GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Dyella japonica UNC79MFTsu3.2

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate N515DRAFT_0492 N515DRAFT_0492 hypothetical protein

Query= reanno::WCS417:GFF2713
         (383 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0492
          Length = 386

 Score =  350 bits (898), Expect = e-101
 Identities = 184/379 (48%), Positives = 257/379 (67%), Gaps = 5/379 (1%)

Query: 3   DIEYTEEQVMIRDMARDFARGEIAPYAQAWEKAGWIDDALVAKMGELGLLGMVVPEEWGG 62
           D  +TE+Q+ I+ +ARDFA+  I P A   +  G      + +MG+LGL+G+ VP E+GG
Sbjct: 2   DFSFTEDQLSIQSIARDFAQKRIVPVAAELDAKGEFPLENIREMGQLGLMGIEVPHEYGG 61

Query: 63  TYVDYVAYALAVEEISAGDGATGALMSIHNSVGCGPILNYGTESQKQTWLADLASGQAIG 122
             +D +AY LA+ EI+A D AT  +MS++NS+ C  IL +G E QKQ ++  +A G+AIG
Sbjct: 62  AGMDPIAYVLAMIEIAAADAATSTVMSVNNSLFCNGILKHGNEEQKQKYVRAIAQGEAIG 121

Query: 123 CFCLTEPQAGSEAHNLRTRAELR-DGHWVITGAKQFVSNGKRAKLAIVFAITDPELGKKG 181
            + LTEPQ+GS+A  + TRA    DG WVI G K ++++G  A+  ++FAI+ P +G +G
Sbjct: 122 AYALTEPQSGSDASAMHTRATKNADGDWVINGKKSWITSGPVARYIVLFAISTPGIGARG 181

Query: 182 ISAFLVPTATPGFVVDRTEHKMGIRASDTCAVTLNQCTVPEANLLGERGKGLAIALSNLE 241
           +SAF++ T  PGF   +TE K+GIRAS TC +  +    P+ NLLGE GKG +IA+  L+
Sbjct: 182 VSAFIIDTQLPGFAAGKTEPKLGIRASATCEIEFSDYVCPKENLLGEEGKGFSIAMGVLD 241

Query: 242 GGRIGIAAQALGIARAAFEAALAYARDRVQFDKAIIEHQSVANLLADMQTQLNAARLLIL 301
            GRIGIA+Q++GIARAA+EA L ++RDR  F +AI   Q     +ADM+ +L+AA LL L
Sbjct: 242 AGRIGIASQSVGIARAAYEATLQWSRDRKAFGQAIGSFQMTQAKIADMKCKLDAATLLTL 301

Query: 302 HAA----RLRSAGKPCLSEASQAKLFASEMAEKVCSSAMQIHGGYGYLEDYPVERYYRDA 357
            AA    +    G    +EAS AKL ASE A  +   A+QIHGG GY ++ P+ERY+RDA
Sbjct: 302 RAAWTKGQAEKNGGRFGTEASVAKLVASEAAMWIAHQAVQIHGGMGYSKEMPLERYFRDA 361

Query: 358 RITQIYEGTSEIQRMVIAR 376
           +IT+IYEGTSEIQR+VIAR
Sbjct: 362 KITEIYEGTSEIQRLVIAR 380


Lambda     K      H
   0.319    0.133    0.390 

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: 345
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: 383
Length of database: 386
Length adjustment: 30
Effective length of query: 353
Effective length of database: 356
Effective search space:   125668
Effective search space used:   125668
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 17 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