GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Paraburkholderia bryophila 376MFSha3.1

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate H281DRAFT_01199 H281DRAFT_01199 Enoyl-CoA hydratase/carnithine racemase

Query= reanno::Cup4G11:RR42_RS28545
         (384 letters)



>FitnessBrowser__Burk376:H281DRAFT_01199
          Length = 386

 Score =  324 bits (830), Expect = 3e-93
 Identities = 180/365 (49%), Positives = 227/365 (62%), Gaps = 5/365 (1%)

Query: 19  ADDEVRFDEINGIGLITLNRPRQLNALSYPMIGLLDAQLAAWAARDDIAAVVLRGAGPKA 78
           A  E++F  IN + +ITLNRP  LNALS+ MI  L   +      D I A+ L+GAG K 
Sbjct: 19  AQREIQFRVINRVAVITLNRPAALNALSHAMIRELAVLVEHCRNDDSIVAIALKGAGHKG 78

Query: 79  FCAGGDIRALYDSFHAGTALHRQFFVDEYQLDYRLHCYPKPVVALMDGIVMGGGMGLAQA 138
           FCAGGD+R ++    +G +    FFVDEY+LDY LH +PKPVVA++DGI MGGGMGL QA
Sbjct: 79  FCAGGDVREVHRLATSGDSRWLAFFVDEYRLDYALHTFPKPVVAILDGIAMGGGMGLGQA 138

Query: 139 AHLRVLTERSRVAMPETGIGLVPDVGASHFLSKLPLALALYVGLTGVTLGAADTLLCKLA 198
           A LRV+TERS++AMPET IG +PDVGA+ FLS +P  L LYVGLTG TL  AD L  +LA
Sbjct: 139 ARLRVVTERSKIAMPETRIGFLPDVGATRFLSVMPAELELYVGLTGATLSGADALRLQLA 198

Query: 199 DIAVPAASLEHFEQTLAAINRTGDVLADLRAALQATPDAGEQAAPLQSVLPAVLRHFRAD 258
           D  VPA  L   EQ L  ++  GD+L+ LR  ++   +    AA +      + RHF   
Sbjct: 199 DQCVPADWLVSCEQRLQHMSHEGDLLSALRGVVEPPCNIVPHAA-ITPFTQLIQRHFDRR 257

Query: 259 ASVAGLLDSLA--AESDP--AYADWAARTLDILRGRSPLMMAVTRELLLRGRDLDLADCF 314
           + V  ++ +L    E DP      W   T D L   SP M+ VTRE LLRGR + LA+CF
Sbjct: 258 SGVDRIMATLRHDLERDPPREVRQWLQSTYDALAAHSPTMLYVTREALLRGRQMTLAECF 317

Query: 315 RMELGVVSHAFSQGDFIEGVRALIVDKDNAPRWRVKDASEVSEAVVQSFFDSPWPREPHP 374
           RMELG+V  A  +GDF EGVRA ++DKD   RW     +EV    V+ F  SPW +E HP
Sbjct: 318 RMELGIVKRAIEEGDFCEGVRAQLIDKDRKGRWAPATLAEVRPERVRHFLSSPWKQEAHP 377

Query: 375 LAMLG 379
           LA LG
Sbjct: 378 LADLG 382


Lambda     K      H
   0.322    0.137    0.405 

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: 402
Number of extensions: 15
Number of successful extensions: 2
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: 384
Length of database: 386
Length adjustment: 30
Effective length of query: 354
Effective length of database: 356
Effective search space:   126024
Effective search space used:   126024
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