GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Sphingomonas histidinilytica UM2

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate WP_079650852.1 B5X82_RS24125 enoyl-CoA hydratase/isomerase family protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2986
         (356 letters)



>NCBI__GCF_900167915.1:WP_079650852.1
          Length = 354

 Score =  231 bits (590), Expect = 2e-65
 Identities = 137/357 (38%), Positives = 191/357 (53%), Gaps = 14/357 (3%)

Query: 2   DAMQNEVLAEVRNHIGHLTLNRPAGLNALTLDMVRNLHRQLDAWAQDSQVHAVVLRGAGE 61
           D + +EVL  V    G + LNRP  ++ALT  +   + R L AWA D  V  V++  A  
Sbjct: 3   DPVNDEVLIFVEGRTGRIRLNRPKAIHALTHPICTAMIRALTAWASDDGVDLVMIDHAEG 62

Query: 62  KAFCAGGDIRSLHDSFKSGDTLHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLV 121
           + FCAGGDIR + DS K   +    FF EEY L+  +  Y KP +A MDG  +GGG+G+ 
Sbjct: 63  RGFCAGGDIRHIADSAKGDGSEGRAFFHEEYRLNHLLFTYAKPTIAFMDGITMGGGVGIS 122

Query: 122 QGADLRVVTEKSRLAMPEVGIGYFPDVGGSYFLSRIPGELGIYLGVSGVQIRAADALYCG 181
           Q   +RVVTE++  AMPE GIG F DVGG  +LSR+PG +G Y+G++G ++  A+ L   
Sbjct: 123 QPCSIRVVTERTMYAMPETGIGLFTDVGGGRYLSRMPGRMGQYVGLTGARLNGAECLALA 182

Query: 182 LADWYLESGKLGVLDEK-LDQLEWHDTPLKDLQGLLAKFAVQQLPDAPLATLRPAIDHFF 240
           L   Y+ES  +  L    L      D  L+         AV  +P AP+   +  ID  F
Sbjct: 183 LGTHYVESDGIEALKAAILGNPGAIDAALRS--------AVSAVPPAPILDRQADIDRLF 234

Query: 241 AQPDVPSIVEQLRQVTVADSHEWAVTTADLLETRSPLAMAVTLEMLRRGREL-PLEQCFA 299
           A      IV  L     AD  +WA+ T   LET+SP A  V L +L     +    +  A
Sbjct: 235 ASDRYEDIVAAL----AADGGDWALATLKTLETKSPQACKVVLRLLAESARIDDFAEEMA 290

Query: 300 LELHLDRQWFERGDLIEGVRALLIDKDKTPRWNPPTLQALDAEHVASFFSEFDRSES 356
           +E  +  +  +R D+IEGVRAL++DKD  PRWNPPT   +    + + F+    SE+
Sbjct: 291 MEYAVVVRVIQRPDIIEGVRALIVDKDNAPRWNPPTAAGVSDADIDAIFAPLPPSEA 347


Lambda     K      H
   0.322    0.139    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: 335
Number of extensions: 16
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: 354
Length adjustment: 29
Effective length of query: 327
Effective length of database: 325
Effective search space:   106275
Effective search space used:   106275
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 24 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