GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Algoriphagus machipongonensis PR1

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_008203176.1 ALPR1_RS19205 acyl-CoA dehydrogenase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2983
         (375 letters)



>NCBI__GCF_000166275.1:WP_008203176.1
          Length = 379

 Score =  319 bits (817), Expect = 9e-92
 Identities = 156/372 (41%), Positives = 241/372 (64%)

Query: 4   NDDQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTG 63
           +++Q+ I DM RDF  + + PF  EWD    FPK+   ++  LG  G+LVP  +GG   G
Sbjct: 6   SENQRMIADMIRDFGAKEITPFRKEWDDTQFFPKDLFKKLGELGLMGVLVPTDFGGAGFG 65

Query: 64  YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFAL 123
           Y  Y  A+ E+   D +    ++ HNS+    IL +G++EQK+++L  LA+  +LGA+ L
Sbjct: 66  YDEYVTAIVEVTKLDPSIGLSLAAHNSLCTGHILLFGSEEQKQKYLPKLATCELLGAWGL 125

Query: 124 TEPQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           TEP  GSDA  +KT A  +GD+++LNG K FIT G +  + +V A T       G++AFI
Sbjct: 126 TEPNTGSDAGNMKTVAVKDGDYWILNGAKNFITHGVSGDLAVVIARTGEVGDSHGMTAFI 185

Query: 184 VPTDSPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVG 243
           V   +PG+K  R EDKLG  AS+T +++FED K+  +  LG  G+G+  ++  L+GGR+ 
Sbjct: 186 VERGTPGFKGGRKEDKLGMRASETAEMIFEDCKIHESQVLGNVGDGFIQSMKVLDGGRIS 245

Query: 244 IASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           IA+ S+G+A  A EA+  Y++ERE FGKPI   Q ++F+LADMATQ+  A+ ++  A+ +
Sbjct: 246 IAALSLGIAEGALEASIQYSKEREQFGKPISRFQGISFKLADMATQVEAAKLLIMKASDM 305

Query: 304 RDSGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGT 363
           ++ G+   + ++ AK +ASE+   V + A+Q  GGYG+  D+PVE+ YRD ++C I EGT
Sbjct: 306 KNRGEKVTLASAQAKYYASEVCVSVSNEAVQIFGGYGFTKDYPVEKYYRDSKLCTIGEGT 365

Query: 364 SDIQRMVISRNL 375
           S+IQ++VI+R +
Sbjct: 366 SEIQKLVIAREV 377


Lambda     K      H
   0.320    0.135    0.394 

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: 342
Number of extensions: 12
Number of successful extensions: 1
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: 379
Length adjustment: 30
Effective length of query: 345
Effective length of database: 349
Effective search space:   120405
Effective search space used:   120405
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