GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00885 in Desulfacinum infernum DSM 9756

Align ABC-type branched-chain amino acid transport system, permease component protein (characterized, see rationale)
to candidate WP_073036690.1 BUB04_RS02685 branched-chain amino acid ABC transporter permease

Query= uniprot:D8IUY4
         (309 letters)



>NCBI__GCF_900129305.1:WP_073036690.1
          Length = 297

 Score =  253 bits (646), Expect = 4e-72
 Identities = 139/307 (45%), Positives = 202/307 (65%), Gaps = 16/307 (5%)

Query: 3   IFIQQIINGLVLGSMYALIALGYTMVYGVLNLINFAHGDILMVGAMVGLSLLKVVQQVAP 62
           IF QQ+ NG+ LGS+YAL+A+GYTMVYG+L LINFAHGD+LMV A   +  + +      
Sbjct: 5   IFFQQLTNGISLGSLYALVAIGYTMVYGILRLINFAHGDLLMVAAYTAIYAVTMFT---- 60

Query: 63  GLPGIVQLVIAIVGAIPVCIVVSLLIERIAYRPLRNAPRLAPLITAIGVSILLQTLAMMI 122
            LP  +   +AI  A+  CI   +L++R+AY+PLR+APR++ LI+AIG S LL+ LA++I
Sbjct: 61  -LPWYLSFPLAI--ALTGCI--GILLDRVAYKPLRDAPRISLLISAIGASFLLENLALVI 115

Query: 123 WGRSPLPFPQV-MPSDPVHIAGALISPTQIMLLALAVLAMVGLVLIVEKTKMGRAMRATA 181
            G  P  FP+  + +  + I G  I    I +  + ++ ++ L+ IV +TK+G+AMRA +
Sbjct: 116 IGGVPKGFPRPDIFAKVIEILGVRIQVLTIYIPLMTLVFLMALLYIVYRTKVGKAMRAAS 175

Query: 182 ENPRIAGLMGVDANKVIVVTFAIGAGLAAIAGVMWAANYSTAQFAMGFVPGLKAFSAAVL 241
           ++     LMG++ +++I +TF +G+ LAA  G+MWA  Y      MG +PGLKAF AAVL
Sbjct: 176 KDIETTRLMGINVDRIIALTFLMGSSLAAAGGIMWAMKYPQVNPFMGVIPGLKAFIAAVL 235

Query: 242 GGIGNIYGAMLGGILLGLIESLGAGYIGDLTGNFLGSNYQDIFAFIVLIIVLTLRPSGIM 301
           GGIGNI GA++GG  LGL E L   +   L      + Y+D FAF++LI+VL  RP+GIM
Sbjct: 236 GGIGNIIGAVVGGFALGLGEILLVAFFPQL------AQYRDAFAFVILILVLLFRPTGIM 289

Query: 302 GERVADR 308
           GE + D+
Sbjct: 290 GEPITDK 296


Lambda     K      H
   0.328    0.144    0.416 

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: 292
Number of extensions: 22
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: 309
Length of database: 297
Length adjustment: 27
Effective length of query: 282
Effective length of database: 270
Effective search space:    76140
Effective search space used:    76140
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