GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Pseudomonas stutzeri RCH2

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 GFF1059 Psest_1092 Branched-chain amino acid ABC-type transport system, permease components

Query= TCDB::Q8YXD0
         (288 letters)



>FitnessBrowser__psRCH2:GFF1059
          Length = 295

 Score =  128 bits (322), Expect = 1e-34
 Identities = 82/278 (29%), Positives = 155/278 (55%), Gaps = 10/278 (3%)

Query: 12  GIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFF-VNTFGVNIWLSMIVA-- 68
           G+  G+  AL ++GL + +G+LR+ NFAHG    LGA++ F  +N  GV+ W ++++A  
Sbjct: 19  GLINGAFYALLSLGLAIIFGLLRIINFAHGAQYMLGAFVAFLGLNYLGVSYWFALVLAPL 78

Query: 69  VVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRNQNYNLP-- 126
           VVG +G+ +  E+ L  R+     +    ++++ GLAL +    + ++G    +Y +P  
Sbjct: 79  VVGCLGMAI--ERGLLRRIAG--EDHLYGLLLTFGLALIVEGSFVKLFGVSGSSYPMPEL 134

Query: 127 ITPALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVADDLDLAKVSGIDV 186
           +    ++  + +P  +  V+  A++   A  Y+++ T++G  +RA  ++  L +  GI+V
Sbjct: 135 LRGGFNLGFMFLPTYRAWVIVAALVVCLATWYVIERTRLGSYLRAGTENPKLMQGFGINV 194

Query: 187 EQVIFWTWLIAGTVTSLGGSMYGLITAVRPNMGWFLILPLFASVILGGIGNPYGAIAAAF 246
             ++  T+     + +  G +   I AV P MG  L++ +FA V++GG+G+  GAI    
Sbjct: 195 PLLVTLTYGYGVALAAFAGVLAAPIYAVTPGMGSNLLIVVFAVVVIGGMGSILGAIVTGI 254

Query: 247 IIGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGLF 284
            +G+++ ++  F   +    V  L+M+ VLLIRP GLF
Sbjct: 255 AMGLIEGLTKVFY-PEAANTVVFLVMVAVLLIRPAGLF 291


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: 270
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: 288
Length of database: 295
Length adjustment: 26
Effective length of query: 262
Effective length of database: 269
Effective search space:    70478
Effective search space used:    70478
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