GapMind for catabolism of small carbon sources

 

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

Align D-arginine dehydrogenase (EC 1.4.99.6) (characterized)
to candidate N515DRAFT_3723 N515DRAFT_3723 D-amino-acid dehydrogenase

Query= BRENDA::Q9HTQ0
         (432 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3723
          Length = 419

 Score =  187 bits (474), Expect = 7e-52
 Identities = 133/419 (31%), Positives = 203/419 (48%), Gaps = 17/419 (4%)

Query: 3   VLVLGSGVIGTASAYYLARAGFEVVVVDRQDGPALETSFANAGQVSPGYASPWAAPGIPL 62
           VL+LG GVIG ASAYYL RAG  V V++ Q  P   +S  N G ++P +A+P A PG+  
Sbjct: 8   VLILGGGVIGLASAYYLLRAGATVRVLE-QGTPGCGSSHGNCGTITPSHAAPLAMPGMVS 66

Query: 63  KAMKWLLEKHAPLAIKLTSDPSQYAWMLQMLRNCTAERYAVNKERMVRLSEYSRDCLDEL 122
            A++ +    APL +    DP +  W+L   R C    +         + + SR  L+ L
Sbjct: 67  VALRSMFRADAPLYLNPRPDPERLRWLLGFARRCNWRDFERATRARSAILQRSRGLLEAL 126

Query: 123 RAETGIAYEGRTLGTTQLFRTQAQLDAAGKDIA-VLERSGVPYEVLDRDGIARVEPALAK 181
             +  +  E    G   ++RT+AQ++A  +  A VL+R G+    L  D +  +EPAL  
Sbjct: 127 VRDEALDCEFVAGGELYVYRTRAQMEADERHHAQVLDRLGIEVNRLRGDEVENLEPAL-- 184

Query: 182 VADKLVGALRLPNDQTGDCQLFTTRLAEMAKGLGVEFRFGQNIERLDFAGDRINGVLVNG 241
               + G L  P D       +   LA   + LG     G  I++      RI+ V    
Sbjct: 185 -LPGVAGGLFHPGDAQLRPNRYAAELARRVRELGGVIESGARIDQFGLQDGRISHVRTTR 243

Query: 242 ELLTADHYVLALGSYSPQLLKPLGIKAPVYPLKGYSLTVPITNPEMAPTSTILDETYKVA 301
            +   +  V+ALG++SP L + L ++ P+ P KGYS+T   T P+ AP   ++     V 
Sbjct: 244 GVFHGEQVVMALGAWSPLLGRLLDLRLPMQPGKGYSIT--YTRPQQAPRHALVLREAAVC 301

Query: 302 ITRFDQRIRVGGMAEIAGFDLSLNPRRRETLEMITTDLY--PEGGDISQATFWTGLRPAT 359
           +T +    R+G   E +G+   LN  R + L          PEG ++ +   W G RP +
Sbjct: 302 VTTWGSGYRLGSTMEFSGYAEGLNRTRLDALRRGAAAALREPEGPEVLEE--WWGWRPMS 359

Query: 360 PDGTPIVG-ATRYRNLFLNTGHGTLGWTMACGSGRYLADLMAKKRPQISTEGLDISRYS 417
            D  PI+G +TR+ NL L T HG LG +M+  +G  +A L  +      T  LD + Y+
Sbjct: 360 MDEVPIIGPSTRWSNLLLATAHGMLGVSMSAATGELVAALAGR-----GTAALDPAPYA 413


Lambda     K      H
   0.318    0.135    0.401 

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: 472
Number of extensions: 26
Number of successful extensions: 7
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: 432
Length of database: 419
Length adjustment: 32
Effective length of query: 400
Effective length of database: 387
Effective search space:   154800
Effective search space used:   154800
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 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