GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Jannaschia aquimarina GSW-M26

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_043919734.1 jaqu_RS14600 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000877395.1:WP_043919734.1
          Length = 329

 Score = 96.3 bits (238), Expect = 8e-25
 Identities = 93/316 (29%), Positives = 145/316 (45%), Gaps = 42/316 (13%)

Query: 7   QLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAY-----------LTFFVN 55
           ++ +NG+  G + +L A+G  L +    + N+A G      A             +  +N
Sbjct: 10  EVALNGLMAGVMYSLVALGFVLIFKASGIFNYAQGVMALFAAMTLVGIQNGQVPFSHLIN 69

Query: 56  T-FGVNI----WLS-MIVAVVGTVGVMLLSEKLLWSRMRSI-----RANSTTLIIISIGL 104
             FG +I    W +  I+A+  TV VM+    L W+  R I           L + +IGL
Sbjct: 70  AIFGTDIHYFGWEAPAILAIALTVVVMIA---LAWAVNRFIFRHLVNQEPIILFMATIGL 126

Query: 105 ALFLRNGIILIWG--------GRNQNYNLPI-TPALDIFGVKVPQNQLLVLA--LAVLSI 153
           A FL     L+WG        G  Q  N  I +   +IFG     + L ++A  +A L +
Sbjct: 127 AYFLEGVADLMWGSEIKTLDVGLPQGINETIDSVTFEIFGYGFFIDNLDIVATVIAALLV 186

Query: 154 GALHYLLQNTKIGKAMRAVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGLITA 213
             L    Q TK G+A+RAVADD   A   GI +  +    W IAG V  + G M+G  + 
Sbjct: 187 LGLVAFSQYTKQGRALRAVADDHQAALSVGISLNFIWVLVWSIAGFVALVAGIMWGAKSG 246

Query: 214 VRPNMGWFLILPLFASVILGGIGNPYGAIAAAFIIGIVQE-----VSTPFLGSQYKQGVA 268
           V+ ++   + L     ++LGG  +  GAI    IIG+ ++     +  PFLG   +   A
Sbjct: 247 VQFSLS-LIALKALPVLMLGGFTSIPGAIVGGLIIGVGEKLFEFAIGQPFLGGATENWFA 305

Query: 269 LLIMILVLLIRPKGLF 284
            ++ +L L+ RP+GLF
Sbjct: 306 YVLALLFLVFRPQGLF 321


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: 295
Number of extensions: 20
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: 329
Length adjustment: 27
Effective length of query: 261
Effective length of database: 302
Effective search space:    78822
Effective search space used:    78822
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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