GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Luteimonas huabeiensis HB2

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

Query= reanno::pseudo3_N2E3:AO353_25670
         (383 letters)



>NCBI__GCF_000559025.1:WP_024890485.1
          Length = 382

 Score =  343 bits (881), Expect = 4e-99
 Identities = 180/371 (48%), Positives = 259/371 (69%), Gaps = 1/371 (0%)

Query: 7   TEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDALVAKMGELGLLGMVVPEEWGGTYVD 66
           +EEQ+MI+D+AR  A+  IAP A+A++++G      +  +GE GL+G+ VP E+GG  +D
Sbjct: 6   SEEQLMIQDVARRIAQERIAPSAEAFDRSGEFPLENIRLLGENGLMGIEVPTEYGGAGMD 65

Query: 67  YVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGTEEQKQTWLADLASGQAIGCFCL 126
            VAY LA+ EI+A D A   +MS++NS+ C  +L +GTE QKQT++  +A G+ IG F L
Sbjct: 66  PVAYVLAMVEIAAADAAHSTIMSVNNSLFCNGILTHGTEAQKQTYVRAIAEGREIGAFAL 125

Query: 127 TEPQAGSEAHNLRTRAELR-DGQWVINGAKQFVSNGRRAKLAIVFAVTDPDLGKKGLSAF 185
           TEPQ+GS+A ++R RA  + DG +V+NG K ++++G  A+  ++FA TDP  G +G++AF
Sbjct: 126 TEPQSGSDATSMRCRAVAQADGSFVVNGKKSWITSGPVARYIVLFATTDPAQGARGITAF 185

Query: 186 LVPTDTPGFIVDRSEHKMGIRASDTCAVTLNNCTIPEANLLGERGKGLAIALSNLEGGRI 245
           LV T   GF   ++E K+GIRAS TC +   +  +    +LG+ G+G  IA+S L+ GRI
Sbjct: 186 LVDTQREGFHRGKTEPKLGIRASATCEIEFQDYVVRADEVLGQPGQGFKIAMSVLDAGRI 245

Query: 246 GIAAQALGIARAAFEAALAYARDRVQFDKPIIEHQSVANMLADMHTRLNAARLLILHAAR 305
           GIA+QA+GIARAA+EA +AY ++R  F +PI   Q     +ADM  +L+A+ LL L AA 
Sbjct: 246 GIASQAIGIARAAYEATIAYVKERKAFGQPIGAFQMTQAKIADMKCKLDASLLLTLRAAW 305

Query: 306 LRSAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVERYYRDARITQIYEG 365
           L+  G+   +EAS AKL ASE A  +   A+QIHGG GY ++ PVERY+RDA+IT+IYEG
Sbjct: 306 LKRQGQRFTTEASVAKLTASEAAMWIAHQAVQIHGGMGYSKEMPVERYFRDAKITEIYEG 365

Query: 366 SSEIQRMVIAR 376
           +SEIQR+VIAR
Sbjct: 366 TSEIQRLVIAR 376


Lambda     K      H
   0.319    0.134    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: 324
Number of extensions: 16
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: 383
Length of database: 382
Length adjustment: 30
Effective length of query: 353
Effective length of database: 352
Effective search space:   124256
Effective search space used:   124256
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