GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00885 in Mesorhizobium ciceri biovar biserrulae WSM1271

Align ABC-type branched-chain amino acid transport system, permease component protein (characterized, see rationale)
to candidate WP_013525177.1 MESCI_RS31055 branched-chain amino acid ABC transporter permease

Query= uniprot:D8IUY4
         (309 letters)



>NCBI__GCF_000185905.1:WP_013525177.1
          Length = 303

 Score =  254 bits (650), Expect = 1e-72
 Identities = 139/309 (44%), Positives = 207/309 (66%), Gaps = 10/309 (3%)

Query: 1   MDIFIQQIINGLVLGSMYALIALGYTMVYGVLNLINFAHGDILMVGAMVGLSLLKVVQ-Q 59
           +D+ IQQ++NGL++GS YALIALGY+MV+GV+ L+NFAHGDI M GA VGL +   V   
Sbjct: 3   LDLLIQQLVNGLIVGSFYALIALGYSMVFGVIKLLNFAHGDIYMNGAFVGLIVFSFVGIW 62

Query: 60  VAPGLPGIVQLVIAIVGAIPVCIVVSLLIERIAYRPLRNAPRLAPLITAIGVSILLQTLA 119
           V  G  G+V    A++ ++ V  ++ ++IER AYRP+RNAPRL+ LITA+G S++L   A
Sbjct: 63  VGNGWLGVV---CALLVSMLVVGLLGVVIERFAYRPMRNAPRLSILITALGASMVLNGTA 119

Query: 120 MMIWGRSPLPFPQVMPSDPVHIAGALISPTQIMLLALAVLAMVGLVLIVEKTKMGRAMRA 179
           + + G     F   +    + I+   I+ TQ++L+A ++  M G+   V +T  G+AMRA
Sbjct: 120 LALTGGRHYAFNTDLGFAGIDISTVHITYTQMVLVAASIALMAGMQAFVSRTMYGKAMRA 179

Query: 180 TAENPRIAGLMGVDANKVIVVTFAIGAGLAAIAGVMWAANYSTAQFAMGFVPGLKAFSAA 239
            + +   + LMG+D ++VI +TF +G+ LAA  GVM  A Y +  F MGF+ GLKAF+AA
Sbjct: 180 VSIDMGASRLMGIDVDRVIALTFFMGSALAAGGGVMAGAYYGSVHFFMGFIMGLKAFTAA 239

Query: 240 VLGGIGNIYGAMLGGILLGLIESLGAGYIGDLTGNFLGSNYQDIFAFIVLIIVLTLRPSG 299
           V+GGIG++ GAMLGG+LLGL+E+ G+         F+GS ++D+F F  LI+ L  +P+G
Sbjct: 240 VIGGIGSVPGAMLGGLLLGLLEAFGSSL------PFVGSEWRDVFVFGTLILFLVFKPTG 293

Query: 300 IMGERVADR 308
           ++G  V +R
Sbjct: 294 LLGRSVVER 302


Lambda     K      H
   0.328    0.144    0.416 

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: 322
Number of extensions: 13
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: 309
Length of database: 303
Length adjustment: 27
Effective length of query: 282
Effective length of database: 276
Effective search space:    77832
Effective search space used:    77832
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 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