GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Desulfobacter vibrioformis DSM 8776

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_084691833.1 Q366_RS13530 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_000745975.1:WP_084691833.1
          Length = 368

 Score =  150 bits (378), Expect = 8e-41
 Identities = 111/346 (32%), Positives = 182/346 (52%), Gaps = 36/346 (10%)

Query: 90  KLFLVALLVLAVAWPFMVSRGT-VDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYAI 148
           K+ L A+L+L +A P ++S  T + I  L   Y  L    N+V G +G+L LG+  F  I
Sbjct: 39  KVLLGAVLILMLALPAVISSPTWLHIIVLIFFYAYLTTSWNMVGGFAGVLPLGHAVFLGI 98

Query: 149 GAYTFALLNHYYGLGFWTCLPIAGLMAAAAGFLLGFPVLRLRGDYLAIVTLGFGEIVRIL 208
           GAYT  +L+  YG+  W  + + G++A AAG ++G P L++RG Y A+ T+ F E VR+ 
Sbjct: 99  GAYTSTVLSLQYGISPWLGMFVGGVLAVAAGMVIGLPTLKMRGAYFALATIAFSEGVRV- 157

Query: 209 LLNNTEITG-----GPNGISQIPKPTLFGLEFSRTAREGGWDTFSNFFGLKYDPSDRVIF 263
           ++ N E  G     GP G+ QIP   +            GW  F          S +V +
Sbjct: 158 MVENIEYLGPFKLNGPRGL-QIPPLNI------------GWANFMF--------SSKVPY 196

Query: 264 LYLVALLLVVLSLFVINRLLRMPLGRAWEALREDEIACRSLGLSPRRIKLTAFTISAAFA 323
            Y++  +L+++ LF+   + R  LG    A  E+  A ++LG++  R K+ A  +S  F 
Sbjct: 197 YYIILAMLLII-LFLTWVVSRSKLGYYLTAGGEEPEAAQALGVNVSRAKVIAMALSCFFT 255

Query: 324 GFAGTLFAARQGFVSPESFTFAESAFVLA-IVVLGGMGSQFAVILAAILLVVSRELMRDF 382
             AGT +A    F+ P+S    + +F +A I ++GG GS    +L A+LL    +L R +
Sbjct: 256 ALAGTFYAQFSLFIHPKSTISLDISFEIAFIALIGGRGSIAGPVLGALLLRPVSDLSRIY 315

Query: 383 -----NEYSMLMLGGLMVLMMIWRPQGLL-PMTRPQLKLKNGAAKG 422
                    +++ G +++L+MI++P+GL  P+TR   ++ N  A G
Sbjct: 316 FGDILPGMHLVIYGVVLILVMIYQPRGLQEPLTRIYDRVINRMADG 361


Lambda     K      H
   0.330    0.145    0.436 

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: 308
Number of extensions: 6
Number of successful extensions: 2
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: 425
Length of database: 368
Length adjustment: 31
Effective length of query: 394
Effective length of database: 337
Effective search space:   132778
Effective search space used:   132778
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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