GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Kyrpidia tusciae DSM 2912

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate WP_013076965.1 BTUS_RS15275 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>NCBI__GCF_000092905.1:WP_013076965.1
          Length = 388

 Score =  180 bits (457), Expect = 5e-50
 Identities = 115/346 (33%), Positives = 175/346 (50%), Gaps = 5/346 (1%)

Query: 22  ADITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILGEKVVLELADDAGEPKQGVS 81
           A + IGL APL+G  A++G   ++ A  A++EIN+ GGILG  +     DD    +  ++
Sbjct: 42  APVKIGLSAPLSGSTASWGTDYRDAAALAIEEINQSGGILGHPIQFVAEDDTMSNEGALN 101

Query: 82  AANKVVGDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTATAPDLTKRGLTNVLRTCGR 141
            A+++V + +  V+GP++S  A+    V ++ GVLM  P A+ P LT+ G  NV R   +
Sbjct: 102 VASRLVDEKVIAVLGPLSSSTAMATEQVYSQGGVLMFPP-ASNPKLTQMGFDNVFRMSPK 160

Query: 142 DDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKATLNAGGITEVVNDAITPGDK 201
           DDQ   + AK   +    K  A+++D   Y KGLA  FK      G   V  +AITPG+K
Sbjct: 161 DDQFGAMDAKVAAERLGAKTAAVIHDNSTYSKGLATYFKDAFEQMGGKVVDFEAITPGEK 220

Query: 202 DFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANATIIGGDGLSNTEFWAIGTDA 261
           D+S + T+IKS   D+ Y+ GY+PEG  L +Q   L      + G+   + +F A+   A
Sbjct: 221 DYSPVLTKIKSMNPDLFYYSGYYPEGAALVKQGKALGLETQYLMGNSNYDQQFIALAGPA 280

Query: 262 AGGTIFTNASDATK-SPDSKAAADALAAKNIPAEAFTLN--AYAAVEVLKAGIEKAGSAE 318
           A   +    +  T  S D      A   +    E   L   AY +V +LK  IEKA S  
Sbjct: 281 AENVVMETLTPVTLISSDQAQKYVARYKEKYGKEPGFLGHLAYDSVHILKQAIEKAHSL- 339

Query: 319 DAEAVATALKDGKEIPTAIGKVTYGETGDLTSQSFSLYKWEAGKIV 364
             +A+ T L+D        GK+T+ + GD+      +   + GK V
Sbjct: 340 SFDAIKTVLRDPGGFQGIAGKITFDKNGDIQGSPSIILTVKNGKFV 385


Lambda     K      H
   0.312    0.131    0.362 

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: 370
Number of extensions: 23
Number of successful extensions: 4
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: 367
Length of database: 388
Length adjustment: 30
Effective length of query: 337
Effective length of database: 358
Effective search space:   120646
Effective search space used:   120646
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 50 (23.9 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