GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Luteimonas huabeiensis HB2

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_024890485.1 Z164_RS0109600 acyl-CoA dehydrogenase

Query= reanno::WCS417:GFF2715
         (375 letters)



>NCBI__GCF_000559025.1:WP_024890485.1
          Length = 382

 Score =  330 bits (847), Expect = 3e-95
 Identities = 176/372 (47%), Positives = 248/372 (66%), Gaps = 1/372 (0%)

Query: 4   NEEQLQISDAARQFAQERLKPFAAEWDREHRFPKEAIGEMAELGFFGMLVPEQWGGCDTG 63
           +EEQL I D AR+ AQER+ P A  +DR   FP E I  + E G  G+ VP ++GG    
Sbjct: 6   SEEQLMIQDVARRIAQERIAPSAEAFDRSGEFPLENIRLLGENGLMGIEVPTEYGGAGMD 65

Query: 64  YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPVLKFGNDQQKEQFLKPLASGAMLGAFAL 123
            +AY +A+ EIAA D A STIMSV+NS+ C  +L  G + QK+ +++ +A G  +GAFAL
Sbjct: 66  PVAYVLAMVEIAAADAAHSTIMSVNNSLFCNGILTHGTEAQKQTYVRAIAEGREIGAFAL 125

Query: 124 TEPQAGSDASSLKTRARLEGD-HYVLNGCKQFITSGQNAGVVIVFAVTDPAAGKRGISAF 182
           TEPQ+GSDA+S++ RA  + D  +V+NG K +ITSG  A  +++FA TDPA G RGI+AF
Sbjct: 126 TEPQSGSDATSMRCRAVAQADGSFVVNGKKSWITSGPVARYIVLFATTDPAQGARGITAF 185

Query: 183 IVPTDSPGYSVARVEDKLGQHASDTCQILFEDVKVPVANRLGEEGEGYKIALANLEGGRV 242
           +V T   G+   + E KLG  AS TC+I F+D  V     LG+ G+G+KIA++ L+ GR+
Sbjct: 186 LVDTQREGFHRGKTEPKLGIRASATCEIEFQDYVVRADEVLGQPGQGFKIAMSVLDAGRI 245

Query: 243 GIASQAVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAA 302
           GIASQA+G+ARAA+EA   Y +ER++FG+PI   Q    ++ADM  ++  +  +   AA 
Sbjct: 246 GIASQAIGIARAAYEATIAYVKERKAFGQPIGAFQMTQAKIADMKCKLDASLLLTLRAAW 305

Query: 303 LRDSGKPALVEASMAKLFASEMAEKVCSAALQTLGGYGYLSDFPLERIYRDVRVCQIYEG 362
           L+  G+    EAS+AKL ASE A  +   A+Q  GG GY  + P+ER +RD ++ +IYEG
Sbjct: 306 LKRQGQRFTTEASVAKLTASEAAMWIAHQAVQIHGGMGYSKEMPVERYFRDAKITEIYEG 365

Query: 363 TSDIQRMVISRN 374
           TS+IQR+VI+RN
Sbjct: 366 TSEIQRLVIARN 377


Lambda     K      H
   0.319    0.134    0.387 

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: 323
Number of extensions: 10
Number of successful extensions: 2
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: 382
Length adjustment: 30
Effective length of query: 345
Effective length of database: 352
Effective search space:   121440
Effective search space used:   121440
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