GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Herbaspirillum seropedicae SmR1

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate HSERO_RS01610 HSERO_RS01610 enoyl-CoA hydratase

Query= reanno::WCS417:GFF2712
         (367 letters)



>FitnessBrowser__HerbieS:HSERO_RS01610
          Length = 386

 Score =  229 bits (585), Expect = 7e-65
 Identities = 144/367 (39%), Positives = 204/367 (55%), Gaps = 21/367 (5%)

Query: 12  AETLQDEVLAEVRNHIGHLTLNRPAGLNAITLNMVRRLASQLKAWADDPQVYAVVLRGAG 71
           A  + +E+ A     IG  TL     L+AI+L MV+ L  QL+ W  DP+V  VVL+  G
Sbjct: 6   APVVFEELTAANGRRIGIATLASEKTLHAISLEMVQLLTPQLQHWQADPEVAMVVLQAQG 65

Query: 72  EKAFCAGGDIRSLYDSFKN-----------GDTLHQDFFVEEYALDLAIHHYRKPVLALM 120
           EKAFCAGGD++ LY S +             +    +FF +EY LD  IH + KP+L   
Sbjct: 66  EKAFCAGGDLQQLYRSMREHHASPAREDIRANRYAAEFFEQEYRLDYLIHSFTKPILCWG 125

Query: 121 DGFVLGGGMGLVQGADLRVVTERSRLAMPEVAIGYFPDVGGSYFLPRIPGELGIYLGVTG 180
            G V+GGG+GL+ G   RVVTE+SRLAMPE+ IG +PDVGGS+FL R+PG++GI+L +TG
Sbjct: 126 HGIVMGGGIGLMAGCSHRVVTEKSRLAMPEITIGLYPDVGGSWFLARMPGKIGIFLALTG 185

Query: 181 VQIRAADALYCGLADWYL-ESSKLADLDNKLDRL--QWHDSPLKD--LQGVLAKLAVQQL 235
             + A DAL+ GLAD+ +  +SK A  D  L +   Q  D+ L D  L G  A    + +
Sbjct: 186 ANLNAQDALFAGLADYGMAHASKAAVFDALLSQPWGQGRDAELLDRVLAGAQAASRREGV 245

Query: 236 PDAPLAVLRPAIDHFFAL---PDVPSIVEQLQQVTVADSHEWALTTAHLMQTRSPLAMAV 292
                + LR   D   AL   P +P IV+ +  V   D+  W L     ++  +P +  +
Sbjct: 246 AAFVPSNLRSHFDQIEALCRRPTLPEIVDAILAVQTDDA--WLLKAQSTLRAGAPGSAWL 303

Query: 293 TLEMLRRGRRLPLEQCFALELHLDRQWFERGDLIEGVRALIIDKDKAPRWNPPTLHGLAL 352
              + ++ R L L + F LE  +      R D +EG+RALII+KD+ P+W P +L     
Sbjct: 304 GYALQKKVRPLSLAEVFRLEFVVSLHCAARPDFVEGIRALIIEKDQKPQWKPASLKQATP 363

Query: 353 SHVESFF 359
           + VE FF
Sbjct: 364 AWVEGFF 370


Lambda     K      H
   0.322    0.138    0.419 

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: 408
Number of extensions: 14
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: 367
Length of database: 386
Length adjustment: 30
Effective length of query: 337
Effective length of database: 356
Effective search space:   119972
Effective search space used:   119972
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 (21.9 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