GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Dyadobacter tibetensis Y620-1

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate WP_025764020.1 X939_RS0114560 acyl-CoA dehydrogenase

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



>NCBI__GCF_000566685.1:WP_025764020.1
          Length = 379

 Score =  226 bits (575), Expect = 1e-63
 Identities = 135/372 (36%), Positives = 205/372 (55%), Gaps = 5/372 (1%)

Query: 18  QLTEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAIFREMGEVGLLGATIPEQYGGSG 77
           +LTEE + ++ +   FA+  L P ++E    ++ DP++ R+MGE+GL+G  + EQYGG G
Sbjct: 4   ELTEEHKAIQQATRDFARTTLLPGIIERDNAQKFDPSLVRQMGEMGLMGMMVEEQYGGGG 63

Query: 78  LNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYLPKLASGEWIGCF 137
           L+ + Y L   E+ +ID+    +MSV +SLV   I ++G+E QKQKYLP LAS + IG F
Sbjct: 64  LDTLSYVLAMEEICKIDASAGVIMSVNNSLVCWGIQQYGSEEQKQKYLPDLASAQKIGAF 123

Query: 138 GLTEPNHGSDPGSMITRARKVDGGYRLTGSKMWITNSPIADVFVVWAKDDA----GDIRG 193
            L+EP  GSD  S  T A      Y L G+K WITN  ++++ +V A+         I  
Sbjct: 124 CLSEPEAGSDATSQHTTAVDQGDYYILNGTKNWITNGNLSEICLVMAQTHPEKRHKGINV 183

Query: 194 FVLEKGWQGLSAPAIHGKVGLRASITGEIVMDNVFVPEEN-IFPDVRGLKGPFTCLNSAR 252
           F++EKG  G +      K+G+RAS T  ++  +V VP+ N I PD  G K     LN  R
Sbjct: 184 FLVEKGIAGFTVGRKEDKMGIRASDTHSLMFADVMVPKGNRIGPDGFGFKFAMDTLNGGR 243

Query: 253 YGISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLALQGCLRLG 312
            GI+  ALG A   +  +  Y   R+ FG+P++ +Q IQ KLA+M T I  A     +  
Sbjct: 244 IGIAAQALGIAAGAYELSLAYAKQRRTFGKPISEHQAIQFKLAEMATRIEAARLLVYKAA 303

Query: 313 RMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNLEVVNTYE 372
             KD G   +   ++ K  +   A+ +   A  + GG G   E+ V RH+ + ++   YE
Sbjct: 304 YTKDVGKDYIGEAAMAKLYASDVAMWVTTEAVQIHGGYGYVKEYHVERHMRDAKITQIYE 363

Query: 373 GTHDVHALILGR 384
           GT ++  L++ R
Sbjct: 364 GTSEIQKLVIAR 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: 374
Number of extensions: 13
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