GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Acidovorax sp. GW101-3H11

Align 3-hydroxy-isobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate Ac3H11_2862 Enoyl-CoA hydratase (EC 4.2.1.17)

Query= reanno::pseudo3_N2E3:AO353_25665
         (368 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2862
          Length = 368

 Score =  271 bits (692), Expect = 3e-77
 Identities = 159/354 (44%), Positives = 219/354 (61%), Gaps = 20/354 (5%)

Query: 18  NDVLAEVRNHIGHLTLNRPAGLNAITLDMVRSLHRQLDAWSKDPHIHAVVLRGAGEK--- 74
           +DVL+EVR  +G +TLNRP  LNA++L MVR L   L AW  D  + AV +RG+ ++   
Sbjct: 11  SDVLSEVRGQVGFITLNRPRALNALSLSMVRDLMAILLAWQNDARVLAVAIRGSNKEGPF 70

Query: 75  -AFCAGGDIRSLYDSFKSGGTLHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLV 133
            AFCAGGDIR L+ +   G    EDFF EEYAL+  IH+Y KP +A MDG V+GGGMG+ 
Sbjct: 71  GAFCAGGDIRFLHQAGSQGNPQLEDFFTEEYALNHLIHNYAKPYIAFMDGIVMGGGMGIS 130

Query: 134 QGADLRVVTERSRLAMPEVAIGYFPDVGGSYFLPRIPGELGIYLGVSGVQIRAADALYCG 193
           QGA LRVVTER+++AMPE AIG FPDVGG YFL R PG +G +L ++G  I A DA+   
Sbjct: 131 QGAALRVVTERTKMAMPETAIGLFPDVGGGYFLSRCPGRVGEWLALTGDTIGAGDAIDSQ 190

Query: 194 LADWYLESQKLAELDQHLDSLEW-HDTPLKDLQGLLAK-LALQQLPDAPLQALRPTIDHF 251
           LAD  L + + A + + L +  +     +KD   + +K +A++ +    L   +  ID +
Sbjct: 191 LADGCLPADQQAAVWEALATQTFASGAAVKDY--VASKFIAIEPM----LSGAKGQIDQY 244

Query: 252 FALPDVPSIVEQLRTVTVADSHDWAMTTADLLDSRSPLAMGVTLEMLRRGRQLSLENCFA 311
           FALP V  IV  L +   ADS DWA  TA  L  RSPL + V LE +RR R + L +   
Sbjct: 245 FALPTVGEIVSALES---ADS-DWARATAATLRKRSPLMLNVVLEQIRRARGMGLADDLR 300

Query: 312 LELHLDRQWF----ERGDLIEGVRALLIDKDKSPRWNPPTVQALDAKHVASFFS 361
           +E  + R  F     + + +EG+RAL +DKD +P+WNP  ++ +  + VA FF+
Sbjct: 301 MERDMVRHCFYLRPGQSETVEGIRALAVDKDHAPKWNPARIEDVTPEMVAPFFA 354


Lambda     K      H
   0.321    0.138    0.418 

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: 348
Number of extensions: 19
Number of successful extensions: 4
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: 368
Length of database: 368
Length adjustment: 30
Effective length of query: 338
Effective length of database: 338
Effective search space:   114244
Effective search space used:   114244
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