GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Chlorobium limicola DSM 245

Align alginate biosynthesis protein AlgA; EC 2.7.7.13; EC 5.3.1.8 (characterized)
to candidate WP_317623571.1 CLIM_RS11050 mannose-1-phosphate guanylyltransferase

Query= CharProtDB::CH_121570
         (483 letters)



>NCBI__GCF_000020465.1:WP_317623571.1
          Length = 375

 Score =  169 bits (429), Expect = 1e-46
 Identities = 109/362 (30%), Positives = 186/362 (51%), Gaps = 15/362 (4%)

Query: 4   VILSGGSGSRLWPLSRKQFPKQFLALTGEHTLFQQTLERLV-FEGMDTPIVVCNKDHRFI 62
           VI++GGS   LWP +RK+ P Q L L    T+F  T+ R+      +  IV+ +++ R  
Sbjct: 15  VIMAGGSAKALWPAARKKQPAQCLELFQLDTMFLLTVRRIASLVPPERIIVISSREGREC 74

Query: 63  VNEQLANRKLECQRILMEPFGRNTAPAVALTAMMLVNEGRDELMLVLPADHVIDDQKALQ 122
           +        +  + I+ EP  RNTAP +AL    +     D + +VLP+DH + D ++  
Sbjct: 75  IIA--GGTDISPENIIAEPSARNTAPCIALATAHIKKRDPDAVTVVLPSDHDVRDVESFI 132

Query: 123 RALALAT-VAAERGEMVLFGVPATRPETGYGYIKSTNDS--LLPEG------VSRVQQFV 173
           + L +   +AAE+  ++  G+  T PET YGYI+S   S  + PE       + RV+ F 
Sbjct: 133 KILEVGIRIAAEKKGLITIGLTPTYPETEYGYIQSAGHSEEMPPEDGEHGYKLFRVKTFA 192

Query: 174 EKPDEKRAVEFVKSGGYFWNSGMFLFRASRFLEELKKHDPDIYDTCVLTLERSEQTADTV 233
           EKPD   AV+F++S  +FWNSG+F++       E ++  P++Y   +   E      +  
Sbjct: 193 EKPDYATAVQFLESRDFFWNSGVFIWHIDAICREFERSMPELYKDLLTIHEHLGTDTEDE 252

Query: 234 TLDDATFACCPDNSIDYAVMEKTQRACVVPLSAGWSDVGCWASLWAVN-DKDIHGNVSKG 292
            ++D  ++     SID+ +MEK     ++    GWSD+ CW  +  ++   +   +  + 
Sbjct: 253 VIED-VYSWIHPVSIDHGIMEKADPVYMLAGDFGWSDLVCWDEVARISASHENPEDTCEL 311

Query: 293 DVVIQDSRNCMIH-GNGKLVSVIGLDNIVVVETKDAMMIAHKDKVQGVKQMVSTLNDQGR 351
           DV+  +S    +    GKLV ++G+ +++VV+T D +MI +K     V  +V  L  + R
Sbjct: 312 DVIRMESSGVFLRKPQGKLVCLLGVKDLIVVDTGDVLMICNKGDTGKVSAIVDLLRRENR 371

Query: 352 SE 353
            E
Sbjct: 372 EE 373


Lambda     K      H
   0.319    0.135    0.405 

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: 473
Number of extensions: 25
Number of successful extensions: 6
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: 483
Length of database: 375
Length adjustment: 32
Effective length of query: 451
Effective length of database: 343
Effective search space:   154693
Effective search space used:   154693
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 51 (24.3 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