GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Desulfacinum infernum DSM 9756

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_073040275.1 BUB04_RS13180 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_900129305.1:WP_073040275.1
          Length = 301

 Score =  189 bits (480), Expect = 6e-53
 Identities = 106/291 (36%), Positives = 176/291 (60%), Gaps = 18/291 (6%)

Query: 7   QLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNTF--------- 57
           Q + NG+AVG I AL A+G T+ YG+L+L NFAHGD  T+G+YL   + T          
Sbjct: 6   QQLTNGLAVGGIYALIALGYTMVYGVLKLINFAHGDLFTIGSYLGLTLLTSLSLTDRLAP 65

Query: 58  --GVNIWLSMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILI 115
             GV +   M++ +V  VG +L  E++ +  +R  ++   + ++ ++G ++F  N ++LI
Sbjct: 66  AAGVLVLAVMVMGLVAVVGALL--ERVAYRPLR--QSPRLSAVVSALGASIFFSNALMLI 121

Query: 116 WGGRNQNYNLPITP--ALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVA 173
           +G R Q Y   I P  A++IFG+ VP  ++L+LA +V+ + AL++ +Q T+IG A+RA A
Sbjct: 122 YGARFQVYPQGILPKVAVNIFGLYVPLVRILILAASVVMMLALYFFIQKTRIGTAIRAAA 181

Query: 174 DDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGL-ITAVRPNMGWFLILPLFASVIL 232
            D D A++ GIDV++VI + +LI   +  + G M GL    +   MGW   L  F + IL
Sbjct: 182 IDQDAARLMGIDVDRVILFVFLIGPALGGVAGLMVGLHYGQINFTMGWVYGLKAFTAAIL 241

Query: 233 GGIGNPYGAIAAAFIIGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGL 283
           GGIGN  GA+    ++G+++ +   +L   +K  +A  ++I++L++RP GL
Sbjct: 242 GGIGNIPGAMVGGILLGVIEALGAAYLSIAWKDAIAFGVLIIILIVRPTGL 292


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: 264
Number of extensions: 19
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: 301
Length adjustment: 26
Effective length of query: 262
Effective length of database: 275
Effective search space:    72050
Effective search space used:    72050
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