ K  +C  A   A  A  + G  G SDE+ V R+L N +   
Sbjct: 301 RAGELKNEGKRNTEETSMAKWQACDFANKAADDAVQVHGAYGYSDEYPVERYLRNSKAPV 360

Query: 370 TYEGTHDVHALI 381
            YEGT +VH L+
Sbjct: 361 IYEGTREVHTLM 372


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: 359
Number of extensions: 17
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: 400
Length adjustment: 31
Effective length of query: 362
Effective length of database: 369
Effective search space:   133578
Effective search space used:   133578
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.

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