GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Magnetospirillum magneticum AMB-1

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_011385250.1 AMB_RS14465 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_000009985.1:WP_011385250.1
          Length = 286

 Score =  141 bits (355), Expect = 2e-38
 Identities = 87/298 (29%), Positives = 153/298 (51%), Gaps = 17/298 (5%)

Query: 3   DIYHFFQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAM 62
           D + F  Q++NG+  G    L+A G T+++GI+G+IN AHG  YM+G+Y+A+        
Sbjct: 2   DFWFFLIQVLNGVQYGLLLFLVASGLTLIFGIMGIINLAHGAFYMLGAYLAYWLARTTGS 61

Query: 63  MGLDSVPLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNT-- 120
           +G         AA + S+ + ++ GY IE +  R L   + L  ++   G+ +       
Sbjct: 62  LG---------AAVLLSLPIAAAIGYGIEALLVRTLYRRDHLDQVLLTYGLILIFNEATR 112

Query: 121 VLLSQDSKDKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLG 180
           ++   D    ++P  +  +  +    ++ V     ++++  V  V  +G+ L I+R+R G
Sbjct: 113 MIWGADVHGVAVPAALNWSIRLTDTLSYPV----YRLMLSGVCAVLAVGMYLVITRTRFG 168

Query: 181 RACRACAEDIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLK 240
              RA A +  M   LGIN   +  + F +GAALA +A   +S     + P  G  V + 
Sbjct: 169 MWVRAGASNRDMVAALGINVKLLFGVVFALGAALAGLAGA-ISTPITSVAPGMGDSVLIL 227

Query: 241 AFTAAVLGGIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGI 298
            F   V+GG+GSI GA LG +++G+A+ FG  +F   +     +G++  VLL++P G+
Sbjct: 228 CFVVVVIGGVGSIKGAFLGAMLIGLADTFG-KVFAPDFASFTVYGVMAAVLLWKPRGL 284


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: 242
Number of extensions: 11
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: 286
Length adjustment: 26
Effective length of query: 281
Effective length of database: 260
Effective search space:    73060
Effective search space used:    73060
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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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