GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Hippea alviniae EP5-r

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_022671209.1 G415_RS0108260 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000420385.1:WP_022671209.1
          Length = 299

 Score =  173 bits (439), Expect = 4e-48
 Identities = 99/290 (34%), Positives = 167/290 (57%), Gaps = 16/290 (5%)

Query: 6   IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAY--LTFFVNTFGVNIWL 63
           +Q +VNG+ +GSI AL A+G T+ YG+L+L NFAHGD + L AY  L   +   G     
Sbjct: 5   LQQLVNGLTIGSIYALVALGYTMVYGVLKLINFAHGDLVALSAYIGLVIMMQLAGALSPA 64

Query: 64  SMIV-------AVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIW 116
           ++I+        ++   GV+L  E+  +  +R  +A   + ++ ++G +L + NGI+LIW
Sbjct: 65  ALIIITFLATMVIIAIAGVIL--ERTAYRPLR--KAPRLSAVVSALGASLVIENGIMLIW 120

Query: 117 GGRNQNYNLPITPAL--DIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVAD 174
           G   + Y   I P +  D+ GV +   Q+LVL ++ + +  L++ +  TK+G AMRA A 
Sbjct: 121 GPMPRIYPASIVPNVNYDLHGVYISLMQILVLVISFVLMIGLYFFVNKTKLGTAMRACAI 180

Query: 175 DLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGL-ITAVRPNMGWFLILPLFASVILG 233
           D D A++ GIDV +VI  T++I   + ++GG   G+    +  NMGW   L  F + I+G
Sbjct: 181 DQDAARLMGIDVNRVIVTTFIIGSALGAVGGLFIGMYYRGITFNMGWIYGLNAFVAAIIG 240

Query: 234 GIGNPYGAIAAAFIIGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGL 283
           GIGN  GA+    ++GI   +   +L S +   +  +++I++++IRP G+
Sbjct: 241 GIGNIPGAMLGGMLLGIFNALIAGYLSSSWAMALTYVLLIVIMIIRPTGI 290


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: 252
Number of extensions: 12
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: 299
Length adjustment: 26
Effective length of query: 262
Effective length of database: 273
Effective search space:    71526
Effective search space used:    71526
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