GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Derxia gummosa DSM 723

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_028310213.1 H566_RS0102680 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000482785.1:WP_028310213.1
          Length = 309

 Score =  140 bits (353), Expect = 4e-38
 Identities = 90/302 (29%), Positives = 167/302 (55%), Gaps = 30/302 (9%)

Query: 6   IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNTF-------- 57
           +Q ++NG+ +GS+ AL A+G T+ YGIL+L NFAHGD L +GA      + F        
Sbjct: 5   LQQLINGLVLGSVYALIALGYTMVYGILQLINFAHGDVLMVGALTALSTSKFLQEAAPWM 64

Query: 58  --GVNIWLSMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILI 115
              + + +++  A+V  V V +  E++ +  +R+  A     +I +IG+++ L+   +LI
Sbjct: 65  PGPLVLLIALAAAIVVCVLVNIGIERVAYRPLRN--APRLAPLITAIGMSITLQTLAMLI 122

Query: 116 WGGRNQNYN-----LPITPALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMR 170
           W   ++NY      LP  P + + G  +   Q++++ L++  +  L  L+  TK+G+AMR
Sbjct: 123 W---SRNYMVFPALLPNAP-MPLGGASITPVQVIIVLLSLALMVGLVLLVNKTKLGRAMR 178

Query: 171 AVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGLITAVRP-NMGWFLILPLFAS 229
           A A++  +A + G+D ++VI  T+ +   + ++ G M     ++    MG+   L  F +
Sbjct: 179 ATAENPRVAALMGVDPDRVIVITFALGAALAAVAGVMIAANYSIAHFYMGFLPGLKAFTA 238

Query: 230 VILGGIGNPYGAIAAAFIIGIVQEVSTPF--------LGSQYKQGVALLIMILVLLIRPK 281
            +LGGIGN YGA+    ++G+++ +   +        LGS Y+   A +++I+VL +RP 
Sbjct: 239 AVLGGIGNLYGAMVGGLLLGLIEALGAGYIGDLTGGVLGSNYQDIFAFIVLIIVLTLRPS 298

Query: 282 GL 283
           G+
Sbjct: 299 GI 300


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: 254
Number of extensions: 17
Number of successful extensions: 4
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: 309
Length adjustment: 27
Effective length of query: 261
Effective length of database: 282
Effective search space:    73602
Effective search space used:    73602
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