GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Desulfarculus baarsii DSM 2075

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_013258865.1 DEBA_RS10275 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_000143965.1:WP_013258865.1
          Length = 288

 Score =  155 bits (393), Expect = 8e-43
 Identities = 95/297 (31%), Positives = 156/297 (52%), Gaps = 13/297 (4%)

Query: 9   QQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGLDSV 68
           Q L+NGL  G  YA  A G ++++G++G++N AHGE+ M+G++V      GL +  L S+
Sbjct: 5   QALINGLLAGGVYAAFATGLSLIFGVMGVLNIAHGELVMLGAFVCAGLFHGLGLGPLWSL 64

Query: 69  PLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNTVLLSQDSK 128
           PL     F        + GY ++R+   P+ G   ++  I   G+ + + N  LL+  + 
Sbjct: 65  PLSFGLMF--------ALGYVMQRLFLAPIAGRPPVMSYILTFGLHLIIANLALLAWSAD 116

Query: 129 DKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACRACAE 188
            +++     G   +   G    L+  M   V +  L  + GL LF+SR+  GRA RA A+
Sbjct: 117 PRAVTTPYSG-AGLRLWGLDLPLLKSM---VCLAALAMVGGLHLFLSRTAWGRAIRATAQ 172

Query: 189 DIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTAAVLG 248
           D + A L+G++   + ALTF +GA L  ++  L++M   V +   G    + AF   V+G
Sbjct: 173 DRQAAELMGVDVGKVFALTFALGAGLTGLSGALVAMVRDV-DVAMGLPYTILAFCVVVVG 231

Query: 249 GIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGILGRPEVE 305
           G+G +PGA++GG +LGV       +    +   + F +L L LL RP G+ G+  VE
Sbjct: 232 GMGYLPGALIGGALLGVVGELCTALISPGWSLAIMFTILYLTLLLRPAGLTGKGMVE 288


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: 251
Number of extensions: 19
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: 288
Length adjustment: 26
Effective length of query: 281
Effective length of database: 262
Effective search space:    73622
Effective search space used:    73622
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