GapMind for catabolism of small carbon sources

 

Alignments for a candidate for antC in Pseudomonas fluorescens FW300-N2E3

Align electron transfer component of the anthranilate 1,2-dioxygenase system (EC 1.14.12.1) (characterized)
to candidate AO353_23545 AO353_23545 NADH oxidase

Query= reanno::WCS417:GFF4631
         (335 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_23545
          Length = 337

 Score =  266 bits (681), Expect = 4e-76
 Identities = 140/338 (41%), Positives = 204/338 (60%), Gaps = 8/338 (2%)

Query: 1   MNHKVAFSFADGKTLFFPVGANEILLDAALRNGIKIPLDCREGVCGTCQGRCESGDYS-- 58
           M H +A +F DG T F      E + DAA R GI IPLDCR+G CGTC+   E+G Y   
Sbjct: 1   MTHSIALNFEDGVTRFVDANPGETVADAAYRQGINIPLDCRDGACGTCKCFAEAGRYDLG 60

Query: 59  QDYVDEEALSSLDLQQRKMLSCQTRVKSDATFYFDFDSSLCNAPGPVQVKGTVSAVEQVS 118
           ++Y+ E+ALSS + ++  +L+CQ R  SD        S +C           +S V Q+S
Sbjct: 61  EEYI-EDALSSDEAEKGFVLTCQMRALSDCVVRVPVSSDVCRTQ-KAHYSAAISQVRQLS 118

Query: 119 ASTAILQVQLD--QALDFLPGQYARLSVPGTDSWRSYSFANLPGN-HLQFLVRLLPDGVM 175
            ST  L ++ +    L FLPGQY  L +PG++  R+YSF++L  +  + FL+R +P G+M
Sbjct: 119 DSTIALSIKGEALSKLAFLPGQYVNLGIPGSEQTRAYSFSSLQRDGEVSFLIRNVPGGLM 178

Query: 176 SNYLRERCQVGDELLMEAPLGAFYLRHVTQPLVLVAGGTGLSALLGMLDQLAANGCEQPV 235
           S++L    + GD + +  PLG+FYLR + +PL+L+AGGTGL+    ML+++A  G E P+
Sbjct: 179 SSFLTGIAKAGDSMSLAGPLGSFYLRDIQRPLLLLAGGTGLAPFTAMLEKIAEQGSEYPL 238

Query: 236 HLYYGVRGAEDLCEAARIRAYAAKIPNLRYTEVLSAPSEEWSGKRGYLTEHFDLAELRDG 295
           HL YGV    DL E  R++A AA+IPN  ++  ++ P      K GY+T+H +   L DG
Sbjct: 239 HLIYGVTNDFDLVELDRLQALAARIPNFSFSACVANPQSAHPLK-GYVTQHIEPKHLNDG 297

Query: 296 SADMYLCGPPPMVESIQQWLADQALDGVQLYYEKFTQS 333
             D+YLCGPPPMVE++ Q++ +Q +     YYEKF  S
Sbjct: 298 DVDVYLCGPPPMVEAVSQFIREQGVSPKNFYYEKFAAS 335


Lambda     K      H
   0.320    0.136    0.412 

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: 338
Number of extensions: 12
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: 335
Length of database: 337
Length adjustment: 28
Effective length of query: 307
Effective length of database: 309
Effective search space:    94863
Effective search space used:    94863
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: 49 (23.5 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