GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Synechococcus elongatus PCC 7942

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 Synpcc7942_2495 Synpcc7942_2495 integral membrane protein of the ABC-type Nat permease for neutral amino acids NatD

Query= TCDB::Q8YXD0
         (288 letters)



>FitnessBrowser__SynE:Synpcc7942_2495
          Length = 313

 Score =  139 bits (349), Expect = 1e-37
 Identities = 91/305 (29%), Positives = 164/305 (53%), Gaps = 29/305 (9%)

Query: 6   IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFV----------- 54
           +Q ++NG+A+G + AL A+G TL + IL + NFAHG   TLGAYLT+ +           
Sbjct: 4   LQPLINGLAIGGVYALFALGYTLVFSILGVINFAHGAVFTLGAYLTYALVGGRFSFNGLL 63

Query: 55  ----NTFGVNIWLSMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRN 110
                 F +   L++++  +   G  LL E++ +  +R  +A+    +I S+G+A+F+ N
Sbjct: 64  ANAALPFSLPFALALLLGSLLAGGASLLIEQVAFRPLRRRQADPLLTLISSLGVAVFIVN 123

Query: 111 GIILIWGGRNQNYNLP------ITPALDIFG----VKVPQNQLLVLALAVLSIGALHYLL 160
            I ++ G   + Y  P      +  A+++      +++   Q+++  +A+     L +L+
Sbjct: 124 LIQILVGA--EIYTFPSNIYGDLPSAINLGSSDRPIQIRTVQIILFVVAIAMFSLLTWLI 181

Query: 161 QNTKIGKAMRAVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGL-ITAVRPNMG 219
             T++G A++AVA+D   A + GID ++ I  T+ ++G +  L G++ G  ++   P  G
Sbjct: 182 NGTRVGHALKAVAEDATTASLLGIDPDRYIRLTFFLSGVLGGLAGTLVGTSVSITGPYFG 241

Query: 220 WFLILPLFASVILGGIGNPYGAIAAAFIIGIVQEVSTPFLGSQYKQGVALLIMILVLLIR 279
               L   + ++LGG+GN  G IA   ++G+  E   P   S Y+  VA  ++  +LLIR
Sbjct: 242 IAYGLKGLSVMVLGGLGNIPGTIAGGLLLGLA-EAWVPPQWSGYRDAVAFALLFAMLLIR 300

Query: 280 PKGLF 284
           P+GLF
Sbjct: 301 PQGLF 305


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: 276
Number of extensions: 23
Number of successful extensions: 5
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: 313
Length adjustment: 27
Effective length of query: 261
Effective length of database: 286
Effective search space:    74646
Effective search space used:    74646
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 17 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