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_2177 Synpcc7942_2177 integral membrane protein of the ABC-type Nat permease for neutral amino acids NatD

Query= TCDB::Q8YXD0
         (288 letters)



>FitnessBrowser__SynE:Synpcc7942_2177
          Length = 296

 Score =  334 bits (856), Expect = 2e-96
 Identities = 163/281 (58%), Positives = 215/281 (76%)

Query: 4   QTIQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNTFGVNIWL 63
           Q  QL +NG+A GS++ALAA GLTL YGILRL+NFA G+FLTLGAY T   N+ G+++WL
Sbjct: 14  QLAQLAINGLATGSLLALAATGLTLIYGILRLTNFAQGEFLTLGAYFTLVANSLGLSLWL 73

Query: 64  SMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRNQNY 123
           ++ +  + T+ + LL E +LW  +R  R N+TTLII++IGL+LFLRN +ILIWG  NQ Y
Sbjct: 74  AIPLGAIATIALCLLGEAVLWEPLRRQRVNTTTLIILTIGLSLFLRNLVILIWGAGNQAY 133

Query: 124 NLPITPALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVADDLDLAKVSG 183
            L + PAL ++G+++  N LLV+  A  ++  LH++LQ T IGK MRA+ADD DLA+VSG
Sbjct: 134 RLAVQPALTLWGLRITLNSLLVVIGAAAALVLLHWVLQRTSIGKGMRAIADDPDLARVSG 193

Query: 184 IDVEQVIFWTWLIAGTVTSLGGSMYGLITAVRPNMGWFLILPLFASVILGGIGNPYGAIA 243
           + VE VI WTW+IAG +T++ G +YGLITAVRP MGW LILPLFAS ILGGIG+PYGAIA
Sbjct: 194 VPVETVIRWTWVIAGGLTAIAGGLYGLITAVRPTMGWNLILPLFASAILGGIGSPYGAIA 253

Query: 244 AAFIIGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGLF 284
              I+G  QE+ST +L ++YK  VA +I+I VL+IRP+GLF
Sbjct: 254 GGLILGFAQELSTYWLPAEYKLAVAFVILIGVLVIRPQGLF 294


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: 295
Number of extensions: 9
Number of successful extensions: 1
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: 296
Length adjustment: 26
Effective length of query: 262
Effective length of database: 270
Effective search space:    70740
Effective search space used:    70740
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