GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Ferroglobus placidus DSM 10642

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_012965508.1 FERP_RS05015 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2397
         (379 letters)



>NCBI__GCF_000025505.1:WP_012965508.1
          Length = 381

 Score =  294 bits (753), Expect = 2e-84
 Identities = 157/377 (41%), Positives = 236/377 (62%), Gaps = 4/377 (1%)

Query: 4   NEDQNAIAEMARQFAQERLKPFAEQWSREHRYPAEAIGEMAALGFFGMLVPEQWGGSDTG 63
           +E+   + E  R+FA++ +KP+  ++  + +YP E   + A LG+ G  VPE++ G+   
Sbjct: 6   SEEHKMLQEAVREFAEKEIKPYGREYDEKKQYPMEIYKKAAKLGYIGASVPEEYDGAGMD 65

Query: 64  YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKSDFLTPLARGEQIGAFAL 123
            LA A+   E    D +  + + +  ++G   +LRFG+E+QK +F+  + RGE   A A+
Sbjct: 66  CLAEAIISMEFCRADSSIGSAIDLA-TLGVPMVLRFGSEEQK-EFVAKVVRGEGPSAIAV 123

Query: 124 TEPQAGSDASSLRTRARRDGDHYVLNGAKQFITSGKHAGTVIVFAVT-DPDAGKGGISAF 182
           TEP  G+D +++RTRA ++GD +V+NG KQFIT+G      +V A T   D    GISAF
Sbjct: 124 TEPDCGTDVAAMRTRAVKEGDEWVINGTKQFITNGSVGIYTVVLAKTAQVDPPHRGISAF 183

Query: 183 IVPTDSPGYQVVRVEDKLGQHASDTCQIAFEDLRVPVANRLGEEGEGYRIALANLEGGRI 242
           +V  D  GY+   +E K+G H  DTC++A +++RVP  + +GEE  G+   +A     R+
Sbjct: 184 LVEQDREGYEARPIE-KMGMHCHDTCEVALKNVRVPADHLIGEENRGFYQLMAFFNESRV 242

Query: 243 GIAAQAVGMARAAFEAARDYARDRETFGKPIIEHQAVAFRLADMATQIAVARQMVHHAAA 302
            IAA   G+A  A+E A +YA++R+ FGKP+IEHQA+ F+LA+M   I  A+ +V  AA 
Sbjct: 243 KIAALHTGIAIGAYERALEYAKERKAFGKPLIEHQAIQFKLAEMFKDIEAAKLLVFKAAW 302

Query: 303 LREVGRPALVEASMAKLFASEMAEKVCSAAIQTLGGYGYLADFPVERIYRDVRVCQIYEG 362
           L + G+P    +S AKLFASEMA KV   A+Q  GGYGY  ++ VER YRD RV  IYEG
Sbjct: 303 LIDQGKPDPALSSAAKLFASEMAVKVTYEAVQIFGGYGYSKEYDVERYYRDARVGTIYEG 362

Query: 363 TSDIQRLVISRNLGGPV 379
           TS+ Q++VI+R + G +
Sbjct: 363 TSEAQKMVIARRIIGKI 379


Lambda     K      H
   0.320    0.135    0.391 

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: 369
Number of extensions: 21
Number of successful extensions: 5
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: 379
Length of database: 381
Length adjustment: 30
Effective length of query: 349
Effective length of database: 351
Effective search space:   122499
Effective search space used:   122499
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