GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Kyrpidia tusciae DSM 2912

Align Branched-chain amino acid ABC transporter permease LivH; SubName: Full=Branched-chain amino acid transporter permease subunit LivH; SubName: Full=L-leucine ABC transporter membrane protein /L-isoleucine ABC transporter membrane protein /L-valine ABC transporter membrane protein (characterized, see rationale)
to candidate WP_013075700.1 BTUS_RS08495 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_000092905.1:WP_013075700.1
          Length = 292

 Score =  258 bits (659), Expect = 1e-73
 Identities = 142/301 (47%), Positives = 201/301 (66%), Gaps = 12/301 (3%)

Query: 7   FFQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGLD 66
           F QQLVNGL+VGS YALIA+GYTMVYGII +INFAHG+V+M+G++VA+ +     +  L 
Sbjct: 4   FIQQLVNGLSVGSIYALIALGYTMVYGIIKLINFAHGDVFMVGAFVAYFSYTVFHLGFLG 63

Query: 67  SVPLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNTVLLSQD 126
           S+ + M A  +  +V        IER AYRPLR S R+  LI+AIG+S+FL+N  +++  
Sbjct: 64  SLIVSMAACAVLGVV--------IERFAYRPLRKSTRIAALITAIGVSLFLENAGIIAVG 115

Query: 127 SKDKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACRAC 186
           ++ +  P+++P N +I  GG   V IS  QI + V+++V M+ L   + R+++G+A RA 
Sbjct: 116 AQARGYPSMLP-NSSINLGG---VTISVQQIGIIVLSVVLMVILQFIVHRTKMGKAMRAV 171

Query: 187 AEDIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTAAV 246
           A D + A L+GI+ +  I+ TF IG+ALAA A V+    Y  I+P  G + GLKAF AAV
Sbjct: 172 AYDAEAAQLMGIDVDRTISFTFAIGSALAAAAGVIYGAYYSAIDPLMGIMPGLKAFIAAV 231

Query: 247 LGGIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGILGRPEVEK 306
           LGGIG IPGAM+GGLVLG+ E     +    ++D VAF LL+L+LL +P G+ G+   EK
Sbjct: 232 LGGIGVIPGAMVGGLVLGMIETLVQSLGFSLWRDAVAFALLILILLVKPEGLFGKHAREK 291

Query: 307 V 307
           V
Sbjct: 292 V 292


Lambda     K      H
   0.327    0.144    0.411 

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: 314
Number of extensions: 13
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: 307
Length of database: 292
Length adjustment: 27
Effective length of query: 280
Effective length of database: 265
Effective search space:    74200
Effective search space used:    74200
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