GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Marinobacter adhaerens HP15

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate GFF930 HP15_909 enoyl-CoA hydratase/isomerase family protein

Query= reanno::pseudo1_N1B4:Pf1N1B4_4790
         (356 letters)



>FitnessBrowser__Marino:GFF930
          Length = 356

 Score =  232 bits (591), Expect = 1e-65
 Identities = 129/335 (38%), Positives = 190/335 (56%), Gaps = 8/335 (2%)

Query: 21  LNRPAGLNAITLDMVRSLQQQLDAWAQDPQVHAVVLRGAGEKAFCAGGDIRSLYDSFKS- 79
           LN P  LN+++L+M+R L  QL  WA+DP + AV L   G+KAFCAGGDI +LY S    
Sbjct: 24  LNTPKALNSLSLEMIRLLTPQLKRWAEDPVIQAVWLESEGDKAFCAGGDIVALYRSMTEP 83

Query: 80  -GDTLHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLVQGADLRVVTERSRLAMP 138
            G +  E FF EEY LD  IH + KP++    G V+GGGMG+++GA  RVVTE S+LAMP
Sbjct: 84  QGASEGEAFFTEEYELDYLIHTFPKPLVCWGHGIVMGGGMGIMEGASHRVVTEGSKLAMP 143

Query: 139 EVAIGYFPDVGGSHFLPRVPGELGIYLGVSGVQIRAADALYCGLADWYLESNKLGTLDEQ 198
           E+ IG +PDV    FL R PG  G++LG++G ++  ADA++ GLAD ++  +    +  +
Sbjct: 144 EITIGLYPDVAAGWFLNRTPGRTGLFLGLTGARLNGADAIFTGLADRFIRHDLKADVIAE 203

Query: 199 LDQLQWH-ETPLKDLQGLLAKLAVQQLPAAPLAALRPAIDHFFALPDVPSM---VEQLRA 254
           L +  W  E P   +  +L +   +   A P + +R   D    + D  S+   V QL+ 
Sbjct: 204 LCKRNWQGEDPHAVVGSVLRRYERESADAMPESPVRTHFDEINRVTDADSLEATVNQLKE 263

Query: 255 VTVADSHEWATATADLLESRSPLAMGVTLEMLRRGRHLSLEQCFALELHLDRQWFERGDL 314
           ++  D   W       L   SP ++ +    L   +H SL++    EL L  +   +G+ 
Sbjct: 264 LSGGDG--WVAKATRSLAGASPTSLALVWRHLHGCKHDSLKEVLDKELVLSTKCLTKGEF 321

Query: 315 IEGVRALLIDKDKNPRWSPPTLQALDAGHVASFFT 349
            EG+RALLIDKD+ PRW   +L  +D+  +  FF+
Sbjct: 322 AEGIRALLIDKDQQPRWRYASLAEMDSAWIDDFFS 356


Lambda     K      H
   0.322    0.138    0.422 

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: 356
Number of extensions: 11
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: 356
Length of database: 356
Length adjustment: 29
Effective length of query: 327
Effective length of database: 327
Effective search space:   106929
Effective search space used:   106929
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: 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