GapMind for catabolism of small carbon sources

 

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

Align Putative acyl-CoA dehydrogenase AidB; EC 1.3.99.- (characterized)
to candidate N515DRAFT_3819 N515DRAFT_3819 Acyl-CoA dehydrogenase

Query= SwissProt::P33224
         (541 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3819
          Length = 546

 Score =  188 bits (478), Expect = 4e-52
 Identities = 137/387 (35%), Positives = 181/387 (46%), Gaps = 20/387 (5%)

Query: 67  PELLRYDAQGRRLDDVRFHPAWHLLMQALCTNRVHNLAWEEDARSGAFVARAARFMLHAQ 126
           P L ++DA GRR+D +   PAW      L T R   LA   +A   A V   AR  L+  
Sbjct: 62  PVLTQWDAWGRRVDRIELTPAWQ--EGPLLTTRHAVLAAGHEAHPEARVEEFARVYLYHL 119

Query: 127 VEAGSLCPITMTFAATPLLLQMLPAPFQDWTTPLLSDRYDSHLLPGGQKRGLLIGMGMTE 186
                 CP+ MT  A   L     A   +   P        H L        L G  MTE
Sbjct: 120 ASEFYTCPLAMTDGAATALKASGNATLIERALP--------HFLSRDPANFWLSGQWMTE 171

Query: 187 KQGGSDVMSNTTRAERLEDGSYRLVGHKWFFSVPQSDAHLVLAQTAG-----GLSCFFVP 241
             GGSDV +  T A R  DG +RL G KWF S    +A L LA+  G     G    F  
Sbjct: 172 NAGGSDVGNTETVARRDVDGQWRLYGRKWFSSAVVGEAALALARPEGAGVGPGALALFYV 231

Query: 242 RFLPDGQRNA-IRLERLKDKLGNRSNASCEVEFQDAIGWLLGLEGEGIRLILKMGGMTRF 300
             + DGQR   + ++RLKDKLG     + E+  +    W +G    G+R +  M  +TR 
Sbjct: 232 ETMDDGQRKPELVIDRLKDKLGTHELPTAEIHLEGLPAWPVGELEHGVRQVAPMLNVTRS 291

Query: 301 DCALGSHAMMRRAFSLAIYHAHQRHVFGNPLIQQPLMRHVLSRMALQLEGQTALLFRLA- 359
             A+ + A M RA  LA  +A +R  FG  L +QPL    L+ M  + E   AL F +A 
Sbjct: 292 WNAICAVASMSRALQLARDYARRRQAFGRTLAEQPLHAQTLAGMQAEFEAAFALSFEVAH 351

Query: 360 ---RAWDRRADAKEALWARLFTPAAKFVICKRGMPFVAEAMEVLGGIGYCEESELPRLYR 416
              R     A  +EA   RL TP AK    K  +   +EA+E  GG GY E++ LP+L R
Sbjct: 352 LLGRTEQHAATPQEAALLRLLTPLAKLWTGKLAIKLCSEALECFGGAGYIEDTGLPQLLR 411

Query: 417 EMPVNSIWEGSGNIMCLDVLRVLNKQA 443
           +  V +IWEG+ N++ LD LR L  +A
Sbjct: 412 DAQVYAIWEGTTNVLSLDALRALAGKA 438


Lambda     K      H
   0.324    0.138    0.428 

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: 675
Number of extensions: 23
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: 541
Length of database: 546
Length adjustment: 35
Effective length of query: 506
Effective length of database: 511
Effective search space:   258566
Effective search space used:   258566
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 52 (24.6 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