GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Saccharomonospora cyanea NA-134

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_043536562.1 SACCYDRAFT_RS16135 acyl-CoA dehydrogenase

Query= reanno::pseudo5_N2C3_1:AO356_26355
         (375 letters)



>NCBI__GCF_000244975.1:WP_043536562.1
          Length = 383

 Score =  278 bits (711), Expect = 2e-79
 Identities = 149/373 (39%), Positives = 220/373 (58%), Gaps = 2/373 (0%)

Query: 4   TEEQTQIRDMARQFAQERLKPFAAEWDREHRFPREAIAEMAELGFFGMLVPEQWGGCDTG 63
           TEE   +RD+AR F +  L P  A W R+    RE   +  E+G   + VPE +GG   G
Sbjct: 12  TEELDDVRDLARTFCRNELAPHQARWARQKHIDREVWTKAGEVGLLALSVPETYGG-GGG 70

Query: 64  YLAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKFGNDEQKAKFLTPLASGAMLGAFAL 123
             A+   L E  A  G  +  ++VHN +    +L + ++E+K ++L  LASG  +GA A+
Sbjct: 71  TFAHEAVLYEEQARSGDSAWGVTVHNGIVAHYLLAYASEEKKREWLPKLASGEYVGAIAM 130

Query: 124 TEPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           TEP  GSD  ++ TRA  +GDHYV+NG K FIT+G  A +V+V   TDP AG RG+S  +
Sbjct: 131 TEPGTGSDLQAISTRAVRDGDHYVVNGAKTFITNGGLADLVVVAVKTDPDAGARGVSLIV 190

Query: 184 VPTDSPGYSVARVEDKLGQHASDTCQILFEEVKVPVGNRLG-EEGEGYKIALANLEGGRV 242
           V T +PG+   RV DK+G H  DT ++ F++V+VP  N LG EEG+G+   +  L   R+
Sbjct: 191 VETSTPGFRRGRVLDKVGMHGQDTAELFFDDVRVPAENLLGDEEGQGFVQLMQQLPQERL 250

Query: 243 GIAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAA 302
            IA  AV    +A E   DY +ER++FG+P+   Q   + LA+ AT+ AVAR  +     
Sbjct: 251 IIAITAVAGMESAIEQTIDYTKERTAFGRPLFGFQNTKYTLAEAATEAAVARAFLDQCIE 310

Query: 303 LRDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYEG 362
               G+  +  A+M KL+++E   KV    +Q  GGYGY+ ++P+ R + DVRV +I+ G
Sbjct: 311 RHLRGELDVQGAAMVKLWSTERVNKVVDDCVQLFGGYGYMTEYPIARAWADVRVSRIFGG 370

Query: 363 TSDIQRMVISRNL 375
           T++I + +ISR L
Sbjct: 371 TNEIMKDIISRTL 383


Lambda     K      H
   0.320    0.134    0.388 

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: 335
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: 375
Length of database: 383
Length adjustment: 30
Effective length of query: 345
Effective length of database: 353
Effective search space:   121785
Effective search space used:   121785
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