GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Shewanella loihica PV-4

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate 5209193 Shew_1671 enoyl-CoA hydratase/isomerase (RefSeq)

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



>FitnessBrowser__PV4:5209193
          Length = 376

 Score =  246 bits (629), Expect = 5e-70
 Identities = 147/349 (42%), Positives = 198/349 (56%), Gaps = 14/349 (4%)

Query: 16  IGHLTLNRPAGLNAITLDMVRSLQQQLDAWAQDPQVHAVVLRGAGEKAFCAGGDIRSLYD 75
           +G  TLN    LNA+ ++MVR+L  QL AWA D  +  VVL GAGEKAFCAGGD+R+LY 
Sbjct: 21  VGVATLNMEKALNALNMEMVRALTTQLTAWADDDAIAMVVLDGAGEKAFCAGGDVRALYQ 80

Query: 76  SFKS--GDT--LHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLVQGADLRVVTE 131
           + +   G+   + +DFF  EY LD  +H + KPVL   DG V+GGG+GL+ GA  RVVTE
Sbjct: 81  AARELPGEIPEVTQDFFTREYFLDHLLHTFDKPVLVWGDGIVMGGGLGLMAGASHRVVTE 140

Query: 132 RSRLAMPEVAIGYFPDVGGSHFLPRVPGELGIYLGVSGVQIRAADALYCGLADWYLESNK 191
           RSR+AMPEV IG +PDVGGS+FL R+PG +G +LG++   +  ADA Y GL + YL S+ 
Sbjct: 141 RSRIAMPEVTIGLYPDVGGSYFLNRMPGHMGRFLGMTAYNMDGADAFYVGLGNHYLNSSD 200

Query: 192 LGTLDEQLDQLQW------HETPLKDLQGLLAKLAVQQLPAAPLAALRPAIDHFFALPDV 245
              L + L  + W      +   L  L   ++    Q +  + L   +  ID   AL D 
Sbjct: 201 KQPLFDALSSIDWENDVCANHGKLNALLEAMSSRCAQPMGESILEQHQAQID---ALMDG 257

Query: 246 PSMVEQLRAVTVADSHEWATATADLLESRSPLAMGVTLEMLRRGRHLSLEQCFALELHLD 305
                  R   V D+  W +     + + SPL++ +  +    G  LSL Q F LEL L 
Sbjct: 258 ELNEIMTRVKAVEDAEPWLSRALSTMLAGSPLSLHLVYQQSLLGTELSLSQVFQLELGLS 317

Query: 306 RQWFERGDLIEGVRALLIDKDKNPRWSPPTLQALDAGHVASFFTG-FDP 353
                 GD  EGVRALLIDKD+ P+W   T++A+    V S  T  +DP
Sbjct: 318 CNCCSIGDFAEGVRALLIDKDRQPQWLYETVEAVPQEMVKSLMTSPWDP 366


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: 382
Number of extensions: 24
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: 376
Length adjustment: 30
Effective length of query: 326
Effective length of database: 346
Effective search space:   112796
Effective search space used:   112796
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