GapMind for catabolism of small carbon sources

 

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

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate N515DRAFT_0941 N515DRAFT_0941 isovaleryl-CoA dehydrogenase

Query= reanno::pseudo3_N2E3:AO353_20350
         (387 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0941
          Length = 385

 Score =  500 bits (1288), Expect = e-146
 Identities = 246/379 (64%), Positives = 302/379 (79%), Gaps = 2/379 (0%)

Query: 8   FALGETIDMLRDQVRAFVSKEIAPRAAQIDIDNLFPADLWRKFGDMGLLGITVPEEYGGA 67
           F+LGE +D+LR+ V AF  KEIAPRA QID DN+FPADLWRKFG+MGLLG+T+PE YGG 
Sbjct: 4   FSLGEELDLLRESVHAFAEKEIAPRATQIDHDNVFPADLWRKFGEMGLLGMTIPEAYGGT 63

Query: 68  GLGYLAHVVAMEEISRGSASVALSYGAHSNLCVNQINRNGTHEQKAKYLPKLISGEHIGA 127
           GLGYLAH+VAMEEISR S SV LSYGAHSNLCV  +  NG  EQ+ KY+P+L SGE++GA
Sbjct: 64  GLGYLAHMVAMEEISRASGSVGLSYGAHSNLCVQNLFHNGNEEQRRKYIPRLCSGEYVGA 123

Query: 128 LAMSEPNAGSDVV-SMKLRADKRGDHYVLNGSKTWITNGPDANTYVIYAKT-DLEKGPHG 185
           LAMSEP AGSDVV SM  +A+ RGD +V NG+K WITNGPDA+  ++Y +T     G   
Sbjct: 124 LAMSEPGAGSDVVGSMSCKAELRGDVWVANGTKMWITNGPDADVLLVYMRTAPRPAGSRC 183

Query: 186 ITAFIVERDWKGFSRSNKFDKLGMRGSNTCELFFDDVEVPEENILGVLNGGVKVLMSGLD 245
           +TAFI+E+  KGFS + K DKLGMRGSNTCEL F+D E+P  NI+G +N GV+VLMSGLD
Sbjct: 184 MTAFIIEKGMKGFSTAQKLDKLGMRGSNTCELVFEDCEIPAANIVGEVNEGVRVLMSGLD 243

Query: 246 YERVVLSGGPTGIMQACMDLIVPYIHDRKQFGQSIGEFQLIQGKVADMYTQLNASRAYLY 305
            ER+VLSGGP G+MQA MDL++PY+ +RKQF   IG F ++Q KVADMYT L +SR + Y
Sbjct: 244 TERLVLSGGPLGLMQAAMDLVLPYVRERKQFNAPIGTFGMMQAKVADMYTALQSSRGFAY 303

Query: 306 AVAQACERGETTRKDAAGVILYSAERATQMALDAIQILGGNGYINEFPAGRLLRDAKLYE 365
            VA+  ++G  +R D A  +L +++ A ++AL+AIQ LGGNGYINEFPAGRLLRDAKLYE
Sbjct: 304 MVAREFDQGSKSRIDPAACLLNASQNAVKVALEAIQALGGNGYINEFPAGRLLRDAKLYE 363

Query: 366 IGAGTSEIRRMLIGRELFN 384
           IGAGT+EIRRMLIGREL++
Sbjct: 364 IGAGTNEIRRMLIGRELYH 382


Lambda     K      H
   0.319    0.137    0.400 

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: 509
Number of extensions: 18
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: 387
Length of database: 385
Length adjustment: 30
Effective length of query: 357
Effective length of database: 355
Effective search space:   126735
Effective search space used:   126735
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 (21.7 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