GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Sulfuritalea hydrogenivorans DSM 22779

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_041099055.1 SUTH_RS10315 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000828635.1:WP_041099055.1
          Length = 294

 Score =  132 bits (331), Expect = 1e-35
 Identities = 88/276 (31%), Positives = 143/276 (51%), Gaps = 7/276 (2%)

Query: 12  GIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTF-FVNTFGVNIWLSMIVAVV 70
           GI  G + ALA +   L +   ++ N A G+ L +GAY  F   +T G  IWL ++VAV+
Sbjct: 15  GIGSGGLYALAGLAFVLIFKATKVVNLAIGEMLMMGAYFFFAMASTLGWPIWLGVLVAVL 74

Query: 71  GTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRNQNYN--LPIT 128
           G+  +  L E+LL   M  +  +  ++ +I+IGL+  L   + LIWG         +P  
Sbjct: 75  GSGALGALVERLLIRPM--LGESPISVFMITIGLSSILVGAVELIWGADQMRLPDFMPSD 132

Query: 129 PALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVADDLDLAKVSGIDVEQ 188
           P L I    VP        +A   I  +  + +  + G A+RA A D   A   GI+V +
Sbjct: 133 PVL-IGEAMVPPKIFYGFLVATSLIAIVLVVFRFWRGGIALRATASDQAAAYSMGINVPR 191

Query: 189 VIFWTWLIAGTVTSLGGSMYGLITAVRPNMGWFLILPLFASVILGGIGNPYGAIAAAFII 248
           V    W++   V ++ G + G I+++ P MG F  L +   VI+GG+ +  GA+    ++
Sbjct: 192 VFSMAWVVGAMVAAIAGIIVGSISSLSPTMGVFG-LSVLVVVIVGGLDSVAGALIGGILV 250

Query: 249 GIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGLF 284
           G+V+  S  +LG +YK      +++LVL++RP GLF
Sbjct: 251 GLVEAWSGTYLGGEYKMLATFSLLVLVLMVRPYGLF 286


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: 271
Number of extensions: 19
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: 294
Length adjustment: 26
Effective length of query: 262
Effective length of database: 268
Effective search space:    70216
Effective search space used:    70216
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