GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Methylobacterium sp. 4-46

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_012335137.1 M446_RS26260 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_000019365.1:WP_012335137.1
          Length = 475

 Score =  261 bits (668), Expect = 2e-74
 Identities = 152/323 (47%), Positives = 202/323 (62%), Gaps = 27/323 (8%)

Query: 29  WVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLFALMASPHLADNFAAFAA 88
           W+ +A L L YV+L  GLNIVVG AGLLDLGYVAFYAVGAY +AL+++            
Sbjct: 147 WIDLAILVLTYVMLGWGLNIVVGLAGLLDLGYVAFYAVGAYTYALLSTT----------- 195

Query: 89  MFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIVTLGFGEIIRIFLNNLDH 148
                   S WI +P+A LLAA +G +LG P L+LRGDYLAIVTL FGEIIR+ L N   
Sbjct: 196 -----FGFSFWICLPLAGLLAACWGMLLGFPVLRLRGDYLAIVTLAFGEIIRLVLINW-- 248

Query: 149 PVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDI-------NSVTLYYYLFLVLVVVSV 201
             + + G  G+  I  V  FGL      + F   +       + V   YYL L L +++ 
Sbjct: 249 -TDFSGGAAGISSIPRVTFFGLPFSADEDGFAATLGIAFSPMHRVVFLYYLILALALLTN 307

Query: 202 IICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGVSGAMFGAFQGF 261
            +  R++   +GRAW A+REDEIA +++GINT N KL AF +GA FGG +G+ F   QGF
Sbjct: 308 GVTLRMRRLPLGRAWEALREDEIACRSLGINTTNTKLTAFALGAMFGGFAGSFFAVRQGF 367

Query: 262 VSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGPLQAMTDGRLDS 321
           VSPESF+ +ES +I+A+VVLGG+G   GV + AV + A PE+LR + G L+A+     D 
Sbjct: 368 VSPESFNFLESAIILAIVVLGGMGSQIGVAIAAVAMVAGPELLRNL-GFLKAVFGEGFDP 426

Query: 322 AILRQLLIALAMIIIMLLRPRGL 344
           +  R LL  LAM+++M+ RPRGL
Sbjct: 427 SEYRLLLFGLAMVLMMIWRPRGL 449


Lambda     K      H
   0.328    0.144    0.430 

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: 462
Number of extensions: 21
Number of successful extensions: 3
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: 358
Length of database: 475
Length adjustment: 31
Effective length of query: 327
Effective length of database: 444
Effective search space:   145188
Effective search space used:   145188
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. 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