GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Paraburkholderia bryophila 376MFSha3.1

Align ABC transporter membrane-spanning permease-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized)
to candidate H281DRAFT_02378 H281DRAFT_02378 amino acid/amide ABC transporter membrane protein 1, HAAT family

Query= TCDB::Q8DQI0
         (292 letters)



>FitnessBrowser__Burk376:H281DRAFT_02378
          Length = 294

 Score =  154 bits (388), Expect = 3e-42
 Identities = 93/285 (32%), Positives = 160/285 (56%), Gaps = 5/285 (1%)

Query: 4   MLQQLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFIGYFLINSFQMNFFV 63
           ML QL+ GL+ GS YA+L+LG  +++G++ +INFAHG ++M+GA + +   + F + ++ 
Sbjct: 11  MLSQLLLGLVNGSFYAILSLGLAVIFGLLNVINFAHGALFMLGAMLAWMGFSYFGVPYWA 70

Query: 64  ALIVAMLATAILGVVIEFLAYRPLRHSTRIAVLITAIGVSFLLEYGMVYLVGANTRAF-- 121
            L++A L   + GV IE    R L     +  L+   G++ ++E     + G++ + +  
Sbjct: 71  MLVLAPLIVGLFGVAIERSMLRWLYKLDHLYGLLLTFGLTLVVEGVFRSIYGSSGQPYDV 130

Query: 122 PQAIQTVRYDLGPISLTNVQLMILGISLILMILLQVIVQKTKMGKAMRAVSVDSDAAQLM 181
           P A+     +LG + L N +  ++  SLI+      +++KT++G  +RA + +    +  
Sbjct: 131 PSALSGAT-NLGFMFLPNYRAWVVVASLIVCFATWFVIEKTRLGAYLRAGTENPKLVEAF 189

Query: 182 GINVNRTISFTFALGSALAGAAGVLIALYYNSLEPLMGVTPGLKSFVAAVLGGIGIIPGA 241
           GINV   I+ T+  G ALA  AGVL A     + PLMG    +  F   V+GG+G I G+
Sbjct: 190 GINVPLMITLTYGFGVALAAFAGVLAAPVI-QVSPLMGQPMIITVFAVVVIGGMGSIMGS 248

Query: 242 ALGGFVIGLLETFATAFGMSDFRDAIVYGILLLILIVRPAGILGK 286
            L G ++G++E     F   +    +V+ I+ L+L+VRPAG+ GK
Sbjct: 249 ILTGLMLGVIEGLTRVF-YPEASATVVFVIMALVLLVRPAGLFGK 292


Lambda     K      H
   0.330    0.146    0.407 

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: 246
Number of extensions: 17
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: 292
Length of database: 294
Length adjustment: 26
Effective length of query: 266
Effective length of database: 268
Effective search space:    71288
Effective search space used:    71288
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 (21.8 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