GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Mesorhizobium ciceri biovar biserrulae WSM1271

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_013525177.1 MESCI_RS31055 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8DQI0
         (292 letters)



>NCBI__GCF_000185905.1:WP_013525177.1
          Length = 303

 Score =  278 bits (710), Expect = 1e-79
 Identities = 143/301 (47%), Positives = 207/301 (68%), Gaps = 9/301 (2%)

Query: 1   MNLMLQQLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFIGYFL------- 53
           ++L++QQLVNGLI+GS YAL+ALGY+MV+G+IKL+NFAHGDIYM GAF+G  +       
Sbjct: 3   LDLLIQQLVNGLIVGSFYALIALGYSMVFGVIKLLNFAHGDIYMNGAFVGLIVFSFVGIW 62

Query: 54  INSFQMNFFVALIVAMLATAILGVVIEFLAYRPLRHSTRIAVLITAIGVSFLLEYGMVYL 113
           + +  +    AL+V+ML   +LGVVIE  AYRP+R++ R+++LITA+G S +L    + L
Sbjct: 63  VGNGWLGVVCALLVSMLVVGLLGVVIERFAYRPMRNAPRLSILITALGASMVLNGTALAL 122

Query: 114 VGANTRAFPQAIQTVRYDLGPISLTNVQLMILGISLILMILLQVIVQKTKMGKAMRAVSV 173
            G    AF   +     D+  + +T  Q++++  S+ LM  +Q  V +T  GKAMRAVS+
Sbjct: 123 TGGRHYAFNTDLGFAGIDISTVHITYTQMVLVAASIALMAGMQAFVSRTMYGKAMRAVSI 182

Query: 174 DSDAAQLMGINVNRTISFTFALGSALAGAAGVLIALYYNSLEPLMGVTPGLKSFVAAVLG 233
           D  A++LMGI+V+R I+ TF +GSALA   GV+   YY S+   MG   GLK+F AAV+G
Sbjct: 183 DMGASRLMGIDVDRVIALTFFMGSALAAGGGVMAGAYYGSVHFFMGFIMGLKAFTAAVIG 242

Query: 234 GIGIIPGAALGGFVIGLLETFATA--FGMSDFRDAIVYGILLLILIVRPAGILGKNVKEK 291
           GIG +PGA LGG ++GLLE F ++  F  S++RD  V+G L+L L+ +P G+LG++V E+
Sbjct: 243 GIGSVPGAMLGGLLLGLLEAFGSSLPFVGSEWRDVFVFGTLILFLVFKPTGLLGRSVVER 302

Query: 292 V 292
           V
Sbjct: 303 V 303


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: 289
Number of extensions: 14
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: 303
Length adjustment: 26
Effective length of query: 266
Effective length of database: 277
Effective search space:    73682
Effective search space used:    73682
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 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