GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00885 in Hydrogenophaga taeniospiralis NBRC 102512

Align ABC transporter permease (characterized, see rationale)
to candidate WP_068173841.1 HTA01S_RS16520 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A165KC95
         (309 letters)



>NCBI__GCF_001592305.1:WP_068173841.1
          Length = 309

 Score =  474 bits (1220), Expect = e-138
 Identities = 240/309 (77%), Positives = 272/309 (88%)

Query: 1   MDILLQQIINGLVLGSMYALIALGYTMVYGIIQLINFAHGEVLMIGALTSWSCIGMMQGA 60
           M+ LLQQIINGLVLGSMYAL+ALGYTMVYGII LINFAHG+VLM+GALTSW+ IG+M+ A
Sbjct: 1   METLLQQIINGLVLGSMYALVALGYTMVYGIIGLINFAHGDVLMVGALTSWTIIGVMREA 60

Query: 61  MPGAPGWVILLLATIIACVVAATLNFVIEKVAYRPLRSSPRLAPLITAIGMSILLQTLAM 120
            PG P W+IL+ AT+IA VV A LN+ IEK+AYRPLR+S RLAPLITAIGMS+LLQT AM
Sbjct: 61  SPGMPLWLILVFATVIAMVVCAALNYTIEKLAYRPLRNSSRLAPLITAIGMSLLLQTFAM 120

Query: 121 IIWKPNYKPYPTMLPSSPFEIGGAFITPTQILILGVTAVALASLVYLVNHTNLGRAMRAT 180
           IIWKPN K YP ML + P  +GGA I+ TQI IL  TAV LA L++LVN TNLGRAMRAT
Sbjct: 121 IIWKPNPKSYPNMLSTDPVHLGGAVISVTQIAILATTAVTLAFLMWLVNRTNLGRAMRAT 180

Query: 181 AENPRVASLMGVKPDMVISATFIIGAVLAAIAGIMYASNYGTAQHTMGFLPGLKAFTAAV 240
           AENPRVA+LMG+KPD+VISATFIIGA+LAAIAGIM+ASNYG+ QH MGF+PGLKAF AAV
Sbjct: 181 AENPRVAALMGIKPDVVISATFIIGAMLAAIAGIMWASNYGSVQHAMGFMPGLKAFVAAV 240

Query: 241 FGGIGNLAGAVVGGILLGLIEAIGSGYIGTLTGGLLGSHYTDIFAFIVLIIILTLRPSGL 300
            GGIGNLAGAVVGGI LGLIE++G+GY+G LTGG+LGS YTDIFAFIVL I+LTLRPSGL
Sbjct: 241 MGGIGNLAGAVVGGIALGLIESLGAGYLGKLTGGVLGSQYTDIFAFIVLAIVLTLRPSGL 300

Query: 301 LGERVADRA 309
           LGERVADRA
Sbjct: 301 LGERVADRA 309


Lambda     K      H
   0.327    0.142    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: 348
Number of extensions: 7
Number of successful extensions: 1
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: 309
Length of database: 309
Length adjustment: 27
Effective length of query: 282
Effective length of database: 282
Effective search space:    79524
Effective search space used:    79524
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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