GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Streptococcus massiliensis 4401825

Align NatD, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized)
to candidate WP_018371595.1 BN415_RS07285 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000341525.1:WP_018371595.1
          Length = 289

 Score =  166 bits (421), Expect = 4e-46
 Identities = 96/281 (34%), Positives = 166/281 (59%), Gaps = 5/281 (1%)

Query: 6   IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFF-VNTFGVNIWLS 64
           +Q +VNG+ +GS+ AL A+G T+ YGI++L NFAHGD   +GA++ ++ + +  +N +L+
Sbjct: 2   LQQLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFMGYYLIGSLHMNFYLA 61

Query: 65  MIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRNQNYN 124
           +IV++VGT  + +L E L +  +R   +     +I +IG++ FL   ++ +     + + 
Sbjct: 62  LIVSMVGTAALGVLIEFLAYRPLR--HSTRIAALITAIGVSFFLEYSMVAVVSANVKAFP 119

Query: 125 LPITPALDIFG-VKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVADDLDLAKVSG 183
             +     + G V V   QL +LA+A++ +  L  ++Q TK+GKAMRAV+ D D A++ G
Sbjct: 120 QVLPSVRFVLGPVSVTSIQLTILAVALILMVLLQLIVQKTKMGKAMRAVSVDSDAAQLMG 179

Query: 184 IDVEQVIFWTWLIAGTVTSLGGSMYGL-ITAVRPNMGWFLILPLFASVILGGIGNPYGAI 242
           I+V Q I +T+ +   +    G +  L   ++ P MG    L  F + ++GGIG   GA 
Sbjct: 180 INVNQTISFTFALGSALAGAAGVLIALYYNSLDPLMGMTPGLKSFVAAVIGGIGIIPGAA 239

Query: 243 AAAFIIGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGL 283
              F+IGI++  +T    S+Y+  +   I+IL+LLIRP G+
Sbjct: 240 LGGFVIGILETFATVINLSEYRDAIVYGILILILLIRPAGI 280


Lambda     K      H
   0.328    0.144    0.426 

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: 243
Number of extensions: 15
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: 288
Length of database: 289
Length adjustment: 26
Effective length of query: 262
Effective length of database: 263
Effective search space:    68906
Effective search space used:    68906
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 Sep 24 2021. 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