GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Cereibacter sphaeroides ATCC 17029

Align ABC transporter membrane-spanning permease-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized)
to candidate WP_002719437.1 RSPH17029_RS04845 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8DQH9
         (318 letters)



>NCBI__GCF_000015985.1:WP_002719437.1
          Length = 358

 Score =  134 bits (337), Expect = 3e-36
 Identities = 100/326 (30%), Positives = 161/326 (49%), Gaps = 38/326 (11%)

Query: 10  LWL-LLLLAGYSLISVLVSVGVLNLFYVQILQQIGINIILAVGLNLIVGFSGQFSLGHAG 68
           LW  + L+ G++++  +++    N   V  L    I  I A+GLN++ G+ GQ SLG  G
Sbjct: 27  LWYQVALVVGFAILPFVINDYWANAVVVPFL----IYAIAAIGLNILTGYCGQVSLGTGG 82

Query: 69  FMAIGAYAAAIIGSKSPTYGAFFGAMLVGALLSGAVALLVGIPTLRLKGDYLAVATLGVS 128
           FMA+GAYA   + +  P        +L GA+ +G V +L G+P+LR+KG YLAVATL  +
Sbjct: 83  FMAVGAYAVYKLMTAFPDVPILIHVILAGAITAG-VGVLFGLPSLRIKGFYLAVATL-AA 140

Query: 129 EIIRIFIIN----------GGSLTNGAAGILGI----PNFTTWQMVYF---FVVITTIAT 171
           +   +++ N           G +T     + GI     N   W    F   F+       
Sbjct: 141 QFFLVWLFNKVPWFYNYSASGQITAPERTMFGIAVTGANTPAWAKYLFCAAFLFALAWIA 200

Query: 172 LNFLRSPIGRSTLSVREDEIAAESVGVNTTKIKIIAFVFGAITASIAGSL-QAGFIGSV- 229
            N  R  IGR  +++R+ +IAAE +GVN    K+ AF   +    IAG+L  A ++G+  
Sbjct: 201 RNLTRGTIGRKWMAIRDMDIAAEIIGVNPLTTKLSAFAVSSFFIGIAGALFFAVYLGAAE 260

Query: 230 VPKDYTFINSINVLIIVVFGGLGSITGAIVSAIVLGILNMLLQDV------------ASV 277
           V + +    S  +L +++ GGLGSI G+   A  L +L + L++V            A +
Sbjct: 261 VGEAFGIQKSFLILFMIIIGGLGSIFGSFAGAAFLVLLPVFLKNVLVGGLGWPSDLAAHI 320

Query: 278 RMIIYALALVLVMIFRPGGLLGTWEL 303
            ++I    ++  +I  P GL   W +
Sbjct: 321 ELMIVGALIIGFLILEPHGLAQLWRV 346


Lambda     K      H
   0.327    0.143    0.403 

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: 256
Number of extensions: 17
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: 318
Length of database: 358
Length adjustment: 28
Effective length of query: 290
Effective length of database: 330
Effective search space:    95700
Effective search space used:    95700
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 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 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